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 15 31217483 31217483 + Missense_Mutation SNP G G T TCGA-OR-A5JA-01A-11D-A29I-10 TCGA-OR-A5JA-10A-01D-A29L-10 g.chr15:31217483G>T c.2326G>T c.(2326-2328)Gat>Tat p.D776Y BLCA 15 31197051 31197051 + Missense_Mutation SNP A A G TCGA-GU-A42R-01A-11D-A23M-08 TCGA-GU-A42R-10A-01D-A23K-08 g.chr15:31197051A>G c.185A>G c.(184-186)gAa>gGa p.E62G BLCA 15 31197389 31197389 + Nonsense_Mutation SNP G G T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr15:31197389G>T c.523G>T c.(523-525)Gaa>Taa p.E175* BLCA 15 31197412 31197412 + Missense_Mutation SNP G G C TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr15:31197412G>C c.546G>C c.(544-546)caG>caC p.Q182H BLCA 15 31197525 31197525 + Missense_Mutation SNP C C G TCGA-DK-A3IT-01A-31D-A20D-08 TCGA-DK-A3IT-10A-01D-A20D-08 g.chr15:31197525C>G c.659C>G c.(658-660)tCt>tGt p.S220C BLCA 15 31197824 31197824 + Missense_Mutation SNP G G C TCGA-DK-AA6L-01A-11D-A391-08 TCGA-DK-AA6L-10A-01D-A394-08 g.chr15:31197824G>C c.958G>C c.(958-960)Gag>Cag p.E320Q BLCA 15 31197966 31197966 + Missense_Mutation SNP G G A TCGA-FD-A3B4-01A-12D-A202-08 TCGA-FD-A3B4-10A-01D-A202-08 g.chr15:31197966G>A c.1100G>A c.(1099-1101)gGt>gAt p.G367D BLCA 15 31210496 31210496 + Silent SNP G G A TCGA-FD-A6TA-01A-12D-A339-08 TCGA-FD-A6TA-10A-21D-A339-08 g.chr15:31210496G>A c.1941G>A c.(1939-1941)ctG>ctA p.L647L BRCA 15 31197787 31197788 + Frame_Shift_Del DEL TG TG - TCGA-BH-A0DP-01A-21W-A071-09 TCGA-BH-A0DP-10A-01W-A071-09 g.chr15:31197787_31197788delTG c.921_922delTG c.(919-924)actgttfs p.V308fs BRCA 15 31197852 31197852 + Missense_Mutation SNP A A T TCGA-AC-A3QP-01A-11D-A22X-09 TCGA-AC-A3QP-10B-01D-A22X-09 g.chr15:31197852A>T c.986A>T c.(985-987)gAt>gTt p.D329V BRCA 15 31206233 31206233 + Missense_Mutation SNP T T A TCGA-A2-A1G4-01A-11D-A13L-09 TCGA-A2-A1G4-10A-01W-A14R-09 g.chr15:31206233T>A c.1750T>A c.(1750-1752)Ttt>Att p.F584I BRCA 15 31206241 31206241 + Missense_Mutation SNP T T G TCGA-E2-A570-01A-11D-A29N-09 TCGA-E2-A570-10A-01D-A29N-09 g.chr15:31206241T>G c.1758T>G c.(1756-1758)agT>agG p.S586R BRCA 15 31212838 31212838 + Missense_Mutation SNP G G C TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr15:31212838G>C c.2034G>C c.(2032-2034)caG>caC p.Q678H BRCA 15 31229326 31229326 + Missense_Mutation SNP T T G TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr15:31229326T>G c.2921T>G c.(2920-2922)gTg>gGg p.V974G BRCA 15 31229382 31229382 + Missense_Mutation SNP G G A TCGA-D8-A1J8-01A-11D-A13L-09 TCGA-D8-A1J8-10A-01D-A13O-09 g.chr15:31229382G>A c.2977G>A c.(2977-2979)Gaa>Aaa p.E993K BRCA 15 31229401 31229401 + Frame_Shift_Del DEL C C - TCGA-A2-A04U-01A-11D-A10Y-09 TCGA-A2-A04U-10A-01D-A110-09 g.chr15:31229401delC c.2996delC c.(2995-2997)gctfs p.A999fs CESC 15 31197287 31197287 + Missense_Mutation SNP G G A TCGA-C5-A1MH-01A-11D-A14W-08 TCGA-C5-A1MH-10A-01D-A14W-08 g.chr15:31197287G>A c.421G>A c.(421-423)Gag>Aag p.E141K CESC 15 31197561 31197561 + Missense_Mutation SNP G G A TCGA-DS-A0VM-01A-11D-A10S-08 TCGA-DS-A0VM-10A-01D-A10S-08 g.chr15:31197561G>A c.695G>A c.(694-696)aGa>aAa p.R232K CESC 15 31197563 31197563 + Nonsense_Mutation SNP G G T TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr15:31197563G>T c.697G>T c.(697-699)Gga>Tga p.G233* CESC 15 31221463 31221463 + Missense_Mutation SNP G G C TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr15:31221463G>C c.2650G>C c.(2650-2652)Gag>Cag p.E884Q COAD 15 31197140 31197140 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr15:31197140G>A c.274G>A c.(274-276)Gtt>Att p.V92I COAD 15 31197239 31197239 + Missense_Mutation SNP A A G TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr15:31197239A>G c.373A>G c.(373-375)Atc>Gtc p.I125V COAD 15 31197830 31197830 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr15:31197830A>C c.964A>C c.(964-966)Aaa>Caa p.K322Q COAD 15 31197927 31197927 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:31197927G>A c.1061G>A c.(1060-1062)aGc>aAc p.S354N COAD 15 31198087 31198087 + Missense_Mutation SNP T T G TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr15:31198087T>G c.1221T>G c.(1219-1221)ttT>ttG p.F407L COAD 15 31200380 31200380 + Missense_Mutation SNP A A G TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:31200380A>G c.1294A>G c.(1294-1296)Acc>Gcc p.T432A COAD 15 31206063 31206063 + Missense_Mutation SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr15:31206063C>T c.1580C>T c.(1579-1581)gCc>gTc p.A527V COAD 15 31206141 31206141 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:31206141C>T c.1658C>T c.(1657-1659)tCg>tTg p.S553L COAD 15 31214475 31214475 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:31214475G>T c.2090G>T c.(2089-2091)aGa>aTa p.R697I COAD 15 31217359 31217359 + Silent SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr15:31217359G>A c.2202G>A c.(2200-2202)gcG>gcA p.A734A COAD 15 31217427 31217427 + Missense_Mutation SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr15:31217427C>T c.2270C>T c.(2269-2271)cCg>cTg p.P757L COAD 15 31217463 31217463 + Missense_Mutation SNP T T C TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr15:31217463T>C c.2306T>C c.(2305-2307)cTc>cCc p.L769P COAD 15 31221463 31221463 + Missense_Mutation SNP G G A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr15:31221463G>A c.2650G>A c.(2650-2652)Gag>Aag p.E884K COAD 15 31221469 31221469 + Missense_Mutation SNP A A G TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr15:31221469A>G c.2656A>G c.(2656-2658)Agg>Ggg p.R886G COAD 15 31221527 31221527 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:31221527C>T c.2714C>T c.(2713-2715)aCg>aTg p.T905M COAD 15 31222790 31222790 + Silent SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr15:31222790C>T c.2832C>T c.(2830-2832)tgC>tgT p.C944C COAD 15 31229421 31229421 + Missense_Mutation SNP G G A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr15:31229421G>A c.3016G>A c.(3016-3018)Gtg>Atg p.V1006M COADREAD 15 31197140 31197140 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr15:31197140G>A c.274G>A c.(274-276)Gtt>Att p.V92I COADREAD 15 31197154 31197154 + Silent SNP T T C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:31197154T>C c.288T>C c.(286-288)gaT>gaC p.D96D COADREAD 15 31197239 31197239 + Missense_Mutation SNP A A G TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr15:31197239A>G c.373A>G c.(373-375)Atc>Gtc p.I125V COADREAD 15 31197830 31197830 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr15:31197830A>C c.964A>C c.(964-966)Aaa>Caa p.K322Q COADREAD 15 31197927 31197927 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:31197927G>A c.1061G>A c.(1060-1062)aGc>aAc p.S354N COADREAD 15 31198087 31198087 + Missense_Mutation SNP T T G TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr15:31198087T>G c.1221T>G c.(1219-1221)ttT>ttG p.F407L COADREAD 15 31200380 31200380 + Missense_Mutation SNP A A G TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr15:31200380A>G c.1294A>G c.(1294-1296)Acc>Gcc p.T432A COADREAD 15 31206063 31206063 + Missense_Mutation SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr15:31206063C>T c.1580C>T c.(1579-1581)gCc>gTc p.A527V COADREAD 15 31206141 31206141 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:31206141C>T c.1658C>T c.(1657-1659)tCg>tTg p.S553L COADREAD 15 31214475 31214475 + Missense_Mutation SNP G G T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr15:31214475G>T c.2090G>T c.(2089-2091)aGa>aTa p.R697I COADREAD 15 31217359 31217359 + Silent SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr15:31217359G>A c.2202G>A c.(2200-2202)gcG>gcA p.A734A COADREAD 15 31217427 31217427 + Missense_Mutation SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr15:31217427C>T c.2270C>T c.(2269-2271)cCg>cTg p.P757L COADREAD 15 31217463 31217463 + Missense_Mutation SNP T T C TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr15:31217463T>C c.2306T>C c.(2305-2307)cTc>cCc p.L769P COADREAD 15 31221463 31221463 + Missense_Mutation SNP G G A TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr15:31221463G>A c.2650G>A c.(2650-2652)Gag>Aag p.E884K COADREAD 15 31221469 31221469 + Missense_Mutation SNP A A G TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr15:31221469A>G c.2656A>G c.(2656-2658)Agg>Ggg p.R886G COADREAD 15 31221527 31221527 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:31221527C>T c.2714C>T c.(2713-2715)aCg>aTg p.T905M COADREAD 15 31222790 31222790 + Silent SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr15:31222790C>T c.2832C>T c.(2830-2832)tgC>tgT p.C944C COADREAD 15 31229421 31229421 + Missense_Mutation SNP G G A TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr15:31229421G>A c.3016G>A c.(3016-3018)Gtg>Atg p.V1006M DLBC 15 31196984 31196984 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr15:31196984G>A c.118G>A c.(118-120)Gct>Act p.A40T ESCA 15 31214550 31214550 + Missense_Mutation SNP T T C TCGA-V5-AASX-01A-11D-A387-09 TCGA-V5-AASX-10A-01D-A38A-09 g.chr15:31214550T>C c.2165T>C c.(2164-2166)cTg>cCg p.L722P GBM 15 31197005 31197005 + Missense_Mutation SNP T T C TCGA-28-2513-01A-01D-1494-08 TCGA-28-2513-10A-01D-1494-08 g.chr15:31197005T>C c.139T>C c.(139-141)Tgc>Cgc p.C47R GBMLGG 15 31196894 31196894 + Frame_Shift_Del DEL A A - TCGA-FN-7833-01A-11D-2086-08 TCGA-FN-7833-10A-01D-2086-08 g.chr15:31196894delA c.28delA c.(28-30)aaafs p.K11fs GBMLGG 15 31197005 31197005 + Missense_Mutation SNP T T C TCGA-28-2513-01A-01D-1494-08 TCGA-28-2513-10A-01D-1494-08 g.chr15:31197005T>C c.139T>C c.(139-141)Tgc>Cgc p.C47R GBMLGG 15 31202868 31202868 + Missense_Mutation SNP A A G TCGA-CS-4944-01A-01D-1468-08 TCGA-CS-4944-10A-01D-1468-08 g.chr15:31202868A>G c.1427A>G c.(1426-1428)gAa>gGa p.E476G GBMLGG 15 31202936 31202936 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:31202936G>A c.1495G>A c.(1495-1497)Gcc>Acc p.A499T GBMLGG 15 31217455 31217455 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:31217455C>A c.2298C>A c.(2296-2298)ttC>ttA p.F766L GBMLGG 15 31221508 31221508 + Missense_Mutation SNP C C T TCGA-FG-A711-01A-21D-A33T-08 TCGA-FG-A711-10A-01D-A33W-08 g.chr15:31221508C>T c.2695C>T c.(2695-2697)Cgg>Tgg p.R899W HNSC 15 31197067 31197067 + Silent SNP T T C TCGA-CV-7429-01A-11D-2129-08 TCGA-CV-7429-10A-01D-2129-08 g.chr15:31197067T>C c.201T>C c.(199-201)aaT>aaC p.N67N HNSC 15 31197880 31197880 + Silent SNP G G A TCGA-CR-7370-01A-11D-2129-08 TCGA-CR-7370-10A-01D-2129-08 g.chr15:31197880G>A c.1014G>A c.(1012-1014)gaG>gaA p.E338E HNSC 15 31202838 31202838 + Missense_Mutation SNP C C T TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr15:31202838C>T c.1397C>T c.(1396-1398)tCt>tTt p.S466F HNSC 15 31202864 31202864 + Missense_Mutation SNP C C G TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr15:31202864C>G c.1423C>G c.(1423-1425)Cct>Gct p.P475A HNSC 15 31210382 31210382 + Silent SNP G G A TCGA-MT-A67F-01A-11D-A30E-08 TCGA-MT-A67F-10A-01D-A30H-08 g.chr15:31210382G>A c.1827G>A c.(1825-1827)acG>acA p.T609T HNSC 15 31210385 31210385 + Silent SNP C C T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr15:31210385C>T c.1830C>T c.(1828-1830)caC>caT p.H610H HNSC 15 31214472 31214473 + Frame_Shift_Del DEL AG AG - TCGA-CR-7398-01A-11D-2012-08 TCGA-CR-7398-10A-01D-2013-08 g.chr15:31214472_31214473delAG c.2087_2088delAG c.(2086-2088)cagfs p.Q696fs HNSC 15 31218129 31218129 + Silent SNP C C T TCGA-BB-4223-01A-01D-1434-08 TCGA-BB-4223-10A-01D-1434-08 g.chr15:31218129C>T c.2475C>T c.(2473-2475)agC>agT p.S825S HNSC 15 31220836 31220836 + Missense_Mutation SNP G G A TCGA-BA-5152-01A-02D-1870-08 TCGA-BA-5152-10A-01D-1870-08 g.chr15:31220836G>A c.2569G>A c.(2569-2571)Gat>Aat p.D857N HNSC 15 31229329 31229329 + Missense_Mutation SNP A A G TCGA-BA-5556-01A-01D-1512-08 TCGA-BA-5556-10A-01D-1512-08 g.chr15:31229329A>G c.2924A>G c.(2923-2925)gAa>gGa p.E975G KIPAN 15 31197838 31197838 + Missense_Mutation SNP T T G TCGA-KV-A6GD-01A-11D-A31X-10 TCGA-KV-A6GD-10A-01D-A31X-10 g.chr15:31197838T>G c.972T>G c.(970-972)caT>caG p.H324Q KIPAN 15 31206244 31206244 + Silent SNP C C T TCGA-CJ-4871-01A-01D-1373-10 TCGA-CJ-4871-11A-01D-1373-10 g.chr15:31206244C>T c.1761C>T c.(1759-1761)taC>taT p.Y587Y KIPAN 15 31221493 31221493 + Missense_Mutation SNP C C T TCGA-BP-4170-01A-02D-1366-10 TCGA-BP-4170-11A-01D-1366-10 g.chr15:31221493C>T c.2680C>T c.(2680-2682)Ccc>Tcc p.P894S KIRC 15 31206244 31206244 + Silent SNP C C T TCGA-CJ-4871-01A-01D-1373-10 TCGA-CJ-4871-11A-01D-1373-10 g.chr15:31206244C>T c.1761C>T c.(1759-1761)taC>taT p.Y587Y KIRC 15 31221493 31221493 + Missense_Mutation SNP C C T TCGA-BP-4170-01A-02D-1366-10 TCGA-BP-4170-11A-01D-1366-10 g.chr15:31221493C>T c.2680C>T c.(2680-2682)Ccc>Tcc p.P894S KIRP 15 31197838 31197838 + Missense_Mutation SNP T T G TCGA-KV-A6GD-01A-11D-A31X-10 TCGA-KV-A6GD-10A-01D-A31X-10 g.chr15:31197838T>G c.972T>G c.(970-972)caT>caG p.H324Q LGG 15 31196894 31196894 + Frame_Shift_Del DEL A A - TCGA-FN-7833-01A-11D-2086-08 TCGA-FN-7833-10A-01D-2086-08 g.chr15:31196894delA c.28delA c.(28-30)aaafs p.K11fs LGG 15 31202868 31202868 + Missense_Mutation SNP A A G TCGA-CS-4944-01A-01D-1468-08 TCGA-CS-4944-10A-01D-1468-08 g.chr15:31202868A>G c.1427A>G c.(1426-1428)gAa>gGa p.E476G LGG 15 31202936 31202936 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:31202936G>A c.1495G>A c.(1495-1497)Gcc>Acc p.A499T LGG 15 31217455 31217455 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:31217455C>A c.2298C>A c.(2296-2298)ttC>ttA p.F766L LGG 15 31221508 31221508 + Missense_Mutation SNP C C T TCGA-FG-A711-01A-21D-A33T-08 TCGA-FG-A711-10A-01D-A33W-08 g.chr15:31221508C>T c.2695C>T c.(2695-2697)Cgg>Tgg p.R899W LIHC 15 31197069 31197069 + Missense_Mutation SNP A A T TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr15:31197069A>T c.203A>T c.(202-204)gAc>gTc p.D68V LIHC 15 31197246 31197246 + Missense_Mutation SNP C C A TCGA-2Y-A9H7-01A-11D-A38X-10 TCGA-2Y-A9H7-10A-01D-A38X-10 g.chr15:31197246C>A c.380C>A c.(379-381)cCc>cAc p.P127H LIHC 15 31203039 31203039 + Intron SNP A A G TCGA-DD-AAE8-01A-11D-A40R-10 TCGA-DD-AAE8-10A-01D-A40U-10 g.chr15:31203039A>G LIHC 15 31221547 31221547 + Missense_Mutation SNP A A G TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr15:31221547A>G c.2734A>G c.(2734-2736)Aga>Gga p.R912G LUAD 15 31197225 31197225 + Missense_Mutation SNP A A G TCGA-17-Z030-01A-01W-0746-08 TCGA-17-Z030-11A-01W-0746-08 g.chr15:31197225A>G c.359A>G c.(358-360)gAa>gGa p.E120G LUAD 15 31197637 31197637 + Silent SNP C C T TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr15:31197637C>T c.771C>T c.(769-771)ttC>ttT p.F257F LUAD 15 31197648 31197648 + Missense_Mutation SNP C C T TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr15:31197648C>T c.782C>T c.(781-783)gCg>gTg p.A261V LUAD 15 31197848 31197848 + Missense_Mutation SNP G G C TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr15:31197848G>C c.982G>C c.(982-984)Gat>Cat p.D328H LUAD 15 31197996 31197996 + Missense_Mutation SNP G G T TCGA-50-7109-01A-11D-2036-08 TCGA-50-7109-11A-01D-2036-08 g.chr15:31197996G>T c.1130G>T c.(1129-1131)cGg>cTg p.R377L LUAD 15 31197997 31197997 + Silent SNP G G T TCGA-50-7109-01A-11D-2036-08 TCGA-50-7109-11A-01D-2036-08 g.chr15:31197997G>T c.1131G>T c.(1129-1131)cgG>cgT p.R377R LUAD 15 31198066 31198066 + Missense_Mutation SNP G G T TCGA-17-Z062-01A-01W-0747-08 TCGA-17-Z062-11A-01W-0747-08 g.chr15:31198066G>T c.1200G>T c.(1198-1200)gaG>gaT p.E400D LUAD 15 31200400 31200400 + Missense_Mutation SNP G G T TCGA-55-A492-01A-11D-A24D-08 TCGA-55-A492-10A-01D-A24F-08 g.chr15:31200400G>T c.1314G>T c.(1312-1314)gaG>gaT p.E438D LUAD 15 31202973 31202973 + Missense_Mutation SNP C C A TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr15:31202973C>A c.1532C>A c.(1531-1533)aCt>aAt p.T511N LUAD 15 31206216 31206216 + Missense_Mutation SNP A A T TCGA-55-8299-01A-11D-2284-08 TCGA-55-8299-10B-01D-2323-08 g.chr15:31206216A>T c.1733A>T c.(1732-1734)aAc>aTc p.N578I LUAD 15 31212784 31212784 + Silent SNP C C T TCGA-78-8640-01A-11D-2393-08 TCGA-78-8640-11A-01D-2393-08 g.chr15:31212784C>T c.1980C>T c.(1978-1980)ttC>ttT p.F660F LUAD 15 31212791 31212791 + Missense_Mutation SNP G G C TCGA-44-8120-01A-11D-2238-08 TCGA-44-8120-10A-01D-2238-08 g.chr15:31212791G>C c.1987G>C c.(1987-1989)Ggg>Cgg p.G663R LUAD 15 31217443 31217443 + Missense_Mutation SNP C C G TCGA-97-A4M5-01A-11D-A24P-08 TCGA-97-A4M5-10A-01D-A24P-08 g.chr15:31217443C>G c.2286C>G c.(2284-2286)ttC>ttG p.F762L LUAD 15 31218081 31218081 + Silent SNP G G T TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr15:31218081G>T c.2427G>T c.(2425-2427)acG>acT p.T809T LUAD 15 31222754 31222754 + Silent SNP C C T TCGA-05-4250-01A-01D-1105-08 TCGA-05-4250-10A-01D-1105-08 g.chr15:31222754C>T c.2796C>T c.(2794-2796)gtC>gtT p.V932V LUAD 15 31222813 31222813 + Missense_Mutation SNP G G A TCGA-73-4668-01A-01D-1265-08 TCGA-73-4668-11A-01D-1265-08 g.chr15:31222813G>A c.2855G>A c.(2854-2856)cGa>cAa p.R952Q LUAD 15 31222863 31222863 + Missense_Mutation SNP C C A TCGA-95-A4VP-01A-21D-A25L-08 TCGA-95-A4VP-10A-01D-A25L-08 g.chr15:31222863C>A c.2905C>A c.(2905-2907)Cgt>Agt p.R969S LUAD 15 31222871 31222871 + Silent SNP T T C TCGA-55-8204-01A-11D-2238-08 TCGA-55-8204-10A-01D-2238-08 g.chr15:31222871T>C c.2913T>C c.(2911-2913)ttT>ttC p.F971F LUSC 15 31197396 31197396 + Missense_Mutation SNP C C T TCGA-34-2596-01A-01D-1522-08 TCGA-34-2596-11A-01D-1522-08 g.chr15:31197396C>T c.530C>T c.(529-531)gCc>gTc p.A177V PAAD 15 31196894 31196894 + Frame_Shift_Del DEL A A - TCGA-2J-AABK-01A-31D-A40W-08 TCGA-2J-AABK-10A-01D-A40W-08 g.chr15:31196894delA c.28delA c.(28-30)aaafs p.K11fs PAAD 15 31196894 31196894 + Frame_Shift_Del DEL A A - TCGA-2L-AAQA-01A-21D-A38G-08 TCGA-2L-AAQA-11A-11D-A38J-08 g.chr15:31196894delA c.28delA c.(28-30)aaafs p.K11fs PAAD 15 31196894 31196894 + Frame_Shift_Del DEL A A - TCGA-HZ-A49I-01A-12D-A26I-08 TCGA-HZ-A49I-10A-01D-A26I-08 g.chr15:31196894delA c.28delA c.(28-30)aaafs p.K11fs PAAD 15 31196894 31196894 + Frame_Shift_Del DEL A A - TCGA-HZ-A8P0-01A-11D-A36O-08 TCGA-HZ-A8P0-10A-01D-A367-08 g.chr15:31196894delA c.28delA c.(28-30)aaafs p.K11fs PAAD 15 31196894 31196894 + Frame_Shift_Del DEL A A - TCGA-IB-AAUU-01A-11D-A377-08 TCGA-IB-AAUU-10A-01D-A37A-08 g.chr15:31196894delA c.28delA c.(28-30)aaafs p.K11fs PAAD 15 31196894 31196894 + Frame_Shift_Del DEL A A - TCGA-LB-A9Q5-01A-11D-A397-08 TCGA-LB-A9Q5-10A-01D-A39A-08 g.chr15:31196894delA c.28delA c.(28-30)aaafs p.K11fs PAAD 15 31196894 31196894 + Frame_Shift_Del DEL A A - TCGA-XD-AAUL-01A-21D-A397-08 TCGA-XD-AAUL-10A-01D-A39A-08 g.chr15:31196894delA c.28delA c.(28-30)aaafs p.K11fs PAAD 15 31202973 31202973 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:31202973C>A c.1532C>A c.(1531-1533)aCt>aAt p.T511N PRAD 15 31196925 31196925 + Missense_Mutation SNP G G T TCGA-HC-8216-01A-11D-A29Q-08 TCGA-HC-8216-10A-01D-A29Q-08 g.chr15:31196925G>T c.59G>T c.(58-60)aGc>aTc p.S20I PRAD 15 31197979 31197979 + Silent SNP T T C TCGA-KK-A59Y-01A-11D-A26M-08 TCGA-KK-A59Y-11A-11D-A26K-08 g.chr15:31197979T>C c.1113T>C c.(1111-1113)ggT>ggC p.G371G PRAD 15 31229359 31229359 + Missense_Mutation SNP A A G TCGA-J4-A67M-01A-11D-A30E-08 TCGA-J4-A67M-10A-01D-A30H-08 g.chr15:31229359A>G c.2954A>G c.(2953-2955)cAt>cGt p.H985R READ 15 31197154 31197154 + Silent SNP T T C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr15:31197154T>C c.288T>C c.(286-288)gaT>gaC p.D96D SARC 15 31217365 31217365 + Silent SNP G G A TCGA-DX-A7EO-01A-11D-A36J-09 TCGA-DX-A7EO-10A-01D-A36M-09 g.chr15:31217365G>A c.2208G>A c.(2206-2208)ccG>ccA p.P736P SKCM 15 31196894 31196894 + Frame_Shift_Del DEL A A - TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr15:31196894delA c.28delA c.(28-30)aaafs p.K11fs SKCM 15 31196961 31196961 + Missense_Mutation SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr15:31196961C>T c.95C>T c.(94-96)tCg>tTg p.S32L SKCM 15 31196991 31196991 + Missense_Mutation SNP T T C TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr15:31196991T>C c.125T>C c.(124-126)cTt>cCt p.L42P SKCM 15 31202912 31202912 + Missense_Mutation SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr15:31202912G>A c.1471G>A c.(1471-1473)Gga>Aga p.G491R SKCM 15 31206141 31206141 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:31206141C>T c.1658C>T c.(1657-1659)tCg>tTg p.S553L SKCM 15 31218060 31218060 + Silent SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr15:31218060G>A c.2406G>A c.(2404-2406)ggG>ggA p.G802G SKCM 15 31220836 31220836 + Missense_Mutation SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr15:31220836G>A c.2569G>A c.(2569-2571)Gat>Aat p.D857N

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 15 31196881 31196881 single base substitution G A exon_variant BLCA-CN 15 31196881 31196881 single base substitution G A intron_variant BLCA-CN 15 31196881 31196881 single base substitution G A synonymous_variant G5G 15G>A BLCA-US 15 31197051 31197051 single base substitution A G exon_variant BLCA-US 15 31197051 31197051 single base substitution A G intron_variant BLCA-US 15 31197051 31197051 single base substitution A G missense_variant E62G 185A>G BLCA-US 15 31197525 31197525 single base substitution C G exon_variant BLCA-US 15 31197525 31197525 single base substitution C G intron_variant BLCA-US 15 31197525 31197525 single base substitution C G missense_variant S220C 659C>G BLCA-US 15 31233969 31233969 single base substitution G A 3_prime_UTR_variant BLCA-US 15 31239356 31239356 single base substitution G A downstream_gene_variant BLCA-US 15 31239408 31239408 single base substitution C T downstream_gene_variant BOCA-FR 15 31192212 31192212 single base substitution G A upstream_gene_variant BOCA-FR 15 31220892 31220892 single base substitution C A intron_variant BOCA-FR 15 31231701 31231701 single base substitution A T intron_variant BRCA-EU 15 31191098 31191098 single base substitution C T upstream_gene_variant BRCA-EU 15 31191349 31191349 deletion of <=200bp T - upstream_gene_variant BRCA-EU 15 31191662 31191662 single base substitution G T upstream_gene_variant BRCA-EU 15 31192065 31192065 single base substitution G C upstream_gene_variant BRCA-EU 15 31192949 31192949 deletion of <=200bp T - upstream_gene_variant BRCA-EU 15 31193947 31193947 single base substitution G A upstream_gene_variant BRCA-EU 15 31194667 31194668 deletion of <=200bp TT - upstream_gene_variant BRCA-EU 15 31195195 31195195 single base substitution G A upstream_gene_variant BRCA-EU 15 31195359 31195359 single base substitution G C upstream_gene_variant BRCA-EU 15 31196398 31196398 single base substitution A G intron_variant BRCA-EU 15 31196398 31196398 single base substitution A G upstream_gene_variant BRCA-EU 15 31196493 31196495 deletion of <=200bp AAG - intron_variant BRCA-EU 15 31196493 31196495 deletion of <=200bp AAG - upstream_gene_variant BRCA-EU 15 31196894 31196894 deletion of <=200bp A - exon_variant BRCA-EU 15 31196894 31196894 deletion of <=200bp A - frameshift_variant K10 BRCA-EU 15 31196894 31196894 deletion of <=200bp A - intron_variant BRCA-EU 15 31197292 31197292 single base substitution G A exon_variant BRCA-EU 15 31197292 31197292 single base substitution G A intron_variant BRCA-EU 15 31197292 31197292 single base substitution G A synonymous_variant L142L 426G>A BRCA-EU 15 31198475 31198475 single base substitution G T intron_variant BRCA-EU 15 31199985 31199985 insertion of <=200bp - T intron_variant BRCA-EU 15 31200313 31200313 single base substitution T C splice_region_variant BRCA-EU 15 31204751 31204751 single base substitution G A downstream_gene_variant BRCA-EU 15 31204751 31204751 single base substitution G A intron_variant BRCA-EU 15 31205230 31205230 single base substitution C A downstream_gene_variant BRCA-EU 15 31205230 31205230 single base substitution C A intron_variant BRCA-EU 15 31208528 31208528 single base substitution C T downstream_gene_variant BRCA-EU 15 31208528 31208528 single base substitution C T intron_variant BRCA-EU 15 31208729 31208729 single base substitution A G downstream_gene_variant BRCA-EU 15 31208729 31208729 single base substitution A G intron_variant BRCA-EU 15 31211646 31211646 single base substitution C T intron_variant BRCA-EU 15 31211646 31211646 single base substitution C T upstream_gene_variant BRCA-EU 15 31211715 31211715 single base substitution G A intron_variant BRCA-EU 15 31211715 31211715 single base substitution G A upstream_gene_variant BRCA-EU 15 31213975 31213975 single base substitution G C intron_variant BRCA-EU 15 31213975 31213975 single base substitution G C upstream_gene_variant BRCA-EU 15 31214870 31214870 single base substitution C T intron_variant BRCA-EU 15 31217845 31217845 single base substitution G C intron_variant BRCA-EU 15 31217845 31217845 single base substitution G C upstream_gene_variant BRCA-EU 15 31219660 31219660 single base substitution G C intron_variant BRCA-EU 15 31219660 31219660 single base substitution G C upstream_gene_variant BRCA-EU 15 31221073 31221073 single base substitution C A intron_variant BRCA-EU 15 31221306 31221306 single base substitution C T intron_variant BRCA-EU 15 31221325 31221325 single base substitution T C intron_variant BRCA-EU 15 31226453 31226453 deletion of <=200bp T - downstream_gene_variant BRCA-EU 15 31226453 31226453 deletion of <=200bp T - intron_variant BRCA-EU 15 31227849 31227849 single base substitution C T downstream_gene_variant BRCA-EU 15 31227849 31227849 single base substitution C T intron_variant BRCA-EU 15 31232358 31232358 single base substitution T G intron_variant BRCA-EU 15 31233247 31233247 single base substitution G A intron_variant BRCA-EU 15 31233844 31233844 single base substitution G T 3_prime_UTR_variant BRCA-EU 15 31234161 31234161 single base substitution G C 3_prime_UTR_variant BRCA-EU 15 31235062 31235062 single base substitution C T 3_prime_UTR_variant BRCA-EU 15 31235372 31235372 single base substitution C G downstream_gene_variant BRCA-EU 15 31236415 31236415 single base substitution T C downstream_gene_variant BRCA-EU 15 31236916 31236916 single base substitution T C downstream_gene_variant BRCA-EU 15 31239854 31239854 single base substitution C G downstream_gene_variant BRCA-FR 15 31192065 31192065 single base substitution G C upstream_gene_variant BRCA-FR 15 31202369 31202369 single base substitution G C intron_variant BRCA-FR 15 31228189 31228189 single base substitution T C intron_variant BRCA-FR 15 31234161 31234161 single base substitution G C 3_prime_UTR_variant BRCA-FR 15 31234749 31234749 single base substitution A G 3_prime_UTR_variant BRCA-UK 15 31191662 31191662 single base substitution G T upstream_gene_variant BRCA-UK 15 31193947 31193947 single base substitution G A upstream_gene_variant BRCA-UK 15 31202976 31202976 single base substitution G C 3_prime_UTR_variant BRCA-UK 15 31202976 31202976 single base substitution G C downstream_gene_variant BRCA-UK 15 31202976 31202976 single base substitution G C missense_variant W512S 1535G>C BRCA-UK 15 31238971 31238971 single base substitution T C downstream_gene_variant BRCA-US 15 31197787 31197788 deletion of <=200bp TG - exon_variant BRCA-US 15 31197787 31197788 deletion of <=200bp TG - frameshift_variant TV307 BRCA-US 15 31197787 31197788 deletion of <=200bp TG - intron_variant BRCA-US 15 31197852 31197852 single base substitution A T exon_variant BRCA-US 15 31197852 31197852 single base substitution A T intron_variant BRCA-US 15 31197852 31197852 single base substitution A T missense_variant D329V 986A>T BRCA-US 15 31206233 31206233 single base substitution T A 3_prime_UTR_variant BRCA-US 15 31206233 31206233 single base substitution T A downstream_gene_variant BRCA-US 15 31206233 31206233 single base substitution T A missense_variant F584I 1750T>A BRCA-US 15 31206241 31206241 single base substitution T G 3_prime_UTR_variant BRCA-US 15 31206241 31206241 single base substitution T G downstream_gene_variant BRCA-US 15 31206241 31206241 single base substitution T G missense_variant S586R 1758T>G BRCA-US 15 31212838 31212838 single base substitution G C 3_prime_UTR_variant BRCA-US 15 31212838 31212838 single base substitution G C missense_variant Q678H 2034G>C BRCA-US 15 31212838 31212838 single base substitution G C upstream_gene_variant BRCA-US 15 31229326 31229326 single base substitution T G 3_prime_UTR_variant BRCA-US 15 31229326 31229326 single base substitution T G missense_variant V974G 2921T>G BRCA-US 15 31229382 31229382 single base substitution G A 3_prime_UTR_variant BRCA-US 15 31229382 31229382 single base substitution G A missense_variant E993K 2977G>A BRCA-US 15 31229401 31229401 deletion of <=200bp C - 3_prime_UTR_variant BRCA-US 15 31229401 31229401 deletion of <=200bp C - frameshift_variant A999 BRCA-US 15 31233955 31233955 single base substitution G C 3_prime_UTR_variant BRCA-US 15 31239429 31239429 single base substitution G C downstream_gene_variant BTCA-JP 15 31214471 31214471 single base substitution C A 3_prime_UTR_variant BTCA-JP 15 31214471 31214471 single base substitution C A exon_variant BTCA-JP 15 31214471 31214471 single base substitution C A missense_variant Q696K 2086C>A BTCA-JP 15 31222709 31222709 single base substitution G A intron_variant BTCA-JP 15 31229498 31229498 single base substitution T G intron_variant CESC-US 15 31197287 31197287 single base substitution G A exon_variant CESC-US 15 31197287 31197287 single base substitution G A intron_variant CESC-US 15 31197287 31197287 single base substitution G A missense_variant E141K 421G>A CESC-US 15 31197561 31197561 single base substitution G A exon_variant CESC-US 15 31197561 31197561 single base substitution G A intron_variant CESC-US 15 31197561 31197561 single base substitution G A missense_variant R232K 695G>A CESC-US 15 31197563 31197563 single base substitution G T exon_variant CESC-US 15 31197563 31197563 single base substitution G T intron_variant CESC-US 15 31197563 31197563 single base substitution G T stop_gained G233* 697G>T CESC-US 15 31221463 31221463 single base substitution G C 3_prime_UTR_variant CESC-US 15 31221463 31221463 single base substitution G C exon_variant CESC-US 15 31221463 31221463 single base substitution G C missense_variant E884Q 2650G>C CESC-US 15 31239429 31239429 single base substitution G T downstream_gene_variant CLLE-ES 15 31195285 31195285 single base substitution G A upstream_gene_variant CLLE-ES 15 31198877 31198877 single base substitution A G intron_variant COAD-US 15 31197140 31197140 single base substitution G A exon_variant COAD-US 15 31197140 31197140 single base substitution G A intron_variant COAD-US 15 31197140 31197140 single base substitution G A missense_variant V92I 274G>A COAD-US 15 31197830 31197830 single base substitution A C exon_variant COAD-US 15 31197830 31197830 single base substitution A C intron_variant COAD-US 15 31197830 31197830 single base substitution A C missense_variant K322Q 964A>C COAD-US 15 31197927 31197927 single base substitution G A exon_variant COAD-US 15 31197927 31197927 single base substitution G A intron_variant COAD-US 15 31197927 31197927 single base substitution G A missense_variant S354N 1061G>A COAD-US 15 31198087 31198087 single base substitution T G exon_variant COAD-US 15 31198087 31198087 single base substitution T G intron_variant COAD-US 15 31198087 31198087 single base substitution T G missense_variant F407L 1221T>G COAD-US 15 31206063 31206063 single base substitution C T downstream_gene_variant COAD-US 15 31206063 31206063 single base substitution C T missense_variant A527V 1580C>T COAD-US 15 31206063 31206063 single base substitution C T splice_region_variant COAD-US 15 31217427 31217427 single base substitution C T 3_prime_UTR_variant COAD-US 15 31217427 31217427 single base substitution C T exon_variant COAD-US 15 31217427 31217427 single base substitution C T missense_variant P757L 2270C>T COAD-US 15 31217427 31217427 single base substitution C T upstream_gene_variant COAD-US 15 31221463 31221463 single base substitution G A 3_prime_UTR_variant COAD-US 15 31221463 31221463 single base substitution G A exon_variant COAD-US 15 31221463 31221463 single base substitution G A missense_variant E884K 2650G>A COAD-US 15 31222790 31222790 single base substitution C T 3_prime_UTR_variant COAD-US 15 31222790 31222790 single base substitution C T exon_variant COAD-US 15 31222790 31222790 single base substitution C T synonymous_variant C944C 2832C>T COAD-US 15 31233725 31233725 deletion of <=200bp A - intron_variant COAD-US 15 31235169 31235169 deletion of <=200bp A - 3_prime_UTR_variant COCA-CN 15 31197503 31197503 single base substitution G T exon_variant COCA-CN 15 31197503 31197503 single base substitution G T intron_variant COCA-CN 15 31197503 31197503 single base substitution G T stop_gained E213* 637G>T COCA-CN 15 31197613 31197613 single base substitution G T exon_variant COCA-CN 15 31197613 31197613 single base substitution G T intron_variant COCA-CN 15 31197613 31197613 single base substitution G T missense_variant E249D 747G>T COCA-CN 15 31216384 31216384 single base substitution G A intron_variant COCA-CN 15 31216384 31216384 single base substitution G A upstream_gene_variant COCA-CN 15 31222863 31222863 single base substitution C T 3_prime_UTR_variant COCA-CN 15 31222863 31222863 single base substitution C T downstream_gene_variant COCA-CN 15 31222863 31222863 single base substitution C T missense_variant R969C 2905C>T COCA-CN 15 31233222 31233222 single base substitution A G intron_variant COCA-CN 15 31233548 31233548 single base substitution G C intron_variant COCA-CN 15 31235116 31235116 single base substitution C T 3_prime_UTR_variant COCA-CN 15 31239254 31239254 single base substitution C T downstream_gene_variant EOPC-DE 15 31234304 31234304 single base substitution G A 3_prime_UTR_variant EOPC-DE 15 31236733 31236733 single base substitution T C downstream_gene_variant ESAD-UK 15 31191311 31191311 single base substitution T G upstream_gene_variant ESAD-UK 15 31193313 31193313 deletion of <=200bp A - upstream_gene_variant ESAD-UK 15 31194553 31194553 single base substitution C T upstream_gene_variant ESAD-UK 15 31195201 31195201 single base substitution C T upstream_gene_variant ESAD-UK 15 31195261 31195261 insertion of <=200bp - C upstream_gene_variant ESAD-UK 15 31196678 31196678 single base substitution A T intron_variant ESAD-UK 15 31196678 31196678 single base substitution A T upstream_gene_variant ESAD-UK 15 31199722 31199722 insertion of <=200bp - A intron_variant ESAD-UK 15 31200228 31200228 single base substitution A G intron_variant ESAD-UK 15 31200814 31200814 single base substitution C T intron_variant ESAD-UK 15 31201045 31201045 insertion of <=200bp - A intron_variant ESAD-UK 15 31203284 31203284 single base substitution G A 3_prime_UTR_variant ESAD-UK 15 31203284 31203284 single base substitution G A downstream_gene_variant ESAD-UK 15 31203284 31203284 single base substitution G A intron_variant ESAD-UK 15 31205626 31205626 single base substitution C T downstream_gene_variant ESAD-UK 15 31205626 31205626 single base substitution C T intron_variant ESAD-UK 15 31206252 31206252 single base substitution A G 3_prime_UTR_variant ESAD-UK 15 31206252 31206252 single base substitution A G downstream_gene_variant ESAD-UK 15 31206252 31206252 single base substitution A G missense_variant N590S 1769A>G ESAD-UK 15 31206606 31206606 single base substitution C T downstream_gene_variant ESAD-UK 15 31206606 31206606 single base substitution C T intron_variant ESAD-UK 15 31208019 31208019 deletion of <=200bp A - downstream_gene_variant ESAD-UK 15 31208019 31208019 deletion of <=200bp A - intron_variant ESAD-UK 15 31208040 31208040 deletion of <=200bp A - downstream_gene_variant ESAD-UK 15 31208040 31208040 deletion of <=200bp A - intron_variant ESAD-UK 15 31210830 31210830 single base substitution G A intron_variant ESAD-UK 15 31210830 31210830 single base substitution G A upstream_gene_variant ESAD-UK 15 31215981 31215981 single base substitution C T intron_variant ESAD-UK 15 31215981 31215981 single base substitution C T upstream_gene_variant ESAD-UK 15 31221951 31221955 deletion of <=200bp ATATA - intron_variant ESAD-UK 15 31225128 31225128 single base substitution G A downstream_gene_variant ESAD-UK 15 31225128 31225128 single base substitution G A intron_variant ESAD-UK 15 31225866 31225866 single base substitution G T downstream_gene_variant ESAD-UK 15 31225866 31225866 single base substitution G T intron_variant ESAD-UK 15 31226310 31226310 single base substitution C T downstream_gene_variant ESAD-UK 15 31226310 31226310 single base substitution C T intron_variant ESAD-UK 15 31227788 31227788 single base substitution G A downstream_gene_variant ESAD-UK 15 31227788 31227788 single base substitution G A intron_variant ESAD-UK 15 31229749 31229749 single base substitution G A intron_variant ESAD-UK 15 31234566 31234566 single base substitution A G 3_prime_UTR_variant ESAD-UK 15 31235733 31235733 single base substitution G A downstream_gene_variant ESAD-UK 15 31236717 31236717 single base substitution C T downstream_gene_variant ESAD-UK 15 31238087 31238087 single base substitution G C downstream_gene_variant ESCA-CN 15 31217329 31217329 single base substitution G C exon_variant ESCA-CN 15 31217329 31217329 single base substitution G C splice_acceptor_variant ESCA-CN 15 31217329 31217329 single base substitution G C upstream_gene_variant GBM-US 15 31197005 31197005 single base substitution T C exon_variant GBM-US 15 31197005 31197005 single base substitution T C intron_variant GBM-US 15 31197005 31197005 single base substitution T C missense_variant C47R 139T>C KIRC-US 15 31206244 31206244 single base substitution C T 3_prime_UTR_variant KIRC-US 15 31206244 31206244 single base substitution C T downstream_gene_variant KIRC-US 15 31206244 31206244 single base substitution C T synonymous_variant Y587Y 1761C>T KIRC-US 15 31221493 31221493 single base substitution C T 3_prime_UTR_variant KIRC-US 15 31221493 31221493 single base substitution C T exon_variant KIRC-US 15 31221493 31221493 single base substitution C T missense_variant P894S 2680C>T KIRP-US 15 31197838 31197838 single base substitution T G exon_variant KIRP-US 15 31197838 31197838 single base substitution T G intron_variant KIRP-US 15 31197838 31197838 single base substitution T G missense_variant H324Q 972T>G LAML-KR 15 31210651 31210651 single base substitution A G intron_variant LAML-KR 15 31210651 31210651 single base substitution A G upstream_gene_variant LAML-KR 15 31212684 31212684 single base substitution G C intron_variant LAML-KR 15 31212684 31212684 single base substitution G C upstream_gene_variant LAML-KR 15 31233934 31233934 single base substitution T A 3_prime_UTR_variant LGG-US 15 31196894 31196894 deletion of <=200bp A - exon_variant LGG-US 15 31196894 31196894 deletion of <=200bp A - frameshift_variant K10 LGG-US 15 31196894 31196894 deletion of <=200bp A - intron_variant LGG-US 15 31202868 31202868 single base substitution A G 3_prime_UTR_variant LGG-US 15 31202868 31202868 single base substitution A G missense_variant E476G 1427A>G LGG-US 15 31202868 31202868 single base substitution A G missense_variant E82G 245A>G LICA-FR 15 31196867 31196867 single base substitution A G exon_variant LICA-FR 15 31196867 31196867 single base substitution A G intron_variant LICA-FR 15 31196867 31196867 single base substitution A G start_lost M1V 1A>G LICA-FR 15 31197960 31197960 single base substitution G A exon_variant LICA-FR 15 31197960 31197960 single base substitution G A intron_variant LICA-FR 15 31197960 31197960 single base substitution G A missense_variant G365D 1094G>A LICA-FR 15 31198145 31198145 single base substitution G A intron_variant LICA-FR 15 31210449 31210449 single base substitution C T 3_prime_UTR_variant LICA-FR 15 31210449 31210449 single base substitution C T stop_gained Q632* 1894C>T LICA-FR 15 31210449 31210449 single base substitution C T upstream_gene_variant LICA-FR 15 31219843 31219843 single base substitution T C intron_variant LICA-FR 15 31219843 31219843 single base substitution T C upstream_gene_variant LICA-FR 15 31220710 31220710 insertion of <=200bp - TGTGTGTGTGTGTGTGTG exon_variant LICA-FR 15 31220710 31220710 insertion of <=200bp - TGTGTGTGTGTGTGTGTG intron_variant LIHC-US 15 31197069 31197069 single base substitution A T exon_variant LIHC-US 15 31197069 31197069 single base substitution A T intron_variant LIHC-US 15 31197069 31197069 single base substitution A T missense_variant D68V 203A>T LIHC-US 15 31221547 31221547 single base substitution A G 3_prime_UTR_variant LIHC-US 15 31221547 31221547 single base substitution A G exon_variant LIHC-US 15 31221547 31221547 single base substitution A G missense_variant R912G 2734A>G LINC-JP 15 31206313 31206313 single base substitution A G downstream_gene_variant LINC-JP 15 31206313 31206313 single base substitution A G intron_variant LINC-JP 15 31217902 31217902 single base substitution A C intron_variant LINC-JP 15 31217902 31217902 single base substitution A C upstream_gene_variant LINC-JP 15 31218130 31218130 single base substitution G A 3_prime_UTR_variant LINC-JP 15 31218130 31218130 single base substitution G A exon_variant LINC-JP 15 31218130 31218130 single base substitution G A missense_variant G826S 2476G>A LINC-JP 15 31218130 31218130 single base substitution G A upstream_gene_variant LINC-JP 15 31219467 31219467 single base substitution A C intron_variant LINC-JP 15 31219467 31219467 single base substitution A C upstream_gene_variant LINC-JP 15 31229429 31229432 deletion of <=200bp AGTT - 3_prime_UTR_variant LINC-JP 15 31229429 31229432 deletion of <=200bp AGTT - frameshift_variant AV1008 LINC-JP 15 31229481 31229481 single base substitution T G intron_variant LINC-JP 15 31229534 31229534 single base substitution T G intron_variant LINC-JP 15 31231361 31231361 insertion of <=200bp - CT intron_variant LINC-JP 15 31233652 31233652 single base substitution A G intron_variant LINC-JP 15 31235298 31235298 single base substitution T A 3_prime_UTR_variant LINC-JP 15 31236764 31236764 single base substitution G A downstream_gene_variant LIRI-JP 15 31191279 31191279 single base substitution G A upstream_gene_variant LIRI-JP 15 31192357 31192357 single base substitution G T upstream_gene_variant LIRI-JP 15 31193987 31193987 single base substitution G A upstream_gene_variant LIRI-JP 15 31195537 31195537 single base substitution A G upstream_gene_variant LIRI-JP 15 31197297 31197297 single base substitution A G exon_variant LIRI-JP 15 31197297 31197297 single base substitution A G intron_variant LIRI-JP 15 31197297 31197297 single base substitution A G missense_variant N144S 431A>G LIRI-JP 15 31200211 31200211 single base substitution G A intron_variant LIRI-JP 15 31200452 31200452 single base substitution C G 3_prime_UTR_variant LIRI-JP 15 31200452 31200452 single base substitution C G missense_variant L456V 1366C>G LIRI-JP 15 31200452 31200452 single base substitution C G missense_variant L62V 184C>G LIRI-JP 15 31202524 31202524 single base substitution G A intron_variant LIRI-JP 15 31203320 31203320 single base substitution T G 3_prime_UTR_variant LIRI-JP 15 31203320 31203320 single base substitution T G downstream_gene_variant LIRI-JP 15 31203320 31203320 single base substitution T G intron_variant LIRI-JP 15 31203646 31203646 single base substitution A G 3_prime_UTR_variant LIRI-JP 15 31203646 31203646 single base substitution A G downstream_gene_variant LIRI-JP 15 31203646 31203646 single base substitution A G intron_variant LIRI-JP 15 31204375 31204375 single base substitution A G downstream_gene_variant LIRI-JP 15 31204375 31204375 single base substitution A G intron_variant LIRI-JP 15 31207439 31207439 single base substitution G A downstream_gene_variant LIRI-JP 15 31207439 31207439 single base substitution G A intron_variant LIRI-JP 15 31208123 31208123 single base substitution A G downstream_gene_variant LIRI-JP 15 31208123 31208123 single base substitution A G intron_variant LIRI-JP 15 31216260 31216260 single base substitution C T intron_variant LIRI-JP 15 31216260 31216260 single base substitution C T upstream_gene_variant LIRI-JP 15 31216758 31216758 single base substitution C A intron_variant LIRI-JP 15 31216758 31216758 single base substitution C A upstream_gene_variant LIRI-JP 15 31217531 31217531 single base substitution G A intron_variant LIRI-JP 15 31217531 31217531 single base substitution G A upstream_gene_variant LIRI-JP 15 31218969 31218969 single base substitution G A intron_variant LIRI-JP 15 31218969 31218969 single base substitution G A upstream_gene_variant LIRI-JP 15 31219166 31219166 single base substitution C T intron_variant LIRI-JP 15 31219166 31219166 single base substitution C T upstream_gene_variant LIRI-JP 15 31219192 31219192 single base substitution A C intron_variant LIRI-JP 15 31219192 31219192 single base substitution A C upstream_gene_variant LIRI-JP 15 31219197 31219197 single base substitution A C intron_variant LIRI-JP 15 31219197 31219197 single base substitution A C upstream_gene_variant LIRI-JP 15 31220848 31220848 single base substitution A C 3_prime_UTR_variant LIRI-JP 15 31220848 31220848 single base substitution A C exon_variant LIRI-JP 15 31220848 31220848 single base substitution A C missense_variant N861H 2581A>C LIRI-JP 15 31221226 31221226 single base substitution T C intron_variant LIRI-JP 15 31225785 31225785 single base substitution A C downstream_gene_variant LIRI-JP 15 31225785 31225785 single base substitution A C intron_variant LIRI-JP 15 31225997 31225997 single base substitution A G downstream_gene_variant LIRI-JP 15 31225997 31225997 single base substitution A G intron_variant LIRI-JP 15 31226726 31226726 single base substitution G A downstream_gene_variant LIRI-JP 15 31226726 31226726 single base substitution G A intron_variant LIRI-JP 15 31230376 31230376 single base substitution G C intron_variant LIRI-JP 15 31230815 31230815 single base substitution T A intron_variant LIRI-JP 15 31231210 31231210 single base substitution A C intron_variant LIRI-JP 15 31237044 31237044 single base substitution A G downstream_gene_variant LIRI-JP 15 31240205 31240205 single base substitution T C downstream_gene_variant LUSC-KR 15 31193093 31193093 single base substitution C A upstream_gene_variant LUSC-KR 15 31195038 31195038 single base substitution C A upstream_gene_variant LUSC-KR 15 31195519 31195519 single base substitution C A upstream_gene_variant LUSC-KR 15 31201898 31201898 single base substitution C G intron_variant LUSC-KR 15 31202483 31202483 single base substitution A T intron_variant LUSC-KR 15 31204129 31204129 single base substitution G T downstream_gene_variant LUSC-KR 15 31204129 31204129 single base substitution G T intron_variant LUSC-KR 15 31205042 31205042 single base substitution G A downstream_gene_variant LUSC-KR 15 31205042 31205042 single base substitution G A intron_variant LUSC-KR 15 31207136 31207136 single base substitution G C downstream_gene_variant LUSC-KR 15 31207136 31207136 single base substitution G C intron_variant LUSC-KR 15 31209691 31209691 single base substitution A C intron_variant LUSC-KR 15 31209691 31209691 single base substitution A C upstream_gene_variant LUSC-KR 15 31209696 31209696 single base substitution A G intron_variant LUSC-KR 15 31209696 31209696 single base substitution A G upstream_gene_variant LUSC-KR 15 31219416 31219416 single base substitution C T intron_variant LUSC-KR 15 31219416 31219416 single base substitution C T upstream_gene_variant LUSC-KR 15 31220890 31220890 single base substitution T C intron_variant LUSC-KR 15 31225285 31225285 single base substitution G C downstream_gene_variant LUSC-KR 15 31225285 31225285 single base substitution G C intron_variant LUSC-KR 15 31226532 31226532 single base substitution C T downstream_gene_variant LUSC-KR 15 31226532 31226532 single base substitution C T intron_variant LUSC-KR 15 31227283 31227283 single base substitution C T downstream_gene_variant LUSC-KR 15 31227283 31227283 single base substitution C T intron_variant LUSC-KR 15 31229405 31229405 single base substitution A C 3_prime_UTR_variant LUSC-KR 15 31229405 31229405 single base substitution A C missense_variant E1000D 3000A>C LUSC-KR 15 31238302 31238302 single base substitution T A downstream_gene_variant LUSC-KR 15 31238937 31238937 single base substitution G T downstream_gene_variant LUSC-US 15 31196869 31196869 single base substitution G A exon_variant LUSC-US 15 31196869 31196869 single base substitution G A intron_variant LUSC-US 15 31196869 31196869 single base substitution G A start_lost M1I 3G>A LUSC-US 15 31197396 31197396 single base substitution C T exon_variant LUSC-US 15 31197396 31197396 single base substitution C T intron_variant LUSC-US 15 31197396 31197396 single base substitution C T missense_variant A177V 530C>T LUSC-US 15 31234047 31234047 single base substitution T C 3_prime_UTR_variant MALY-DE 15 31192917 31192917 single base substitution A T upstream_gene_variant MALY-DE 15 31200007 31200007 single base substitution G A intron_variant MALY-DE 15 31201870 31201870 single base substitution C T intron_variant MALY-DE 15 31207863 31207863 single base substitution A G downstream_gene_variant MALY-DE 15 31207863 31207863 single base substitution A G intron_variant MALY-DE 15 31208404 31208404 single base substitution C T downstream_gene_variant MALY-DE 15 31208404 31208404 single base substitution C T intron_variant MALY-DE 15 31215036 31215036 single base substitution G T intron_variant MALY-DE 15 31217377 31217377 single base substitution G A 3_prime_UTR_variant MALY-DE 15 31217377 31217377 single base substitution G A exon_variant MALY-DE 15 31217377 31217377 single base substitution G A synonymous_variant T740T 2220G>A MALY-DE 15 31217377 31217377 single base substitution G A upstream_gene_variant MALY-DE 15 31219264 31219264 single base substitution C A intron_variant MALY-DE 15 31219264 31219264 single base substitution C A upstream_gene_variant MALY-DE 15 31220097 31220097 single base substitution T G intron_variant MALY-DE 15 31220097 31220097 single base substitution T G upstream_gene_variant MALY-DE 15 31221745 31221745 single base substitution C A intron_variant MALY-DE 15 31223235 31223235 single base substitution G A downstream_gene_variant MALY-DE 15 31223235 31223235 single base substitution G A intron_variant MALY-DE 15 31225337 31225337 single base substitution G A downstream_gene_variant MALY-DE 15 31225337 31225337 single base substitution G A intron_variant MALY-DE 15 31228459 31228459 single base substitution T G intron_variant MALY-DE 15 31229159 31229159 single base substitution C T intron_variant MELA-AU 15 31191532 31191532 single base substitution C T upstream_gene_variant MELA-AU 15 31192522 31192522 single base substitution G A upstream_gene_variant MELA-AU 15 31193228 31193228 single base substitution C T upstream_gene_variant MELA-AU 15 31193333 31193333 single base substitution C T upstream_gene_variant MELA-AU 15 31193686 31193686 single base substitution C T upstream_gene_variant MELA-AU 15 31193822 31193822 single base substitution G A upstream_gene_variant MELA-AU 15 31194178 31194178 single base substitution C T upstream_gene_variant MELA-AU 15 31195408 31195408 single base substitution G A upstream_gene_variant MELA-AU 15 31196952 31196952 single base substitution C T exon_variant MELA-AU 15 31196952 31196952 single base substitution C T intron_variant MELA-AU 15 31196952 31196952 single base substitution C T missense_variant S29F 86C>T MELA-AU 15 31196991 31196991 single base substitution T C exon_variant MELA-AU 15 31196991 31196991 single base substitution T C intron_variant MELA-AU 15 31196991 31196991 single base substitution T C missense_variant L42P 125T>C MELA-AU 15 31197848 31197848 single base substitution G A exon_variant MELA-AU 15 31197848 31197848 single base substitution G A intron_variant MELA-AU 15 31197848 31197848 single base substitution G A missense_variant D328N 982G>A MELA-AU 15 31198576 31198576 single base substitution T C intron_variant MELA-AU 15 31198576 31198576 single base substitution T C splice_region_variant MELA-AU 15 31199741 31199741 single base substitution C A intron_variant MELA-AU 15 31199743 31199743 single base substitution A C intron_variant MELA-AU 15 31199786 31199786 single base substitution C T intron_variant MELA-AU 15 31199969 31199969 single base substitution C T intron_variant MELA-AU 15 31200765 31200765 single base substitution C T intron_variant MELA-AU 15 31200775 31200776 multiple base substitution (>=2bp and <=200bp) AC GT intron_variant MELA-AU 15 31200885 31200902 deletion of <=200bp CTAAAAATACAAAATTAG - intron_variant MELA-AU 15 31201435 31201435 single base substitution T A intron_variant MELA-AU 15 31201829 31201829 single base substitution C T intron_variant MELA-AU 15 31202005 31202005 single base substitution C T intron_variant MELA-AU 15 31202154 31202154 single base substitution C T intron_variant MELA-AU 15 31202855 31202855 single base substitution C T 3_prime_UTR_variant MELA-AU 15 31202855 31202855 single base substitution C T missense_variant L472F 1414C>T MELA-AU 15 31202855 31202855 single base substitution C T missense_variant L78F 232C>T MELA-AU 15 31205544 31205544 single base substitution C T downstream_gene_variant MELA-AU 15 31205544 31205544 single base substitution C T intron_variant MELA-AU 15 31205704 31205704 single base substitution A G downstream_gene_variant MELA-AU 15 31205704 31205704 single base substitution A G intron_variant MELA-AU 15 31205924 31205924 single base substitution C T downstream_gene_variant MELA-AU 15 31205924 31205924 single base substitution C T intron_variant MELA-AU 15 31205974 31205974 single base substitution C T downstream_gene_variant MELA-AU 15 31205974 31205974 single base substitution C T intron_variant MELA-AU 15 31206236 31206236 single base substitution C T 3_prime_UTR_variant MELA-AU 15 31206236 31206236 single base substitution C T downstream_gene_variant MELA-AU 15 31206236 31206236 single base substitution C T missense_variant P585S 1753C>T MELA-AU 15 31206465 31206465 single base substitution G A downstream_gene_variant MELA-AU 15 31206465 31206465 single base substitution G A intron_variant MELA-AU 15 31207950 31207950 single base substitution C T downstream_gene_variant MELA-AU 15 31207950 31207950 single base substitution C T intron_variant MELA-AU 15 31208079 31208079 single base substitution C T downstream_gene_variant MELA-AU 15 31208079 31208079 single base substitution C T intron_variant MELA-AU 15 31210997 31210997 single base substitution C T intron_variant MELA-AU 15 31210997 31210997 single base substitution C T upstream_gene_variant MELA-AU 15 31211331 31211331 single base substitution C T intron_variant MELA-AU 15 31211331 31211331 single base substitution C T upstream_gene_variant MELA-AU 15 31211443 31211443 single base substitution C T intron_variant MELA-AU 15 31211443 31211443 single base substitution C T upstream_gene_variant MELA-AU 15 31212106 31212106 single base substitution C T intron_variant MELA-AU 15 31212106 31212106 single base substitution C T upstream_gene_variant MELA-AU 15 31213996 31213996 single base substitution G A intron_variant MELA-AU 15 31213996 31213996 single base substitution G A upstream_gene_variant MELA-AU 15 31214029 31214029 single base substitution C T intron_variant MELA-AU 15 31214029 31214029 single base substitution C T upstream_gene_variant MELA-AU 15 31214645 31214645 single base substitution A G intron_variant MELA-AU 15 31214976 31214976 single base substitution C T intron_variant MELA-AU 15 31217499 31217499 single base substitution G A splice_region_variant MELA-AU 15 31217499 31217499 single base substitution G A upstream_gene_variant MELA-AU 15 31218115 31218115 single base substitution C T 3_prime_UTR_variant MELA-AU 15 31218115 31218115 single base substitution C T exon_variant MELA-AU 15 31218115 31218115 single base substitution C T missense_variant H821Y 2461C>T MELA-AU 15 31218115 31218115 single base substitution C T upstream_gene_variant MELA-AU 15 31218229 31218229 single base substitution C T intron_variant MELA-AU 15 31218229 31218229 single base substitution C T upstream_gene_variant MELA-AU 15 31219141 31219141 single base substitution C T intron_variant MELA-AU 15 31219141 31219141 single base substitution C T upstream_gene_variant MELA-AU 15 31220577 31220577 single base substitution C T intron_variant MELA-AU 15 31220577 31220577 single base substitution C T upstream_gene_variant MELA-AU 15 31221540 31221541 multiple base substitution (>=2bp and <=200bp) GG TA 3_prime_UTR_variant MELA-AU 15 31221540 31221541 multiple base substitution (>=2bp and <=200bp) GG TA exon_variant MELA-AU 15 31221540 31221541 multiple base substitution (>=2bp and <=200bp) GG TA missense_variant QE909HK MELA-AU 15 31223003 31223003 single base substitution C T downstream_gene_variant MELA-AU 15 31223003 31223003 single base substitution C T intron_variant MELA-AU 15 31224227 31224227 single base substitution C T downstream_gene_variant MELA-AU 15 31224227 31224227 single base substitution C T intron_variant MELA-AU 15 31224529 31224529 single base substitution C T downstream_gene_variant MELA-AU 15 31224529 31224529 single base substitution C T intron_variant MELA-AU 15 31225294 31225294 insertion of <=200bp - A downstream_gene_variant MELA-AU 15 31225294 31225294 insertion of <=200bp - A intron_variant MELA-AU 15 31228239 31228239 single base substitution C T intron_variant MELA-AU 15 31228901 31228901 single base substitution C G intron_variant MELA-AU 15 31231502 31231502 single base substitution A T intron_variant MELA-AU 15 31231558 31231558 single base substitution G A intron_variant MELA-AU 15 31233323 31233324 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 31234951 31234951 single base substitution G A 3_prime_UTR_variant MELA-AU 15 31235757 31235757 single base substitution C T downstream_gene_variant MELA-AU 15 31236412 31236412 single base substitution G A downstream_gene_variant MELA-AU 15 31236788 31236788 deletion of <=200bp T - downstream_gene_variant MELA-AU 15 31238714 31238714 single base substitution C A downstream_gene_variant MELA-AU 15 31238878 31238878 single base substitution G A downstream_gene_variant MELA-AU 15 31240182 31240182 single base substitution A T downstream_gene_variant ORCA-IN 15 31199725 31199735 deletion of <=200bp AAAAACAAAAC - intron_variant ORCA-IN 15 31201406 31201406 single base substitution G C intron_variant ORCA-IN 15 31229718 31229718 single base substitution G C intron_variant ORCA-IN 15 31239350 31239350 single base substitution G A downstream_gene_variant OV-AU 15 31219951 31219951 single base substitution G A intron_variant OV-AU 15 31219951 31219951 single base substitution G A upstream_gene_variant OV-AU 15 31225597 31225597 single base substitution A C downstream_gene_variant OV-AU 15 31225597 31225597 single base substitution A C intron_variant OV-AU 15 31236361 31236361 single base substitution G C downstream_gene_variant PACA-AU 15 31193157 31193157 single base substitution A G upstream_gene_variant PACA-AU 15 31199741 31199741 single base substitution C A intron_variant PACA-AU 15 31199743 31199743 single base substitution A C intron_variant PACA-AU 15 31202509 31202509 single base substitution G A intron_variant PACA-AU 15 31215044 31215044 single base substitution A T intron_variant PACA-AU 15 31220796 31220798 deletion of <=200bp CCT - 3_prime_UTR_variant PACA-AU 15 31220796 31220798 deletion of <=200bp CCT - exon_variant PACA-AU 15 31220796 31220798 deletion of <=200bp CCT - inframe_deletion GL843G PACA-AU 15 31222256 31222256 single base substitution A G intron_variant PACA-AU 15 31223403 31223403 single base substitution C G downstream_gene_variant PACA-AU 15 31223403 31223403 single base substitution C G intron_variant PACA-AU 15 31224270 31224270 deletion of <=200bp A - downstream_gene_variant PACA-AU 15 31224270 31224270 deletion of <=200bp A - intron_variant PACA-AU 15 31228832 31228832 single base substitution A G intron_variant PACA-AU 15 31231505 31231505 single base substitution A G intron_variant PACA-AU 15 31233939 31233939 single base substitution C T 3_prime_UTR_variant PACA-AU 15 31237626 31237626 single base substitution G C downstream_gene_variant PACA-AU 15 31238798 31238798 single base substitution C A downstream_gene_variant PACA-CA 15 31192521 31192521 deletion of <=200bp G - upstream_gene_variant PACA-CA 15 31192890 31192890 single base substitution G A upstream_gene_variant PACA-CA 15 31193292 31193292 single base substitution C T upstream_gene_variant PACA-CA 15 31196894 31196897 deletion of <=200bp AAAA - exon_variant PACA-CA 15 31196894 31196897 deletion of <=200bp AAAA - frameshift_variant KK10 PACA-CA 15 31196894 31196897 deletion of <=200bp AAAA - intron_variant PACA-CA 15 31199616 31199616 single base substitution G C intron_variant PACA-CA 15 31215332 31215332 single base substitution G A intron_variant PACA-CA 15 31221621 31221621 single base substitution C T intron_variant PACA-CA 15 31225568 31225568 single base substitution A G downstream_gene_variant PACA-CA 15 31225568 31225568 single base substitution A G intron_variant PACA-CA 15 31230399 31230399 single base substitution A T intron_variant PACA-CA 15 31230400 31230400 deletion of <=200bp T - intron_variant PACA-CA 15 31231513 31231513 single base substitution G A intron_variant PACA-CA 15 31235104 31235104 insertion of <=200bp - A 3_prime_UTR_variant PACA-CA 15 31239817 31239817 single base substitution C A downstream_gene_variant PAEN-AU 15 31192362 31192362 single base substitution G A upstream_gene_variant PAEN-AU 15 31206659 31206659 single base substitution C A downstream_gene_variant PAEN-AU 15 31206659 31206659 single base substitution C A intron_variant PBCA-DE 15 31201191 31201191 single base substitution C T intron_variant PBCA-DE 15 31213376 31213376 single base substitution G T intron_variant PBCA-DE 15 31213376 31213376 single base substitution G T upstream_gene_variant PBCA-DE 15 31224577 31224577 single base substitution T G downstream_gene_variant PBCA-DE 15 31224577 31224577 single base substitution T G intron_variant PBCA-DE 15 31237402 31237402 single base substitution C T downstream_gene_variant PRAD-CA 15 31239891 31239891 single base substitution C G downstream_gene_variant PRAD-UK 15 31192317 31192317 single base substitution A G upstream_gene_variant PRAD-UK 15 31197092 31197092 single base substitution C T exon_variant PRAD-UK 15 31197092 31197092 single base substitution C T intron_variant PRAD-UK 15 31197092 31197092 single base substitution C T stop_gained Q76* 226C>T PRAD-UK 15 31199588 31199588 single base substitution G T intron_variant PRAD-UK 15 31207347 31207347 single base substitution C T downstream_gene_variant PRAD-UK 15 31207347 31207347 single base substitution C T intron_variant PRAD-UK 15 31211673 31211673 single base substitution C T intron_variant PRAD-UK 15 31211673 31211673 single base substitution C T upstream_gene_variant PRAD-UK 15 31220056 31220056 single base substitution C A intron_variant PRAD-UK 15 31220056 31220056 single base substitution C A upstream_gene_variant PRAD-UK 15 31235901 31235911 deletion of <=200bp GGGCGGGTGCA - downstream_gene_variant PRAD-US 15 31196925 31196925 single base substitution G T exon_variant PRAD-US 15 31196925 31196925 single base substitution G T intron_variant PRAD-US 15 31196925 31196925 single base substitution G T missense_variant S20I 59G>T PRAD-US 15 31197979 31197979 single base substitution T C exon_variant PRAD-US 15 31197979 31197979 single base substitution T C intron_variant PRAD-US 15 31197979 31197979 single base substitution T C synonymous_variant G371G 1113T>C PRAD-US 15 31229359 31229359 single base substitution A G 3_prime_UTR_variant PRAD-US 15 31229359 31229359 single base substitution A G missense_variant H985R 2954A>G READ-US 15 31212812 31212812 single base substitution T G 3_prime_UTR_variant READ-US 15 31212812 31212812 single base substitution T G missense_variant L670V 2008T>G READ-US 15 31212812 31212812 single base substitution T G upstream_gene_variant READ-US 15 31234044 31234044 single base substitution T G 3_prime_UTR_variant READ-US 15 31234231 31234231 single base substitution C A 3_prime_UTR_variant RECA-EU 15 31198802 31198802 single base substitution T C intron_variant RECA-EU 15 31203333 31203333 single base substitution T G 3_prime_UTR_variant RECA-EU 15 31203333 31203333 single base substitution T G downstream_gene_variant RECA-EU 15 31203333 31203333 single base substitution T G intron_variant RECA-EU 15 31207192 31207192 single base substitution A C downstream_gene_variant RECA-EU 15 31207192 31207192 single base substitution A C intron_variant RECA-EU 15 31208551 31208551 single base substitution T G downstream_gene_variant RECA-EU 15 31208551 31208551 single base substitution T G intron_variant RECA-EU 15 31217119 31217119 single base substitution C A intron_variant RECA-EU 15 31217119 31217119 single base substitution C A upstream_gene_variant RECA-EU 15 31226244 31226244 single base substitution T G downstream_gene_variant RECA-EU 15 31226244 31226244 single base substitution T G intron_variant RECA-EU 15 31227717 31227717 single base substitution C A downstream_gene_variant RECA-EU 15 31227717 31227717 single base substitution C A intron_variant RECA-EU 15 31240026 31240026 single base substitution T G downstream_gene_variant SKCA-BR 15 31193802 31193802 insertion of <=200bp - CT upstream_gene_variant SKCA-BR 15 31196213 31196213 single base substitution A C 5_prime_UTR_variant SKCA-BR 15 31196213 31196213 single base substitution A C intron_variant SKCA-BR 15 31196213 31196213 single base substitution A C splice_region_variant SKCA-BR 15 31196213 31196213 single base substitution A C upstream_gene_variant SKCA-BR 15 31197382 31197382 single base substitution G A exon_variant SKCA-BR 15 31197382 31197382 single base substitution G A intron_variant SKCA-BR 15 31197382 31197382 single base substitution G A synonymous_variant K172K 516G>A SKCA-BR 15 31199426 31199426 single base substitution A G intron_variant SKCA-BR 15 31202497 31202497 single base substitution G A intron_variant SKCA-BR 15 31204264 31204266 deletion of <=200bp CAA - downstream_gene_variant SKCA-BR 15 31204264 31204266 deletion of <=200bp CAA - intron_variant SKCA-BR 15 31204426 31204426 single base substitution G C downstream_gene_variant SKCA-BR 15 31204426 31204426 single base substitution G C intron_variant SKCA-BR 15 31210651 31210651 single base substitution A G intron_variant SKCA-BR 15 31210651 31210651 single base substitution A G upstream_gene_variant SKCA-BR 15 31216904 31216904 single base substitution G A intron_variant SKCA-BR 15 31216904 31216904 single base substitution G A upstream_gene_variant SKCA-BR 15 31219404 31219404 single base substitution C T intron_variant SKCA-BR 15 31219404 31219404 single base substitution C T upstream_gene_variant SKCA-BR 15 31220709 31220709 insertion of <=200bp - TTGTGTG exon_variant SKCA-BR 15 31220709 31220709 insertion of <=200bp - TTGTGTG intron_variant SKCA-BR 15 31221757 31221762 deletion of <=200bp ATATAT - intron_variant SKCA-BR 15 31222617 31222617 single base substitution G A intron_variant SKCA-BR 15 31223026 31223026 single base substitution C G downstream_gene_variant SKCA-BR 15 31223026 31223026 single base substitution C G intron_variant SKCA-BR 15 31223055 31223055 single base substitution T G downstream_gene_variant SKCA-BR 15 31223055 31223055 single base substitution T G intron_variant SKCA-BR 15 31223214 31223214 single base substitution G A downstream_gene_variant SKCA-BR 15 31223214 31223214 single base substitution G A intron_variant SKCA-BR 15 31224424 31224425 deletion of <=200bp CA - downstream_gene_variant SKCA-BR 15 31224424 31224425 deletion of <=200bp CA - intron_variant SKCA-BR 15 31227343 31227343 single base substitution C T downstream_gene_variant SKCA-BR 15 31227343 31227343 single base substitution C T intron_variant SKCA-BR 15 31233220 31233220 single base substitution C T intron_variant SKCM-US 15 31196894 31196894 deletion of <=200bp A - exon_variant SKCM-US 15 31196894 31196894 deletion of <=200bp A - frameshift_variant K10 SKCM-US 15 31196894 31196894 deletion of <=200bp A - intron_variant SKCM-US 15 31196961 31196961 single base substitution C T exon_variant SKCM-US 15 31196961 31196961 single base substitution C T intron_variant SKCM-US 15 31196961 31196961 single base substitution C T missense_variant S32L 95C>T SKCM-US 15 31196991 31196991 single base substitution T C exon_variant SKCM-US 15 31196991 31196991 single base substitution T C intron_variant SKCM-US 15 31196991 31196991 single base substitution T C missense_variant L42P 125T>C SKCM-US 15 31202912 31202912 single base substitution G A 3_prime_UTR_variant SKCM-US 15 31202912 31202912 single base substitution G A missense_variant G491R 1471G>A SKCM-US 15 31202912 31202912 single base substitution G A missense_variant G97R 289G>A SKCM-US 15 31206141 31206141 single base substitution C T 3_prime_UTR_variant SKCM-US 15 31206141 31206141 single base substitution C T downstream_gene_variant SKCM-US 15 31206141 31206141 single base substitution C T missense_variant S553L 1658C>T SKCM-US 15 31218056 31218056 single base substitution C T 3_prime_UTR_variant SKCM-US 15 31218056 31218056 single base substitution C T exon_variant SKCM-US 15 31218056 31218056 single base substitution C T missense_variant A801V 2402C>T SKCM-US 15 31218056 31218056 single base substitution C T upstream_gene_variant SKCM-US 15 31218060 31218060 single base substitution G A 3_prime_UTR_variant SKCM-US 15 31218060 31218060 single base substitution G A exon_variant SKCM-US 15 31218060 31218060 single base substitution G A synonymous_variant G802G 2406G>A SKCM-US 15 31218060 31218060 single base substitution G A upstream_gene_variant SKCM-US 15 31220836 31220836 single base substitution G A 3_prime_UTR_variant SKCM-US 15 31220836 31220836 single base substitution G A exon_variant SKCM-US 15 31220836 31220836 single base substitution G A missense_variant D857N 2569G>A SKCM-US 15 31221449 31221449 single base substitution G A 3_prime_UTR_variant SKCM-US 15 31221449 31221449 single base substitution G A exon_variant SKCM-US 15 31221449 31221449 single base substitution G A missense_variant R879K 2636G>A SKCM-US 15 31234080 31234080 single base substitution C T 3_prime_UTR_variant SKCM-US 15 31234118 31234118 single base substitution T C 3_prime_UTR_variant SKCM-US 15 31239361 31239361 single base substitution G T downstream_gene_variant SKCM-US 15 31239448 31239448 single base substitution G A downstream_gene_variant STAD-US 15 31196885 31196887 deletion of <=200bp CCT - exon_variant STAD-US 15 31196885 31196887 deletion of <=200bp CCT - inframe_deletion P7 STAD-US 15 31196885 31196887 deletion of <=200bp CCT - intron_variant STAD-US 15 31197145 31197145 single base substitution C A exon_variant STAD-US 15 31197145 31197145 single base substitution C A intron_variant STAD-US 15 31197145 31197145 single base substitution C A synonymous_variant T93T 279C>A STAD-US 15 31197648 31197648 single base substitution C T exon_variant STAD-US 15 31197648 31197648 single base substitution C T intron_variant STAD-US 15 31197648 31197648 single base substitution C T missense_variant A261V 782C>T STAD-US 15 31197803 31197803 single base substitution A G exon_variant STAD-US 15 31197803 31197803 single base substitution A G intron_variant STAD-US 15 31197803 31197803 single base substitution A G missense_variant K313E 937A>G STAD-US 15 31197974 31197974 single base substitution A G exon_variant STAD-US 15 31197974 31197974 single base substitution A G intron_variant STAD-US 15 31197974 31197974 single base substitution A G missense_variant T370A 1108A>G STAD-US 15 31202890 31202890 single base substitution C A 3_prime_UTR_variant STAD-US 15 31202890 31202890 single base substitution C A synonymous_variant T483T 1449C>A STAD-US 15 31202890 31202890 single base substitution C A synonymous_variant T89T 267C>A STAD-US 15 31206224 31206224 single base substitution C T 3_prime_UTR_variant STAD-US 15 31206224 31206224 single base substitution C T downstream_gene_variant STAD-US 15 31206224 31206224 single base substitution C T stop_gained R581* 1741C>T STAD-US 15 31206262 31206262 single base substitution C T 3_prime_UTR_variant STAD-US 15 31206262 31206262 single base substitution C T downstream_gene_variant STAD-US 15 31206262 31206262 single base substitution C T synonymous_variant T593T 1779C>T STAD-US 15 31210380 31210380 single base substitution A G 3_prime_UTR_variant STAD-US 15 31210380 31210380 single base substitution A G missense_variant T609A 1825A>G STAD-US 15 31210380 31210380 single base substitution A G upstream_gene_variant STAD-US 15 31214442 31214442 single base substitution C T 3_prime_UTR_variant STAD-US 15 31214442 31214442 single base substitution C T missense_variant A686V 2057C>T STAD-US 15 31214442 31214442 single base substitution C T upstream_gene_variant STAD-US 15 31217442 31217442 single base substitution T C 3_prime_UTR_variant STAD-US 15 31217442 31217442 single base substitution T C exon_variant STAD-US 15 31217442 31217442 single base substitution T C missense_variant F762S 2285T>C STAD-US 15 31217442 31217442 single base substitution T C upstream_gene_variant STAD-US 15 31218089 31218089 single base substitution G A 3_prime_UTR_variant STAD-US 15 31218089 31218089 single base substitution G A exon_variant STAD-US 15 31218089 31218089 single base substitution G A missense_variant C812Y 2435G>A STAD-US 15 31218089 31218089 single base substitution G A upstream_gene_variant STAD-US 15 31222835 31222835 single base substitution C T 3_prime_UTR_variant STAD-US 15 31222835 31222835 single base substitution C T exon_variant STAD-US 15 31222835 31222835 single base substitution C T synonymous_variant P959P 2877C>T STAD-US 15 31233850 31233850 single base substitution G A 3_prime_UTR_variant STAD-US 15 31234015 31234015 single base substitution C G 3_prime_UTR_variant STAD-US 15 31234037 31234038 deletion of <=200bp CA - 3_prime_UTR_variant STAD-US 15 31239334 31239334 single base substitution G A downstream_gene_variant STAD-US 15 31239370 31239370 single base substitution A G downstream_gene_variant THCA-SA 15 31197564 31197564 single base substitution G A exon_variant THCA-SA 15 31197564 31197564 single base substitution G A intron_variant THCA-SA 15 31197564 31197564 single base substitution G A missense_variant G233E 698G>A THCA-SA 15 31203093 31203093 single base substitution C T 3_prime_UTR_variant THCA-SA 15 31203093 31203093 single base substitution C T downstream_gene_variant THCA-SA 15 31203093 31203093 single base substitution C T intron_variant THCA-SA 15 31229420 31229420 single base substitution T C 3_prime_UTR_variant THCA-SA 15 31229420 31229420 single base substitution T C synonymous_variant H1005H 3015T>C THCA-SA 15 31231255 31231255 single base substitution A G intron_variant THCA-US 15 31202968 31202968 single base substitution C T 3_prime_UTR_variant THCA-US 15 31202968 31202968 single base substitution C T downstream_gene_variant THCA-US 15 31202968 31202968 single base substitution C T synonymous_variant V509V 1527C>T UCEC-US 15 31196980 31196980 single base substitution A G exon_variant UCEC-US 15 31196980 31196980 single base substitution A G intron_variant UCEC-US 15 31196980 31196980 single base substitution A G synonymous_variant P38P 114A>G UCEC-US 15 31197155 31197155 single base substitution G A exon_variant UCEC-US 15 31197155 31197155 single base substitution G A intron_variant UCEC-US 15 31197155 31197155 single base substitution G A missense_variant V97I 289G>A UCEC-US 15 31197344 31197344 single base substitution T C exon_variant UCEC-US 15 31197344 31197344 single base substitution T C intron_variant UCEC-US 15 31197344 31197344 single base substitution T C missense_variant S160P 478T>C UCEC-US 15 31197563 31197563 single base substitution G A exon_variant UCEC-US 15 31197563 31197563 single base substitution G A intron_variant UCEC-US 15 31197563 31197563 single base substitution G A missense_variant G233R 697G>A UCEC-US 15 31197599 31197599 single base substitution A G exon_variant UCEC-US 15 31197599 31197599 single base substitution A G intron_variant UCEC-US 15 31197599 31197599 single base substitution A G missense_variant T245A 733A>G UCEC-US 15 31197803 31197803 single base substitution A G exon_variant UCEC-US 15 31197803 31197803 single base substitution A G intron_variant UCEC-US 15 31197803 31197803 single base substitution A G missense_variant K313E 937A>G UCEC-US 15 31203041 31203041 single base substitution T G downstream_gene_variant UCEC-US 15 31203041 31203041 single base substitution T G intron_variant UCEC-US 15 31203041 31203041 single base substitution T G stop_lost *534E 1600T>G UCEC-US 15 31206105 31206105 single base substitution C A 3_prime_UTR_variant UCEC-US 15 31206105 31206105 single base substitution C A downstream_gene_variant UCEC-US 15 31206105 31206105 single base substitution C A missense_variant P541H 1622C>A UCEC-US 15 31212806 31212806 single base substitution A G 3_prime_UTR_variant UCEC-US 15 31212806 31212806 single base substitution A G missense_variant R668G 2002A>G UCEC-US 15 31212806 31212806 single base substitution A G upstream_gene_variant UCEC-US 15 31221496 31221496 single base substitution G A 3_prime_UTR_variant UCEC-US 15 31221496 31221496 single base substitution G A exon_variant UCEC-US 15 31221496 31221496 single base substitution G A missense_variant E895K 2683G>A UCEC-US 15 31233730 31233730 single base substitution T G intron_variant UCEC-US 15 31234193 31234193 single base substitution C A 3_prime_UTR_variant UCEC-US 15 31235126 31235126 single base substitution C A 3_prime_UTR_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand CHC1763T COSM4789708 c.1A>G p.M1V Substitution - Missense 15:30904664-30904664 + ESCC-F40 COSM5047731 c.1483C>G p.Q495E Substitution - Missense 15:30910721-30910721 + TCGA-JW-A5VL-01 COSM4847908 c.2650G>C p.E884Q Substitution - Missense 15:30929260-30929260 + TCGA-CD-A4MG-01 COSM4053930 c.1779C>T p.T593T Substitution - coding silent 15:30914059-30914059 + TCGA-DS-A0VM-01 COSM459059 c.695G>A p.R232K Substitution - Missense 15:30905358-30905358 + TCGA-AD-6964-01 COSM1372316 c.1580C>T p.A527V Substitution - Missense 15:30913860-30913860 + Z138 COSM1740219 c.1535G>C p.W512S Substitution - Missense 15:30910773-30910773 + YUKADI COSM1707964 c.1066C>T p.P356S Substitution - Missense 15:30905729-30905729 + RK169_C01 COSM3700935 c.431A>G p.N144S Substitution - Missense 15:30905094-30905094 + 3N57-VS-3T57 COSM4983934 c.36G>T p.R12S Substitution - Missense 15:30904699-30904699 + T2269 COSM1215699 c.2090G>T p.R697I Substitution - Missense 15:30922272-30922272 + CSCC-31-T COSM4465127 c.1369C>T p.Q457* Substitution - Nonsense 15:30908252-30908252 + CHC892T COSM4960696 c.1094G>A p.G365D Substitution - Missense 15:30905757-30905757 + B109 COSM1749093 c.15G>A p.G5G Substitution - coding silent 15:30904678-30904678 + CSCC-31-T COSM4465128 c.1369C>T p.Q457* Substitution - Nonsense 15:30908252-30908252 + TCGA-D1-A0ZP-01 COSM960352 c.289G>A p.V97I Substitution - Missense 15:30904952-30904952 + S02219 COSM5675613 c.1303G>A p.E435K Substitution - Missense 15:30908186-30908186 + KM12 COSM1678326 c.1484A>C p.Q495P Substitution - Missense 15:30910722-30910722 + N170T COSM236640 c.2041C>A p.H681N Substitution - Missense 15:30920642-30920642 + SJHGG093_A COSM4971589 c.1366C>A p.L456I Substitution - Missense 15:30908249-30908249 + S00934 COSM5662729 c.479C>G p.S160C Substitution - Missense 15:30905142-30905142 + CSCC-57-T COSM4449541 c.2593-1G>A p.? Unknown 15:30929202-30929202 + TCGA-AZ-4315-01 COSM5828211 c.1061G>A p.S354N Substitution - Missense 15:30905724-30905724 + TCGA-EL-A3CR-01 COSM3370136 c.1527C>T p.V509V Substitution - coding silent 15:30910765-30910765 + CSCC-41-T COSM4510234 c.830C>T p.S277F Substitution - Missense 15:30905493-30905493 + T3306 COSM4683332 c.642C>T p.N214N Substitution - coding silent 15:30905305-30905305 + CHC892T COSM4960696 c.1094G>A p.G365D Substitution - Missense 15:30905757-30905757 + TCGA-BR-8284-01 COSM4053922 c.782C>T p.A261V Substitution - Missense 15:30905445-30905445 + PTC-7C COSM3734135 c.698G>A p.G233E Substitution - Missense 15:30905361-30905361 + TCGA-KK-A59Y-01 COSM4877947 c.1113T>C p.G371G Substitution - coding silent 15:30905776-30905776 + HT115 COSM2084271 c.95C>T p.S32L Substitution - Missense 15:30904758-30904758 + S02296 COSM5689402 c.545A>G p.Q182R Substitution - Missense 15:30905208-30905208 + 391 COSM4427893 c.1974G>T p.R658R Substitution - coding silent 15:30920575-30920575 + TCGA-A2-A04U-01 COSM5193204 c.2996delC p.A999fs*3 Deletion - Frameshift 15:30937198-30937198 + S02219 COSM5675615 c.1662G>A p.L554L Substitution - coding silent 15:30913942-30913942 + 2492723 COSM5722274 c.1850C>T p.S617F Substitution - Missense 15:30918202-30918202 + TCGA-GU-A42R-01 COSM3794064 c.185A>G p.E62G Substitution - Missense 15:30904848-30904848 + TCGA-KV-A6GD-01 COSM3987897 c.972T>G p.H324Q Substitution - Missense 15:30905635-30905635 + BN24T COSM1608233 c.2476G>A p.G826S Substitution - Missense 15:30925927-30925927 + PT48 COSM5933360 c.1436C>T p.S479F Substitution - Missense 15:30910674-30910674 + BN06T COSM1608234 c.3024_3027delAGTT p.V1009fs*>8 Deletion - Frameshift 15:30937226-30937229 + S02219 COSM1749094 c.15G>A p.G5G Substitution - coding silent 15:30904678-30904678 + CHC892T COSM4960695 c.1094G>A p.G365D Substitution - Missense 15:30905757-30905757 + TCGA-33-4533-01 COSM700210 c.3G>A p.M1I Substitution - Missense 15:30904666-30904666 + CHC1742T COSM4792229 c.1894C>T p.Q632* Substitution - Nonsense 15:30918246-30918246 + E61 COSM1717609 c.1921C>A p.L641M Substitution - Missense 15:30918273-30918273 + 49M COSM5590916 c.1932C>T p.H644H Substitution - coding silent 15:30918284-30918284 + ME011T COSM224480 c.1914G>A p.W638* Substitution - Nonsense 15:30918266-30918266 + ESCC_60 COSM5632697 c.2315T>C p.M772T Substitution - Missense 15:30925269-30925269 + I2L-P7-Tumor-Organoid COSM5363117 c.2982G>A p.L994L Substitution - coding silent 15:30937184-30937184 + LC_C29 COSM1188942 c.918G>T p.M306I Substitution - Missense 15:30905581-30905581 + TCGA-AP-A0LM-01 COSM960356 c.937A>G p.K313E Substitution - Missense 15:30905600-30905600 + TCGA-CA-6718-01 COSM5144579 c.964A>C p.K322Q Substitution - Missense 15:30905627-30905627 + S02296 COSM5689403 c.545A>G p.Q182R Substitution - Missense 15:30905208-30905208 + LUAD-NYU315 COSM373576 c.1651C>G p.L551V Substitution - Missense 15:30913931-30913931 + TCGA-EE-A3AA-06 COSM3500344 c.125T>C p.L42P Substitution - Missense 15:30904788-30904788 + ESCC-F87 COSM5048957 c.1027G>A p.D343N Substitution - Missense 15:30905690-30905690 + TCGA-KK-A59Y-01 COSM4877948 c.1113T>C p.G371G Substitution - coding silent 15:30905776-30905776 + CHC1763T COSM4789708 c.1A>G p.M1V Substitution - Missense 15:30904664-30904664 + TCGA-EE-A2GI-06 COSM3500345 c.1471G>A p.G491R Substitution - Missense 15:30910709-30910709 + TCGA-AD-6889-01 COSM1372318 c.2270C>T p.P757L Substitution - Missense 15:30925224-30925224 + TCGA-BG-A0VZ-01 COSM960359 c.2683G>A p.E895K Substitution - Missense 15:30929293-30929293 + T3080 COSM4683329 c.63G>T p.K21N Substitution - Missense 15:30904726-30904726 + TCGA-CG-5721-01 COSM960356 c.937A>G p.K313E Substitution - Missense 15:30905600-30905600 + TCGA-CJ-4913-01 COSM470486 c.2546T>G p.I849S Substitution - Missense 15:30928610-30928610 + TCGA-34-2596-01 COSM1646665 c.530C>T p.A177V Substitution - Missense 15:30905193-30905193 + TCGA-AA-A00N-01 COSM275086 c.2714C>T p.T905M Substitution - Missense 15:30929324-30929324 + EGC8 COSM4613382 c.28delA p.R12fs*45 Deletion - Frameshift 15:30904691-30904691 + TCGA-HU-A4GT-01 COSM4053932 c.2057C>T p.A686V Substitution - Missense 15:30922239-30922239 + B109-Tumor COSM1749093 c.15G>A p.G5G Substitution - coding silent 15:30904678-30904678 + 381T COSM4386014 c.2876C>A p.P959H Substitution - Missense 15:30930631-30930631 + TCGA-CG-4305-01 COSM4053920 c.279C>A p.T93T Substitution - coding silent 15:30904942-30904942 + TCGA-D1-A174-01 COSM960357 c.1622C>A p.P541H Substitution - Missense 15:30913902-30913902 + pfg029T COSM1640203 c.1705G>C p.G569R Substitution - Missense 15:30913985-30913985 + CSCC-41-T COSM4510233 c.830C>T p.S277F Substitution - Missense 15:30905493-30905493 + B109-Tumor COSM1749094 c.15G>A p.G5G Substitution - coding silent 15:30904678-30904678 + BN24 COSM1608233 c.2476G>A p.G826S Substitution - Missense 15:30925927-30925927 + SC_9005 COSM5568001 c.86C>G p.S29C Substitution - Missense 15:30904749-30904749 + T578 COSM4683333 c.2065G>T p.E689* Substitution - Nonsense 15:30922247-30922247 + TCGA-FU-A3HZ-01 COSM4839720 c.697G>T p.G233* Substitution - Nonsense 15:30905360-30905360 + TCGA-BH-A0DP-01 COSM433692 c.921_922delTG p.V308fs*5 Deletion - Frameshift 15:30905584-30905585 + TCGA-AC-A3QP-01 COSM3815816 c.986A>T p.D329V Substitution - Missense 15:30905649-30905649 + TCGA-E2-A570-01 COSM3815818 c.1758T>G p.S586R Substitution - Missense 15:30914038-30914038 + 2492720 COSM5722274 c.1850C>T p.S617F Substitution - Missense 15:30918202-30918202 + 4P2 COSM3734136 c.698G>A p.G233E Substitution - Missense 15:30905361-30905361 + HT115 COSM2084272 c.95C>T p.S32L Substitution - Missense 15:30904758-30904758 + RK169_C01 COSM3700934 c.431A>G p.N144S Substitution - Missense 15:30905094-30905094 + ESCC-D13 COSM5045365 c.1796G>C p.R599T Substitution - Missense 15:30914076-30914076 + 3844_T COSM3956541 c.995C>T p.A332V Substitution - Missense 15:30905658-30905658 + TCGA-EE-A2GO-06 COSM3500348 c.2406G>A p.G802G Substitution - coding silent 15:30925857-30925857 + TCGA-FW-A3R5-06 COSM275085 c.1658C>T p.S553L Substitution - Missense 15:30913938-30913938 + 2492722 COSM5722274 c.1850C>T p.S617F Substitution - Missense 15:30918202-30918202 + KM12 COSM1678326 c.1484A>C p.Q495P Substitution - Missense 15:30910722-30910722 + T2944 COSM4683335 c.2404G>A p.G802R Substitution - Missense 15:30925855-30925855 + TCGA-BR-8361-01 COSM4053931 c.1825A>G p.T609A Substitution - Missense 15:30918177-30918177 + pfg057T COSM4746899 c.561_570del10 p.V188fs*2 Deletion - Frameshift 15:30905224-30905233 + 587256 COSM1215701 c.2860T>C p.C954R Substitution - Missense 15:30930615-30930615 + TCGA-HC-8216-01 COSM3672018 c.59G>T p.S20I Substitution - Missense 15:30904722-30904722 + CH-109-T2 COSM5650655 c.1900G>A p.A634T Substitution - Missense 15:30918252-30918252 + 255 COSM3732247 c.2227C>T p.R743C Substitution - Missense 15:30925181-30925181 + ESCC-152T COSM3936715 c.2173-1G>C p.? Unknown 15:30925126-30925126 + CSCC-31-T COSM4480576 c.2431C>T p.L811L Substitution - coding silent 15:30925882-30925882 + CHC1742T COSM4792229 c.1894C>T p.Q632* Substitution - Nonsense 15:30918246-30918246 + ESCC_170 COSM5649213 c.2985G>A p.Q995Q Substitution - coding silent 15:30937187-30937187 + TCGA-CS-4944-01 COSM3969056 c.1427A>G p.E476G Substitution - Missense 15:30910665-30910665 + TCGA-D9-A4Z3-01 COSM3500350 c.2636G>A p.R879K Substitution - Missense 15:30929246-30929246 + TCGA-A5-A0G5-01 COSM960350 c.114A>G p.P38P Substitution - coding silent 15:30904777-30904777 + TCGA-BR-8363-01 COSM4053933 c.2285T>C p.F762S Substitution - Missense 15:30925239-30925239 + CSCC-55-T COSM4516979 c.2600_2601CC>TT p.P867L Substitution - Missense 15:30929210-30929211 + TCGA-CS-4944-01 COSM3969057 c.1427A>G p.E476G Substitution - Missense 15:30910665-30910665 + T3062 COSM4683334 c.2276G>A p.C759Y Substitution - Missense 15:30925230-30925230 + TCGA-C5-A1MH-01 COSM4821086 c.421G>A p.E141K Substitution - Missense 15:30905084-30905084 + 0077_CRUK_PC_0077_T1_DNA COSM4419365 c.226C>T p.Q76* Substitution - Nonsense 15:30904889-30904889 + 1N05-VS-1T05 COSM4972824 c.570G>C p.K190N Substitution - Missense 15:30905233-30905233 + LUAD-NYU259 COSM371749 c.652T>C p.C218R Substitution - Missense 15:30905315-30905315 + LIM2405 COSM4613381 c.28delA p.R12fs*45 Deletion - Frameshift 15:30904691-30904691 + TCGA-J4-A67M-01 COSM3782865 c.2954A>G p.H985R Substitution - Missense 15:30937156-30937156 + TCGA-EE-A29M-06 COSM2084272 c.95C>T p.S32L Substitution - Missense 15:30904758-30904758 + PD4006a COSM1740218 c.1535G>C p.W512S Substitution - Missense 15:30910773-30910773 + 3844_T COSM3956542 c.995C>T p.A332V Substitution - Missense 15:30905658-30905658 + T3090 COSM4683336 c.2805delG p.G937fs*52 Deletion - Frameshift 15:30930560-30930560 + S02219 COSM5675616 c.1675G>A p.E559K Substitution - Missense 15:30913955-30913955 + TCGA-A2-A1G4-01 COSM1478033 c.1750T>A p.F584I Substitution - Missense 15:30914030-30914030 + 587256 COSM1215700 c.994G>A p.A332T Substitution - Missense 15:30905657-30905657 + TCGA-AA-A00N-01 COSM275085 c.1658C>T p.S553L Substitution - Missense 15:30913938-30913938 + TCGA-CG-4305-01 COSM4053921 c.279C>A p.T93T Substitution - coding silent 15:30904942-30904942 + TCGA-AZ-4315-01 COSM1372314 c.1061G>A p.S354N Substitution - Missense 15:30905724-30905724 + 49M COSM5590914 c.207C>T p.F69F Substitution - coding silent 15:30904870-30904870 + TCGA-AC-A3QP-01 COSM3815817 c.986A>T p.D329V Substitution - Missense 15:30905649-30905649 + S02219 COSM5675614 c.1303G>A p.E435K Substitution - Missense 15:30908186-30908186 + TCGA-BR-8368-01 COSM4053935 c.2877C>T p.P959P Substitution - coding silent 15:30930632-30930632 + LS411 COSM2084277 c.277A>G p.T93A Substitution - Missense 15:30904940-30904940 + EGC8 COSM4613381 c.28delA p.R12fs*45 Deletion - Frameshift 15:30904691-30904691 + 3N04-VS-3T04 COSM4978669 c.2613C>T p.C871C Substitution - coding silent 15:30929223-30929223 + T27 COSM1177709 c.686A>G p.H229R Substitution - Missense 15:30905349-30905349 + YUKADI COSM1707963 c.1066C>T p.P356S Substitution - Missense 15:30905729-30905729 + LS411 COSM2084278 c.277A>G p.T93A Substitution - Missense 15:30904940-30904940 + CHC1763T COSM4789709 c.1A>G p.M1V Substitution - Missense 15:30904664-30904664 + S02219 COSM5675611 c.546G>C p.Q182H Substitution - Missense 15:30905209-30905209 + TCGA-AP-A05N-01 COSM960355 c.733A>G p.T245A Substitution - Missense 15:30905396-30905396 + RK197_C01 COSM3744544 c.1366C>G p.L456V Substitution - Missense 15:30908249-30908249 + ESCC-F87 COSM5048956 c.1027G>A p.D343N Substitution - Missense 15:30905690-30905690 + 587376 COSM1215699 c.2090G>T p.R697I Substitution - Missense 15:30922272-30922272 + S00934 COSM5662728 c.479C>G p.S160C Substitution - Missense 15:30905142-30905142 + TCGA-AP-A05J-01 COSM960360 c.2898C>T p.S966S Substitution - coding silent 15:30930653-30930653 + T3104 COSM4683327 c.27_28insA p.R12fs*4 Insertion - Frameshift 15:30904690-30904691 + YUKAT COSM5383128 c.602A>G p.D201G Substitution - Missense 15:30905265-30905265 + T3306 COSM4683331 c.642C>T p.N214N Substitution - coding silent 15:30905305-30905305 + TCGA-EE-A2A2-06 COSM3500349 c.2569G>A p.D857N Substitution - Missense 15:30928633-30928633 + TCGA-DI-A0WH-01 COSM960351 c.237A>G p.L79L Substitution - coding silent 15:30904900-30904900 + 397 COSM4428912 c.2705T>A p.V902E Substitution - Missense 15:30929315-30929315 + SA077 COSM214205 c.2671C>A p.H891N Substitution - Missense 15:30929281-30929281 + TCGA-EE-A3AA-06 COSM3500343 c.125T>C p.L42P Substitution - Missense 15:30904788-30904788 + TCGA-BR-8081-01 COSM4053927 c.1449C>A p.T483T Substitution - coding silent 15:30910687-30910687 + TCGA-FU-A3HZ-01 COSM4839719 c.697G>T p.G233* Substitution - Nonsense 15:30905360-30905360 + TCGA-BR-4368-01 COSM4053929 c.1741C>T p.R581* Substitution - Nonsense 15:30914021-30914021 + TCGA-KV-A6GD-01 COSM3987896 c.972T>G p.H324Q Substitution - Missense 15:30905635-30905635 + TCGA-HC-8216-01 COSM3672019 c.59G>T p.S20I Substitution - Missense 15:30904722-30904722 + TCGA-G4-6628-01 COSM1372322 c.2832C>T p.C944C Substitution - coding silent 15:30930587-30930587 + SF295 COSM1678328 c.2264A>T p.E755V Substitution - Missense 15:30925218-30925218 + ESCC_17 COSM5625913 c.1836G>C p.L612L Substitution - coding silent 15:30918188-30918188 + KM12 COSM1678327 c.1484A>C p.Q495P Substitution - Missense 15:30910722-30910722 + CHC1763T COSM4789709 c.1A>G p.M1V Substitution - Missense 15:30904664-30904664 + TCGA-AG-A002-01 COSM260833 c.288T>C p.D96D Substitution - coding silent 15:30904951-30904951 + T3104 COSM4683328 c.27_28insA p.R12fs*4 Insertion - Frameshift 15:30904690-30904691 + TCGA-AC-A5XS-01 COSM4391145 c.2034G>C p.Q678H Substitution - Missense 15:30920635-30920635 + TCGA-DR-A0ZM-01 COSM459058 c.2071G>A p.E691K Substitution - Missense 15:30922253-30922253 + TCGA-CG-5721-01 COSM4053924 c.937A>G p.K313E Substitution - Missense 15:30905600-30905600 + U343 COSM5712682 c.2412C>T p.A804A Substitution - coding silent 15:30925863-30925863 + DLD1 COSM4623073 c.1823C>T p.A608V Substitution - Missense 15:30918175-30918175 + KM12 COSM1678327 c.1484A>C p.Q495P Substitution - Missense 15:30910722-30910722 + RK182_C01 COSM1629495 c.2581A>C p.N861H Substitution - Missense 15:30928645-30928645 + LIM2405 COSM4613382 c.28delA p.R12fs*45 Deletion - Frameshift 15:30904691-30904691 + TCGA-EE-A2GI-06 COSM3500346 c.1471G>A p.G491R Substitution - Missense 15:30910709-30910709 + 4P2 COSM3734135 c.698G>A p.G233E Substitution - Missense 15:30905361-30905361 + S02219 COSM1749093 c.15G>A p.G5G Substitution - coding silent 15:30904678-30904678 + 4T COSM3734136 c.698G>A p.G233E Substitution - Missense 15:30905361-30905361 + TCGA-DK-A3IT-01 COSM1301015 c.659C>G p.S220C Substitution - Missense 15:30905322-30905322 + TCGA-AX-A0J0-01 COSM960358 c.2002A>G p.R668G Substitution - Missense 15:30920603-30920603 + PTC-7C COSM4148615 c.990T>C p.A330A Substitution - coding silent 15:30905653-30905653 + sysucc-1317T COSM5448724 c.2905C>T p.R969C Substitution - Missense 15:30930660-30930660 + TCGA-ES-A2HT-01 COSM4938763 c.2734A>G p.R912G Substitution - Missense 15:30929344-30929344 + SC_9076 COSM5559984 c.2230C>T p.L744F Substitution - Missense 15:30925184-30925184 + TCGA-BR-4361-01 COSM4053926 c.1108A>G p.T370A Substitution - Missense 15:30905771-30905771 + TCGA-AP-A0LM-01 COSM960353 c.478T>C p.S160P Substitution - Missense 15:30905141-30905141 + TCGA-A6-6653-01 COSM5092089 c.274G>A p.V92I Substitution - Missense 15:30904937-30904937 + T155 COSM1177379 c.72A>G p.K24K Substitution - coding silent 15:30904735-30904735 + TCGA-G4-6628-01 COSM1372315 c.1221T>G p.F407L Substitution - Missense 15:30905884-30905884 + TCGA-HU-A4G3-01 COSM4053934 c.2435G>A p.C812Y Substitution - Missense 15:30925886-30925886 + TCGA-BP-4170-01 COSM3773718 c.2680C>T p.P894S Substitution - Missense 15:30929290-30929290 + TCGA-28-2513-01 COSM3401666 c.139T>C p.C47R Substitution - Missense 15:30904802-30904802 + TCGA-FD-A3B4-01 COSM1301016 c.1100G>A p.G367D Substitution - Missense 15:30905763-30905763 + H1155 COSM1195581 c.757C>A p.L253I Substitution - Missense 15:30905420-30905420 + S02219 COSM5675612 c.546G>C p.Q182H Substitution - Missense 15:30905209-30905209 + ESCC_11 COSM5624291 c.2059G>C p.V687L Substitution - Missense 15:30922241-30922241 + 587222 COSM1215697 c.1446G>T p.K482N Substitution - Missense 15:30910684-30910684 + TCGA-G4-6628-01 COSM5180062 c.1221T>G p.F407L Substitution - Missense 15:30905884-30905884 + TCGA-D8-A1J8-01 COSM3815820 c.2977G>A p.E993K Substitution - Missense 15:30937179-30937179 + CHC892T COSM4960695 c.1094G>A p.G365D Substitution - Missense 15:30905757-30905757 + 3N57-VS-3T57 COSM4983933 c.36G>T p.R12S Substitution - Missense 15:30904699-30904699 + TCGA-BR-4361-01 COSM4053925 c.1108A>G p.T370A Substitution - Missense 15:30905771-30905771 + 587376 COSM1215698 c.615T>G p.I205M Substitution - Missense 15:30905278-30905278 + TCGA-BH-A0DP-01 COSM5215903 c.921_922delTG p.V308fs*5 Deletion - Frameshift 15:30905584-30905585 + SJHGG093_A COSM4971588 c.1366C>A p.L456I Substitution - Missense 15:30908249-30908249 + TCGA-28-2513-01 COSM3401667 c.139T>C p.C47R Substitution - Missense 15:30904802-30904802 + TCGA-BR-8284-01 COSM4053923 c.782C>T p.A261V Substitution - Missense 15:30905445-30905445 + TCGA-CA-6718-01 COSM1372313 c.964A>C p.K322Q Substitution - Missense 15:30905627-30905627 + TCGA-33-4533-01 COSM1646666 c.3G>A p.M1I Substitution - Missense 15:30904666-30904666 + B109 COSM1749094 c.15G>A p.G5G Substitution - coding silent 15:30904678-30904678 + 49M COSM5590915 c.207C>T p.F69F Substitution - coding silent 15:30904870-30904870 + TCGA-A6-6653-01 COSM1372312 c.274G>A p.V92I Substitution - Missense 15:30904937-30904937 + TCGA-EL-A3CR-01 COSM3370135 c.1527C>T p.V509V Substitution - coding silent 15:30910765-30910765 + TCGA-GU-A42R-01 COSM3794063 c.185A>G p.E62G Substitution - Missense 15:30904848-30904848 + TCGA-CJ-4871-01 COSM3361337 c.1761C>T p.Y587Y Substitution - coding silent 15:30914041-30914041 + TCGA-34-2596-01 COSM700209 c.530C>T p.A177V Substitution - Missense 15:30905193-30905193 + TCGA-EE-A29M-06 COSM2084271 c.95C>T p.S32L Substitution - Missense 15:30904758-30904758 + TCGA-AA-3715-01 COSM269143 c.1294A>G p.T432A Substitution - Missense 15:30908177-30908177 + PTC-7C COSM4148616 c.990T>C p.A330A Substitution - coding silent 15:30905653-30905653 + RK197_C01 COSM3744543 c.1366C>G p.L456V Substitution - Missense 15:30908249-30908249 + TCGA-GN-A26C-01 COSM3500347 c.2402C>T p.A801V Substitution - Missense 15:30925853-30925853 + TCGA-AX-A05Z-01 COSM960354 c.697G>A p.G233R Substitution - Missense 15:30905360-30905360 + TCGA-F5-6814-01 COSM3420224 c.2008T>G p.L670V Substitution - Missense 15:30920609-30920609 + PD4006a COSM1740219 c.1535G>C p.W512S Substitution - Missense 15:30910773-30910773 + pfg057T COSM4746900 c.561_570del10 p.V188fs*2 Deletion - Frameshift 15:30905224-30905233 + TCGA-A2-A0T5-01 COSM3815819 c.2921T>G p.V974G Substitution - Missense 15:30937123-30937123 + LUAD-RT-S01777 COSM381952 c.825A>G p.L275L Substitution - coding silent 15:30905488-30905488 + ESCC-F40 COSM5047730 c.1483C>G p.Q495E Substitution - Missense 15:30910721-30910721 + 2492721 COSM5722274 c.1850C>T p.S617F Substitution - Missense 15:30918202-30918202 + YUKAT COSM5383127 c.602A>G p.D201G Substitution - Missense 15:30905265-30905265 + ESCC_11 COSM5624292 c.2171C>G p.P724R Substitution - Missense 15:30922353-30922353 + SC_9005 COSM5568000 c.86C>G p.S29C Substitution - Missense 15:30904749-30904749 + PTC-7C COSM3734136 c.698G>A p.G233E Substitution - Missense 15:30905361-30905361 + T3080 COSM4683330 c.63G>T p.K21N Substitution - Missense 15:30904726-30904726 + TCGA-D1-A17Q-01 COSM1587788 c.1600T>G p.*534E Nonstop extension 15:30910838-30910838 + PT52 COSM5940509 c.2014C>T p.R672W Substitution - Missense 15:30920615-30920615 + TCGA-BR-8081-01 COSM4053928 c.1449C>A p.T483T Substitution - coding silent 15:30910687-30910687 + TCGA-UB-A7MB-01 COSM4931743 c.203A>T p.D68V Substitution - Missense 15:30904866-30904866 + Z138 COSM1740218 c.1535G>C p.W512S Substitution - Missense 15:30910773-30910773 + PT48 COSM5933359 c.1436C>T p.S479F Substitution - Missense 15:30910674-30910674 + 4T COSM3734135 c.698G>A p.G233E Substitution - Missense 15:30905361-30905361 + 0077_CRUK_PC_0077_T1_DNA COSM4419366 c.226C>T p.Q76* Substitution - Nonsense 15:30904889-30904889 + 98711 COSM325863 c.529G>T p.A177S Substitution - Missense 15:30905192-30905192 + TCGA-C5-A1MH-01 COSM4821085 c.421G>A p.E141K Substitution - Missense 15:30905084-30905084 + 587316 COSM1215696 c.2470C>T p.R824C Substitution - Missense 15:30925921-30925921 + N576T COSM236639 c.2384C>G p.S795C Substitution - Missense 15:30925835-30925835 + 1N05-VS-1T05 COSM4972825 c.570G>C p.K190N Substitution - Missense 15:30905233-30905233 + TCGA-AD-5900-01 COSM1372320 c.2650G>A p.E884K Substitution - Missense 15:30929260-30929260 + TCGA-UB-A7MB-01 COSM4931742 c.203A>T p.D68V Substitution - Missense 15:30904866-30904866 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.584863 15q13.2-q13.3 613534 2443776|CGAP|BC047882|A/G|non-coding||2535|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - Frameshift p.R12Gfs*45 c.34delA 15 31196894 CM A - Frameshift p.R12Gfs*45 c.34delA 15 31196894 LGG AG - Frameshift p.R697Nfs*5 c.2090_2091delGA 15 31214472 HNSC A G IntronicSNV . c.1577+628A>G 15 31203646 HC A G Missense p.E120G c.359A>G 15 31197225 LUAD A G Missense p.E476G c.1427A>G 15 31202868 LGG A G Missense p.E975G c.2924A>G 15 31229329 HNSC A G Missense p.H985R c.2954A>G 15 31229359 PRAD A G Missense p.I170M c.510A>G 15 31197376 CM A G Missense p.Q987R c.2960A>G 15 31229365 CM A G Missense p.T245A c.733A>G 15 31197599 UCEC A G Synonymous p.P38P c.114A>G 15 31196980 UCEC C A Missense p.H891N c.2671C>A 15 31221484 BRCA C A Missense p.P541H c.1622C>A 15 31206105 UCEC C A Missense p.T511N c.1532C>A 15 31202973 LUAD C A Synonymous p.T93T c.279C>A 15 31197145 STAD C G Missense p.S220C c.659C>G 15 31197525 BLCA C T IntronicSNV . c.1577+101C>T 15 31203119 CM C T Missense p.A177V c.530C>T 15 31197396 LUSC C T Missense p.A801V c.2402C>T 15 31218056 CM C T Missense p.S32L c.95C>T 15 31196961 CM C T Missense p.S553L c.1658C>T 15 31206141 CM C T Nonsense p.R581* c.1741C>T 15 31206224 STAD C T Synonymous p.D498D c.1494C>T 15 31202935 BRCA C T Synonymous p.S825S c.2475C>T 15 31218129 HNSC C T Synonymous p.V509V c.1527C>T 15 31202968 THCA C T Synonymous p.V932V c.2796C>T 15 31222754 LUAD C T Synonymous p.Y587Y c.1761C>T 15 31206244 RCCC G A Missense p.D857N c.2569G>A 15 31220836 CM G A Missense p.D857N c.2569G>A 15 31220836 HNSC G A Missense p.E895K c.2683G>A 15 31221496 UCEC G A Missense p.G367D c.1100G>A 15 31197966 BLCA G A Missense p.G491R c.1471G>A 15 31202912 CM G A Missense p.M1I c.3G>A 15 31196869 LUSC G A Missense p.R952Q c.2855G>A 15 31222813 LUAD G A Missense p.V97I c.289G>A 15 31197155 UCEC G A Nonsense p.W638* c.1914G>A 15 31210469 CM G A Synonymous p.E338E c.1014G>A 15 31197880 HNSC G A Synonymous p.G802G c.2406G>A 15 31218060 CM G C Missense p.G569R c.1705G>C 15 31206188 STAD G C Missense p.G802A c.2405G>C 15 31218059 CM G T Missense p.A177S c.529G>T 15 31197395 SCLC G T Missense p.E400D c.1200G>T 15 31198066 LUAD G T Missense p.G830V c.2489G>T 15 31220756 COREAD G T Missense p.K101N c.303G>T 15 31197169 CM G T Missense p.R591L c.1772G>T 15 31206255 STAD G T Missense p.S20I c.59G>T 15 31196925 PRAD T A Missense p.F584I c.1750T>A 15 31206233 BRCA T C Missense p.C47R c.139T>C 15 31197005 GBM T C Missense p.L42P c.125T>C 15 31196991 CM T C Synonymous p.G371G c.1113T>C 15 31197979 PRAD T C Synonymous p.N67N c.201T>C 15 31197067 HNSC TG - Frameshift p.V308Cfs*5 c.922_923delGT 15 31197787 BRCA TG - IntronicDeletion . c.2917-991_2917-990delGT 15 31228328 CM T G IntronicSNV . c.1577+302T>G 15 31203320 HC TTCGTTGACCGACTCAATG - Frameshift p.F552Lfs*55 c.1656_1674delTTCGTTGACCGACTCAATG 15 31206139 BRCA