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 6 53519456 53519456 + Silent SNP C C A TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr6:53519456C>A c.615G>T c.(613-615)tcG>tcT p.S205S BLCA 6 53516582 53516582 + Nonsense_Mutation SNP C C T TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr6:53516582C>T c.1719G>A c.(1717-1719)tgG>tgA p.W573* BLCA 6 53516760 53516760 + Missense_Mutation SNP C C G TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr6:53516760C>G c.1541G>C c.(1540-1542)aGa>aCa p.R514T BLCA 6 53516997 53516997 + Missense_Mutation SNP G G A TCGA-4Z-AA7R-01A-11D-A391-08 TCGA-4Z-AA7R-10A-01D-A394-08 g.chr6:53516997G>A c.1304C>T c.(1303-1305)tCg>tTg p.S435L BLCA 6 53519742 53519742 + Missense_Mutation SNP C C A TCGA-XF-A9T4-01A-11D-A391-08 TCGA-XF-A9T4-10A-01D-A394-08 g.chr6:53519742C>A c.329G>T c.(328-330)aGg>aTg p.R110M BLCA 6 53519801 53519801 + Silent SNP G G C TCGA-BT-A42E-01A-11D-A23U-08 TCGA-BT-A42E-10A-01D-A23U-08 g.chr6:53519801G>C c.270C>G c.(268-270)gtC>gtG p.V90V BRCA 6 53519409 53519409 + Missense_Mutation SNP A A C TCGA-E2-A1IF-01A-11D-A142-09 TCGA-E2-A1IF-10A-01D-A142-09 g.chr6:53519409A>C c.662T>G c.(661-663)aTa>aGa p.I221R BRCA 6 53519444 53519444 + Missense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr6:53519444C>A c.627G>T c.(625-627)atG>atT p.M209I BRCA 6 53519444 53519444 + Missense_Mutation SNP C C G TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chr6:53519444C>G c.627G>C c.(625-627)atG>atC p.M209I BRCA 6 53519520 53519520 + Missense_Mutation SNP A A G TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr6:53519520A>G c.551T>C c.(550-552)cTa>cCa p.L184P BRCA 6 53519578 53519578 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr6:53519578G>A c.493C>T c.(493-495)Cgg>Tgg p.R165W BRCA 6 53519885 53519885 + Silent SNP A A G TCGA-AN-A0AK-01A-21W-A019-09 TCGA-AN-A0AK-10A-01W-A021-09 g.chr6:53519885A>G c.186T>C c.(184-186)ggT>ggC p.G62G CESC 6 53519746 53519746 + Missense_Mutation SNP G G C TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr6:53519746G>C c.325C>G c.(325-327)Cag>Gag p.Q109E CHOL 6 53519100 53519100 + Missense_Mutation SNP C C A TCGA-YR-A95A-01A-12D-A417-09 TCGA-YR-A95A-10A-01D-A41A-09 g.chr6:53519100C>A c.971G>T c.(970-972)cGc>cTc p.R324L CHOL 6 53519311 53519311 + Missense_Mutation SNP G G T TCGA-4G-AAZO-01A-12D-A417-09 TCGA-4G-AAZO-11A-11D-A41A-09 g.chr6:53519311G>T c.760C>A c.(760-762)Ctt>Att p.L254I COAD 6 53518912 53518912 + Missense_Mutation SNP T T C TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr6:53518912T>C c.1159A>G c.(1159-1161)Agc>Ggc p.S387G COAD 6 53519024 53519024 + Silent SNP C C T TCGA-D5-6926-01A-11D-1924-10 TCGA-D5-6926-10A-01D-1924-10 g.chr6:53519024C>T c.1047G>A c.(1045-1047)acG>acA p.T349T COAD 6 53519149 53519149 + Nonsense_Mutation SNP G G A TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr6:53519149G>A c.922C>T c.(922-924)Cga>Tga p.R308* COAD 6 53519321 53519321 + Silent SNP G G A TCGA-AA-A01Z-01A-11W-A096-10 TCGA-AA-A01Z-11A-11W-A096-10 g.chr6:53519321G>A c.750C>T c.(748-750)taC>taT p.Y250Y COADREAD 6 53518912 53518912 + Missense_Mutation SNP T T C TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr6:53518912T>C c.1159A>G c.(1159-1161)Agc>Ggc p.S387G COADREAD 6 53518999 53518999 + Missense_Mutation SNP G G T TCGA-EI-6506-01A-11D-1733-10 TCGA-EI-6506-10A-01D-1733-10 g.chr6:53518999G>T c.1072C>A c.(1072-1074)Cag>Aag p.Q358K COADREAD 6 53519024 53519024 + Silent SNP C C T TCGA-D5-6926-01A-11D-1924-10 TCGA-D5-6926-10A-01D-1924-10 g.chr6:53519024C>T c.1047G>A c.(1045-1047)acG>acA p.T349T COADREAD 6 53519149 53519149 + Nonsense_Mutation SNP G G A TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr6:53519149G>A c.922C>T c.(922-924)Cga>Tga p.R308* COADREAD 6 53519321 53519321 + Silent SNP G G A TCGA-AA-A01Z-01A-11W-A096-10 TCGA-AA-A01Z-11A-11W-A096-10 g.chr6:53519321G>A c.750C>T c.(748-750)taC>taT p.Y250Y ESCA 6 53516583 53516583 + Nonsense_Mutation SNP C C T TCGA-2H-A9GI-01A-11D-A37C-09 TCGA-2H-A9GI-11A-11D-A37F-09 g.chr6:53516583C>T c.1718G>A c.(1717-1719)tGg>tAg p.W573* HNSC 6 53516534 53516534 + Frame_Shift_Del DEL G G - TCGA-BA-4074-01A-01D-1434-08 TCGA-BA-4074-10A-01D-1434-08 g.chr6:53516534delG c.1767delC c.(1765-1767)cccfs p.P589fs HNSC 6 53516703 53516703 + Missense_Mutation SNP A A G TCGA-CV-7089-01A-11D-2012-08 TCGA-CV-7089-10A-01D-2013-08 g.chr6:53516703A>G c.1598T>C c.(1597-1599)cTc>cCc p.L533P HNSC 6 53519101 53519101 + Missense_Mutation SNP G G A TCGA-CV-5431-01A-01D-1512-08 TCGA-CV-5431-11A-01D-1512-08 g.chr6:53519101G>A c.970C>T c.(970-972)Cgc>Tgc p.R324C HNSC 6 53519325 53519325 + Missense_Mutation SNP T T C TCGA-CV-7429-01A-11D-2129-08 TCGA-CV-7429-10A-01D-2129-08 g.chr6:53519325T>C c.746A>G c.(745-747)aAa>aGa p.K249R HNSC 6 53519396 53519396 + Silent SNP T T C TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr6:53519396T>C c.675A>G c.(673-675)ttA>ttG p.L225L HNSC 6 53519582 53519582 + Silent SNP C C T TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chr6:53519582C>T c.489G>A c.(487-489)ctG>ctA p.L163L HNSC 6 53519694 53519694 + Missense_Mutation SNP G G A TCGA-CQ-5332-01A-01D-1683-08 TCGA-CQ-5332-10A-01D-1683-08 g.chr6:53519694G>A c.377C>T c.(376-378)gCa>gTa p.A126V KIPAN 6 53516418 53516418 + Missense_Mutation SNP G G T TCGA-CJ-4644-01A-02D-1386-10 TCGA-CJ-4644-11A-01D-1251-10 g.chr6:53516418G>T c.1883C>A c.(1882-1884)tCt>tAt p.S628Y KIPAN 6 53516723 53516723 + Silent SNP G G A TCGA-IA-A83W-01A-11D-A34Z-10 TCGA-IA-A83W-11A-11D-A34Z-10 g.chr6:53516723G>A c.1578C>T c.(1576-1578)cgC>cgT p.R526R KIPAN 6 53519514 53519514 + Frame_Shift_Del DEL T T - TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr6:53519514delT c.557delA c.(556-558)aatfs p.N186fs KIPAN 6 53520057 53520057 + Missense_Mutation SNP T T A TCGA-BP-5010-01A-02D-1421-08 TCGA-BP-5010-11A-01D-1421-08 g.chr6:53520057T>A c.14A>T c.(13-15)aAg>aTg p.K5M KIRC 6 53516418 53516418 + Missense_Mutation SNP G G T TCGA-CJ-4644-01A-02D-1386-10 TCGA-CJ-4644-11A-01D-1251-10 g.chr6:53516418G>T c.1883C>A c.(1882-1884)tCt>tAt p.S628Y KIRC 6 53519514 53519514 + Frame_Shift_Del DEL T T - TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr6:53519514delT c.557delA c.(556-558)aatfs p.N186fs KIRC 6 53520057 53520057 + Missense_Mutation SNP T T A TCGA-BP-5010-01A-02D-1421-08 TCGA-BP-5010-11A-01D-1421-08 g.chr6:53520057T>A c.14A>T c.(13-15)aAg>aTg p.K5M KIRP 6 53516723 53516723 + Silent SNP G G A TCGA-IA-A83W-01A-11D-A34Z-10 TCGA-IA-A83W-11A-11D-A34Z-10 g.chr6:53516723G>A c.1578C>T c.(1576-1578)cgC>cgT p.R526R LIHC 6 53516499 53516499 + Missense_Mutation SNP G G T TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr6:53516499G>T c.1802C>A c.(1801-1803)cCc>cAc p.P601H LUAD 6 53516497 53516497 + Missense_Mutation SNP C C T TCGA-NJ-A4YP-01A-11D-A25L-08 TCGA-NJ-A4YP-10A-01D-A25L-08 g.chr6:53516497C>T c.1804G>A c.(1804-1806)Gag>Aag p.E602K LUAD 6 53516934 53516934 + Missense_Mutation SNP C C A TCGA-73-4666-01A-01D-1265-08 TCGA-73-4666-11A-01D-1265-08 g.chr6:53516934C>A c.1367G>T c.(1366-1368)cGc>cTc p.R456L LUAD 6 53516940 53516940 + Missense_Mutation SNP A A G TCGA-86-8281-01A-11D-2284-08 TCGA-86-8281-10A-01D-2284-08 g.chr6:53516940A>G c.1361T>C c.(1360-1362)gTg>gCg p.V454A LUAD 6 53518930 53518930 + Nonsense_Mutation SNP G G A TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr6:53518930G>A c.1141C>T c.(1141-1143)Caa>Taa p.Q381* LUAD 6 53519011 53519011 + Missense_Mutation SNP T T G TCGA-44-6778-01A-11D-1855-08 TCGA-44-6778-10A-01D-1855-08 g.chr6:53519011T>G c.1060A>C c.(1060-1062)Aaa>Caa p.K354Q LUAD 6 53519729 53519729 + Silent SNP A A G TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr6:53519729A>G c.342T>C c.(340-342)aaT>aaC p.N114N LUAD 6 53519984 53519984 + Silent SNP T T C TCGA-38-4626-01A-01D-1553-08 TCGA-38-4626-11A-01D-1553-08 g.chr6:53519984T>C c.87A>G c.(85-87)aaA>aaG p.K29K LUAD 6 53519990 53519991 + Frame_Shift_Ins INS - - A TCGA-44-6778-01A-11D-1855-08 TCGA-44-6778-10A-01D-1855-08 g.chr6:53519990_53519991insA c.80_81insT c.(79-81)ctafs p.L27fs LUSC 6 53517037 53517037 + Missense_Mutation SNP A A T TCGA-21-5786-01A-01D-1632-08 TCGA-21-5786-10A-01D-1632-08 g.chr6:53517037A>T c.1264T>A c.(1264-1266)Tac>Aac p.Y422N LUSC 6 53517046 53517046 + Missense_Mutation SNP C C G TCGA-66-2754-01A-01D-0983-08 TCGA-66-2754-11A-01D-0983-08 g.chr6:53517046C>G c.1255G>C c.(1255-1257)Ggg>Cgg p.G419R LUSC 6 53519311 53519311 + Missense_Mutation SNP G G T TCGA-22-5485-01A-01D-1632-08 TCGA-22-5485-11A-01D-1632-08 g.chr6:53519311G>T c.760C>A c.(760-762)Ctt>Att p.L254I LUSC 6 53519386 53519386 + Missense_Mutation SNP A A C TCGA-60-2726-01A-01D-1522-08 TCGA-60-2726-11A-01D-1522-08 g.chr6:53519386A>C c.685T>G c.(685-687)Tct>Gct p.S229A OV 6 53518977 53518977 + Missense_Mutation SNP C C T TCGA-29-1768-01A-01W-0633-09 TCGA-29-1768-10A-01W-0634-09 g.chr6:53518977C>T c.1094G>A c.(1093-1095)gGa>gAa p.G365E OV 6 53518999 53518999 + Nonsense_Mutation SNP G G A TCGA-24-2298-01A-01W-0799-08 TCGA-24-2298-11A-01W-0799-08 g.chr6:53518999G>A c.1072C>T c.(1072-1074)Cag>Tag p.Q358* PAAD 6 53519025 53519025 + Missense_Mutation SNP G G A TCGA-2J-AAB4-01A-12D-A40W-08 TCGA-2J-AAB4-10A-01D-A40W-08 g.chr6:53519025G>A c.1046C>T c.(1045-1047)aCg>aTg p.T349M PAAD 6 53519025 53519025 + Missense_Mutation SNP G G A TCGA-HZ-A8P0-01A-11D-A36O-08 TCGA-HZ-A8P0-10A-01D-A367-08 g.chr6:53519025G>A c.1046C>T c.(1045-1047)aCg>aTg p.T349M PAAD 6 53519407 53519407 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:53519407C>A c.664G>T c.(664-666)Gat>Tat p.D222Y PAAD 6 53519553 53519553 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:53519553A>G c.518T>C c.(517-519)aTg>aCg p.M173T PRAD 6 53519296 53519296 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:53519296G>A c.775C>T c.(775-777)Cgc>Tgc p.R259C PRAD 6 53520007 53520007 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:53520007C>T c.64G>A c.(64-66)Gta>Ata p.V22I READ 6 53518999 53518999 + Missense_Mutation SNP G G T TCGA-EI-6506-01A-11D-1733-10 TCGA-EI-6506-10A-01D-1733-10 g.chr6:53518999G>T c.1072C>A c.(1072-1074)Cag>Aag p.Q358K SKCM 6 53517009 53517009 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr6:53517009C>T c.1292G>A c.(1291-1293)gGa>gAa p.G431E SKCM 6 53519023 53519023 + Missense_Mutation SNP C C T TCGA-D3-A51R-06A-11D-A25O-08 TCGA-D3-A51R-10A-01D-A25O-08 g.chr6:53519023C>T c.1048G>A c.(1048-1050)Gaa>Aaa p.E350K SKCM 6 53519041 53519041 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr6:53519041C>T c.1030G>A c.(1030-1032)Gga>Aga p.G344R SKCM 6 53519078 53519078 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr6:53519078G>A c.993C>T c.(991-993)tcC>tcT p.S331S SKCM 6 53519241 53519241 + Missense_Mutation SNP C C T TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr6:53519241C>T c.830G>A c.(829-831)aGa>aAa p.R277K SKCM 6 53519485 53519485 + Missense_Mutation SNP G G A TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr6:53519485G>A c.586C>T c.(586-588)Cgg>Tgg p.R196W SKCM 6 53519497 53519497 + Nonsense_Mutation SNP G G A TCGA-D3-A51J-06A-11D-A25O-08 TCGA-D3-A51J-10A-01D-A25O-08 g.chr6:53519497G>A c.574C>T c.(574-576)Cag>Tag p.Q192* SKCM 6 53519498 53519498 + Silent SNP G G A TCGA-D3-A51J-06A-11D-A25O-08 TCGA-D3-A51J-10A-01D-A25O-08 g.chr6:53519498G>A c.573C>T c.(571-573)gcC>gcT p.A191A SKCM 6 53519576 53519576 + Silent SNP C C T TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr6:53519576C>T c.495G>A c.(493-495)cgG>cgA p.R165R SKCM 6 53519615 53519615 + Silent SNP G G A TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr6:53519615G>A c.456C>T c.(454-456)atC>atT p.I152I SKCM 6 53519768 53519768 + Silent SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr6:53519768G>A c.303C>T c.(301-303)atC>atT p.I101I SKCM 6 53519866 53519866 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr6:53519866C>T c.205G>A c.(205-207)Gag>Aag p.E69K SKCM 6 53519959 53519959 + Missense_Mutation SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr6:53519959C>T c.112G>A c.(112-114)Gag>Aag p.E38K SKCM 6 53520004 53520004 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr6:53520004C>T c.67G>A c.(67-69)Gaa>Aaa p.E23K

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 6 53516582 53516582 single base substitution C T stop_gained W573* 1719G>A BLCA-US 6 53516760 53516760 single base substitution C G missense_variant R514T 1541G>C BOCA-FR 6 53517548 53517548 single base substitution T C intron_variant BRCA-EU 6 53508235 53508235 single base substitution C G downstream_gene_variant BRCA-EU 6 53510535 53510535 deletion of <=200bp A - downstream_gene_variant BRCA-EU 6 53510877 53510877 single base substitution C T downstream_gene_variant BRCA-EU 6 53513106 53513106 single base substitution G T 3_prime_UTR_variant BRCA-EU 6 53513106 53513106 single base substitution G T downstream_gene_variant BRCA-EU 6 53513796 53513796 single base substitution A C 3_prime_UTR_variant BRCA-EU 6 53513796 53513796 single base substitution A C downstream_gene_variant BRCA-EU 6 53513883 53513883 single base substitution A C 3_prime_UTR_variant BRCA-EU 6 53513883 53513883 single base substitution A C downstream_gene_variant BRCA-EU 6 53515739 53515739 single base substitution G A 3_prime_UTR_variant BRCA-EU 6 53515739 53515739 single base substitution G A downstream_gene_variant BRCA-EU 6 53516320 53516320 single base substitution C T 3_prime_UTR_variant BRCA-EU 6 53516320 53516320 single base substitution C T downstream_gene_variant BRCA-EU 6 53517330 53517330 single base substitution C T intron_variant BRCA-EU 6 53517541 53517541 single base substitution G T intron_variant BRCA-EU 6 53517731 53517733 deletion of <=200bp GAC - intron_variant BRCA-EU 6 53518467 53518467 single base substitution G C intron_variant BRCA-EU 6 53518529 53518529 single base substitution G T intron_variant BRCA-EU 6 53518863 53518863 single base substitution T C intron_variant BRCA-EU 6 53519514 53519514 deletion of <=200bp T - frameshift_variant N186 BRCA-EU 6 53520272 53520272 single base substitution T C intron_variant BRCA-EU 6 53520272 53520272 single base substitution T C upstream_gene_variant BRCA-EU 6 53520550 53520550 single base substitution G T intron_variant BRCA-EU 6 53520550 53520550 single base substitution G T upstream_gene_variant BRCA-EU 6 53524394 53524394 single base substitution G A intron_variant BRCA-EU 6 53524394 53524394 single base substitution G A upstream_gene_variant BRCA-EU 6 53526443 53526443 single base substitution G C intron_variant BRCA-EU 6 53526768 53526768 deletion of <=200bp T - intron_variant BRCA-EU 6 53526854 53526854 single base substitution T C intron_variant BRCA-EU 6 53529300 53529300 single base substitution G T intron_variant BRCA-EU 6 53530413 53530413 single base substitution G A 5_prime_UTR_variant BRCA-EU 6 53533868 53533868 single base substitution C T upstream_gene_variant BRCA-FR 6 53519142 53519142 single base substitution C G missense_variant R310T 929G>C BRCA-US 6 53519409 53519409 single base substitution A C missense_variant I221R 662T>G BRCA-US 6 53519444 53519444 single base substitution C A missense_variant M209I 627G>T BRCA-US 6 53519444 53519444 single base substitution C G missense_variant M209I 627G>C BRCA-US 6 53519520 53519520 single base substitution A G missense_variant L184P 551T>C BRCA-US 6 53519578 53519578 single base substitution G A missense_variant R165W 493C>T BRCA-US 6 53519885 53519885 single base substitution A G synonymous_variant G62G 186T>C BTCA-JP 6 53516409 53516409 single base substitution G A missense_variant P631L 1892C>T BTCA-JP 6 53516512 53516512 single base substitution C A missense_variant D597Y 1789G>T BTCA-JP 6 53516937 53516937 single base substitution G A missense_variant A455V 1364C>T BTCA-JP 6 53517122 53517122 single base substitution A T missense_variant D393E 1179T>A BTCA-JP 6 53519796 53519796 single base substitution G T missense_variant A92D 275C>A CESC-US 6 53519746 53519746 single base substitution G C missense_variant Q109E 325C>G COAD-US 6 53516876 53516876 single base substitution T G synonymous_variant I475I 1425A>C COAD-US 6 53517035 53517035 single base substitution G A synonymous_variant Y422Y 1266C>T COAD-US 6 53519024 53519024 single base substitution C T synonymous_variant T349T 1047G>A COAD-US 6 53519149 53519149 single base substitution G A stop_gained R308* 922C>T COCA-CN 6 53515930 53515930 single base substitution C T 3_prime_UTR_variant COCA-CN 6 53515930 53515930 single base substitution C T downstream_gene_variant COCA-CN 6 53516616 53516616 single base substitution G A missense_variant A562V 1685C>T COCA-CN 6 53518973 53518973 single base substitution A G synonymous_variant F366F 1098T>C COCA-CN 6 53519053 53519053 single base substitution C T missense_variant D340N 1018G>A COCA-CN 6 53519116 53519116 single base substitution C T missense_variant V319I 955G>A COCA-CN 6 53519457 53519457 single base substitution G A missense_variant S205L 614C>T COCA-CN 6 53519618 53519618 single base substitution C A missense_variant Q151H 453G>T COCA-CN 6 53520003 53520003 single base substitution T G missense_variant E23A 68A>C COCA-CN 6 53520114 53520114 single base substitution A G intron_variant COCA-CN 6 53520114 53520114 single base substitution A G upstream_gene_variant COCA-CN 6 53530773 53530773 single base substitution A G upstream_gene_variant COCA-CN 6 53530821 53530821 single base substitution G A upstream_gene_variant COCA-CN 6 53530865 53530865 single base substitution A G upstream_gene_variant COCA-CN 6 53530869 53530869 single base substitution A G upstream_gene_variant EOPC-DE 6 53508575 53508575 single base substitution G T downstream_gene_variant ESAD-UK 6 53508149 53508149 single base substitution C T downstream_gene_variant ESAD-UK 6 53508325 53508325 single base substitution T C downstream_gene_variant ESAD-UK 6 53511934 53511934 single base substitution T C downstream_gene_variant ESAD-UK 6 53518006 53518008 deletion of <=200bp CTT - intron_variant ESAD-UK 6 53518841 53518841 single base substitution T C intron_variant ESAD-UK 6 53519707 53519707 single base substitution C T missense_variant A122T 364G>A ESAD-UK 6 53521310 53521310 single base substitution A T intron_variant ESAD-UK 6 53521310 53521310 single base substitution A T upstream_gene_variant ESAD-UK 6 53522911 53522911 single base substitution T C intron_variant ESAD-UK 6 53522911 53522911 single base substitution T C upstream_gene_variant ESAD-UK 6 53523910 53523910 single base substitution T C intron_variant ESAD-UK 6 53523910 53523910 single base substitution T C upstream_gene_variant ESAD-UK 6 53525964 53525964 single base substitution C T intron_variant ESAD-UK 6 53526227 53526227 single base substitution C T intron_variant ESAD-UK 6 53527531 53527531 single base substitution C T intron_variant ESAD-UK 6 53528725 53528725 single base substitution T C intron_variant ESAD-UK 6 53529171 53529171 single base substitution A C intron_variant ESAD-UK 6 53530550 53530550 single base substitution T A upstream_gene_variant ESAD-UK 6 53532219 53532219 single base substitution T A upstream_gene_variant ESAD-UK 6 53535105 53535105 single base substitution G A upstream_gene_variant ESCA-CN 6 53516510 53516510 single base substitution G A synonymous_variant D597D 1791C>T ESCA-CN 6 53516617 53516617 single base substitution C T missense_variant A562T 1684G>A KIRC-US 6 53516418 53516418 single base substitution G T missense_variant S628Y 1883C>A KIRC-US 6 53520057 53520057 single base substitution T A missense_variant K5M 14A>T KIRP-US 6 53517013 53517013 single base substitution C T missense_variant E430K 1288G>A LICA-CN 6 53516826 53516826 single base substitution G C missense_variant S492W 1475C>G LIHC-US 6 53517092 53517092 single base substitution G T synonymous_variant A403A 1209C>A LINC-JP 6 53510252 53510252 single base substitution G T downstream_gene_variant LINC-JP 6 53516721 53516721 single base substitution C A missense_variant G527V 1580G>T LINC-JP 6 53517296 53517296 single base substitution G C intron_variant LINC-JP 6 53519053 53519053 single base substitution C G missense_variant D340H 1018G>C LINC-JP 6 53519299 53519299 single base substitution T C missense_variant I258V 772A>G LINC-JP 6 53519518 53519518 single base substitution T A stop_gained K185* 553A>T LIRI-JP 6 53509990 53509990 single base substitution A G downstream_gene_variant LIRI-JP 6 53512686 53512686 single base substitution T C downstream_gene_variant LIRI-JP 6 53513474 53513474 single base substitution T C 3_prime_UTR_variant LIRI-JP 6 53513474 53513474 single base substitution T C downstream_gene_variant LIRI-JP 6 53513819 53513819 single base substitution A C 3_prime_UTR_variant LIRI-JP 6 53513819 53513819 single base substitution A C downstream_gene_variant LIRI-JP 6 53513832 53513832 single base substitution A C 3_prime_UTR_variant LIRI-JP 6 53513832 53513832 single base substitution A C downstream_gene_variant LIRI-JP 6 53514346 53514346 single base substitution T C 3_prime_UTR_variant LIRI-JP 6 53514346 53514346 single base substitution T C downstream_gene_variant LIRI-JP 6 53515799 53515799 single base substitution A G 3_prime_UTR_variant LIRI-JP 6 53515799 53515799 single base substitution A G downstream_gene_variant LIRI-JP 6 53516301 53516302 deletion of <=200bp TG - 3_prime_UTR_variant LIRI-JP 6 53516301 53516302 deletion of <=200bp TG - downstream_gene_variant LIRI-JP 6 53518110 53518110 single base substitution A T intron_variant LIRI-JP 6 53519114 53519114 single base substitution G A synonymous_variant V319V 957C>T LIRI-JP 6 53522062 53522062 single base substitution A G intron_variant LIRI-JP 6 53522062 53522062 single base substitution A G upstream_gene_variant LIRI-JP 6 53528530 53528530 single base substitution T G intron_variant LIRI-JP 6 53530189 53530189 single base substitution A C intron_variant LIRI-JP 6 53530742 53530746 deletion of <=200bp AAAAG - upstream_gene_variant LIRI-JP 6 53531620 53531620 single base substitution G A upstream_gene_variant LIRI-JP 6 53532651 53532651 single base substitution A G upstream_gene_variant LIRI-JP 6 53533217 53533217 single base substitution A G upstream_gene_variant LIRI-JP 6 53533540 53533540 single base substitution T C upstream_gene_variant LUSC-KR 6 53507980 53507980 single base substitution C A downstream_gene_variant LUSC-KR 6 53519563 53519563 single base substitution C G missense_variant E170Q 508G>C LUSC-KR 6 53530793 53530793 single base substitution A G upstream_gene_variant LUSC-KR 6 53530865 53530865 single base substitution A G upstream_gene_variant LUSC-US 6 53517037 53517037 single base substitution A T missense_variant Y422N 1264T>A LUSC-US 6 53517046 53517046 single base substitution C G missense_variant G419R 1255G>C LUSC-US 6 53519311 53519311 single base substitution G T missense_variant L254I 760C>A LUSC-US 6 53519386 53519386 single base substitution A C missense_variant S229A 685T>G MALY-DE 6 53508228 53508228 single base substitution G A downstream_gene_variant MALY-DE 6 53515323 53515323 single base substitution C A 3_prime_UTR_variant MALY-DE 6 53515323 53515323 single base substitution C A downstream_gene_variant MALY-DE 6 53515343 53515343 single base substitution A G 3_prime_UTR_variant MALY-DE 6 53515343 53515343 single base substitution A G downstream_gene_variant MALY-DE 6 53528654 53528654 single base substitution T C intron_variant MALY-DE 6 53528694 53528694 single base substitution T C intron_variant MALY-DE 6 53529406 53529406 single base substitution G A intron_variant MALY-DE 6 53532571 53532571 single base substitution A C upstream_gene_variant MALY-DE 6 53534114 53534114 single base substitution G T upstream_gene_variant MELA-AU 6 53507859 53507859 single base substitution G A downstream_gene_variant MELA-AU 6 53507900 53507900 single base substitution G A downstream_gene_variant MELA-AU 6 53508045 53508045 single base substitution C T downstream_gene_variant MELA-AU 6 53508123 53508123 single base substitution C T downstream_gene_variant MELA-AU 6 53509065 53509065 single base substitution C T downstream_gene_variant MELA-AU 6 53509341 53509341 single base substitution G A downstream_gene_variant MELA-AU 6 53509552 53509552 single base substitution A G downstream_gene_variant MELA-AU 6 53509594 53509594 single base substitution G A downstream_gene_variant MELA-AU 6 53509658 53509658 single base substitution G A downstream_gene_variant MELA-AU 6 53509787 53509787 single base substitution C T downstream_gene_variant MELA-AU 6 53509788 53509788 single base substitution C T downstream_gene_variant MELA-AU 6 53509862 53509862 single base substitution C T downstream_gene_variant MELA-AU 6 53509911 53509911 single base substitution G A downstream_gene_variant MELA-AU 6 53510106 53510106 single base substitution A T downstream_gene_variant MELA-AU 6 53510371 53510371 single base substitution C T downstream_gene_variant MELA-AU 6 53510504 53510504 single base substitution A T downstream_gene_variant MELA-AU 6 53510620 53510620 single base substitution G A downstream_gene_variant MELA-AU 6 53510661 53510661 single base substitution G A downstream_gene_variant MELA-AU 6 53510970 53510970 single base substitution G A downstream_gene_variant MELA-AU 6 53511020 53511020 single base substitution G A downstream_gene_variant MELA-AU 6 53511063 53511063 single base substitution G A downstream_gene_variant MELA-AU 6 53511100 53511100 single base substitution A G downstream_gene_variant MELA-AU 6 53511418 53511418 single base substitution G A downstream_gene_variant MELA-AU 6 53511538 53511538 single base substitution G A downstream_gene_variant MELA-AU 6 53511789 53511789 single base substitution G A downstream_gene_variant MELA-AU 6 53512160 53512160 single base substitution G A downstream_gene_variant MELA-AU 6 53512249 53512270 deletion of <=200bp AGTACTACATTAGATCAAAGGT - downstream_gene_variant MELA-AU 6 53512493 53512493 single base substitution C T downstream_gene_variant MELA-AU 6 53512953 53512953 single base substitution G A 3_prime_UTR_variant MELA-AU 6 53512953 53512953 single base substitution G A downstream_gene_variant MELA-AU 6 53512995 53512995 single base substitution G A 3_prime_UTR_variant MELA-AU 6 53512995 53512995 single base substitution G A downstream_gene_variant MELA-AU 6 53513166 53513166 single base substitution G A 3_prime_UTR_variant MELA-AU 6 53513166 53513166 single base substitution G A downstream_gene_variant MELA-AU 6 53513174 53513174 single base substitution T A 3_prime_UTR_variant MELA-AU 6 53513174 53513174 single base substitution T A downstream_gene_variant MELA-AU 6 53513199 53513199 single base substitution C T 3_prime_UTR_variant MELA-AU 6 53513199 53513199 single base substitution C T downstream_gene_variant MELA-AU 6 53513213 53513213 single base substitution G A 3_prime_UTR_variant MELA-AU 6 53513213 53513213 single base substitution G A downstream_gene_variant MELA-AU 6 53513798 53513798 single base substitution G A 3_prime_UTR_variant MELA-AU 6 53513798 53513798 single base substitution G A downstream_gene_variant MELA-AU 6 53514033 53514033 single base substitution C T 3_prime_UTR_variant MELA-AU 6 53514033 53514033 single base substitution C T downstream_gene_variant MELA-AU 6 53514139 53514139 single base substitution G A 3_prime_UTR_variant MELA-AU 6 53514139 53514139 single base substitution G A downstream_gene_variant MELA-AU 6 53514668 53514668 single base substitution G A 3_prime_UTR_variant MELA-AU 6 53514668 53514668 single base substitution G A downstream_gene_variant MELA-AU 6 53514828 53514828 single base substitution A G 3_prime_UTR_variant MELA-AU 6 53514828 53514828 single base substitution A G downstream_gene_variant MELA-AU 6 53514912 53514912 single base substitution A C 3_prime_UTR_variant MELA-AU 6 53514912 53514912 single base substitution A C downstream_gene_variant MELA-AU 6 53515730 53515730 single base substitution G A 3_prime_UTR_variant MELA-AU 6 53515730 53515730 single base substitution G A downstream_gene_variant MELA-AU 6 53515773 53515773 single base substitution G A 3_prime_UTR_variant MELA-AU 6 53515773 53515773 single base substitution G A downstream_gene_variant MELA-AU 6 53515837 53515837 single base substitution T A 3_prime_UTR_variant MELA-AU 6 53515837 53515837 single base substitution T A downstream_gene_variant MELA-AU 6 53516131 53516131 single base substitution C T 3_prime_UTR_variant MELA-AU 6 53516131 53516131 single base substitution C T downstream_gene_variant MELA-AU 6 53517683 53517683 single base substitution A T intron_variant MELA-AU 6 53517841 53517841 single base substitution T A intron_variant MELA-AU 6 53518324 53518324 single base substitution C T intron_variant MELA-AU 6 53518675 53518675 single base substitution C T intron_variant MELA-AU 6 53519495 53519495 single base substitution C T synonymous_variant Q192Q 576G>A MELA-AU 6 53519959 53519959 single base substitution C T missense_variant E38K 112G>A MELA-AU 6 53520468 53520468 single base substitution G A intron_variant MELA-AU 6 53520468 53520468 single base substitution G A upstream_gene_variant MELA-AU 6 53520485 53520485 single base substitution A G intron_variant MELA-AU 6 53520485 53520485 single base substitution A G upstream_gene_variant MELA-AU 6 53520651 53520651 single base substitution C T intron_variant MELA-AU 6 53520651 53520651 single base substitution C T upstream_gene_variant MELA-AU 6 53520803 53520803 single base substitution G A intron_variant MELA-AU 6 53520803 53520803 single base substitution G A upstream_gene_variant MELA-AU 6 53521086 53521086 single base substitution G A intron_variant MELA-AU 6 53521086 53521086 single base substitution G A upstream_gene_variant MELA-AU 6 53521217 53521217 single base substitution C T intron_variant MELA-AU 6 53521217 53521217 single base substitution C T upstream_gene_variant MELA-AU 6 53521446 53521446 single base substitution G A intron_variant MELA-AU 6 53521446 53521446 single base substitution G A upstream_gene_variant MELA-AU 6 53521754 53521754 single base substitution C T intron_variant MELA-AU 6 53521754 53521754 single base substitution C T upstream_gene_variant MELA-AU 6 53521967 53521967 single base substitution G A intron_variant MELA-AU 6 53521967 53521967 single base substitution G A upstream_gene_variant MELA-AU 6 53522024 53522024 single base substitution A T intron_variant MELA-AU 6 53522024 53522024 single base substitution A T upstream_gene_variant MELA-AU 6 53522408 53522408 single base substitution T G intron_variant MELA-AU 6 53522408 53522408 single base substitution T G upstream_gene_variant MELA-AU 6 53522477 53522477 single base substitution C T intron_variant MELA-AU 6 53522477 53522477 single base substitution C T upstream_gene_variant MELA-AU 6 53522662 53522662 single base substitution C T intron_variant MELA-AU 6 53522662 53522662 single base substitution C T upstream_gene_variant MELA-AU 6 53522859 53522859 single base substitution G A intron_variant MELA-AU 6 53522859 53522859 single base substitution G A upstream_gene_variant MELA-AU 6 53522902 53522902 single base substitution C T intron_variant MELA-AU 6 53522902 53522902 single base substitution C T upstream_gene_variant MELA-AU 6 53523069 53523069 single base substitution C T intron_variant MELA-AU 6 53523069 53523069 single base substitution C T upstream_gene_variant MELA-AU 6 53523268 53523268 single base substitution T A intron_variant MELA-AU 6 53523268 53523268 single base substitution T A upstream_gene_variant MELA-AU 6 53523918 53523918 single base substitution G A intron_variant MELA-AU 6 53523918 53523918 single base substitution G A upstream_gene_variant MELA-AU 6 53524316 53524316 single base substitution G A intron_variant MELA-AU 6 53524316 53524316 single base substitution G A upstream_gene_variant MELA-AU 6 53524389 53524389 single base substitution G A intron_variant MELA-AU 6 53524389 53524389 single base substitution G A upstream_gene_variant MELA-AU 6 53524529 53524529 single base substitution T C intron_variant MELA-AU 6 53524529 53524529 single base substitution T C upstream_gene_variant MELA-AU 6 53524705 53524705 single base substitution C T intron_variant MELA-AU 6 53524705 53524705 single base substitution C T upstream_gene_variant MELA-AU 6 53525437 53525437 single base substitution C T intron_variant MELA-AU 6 53525522 53525522 single base substitution G A intron_variant MELA-AU 6 53525539 53525539 single base substitution G A intron_variant MELA-AU 6 53525636 53525636 single base substitution G A intron_variant MELA-AU 6 53525670 53525670 single base substitution G A intron_variant MELA-AU 6 53526020 53526020 single base substitution A G intron_variant MELA-AU 6 53526628 53526628 single base substitution G A intron_variant MELA-AU 6 53526728 53526728 single base substitution T C intron_variant MELA-AU 6 53526789 53526789 single base substitution C T intron_variant MELA-AU 6 53526949 53526949 single base substitution C T intron_variant MELA-AU 6 53527183 53527183 single base substitution T C intron_variant MELA-AU 6 53527197 53527197 single base substitution G A intron_variant MELA-AU 6 53527248 53527248 single base substitution C T intron_variant MELA-AU 6 53527324 53527324 single base substitution C T intron_variant MELA-AU 6 53527499 53527499 single base substitution C T intron_variant MELA-AU 6 53527601 53527601 single base substitution C T intron_variant MELA-AU 6 53527663 53527663 single base substitution G A intron_variant MELA-AU 6 53528393 53528393 single base substitution G A intron_variant MELA-AU 6 53528817 53528817 single base substitution C T intron_variant MELA-AU 6 53528886 53528886 single base substitution G A intron_variant MELA-AU 6 53529269 53529269 single base substitution G A intron_variant MELA-AU 6 53529330 53529330 single base substitution G A intron_variant MELA-AU 6 53529366 53529366 single base substitution C T intron_variant MELA-AU 6 53529379 53529379 single base substitution G A intron_variant MELA-AU 6 53529400 53529400 single base substitution G T intron_variant MELA-AU 6 53529603 53529603 single base substitution C T intron_variant MELA-AU 6 53530052 53530052 single base substitution C T intron_variant MELA-AU 6 53530079 53530079 single base substitution G A intron_variant MELA-AU 6 53530242 53530242 single base substitution G A intron_variant MELA-AU 6 53530254 53530254 single base substitution G A intron_variant MELA-AU 6 53530350 53530350 single base substitution C T intron_variant MELA-AU 6 53530471 53530471 single base substitution C T 5_prime_UTR_variant MELA-AU 6 53530655 53530655 single base substitution A G upstream_gene_variant MELA-AU 6 53530793 53530793 single base substitution A G upstream_gene_variant MELA-AU 6 53530929 53530929 single base substitution G A upstream_gene_variant MELA-AU 6 53530971 53530971 single base substitution G A upstream_gene_variant MELA-AU 6 53531203 53531203 single base substitution G A upstream_gene_variant MELA-AU 6 53531297 53531297 single base substitution A T upstream_gene_variant MELA-AU 6 53531717 53531717 single base substitution A C upstream_gene_variant MELA-AU 6 53532075 53532075 single base substitution G A upstream_gene_variant MELA-AU 6 53532101 53532101 single base substitution G A upstream_gene_variant MELA-AU 6 53532112 53532112 single base substitution G A upstream_gene_variant MELA-AU 6 53532138 53532138 single base substitution G T upstream_gene_variant MELA-AU 6 53532264 53532264 single base substitution G A upstream_gene_variant MELA-AU 6 53532453 53532453 single base substitution C T upstream_gene_variant MELA-AU 6 53532488 53532488 single base substitution G A upstream_gene_variant MELA-AU 6 53532675 53532675 single base substitution G A upstream_gene_variant MELA-AU 6 53532740 53532740 single base substitution G A upstream_gene_variant MELA-AU 6 53532805 53532805 single base substitution C T upstream_gene_variant MELA-AU 6 53533278 53533278 single base substitution C T upstream_gene_variant MELA-AU 6 53533377 53533377 single base substitution C T upstream_gene_variant MELA-AU 6 53533610 53533610 single base substitution G T upstream_gene_variant MELA-AU 6 53533778 53533778 single base substitution C T upstream_gene_variant MELA-AU 6 53533879 53533879 single base substitution G A upstream_gene_variant MELA-AU 6 53534735 53534735 single base substitution G A upstream_gene_variant MELA-AU 6 53534919 53534919 single base substitution G A upstream_gene_variant MELA-AU 6 53535186 53535186 single base substitution G A upstream_gene_variant MELA-AU 6 53535348 53535348 single base substitution C T upstream_gene_variant MELA-AU 6 53535432 53535432 single base substitution T A upstream_gene_variant ORCA-IN 6 53516636 53516636 single base substitution C G synonymous_variant V555V 1665G>C ORCA-IN 6 53516896 53516896 single base substitution G T missense_variant L469M 1405C>A ORCA-IN 6 53520113 53520113 deletion of <=200bp G - intron_variant ORCA-IN 6 53520113 53520113 deletion of <=200bp G - upstream_gene_variant OV-AU 6 53508117 53508117 single base substitution A G downstream_gene_variant OV-AU 6 53515713 53515713 single base substitution T A 3_prime_UTR_variant OV-AU 6 53515713 53515713 single base substitution T A downstream_gene_variant OV-AU 6 53516789 53516789 single base substitution G A synonymous_variant G504G 1512C>T OV-AU 6 53521874 53521874 single base substitution G A intron_variant OV-AU 6 53521874 53521874 single base substitution G A upstream_gene_variant OV-AU 6 53522737 53522737 single base substitution C A intron_variant OV-AU 6 53522737 53522737 single base substitution C A upstream_gene_variant OV-AU 6 53532336 53532336 single base substitution A G upstream_gene_variant PACA-AU 6 53507977 53507977 single base substitution T C downstream_gene_variant PACA-AU 6 53515178 53515178 single base substitution A T 3_prime_UTR_variant PACA-AU 6 53515178 53515178 single base substitution A T downstream_gene_variant PACA-AU 6 53515413 53515413 single base substitution G A 3_prime_UTR_variant PACA-AU 6 53515413 53515413 single base substitution G A downstream_gene_variant PACA-AU 6 53524094 53524094 deletion of <=200bp A - intron_variant PACA-AU 6 53524094 53524094 deletion of <=200bp A - upstream_gene_variant PACA-AU 6 53531702 53531702 single base substitution G A upstream_gene_variant PACA-AU 6 53532692 53532692 single base substitution G A upstream_gene_variant PACA-CA 6 53509036 53509036 single base substitution G A downstream_gene_variant PACA-CA 6 53512078 53512078 single base substitution C T downstream_gene_variant PACA-CA 6 53514386 53514386 single base substitution T C 3_prime_UTR_variant PACA-CA 6 53514386 53514386 single base substitution T C downstream_gene_variant PACA-CA 6 53516246 53516246 single base substitution A T 3_prime_UTR_variant PACA-CA 6 53516246 53516246 single base substitution A T downstream_gene_variant PACA-CA 6 53516937 53516937 single base substitution G A missense_variant A455V 1364C>T PACA-CA 6 53519206 53519206 single base substitution C T missense_variant V289I 865G>A PACA-CA 6 53519717 53519717 single base substitution T C synonymous_variant P118P 354A>G PACA-CA 6 53520585 53520585 single base substitution G C intron_variant PACA-CA 6 53520585 53520585 single base substitution G C upstream_gene_variant PACA-CA 6 53524614 53524614 single base substitution G A intron_variant PACA-CA 6 53524614 53524614 single base substitution G A upstream_gene_variant PACA-CA 6 53525574 53525595 deletion of <=200bp CACTGCCCTCCAGCCTGGGCAA - intron_variant PACA-CA 6 53525669 53525669 single base substitution C T intron_variant PACA-CA 6 53526587 53526587 single base substitution A T intron_variant PACA-CA 6 53531112 53531112 single base substitution C T upstream_gene_variant PACA-CA 6 53535268 53535268 single base substitution G T upstream_gene_variant PAEN-AU 6 53530964 53530964 single base substitution G C upstream_gene_variant PAEN-IT 6 53523914 53523914 single base substitution G T intron_variant PAEN-IT 6 53523914 53523914 single base substitution G T upstream_gene_variant PBCA-DE 6 53530564 53530564 single base substitution C T upstream_gene_variant PBCA-DE 6 53532525 53532525 single base substitution T C upstream_gene_variant PRAD-UK 6 53518250 53518250 single base substitution G T intron_variant PRAD-UK 6 53532367 53532367 single base substitution G A upstream_gene_variant READ-US 6 53516876 53516876 single base substitution T G synonymous_variant I475I 1425A>C READ-US 6 53517004 53517005 deletion of <=200bp GG - frameshift_variant SL432 READ-US 6 53517006 53517006 insertion of <=200bp - T frameshift_variant S432R? READ-US 6 53519148 53519148 single base substitution C T missense_variant R308Q 923G>A READ-US 6 53519457 53519457 single base substitution G A missense_variant S205L 614C>T READ-US 6 53519561 53519561 single base substitution C T synonymous_variant E170E 510G>A READ-US 6 53519662 53519662 single base substitution A G synonymous_variant L137L 409T>C RECA-EU 6 53509440 53509440 single base substitution G A downstream_gene_variant RECA-EU 6 53509545 53509545 single base substitution T C downstream_gene_variant RECA-EU 6 53514207 53514207 single base substitution T C 3_prime_UTR_variant RECA-EU 6 53514207 53514207 single base substitution T C downstream_gene_variant RECA-EU 6 53530773 53530773 single base substitution A G upstream_gene_variant SKCA-BR 6 53507786 53507786 single base substitution C T downstream_gene_variant SKCA-BR 6 53508983 53508983 single base substitution G A downstream_gene_variant SKCA-BR 6 53509651 53509651 single base substitution C T downstream_gene_variant SKCA-BR 6 53511010 53511010 single base substitution G A downstream_gene_variant SKCA-BR 6 53516641 53516641 single base substitution C T missense_variant G554R 1660G>A SKCA-BR 6 53516797 53516797 single base substitution G A missense_variant P502S 1504C>T SKCA-BR 6 53518135 53518135 single base substitution T A intron_variant SKCA-BR 6 53518955 53518955 single base substitution A C synonymous_variant G372G 1116T>G SKCA-BR 6 53523337 53523337 single base substitution G C intron_variant SKCA-BR 6 53523337 53523337 single base substitution G C upstream_gene_variant SKCA-BR 6 53523826 53523826 single base substitution G A intron_variant SKCA-BR 6 53523826 53523826 single base substitution G A upstream_gene_variant SKCA-BR 6 53528837 53528837 single base substitution C T intron_variant SKCA-BR 6 53530777 53530777 insertion of <=200bp - GGAAAGAAA upstream_gene_variant SKCA-BR 6 53530865 53530865 single base substitution A G upstream_gene_variant SKCA-BR 6 53532860 53532860 single base substitution G A upstream_gene_variant SKCA-BR 6 53533149 53533149 single base substitution G A upstream_gene_variant SKCA-BR 6 53534364 53534364 single base substitution G A upstream_gene_variant SKCA-BR 6 53534365 53534365 single base substitution G A upstream_gene_variant SKCA-BR 6 53535173 53535173 single base substitution G A upstream_gene_variant SKCM-US 6 53517009 53517009 single base substitution C T missense_variant G431E 1292G>A SKCM-US 6 53519023 53519023 single base substitution C T missense_variant E350K 1048G>A SKCM-US 6 53519041 53519041 single base substitution C T missense_variant G344R 1030G>A SKCM-US 6 53519078 53519078 single base substitution G A synonymous_variant S331S 993C>T SKCM-US 6 53519241 53519241 single base substitution C T missense_variant R277K 830G>A SKCM-US 6 53519485 53519485 single base substitution G A missense_variant R196W 586C>T SKCM-US 6 53519576 53519576 single base substitution C T synonymous_variant R165R 495G>A SKCM-US 6 53519615 53519615 single base substitution G A synonymous_variant I152I 456C>T SKCM-US 6 53519768 53519768 single base substitution G A synonymous_variant I101I 303C>T SKCM-US 6 53519866 53519866 single base substitution C T missense_variant E69K 205G>A SKCM-US 6 53519959 53519959 single base substitution C T missense_variant E38K 112G>A SKCM-US 6 53520004 53520004 single base substitution C T missense_variant E23K 67G>A STAD-US 6 53516493 53516493 single base substitution G A missense_variant A603V 1808C>T STAD-US 6 53516564 53516566 deletion of <=200bp CTT - inframe_deletion K579 STAD-US 6 53516915 53516915 single base substitution C G synonymous_variant A462A 1386G>C STAD-US 6 53519514 53519514 insertion of <=200bp - T frameshift_variant N186K? STAD-US 6 53519759 53519759 insertion of <=200bp - T frameshift_variant K104K? STAD-US 6 53519830 53519830 single base substitution T G missense_variant T81P 241A>C UCEC-US 6 53516539 53516539 single base substitution T G missense_variant S588R 1762A>C UCEC-US 6 53519100 53519100 single base substitution C T missense_variant R324H 971G>A UCEC-US 6 53519187 53519187 single base substitution T C missense_variant H295R 884A>G UCEC-US 6 53519255 53519255 single base substitution A G synonymous_variant V272V 816T>C UCEC-US 6 53519485 53519485 single base substitution G A missense_variant R196W 586C>T UCEC-US 6 53519561 53519561 single base substitution C A missense_variant E170D 510G>T UCEC-US 6 53519578 53519578 single base substitution G A missense_variant R165W 493C>T UCEC-US 6 53519933 53519933 single base substitution A C missense_variant I46M 138T>G

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand AOCS-001-1-7 COSM4153539 c.1512C>T p.G504G Substitution - coding silent 6:53651991-53651991 - TCGA-E2-A1IF-01 COSM1487851 c.662T>G p.I221R Substitution - Missense 6:53654611-53654611 - PCSI_0230_Pa_P_526 COSM4966017 c.865G>A p.V289I Substitution - Missense 6:53654408-53654408 - sysucc-1397T COSM5474960 c.1018G>A p.D340N Substitution - Missense 6:53654255-53654255 - BD179T COSM5499828 c.275C>A p.A92D Substitution - Missense 6:53654998-53654998 - CRC-03T COSM5451873 c.955G>A p.V319I Substitution - Missense 6:53654318-53654318 - TCGA-AN-A046-01 COSM1080343 c.493C>T p.R165W Substitution - Missense 6:53654780-53654780 - PT52 COSM5939547 c.751G>A p.A251T Substitution - Missense 6:53654522-53654522 - ccRCC-23 COSM1662509 c.892C>A p.P298T Substitution - Missense 6:53654381-53654381 - C13 COSM3430759 c.614C>T p.S205L Substitution - Missense 6:53654659-53654659 - 587228 COSM1212643 c.199C>T p.R67W Substitution - Missense 6:53655074-53655074 - TCGA-AX-A05Z-01 COSM1080340 c.816T>C p.V272V Substitution - coding silent 6:53654457-53654457 - CRC-06T COSM5457273 c.1685C>T p.A562V Substitution - Missense 6:53651818-53651818 - C391 COSM4441824 c.1784C>T p.T595M Substitution - Missense 6:53651719-53651719 - TCGA-F5-6814-01 COSM3430760 c.510G>A p.E170E Substitution - coding silent 6:53654763-53654763 - ESO-0023 COSM1255979 c.414T>C p.Y138Y Substitution - coding silent 6:53654859-53654859 - TCGA-CJ-4644-01 COSM1137548 c.1883C>A p.S628Y Substitution - Missense 6:53651620-53651620 - ESCC_54 COSM5631574 c.829delA p.R277fs*2 Deletion - Frameshift 6:53654444-53654444 - Au9 COSM5607471 c.213C>T p.F71F Substitution - coding silent 6:53655060-53655060 - TCGA-F5-6464-01 COSM5826374 c.1296_1297delCC p.L433fs*28 Deletion - Frameshift 6:53652206-53652207 - Z138 COSM1739238 c.878A>G p.N293S Substitution - Missense 6:53654395-53654395 - I2L-P19Ta-Tumor-Biopsy COSM3355395 c.557delA p.N186fs*24 Deletion - Frameshift 6:53654716-53654716 - SH-0622 COSM1445208 c.312delA p.D105fs*15 Deletion - Frameshift 6:53654961-53654961 - NOKSI COSM4596269 c.868G>A p.D290N Substitution - Missense 6:53654405-53654405 - HCC64 COSM1621772 c.1580G>T p.G527V Substitution - Missense 6:53651923-53651923 - Pat_01_B COSM5870921 c.494G>A p.R165Q Substitution - Missense 6:53654779-53654779 - Pat_07_A COSM5870920 c.835A>G p.M279V Substitution - Missense 6:53654438-53654438 - N459T COSM236468 c.427A>T p.I143F Substitution - Missense 6:53654846-53654846 - SNU-C4 COSM4654118 c.1521C>T p.C507C Substitution - coding silent 6:53651982-53651982 - TCGA-F5-6814-01 COSM3430761 c.409T>C p.L137L Substitution - coding silent 6:53654864-53654864 - TCGA-EE-A3JA-06 COSM3628561 c.456C>T p.I152I Substitution - coding silent 6:53654817-53654817 - ORL-48 COSM4596565 c.1279C>A p.R427S Substitution - Missense 6:53652224-53652224 - TCGA-EE-A181-06 COSM3628559 c.1292G>A p.G431E Substitution - Missense 6:53652211-53652211 - TCGA-FW-A3R5-06 COSM3921977 c.67G>A p.E23K Substitution - Missense 6:53655206-53655206 - TCGA-60-2726-01 COSM742503 c.685T>G p.S229A Substitution - Missense 6:53654588-53654588 - LS411 COSM4614556 c.79_80insC p.L27fs*18 Insertion - Frameshift 6:53655193-53655194 - LUAD-F00368 COSM367735 c.1573C>A p.P525T Substitution - Missense 6:53651930-53651930 - TCGA-AA-3662-01 COSM3749983 c.1425A>C p.I475I Substitution - coding silent 6:53652078-53652078 - LUAD-E01014 COSM394037 c.536C>T p.A179V Substitution - Missense 6:53654737-53654737 - TCGA-BR-6452-01 COSM3874817 c.241A>C p.T81P Substitution - Missense 6:53655032-53655032 - RK136_C01 COSM3745299 c.957C>T p.V319V Substitution - coding silent 6:53654316-53654316 - TCGA-G4-6302-01 COSM3749983 c.1425A>C p.I475I Substitution - coding silent 6:53652078-53652078 - SJHGG102_D COSM4969919 c.661_662delAT p.I221fs*2 Deletion - Frameshift 6:53654611-53654612 - TCGA-DC-6681-01 COSM3749983 c.1425A>C p.I475I Substitution - coding silent 6:53652078-53652078 - TCGA-HU-A4H0-01 COSM3874816 c.1386G>C p.A462A Substitution - coding silent 6:53652117-53652117 - ESCC_122 COSM5640793 c.1509G>T p.R503R Substitution - coding silent 6:53651994-53651994 - TCGA-B5-A0K9-01 COSM1080337 c.1360G>A p.V454M Substitution - Missense 6:53652143-53652143 - TCGA-C8-A26Y-01 COSM3830783 c.627G>C p.M209I Substitution - Missense 6:53654646-53654646 - HT115 COSM3355392 c.771T>C p.N257N Substitution - coding silent 6:53654502-53654502 - ESCC_BICR_047T COSM5430450 c.1684G>A p.A562T Substitution - Missense 6:53651819-53651819 - HCC5T COSM3662627 c.1018G>C p.D340H Substitution - Missense 6:53654255-53654255 - TCGA-BS-A0UV-01 COSM1080342 c.510G>T p.E170D Substitution - Missense 6:53654763-53654763 - TCGA-BR-4184-01 COSM3355376 c.1808C>T p.A603V Substitution - Missense 6:53651695-53651695 - TCGA-24-2298-01 COSM78974 c.1072C>T p.Q358* Substitution - Nonsense 6:53654201-53654201 - TCGA-EE-A3AF-06 COSM3921976 c.830G>A p.R277K Substitution - Missense 6:53654443-53654443 - PTC-7C COSM3749983 c.1425A>C p.I475I Substitution - coding silent 6:53652078-53652078 - TCGA-D3-A51R-06 COSM3628560 c.1048G>A p.E350K Substitution - Missense 6:53654225-53654225 - TCGA-GF-A6C9-06 COSM4900380 c.303C>T p.I101I Substitution - coding silent 6:53654970-53654970 - TCGA-F5-6464-01 COSM5826375 c.1294_1295insA p.S432fs*30 Insertion - Frameshift 6:53652208-53652209 - TCGA-IR-A3LA-01 COSM4845468 c.325C>G p.Q109E Substitution - Missense 6:53654948-53654948 - TCGA-AA-3697-01 COSM3749983 c.1425A>C p.I475I Substitution - coding silent 6:53652078-53652078 - Pat_07_B COSM5870920 c.835A>G p.M279V Substitution - Missense 6:53654438-53654438 - TCGA-F5-6814-01 COSM3430759 c.614C>T p.S205L Substitution - Missense 6:53654659-53654659 - HX29T COSM3662628 c.772A>G p.I258V Substitution - Missense 6:53654501-53654501 - BK0004 COSM4185519 c.1771C>T p.L591F Substitution - Missense 6:53651732-53651732 - S02139 COSM5674570 c.199C>A p.R67R Substitution - coding silent 6:53655074-53655074 - TCGA-AA-A01Z-01 COSM300421 c.750C>T p.Y250Y Substitution - coding silent 6:53654523-53654523 - MX02 COSM5759581 c.372C>T p.V124V Substitution - coding silent 6:53654901-53654901 - TCGA-FW-A3R5-06 COSM3921975 c.993C>T p.S331S Substitution - coding silent 6:53654280-53654280 - TCGA-EE-A3JA-06 COSM1080341 c.586C>T p.R196W Substitution - Missense 6:53654687-53654687 - TCGA-GV-A3JZ-01 COSM1312310 c.1719G>A p.W573* Substitution - Nonsense 6:53651784-53651784 - TCGA-AX-A06H-01 COSM1080343 c.493C>T p.R165W Substitution - Missense 6:53654780-53654780 - T3658 COSM3355395 c.557delA p.N186fs*24 Deletion - Frameshift 6:53654716-53654716 - TCGA-F5-6702-01 COSM3749983 c.1425A>C p.I475I Substitution - coding silent 6:53652078-53652078 - HCC120T COSM3662629 c.553A>T p.K185* Substitution - Nonsense 6:53654720-53654720 - TCGA-DD-A1EL-01 COSM4925947 c.1209C>A p.A403A Substitution - coding silent 6:53652294-53652294 - HSJD_DIPG001 COSM4746160 c.210C>A p.N70K Substitution - Missense 6:53655063-53655063 - RKO COSM3355395 c.557delA p.N186fs*24 Deletion - Frameshift 6:53654716-53654716 - Pat_36_B COSM1445208 c.312delA p.D105fs*15 Deletion - Frameshift 6:53654961-53654961 - TCGA-22-5485-01 COSM742504 c.760C>A p.L254I Substitution - Missense 6:53654513-53654513 - TCGA-A5-A0G9-01 COSM1080339 c.884A>G p.H295R Substitution - Missense 6:53654389-53654389 - 587376 COSM1080341 c.586C>T p.R196W Substitution - Missense 6:53654687-53654687 - RMS111_ COSM1312311 c.1541G>C p.R514T Substitution - Missense 6:53651962-53651962 - TCGA-GV-A3JZ-01 COSM1312311 c.1541G>C p.R514T Substitution - Missense 6:53651962-53651962 - SK-MEL-2 COSM1672508 c.868G>T p.D290Y Substitution - Missense 6:53654405-53654405 - SNUH_G76_S1 COSM3762137 c.1266C>T p.Y422Y Substitution - coding silent 6:53652237-53652237 - TCGA-AF-2693-01 COSM3749983 c.1425A>C p.I475I Substitution - coding silent 6:53652078-53652078 - TCGA-EE-A2MR-06 COSM3628562 c.205G>A p.E69K Substitution - Missense 6:53655068-53655068 - TCGA-BS-A0UV-01 COSM1080341 c.586C>T p.R196W Substitution - Missense 6:53654687-53654687 - TCGA-21-5786-01 COSM742506 c.1264T>A p.Y422N Substitution - Missense 6:53652239-53652239 - 2237 COSM1644719 c.740G>C p.R247T Substitution - Missense 6:53654533-53654533 - TCGA-G4-6311-01 COSM3749983 c.1425A>C p.I475I Substitution - coding silent 6:53652078-53652078 - HCC5 COSM3662627 c.1018G>C p.D340H Substitution - Missense 6:53654255-53654255 - YUOTHO COSM5405581 c.714G>A p.M238I Substitution - Missense 6:53654559-53654559 - TCGA-EE-A3AA-06 COSM3628563 c.112G>A p.E38K Substitution - Missense 6:53655161-53655161 - HCA7 COSM4631129 c.1577G>A p.R526H Substitution - Missense 6:53651926-53651926 - I2L-P25-Tumor-Organoid COSM5357570 c.1432G>T p.A478S Substitution - Missense 6:53652071-53652071 - TCGA-29-1768-01 COSM1329624 c.1094G>A p.G365E Substitution - Missense 6:53654179-53654179 - TCGA-AN-A0AK-01 COSM3830785 c.186T>C p.G62G Substitution - coding silent 6:53655087-53655087 - MX02 COSM5759582 c.228C>G p.V76V Substitution - coding silent 6:53655045-53655045 - BD119T COSM5520876 c.1179T>A p.D393E Substitution - Missense 6:53652324-53652324 - TCGA-FW-A3R5-06 COSM3921974 c.1030G>A p.G344R Substitution - Missense 6:53654243-53654243 - MT-439-T2 COSM5651554 c.1392C>T p.A464A Substitution - coding silent 6:53652111-53652111 - TCGA-D5-6926-01 COSM1445206 c.1047G>A p.T349T Substitution - coding silent 6:53654226-53654226 - BD245T COSM5519986 c.1789G>T p.D597Y Substitution - Missense 6:53651714-53651714 - TCGA-CK-4950-01 COSM3749983 c.1425A>C p.I475I Substitution - coding silent 6:53652078-53652078 - J90_T COSM3949339 c.508G>C p.E170Q Substitution - Missense 6:53654765-53654765 - PR-1024 COSM242554 c.193A>G p.K65E Substitution - Missense 6:53655080-53655080 - TCGA-AM-5821-01 COSM3762137 c.1266C>T p.Y422Y Substitution - coding silent 6:53652237-53652237 - TCGA-B0-5692-01 COSM484211 c.1110C>T p.A370A Substitution - coding silent 6:53654163-53654163 - ESCC_BICR_020T COSM5429253 c.1791C>T p.D597D Substitution - coding silent 6:53651712-53651712 - TCGA-BH-A18G-01 COSM3830784 c.551T>C p.L184P Substitution - Missense 6:53654722-53654722 - 9227_T COSM5039459 c.872C>T p.A291V Substitution - Missense 6:53654401-53654401 - PR-3035 COSM245318 c.692T>C p.I231T Substitution - Missense 6:53654581-53654581 - YUGURT COSM5405580 c.1099C>T p.L367F Substitution - Missense 6:53654174-53654174 - sysucc-1317T COSM5450275 c.1098T>C p.F366F Substitution - coding silent 6:53654175-53654175 - TCGA-66-2754-01 COSM742505 c.1255G>C p.G419R Substitution - Missense 6:53652248-53652248 - ACINAR28 COSM1734861 c.748T>C p.Y250H Substitution - Missense 6:53654525-53654525 - TCGA-BS-A0UV-01 COSM1080336 c.1762A>C p.S588R Substitution - Missense 6:53651741-53651741 - TCGA-BQ-5894-01 COSM3995063 c.1288G>A p.E430K Substitution - Missense 6:53652215-53652215 - MX02 COSM5759580 c.434C>T p.S145F Substitution - Missense 6:53654839-53654839 - pfg122T COSM4755412 c.137T>A p.I46N Substitution - Missense 6:53655136-53655136 - LIM1899 COSM4640733 c.1334A>G p.Q445R Substitution - Missense 6:53652169-53652169 - TCGA-AX-A0J1-01 COSM1080338 c.971G>A p.R324H Substitution - Missense 6:53654302-53654302 - HCC120 COSM3662629 c.553A>T p.K185* Substitution - Nonsense 6:53654720-53654720 - WA40 COSM240427 c.1001G>C p.R334T Substitution - Missense 6:53654272-53654272 - ESO-0129 COSM1255980 c.64G>A p.V22I Substitution - Missense 6:53655209-53655209 - TCGA-RP-A695-06 COSM4896854 c.495G>A p.R165R Substitution - coding silent 6:53654778-53654778 - DN1401F COSM5960881 c.929G>C p.R310T Substitution - Missense 6:53654344-53654344 - TCGA-BP-5010-01 COSM484212 c.14A>T p.K5M Substitution - Missense 6:53655259-53655259 - OSCC-GB_01050111 COSM4889882 c.1665G>C p.V555V Substitution - coding silent 6:53651838-53651838 - 49M COSM5591559 c.175C>T p.L59F Substitution - Missense 6:53655098-53655098 - pfg016T COSM1643112 c.384C>A p.A128A Substitution - coding silent 6:53654889-53654889 - PCSI_0139_Pa_X COSM3381631 c.354A>G p.P118P Substitution - coding silent 6:53654919-53654919 - TCGA-A6-5667-01 COSM3749983 c.1425A>C p.I475I Substitution - coding silent 6:53652078-53652078 - TCGA-CK-5916-01 COSM1445207 c.922C>T p.R308* Substitution - Nonsense 6:53654351-53654351 - HCC123T COSM5816877 c.1475C>G p.S492W Substitution - Missense 6:53652028-53652028 - TCGA-AP-A056-01 COSM1080344 c.138T>G p.I46M Substitution - Missense 6:53655135-53655135 - HCC64T COSM1621772 c.1580G>T p.G527V Substitution - Missense 6:53651923-53651923 - OSCC-GB_00600111 COSM4890333 c.1405C>A p.L469M Substitution - Missense 6:53652098-53652098 - TCGA-AN-A046-01 COSM3830782 c.627G>T p.M209I Substitution - Missense 6:53654646-53654646 - TCGA-EI-6917-01 COSM3430758 c.923G>A p.R308Q Substitution - Missense 6:53654350-53654350 - I2L-P19Ta-Tumor-Organoid COSM3355395 c.557delA p.N186fs*24 Deletion - Frameshift 6:53654716-53654716 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.131057;Hs.131064 6p12.1 610749

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C 3-UTRSNV . c.1902+2567T>G 6 53513832 HC A C 3-UTRSNV . c.1902+2580T>G 6 53513819 HC A C Missense p.I221R c.662T>G 6 53519409 BRCA A C Missense p.S229A c.685T>G 6 53519386 LUSC - A Frameshift p.N28Kfs*17 c.80dupT 6 53519991 LUAD A G Missense p.L533P c.1598T>C 6 53516703 HNSC A G Synonymous p.Y138Y c.414T>C 6 53519657 ESCA A T Missense p.Y422N c.1264T>A 6 53517037 LUSC C A Missense p.R456L c.1367G>T 6 53516934 LUAD C G Missense p.G419R c.1255G>C 6 53517046 LUSC C G Missense p.R514T c.1541G>C 6 53516760 BLCA C T Missense p.E38K c.112G>A 6 53519959 CM C T Missense p.G431E c.1292G>A 6 53517009 CM C T Missense p.R196Q c.587G>A 6 53519484 BRCA C T Missense p.R277K c.830G>A 6 53519241 CM C T Missense p.V22I c.64G>A 6 53520007 ESCA C T Nonsense p.W573* c.1719G>A 6 53516582 BLCA G A Missense p.A126V c.377C>T 6 53519694 HNSC G A Missense p.R165W c.493C>T 6 53519578 UCEC G A Missense p.R196W c.586C>T 6 53519485 CM G A Missense p.R324C c.970C>T 6 53519101 HNSC G A Nonsense p.Q358* c.1072C>T 6 53518999 OV G A Synonymous p.F71F c.213C>T 6 53519858 CM G A Synonymous p.I152I c.456C>T 6 53519615 CM G A Synonymous p.I21I c.63C>T 6 53520008 CM G A Synonymous p.I336I c.1008C>T 6 53519063 CM G A Synonymous p.P394P c.1182C>T 6 53517119 CM G A Synonymous p.Y250Y c.750C>T 6 53519321 COREAD G - Frameshift p.E590Sfs*29 c.1767delC 6 53516534 HNSC G T Missense p.L254I c.760C>A 6 53519311 LUSC G T Missense p.S628Y c.1883C>A 6 53516418 RCCC G T Synonymous p.A128A c.384C>A 6 53519687 STAD T A Missense p.K5M c.14A>T 6 53520057 RCCC T C 3-UTRSNV . c.1902+2925A>G 6 53513474 HC T C Missense p.H295R c.884A>G 6 53519187 UCEC T C Missense p.K249R c.746A>G 6 53519325 HNSC T C Synonymous p.K29K c.87A>G 6 53519984 LUAD T - Frameshift p.N186Mfs*24 c.557delA 6 53519514 STAD T G Missense p.K354Q c.1060A>C 6 53519011 LUAD