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 BLCA 11 58352328 58352328 + Splice_Site SNP G G A TCGA-DK-AA6L-01A-11D-A391-08 TCGA-DK-AA6L-10A-01D-A394-08 g.chr11:58352328G>A c.e2-1 BLCA 11 58352336 58352336 + Missense_Mutation SNP G G C TCGA-DK-AA6L-01A-11D-A391-08 TCGA-DK-AA6L-10A-01D-A394-08 g.chr11:58352336G>C c.349G>C c.(349-351)Gaa>Caa p.E117Q BLCA 11 58377337 58377337 + Silent SNP T T A TCGA-ZF-AA58-01A-12D-A42E-08 TCGA-ZF-AA58-10A-01D-A42H-08 g.chr11:58377337T>A c.405T>A c.(403-405)tcT>tcA p.S135S BLCA 11 58377347 58377347 + Missense_Mutation SNP C C G TCGA-ZF-AA58-01A-12D-A42E-08 TCGA-ZF-AA58-10A-01D-A42H-08 g.chr11:58377347C>G c.415C>G c.(415-417)Cag>Gag p.Q139E BLCA 11 58379117 58379117 + Missense_Mutation SNP G G C TCGA-GC-A3RB-01A-12D-A21Z-08 TCGA-GC-A3RB-10A-01D-A21Z-08 g.chr11:58379117G>C c.763G>C c.(763-765)Gaa>Caa p.E255Q BLCA 11 58384270 58384270 + Missense_Mutation SNP C C A TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr11:58384270C>A c.1184C>A c.(1183-1185)aCt>aAt p.T395N BLCA 11 58384283 58384283 + Silent SNP A A G TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr11:58384283A>G c.1197A>G c.(1195-1197)ccA>ccG p.P399P BLCA 11 58384940 58384940 + Missense_Mutation SNP C C T TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr11:58384940C>T c.1474C>T c.(1474-1476)Ctt>Ttt p.L492F BLCA 11 58385156 58385156 + Missense_Mutation SNP G G C TCGA-4Z-AA7Q-01A-11D-A391-08 TCGA-4Z-AA7Q-10A-01D-A394-08 g.chr11:58385156G>C c.1690G>C c.(1690-1692)Gat>Cat p.D564H BRCA 11 58347039 58347039 + Silent SNP G G A TCGA-AR-A5QQ-01A-11D-A28B-09 TCGA-AR-A5QQ-10A-01D-A28E-09 g.chr11:58347039G>A c.285G>A c.(283-285)caG>caA p.Q95Q BRCA 11 58381720 58381720 + Missense_Mutation SNP C C T TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr11:58381720C>T c.1006C>T c.(1006-1008)Cat>Tat p.H336Y BRCA 11 58381738 58381738 + Missense_Mutation SNP T T A TCGA-A1-A0SD-01A-11D-A10Y-09 TCGA-A1-A0SD-10A-01D-A110-09 g.chr11:58381738T>A c.1024T>A c.(1024-1026)Tat>Aat p.Y342N BRCA 11 58384237 58384237 + Missense_Mutation SNP C C T TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr11:58384237C>T c.1151C>T c.(1150-1152)tCc>tTc p.S384F BRCA 11 58384773 58384773 + Missense_Mutation SNP G G C TCGA-A7-A2KD-01A-31D-A21Q-09 TCGA-A7-A2KD-10A-01D-A21Q-09 g.chr11:58384773G>C c.1307G>C c.(1306-1308)gGc>gCc p.G436A BRCA 11 58384774 58384775 + Frame_Shift_Ins INS - - A TCGA-AN-A04D-01A-21W-A050-09 TCGA-AN-A04D-10A-01W-A055-09 g.chr11:58384774_58384775insA c.1308_1309insA c.(1309-1311)aaafs p.K437fs BRCA 11 58384907 58384907 + Missense_Mutation SNP G G A TCGA-D8-A1JD-01A-11D-A13L-09 TCGA-D8-A1JD-10A-01D-A13O-09 g.chr11:58384907G>A c.1441G>A c.(1441-1443)Gag>Aag p.E481K BRCA 11 58385028 58385028 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr11:58385028G>A c.1562G>A c.(1561-1563)aGt>aAt p.S521N CESC 11 58378523 58378523 + Missense_Mutation SNP G G C TCGA-DR-A0ZM-01A-12D-A10S-08 TCGA-DR-A0ZM-10A-01D-A10S-08 g.chr11:58378523G>C c.718G>C c.(718-720)Gaa>Caa p.E240Q COAD 11 58377414 58377414 + Missense_Mutation SNP G G A TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:58377414G>A c.482G>A c.(481-483)cGc>cAc p.R161H COAD 11 58377433 58377433 + Silent SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr11:58377433C>T c.501C>T c.(499-501)aaC>aaT p.N167N COAD 11 58377437 58377437 + Nonsense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:58377437C>T c.505C>T c.(505-507)Cga>Tga p.R169* COAD 11 58380290 58380290 + Missense_Mutation SNP C C T TCGA-AA-A00L-01A-01W-A005-10 TCGA-AA-A00L-10A-01W-A005-10 g.chr11:58380290C>T c.964C>T c.(964-966)Ctt>Ttt p.L322F COAD 11 58384886 58384886 + Missense_Mutation SNP G G C TCGA-AA-3860-01A-02W-0900-09 TCGA-AA-3860-10A-01W-0902-09 g.chr11:58384886G>C c.1420G>C c.(1420-1422)Gat>Cat p.D474H COAD 11 58384962 58384962 + Missense_Mutation SNP T T C TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr11:58384962T>C c.1496T>C c.(1495-1497)tTg>tCg p.L499S COAD 11 58384963 58384963 + Missense_Mutation SNP G G T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr11:58384963G>T c.1497G>T c.(1495-1497)ttG>ttT p.L499F COAD 11 58384963 58384963 + Missense_Mutation SNP G G T TCGA-DM-A28G-01A-11D-A16V-10 TCGA-DM-A28G-10A-01D-A16V-10 g.chr11:58384963G>T c.1497G>T c.(1495-1497)ttG>ttT p.L499F COAD 11 58384963 58384963 + Silent SNP G G A TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr11:58384963G>A c.1497G>A c.(1495-1497)ttG>ttA p.L499L COADREAD 11 58377414 58377414 + Missense_Mutation SNP G G A TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:58377414G>A c.482G>A c.(481-483)cGc>cAc p.R161H COADREAD 11 58377433 58377433 + Silent SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr11:58377433C>T c.501C>T c.(499-501)aaC>aaT p.N167N COADREAD 11 58377437 58377437 + Nonsense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:58377437C>T c.505C>T c.(505-507)Cga>Tga p.R169* COADREAD 11 58380290 58380290 + Missense_Mutation SNP C C T TCGA-AA-A00L-01A-01W-A005-10 TCGA-AA-A00L-10A-01W-A005-10 g.chr11:58380290C>T c.964C>T c.(964-966)Ctt>Ttt p.L322F COADREAD 11 58384886 58384886 + Missense_Mutation SNP G G C TCGA-AA-3860-01A-02W-0900-09 TCGA-AA-3860-10A-01W-0902-09 g.chr11:58384886G>C c.1420G>C c.(1420-1422)Gat>Cat p.D474H COADREAD 11 58384962 58384962 + Missense_Mutation SNP T T C TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr11:58384962T>C c.1496T>C c.(1495-1497)tTg>tCg p.L499S COADREAD 11 58384963 58384963 + Missense_Mutation SNP G G T TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr11:58384963G>T c.1497G>T c.(1495-1497)ttG>ttT p.L499F COADREAD 11 58384963 58384963 + Missense_Mutation SNP G G T TCGA-DM-A28G-01A-11D-A16V-10 TCGA-DM-A28G-10A-01D-A16V-10 g.chr11:58384963G>T c.1497G>T c.(1495-1497)ttG>ttT p.L499F COADREAD 11 58384963 58384963 + Silent SNP G G A TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr11:58384963G>A c.1497G>A c.(1495-1497)ttG>ttA p.L499L COADREAD 11 58384980 58384980 + Missense_Mutation SNP G G C TCGA-DT-5265-01A-21D-1826-10 TCGA-DT-5265-10A-01D-1826-10 g.chr11:58384980G>C c.1514G>C c.(1513-1515)gGa>gCa p.G505A COADREAD 11 58385068 58385068 + Silent SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:58385068C>A c.1602C>A c.(1600-1602)atC>atA p.I534I ESCA 11 58381734 58381734 + Missense_Mutation SNP G G T TCGA-L7-A6VZ-01A-12D-A33E-09 TCGA-L7-A6VZ-10A-01D-A33H-09 g.chr11:58381734G>T c.1020G>T c.(1018-1020)aaG>aaT p.K340N ESCA 11 58384873 58384873 + Silent SNP C C T TCGA-VR-AA7B-01A-31D-A403-09 TCGA-VR-AA7B-10A-01D-A403-09 g.chr11:58384873C>T c.1407C>T c.(1405-1407)ctC>ctT p.L469L ESCA 11 58384886 58384886 + Missense_Mutation SNP G G T TCGA-LN-A5U6-01A-11D-A28B-09 TCGA-LN-A5U6-10A-01D-A28E-09 g.chr11:58384886G>T c.1420G>T c.(1420-1422)Gat>Tat p.D474Y GBMLGG 11 58379786 58379786 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:58379786G>A c.893G>A c.(892-894)cGt>cAt p.R298H GBMLGG 11 58380261 58380261 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:58380261G>A c.935G>A c.(934-936)cGt>cAt p.R312H HNSC 11 58378451 58378451 + Missense_Mutation SNP G G A TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr11:58378451G>A c.646G>A c.(646-648)Gag>Aag p.E216K HNSC 11 58379154 58379154 + Missense_Mutation SNP A A T TCGA-CN-4729-01A-01D-1434-08 TCGA-CN-4729-10A-01D-1434-08 g.chr11:58379154A>T c.800A>T c.(799-801)gAg>gTg p.E267V HNSC 11 58384240 58384240 + Missense_Mutation SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:58384240A>G c.1154A>G c.(1153-1155)cAc>cGc p.H385R HNSC 11 58384258 58384258 + Missense_Mutation SNP G G A TCGA-CR-7398-01A-11D-2012-08 TCGA-CR-7398-10A-01D-2013-08 g.chr11:58384258G>A c.1172G>A c.(1171-1173)cGg>cAg p.R391Q HNSC 11 58384275 58384275 + Missense_Mutation SNP G G A TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr11:58384275G>A c.1189G>A c.(1189-1191)Gag>Aag p.E397K HNSC 11 58384695 58384695 + Missense_Mutation SNP G G T TCGA-CN-4725-01A-01D-1434-08 TCGA-CN-4725-10A-01D-1434-08 g.chr11:58384695G>T c.1229G>T c.(1228-1230)cGa>cTa p.R410L HNSC 11 58384739 58384739 + Missense_Mutation SNP G G A TCGA-CN-5359-01A-01D-1434-08 TCGA-CN-5359-10A-01D-1434-08 g.chr11:58384739G>A c.1273G>A c.(1273-1275)Gac>Aac p.D425N HNSC 11 58384768 58384768 + Silent SNP C C T TCGA-P3-A5Q5-01A-11D-A28R-08 TCGA-P3-A5Q5-10A-01D-A28U-08 g.chr11:58384768C>T c.1302C>T c.(1300-1302)atC>atT p.I434I KIPAN 11 58346868 58346868 + Silent SNP G G A TCGA-P4-A5E6-01A-11D-A28G-10 TCGA-P4-A5E6-11A-22D-A28G-10 g.chr11:58346868G>A c.114G>A c.(112-114)gcG>gcA p.A38A KIPAN 11 58377371 58377371 + Missense_Mutation SNP A A G TCGA-BP-5199-01A-01D-1429-08 TCGA-BP-5199-11A-01D-1429-08 g.chr11:58377371A>G c.439A>G c.(439-441)Aga>Gga p.R147G KIPAN 11 58381764 58381764 + Silent SNP A A G TCGA-AK-3430-01A-01D-1251-10 TCGA-AK-3430-10A-01D-1251-10 g.chr11:58381764A>G c.1050A>G c.(1048-1050)ggA>ggG p.G350G KIPAN 11 58384897 58384897 + Silent SNP C C A TCGA-A3-3326-01A-01D-0966-08 TCGA-A3-3326-11A-01D-0966-08 g.chr11:58384897C>A c.1431C>A c.(1429-1431)ggC>ggA p.G477G KIRC 11 58377371 58377371 + Missense_Mutation SNP A A G TCGA-BP-5199-01A-01D-1429-08 TCGA-BP-5199-11A-01D-1429-08 g.chr11:58377371A>G c.439A>G c.(439-441)Aga>Gga p.R147G KIRC 11 58381764 58381764 + Silent SNP A A G TCGA-AK-3430-01A-01D-1251-10 TCGA-AK-3430-10A-01D-1251-10 g.chr11:58381764A>G c.1050A>G c.(1048-1050)ggA>ggG p.G350G KIRC 11 58384897 58384897 + Silent SNP C C A TCGA-A3-3326-01A-01D-0966-08 TCGA-A3-3326-11A-01D-0966-08 g.chr11:58384897C>A c.1431C>A c.(1429-1431)ggC>ggA p.G477G KIRP 11 58346868 58346868 + Silent SNP G G A TCGA-P4-A5E6-01A-11D-A28G-10 TCGA-P4-A5E6-11A-22D-A28G-10 g.chr11:58346868G>A c.114G>A c.(112-114)gcG>gcA p.A38A LGG 11 58379786 58379786 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:58379786G>A c.893G>A c.(892-894)cGt>cAt p.R298H LGG 11 58380261 58380261 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:58380261G>A c.935G>A c.(934-936)cGt>cAt p.R312H LIHC 11 58347078 58347078 + Silent SNP G G A TCGA-LG-A6GG-01A-11D-A30V-10 TCGA-LG-A6GG-10A-01D-A30V-10 g.chr11:58347078G>A c.324G>A c.(322-324)aaG>aaA p.K108K LIHC 11 58381796 58381796 + Missense_Mutation SNP G G T TCGA-DD-AADG-01A-11D-A40R-10 TCGA-DD-AADG-10A-01D-A40U-10 g.chr11:58381796G>T c.1082G>T c.(1081-1083)cGa>cTa p.R361L LIHC 11 58384203 58384203 + Missense_Mutation SNP A A G TCGA-CC-A7II-01A-11D-A33K-10 TCGA-CC-A7II-10A-01D-A33K-10 g.chr11:58384203A>G c.1117A>G c.(1117-1119)Atc>Gtc p.I373V LUAD 11 58378451 58378451 + Missense_Mutation SNP G G A TCGA-44-6775-01A-11D-1855-08 TCGA-44-6775-10A-01D-1855-08 g.chr11:58378451G>A c.646G>A c.(646-648)Gag>Aag p.E216K LUAD 11 58378469 58378469 + Missense_Mutation SNP G G C TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr11:58378469G>C c.664G>C c.(664-666)Gag>Cag p.E222Q LUAD 11 58380279 58380279 + Missense_Mutation SNP G G T TCGA-91-6831-01A-11D-1855-08 TCGA-91-6831-11A-02D-1855-08 g.chr11:58380279G>T c.953G>T c.(952-954)tGt>tTt p.C318F LUAD 11 58381734 58381734 + Missense_Mutation SNP G G C TCGA-49-4490-01A-21D-1855-08 TCGA-49-4490-11A-01D-1855-08 g.chr11:58381734G>C c.1020G>C c.(1018-1020)aaG>aaC p.K340N LUAD 11 58384671 58384671 + Missense_Mutation SNP G G A TCGA-50-5045-01A-01D-1625-08 TCGA-50-5045-10A-01D-1625-08 g.chr11:58384671G>A c.1205G>A c.(1204-1206)tGt>tAt p.C402Y LUAD 11 58384721 58384721 + Missense_Mutation SNP A A G TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr11:58384721A>G c.1255A>G c.(1255-1257)Atg>Gtg p.M419V LUAD 11 58385171 58385171 + Nonsense_Mutation SNP G G T TCGA-49-4488-01A-01D-1753-08 TCGA-49-4488-11A-01D-1753-08 g.chr11:58385171G>T c.1705G>T c.(1705-1707)Gga>Tga p.G569* LUSC 11 58377407 58377407 + Missense_Mutation SNP G G T TCGA-66-2756-01A-01D-1522-08 TCGA-66-2756-11A-01D-1522-08 g.chr11:58377407G>T c.475G>T c.(475-477)Gtt>Ttt p.V159F LUSC 11 58384221 58384221 + Missense_Mutation SNP C C G TCGA-34-2608-01A-02D-1522-08 TCGA-34-2608-11A-01D-1522-08 g.chr11:58384221C>G c.1135C>G c.(1135-1137)Cgg>Ggg p.R379G LUSC 11 58384716 58384716 + Nonsense_Mutation SNP G G A TCGA-18-3414-01A-01D-0983-08 TCGA-18-3414-11A-01D-0983-08 g.chr11:58384716G>A c.1250G>A c.(1249-1251)tGg>tAg p.W417* LUSC 11 58385039 58385039 + Silent SNP C C A TCGA-39-5028-01A-01D-1441-08 TCGA-39-5028-11A-01D-1441-08 g.chr11:58385039C>A c.1573C>A c.(1573-1575)Cgg>Agg p.R525R OV 11 58384963 58384963 + Missense_Mutation SNP G G C TCGA-13-0883-01A-02W-0420-08 TCGA-13-0883-10A-01D-0399-08 g.chr11:58384963G>C c.1497G>C c.(1495-1497)ttG>ttC p.L499F PAAD 11 58347089 58347089 + Missense_Mutation SNP G G A TCGA-IB-7885-01A-11D-2154-08 TCGA-IB-7885-10A-01D-2154-08 g.chr11:58347089G>A c.335G>A c.(334-336)cGa>cAa p.R112Q PAAD 11 58379764 58379764 + Nonsense_Mutation SNP C C T TCGA-XN-A8T3-01A-11D-A36O-08 TCGA-XN-A8T3-10A-01D-A367-08 g.chr11:58379764C>T c.871C>T c.(871-873)Cga>Tga p.R291* PAAD 11 58381795 58381795 + Nonsense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:58381795C>T c.1081C>T c.(1081-1083)Cga>Tga p.R361* PAAD 11 58384868 58384868 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:58384868G>A c.1402G>A c.(1402-1404)Gcc>Acc p.A468T PAAD 11 58385162 58385162 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:58385162G>T c.1696G>T c.(1696-1698)Gac>Tac p.D566Y READ 11 58384980 58384980 + Missense_Mutation SNP G G C TCGA-DT-5265-01A-21D-1826-10 TCGA-DT-5265-10A-01D-1826-10 g.chr11:58384980G>C c.1514G>C c.(1513-1515)gGa>gCa p.G505A READ 11 58385068 58385068 + Silent SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:58385068C>A c.1602C>A c.(1600-1602)atC>atA p.I534I SKCM 11 58347022 58347022 + Missense_Mutation SNP G G A TCGA-GF-A3OT-06A-23D-A23B-08 TCGA-GF-A3OT-10A-01D-A23B-08 g.chr11:58347022G>A c.268G>A c.(268-270)Gac>Aac p.D90N SKCM 11 58379782 58379782 + Missense_Mutation SNP C C T TCGA-ER-A195-06A-11D-A196-08 TCGA-ER-A195-10A-01D-A198-08 g.chr11:58379782C>T c.889C>T c.(889-891)Cca>Tca p.P297S SKCM 11 58380311 58380311 + Nonsense_Mutation SNP C C T TCGA-EE-A29S-06A-11D-A197-08 TCGA-EE-A29S-10A-01D-A199-08 g.chr11:58380311C>T c.985C>T c.(985-987)Cag>Tag p.Q329* SKCM 11 58384275 58384275 + Missense_Mutation SNP G G A TCGA-OD-A75X-06A-12D-A32N-08 TCGA-OD-A75X-10A-01D-A32N-08 g.chr11:58384275G>A c.1189G>A c.(1189-1191)Gag>Aag p.E397K

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 11 58385036 58385036 single base substitution G C missense_variant E524Q 1570G>C BLCA-US 11 58379117 58379117 single base substitution G C missense_variant E255Q 763G>C BLCA-US 11 58384270 58384270 single base substitution C A missense_variant T395N 1184C>A BLCA-US 11 58384283 58384283 single base substitution A G synonymous_variant P399P 1197A>G BLCA-US 11 58391557 58391557 single base substitution G A downstream_gene_variant BLCA-US 11 58391595 58391595 single base substitution C A downstream_gene_variant BOCA-FR 11 58392887 58392887 single base substitution G T downstream_gene_variant BOCA-UK 11 58384982 58384982 single base substitution G A missense_variant E506K 1516G>A BRCA-EU 11 58342282 58342282 single base substitution T G upstream_gene_variant BRCA-EU 11 58342809 58342809 single base substitution G C upstream_gene_variant BRCA-EU 11 58342886 58342886 single base substitution C A upstream_gene_variant BRCA-EU 11 58343256 58343256 single base substitution C T upstream_gene_variant BRCA-EU 11 58344294 58344294 single base substitution C T upstream_gene_variant BRCA-EU 11 58344621 58344621 deletion of <=200bp T - upstream_gene_variant BRCA-EU 11 58345925 58345925 single base substitution C G upstream_gene_variant BRCA-EU 11 58347116 58347116 single base substitution C A intron_variant BRCA-EU 11 58347781 58347781 single base substitution C T intron_variant BRCA-EU 11 58348441 58348441 single base substitution C T intron_variant BRCA-EU 11 58348919 58348919 single base substitution C T intron_variant BRCA-EU 11 58349722 58349722 single base substitution C G intron_variant BRCA-EU 11 58350620 58350620 single base substitution G C intron_variant BRCA-EU 11 58353207 58353207 single base substitution G C intron_variant BRCA-EU 11 58353699 58353699 single base substitution A G intron_variant BRCA-EU 11 58355255 58355255 deletion of <=200bp T - intron_variant BRCA-EU 11 58356545 58356545 deletion of <=200bp T - intron_variant BRCA-EU 11 58356832 58356832 single base substitution C A intron_variant BRCA-EU 11 58357264 58357264 single base substitution C G intron_variant BRCA-EU 11 58358243 58358243 single base substitution A C intron_variant BRCA-EU 11 58358492 58358492 single base substitution C A intron_variant BRCA-EU 11 58359031 58359031 single base substitution C G intron_variant BRCA-EU 11 58359447 58359447 single base substitution C T intron_variant BRCA-EU 11 58359516 58359516 single base substitution G A intron_variant BRCA-EU 11 58360602 58360602 single base substitution G A intron_variant BRCA-EU 11 58361996 58361996 single base substitution G C intron_variant BRCA-EU 11 58362409 58362409 single base substitution C G intron_variant BRCA-EU 11 58362783 58362783 single base substitution G C intron_variant BRCA-EU 11 58363913 58363913 single base substitution G C intron_variant BRCA-EU 11 58364016 58364016 single base substitution C A intron_variant BRCA-EU 11 58366283 58366283 deletion of <=200bp A - intron_variant BRCA-EU 11 58367256 58367256 single base substitution A G intron_variant BRCA-EU 11 58368679 58368679 single base substitution A G intron_variant BRCA-EU 11 58369248 58369248 single base substitution A G intron_variant BRCA-EU 11 58369339 58369339 single base substitution G A intron_variant BRCA-EU 11 58369357 58369357 single base substitution G C intron_variant BRCA-EU 11 58369358 58369358 single base substitution C A intron_variant BRCA-EU 11 58369889 58369889 single base substitution A G intron_variant BRCA-EU 11 58369915 58369915 single base substitution G A intron_variant BRCA-EU 11 58372048 58372048 single base substitution G A intron_variant BRCA-EU 11 58375370 58375370 single base substitution T C intron_variant BRCA-EU 11 58376102 58376102 single base substitution G A intron_variant BRCA-EU 11 58376530 58376530 single base substitution T G intron_variant BRCA-EU 11 58378156 58378156 single base substitution G A intron_variant BRCA-EU 11 58379385 58379385 deletion of <=200bp A - intron_variant BRCA-EU 11 58380142 58380142 single base substitution G C intron_variant BRCA-EU 11 58381387 58381387 single base substitution G A intron_variant BRCA-EU 11 58382808 58382808 single base substitution C G intron_variant BRCA-EU 11 58383123 58383123 single base substitution T C intron_variant BRCA-EU 11 58383696 58383696 single base substitution G T intron_variant BRCA-EU 11 58384176 58384176 single base substitution A T intron_variant BRCA-EU 11 58385760 58385760 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 58385857 58385857 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 58385945 58385945 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 58386041 58386041 single base substitution G T 3_prime_UTR_variant BRCA-EU 11 58386356 58386356 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 58386395 58386395 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 58386428 58386429 deletion of <=200bp TT - 3_prime_UTR_variant BRCA-EU 11 58386631 58386631 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 58387204 58387204 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 58387304 58387304 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 58389313 58389313 single base substitution G C downstream_gene_variant BRCA-EU 11 58389884 58389884 single base substitution G T downstream_gene_variant BRCA-EU 11 58390371 58390371 single base substitution C T downstream_gene_variant BRCA-EU 11 58391702 58391702 single base substitution G T downstream_gene_variant BRCA-EU 11 58391758 58391758 single base substitution G A downstream_gene_variant BRCA-EU 11 58391773 58391773 single base substitution G A downstream_gene_variant BRCA-EU 11 58391804 58391804 single base substitution G A downstream_gene_variant BRCA-EU 11 58392730 58392730 single base substitution G C downstream_gene_variant BRCA-EU 11 58392887 58392887 single base substitution G C downstream_gene_variant BRCA-EU 11 58392933 58392933 single base substitution G C downstream_gene_variant BRCA-FR 11 58342282 58342282 single base substitution T G upstream_gene_variant BRCA-FR 11 58348441 58348441 single base substitution C T intron_variant BRCA-FR 11 58350620 58350620 single base substitution G C intron_variant BRCA-FR 11 58351919 58351919 single base substitution T C intron_variant BRCA-FR 11 58359447 58359447 single base substitution C T intron_variant BRCA-FR 11 58360602 58360602 single base substitution G A intron_variant BRCA-FR 11 58361996 58361996 single base substitution G C intron_variant BRCA-FR 11 58362409 58362409 single base substitution C G intron_variant BRCA-FR 11 58362783 58362783 single base substitution G C intron_variant BRCA-FR 11 58366316 58366316 single base substitution A G intron_variant BRCA-FR 11 58368679 58368679 single base substitution A G intron_variant BRCA-FR 11 58375370 58375370 single base substitution T C intron_variant BRCA-FR 11 58376530 58376530 single base substitution T G intron_variant BRCA-FR 11 58376983 58376983 single base substitution C A intron_variant BRCA-FR 11 58382808 58382808 single base substitution C G intron_variant BRCA-FR 11 58387304 58387304 single base substitution G A 3_prime_UTR_variant BRCA-FR 11 58390371 58390371 single base substitution C T downstream_gene_variant BRCA-KR 11 58377320 58377320 single base substitution G C missense_variant E130Q 388G>C BRCA-KR 11 58384150 58384150 single base substitution T C intron_variant BRCA-KR 11 58391666 58391666 single base substitution G A downstream_gene_variant BRCA-UK 11 58342809 58342809 single base substitution G C upstream_gene_variant BRCA-UK 11 58390318 58390318 single base substitution G A downstream_gene_variant BRCA-UK 11 58391762 58391762 single base substitution G A downstream_gene_variant BRCA-US 11 58345493 58345493 single base substitution G A upstream_gene_variant BRCA-US 11 58345513 58345513 single base substitution T C upstream_gene_variant BRCA-US 11 58347039 58347039 single base substitution G A synonymous_variant Q95Q 285G>A BRCA-US 11 58381720 58381720 single base substitution C T missense_variant H336Y 1006C>T BRCA-US 11 58381738 58381738 single base substitution T A missense_variant Y342N 1024T>A BRCA-US 11 58384237 58384237 single base substitution C T missense_variant S384F 1151C>T BRCA-US 11 58384773 58384773 single base substitution G C missense_variant G436A 1307G>C BRCA-US 11 58384774 58384774 insertion of <=200bp - A frameshift_variant G436G? BRCA-US 11 58384907 58384907 single base substitution G A missense_variant E481K 1441G>A BRCA-US 11 58385028 58385028 single base substitution G A missense_variant S521N 1562G>A BTCA-JP 11 58343108 58343108 single base substitution G A upstream_gene_variant BTCA-JP 11 58379887 58379887 single base substitution C T intron_variant BTCA-JP 11 58381664 58381664 insertion of <=200bp - T intron_variant BTCA-JP 11 58381795 58381795 single base substitution C T stop_gained R361* 1081C>T BTCA-JP 11 58381825 58381825 insertion of <=200bp - A intron_variant BTCA-JP 11 58384645 58384645 single base substitution C T intron_variant BTCA-JP 11 58384729 58384729 single base substitution A G synonymous_variant K421K 1263A>G CESC-US 11 58378523 58378523 single base substitution G C missense_variant E240Q 718G>C CESC-US 11 58391849 58391849 single base substitution G C downstream_gene_variant CESC-US 11 58391931 58391931 single base substitution C A downstream_gene_variant CLLE-ES 11 58381056 58381056 deletion of <=200bp A - intron_variant CLLE-ES 11 58383746 58383751 deletion of <=200bp GTTCTT - intron_variant CLLE-ES 11 58389302 58389302 single base substitution C T downstream_gene_variant COAD-US 11 58377414 58377414 single base substitution G A missense_variant R161H 482G>A COAD-US 11 58377433 58377433 single base substitution C T synonymous_variant N167N 501C>T COAD-US 11 58377809 58377809 insertion of <=200bp - A splice_donor_variant COAD-US 11 58377810 58377810 deletion of <=200bp A - splice_region_variant COAD-US 11 58378422 58378422 single base substitution G A splice_acceptor_variant COAD-US 11 58378424 58378424 single base substitution A G missense_variant S207G 619A>G COAD-US 11 58384221 58384221 single base substitution C G missense_variant R379G 1135C>G COAD-US 11 58391699 58391699 single base substitution G T downstream_gene_variant COAD-US 11 58391957 58391957 single base substitution C T downstream_gene_variant COCA-CN 11 58377415 58377415 single base substitution C T synonymous_variant R161R 483C>T COCA-CN 11 58377437 58377437 single base substitution C T stop_gained R169* 505C>T COCA-CN 11 58377716 58377716 single base substitution G T intron_variant COCA-CN 11 58384166 58384166 single base substitution T C intron_variant COCA-CN 11 58386071 58386071 single base substitution G T 3_prime_UTR_variant COCA-CN 11 58391799 58391799 single base substitution G A downstream_gene_variant EOPC-DE 11 58355475 58355475 single base substitution A G intron_variant EOPC-DE 11 58372329 58372329 single base substitution G C intron_variant ESAD-UK 11 58342316 58342316 deletion of <=200bp T - upstream_gene_variant ESAD-UK 11 58344193 58344193 single base substitution G A upstream_gene_variant ESAD-UK 11 58344574 58344574 single base substitution T G upstream_gene_variant ESAD-UK 11 58347410 58347410 single base substitution C G intron_variant ESAD-UK 11 58347699 58347699 single base substitution T G intron_variant ESAD-UK 11 58350136 58350136 single base substitution G C intron_variant ESAD-UK 11 58351581 58351581 single base substitution T G intron_variant ESAD-UK 11 58351586 58351586 single base substitution G T intron_variant ESAD-UK 11 58351877 58351877 single base substitution G A intron_variant ESAD-UK 11 58353814 58353814 insertion of <=200bp - T intron_variant ESAD-UK 11 58355709 58355709 single base substitution T G intron_variant ESAD-UK 11 58358437 58358437 single base substitution A G intron_variant ESAD-UK 11 58358462 58358462 single base substitution A G intron_variant ESAD-UK 11 58359094 58359094 single base substitution A G intron_variant ESAD-UK 11 58359208 58359208 single base substitution A T intron_variant ESAD-UK 11 58359678 58359678 single base substitution C T intron_variant ESAD-UK 11 58360657 58360657 single base substitution A G intron_variant ESAD-UK 11 58361931 58361931 single base substitution T G intron_variant ESAD-UK 11 58362223 58362223 single base substitution T A intron_variant ESAD-UK 11 58362331 58362331 single base substitution C T intron_variant ESAD-UK 11 58362728 58362728 single base substitution C G intron_variant ESAD-UK 11 58363196 58363196 single base substitution C T intron_variant ESAD-UK 11 58366450 58366450 single base substitution G A intron_variant ESAD-UK 11 58367176 58367176 single base substitution T C intron_variant ESAD-UK 11 58368767 58368767 single base substitution G T intron_variant ESAD-UK 11 58371526 58371526 single base substitution A G intron_variant ESAD-UK 11 58372507 58372507 single base substitution T G intron_variant ESAD-UK 11 58373548 58373548 deletion of <=200bp G - intron_variant ESAD-UK 11 58375540 58375540 insertion of <=200bp - AT intron_variant ESAD-UK 11 58378268 58378268 single base substitution A G intron_variant ESAD-UK 11 58380536 58380536 single base substitution C A intron_variant ESAD-UK 11 58380761 58380761 single base substitution A C intron_variant ESAD-UK 11 58381519 58381519 single base substitution G C intron_variant ESAD-UK 11 58389406 58389406 single base substitution T G downstream_gene_variant ESAD-UK 11 58389890 58389890 single base substitution T C downstream_gene_variant ESAD-UK 11 58389998 58389998 deletion of <=200bp A - downstream_gene_variant ESAD-UK 11 58390901 58390901 single base substitution T G downstream_gene_variant ESAD-UK 11 58392266 58392266 single base substitution G A downstream_gene_variant ESCA-CN 11 58384726 58384726 single base substitution G A synonymous_variant K420K 1260G>A ESCA-CN 11 58391838 58391838 insertion of <=200bp - TGGT downstream_gene_variant KIRC-US 11 58377371 58377371 single base substitution A G missense_variant R147G 439A>G KIRC-US 11 58381764 58381764 single base substitution A G synonymous_variant G350G 1050A>G KIRC-US 11 58384897 58384897 single base substitution C A synonymous_variant G477G 1431C>A KIRP-US 11 58391968 58391968 deletion of <=200bp T - downstream_gene_variant LAML-KR 11 58366241 58366241 single base substitution G T intron_variant LAML-KR 11 58378424 58378424 single base substitution A G missense_variant S207G 619A>G LAML-KR 11 58380206 58380206 single base substitution C T intron_variant LAML-KR 11 58381686 58381686 single base substitution A G intron_variant LAML-KR 11 58385956 58385956 single base substitution A G 3_prime_UTR_variant LAML-KR 11 58386177 58386177 single base substitution G A 3_prime_UTR_variant LICA-FR 11 58343474 58343474 single base substitution T C upstream_gene_variant LICA-FR 11 58346941 58346941 single base substitution G A missense_variant A63T 187G>A LICA-FR 11 58377406 58377406 single base substitution T A synonymous_variant S158S 474T>A LICA-FR 11 58380881 58380881 single base substitution A G intron_variant LICA-FR 11 58382816 58382816 single base substitution T A intron_variant LIHC-US 11 58347078 58347078 single base substitution G A synonymous_variant K108K 324G>A LIHC-US 11 58384203 58384203 single base substitution A G missense_variant I373V 1117A>G LINC-JP 11 58350481 58350481 single base substitution A G intron_variant LINC-JP 11 58352093 58352093 single base substitution A C intron_variant LINC-JP 11 58352268 58352268 single base substitution A G intron_variant LINC-JP 11 58352331 58352331 single base substitution G C missense_variant C115S 344G>C LINC-JP 11 58355634 58355634 single base substitution A G intron_variant LINC-JP 11 58357704 58357704 single base substitution A G intron_variant LINC-JP 11 58372200 58372200 single base substitution A G intron_variant LINC-JP 11 58380205 58380205 single base substitution G T intron_variant LIRI-JP 11 58343108 58343108 single base substitution G C upstream_gene_variant LIRI-JP 11 58344788 58344788 single base substitution T C upstream_gene_variant LIRI-JP 11 58347622 58347622 single base substitution A G intron_variant LIRI-JP 11 58348029 58348029 single base substitution G T intron_variant LIRI-JP 11 58348536 58348536 single base substitution A C intron_variant LIRI-JP 11 58348568 58348568 single base substitution G A intron_variant LIRI-JP 11 58349941 58349941 single base substitution A G intron_variant LIRI-JP 11 58350051 58350051 deletion of <=200bp C - intron_variant LIRI-JP 11 58350850 58350850 deletion of <=200bp T - intron_variant LIRI-JP 11 58353091 58353091 single base substitution G A intron_variant LIRI-JP 11 58355664 58355664 single base substitution A G intron_variant LIRI-JP 11 58357837 58357837 single base substitution A G intron_variant LIRI-JP 11 58358693 58358693 single base substitution A G intron_variant LIRI-JP 11 58360065 58360065 single base substitution G T intron_variant LIRI-JP 11 58362859 58362859 single base substitution G A intron_variant LIRI-JP 11 58363565 58363565 single base substitution A G intron_variant LIRI-JP 11 58364655 58364655 single base substitution A G intron_variant LIRI-JP 11 58366019 58366019 single base substitution G T intron_variant LIRI-JP 11 58370632 58370632 single base substitution C G intron_variant LIRI-JP 11 58373003 58373003 single base substitution A G intron_variant LIRI-JP 11 58374433 58374433 single base substitution T G intron_variant LIRI-JP 11 58375054 58375054 single base substitution G T intron_variant LIRI-JP 11 58375169 58375169 single base substitution A G intron_variant LIRI-JP 11 58375667 58375681 deletion of <=200bp TATATATATCTTACA - intron_variant LIRI-JP 11 58378170 58378170 single base substitution G A intron_variant LIRI-JP 11 58378765 58378765 single base substitution A G intron_variant LIRI-JP 11 58378942 58378942 single base substitution G A intron_variant LIRI-JP 11 58380055 58380055 single base substitution A G intron_variant LIRI-JP 11 58381218 58381218 insertion of <=200bp - A intron_variant LIRI-JP 11 58381859 58381859 single base substitution C T intron_variant LIRI-JP 11 58382121 58382121 single base substitution A G intron_variant LIRI-JP 11 58383749 58383749 deletion of <=200bp C - intron_variant LIRI-JP 11 58383773 58383773 single base substitution T G intron_variant LIRI-JP 11 58384577 58384577 single base substitution A G intron_variant LIRI-JP 11 58385453 58385453 single base substitution A G 3_prime_UTR_variant LIRI-JP 11 58385463 58385463 single base substitution A G 3_prime_UTR_variant LIRI-JP 11 58386474 58386474 single base substitution C T 3_prime_UTR_variant LIRI-JP 11 58386771 58386771 single base substitution G A 3_prime_UTR_variant LIRI-JP 11 58388882 58388882 single base substitution A T downstream_gene_variant LIRI-JP 11 58389024 58389024 single base substitution T C downstream_gene_variant LIRI-JP 11 58389309 58389309 deletion of <=200bp T - downstream_gene_variant LIRI-JP 11 58389531 58389531 single base substitution A G downstream_gene_variant LIRI-JP 11 58390577 58390577 single base substitution G C downstream_gene_variant LIRI-JP 11 58392836 58392836 single base substitution C T downstream_gene_variant LUSC-KR 11 58342107 58342107 single base substitution C G upstream_gene_variant LUSC-KR 11 58343996 58343996 single base substitution A G upstream_gene_variant LUSC-KR 11 58346021 58346021 single base substitution G T upstream_gene_variant LUSC-KR 11 58347144 58347144 single base substitution C G intron_variant LUSC-KR 11 58349843 58349843 single base substitution A C intron_variant LUSC-KR 11 58360309 58360309 single base substitution C T intron_variant LUSC-KR 11 58366166 58366166 single base substitution G T intron_variant LUSC-KR 11 58374863 58374863 single base substitution A G intron_variant LUSC-KR 11 58375426 58375426 single base substitution A G intron_variant LUSC-KR 11 58387598 58387598 single base substitution T G 3_prime_UTR_variant LUSC-KR 11 58388981 58388981 single base substitution C T downstream_gene_variant LUSC-KR 11 58393371 58393371 single base substitution G A downstream_gene_variant LUSC-US 11 58343234 58343234 single base substitution T G upstream_gene_variant LUSC-US 11 58377407 58377407 single base substitution G T missense_variant V159F 475G>T LUSC-US 11 58384221 58384221 single base substitution C G missense_variant R379G 1135C>G LUSC-US 11 58384716 58384716 single base substitution G A stop_gained W417* 1250G>A LUSC-US 11 58385039 58385039 single base substitution C A synonymous_variant R525R 1573C>A MALY-DE 11 58345357 58345357 single base substitution T A upstream_gene_variant MALY-DE 11 58354077 58354077 single base substitution G A intron_variant MALY-DE 11 58356283 58356283 single base substitution T C intron_variant MALY-DE 11 58356879 58356879 single base substitution A G intron_variant MALY-DE 11 58361699 58361699 single base substitution C G intron_variant MALY-DE 11 58369245 58369245 single base substitution T C intron_variant MALY-DE 11 58374660 58374660 single base substitution A G intron_variant MALY-DE 11 58379664 58379665 deletion of <=200bp GT - intron_variant MALY-DE 11 58384544 58384545 deletion of <=200bp TG - intron_variant MALY-DE 11 58385079 58385079 single base substitution G T missense_variant S538I 1613G>T MELA-AU 11 58341717 58341717 single base substitution G A upstream_gene_variant MELA-AU 11 58342904 58342904 single base substitution G A upstream_gene_variant MELA-AU 11 58343583 58343583 single base substitution G A upstream_gene_variant MELA-AU 11 58343676 58343676 single base substitution G A upstream_gene_variant MELA-AU 11 58344207 58344207 single base substitution T C upstream_gene_variant MELA-AU 11 58345854 58345854 single base substitution G A upstream_gene_variant MELA-AU 11 58345922 58345922 single base substitution C T upstream_gene_variant MELA-AU 11 58345931 58345931 single base substitution C T upstream_gene_variant MELA-AU 11 58345995 58345996 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 58346404 58346404 single base substitution C T upstream_gene_variant MELA-AU 11 58347456 58347456 single base substitution T C intron_variant MELA-AU 11 58347490 58347491 multiple base substitution (>=2bp and <=200bp) AT GA intron_variant MELA-AU 11 58348450 58348450 single base substitution C T intron_variant MELA-AU 11 58348479 58348479 single base substitution C T intron_variant MELA-AU 11 58349233 58349233 single base substitution T G intron_variant MELA-AU 11 58349854 58349854 single base substitution G A intron_variant MELA-AU 11 58349907 58349907 single base substitution C T intron_variant MELA-AU 11 58350602 58350602 single base substitution C T intron_variant MELA-AU 11 58352183 58352183 single base substitution T A intron_variant MELA-AU 11 58352485 58352485 single base substitution T C intron_variant MELA-AU 11 58352725 58352725 single base substitution C T intron_variant MELA-AU 11 58352860 58352860 single base substitution C T intron_variant MELA-AU 11 58353018 58353018 single base substitution C T intron_variant MELA-AU 11 58354179 58354179 single base substitution C T intron_variant MELA-AU 11 58354191 58354191 single base substitution C T intron_variant MELA-AU 11 58354561 58354584 deletion of <=200bp AAGTTGCAACTTAAAAAAAAAGTT - intron_variant MELA-AU 11 58355642 58355642 single base substitution C T intron_variant MELA-AU 11 58356078 58356078 single base substitution C T intron_variant MELA-AU 11 58358084 58358084 single base substitution C T intron_variant MELA-AU 11 58358595 58358596 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 58359081 58359081 single base substitution C T intron_variant MELA-AU 11 58359408 58359408 single base substitution C A intron_variant MELA-AU 11 58359868 58359868 single base substitution C A intron_variant MELA-AU 11 58359947 58359947 single base substitution C T intron_variant MELA-AU 11 58360583 58360583 single base substitution A T intron_variant MELA-AU 11 58360755 58360755 single base substitution C T intron_variant MELA-AU 11 58361019 58361019 single base substitution G A intron_variant MELA-AU 11 58361315 58361315 single base substitution C T intron_variant MELA-AU 11 58363119 58363119 single base substitution C T intron_variant MELA-AU 11 58364040 58364040 single base substitution C T intron_variant MELA-AU 11 58364323 58364323 single base substitution C T intron_variant MELA-AU 11 58364891 58364891 single base substitution C T intron_variant MELA-AU 11 58365061 58365061 single base substitution A G intron_variant MELA-AU 11 58366798 58366798 single base substitution G A intron_variant MELA-AU 11 58367055 58367055 single base substitution C T intron_variant MELA-AU 11 58367136 58367136 single base substitution C A intron_variant MELA-AU 11 58367748 58367748 single base substitution C T intron_variant MELA-AU 11 58369408 58369408 single base substitution C T intron_variant MELA-AU 11 58369723 58369723 single base substitution C T intron_variant MELA-AU 11 58369775 58369775 single base substitution C T intron_variant MELA-AU 11 58370160 58370160 single base substitution C T intron_variant MELA-AU 11 58370839 58370839 single base substitution C T intron_variant MELA-AU 11 58370982 58370982 single base substitution C T intron_variant MELA-AU 11 58371279 58371279 single base substitution C T intron_variant MELA-AU 11 58371295 58371295 single base substitution C T intron_variant MELA-AU 11 58372445 58372446 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 58372688 58372688 single base substitution A T intron_variant MELA-AU 11 58373125 58373125 single base substitution C T intron_variant MELA-AU 11 58373389 58373389 single base substitution C T intron_variant MELA-AU 11 58374770 58374770 single base substitution C T intron_variant MELA-AU 11 58375328 58375328 single base substitution A G intron_variant MELA-AU 11 58375482 58375482 single base substitution T C intron_variant MELA-AU 11 58375750 58375750 single base substitution T C intron_variant MELA-AU 11 58376619 58376619 single base substitution C T intron_variant MELA-AU 11 58377306 58377306 single base substitution C T missense_variant P125L 374C>T MELA-AU 11 58377436 58377436 single base substitution C T synonymous_variant T168T 504C>T MELA-AU 11 58378442 58378442 single base substitution G A missense_variant E213K 637G>A MELA-AU 11 58378964 58378964 single base substitution C T intron_variant MELA-AU 11 58379664 58379664 insertion of <=200bp - GT intron_variant MELA-AU 11 58380671 58380671 single base substitution T A intron_variant MELA-AU 11 58380703 58380703 single base substitution C T intron_variant MELA-AU 11 58380705 58380705 single base substitution A G intron_variant MELA-AU 11 58380963 58380963 single base substitution G A intron_variant MELA-AU 11 58381565 58381565 single base substitution T C intron_variant MELA-AU 11 58382502 58382502 single base substitution G T intron_variant MELA-AU 11 58382911 58382911 single base substitution C A intron_variant MELA-AU 11 58383300 58383300 single base substitution G T intron_variant MELA-AU 11 58384912 58384912 single base substitution C T synonymous_variant S482S 1446C>T MELA-AU 11 58384960 58384960 single base substitution C T synonymous_variant P498P 1494C>T MELA-AU 11 58385218 58385218 single base substitution T A 3_prime_UTR_variant MELA-AU 11 58385520 58385520 single base substitution A G 3_prime_UTR_variant MELA-AU 11 58385644 58385644 single base substitution C T 3_prime_UTR_variant MELA-AU 11 58386861 58386861 single base substitution C T 3_prime_UTR_variant MELA-AU 11 58387009 58387009 single base substitution C T 3_prime_UTR_variant MELA-AU 11 58387131 58387131 single base substitution C T 3_prime_UTR_variant MELA-AU 11 58387259 58387259 single base substitution T A 3_prime_UTR_variant MELA-AU 11 58387702 58387702 single base substitution C T 3_prime_UTR_variant MELA-AU 11 58388309 58388309 single base substitution C T 3_prime_UTR_variant MELA-AU 11 58388933 58388933 single base substitution C T downstream_gene_variant MELA-AU 11 58389446 58389446 single base substitution T A downstream_gene_variant MELA-AU 11 58390462 58390462 single base substitution T G downstream_gene_variant MELA-AU 11 58390609 58390609 single base substitution A T downstream_gene_variant MELA-AU 11 58390757 58390757 single base substitution A C downstream_gene_variant ORCA-IN 11 58376700 58376700 single base substitution C T intron_variant OV-AU 11 58344022 58344022 single base substitution T A upstream_gene_variant OV-AU 11 58344109 58344109 single base substitution C A upstream_gene_variant OV-AU 11 58345668 58345668 single base substitution T A upstream_gene_variant OV-AU 11 58347212 58347212 single base substitution C G intron_variant OV-AU 11 58353074 58353074 single base substitution G C intron_variant OV-AU 11 58357575 58357575 single base substitution A T intron_variant OV-AU 11 58362594 58362594 single base substitution G C intron_variant OV-AU 11 58365886 58365886 single base substitution T C intron_variant OV-AU 11 58370511 58370511 single base substitution A T intron_variant OV-AU 11 58371362 58371362 single base substitution T G intron_variant OV-AU 11 58377425 58377425 single base substitution A G missense_variant T165A 493A>G OV-AU 11 58377627 58377627 single base substitution G T intron_variant OV-AU 11 58381281 58381281 single base substitution C T intron_variant PACA-AU 11 58342352 58342352 single base substitution T A upstream_gene_variant PACA-AU 11 58342493 58342493 single base substitution G C upstream_gene_variant PACA-AU 11 58344902 58344902 single base substitution T C upstream_gene_variant PACA-AU 11 58345625 58345625 single base substitution A G upstream_gene_variant PACA-AU 11 58346737 58346737 single base substitution G T 5_prime_UTR_variant PACA-AU 11 58347168 58347168 single base substitution G A intron_variant PACA-AU 11 58350171 58350185 deletion of <=200bp CTTCATTTATAATTG - intron_variant PACA-AU 11 58353476 58353476 single base substitution T A intron_variant PACA-AU 11 58354907 58354907 single base substitution G C intron_variant PACA-AU 11 58356503 58356503 single base substitution C T intron_variant PACA-AU 11 58357190 58357190 single base substitution A G intron_variant PACA-AU 11 58357754 58357754 single base substitution A G intron_variant PACA-AU 11 58361934 58361934 single base substitution T G intron_variant PACA-AU 11 58366319 58366319 single base substitution C T intron_variant PACA-AU 11 58367860 58367861 deletion of <=200bp TG - intron_variant PACA-AU 11 58370978 58370978 single base substitution G A intron_variant PACA-AU 11 58375507 58375507 single base substitution A G intron_variant PACA-AU 11 58376576 58376576 single base substitution G A intron_variant PACA-AU 11 58379664 58379665 deletion of <=200bp GT - intron_variant PACA-AU 11 58383760 58383760 insertion of <=200bp - T intron_variant PACA-AU 11 58384781 58384781 single base substitution T A missense_variant F439I 1315T>A PACA-AU 11 58384971 58384971 single base substitution C A stop_gained S502* 1505C>A PACA-AU 11 58391905 58391905 single base substitution G A downstream_gene_variant PACA-CA 11 58341979 58341979 single base substitution A C upstream_gene_variant PACA-CA 11 58342315 58342315 insertion of <=200bp - T upstream_gene_variant PACA-CA 11 58342502 58342502 deletion of <=200bp A - upstream_gene_variant PACA-CA 11 58348405 58348405 single base substitution G T intron_variant PACA-CA 11 58349421 58349421 single base substitution C T intron_variant PACA-CA 11 58351298 58351298 single base substitution T A intron_variant PACA-CA 11 58354401 58354401 deletion of <=200bp T - intron_variant PACA-CA 11 58355540 58355540 single base substitution G A intron_variant PACA-CA 11 58356133 58356133 single base substitution C A intron_variant PACA-CA 11 58366309 58366309 single base substitution G C intron_variant PACA-CA 11 58366461 58366461 single base substitution C G intron_variant PACA-CA 11 58367411 58367411 insertion of <=200bp - C intron_variant PACA-CA 11 58367968 58367968 single base substitution C T intron_variant PACA-CA 11 58369955 58369955 single base substitution G T intron_variant PACA-CA 11 58371962 58371962 single base substitution G C intron_variant PACA-CA 11 58373341 58373341 single base substitution T C intron_variant PACA-CA 11 58373369 58373369 single base substitution G A intron_variant PACA-CA 11 58376323 58376323 single base substitution G A intron_variant PACA-CA 11 58376503 58376508 deletion of <=200bp TGAGTT - intron_variant PACA-CA 11 58380346 58380346 single base substitution G T intron_variant PACA-CA 11 58382901 58382901 single base substitution G A intron_variant PACA-CA 11 58384774 58384774 insertion of <=200bp - A frameshift_variant G436G? PACA-CA 11 58385241 58385241 single base substitution A C 3_prime_UTR_variant PACA-CA 11 58387520 58387520 single base substitution C G 3_prime_UTR_variant PACA-CA 11 58389998 58389998 deletion of <=200bp A - downstream_gene_variant PACA-CA 11 58392679 58392679 single base substitution T G downstream_gene_variant PACA-CA 11 58392956 58392956 single base substitution A G downstream_gene_variant PAEN-IT 11 58384162 58384162 single base substitution A T intron_variant PBCA-DE 11 58352047 58352047 single base substitution G A intron_variant PBCA-DE 11 58353337 58353337 single base substitution T A intron_variant PBCA-DE 11 58369398 58369398 single base substitution T C intron_variant PBCA-DE 11 58375621 58375622 deletion of <=200bp TA - intron_variant PBCA-DE 11 58376588 58376588 single base substitution G A intron_variant PBCA-DE 11 58379664 58379665 deletion of <=200bp GT - intron_variant PBCA-DE 11 58391975 58391975 single base substitution G T downstream_gene_variant PRAD-CA 11 58348437 58348437 single base substitution A G intron_variant PRAD-CA 11 58364242 58364242 single base substitution C T intron_variant PRAD-CA 11 58370762 58370762 single base substitution G T intron_variant PRAD-CA 11 58384202 58384202 single base substitution T G stop_gained Y372* 1116T>G PRAD-CA 11 58388695 58388695 single base substitution A G downstream_gene_variant PRAD-UK 11 58357480 58357480 single base substitution C T intron_variant PRAD-UK 11 58359029 58359029 single base substitution C T intron_variant PRAD-UK 11 58363113 58363113 single base substitution C T intron_variant PRAD-UK 11 58368837 58368837 single base substitution T C intron_variant PRAD-UK 11 58373970 58373970 single base substitution T C intron_variant PRAD-UK 11 58383855 58383855 single base substitution T C intron_variant PRAD-US 11 58391921 58391921 single base substitution C T downstream_gene_variant READ-US 11 58345490 58345490 single base substitution A T upstream_gene_variant READ-US 11 58384891 58384891 single base substitution C A synonymous_variant I475I 1425C>A READ-US 11 58384980 58384980 single base substitution G C missense_variant G505A 1514G>C RECA-EU 11 58343267 58343267 single base substitution T A upstream_gene_variant RECA-EU 11 58352100 58352100 single base substitution T C intron_variant RECA-EU 11 58355581 58355581 single base substitution G A intron_variant RECA-EU 11 58367843 58367843 single base substitution T C intron_variant RECA-EU 11 58375090 58375090 single base substitution A C intron_variant RECA-EU 11 58380795 58380795 single base substitution A G intron_variant RECA-EU 11 58386442 58386442 single base substitution T C 3_prime_UTR_variant RECA-EU 11 58388129 58388129 single base substitution T C 3_prime_UTR_variant SKCA-BR 11 58345938 58345938 single base substitution A C upstream_gene_variant SKCA-BR 11 58346153 58346153 single base substitution T C upstream_gene_variant SKCA-BR 11 58346246 58346246 single base substitution A T upstream_gene_variant SKCA-BR 11 58346256 58346256 single base substitution A C upstream_gene_variant SKCA-BR 11 58346729 58346729 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant SKCA-BR 11 58363562 58363562 single base substitution C T intron_variant SKCA-BR 11 58364175 58364175 insertion of <=200bp - CT intron_variant SKCA-BR 11 58365511 58365511 single base substitution C T intron_variant SKCA-BR 11 58368699 58368699 single base substitution A T intron_variant SKCA-BR 11 58369238 58369238 single base substitution C T intron_variant SKCA-BR 11 58372825 58372825 insertion of <=200bp - AT intron_variant SKCA-BR 11 58379663 58379663 insertion of <=200bp - CGT intron_variant SKCA-BR 11 58381838 58381838 single base substitution C T intron_variant SKCA-BR 11 58387538 58387538 single base substitution C T 3_prime_UTR_variant SKCM-US 11 58347022 58347022 single base substitution G A missense_variant D90N 268G>A SKCM-US 11 58379782 58379782 single base substitution C T missense_variant P297S 889C>T SKCM-US 11 58380311 58380311 single base substitution C T stop_gained Q329* 985C>T SKCM-US 11 58384678 58384678 single base substitution C A synonymous_variant I404I 1212C>A SKCM-US 11 58391524 58391524 single base substitution G A downstream_gene_variant SKCM-US 11 58391897 58391897 single base substitution A G downstream_gene_variant SKCM-US 11 58391965 58391965 single base substitution C T downstream_gene_variant STAD-US 11 58377501 58377501 single base substitution A G missense_variant Q190R 569A>G STAD-US 11 58377810 58377810 deletion of <=200bp A - splice_region_variant STAD-US 11 58377810 58377810 insertion of <=200bp - A splice_region_variant STAD-US 11 58378437 58378437 single base substitution A T missense_variant E211V 632A>T STAD-US 11 58379103 58379103 single base substitution C T missense_variant S250L 749C>T STAD-US 11 58384785 58384787 deletion of <=200bp AGA - inframe_deletion EK440E STAD-US 11 58385066 58385066 single base substitution A T missense_variant I534F 1600A>T STAD-US 11 58391516 58391516 single base substitution C T downstream_gene_variant STAD-US 11 58391580 58391580 single base substitution A G downstream_gene_variant STAD-US 11 58391663 58391663 single base substitution T C downstream_gene_variant STAD-US 11 58391931 58391931 single base substitution C A downstream_gene_variant THCA-US 11 58390308 58390308 single base substitution G A downstream_gene_variant UCEC-US 11 58377331 58377331 single base substitution C T synonymous_variant D133D 399C>T UCEC-US 11 58377419 58377419 single base substitution C T missense_variant R163C 487C>T UCEC-US 11 58377446 58377446 single base substitution C T missense_variant R172W 514C>T UCEC-US 11 58377457 58377457 single base substitution C T synonymous_variant T175T 525C>T UCEC-US 11 58378437 58378437 single base substitution A C missense_variant E211A 632A>C UCEC-US 11 58379202 58379202 single base substitution C A missense_variant P283H 848C>A UCEC-US 11 58380260 58380260 single base substitution C A missense_variant R312S 934C>A UCEC-US 11 58380282 58380282 single base substitution G T missense_variant G319V 956G>T UCEC-US 11 58381795 58381795 single base substitution C T stop_gained R361* 1081C>T UCEC-US 11 58384219 58384219 single base substitution C A missense_variant A378D 1133C>A UCEC-US 11 58384226 58384226 single base substitution C G synonymous_variant A380A 1140C>G UCEC-US 11 58384736 58384736 single base substitution G A missense_variant A424T 1270G>A UCEC-US 11 58384744 58384744 single base substitution C A synonymous_variant S426S 1278C>A UCEC-US 11 58385068 58385068 single base substitution C A synonymous_variant I534I 1602C>A UCEC-US 11 58385170 58385170 single base substitution C T synonymous_variant A568A 1704C>T UCEC-US 11 58390264 58390264 single base substitution T C downstream_gene_variant UCEC-US 11 58391729 58391729 single base substitution C A downstream_gene_variant UCEC-US 11 58391858 58391858 single base substitution C T downstream_gene_variant UCEC-US 11 58391865 58391865 single base substitution G A downstream_gene_variant UCEC-US 11 58391921 58391921 single base substitution C T downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-F5-6814-01 COSM3416013 c.1425C>A p.I475I Substitution - coding silent 11:58617418-58617418 + S02244 COSM5678080 c.1343A>G p.H448R Substitution - Missense 11:58617336-58617336 + RMS109_ COSM3752520 c.619A>G p.S207G Substitution - Missense 11:58610951-58610951 + 2492710 COSM5717577 c.1206T>G p.C402W Substitution - Missense 11:58617199-58617199 + CHC1616T COSM4803673 c.187G>A p.A63T Substitution - Missense 11:58579468-58579468 + TCGA-B0-5692-01 COSM467021 c.1192A>G p.K398E Substitution - Missense 11:58616805-58616805 + ESCC_BICR_032T COSM5431891 c.1260G>A p.K420K Substitution - coding silent 11:58617253-58617253 + TCGA-A7-A2KD-01 COSM3809636 c.1307G>C p.G436A Substitution - Missense 11:58617300-58617300 + RD COSM3752520 c.619A>G p.S207G Substitution - Missense 11:58610951-58610951 + TCGA-AP-A059-01 COSM928892 c.1270G>A p.A424T Substitution - Missense 11:58617263-58617263 + Pat_16_B COSM5838864 c.925C>T p.Q309* Substitution - Nonsense 11:58612778-58612778 + TCGA-AP-A056-01 COSM928884 c.956G>T p.G319V Substitution - Missense 11:58612809-58612809 + 2492709 COSM5717577 c.1206T>G p.C402W Substitution - Missense 11:58617199-58617199 + pfg020T COSM1289051 c.682G>A p.D228N Substitution - Missense 11:58611014-58611014 + TCGA-B5-A0JY-01 COSM928874 c.514C>T p.R172W Substitution - Missense 11:58609973-58609973 + TCGA-A8-A09Z-01 COSM3809634 c.1006C>T p.H336Y Substitution - Missense 11:58614247-58614247 + TCGA-D1-A17H-01 COSM928882 c.854G>T p.R285M Substitution - Missense 11:58611735-58611735 + TCGA-AM-5821-01 COSM3752520 c.619A>G p.S207G Substitution - Missense 11:58610951-58610951 + TCGA-GC-A3RB-01 COSM1298228 c.763G>C p.E255Q Substitution - Missense 11:58611644-58611644 + TCGA-A1-A0SD-01 COSM429311 c.1024T>A p.Y342N Substitution - Missense 11:58614265-58614265 + PTC-14C COSM4145922 c.243G>T p.R81S Substitution - Missense 11:58579524-58579524 + RMS111_ COSM3752520 c.619A>G p.S207G Substitution - Missense 11:58610951-58610951 + TCGA-A3-3326-01 COSM467023 c.1431C>A p.G477G Substitution - coding silent 11:58617424-58617424 + AOCS-166-1-2 COSM3980453 c.493A>G p.T165A Substitution - Missense 11:58609952-58609952 + TCGA-BR-8680-01 COSM4034195 c.569A>G p.Q190R Substitution - Missense 11:58610028-58610028 + TCGA-CC-A7II-01 COSM4937721 c.1117A>G p.I373V Substitution - Missense 11:58616730-58616730 + TCGA-34-2608-01 COSM688239 c.1135C>G p.R379G Substitution - Missense 11:58616748-58616748 + PD6755a COSM1637894 c.1516G>A p.E506K Substitution - Missense 11:58617509-58617509 + T3091 COSM4742682 c.909delA p.K305fs*34 Deletion - Frameshift 11:58612762-58612762 + RMS10_ COSM3752520 c.619A>G p.S207G Substitution - Missense 11:58610951-58610951 + TCGA-D1-A103-01 COSM928870 c.399C>T p.D133D Substitution - coding silent 11:58609858-58609858 + CN-AML-NR-08-Dx COSM3752520 c.619A>G p.S207G Substitution - Missense 11:58610951-58610951 + TCGA-66-2756-01 COSM688241 c.475G>T p.V159F Substitution - Missense 11:58609934-58609934 + TCGA-13-0883-01 COSM73366 c.1497G>C p.L499F Substitution - Missense 11:58617490-58617490 + TCGA-AP-A051-01 COSM928886 c.1081C>T p.R361* Substitution - Nonsense 11:58614322-58614322 + TCGA-AD-6964-01 COSM1354927 c.501C>T p.N167N Substitution - coding silent 11:58609960-58609960 + Pat_16_A COSM5838864 c.925C>T p.Q309* Substitution - Nonsense 11:58612778-58612778 + TCGA-F4-6570-01 COSM5826981 c.617+3delA p.? Unknown 11:58610337-58610337 + NCI-H322M COSM1194869 c.1465G>A p.G489S Substitution - Missense 11:58617458-58617458 + ESCC_41 COSM5629507 c.1568C>T p.T523M Substitution - Missense 11:58617561-58617561 + BD121T COSM928886 c.1081C>T p.R361* Substitution - Nonsense 11:58614322-58614322 + CN-AML-08-T COSM3752520 c.619A>G p.S207G Substitution - Missense 11:58610951-58610951 + S02219 COSM5675564 c.371-3T>G p.? Unknown 11:58609827-58609827 + TCGA-GF-A3OT-06 COSM3450009 c.268G>A p.D90N Substitution - Missense 11:58579549-58579549 + TCGA-EB-A3Y7-01 COSM3450015 c.1212C>A p.I404I Substitution - coding silent 11:58617205-58617205 + 19685 COSM5346474 c.728C>T p.T243I Substitution - Missense 11:58611609-58611609 + TCGA-DR-A0ZM-01 COSM458522 c.718G>C p.E240Q Substitution - Missense 11:58611050-58611050 + B86-Tumor COSM1746349 c.1570G>C p.E524Q Substitution - Missense 11:58617563-58617563 + CSCC-55-T COSM4560883 c.860G>A p.R287K Substitution - Missense 11:58612280-58612280 + T154 COSM1177859 c.1039C>G p.P347A Substitution - Missense 11:58614280-58614280 + TCGA-AN-A04D-01 COSM5205641 c.1308_1309insA p.F439fs*2 Insertion - Frameshift 11:58617301-58617302 + TCGA-BR-7851-01 COSM4034201 c.1600A>T p.I534F Substitution - Missense 11:58617593-58617593 + KPOPBR-03-T COSM5965801 c.388G>C p.E130Q Substitution - Missense 11:58609847-58609847 + TCGA-AX-A0J1-01 COSM177249 c.1602C>A p.I534I Substitution - coding silent 11:58617595-58617595 + 2293755 COSM4606788 c.379G>A p.E127K Substitution - Missense 11:58609838-58609838 + CHC1616T COSM4803673 c.187G>A p.A63T Substitution - Missense 11:58579468-58579468 + TCGA-ER-A195-06 COSM3450011 c.889C>T p.P297S Substitution - Missense 11:58612309-58612309 + HN_62854 COSM128531 c.1152C>G p.S384S Substitution - coding silent 11:58616765-58616765 + TCGA-BS-A0U5-01 COSM928872 c.487C>T p.R163C Substitution - Missense 11:58609946-58609946 + sysucc-826T COSM192859 c.505C>T p.R169* Substitution - Nonsense 11:58609964-58609964 + TCGA-AP-A051-01 COSM928880 c.848C>A p.P283H Substitution - Missense 11:58611729-58611729 + 3N24-VS-3T24 COSM4979678 c.940G>C p.E314Q Substitution - Missense 11:58612793-58612793 + ME009T COSM223467 c.757G>A p.V253I Substitution - Missense 11:58611638-58611638 + RMS80_ COSM3752520 c.619A>G p.S207G Substitution - Missense 11:58610951-58610951 + sysucc-1370T COSM5469663 c.483C>T p.R161R Substitution - coding silent 11:58609942-58609942 + TCGA-EE-A29S-06 COSM3450013 c.985C>T p.Q329* Substitution - Nonsense 11:58612838-58612838 + SCMC_RM2_ COSM3752520 c.619A>G p.S207G Substitution - Missense 11:58610951-58610951 + 18 COSM5745117 c.1172G>T p.R391L Substitution - Missense 11:58616785-58616785 + LUAD-NYU739 COSM376242 c.1664G>C p.G555A Substitution - Missense 11:58617657-58617657 + TCGA-BS-A0UJ-01 COSM543760 c.934C>A p.R312S Substitution - Missense 11:58612787-58612787 + TCGA-AX-A05Z-01 COSM928876 c.525C>T p.T175T Substitution - coding silent 11:58609984-58609984 + H322T COSM1194869 c.1465G>A p.G489S Substitution - Missense 11:58617458-58617458 + 8035834 COSM4407738 c.1315T>A p.F439I Substitution - Missense 11:58617308-58617308 + TCGA-F4-6459-01 COSM688239 c.1135C>G p.R379G Substitution - Missense 11:58616748-58616748 + HCC31 COSM3666431 c.344G>C p.C115S Substitution - Missense 11:58584858-58584858 + PT38 COSM5922937 c.1040C>T p.P347L Substitution - Missense 11:58614281-58614281 + TCGA-D7-6526-01 COSM4034199 c.749C>T p.S250L Substitution - Missense 11:58611630-58611630 + YUMOOK COSM1704041 c.1105C>T p.Q369* Substitution - Nonsense 11:58616718-58616718 + HCC31T COSM3666431 c.344G>C p.C115S Substitution - Missense 11:58584858-58584858 + TCGA-A5-A0GA-01 COSM928896 c.1704C>T p.A568A Substitution - coding silent 11:58617697-58617697 + TCGA-DT-5265-01 COSM1561328 c.1514G>C p.G505A Substitution - Missense 11:58617507-58617507 + CHC912T COSM4806485 c.474T>A p.S158S Substitution - coding silent 11:58609933-58609933 + 2492708 COSM5717577 c.1206T>G p.C402W Substitution - Missense 11:58617199-58617199 + BK0060 COSM4188385 c.1122T>A p.C374* Substitution - Nonsense 11:58616735-58616735 + TCGA-AC-A23H-01 COSM3809638 c.1562G>A p.S521N Substitution - Missense 11:58617555-58617555 + BD72T COSM5512787 c.1102+9_1102+10insA p.? Unknown 11:58614352-58614353 + B86 COSM1746349 c.1570G>C p.E524Q Substitution - Missense 11:58617563-58617563 + LC_S51 COSM1188235 c.971A>G p.H324R Substitution - Missense 11:58612824-58612824 + CHC912T COSM4806485 c.474T>A p.S158S Substitution - coding silent 11:58609933-58609933 + TARGET-30-PASXIE COSM1289051 c.682G>A p.D228N Substitution - Missense 11:58611014-58611014 + CSCC-6-T COSM4510914 c.851C>T p.P284L Substitution - Missense 11:58611732-58611732 + LUAD-S01345 COSM396856 c.631G>A p.E211K Substitution - Missense 11:58610963-58610963 + TCGA-BG-A0M2-01 COSM928890 c.1140C>G p.A380A Substitution - coding silent 11:58616753-58616753 + TCGA-BT-A2LB-01 COSM3791609 c.1184C>A p.T395N Substitution - Missense 11:58616797-58616797 + 587220 COSM1233420 c.482G>A p.R161H Substitution - Missense 11:58609941-58609941 + TCGA-EB-A431-01 COSM3450011 c.889C>T p.P297S Substitution - Missense 11:58612309-58612309 + TCGA-AX-A0J1-01 COSM928888 c.1133C>A p.A378D Substitution - Missense 11:58616746-58616746 + TCGA-AC-A5XS-01 COSM4391209 c.1151C>T p.S384F Substitution - Missense 11:58616764-58616764 + TCGA-AY-6197-01 COSM5826979 c.617+2_617+3insA p.? Unknown 11:58610336-58610337 + TCGA-AA-3860-01 COSM295967 c.1420G>C p.D474H Substitution - Missense 11:58617413-58617413 + S02296 COSM5689365 c.1154A>G p.H385R Substitution - Missense 11:58616767-58616767 + ESO-916 COSM1270895 c.882C>A p.D294E Substitution - Missense 11:58612302-58612302 + TCGA-D8-A1JD-01 COSM1475585 c.1441G>A p.E481K Substitution - Missense 11:58617434-58617434 + 721LT COSM4381642 c.1543A>T p.M515L Substitution - Missense 11:58617536-58617536 + TCGA-BP-5199-01 COSM467017 c.439A>G p.R147G Substitution - Missense 11:58609898-58609898 + TCGA-BT-A2LB-01 COSM3791611 c.1197A>G p.P399P Substitution - coding silent 11:58616810-58616810 + T3064 COSM4742680 c.526G>A p.G176S Substitution - Missense 11:58609985-58609985 + TCGA-AK-3430-01 COSM467019 c.1050A>G p.G350G Substitution - coding silent 11:58614291-58614291 + ESO-1059 COSM1270893 c.678C>T p.F226F Substitution - coding silent 11:58611010-58611010 + TCGA-18-3414-01 COSM688237 c.1250G>A p.W417* Substitution - Nonsense 11:58617243-58617243 + 587284 COSM1233422 c.977G>A p.R326H Substitution - Missense 11:58612830-58612830 + 3N52-VS-3T52 COSM4983394 c.1505C>G p.S502* Substitution - Nonsense 11:58617498-58617498 + TCGA-AM-5821-01 COSM3687396 c.618-1G>A p.? Unknown 11:58610949-58610949 + YUKLAB COSM1704043 c.1372A>T p.I458F Substitution - Missense 11:58617365-58617365 + TCGA-B5-A11E-01 COSM928894 c.1278C>A p.S426S Substitution - coding silent 11:58617271-58617271 + 440 COSM4434383 c.490G>A p.D164N Substitution - Missense 11:58609949-58609949 + YUDAB COSM1704039 c.479C>G p.S160C Substitution - Missense 11:58609938-58609938 + TCGA-A6-5661-01 COSM1233420 c.482G>A p.R161H Substitution - Missense 11:58609941-58609941 + S02255 COSM5680417 c.1333G>C p.V445L Substitution - Missense 11:58617326-58617326 + TCGA-39-5028-01 COSM688235 c.1573C>A p.R525R Substitution - coding silent 11:58617566-58617566 + TCGA-CG-4465-01 COSM4034197 c.632A>T p.E211V Substitution - Missense 11:58610964-58610964 + RMS77_ COSM3752520 c.619A>G p.S207G Substitution - Missense 11:58610951-58610951 + tumor_4159421 COSM5946704 c.1613G>T p.S538I Substitution - Missense 11:58617606-58617606 + TCGA-D1-A167-01 COSM928878 c.632A>C p.E211A Substitution - Missense 11:58610964-58610964 + 8033471 COSM3383610 c.1505C>A p.S502* Substitution - Nonsense 11:58617498-58617498 + 2318502 COSM4777341 c.1304G>T p.C435F Substitution - Missense 11:58617297-58617297 + SR COSM1676046 c.308C>T p.S103F Substitution - Missense 11:58579589-58579589 + T3021 COSM4742684 c.1185T>C p.T395T Substitution - coding silent 11:58616798-58616798 + TCGA-AR-A5QQ-01 COSM3809632 c.285G>A p.Q95Q Substitution - coding silent 11:58579566-58579566 + TCGA-LG-A6GG-01 COSM4939637 c.324G>A p.K108K Substitution - coding silent 11:58579605-58579605 +

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.Q429P c.1286A>C 11 58384752 CM A G 3-UTRSNV . c.1710+277A>G 11 58385453 HC A G 3-UTRSNV . c.1710+287A>G 11 58385463 HC A G Missense p.R147G c.439A>G 11 58377371 RCCC A G Synonymous p.G350G c.1050A>G 11 58381764 RCCC A G Synonymous p.P399P c.1197A>G 11 58384283 BLCA A T IntronicSNV . c.1103-16A>T 11 58384173 NSCLC A T Missense p.E211V c.632A>T 11 58378437 STAD A T Missense p.E267V c.800A>T 11 58379154 HNSC CA - IntronicDeletion . c.988-647_988-646delCA 11 58381055 CLL C A Missense p.D294E c.882C>A 11 58379775 ESCA C A Missense p.T395N c.1184C>A 11 58384270 BLCA C A Synonymous p.G477G c.1431C>A 11 58384897 RCCC C A Synonymous p.R525R c.1573C>A 11 58385039 LUSC C G Missense p.L387V c.1159C>G 11 58384245 BRCA C G Missense p.R379G c.1135C>G 11 58384221 LUSC C G Synonymous p.A380A c.1140C>G 11 58384226 UCEC C G Synonymous p.S384S c.1152C>G 11 58384238 HNSC C T Missense p.L322F c.964C>T 11 58380290 COREAD C T Missense p.P138S c.412C>T 11 58377344 CM C T Missense p.P297S c.889C>T 11 58379782 CM C T Missense p.R163C c.487C>T 11 58377419 UCEC C T Missense p.S250L c.749C>T 11 58379103 STAD C T Nonsense p.Q329* c.985C>T 11 58380311 CM C T Synonymous p.A568A c.1704C>T 11 58385170 UCEC C T Synonymous p.F226F c.678C>T 11 58378483 ESCA C T Synonymous p.F427F c.1281C>T 11 58384747 BRCA G A 3-UTRSNV . c.1710+1595G>A 11 58386771 HC G A Missense p.C402Y c.1205G>A 11 58384671 LUAD G A Missense p.D228N c.682G>A 11 58378487 NB G A Missense p.D228N c.682G>A 11 58378487 STAD G A Missense p.D425N c.1273G>A 11 58384739 HNSC G A Missense p.E216K c.646G>A 11 58378451 LUAD G A Missense p.E481K c.1441G>A 11 58384907 BRCA G A Missense p.R391Q c.1172G>A 11 58384258 HNSC G A Missense p.V253I c.757G>A 11 58379111 CM G A Nonsense p.W417* c.1250G>A 11 58384716 LUSC G C Missense p.D474H c.1420G>C 11 58384886 COREAD G C Missense p.E255Q c.763G>C 11 58379117 BLCA G C Missense p.K340N c.1020G>C 11 58381734 LUAD G C Missense p.L499F c.1497G>C 11 58384963 OV G T Missense p.C318F c.953G>T 11 58380279 LUAD G T Missense p.R410L c.1229G>T 11 58384695 HNSC G T Missense p.V159F c.475G>T 11 58377407 LUSC G T Nonsense p.G569* c.1705G>T 11 58385171 LUAD T A Missense p.Y342N c.1024T>A 11 58381738 BRCA