Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 17 16285604 16285604 + Missense_Mutation SNP A A G TCGA-P6-A5OH-01A-11D-A30A-10 TCGA-P6-A5OH-11A-01D-A30A-10 g.chr17:16285604A>G c.383A>G c.(382-384)gAt>gGt p.D128G BLCA 17 16285353 16285353 + Silent SNP C C T TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr17:16285353C>T c.132C>T c.(130-132)atC>atT p.I44I BLCA 17 16285491 16285491 + Silent SNP C C T TCGA-CF-A3MH-01A-11D-A20D-08 TCGA-CF-A3MH-10A-01D-A20D-08 g.chr17:16285491C>T c.270C>T c.(268-270)acC>acT p.T90T BLCA 17 16285560 16285560 + Silent SNP T T C TCGA-SY-A9G0-01A-12D-A38G-08 TCGA-SY-A9G0-10A-01D-A38J-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P BLCA 17 16285560 16285560 + Silent SNP T T C TCGA-UY-A9PD-01A-11D-A38G-08 TCGA-UY-A9PD-10A-01D-A38J-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P BLCA 17 16285560 16285560 + Silent SNP T T C TCGA-XF-A9SH-01A-11D-A391-08 TCGA-XF-A9SH-10A-01D-A394-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P BLCA 17 16285578 16285578 + Silent SNP C C A TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr17:16285578C>A c.357C>A c.(355-357)ctC>ctA p.L119L COAD 17 16285785 16285785 + Frame_Shift_Del DEL C C - TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr17:16285785delC c.564delC c.(562-564)atcfs p.I188fs COAD 17 16285785 16285785 + Frame_Shift_Del DEL C C - TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr17:16285785delC c.564delC c.(562-564)atcfs p.I188fs COADREAD 17 16285609 16285609 + Missense_Mutation SNP C C T TCGA-AG-A01Y-01A-41W-A096-10 TCGA-AG-A01Y-11A-11W-A096-10 g.chr17:16285609C>T c.388C>T c.(388-390)Cgc>Tgc p.R130C COADREAD 17 16285785 16285785 + Frame_Shift_Del DEL C C - TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr17:16285785delC c.564delC c.(562-564)atcfs p.I188fs COADREAD 17 16285785 16285785 + Frame_Shift_Del DEL C C - TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr17:16285785delC c.564delC c.(562-564)atcfs p.I188fs DLBC 17 16285294 16285294 + Missense_Mutation SNP A A T TCGA-GS-A9TW-01A-11D-A382-10 TCGA-GS-A9TW-10A-01D-A385-10 g.chr17:16285294A>T c.73A>T c.(73-75)Aat>Tat p.N25Y GBMLGG 17 16285491 16285491 + Silent SNP C C T TCGA-FG-8185-01A-11D-2253-08 TCGA-FG-8185-10A-01D-2253-08 g.chr17:16285491C>T c.270C>T c.(268-270)acC>acT p.T90T GBMLGG 17 16285560 16285560 + Silent SNP T T C TCGA-P5-A5F4-01A-11D-A289-08 TCGA-P5-A5F4-10A-01D-A289-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P HNSC 17 16285753 16285753 + Missense_Mutation SNP G G A TCGA-BA-6869-01A-11D-1870-08 TCGA-BA-6869-10A-01D-1870-08 g.chr17:16285753G>A c.532G>A c.(532-534)Gtg>Atg p.V178M HNSC 17 16285800 16285800 + Silent SNP G G A TCGA-CV-A45Q-01A-11D-A24D-08 TCGA-CV-A45Q-10A-01D-A24F-08 g.chr17:16285800G>A c.579G>A c.(577-579)caG>caA p.Q193Q KIPAN 17 16285560 16285560 + Silent SNP T T C TCGA-CJ-4643-01A-02D-1386-10 TCGA-CJ-4643-11A-01D-1251-10 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P KIPAN 17 16285911 16285911 + Silent SNP A A G TCGA-DV-5565-01A-01D-1534-10 TCGA-DV-5565-10A-01D-1535-10 g.chr17:16285911A>G c.690A>G c.(688-690)taA>taG p.*230* KIRC 17 16285560 16285560 + Silent SNP T T C TCGA-CJ-4643-01A-02D-1386-10 TCGA-CJ-4643-11A-01D-1251-10 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P KIRC 17 16285911 16285911 + Silent SNP A A G TCGA-DV-5565-01A-01D-1534-10 TCGA-DV-5565-10A-01D-1535-10 g.chr17:16285911A>G c.690A>G c.(688-690)taA>taG p.*230* LGG 17 16285491 16285491 + Silent SNP C C T TCGA-FG-8185-01A-11D-2253-08 TCGA-FG-8185-10A-01D-2253-08 g.chr17:16285491C>T c.270C>T c.(268-270)acC>acT p.T90T LGG 17 16285560 16285560 + Silent SNP T T C TCGA-P5-A5F4-01A-11D-A289-08 TCGA-P5-A5F4-10A-01D-A289-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P LUAD 17 16285380 16285380 + Silent SNP C C A TCGA-99-8025-01A-11D-2238-08 TCGA-99-8025-10A-01D-2238-08 g.chr17:16285380C>A c.159C>A c.(157-159)ggC>ggA p.G53G LUAD 17 16285497 16285497 + Silent SNP A A G TCGA-78-7159-01A-11D-2036-08 TCGA-78-7159-10A-01D-2036-08 g.chr17:16285497A>G c.276A>G c.(274-276)gaA>gaG p.E92E LUAD 17 16285701 16285701 + Silent SNP G G T TCGA-50-8457-01A-11D-2323-08 TCGA-50-8457-10A-01D-2323-08 g.chr17:16285701G>T c.480G>T c.(478-480)ctG>ctT p.L160L LUAD 17 16285719 16285719 + Silent SNP T T C TCGA-55-7914-01A-11D-2167-08 TCGA-55-7914-10A-01D-2167-08 g.chr17:16285719T>C c.498T>C c.(496-498)acT>acC p.T166T LUSC 17 16285361 16285361 + Missense_Mutation SNP G G T TCGA-66-2771-01A-01D-0983-08 TCGA-66-2771-11A-01D-0983-08 g.chr17:16285361G>T c.140G>T c.(139-141)gGc>gTc p.G47V LUSC 17 16285542 16285542 + Silent SNP G G A TCGA-60-2725-01A-01D-1267-08 TCGA-60-2725-11A-01D-1267-08 g.chr17:16285542G>A c.321G>A c.(319-321)caG>caA p.Q107Q LUSC 17 16285604 16285604 + Missense_Mutation SNP A A G TCGA-60-2726-01A-01D-1522-08 TCGA-60-2726-11A-01D-1522-08 g.chr17:16285604A>G c.383A>G c.(382-384)gAt>gGt p.D128G PAAD 17 16285438 16285438 + Missense_Mutation SNP C C G TCGA-HZ-A77P-01A-11D-A33T-08 TCGA-HZ-A77P-10A-01D-A33W-08 g.chr17:16285438C>G c.217C>G c.(217-219)Ctg>Gtg p.L73V PAAD 17 16285491 16285491 + Silent SNP C C T TCGA-HZ-A77Q-01A-11D-A36O-08 TCGA-HZ-A77Q-10A-01D-A367-08 g.chr17:16285491C>T c.270C>T c.(268-270)acC>acT p.T90T PAAD 17 16285497 16285497 + Silent SNP A A G TCGA-FB-AAPQ-01A-11D-A40W-08 TCGA-FB-AAPQ-11A-11D-A40W-08 g.chr17:16285497A>G c.276A>G c.(274-276)gaA>gaG p.E92E PAAD 17 16285497 16285497 + Silent SNP A A G TCGA-Q3-AA2A-01A-11D-A377-08 TCGA-Q3-AA2A-10A-01D-A37A-08 g.chr17:16285497A>G c.276A>G c.(274-276)gaA>gaG p.E92E PAAD 17 16285497 16285497 + Silent SNP A A G TCGA-US-A776-01A-13D-A33T-08 TCGA-US-A776-11A-11D-A33W-08 g.chr17:16285497A>G c.276A>G c.(274-276)gaA>gaG p.E92E PAAD 17 16285497 16285497 + Silent SNP A A G TCGA-US-A77J-01A-11D-A32N-08 TCGA-US-A77J-11A-11D-A32N-08 g.chr17:16285497A>G c.276A>G c.(274-276)gaA>gaG p.E92E PAAD 17 16285497 16285497 + Silent SNP A A G TCGA-XN-A8T5-01A-12D-A36O-08 TCGA-XN-A8T5-10A-01D-A367-08 g.chr17:16285497A>G c.276A>G c.(274-276)gaA>gaG p.E92E PAAD 17 16285497 16285497 + Silent SNP A A G TCGA-YB-A89D-01A-12D-A36O-08 TCGA-YB-A89D-11A-11D-A36O-08 g.chr17:16285497A>G c.276A>G c.(274-276)gaA>gaG p.E92E PAAD 17 16285542 16285542 + Silent SNP G G A TCGA-2J-AABA-01A-21D-A40W-08 TCGA-2J-AABA-10A-01D-A40W-08 g.chr17:16285542G>A c.321G>A c.(319-321)caG>caA p.Q107Q PAAD 17 16285560 16285560 + Silent SNP T T C TCGA-3A-A9IO-01A-11D-A38G-08 TCGA-3A-A9IO-10A-01D-A38J-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P PAAD 17 16285560 16285560 + Silent SNP T T C TCGA-IB-A5SO-01A-11D-A32N-08 TCGA-IB-A5SO-10A-01D-A32N-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P PAAD 17 16285560 16285560 + Silent SNP T T C TCGA-IB-A7LX-01A-12D-A36O-08 TCGA-IB-A7LX-10A-01D-A367-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P PAAD 17 16285560 16285560 + Silent SNP T T C TCGA-US-A77E-01A-11D-A32N-08 TCGA-US-A77E-11A-11D-A32N-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P PAAD 17 16285560 16285560 + Silent SNP T T C TCGA-XD-AAUI-01A-42D-A40W-08 TCGA-XD-AAUI-10A-01D-A40W-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P PAAD 17 16285560 16285560 + Silent SNP T T C TCGA-YY-A8LH-01A-11D-A36O-08 TCGA-YY-A8LH-10A-01D-A367-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P PAAD 17 16285638 16285638 + Silent SNP G G A TCGA-3A-A9IJ-01A-11D-A397-08 TCGA-3A-A9IJ-10A-01D-A39A-08 g.chr17:16285638G>A c.417G>A c.(415-417)aaG>aaA p.K139K PAAD 17 16285638 16285638 + Silent SNP G G A TCGA-HV-A7OP-01A-11D-A33T-08 TCGA-HV-A7OP-10A-01D-A33W-08 g.chr17:16285638G>A c.417G>A c.(415-417)aaG>aaA p.K139K PCPG 17 16285491 16285491 + Silent SNP C C T TCGA-QR-A6H5-01A-11D-A35D-08 TCGA-QR-A6H5-10A-01D-A35B-08 g.chr17:16285491C>T c.270C>T c.(268-270)acC>acT p.T90T PRAD 17 16285491 16285491 + Silent SNP C C T TCGA-KK-A7AQ-01A-11D-A33T-08 TCGA-KK-A7AQ-11A-11D-A33W-08 g.chr17:16285491C>T c.270C>T c.(268-270)acC>acT p.T90T PRAD 17 16285497 16285497 + Silent SNP A A G TCGA-G9-7523-01A-11D-2260-08 TCGA-G9-7523-10A-01D-2260-08 g.chr17:16285497A>G c.276A>G c.(274-276)gaA>gaG p.E92E PRAD 17 16285560 16285560 + Silent SNP T T C TCGA-EJ-A65F-01A-21D-A30X-08 TCGA-EJ-A65F-10A-01D-A30X-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P PRAD 17 16285560 16285560 + Silent SNP T T C TCGA-HC-A76W-01A-11D-A33T-08 TCGA-HC-A76W-10A-01D-A33W-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P PRAD 17 16285560 16285560 + Silent SNP T T C TCGA-SU-A7E7-01A-22D-A33T-08 TCGA-SU-A7E7-10A-01D-A33W-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P PRAD 17 16285560 16285560 + Silent SNP T T C TCGA-VN-A88I-01A-11D-A34U-08 TCGA-VN-A88I-10A-01D-A34X-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P PRAD 17 16285790 16285790 + Missense_Mutation SNP C C A TCGA-EJ-5518-01A-01D-1576-08 TCGA-EJ-5518-10A-01D-1577-08 g.chr17:16285790C>A c.569C>A c.(568-570)cCc>cAc p.P190H READ 17 16285609 16285609 + Missense_Mutation SNP C C T TCGA-AG-A01Y-01A-41W-A096-10 TCGA-AG-A01Y-11A-11W-A096-10 g.chr17:16285609C>T c.388C>T c.(388-390)Cgc>Tgc p.R130C SARC 17 16285594 16285594 + Nonsense_Mutation SNP C C T TCGA-DX-A1L2-01A-22D-A24N-09 TCGA-DX-A1L2-10A-01D-A24N-09 g.chr17:16285594C>T c.373C>T c.(373-375)Cag>Tag p.Q125* SARC 17 16285600 16285600 + Missense_Mutation SNP G G A TCGA-DX-A8BQ-01A-11D-A37C-09 TCGA-DX-A8BQ-10A-01D-A37F-09 g.chr17:16285600G>A c.379G>A c.(379-381)Gaa>Aaa p.E127K SKCM 17 16285329 16285329 + Silent SNP T T C TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr17:16285329T>C c.108T>C c.(106-108)atT>atC p.I36I SKCM 17 16285382 16285382 + Missense_Mutation SNP G G A TCGA-EE-A3JH-06A-11D-A21A-08 TCGA-EE-A3JH-10A-01D-A21A-08 g.chr17:16285382G>A c.161G>A c.(160-162)cGt>cAt p.R54H SKCM 17 16285497 16285497 + Silent SNP A A G TCGA-ER-A1A1-06A-11D-A197-08 TCGA-ER-A1A1-10A-01D-A199-08 g.chr17:16285497A>G c.276A>G c.(274-276)gaA>gaG p.E92E SKCM 17 16285560 16285560 + Silent SNP T T C TCGA-FS-A1ZP-06A-11D-A197-08 TCGA-FS-A1ZP-10A-01D-A199-08 g.chr17:16285560T>C c.339T>C c.(337-339)ccT>ccC p.P113P

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 17 16285291 16285291 single base substitution G A intron_variant BLCA-CN 17 16285291 16285291 single base substitution G A missense_variant E24K 70G>A BLCA-US 17 16285453 16285453 single base substitution C A downstream_gene_variant BLCA-US 17 16285453 16285453 single base substitution C A intron_variant BLCA-US 17 16285453 16285453 single base substitution C A missense_variant Q78K 232C>A BLCA-US 17 16285681 16285681 single base substitution C A downstream_gene_variant BLCA-US 17 16285681 16285681 single base substitution C A exon_variant BLCA-US 17 16285681 16285681 single base substitution C A missense_variant Q154K 460C>A BLCA-US 17 16285681 16285681 single base substitution C A missense_variant Q78K 232C>A BLCA-US 17 16285788 16285788 single base substitution C T downstream_gene_variant BLCA-US 17 16285788 16285788 single base substitution C T exon_variant BLCA-US 17 16285788 16285788 single base substitution C T synonymous_variant P113P 339C>T BLCA-US 17 16285788 16285788 single base substitution C T synonymous_variant P189P 567C>T BRCA-EU 17 16280273 16280273 single base substitution C G upstream_gene_variant BRCA-EU 17 16281957 16281957 single base substitution C T upstream_gene_variant BRCA-EU 17 16282146 16282146 single base substitution C A upstream_gene_variant BRCA-EU 17 16282675 16282675 deletion of <=200bp G - upstream_gene_variant BRCA-EU 17 16282813 16282813 single base substitution C T upstream_gene_variant BRCA-EU 17 16282818 16282818 single base substitution G A upstream_gene_variant BRCA-EU 17 16283528 16283528 single base substitution G A upstream_gene_variant BRCA-EU 17 16284404 16284404 single base substitution C G 5_prime_UTR_variant BRCA-EU 17 16284404 16284404 single base substitution C G intron_variant BRCA-EU 17 16284404 16284404 single base substitution C G upstream_gene_variant BRCA-EU 17 16284818 16284818 single base substitution A C 5_prime_UTR_variant BRCA-EU 17 16284818 16284818 single base substitution A C intron_variant BRCA-EU 17 16285440 16285440 single base substitution G C downstream_gene_variant BRCA-EU 17 16285440 16285440 single base substitution G C intron_variant BRCA-EU 17 16285440 16285440 single base substitution G C synonymous_variant L73L 219G>C BRCA-EU 17 16285611 16285611 single base substitution C T downstream_gene_variant BRCA-EU 17 16285611 16285611 single base substitution C T intron_variant BRCA-EU 17 16285611 16285611 single base substitution C T synonymous_variant R130R 390C>T BRCA-EU 17 16285837 16285837 single base substitution C G downstream_gene_variant BRCA-EU 17 16285837 16285837 single base substitution C G exon_variant BRCA-EU 17 16285837 16285837 single base substitution C G missense_variant R130G 388C>G BRCA-EU 17 16285837 16285837 single base substitution C G missense_variant R206G 616C>G BRCA-EU 17 16288811 16288811 single base substitution G A downstream_gene_variant BRCA-EU 17 16289151 16289151 single base substitution C T downstream_gene_variant BRCA-EU 17 16289589 16289589 single base substitution A C downstream_gene_variant BRCA-EU 17 16289780 16289780 single base substitution G C downstream_gene_variant BRCA-EU 17 16289855 16289855 single base substitution C A downstream_gene_variant BRCA-FR 17 16281957 16281957 single base substitution C T upstream_gene_variant BRCA-UK 17 16283268 16283268 single base substitution C T upstream_gene_variant BRCA-UK 17 16285488 16285488 single base substitution C T downstream_gene_variant BRCA-UK 17 16285488 16285488 single base substitution C T intron_variant BRCA-UK 17 16285488 16285488 single base substitution C T synonymous_variant I89I 267C>T BRCA-UK 17 16286073 16286073 single base substitution C T downstream_gene_variant BRCA-UK 17 16286656 16286656 single base substitution G A downstream_gene_variant BRCA-UK 17 16288019 16288019 single base substitution C G downstream_gene_variant BRCA-UK 17 16288703 16288703 single base substitution C T downstream_gene_variant BRCA-UK 17 16289123 16289123 single base substitution C T downstream_gene_variant BRCA-UK 17 16290205 16290205 single base substitution C G downstream_gene_variant BRCA-UK 17 16290361 16290361 single base substitution C G downstream_gene_variant CLLE-ES 17 16286260 16286260 single base substitution A G downstream_gene_variant COAD-US 17 16285383 16285383 single base substitution T C downstream_gene_variant COAD-US 17 16285383 16285383 single base substitution T C intron_variant COAD-US 17 16285383 16285383 single base substitution T C synonymous_variant R54R 162T>C COAD-US 17 16285785 16285785 deletion of <=200bp C - downstream_gene_variant COAD-US 17 16285785 16285785 deletion of <=200bp C - exon_variant COAD-US 17 16285785 16285785 deletion of <=200bp C - frameshift_variant I112 COAD-US 17 16285785 16285785 deletion of <=200bp C - frameshift_variant I188 COCA-CN 17 16285168 16285168 single base substitution A C intron_variant COCA-CN 17 16285784 16285784 single base substitution T C downstream_gene_variant COCA-CN 17 16285784 16285784 single base substitution T C exon_variant COCA-CN 17 16285784 16285784 single base substitution T C missense_variant I112T 335T>C COCA-CN 17 16285784 16285784 single base substitution T C missense_variant I188T 563T>C ESAD-UK 17 16282163 16282163 single base substitution G T upstream_gene_variant ESAD-UK 17 16282940 16282940 single base substitution C T upstream_gene_variant ESAD-UK 17 16283444 16283444 single base substitution G A upstream_gene_variant ESAD-UK 17 16283946 16283946 single base substitution T A upstream_gene_variant ESAD-UK 17 16283947 16283947 single base substitution C T upstream_gene_variant ESAD-UK 17 16288819 16288819 single base substitution T A downstream_gene_variant ESAD-UK 17 16290369 16290369 insertion of <=200bp - TGGG downstream_gene_variant GBM-US 17 16285788 16285788 single base substitution C T downstream_gene_variant GBM-US 17 16285788 16285788 single base substitution C T exon_variant GBM-US 17 16285788 16285788 single base substitution C T synonymous_variant P113P 339C>T GBM-US 17 16285788 16285788 single base substitution C T synonymous_variant P189P 567C>T KIRC-US 17 16285560 16285560 single base substitution T C downstream_gene_variant KIRC-US 17 16285560 16285560 single base substitution T C intron_variant KIRC-US 17 16285560 16285560 single base substitution T C synonymous_variant P113P 339T>C KIRC-US 17 16285911 16285911 single base substitution A G downstream_gene_variant KIRC-US 17 16285911 16285911 single base substitution A G exon_variant KIRC-US 17 16285911 16285911 single base substitution A G stop_retained_variant *154* 462A>G KIRC-US 17 16285911 16285911 single base substitution A G stop_retained_variant *230* 690A>G KIRP-US 17 16285476 16285476 single base substitution C G downstream_gene_variant KIRP-US 17 16285476 16285476 single base substitution C G intron_variant KIRP-US 17 16285476 16285476 single base substitution C G synonymous_variant T85T 255C>G LAML-KR 17 16285329 16285329 single base substitution T C intron_variant LAML-KR 17 16285329 16285329 single base substitution T C synonymous_variant I36I 108T>C LAML-KR 17 16285332 16285332 single base substitution C T intron_variant LAML-KR 17 16285332 16285332 single base substitution C T synonymous_variant P37P 111C>T LAML-KR 17 16285383 16285383 single base substitution T C downstream_gene_variant LAML-KR 17 16285383 16285383 single base substitution T C intron_variant LAML-KR 17 16285383 16285383 single base substitution T C synonymous_variant R54R 162T>C LAML-KR 17 16285467 16285467 single base substitution G A downstream_gene_variant LAML-KR 17 16285467 16285467 single base substitution G A intron_variant LAML-KR 17 16285467 16285467 single base substitution G A synonymous_variant K82K 246G>A LAML-KR 17 16285494 16285494 single base substitution G T downstream_gene_variant LAML-KR 17 16285494 16285494 single base substitution G T intron_variant LAML-KR 17 16285494 16285494 single base substitution G T synonymous_variant L91L 273G>T LAML-KR 17 16285611 16285611 single base substitution C T downstream_gene_variant LAML-KR 17 16285611 16285611 single base substitution C T intron_variant LAML-KR 17 16285611 16285611 single base substitution C T synonymous_variant R130R 390C>T LAML-KR 17 16285725 16285725 single base substitution G A downstream_gene_variant LAML-KR 17 16285725 16285725 single base substitution G A exon_variant LAML-KR 17 16285725 16285725 single base substitution G A synonymous_variant E168E 504G>A LAML-KR 17 16285725 16285725 single base substitution G A synonymous_variant E92E 276G>A LAML-KR 17 16285770 16285770 single base substitution A G downstream_gene_variant LAML-KR 17 16285770 16285770 single base substitution A G exon_variant LAML-KR 17 16285770 16285770 single base substitution A G synonymous_variant Q107Q 321A>G LAML-KR 17 16285770 16285770 single base substitution A G synonymous_variant Q183Q 549A>G LAML-KR 17 16285788 16285788 single base substitution C T downstream_gene_variant LAML-KR 17 16285788 16285788 single base substitution C T exon_variant LAML-KR 17 16285788 16285788 single base substitution C T synonymous_variant P113P 339C>T LAML-KR 17 16285788 16285788 single base substitution C T synonymous_variant P189P 567C>T LAML-KR 17 16285841 16285841 single base substitution C G downstream_gene_variant LAML-KR 17 16285841 16285841 single base substitution C G exon_variant LAML-KR 17 16285841 16285841 single base substitution C G missense_variant T131S 392C>G LAML-KR 17 16285841 16285841 single base substitution C G missense_variant T207S 620C>G LGG-US 17 16285491 16285491 single base substitution C T downstream_gene_variant LGG-US 17 16285491 16285491 single base substitution C T intron_variant LGG-US 17 16285491 16285491 single base substitution C T synonymous_variant T90T 270C>T LINC-JP 17 16285785 16285785 deletion of <=200bp C - downstream_gene_variant LINC-JP 17 16285785 16285785 deletion of <=200bp C - exon_variant LINC-JP 17 16285785 16285785 deletion of <=200bp C - frameshift_variant I112 LINC-JP 17 16285785 16285785 deletion of <=200bp C - frameshift_variant I188 LINC-JP 17 16288955 16288955 single base substitution A C downstream_gene_variant LIRI-JP 17 16279560 16279560 single base substitution C T upstream_gene_variant LIRI-JP 17 16281617 16281617 single base substitution A C upstream_gene_variant LIRI-JP 17 16282168 16282168 single base substitution A G upstream_gene_variant LIRI-JP 17 16284029 16284029 single base substitution A G upstream_gene_variant LIRI-JP 17 16284208 16284208 single base substitution G A 5_prime_UTR_variant LIRI-JP 17 16284208 16284208 single base substitution G A upstream_gene_variant LIRI-JP 17 16285383 16285383 single base substitution T C downstream_gene_variant LIRI-JP 17 16285383 16285383 single base substitution T C intron_variant LIRI-JP 17 16285383 16285383 single base substitution T C synonymous_variant R54R 162T>C LIRI-JP 17 16290016 16290016 single base substitution G A downstream_gene_variant LUSC-KR 17 16280947 16280947 single base substitution C A upstream_gene_variant LUSC-KR 17 16283818 16283818 single base substitution G A upstream_gene_variant LUSC-KR 17 16284162 16284162 single base substitution G C 5_prime_UTR_variant LUSC-KR 17 16284162 16284162 single base substitution G C upstream_gene_variant LUSC-KR 17 16285383 16285383 single base substitution T C downstream_gene_variant LUSC-KR 17 16285383 16285383 single base substitution T C intron_variant LUSC-KR 17 16285383 16285383 single base substitution T C synonymous_variant R54R 162T>C LUSC-KR 17 16285638 16285638 single base substitution G A downstream_gene_variant LUSC-KR 17 16285638 16285638 single base substitution G A intron_variant LUSC-KR 17 16285638 16285638 single base substitution G A synonymous_variant K139K 417G>A LUSC-KR 17 16285770 16285770 single base substitution A G downstream_gene_variant LUSC-KR 17 16285770 16285770 single base substitution A G exon_variant LUSC-KR 17 16285770 16285770 single base substitution A G synonymous_variant Q107Q 321A>G LUSC-KR 17 16285770 16285770 single base substitution A G synonymous_variant Q183Q 549A>G LUSC-KR 17 16285788 16285788 single base substitution C T downstream_gene_variant LUSC-KR 17 16285788 16285788 single base substitution C T exon_variant LUSC-KR 17 16285788 16285788 single base substitution C T synonymous_variant P113P 339C>T LUSC-KR 17 16285788 16285788 single base substitution C T synonymous_variant P189P 567C>T LUSC-KR 17 16285866 16285866 single base substitution A G downstream_gene_variant LUSC-KR 17 16285866 16285866 single base substitution A G exon_variant LUSC-KR 17 16285866 16285866 single base substitution A G synonymous_variant K139K 417A>G LUSC-KR 17 16285866 16285866 single base substitution A G synonymous_variant K215K 645A>G LUSC-KR 17 16287314 16287314 single base substitution C T downstream_gene_variant LUSC-KR 17 16287315 16287315 single base substitution G T downstream_gene_variant LUSC-KR 17 16288133 16288133 single base substitution G A downstream_gene_variant LUSC-KR 17 16288980 16288980 single base substitution A G downstream_gene_variant LUSC-KR 17 16290006 16290006 single base substitution C G downstream_gene_variant LUSC-US 17 16285361 16285361 single base substitution G T downstream_gene_variant LUSC-US 17 16285361 16285361 single base substitution G T intron_variant LUSC-US 17 16285361 16285361 single base substitution G T missense_variant G47V 140G>T LUSC-US 17 16285542 16285542 single base substitution G A downstream_gene_variant LUSC-US 17 16285542 16285542 single base substitution G A intron_variant LUSC-US 17 16285542 16285542 single base substitution G A synonymous_variant Q107Q 321G>A LUSC-US 17 16285604 16285604 single base substitution A G downstream_gene_variant LUSC-US 17 16285604 16285604 single base substitution A G intron_variant LUSC-US 17 16285604 16285604 single base substitution A G missense_variant D128G 383A>G MALY-DE 17 16280050 16280050 single base substitution G A upstream_gene_variant MALY-DE 17 16281876 16281876 single base substitution A G upstream_gene_variant MELA-AU 17 16280135 16280135 single base substitution C T upstream_gene_variant MELA-AU 17 16282931 16282931 single base substitution A C upstream_gene_variant MELA-AU 17 16283003 16283003 single base substitution C T upstream_gene_variant MELA-AU 17 16283870 16283870 single base substitution G A upstream_gene_variant MELA-AU 17 16284191 16284191 single base substitution G A 5_prime_UTR_variant MELA-AU 17 16284191 16284191 single base substitution G A upstream_gene_variant MELA-AU 17 16284208 16284208 single base substitution G A 5_prime_UTR_variant MELA-AU 17 16284208 16284208 single base substitution G A upstream_gene_variant MELA-AU 17 16284293 16284293 single base substitution G A 5_prime_UTR_variant MELA-AU 17 16284293 16284293 single base substitution G A upstream_gene_variant MELA-AU 17 16284371 16284371 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 17 16284371 16284371 single base substitution C T intron_variant MELA-AU 17 16284371 16284371 single base substitution C T upstream_gene_variant MELA-AU 17 16285557 16285557 single base substitution C T downstream_gene_variant MELA-AU 17 16285557 16285557 single base substitution C T intron_variant MELA-AU 17 16285557 16285557 single base substitution C T synonymous_variant I112I 336C>T MELA-AU 17 16285559 16285559 single base substitution C T downstream_gene_variant MELA-AU 17 16285559 16285559 single base substitution C T intron_variant MELA-AU 17 16285559 16285559 single base substitution C T missense_variant P113L 338C>T MELA-AU 17 16286444 16286444 single base substitution C T downstream_gene_variant MELA-AU 17 16287061 16287061 single base substitution C T downstream_gene_variant MELA-AU 17 16287394 16287394 single base substitution A T downstream_gene_variant MELA-AU 17 16288751 16288751 single base substitution G C downstream_gene_variant MELA-AU 17 16289541 16289541 single base substitution C T downstream_gene_variant MELA-AU 17 16289748 16289748 single base substitution G A downstream_gene_variant MELA-AU 17 16290711 16290711 single base substitution C T downstream_gene_variant ORCA-IN 17 16283017 16283017 single base substitution G C upstream_gene_variant OV-AU 17 16282383 16282383 single base substitution G A upstream_gene_variant OV-AU 17 16284123 16284123 single base substitution C T 5_prime_UTR_variant OV-AU 17 16284123 16284123 single base substitution C T upstream_gene_variant OV-AU 17 16285905 16285905 single base substitution C T downstream_gene_variant OV-AU 17 16285905 16285905 single base substitution C T exon_variant OV-AU 17 16285905 16285905 single base substitution C T synonymous_variant G152G 456C>T OV-AU 17 16285905 16285905 single base substitution C T synonymous_variant G228G 684C>T OV-AU 17 16287169 16287169 single base substitution A T downstream_gene_variant PACA-AU 17 16287662 16287662 single base substitution A G downstream_gene_variant PACA-AU 17 16289604 16289604 single base substitution C T downstream_gene_variant PACA-CA 17 16279919 16279919 single base substitution G A upstream_gene_variant PACA-CA 17 16283635 16283635 single base substitution C T upstream_gene_variant PACA-CA 17 16288064 16288064 single base substitution C A downstream_gene_variant PAEN-AU 17 16284611 16284611 single base substitution A G 5_prime_UTR_variant PAEN-AU 17 16284611 16284611 single base substitution A G intron_variant PAEN-AU 17 16284611 16284611 single base substitution A G upstream_gene_variant PAEN-IT 17 16290160 16290160 single base substitution G A downstream_gene_variant PBCA-DE 17 16284361 16284361 single base substitution A G 5_prime_UTR_variant PBCA-DE 17 16284361 16284361 single base substitution A G intron_variant PBCA-DE 17 16284361 16284361 single base substitution A G upstream_gene_variant PBCA-DE 17 16285497 16285497 single base substitution A G downstream_gene_variant PBCA-DE 17 16285497 16285497 single base substitution A G intron_variant PBCA-DE 17 16285497 16285497 single base substitution A G synonymous_variant E92E 276A>G PRAD-CA 17 16290738 16290738 single base substitution C A downstream_gene_variant PRAD-UK 17 16288819 16288819 single base substitution T A downstream_gene_variant PRAD-US 17 16285497 16285497 single base substitution A G downstream_gene_variant PRAD-US 17 16285497 16285497 single base substitution A G intron_variant PRAD-US 17 16285497 16285497 single base substitution A G synonymous_variant E92E 276A>G PRAD-US 17 16285560 16285560 single base substitution T C downstream_gene_variant PRAD-US 17 16285560 16285560 single base substitution T C intron_variant PRAD-US 17 16285560 16285560 single base substitution T C synonymous_variant P113P 339T>C PRAD-US 17 16285790 16285790 single base substitution C A downstream_gene_variant PRAD-US 17 16285790 16285790 single base substitution C A exon_variant PRAD-US 17 16285790 16285790 single base substitution C A missense_variant P114H 341C>A PRAD-US 17 16285790 16285790 single base substitution C A missense_variant P190H 569C>A RECA-EU 17 16289003 16289003 single base substitution T C downstream_gene_variant SKCA-BR 17 16282682 16282682 single base substitution C T upstream_gene_variant SKCA-BR 17 16283911 16283911 single base substitution A C upstream_gene_variant SKCA-BR 17 16288912 16288912 single base substitution T C downstream_gene_variant SKCA-BR 17 16288989 16288992 deletion of <=200bp TTTC - downstream_gene_variant SKCA-BR 17 16289001 16289001 single base substitution C T downstream_gene_variant SKCA-BR 17 16289653 16289653 single base substitution C T downstream_gene_variant SKCA-BR 17 16289860 16289863 deletion of <=200bp CAAA - downstream_gene_variant SKCM-US 17 16285497 16285497 single base substitution A G downstream_gene_variant SKCM-US 17 16285497 16285497 single base substitution A G intron_variant SKCM-US 17 16285497 16285497 single base substitution A G synonymous_variant E92E 276A>G SKCM-US 17 16285560 16285560 single base substitution T C downstream_gene_variant SKCM-US 17 16285560 16285560 single base substitution T C intron_variant SKCM-US 17 16285560 16285560 single base substitution T C synonymous_variant P113P 339T>C UCEC-US 17 16285549 16285549 single base substitution G T downstream_gene_variant UCEC-US 17 16285549 16285549 single base substitution G T intron_variant UCEC-US 17 16285549 16285549 single base substitution G T stop_gained E110* 328G>T UCEC-US 17 16285581 16285581 single base substitution C T downstream_gene_variant UCEC-US 17 16285581 16285581 single base substitution C T intron_variant UCEC-US 17 16285581 16285581 single base substitution C T synonymous_variant I120I 360C>T UCEC-US 17 16285838 16285838 single base substitution G A downstream_gene_variant UCEC-US 17 16285838 16285838 single base substitution G A exon_variant UCEC-US 17 16285838 16285838 single base substitution G A missense_variant R130H 389G>A UCEC-US 17 16285838 16285838 single base substitution G A missense_variant R206H 617G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand AML_14y_01_DX COSM417179 c.567C>T p.P189P Substitution - coding silent 17:16382474-16382474 + TCGA-60-2726-01 COSM704893 c.383A>G p.D128G Substitution - Missense 17:16382290-16382290 + BZ24 COSM1302430 c.270C>T p.T90T Substitution - coding silent 17:16382177-16382177 + TCGA-AP-A056-01 COSM975897 c.360C>T p.I120I Substitution - coding silent 17:16382267-16382267 + B98 COSM1749881 c.70G>A p.E24K Substitution - Missense 17:16381977-16381977 + TCGA-DK-A3IS-01 COSM1302429 c.232C>A p.Q78K Substitution - Missense 17:16382139-16382139 + TCGA-DK-A1A5-01 COSM417179 c.567C>T p.P189P Substitution - coding silent 17:16382474-16382474 + TCGA-12-3649-01 COSM417179 c.567C>T p.P189P Substitution - coding silent 17:16382474-16382474 + TCGA-DK-A3IU-01 COSM417179 c.567C>T p.P189P Substitution - coding silent 17:16382474-16382474 + PD24223a COSM5795084 c.616C>G p.R206G Substitution - Missense 17:16382523-16382523 + AML_14y_09_DX COSM5956418 c.504G>A p.E168E Substitution - coding silent 17:16382411-16382411 + TCGA-CF-A3MH-01 COSM307160 c.276A>G p.E92E Substitution - coding silent 17:16382183-16382183 + 24T COSM109788 c.150G>A p.L50L Substitution - coding silent 17:16382057-16382057 + AML_14y_08_DX COSM5956907 c.111C>T p.P37P Substitution - coding silent 17:16382018-16382018 + TCGA-AA-3877-01 COSM296534 c.564delC p.D191fs*35 Deletion - Frameshift 17:16382471-16382471 + I2L-P19Ta-Tumor-Organoid COSM2739149 c.677delG p.G227fs*>3 Deletion - Frameshift 17:16382584-16382584 + MedB-1 COSM4738652 c.368G>A p.G123D Substitution - Missense 17:16382275-16382275 + TCGA-EJ-5504-01 COSM1128819 c.162T>C p.R54R Substitution - coding silent 17:16382069-16382069 + AML_14y_10_DX COSM417179 c.567C>T p.P189P Substitution - coding silent 17:16382474-16382474 + TCGA-AG-A023-01 COSM5073837 c.563_564insC p.D191fs*20 Insertion - Frameshift 17:16382470-16382471 + sysucc-880T COSM5462603 c.563T>C p.I188T Substitution - Missense 17:16382470-16382470 + AML_14y_06_DX COSM5956732 c.246G>A p.K82K Substitution - coding silent 17:16382153-16382153 + pfg068T COSM296534 c.564delC p.D191fs*35 Deletion - Frameshift 17:16382471-16382471 + TCGA-ER-A1A1-06 COSM307160 c.276A>G p.E92E Substitution - coding silent 17:16382183-16382183 + TCGA-AA-3864-01 COSM5114610 c.256G>A p.G86S Substitution - Missense 17:16382163-16382163 + TCGA-BP-4976-01 COSM417179 c.567C>T p.P189P Substitution - coding silent 17:16382474-16382474 + 24T COSM109854 c.160C>T p.R54C Substitution - Missense 17:16382067-16382067 + AML_14y_05_DX COSM400523 c.390C>T p.R130R Substitution - coding silent 17:16382297-16382297 + U343 COSM5712785 c.18A>G p.K6K Substitution - coding silent 17:16381925-16381925 + TCGA-BS-A0U8-01 COSM307160 c.276A>G p.E92E Substitution - coding silent 17:16382183-16382183 + LUAD-2GUGK COSM400523 c.390C>T p.R130R Substitution - coding silent 17:16382297-16382297 + TCGA-D5-6540-01 COSM296534 c.564delC p.D191fs*35 Deletion - Frameshift 17:16382471-16382471 + T2950 COSM4738652 c.368G>A p.G123D Substitution - Missense 17:16382275-16382275 + TCGA-FG-8185-01 COSM1302430 c.270C>T p.T90T Substitution - coding silent 17:16382177-16382177 + 4132_T COSM3958054 c.67A>C p.I23L Substitution - Missense 17:16381974-16381974 + TCGA-D3-A5GN-06 COSM307160 c.276A>G p.E92E Substitution - coding silent 17:16382183-16382183 + I2L-P19Ta-Tumor-Biopsy COSM2739149 c.677delG p.G227fs*>3 Deletion - Frameshift 17:16382584-16382584 + TCGA-AA-A022-01 COSM5073837 c.563_564insC p.D191fs*20 Insertion - Frameshift 17:16382470-16382471 + TCGA-CM-6171-01 COSM1128819 c.162T>C p.R54R Substitution - coding silent 17:16382069-16382069 + U343 COSM5712786 c.24T>G p.L8L Substitution - coding silent 17:16381931-16381931 + TCGA-EJ-A65F-01 COSM2739144 c.339T>C p.P113P Substitution - coding silent 17:16382246-16382246 + 2_PRE-TREATMENT COSM307160 c.276A>G p.E92E Substitution - coding silent 17:16382183-16382183 + TCGA-QG-A5Z2-01 COSM5187271 c.65C>T p.T22I Substitution - Missense 17:16381972-16381972 + CHEWS015 COSM4579470 c.441G>A p.L147L Substitution - coding silent 17:16382348-16382348 + 24T COSM107825 c.143A>T p.K48M Substitution - Missense 17:16382050-16382050 + TCGA-BS-A0UV-01 COSM975896 c.328G>T p.E110* Substitution - Nonsense 17:16382235-16382235 + TCGA-AG-A01Y-01 COSM290295 c.388C>T p.R130C Substitution - Missense 17:16382295-16382295 + AOCS-107-1-4 COSM3983278 c.684C>T p.G228G Substitution - coding silent 17:16382591-16382591 + AML_14y_04_DX COSM1128819 c.162T>C p.R54R Substitution - coding silent 17:16382069-16382069 + AML_14y_08_DX COSM5956835 c.108T>C p.I36I Substitution - coding silent 17:16382015-16382015 + RK241_C01 COSM1128819 c.162T>C p.R54R Substitution - coding silent 17:16382069-16382069 + TCGA-AP-A056-01 COSM975898 c.617G>A p.R206H Substitution - Missense 17:16382524-16382524 + T2769 COSM2739144 c.339T>C p.P113P Substitution - coding silent 17:16382246-16382246 + TCGA-AA-A01P-01 COSM296534 c.564delC p.D191fs*35 Deletion - Frameshift 17:16382471-16382471 + TCGA-DK-A3IS-01 COSM1302431 c.460C>A p.Q154K Substitution - Missense 17:16382367-16382367 + TCGA-CM-5862-01 COSM1128819 c.162T>C p.R54R Substitution - coding silent 17:16382069-16382069 + 1_RESISTANT COSM307160 c.276A>G p.E92E Substitution - coding silent 17:16382183-16382183 + AML_14y_05_DX COSM5956293 c.620C>G p.T207S Substitution - Missense 17:16382527-16382527 + BZ24 COSM307160 c.276A>G p.E92E Substitution - coding silent 17:16382183-16382183 + LFS_MB1 COSM307160 c.276A>G p.E92E Substitution - coding silent 17:16382183-16382183 + CSB1 COSM5028231 c.525C>T p.I175I Substitution - coding silent 17:16382432-16382432 + PD18031a COSM400523 c.390C>T p.R130R Substitution - coding silent 17:16382297-16382297 + 116 COSM5013112 c.320A>G p.Q107R Substitution - Missense 17:16382227-16382227 + T3336 COSM4738653 c.671G>A p.R224H Substitution - Missense 17:16382578-16382578 + T3262 COSM4738650 c.258C>T p.G86G Substitution - coding silent 17:16382165-16382165 + Patient_2_Relapse COSM5414997 c.215G>A p.R72H Substitution - Missense 17:16382122-16382122 + AML_14y_01_DX COSM5956783 c.273G>T p.L91L Substitution - coding silent 17:16382180-16382180 + TCGA-CJ-4643-01 COSM2739144 c.339T>C p.P113P Substitution - coding silent 17:16382246-16382246 + TCGA-FS-A1ZP-06 COSM2739144 c.339T>C p.P113P Substitution - coding silent 17:16382246-16382246 + TCGA-66-2771-01 COSM704895 c.140G>T p.G47V Substitution - Missense 17:16382047-16382047 + TCGA-HE-7129-01 COSM3988791 c.255C>G p.T85T Substitution - coding silent 17:16382162-16382162 + PD4120a COSM165366 c.267C>T p.I89I Substitution - coding silent 17:16382174-16382174 + TCGA-DV-5565-01 COSM3361999 c.690A>G p.*230* Substitution - coding silent 17:16382597-16382597 + AML_14y_01_DX COSM1128819 c.162T>C p.R54R Substitution - coding silent 17:16382069-16382069 + 076T COSM107825 c.143A>T p.K48M Substitution - Missense 17:16382050-16382050 + T368 COSM4738651 c.363T>C p.F121F Substitution - coding silent 17:16382270-16382270 + AML_14y_09_DX COSM5956416 c.549A>G p.Q183Q Substitution - coding silent 17:16382456-16382456 + HN_62854 COSM128427 c.534G>A p.V178V Substitution - coding silent 17:16382441-16382441 + TCGA-60-2725-01 COSM704894 c.321G>A p.Q107Q Substitution - coding silent 17:16382228-16382228 + Pat_15_B COSM1302429 c.232C>A p.Q78K Substitution - Missense 17:16382139-16382139 + TCGA-CF-A3MH-01 COSM1302430 c.270C>T p.T90T Substitution - coding silent 17:16382177-16382177 + TCGA-AX-A2H5-01 COSM975895 c.93G>T p.Q31H Substitution - Missense 17:16382000-16382000 + TCGA-G9-7523-01 COSM307160 c.276A>G p.E92E Substitution - coding silent 17:16382183-16382183 + AML_14y_01_DX COSM5956418 c.504G>A p.E168E Substitution - coding silent 17:16382411-16382411 + TCGA-EJ-5518-01 COSM1128818 c.569C>A p.P190H Substitution - Missense 17:16382476-16382476 + BZ12 COSM307160 c.276A>G p.E92E Substitution - coding silent 17:16382183-16382183 + 1_RESISTANT COSM1302430 c.270C>T p.T90T Substitution - coding silent 17:16382177-16382177 + B98-Tumor COSM1749881 c.70G>A p.E24K Substitution - Missense 17:16381977-16381977 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.356190 17p12-p11.2 191339 2449747|CGAP|BC000379|C/T|coding|Ile137Ile|548|Candidate; 2449747|CGAP|BC000379|C/T|coding|Ile213Ile|776|Candidate; 2449747|CGAP|BC000379|C/T|coding|Ile61Ile|320|Candidate; 2449747|CGAP|BC009301|C/T|coding|Ile137Ile|494|Candidate; 2449747|CGAP|BC009301|C/T|coding|Ile213Ile|722|Candidate; 2449747|CGAP|BC009301|C/T|coding|Ile61Ile|266|Candidate; 2449747|CGAP|BC015127|C/T|coding|Ile137Ile|510|Candidate; 2449747|CGAP|BC015127|C/T|coding|Ile213Ile|738|Candidate; 2449747|CGAP|BC015127|C/T|coding|Ile61Ile|282|Candidate; 2449747|CGAP|BC026301|C/T|coding|Ile137Ile|506|Candidate; 2449747|CGAP|BC026301|C/T|coding|Ile213Ile|734|Candidate; 2449747|CGAP|BC026301|C/T|coding|Ile61Ile|278|Candidate; 2449747|CGAP|BC031027|C/T|coding|Ile137Ile|508|Candidate; 2449747|CGAP|BC031027|C/T|coding|Ile213Ile|736|Candidate; 2449747|CGAP|BC031027|C/T|coding|Ile61Ile|280|Candidate; 2449747|CGAP|BC038999|C/T|coding|Ile137Ile|517|Candidate; 2449747|CGAP|BC038999|C/T|coding|Ile213Ile|745|Candidate; 2449747|CGAP|BC038999|C/T|coding|Ile61Ile|289|Candidate; 2449747|CGAP|BC046123|C/T|coding|Ile137Ile|496|Candidate; 2449747|CGAP|BC046123|C/T|coding|Ile213Ile|724|Candidate; 2449747|CGAP|BC046123|C/T|coding|Ile61Ile|268|Candidate; 2449751|CGAP|BC000379|C/T|coding|Ile13Ile|176|Candidate; 2449751|CGAP|BC009301|C/T|coding|Ile13Ile|122|Candidate; 2449751|CGAP|BC015127|C/T|coding|Ile13Ile|138|Candidate; 2449751|CGAP|BC026301|C/T|coding|Ile13Ile|134|Candidate; 2449751|CGAP|BC031027|C/T|coding|Ile13Ile|136|Candidate; 2449751|CGAP|BC038999|C/T|codi

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G 3-UTRSNV . c.687+3A>G 17 16285911 RCCC A G Missense p.D128G c.383A>G 17 16285604 LUSC A G Synonymous p.E92E c.276A>G 17 16285497 BLCA A G Synonymous p.E92E c.276A>G 17 16285497 CM A G Synonymous p.E92E c.276A>G 17 16285497 LGG A G Synonymous p.E92E c.276A>G 17 16285497 STAD C A Missense p.P190H c.569C>A 17 16285790 PRAD C A Missense p.Q154K c.460C>A 17 16285681 BLCA C A Missense p.Q78K c.232C>A 17 16285453 BLCA C T Missense p.R130C c.388C>T 17 16285609 COREAD C T Synonymous p.I175I c.525C>T 17 16285746 BRCA C T Synonymous p.I89I c.267C>T 17 16285488 BRCA C T Synonymous p.P189P c.567C>T 17 16285788 BLCA C T Synonymous p.P189P c.567C>T 17 16285788 GBM C T Synonymous p.R130R c.390C>T 17 16285611 BRCA G A Missense p.R54H c.161G>A 17 16285382 CM G A Missense p.V178M c.532G>A 17 16285753 HNSC G A Synonymous p.Q107Q c.321G>A 17 16285542 LUSC G A Synonymous p.V178V c.534G>A 17 16285755 HNSC G T Missense p.G47V c.140G>T 17 16285361 LUSC T C Synonymous p.I36I c.108T>C 17 16285329 CM T C Synonymous p.P113P c.339T>C 17 16285560 CM T C Synonymous p.P113P c.339T>C 17 16285560 RCCC T C Synonymous p.P113P c.339T>C 17 16285560 THCA