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 103907682 103907682 + Missense_Mutation SNP G G T TCGA-E7-A5KF-01A-11D-A289-08 TCGA-E7-A5KF-10A-01D-A289-08 g.chr11:103907682G>T c.132G>T c.(130-132)gaG>gaT p.E44D BLCA 11 103907712 103907712 + Silent SNP C C T TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chr11:103907712C>T c.162C>T c.(160-162)ctC>ctT p.L54L BLCA 11 103908030 103908030 + Silent SNP C C G TCGA-C4-A0F6-01A-11D-A10S-08 TCGA-C4-A0F6-10A-01D-A10S-08 g.chr11:103908030C>G c.480C>G c.(478-480)ctC>ctG p.L160L BLCA 11 103908223 103908223 + Missense_Mutation SNP G G A TCGA-2F-A9KT-01A-11D-A38G-08 TCGA-2F-A9KT-10A-01D-A38J-08 g.chr11:103908223G>A c.673G>A c.(673-675)Gaa>Aaa p.E225K BLCA 11 103908332 103908332 + Missense_Mutation SNP C C T TCGA-K4-A5RH-01A-11D-A30E-08 TCGA-K4-A5RH-10A-01D-A30H-08 g.chr11:103908332C>T c.782C>T c.(781-783)tCg>tTg p.S261L BLCA 11 103908440 103908440 + Missense_Mutation SNP G G C TCGA-DK-AA6R-01A-11D-A42E-08 TCGA-DK-AA6R-10A-01D-A42H-08 g.chr11:103908440G>C c.890G>C c.(889-891)aGa>aCa p.R297T BLCA 11 103908506 103908506 + Missense_Mutation SNP C C G TCGA-G2-A2EJ-01A-11D-A17V-08 TCGA-G2-A2EJ-10A-01D-A17V-08 g.chr11:103908506C>G c.956C>G c.(955-957)tCc>tGc p.S319C BLCA 11 103908520 103908520 + Missense_Mutation SNP C C A TCGA-E7-A3Y1-01A-11D-A22Z-08 TCGA-E7-A3Y1-10A-01D-A22Z-08 g.chr11:103908520C>A c.970C>A c.(970-972)Caa>Aaa p.Q324K BLCA 11 103908679 103908679 + Missense_Mutation SNP G G C TCGA-G2-AA3C-01A-21D-A391-08 TCGA-G2-AA3C-10A-01D-A394-08 g.chr11:103908679G>C c.1129G>C c.(1129-1131)Gat>Cat p.D377H BRCA 11 103907556 103907556 + Silent SNP G G A TCGA-E2-A1LB-01A-11D-A142-09 TCGA-E2-A1LB-11A-22D-A142-09 g.chr11:103907556G>A c.6G>A c.(4-6)ctG>ctA p.L2L BRCA 11 103907921 103907921 + Missense_Mutation SNP G G A TCGA-EW-A1PB-01A-11D-A142-09 TCGA-EW-A1PB-10A-01D-A142-09 g.chr11:103907921G>A c.371G>A c.(370-372)cGg>cAg p.R124Q BRCA 11 103908037 103908037 + Missense_Mutation SNP C C T TCGA-C8-A12T-01A-11D-A10Y-09 TCGA-C8-A12T-10A-01D-A110-09 g.chr11:103908037C>T c.487C>T c.(487-489)Cgc>Tgc p.R163C BRCA 11 103908260 103908260 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:103908260G>T c.710G>T c.(709-711)aGt>aTt p.S237I BRCA 11 103908332 103908332 + Missense_Mutation SNP C C T TCGA-BH-A204-01A-11D-A159-09 TCGA-BH-A204-11A-53D-A159-09 g.chr11:103908332C>T c.782C>T c.(781-783)tCg>tTg p.S261L BRCA 11 103908577 103908577 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:103908577G>A c.1027G>A c.(1027-1029)Gat>Aat p.D343N CESC 11 103908011 103908011 + Missense_Mutation SNP C C T TCGA-EK-A2RJ-01A-11D-A18J-09 TCGA-EK-A2RJ-10A-01D-A18J-09 g.chr11:103908011C>T c.461C>T c.(460-462)cCc>cTc p.P154L CESC 11 103908368 103908368 + Missense_Mutation SNP C C T TCGA-C5-A1BI-01B-11D-A13W-08 TCGA-C5-A1BI-10A-01D-A13W-08 g.chr11:103908368C>T c.818C>T c.(817-819)gCc>gTc p.A273V CHOL 11 103908641 103908641 + Missense_Mutation SNP G G T TCGA-ZD-A8I3-01A-11D-A417-09 TCGA-ZD-A8I3-10A-01D-A41A-09 g.chr11:103908641G>T c.1091G>T c.(1090-1092)gGa>gTa p.G364V COAD 11 103907571 103907571 + Silent SNP C C T TCGA-D5-6898-01A-11D-1924-10 TCGA-D5-6898-10A-01D-1924-10 g.chr11:103907571C>T c.21C>T c.(19-21)tgC>tgT p.C7C COAD 11 103907586 103907586 + Silent SNP C C T TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr11:103907586C>T c.36C>T c.(34-36)ctC>ctT p.L12L COAD 11 103907674 103907674 + Missense_Mutation SNP G G A TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr11:103907674G>A c.124G>A c.(124-126)Gtc>Atc p.V42I COAD 11 103907676 103907676 + Silent SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr11:103907676C>T c.126C>T c.(124-126)gtC>gtT p.V42V COAD 11 103907716 103907716 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:103907716G>A c.166G>A c.(166-168)Gag>Aag p.E56K COAD 11 103907731 103907731 + Missense_Mutation SNP C C A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr11:103907731C>A c.181C>A c.(181-183)Ctg>Atg p.L61M COAD 11 103907742 103907742 + Silent SNP C C T TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr11:103907742C>T c.192C>T c.(190-192)taC>taT p.Y64Y COAD 11 103907810 103907810 + Missense_Mutation SNP G G A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr11:103907810G>A c.260G>A c.(259-261)cGt>cAt p.R87H COAD 11 103907872 103907872 + Missense_Mutation SNP C C T TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr11:103907872C>T c.322C>T c.(322-324)Cgt>Tgt p.R108C COAD 11 103907882 103907882 + Missense_Mutation SNP A A T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:103907882A>T c.332A>T c.(331-333)cAc>cTc p.H111L COAD 11 103907902 103907902 + Missense_Mutation SNP C C T TCGA-AA-A02K-01A-21W-A096-10 TCGA-AA-A02K-10A-01W-A096-10 g.chr11:103907902C>T c.352C>T c.(352-354)Cgc>Tgc p.R118C COAD 11 103907979 103907979 + Silent SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr11:103907979C>T c.429C>T c.(427-429)ccC>ccT p.P143P COAD 11 103908038 103908038 + Missense_Mutation SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr11:103908038G>A c.488G>A c.(487-489)cGc>cAc p.R163H COAD 11 103908145 103908145 + Missense_Mutation SNP C C A TCGA-F4-6855-01A-11D-1924-10 TCGA-F4-6855-10A-01D-1924-10 g.chr11:103908145C>A c.595C>A c.(595-597)Cgt>Agt p.R199S COAD 11 103908146 103908146 + Missense_Mutation SNP G G A TCGA-AA-3870-01A-01W-0995-10 TCGA-AA-3870-10A-01W-0995-10 g.chr11:103908146G>A c.596G>A c.(595-597)cGt>cAt p.R199H COAD 11 103908323 103908323 + Missense_Mutation SNP T T C TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr11:103908323T>C c.773T>C c.(772-774)tTt>tCt p.F258S COAD 11 103908374 103908374 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:103908374G>A c.824G>A c.(823-825)cGa>cAa p.R275Q COAD 11 103908374 103908374 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:103908374G>A c.824G>A c.(823-825)cGa>cAa p.R275Q COAD 11 103908452 103908452 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:103908452G>A c.902G>A c.(901-903)cGt>cAt p.R301H COAD 11 103908691 103908691 + Missense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr11:103908691G>T c.1141G>T c.(1141-1143)Gac>Tac p.D381Y COAD 11 103908700 103908700 + Missense_Mutation SNP A A G TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:103908700A>G c.1150A>G c.(1150-1152)Att>Gtt p.I384V COAD 11 103908728 103908728 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:103908728G>A c.1178G>A c.(1177-1179)cGa>cAa p.R393Q COADREAD 11 103907571 103907571 + Silent SNP C C T TCGA-D5-6898-01A-11D-1924-10 TCGA-D5-6898-10A-01D-1924-10 g.chr11:103907571C>T c.21C>T c.(19-21)tgC>tgT p.C7C COADREAD 11 103907586 103907586 + Silent SNP C C T TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr11:103907586C>T c.36C>T c.(34-36)ctC>ctT p.L12L COADREAD 11 103907674 103907674 + Missense_Mutation SNP G G A TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr11:103907674G>A c.124G>A c.(124-126)Gtc>Atc p.V42I COADREAD 11 103907676 103907676 + Silent SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr11:103907676C>T c.126C>T c.(124-126)gtC>gtT p.V42V COADREAD 11 103907716 103907716 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:103907716G>A c.166G>A c.(166-168)Gag>Aag p.E56K COADREAD 11 103907731 103907731 + Missense_Mutation SNP C C A TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr11:103907731C>A c.181C>A c.(181-183)Ctg>Atg p.L61M COADREAD 11 103907742 103907742 + Silent SNP C C T TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr11:103907742C>T c.192C>T c.(190-192)taC>taT p.Y64Y COADREAD 11 103907810 103907810 + Missense_Mutation SNP G G A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr11:103907810G>A c.260G>A c.(259-261)cGt>cAt p.R87H COADREAD 11 103907872 103907872 + Missense_Mutation SNP C C T TCGA-AA-A01P-01A-21W-A096-10 TCGA-AA-A01P-11A-11W-A096-10 g.chr11:103907872C>T c.322C>T c.(322-324)Cgt>Tgt p.R108C COADREAD 11 103907882 103907882 + Missense_Mutation SNP A A T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr11:103907882A>T c.332A>T c.(331-333)cAc>cTc p.H111L COADREAD 11 103907902 103907902 + Missense_Mutation SNP C C T TCGA-AA-A02K-01A-21W-A096-10 TCGA-AA-A02K-10A-01W-A096-10 g.chr11:103907902C>T c.352C>T c.(352-354)Cgc>Tgc p.R118C COADREAD 11 103907979 103907979 + Silent SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr11:103907979C>T c.429C>T c.(427-429)ccC>ccT p.P143P COADREAD 11 103908038 103908038 + Missense_Mutation SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr11:103908038G>A c.488G>A c.(487-489)cGc>cAc p.R163H COADREAD 11 103908145 103908145 + Missense_Mutation SNP C C A TCGA-F4-6855-01A-11D-1924-10 TCGA-F4-6855-10A-01D-1924-10 g.chr11:103908145C>A c.595C>A c.(595-597)Cgt>Agt p.R199S COADREAD 11 103908146 103908146 + Missense_Mutation SNP G G A TCGA-AA-3870-01A-01W-0995-10 TCGA-AA-3870-10A-01W-0995-10 g.chr11:103908146G>A c.596G>A c.(595-597)cGt>cAt p.R199H COADREAD 11 103908323 103908323 + Missense_Mutation SNP T T C TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr11:103908323T>C c.773T>C c.(772-774)tTt>tCt p.F258S COADREAD 11 103908374 103908374 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:103908374G>A c.824G>A c.(823-825)cGa>cAa p.R275Q COADREAD 11 103908374 103908374 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:103908374G>A c.824G>A c.(823-825)cGa>cAa p.R275Q COADREAD 11 103908452 103908452 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:103908452G>A c.902G>A c.(901-903)cGt>cAt p.R301H COADREAD 11 103908679 103908679 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:103908679G>A c.1129G>A c.(1129-1131)Gat>Aat p.D377N COADREAD 11 103908691 103908691 + Missense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr11:103908691G>T c.1141G>T c.(1141-1143)Gac>Tac p.D381Y COADREAD 11 103908700 103908700 + Missense_Mutation SNP A A G TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:103908700A>G c.1150A>G c.(1150-1152)Att>Gtt p.I384V COADREAD 11 103908728 103908728 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:103908728G>A c.1178G>A c.(1177-1179)cGa>cAa p.R393Q DLBC 11 103908517 103908517 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr11:103908517G>A c.967G>A c.(967-969)Gat>Aat p.D323N ESCA 11 103908168 103908168 + Silent SNP G G T TCGA-2H-A9GH-01A-11D-A37C-09 TCGA-2H-A9GH-11A-11D-A37F-09 g.chr11:103908168G>T c.618G>T c.(616-618)ctG>ctT p.L206L ESCA 11 103908222 103908222 + Missense_Mutation SNP A A T TCGA-2H-A9GR-01A-12D-A37C-09 TCGA-2H-A9GR-11A-11D-A37F-09 g.chr11:103908222A>T c.672A>T c.(670-672)gaA>gaT p.E224D ESCA 11 103908556 103908556 + Missense_Mutation SNP C C T TCGA-LN-A8HZ-01A-11D-A36J-09 TCGA-LN-A8HZ-10A-01D-A36M-09 g.chr11:103908556C>T c.1006C>T c.(1006-1008)Cgg>Tgg p.R336W ESCA 11 103908640 103908640 + Nonsense_Mutation SNP G G T TCGA-2H-A9GJ-01A-11D-A37C-09 TCGA-2H-A9GJ-11A-11D-A37F-09 g.chr11:103908640G>T c.1090G>T c.(1090-1092)Gga>Tga p.G364* GBM 11 103908056 103908056 + Missense_Mutation SNP A A C TCGA-06-0192-01B-01W-0348-08 TCGA-06-0192-10A-01W-0348-08 g.chr11:103908056A>C c.506A>C c.(505-507)gAa>gCa p.E169A GBM 11 103908142 103908142 + Missense_Mutation SNP C C G TCGA-28-2513-01A-01D-1494-08 TCGA-28-2513-10A-01D-1494-08 g.chr11:103908142C>G c.592C>G c.(592-594)Ctt>Gtt p.L198V GBM 11 103908618 103908618 + Silent SNP G G A TCGA-74-6584-01A-11D-1845-08 TCGA-74-6584-10A-01D-1845-08 g.chr11:103908618G>A c.1068G>A c.(1066-1068)acG>acA p.T356T GBMLGG 11 103907867 103907867 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:103907867G>A c.317G>A c.(316-318)aGc>aAc p.S106N GBMLGG 11 103907873 103907873 + Missense_Mutation SNP G G A TCGA-DU-7012-01A-11D-2024-08 TCGA-DU-7012-10A-01D-2024-08 g.chr11:103907873G>A c.323G>A c.(322-324)cGt>cAt p.R108H GBMLGG 11 103908056 103908056 + Missense_Mutation SNP A A C TCGA-06-0192-01B-01W-0348-08 TCGA-06-0192-10A-01W-0348-08 g.chr11:103908056A>C c.506A>C c.(505-507)gAa>gCa p.E169A GBMLGG 11 103908142 103908142 + Missense_Mutation SNP C C G TCGA-28-2513-01A-01D-1494-08 TCGA-28-2513-10A-01D-1494-08 g.chr11:103908142C>G c.592C>G c.(592-594)Ctt>Gtt p.L198V GBMLGG 11 103908169 103908169 + Missense_Mutation SNP G G C TCGA-P5-A5EV-01A-11D-A27K-08 TCGA-P5-A5EV-10A-01D-A27N-08 g.chr11:103908169G>C c.619G>C c.(619-621)Gat>Cat p.D207H GBMLGG 11 103908442 103908442 + Missense_Mutation SNP A A T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:103908442A>T c.892A>T c.(892-894)Att>Ttt p.I298F GBMLGG 11 103908618 103908618 + Silent SNP G G A TCGA-74-6584-01A-11D-1845-08 TCGA-74-6584-10A-01D-1845-08 g.chr11:103908618G>A c.1068G>A c.(1066-1068)acG>acA p.T356T GBMLGG 11 103908727 103908727 + Nonsense_Mutation SNP C C T TCGA-E1-A7YN-01A-11D-A34A-08 TCGA-E1-A7YN-10A-01D-A34A-08 g.chr11:103908727C>T c.1177C>T c.(1177-1179)Cga>Tga p.R393* HNSC 11 103907963 103907963 + Missense_Mutation SNP A A G TCGA-CV-7446-01A-11D-2229-08 TCGA-CV-7446-10A-01D-2229-08 g.chr11:103907963A>G c.413A>G c.(412-414)cAa>cGa p.Q138R HNSC 11 103908268 103908268 + Missense_Mutation SNP C C A TCGA-HD-7229-01A-11D-2012-08 TCGA-HD-7229-10A-01D-2013-08 g.chr11:103908268C>A c.718C>A c.(718-720)Caa>Aaa p.Q240K HNSC 11 103908425 103908425 + Missense_Mutation SNP G G A TCGA-BA-6871-01A-11D-1870-08 TCGA-BA-6871-10A-01D-1870-08 g.chr11:103908425G>A c.875G>A c.(874-876)gGa>gAa p.G292E HNSC 11 103908508 103908508 + Missense_Mutation SNP A A G TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr11:103908508A>G c.958A>G c.(958-960)Ata>Gta p.I320V HNSC 11 103908514 103908514 + Missense_Mutation SNP G G A TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr11:103908514G>A c.964G>A c.(964-966)Gag>Aag p.E322K KICH 11 103908145 103908145 + Missense_Mutation SNP C C T TCGA-KO-8408-01A-11D-2310-10 TCGA-KO-8408-11A-01D-2311-10 g.chr11:103908145C>T c.595C>T c.(595-597)Cgt>Tgt p.R199C KIPAN 11 103907571 103907571 + Silent SNP C C T TCGA-G7-A8LC-01A-11D-A35Z-10 TCGA-G7-A8LC-10A-01D-A35Z-10 g.chr11:103907571C>T c.21C>T c.(19-21)tgC>tgT p.C7C KIPAN 11 103908145 103908145 + Missense_Mutation SNP C C T TCGA-KO-8408-01A-11D-2310-10 TCGA-KO-8408-11A-01D-2311-10 g.chr11:103908145C>T c.595C>T c.(595-597)Cgt>Tgt p.R199C KIPAN 11 103908554 103908554 + Missense_Mutation SNP T T C TCGA-BP-4975-01A-01D-1462-08 TCGA-BP-4975-11A-01D-1462-08 g.chr11:103908554T>C c.1004T>C c.(1003-1005)cTc>cCc p.L335P KIPAN 11 103908556 103908556 + Missense_Mutation SNP C C T TCGA-BP-4164-01A-02D-1386-10 TCGA-BP-4164-11A-01D-1251-10 g.chr11:103908556C>T c.1006C>T c.(1006-1008)Cgg>Tgg p.R336W KIRC 11 103908554 103908554 + Missense_Mutation SNP T T C TCGA-BP-4975-01A-01D-1462-08 TCGA-BP-4975-11A-01D-1462-08 g.chr11:103908554T>C c.1004T>C c.(1003-1005)cTc>cCc p.L335P KIRC 11 103908556 103908556 + Missense_Mutation SNP C C T TCGA-BP-4164-01A-02D-1386-10 TCGA-BP-4164-11A-01D-1251-10 g.chr11:103908556C>T c.1006C>T c.(1006-1008)Cgg>Tgg p.R336W KIRP 11 103907571 103907571 + Silent SNP C C T TCGA-G7-A8LC-01A-11D-A35Z-10 TCGA-G7-A8LC-10A-01D-A35Z-10 g.chr11:103907571C>T c.21C>T c.(19-21)tgC>tgT p.C7C LGG 11 103907867 103907867 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:103907867G>A c.317G>A c.(316-318)aGc>aAc p.S106N LGG 11 103907873 103907873 + Missense_Mutation SNP G G A TCGA-DU-7012-01A-11D-2024-08 TCGA-DU-7012-10A-01D-2024-08 g.chr11:103907873G>A c.323G>A c.(322-324)cGt>cAt p.R108H LGG 11 103908169 103908169 + Missense_Mutation SNP G G C TCGA-P5-A5EV-01A-11D-A27K-08 TCGA-P5-A5EV-10A-01D-A27N-08 g.chr11:103908169G>C c.619G>C c.(619-621)Gat>Cat p.D207H LGG 11 103908442 103908442 + Missense_Mutation SNP A A T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:103908442A>T c.892A>T c.(892-894)Att>Ttt p.I298F LGG 11 103908727 103908727 + Nonsense_Mutation SNP C C T TCGA-E1-A7YN-01A-11D-A34A-08 TCGA-E1-A7YN-10A-01D-A34A-08 g.chr11:103908727C>T c.1177C>T c.(1177-1179)Cga>Tga p.R393* LIHC 11 103908038 103908038 + Missense_Mutation SNP G G A TCGA-CC-A5UE-01A-11D-A28X-10 TCGA-CC-A5UE-10A-01D-A28X-10 g.chr11:103908038G>A c.488G>A c.(487-489)cGc>cAc p.R163H LIHC 11 103908147 103908147 + Silent SNP T T C TCGA-CC-A3MB-01A-11D-A20W-10 TCGA-CC-A3MB-10A-01D-A20W-10 g.chr11:103908147T>C c.597T>C c.(595-597)cgT>cgC p.R199R LIHC 11 103908223 103908223 + Missense_Mutation SNP G G C TCGA-DD-AAE3-01A-11D-A40R-10 TCGA-DD-AAE3-10A-01D-A40U-10 g.chr11:103908223G>C c.673G>C c.(673-675)Gaa>Caa p.E225Q LIHC 11 103908253 103908253 + Missense_Mutation SNP C C A TCGA-MI-A75G-01A-11D-A32G-10 TCGA-MI-A75G-10A-01D-A32G-10 g.chr11:103908253C>A c.703C>A c.(703-705)Ccc>Acc p.P235T LIHC 11 103908514 103908514 + Missense_Mutation SNP G G A TCGA-DD-AADM-01A-11D-A40R-10 TCGA-DD-AADM-10A-01D-A40U-10 g.chr11:103908514G>A c.964G>A c.(964-966)Gag>Aag p.E322K LUAD 11 103907614 103907614 + Frame_Shift_Del DEL A A - TCGA-55-8208-01A-11D-2238-08 TCGA-55-8208-10A-01D-2238-08 g.chr11:103907614delA c.64delA c.(64-66)agcfs p.S22fs LUAD 11 103907619 103907619 + Silent SNP C C A TCGA-55-8299-01A-11D-2284-08 TCGA-55-8299-10B-01D-2323-08 g.chr11:103907619C>A c.69C>A c.(67-69)ccC>ccA p.P23P LUAD 11 103907640 103907640 + Missense_Mutation SNP C C A TCGA-50-6593-01A-11D-1753-08 TCGA-50-6593-11A-01D-1753-08 g.chr11:103907640C>A c.90C>A c.(88-90)ttC>ttA p.F30L LUAD 11 103907653 103907653 + Missense_Mutation SNP G G A TCGA-86-7954-01A-11D-2184-08 TCGA-86-7954-10A-01D-2184-08 g.chr11:103907653G>A c.103G>A c.(103-105)Gaa>Aaa p.E35K LUAD 11 103907700 103907700 + Missense_Mutation SNP G G A TCGA-55-8507-01A-11D-2393-08 TCGA-55-8507-10A-01D-2393-08 g.chr11:103907700G>A c.150G>A c.(148-150)atG>atA p.M50I LUAD 11 103907704 103907704 + Silent SNP C C A TCGA-64-5774-01A-01D-1625-08 TCGA-64-5774-10A-01D-1625-08 g.chr11:103907704C>A c.154C>A c.(154-156)Cga>Aga p.R52R LUAD 11 103907790 103907790 + Silent SNP G G T TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chr11:103907790G>T c.240G>T c.(238-240)gtG>gtT p.V80V LUAD 11 103907842 103907842 + Missense_Mutation SNP G G A TCGA-78-7158-01A-11D-2036-08 TCGA-78-7158-10A-01D-2036-08 g.chr11:103907842G>A c.292G>A c.(292-294)Ggc>Agc p.G98S LUAD 11 103907855 103907855 + Missense_Mutation SNP C C A TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr11:103907855C>A c.305C>A c.(304-306)cCt>cAt p.P102H LUAD 11 103907872 103907872 + Missense_Mutation SNP C C A TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr11:103907872C>A c.322C>A c.(322-324)Cgt>Agt p.R108S LUAD 11 103907872 103907872 + Missense_Mutation SNP C C G TCGA-78-7148-01A-11D-2036-08 TCGA-78-7148-10A-01D-2036-08 g.chr11:103907872C>G c.322C>G c.(322-324)Cgt>Ggt p.R108G LUAD 11 103907912 103907912 + Missense_Mutation SNP C C T TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr11:103907912C>T c.362C>T c.(361-363)gCt>gTt p.A121V LUAD 11 103908003 103908003 + Silent SNP C C A TCGA-17-Z005-01A-01W-0746-08 TCGA-17-Z005-11A-01W-0746-08 g.chr11:103908003C>A c.453C>A c.(451-453)ctC>ctA p.L151L LUAD 11 103908012 103908012 + Silent SNP C C A TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chr11:103908012C>A c.462C>A c.(460-462)ccC>ccA p.P154P LUAD 11 103908038 103908038 + Missense_Mutation SNP G G T TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr11:103908038G>T c.488G>T c.(487-489)cGc>cTc p.R163L LUAD 11 103908057 103908057 + Missense_Mutation SNP A A C TCGA-49-6742-01A-11D-1855-08 TCGA-49-6742-11A-01D-1855-08 g.chr11:103908057A>C c.507A>C c.(505-507)gaA>gaC p.E169D LUAD 11 103908104 103908104 + Missense_Mutation SNP A A G TCGA-17-Z009-01A-01W-0746-08 TCGA-17-Z009-11A-01W-0746-08 g.chr11:103908104A>G c.554A>G c.(553-555)gAg>gGg p.E185G LUAD 11 103908164 103908164 + Missense_Mutation SNP C C A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr11:103908164C>A c.614C>A c.(613-615)cCa>cAa p.P205Q LUAD 11 103908255 103908255 + Silent SNP C C A TCGA-64-1676-01A-01D-0969-08 TCGA-64-1676-10A-01D-0969-08 g.chr11:103908255C>A c.705C>A c.(703-705)ccC>ccA p.P235P LUAD 11 103908282 103908282 + Silent SNP C C G TCGA-49-4487-01A-21D-1855-08 TCGA-49-4487-11A-01D-1855-08 g.chr11:103908282C>G c.732C>G c.(730-732)ctC>ctG p.L244L LUAD 11 103908338 103908338 + Missense_Mutation SNP C C A TCGA-50-6594-01A-11D-1753-08 TCGA-50-6594-11A-01D-1753-08 g.chr11:103908338C>A c.788C>A c.(787-789)gCc>gAc p.A263D LUAD 11 103908369 103908369 + Silent SNP C C A TCGA-64-1679-01A-21D-2063-08 TCGA-64-1679-10A-01D-2063-08 g.chr11:103908369C>A c.819C>A c.(817-819)gcC>gcA p.A273A LUAD 11 103908410 103908410 + Missense_Mutation SNP C C A TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr11:103908410C>A c.860C>A c.(859-861)gCt>gAt p.A287D LUAD 11 103908471 103908471 + Silent SNP T T A TCGA-55-7283-01A-11D-2036-08 TCGA-55-7283-10A-01D-2036-08 g.chr11:103908471T>A c.921T>A c.(919-921)atT>atA p.I307I LUAD 11 103908544 103908544 + Missense_Mutation SNP C C A TCGA-44-6144-01A-11D-1753-08 TCGA-44-6144-10A-01D-1753-08 g.chr11:103908544C>A c.994C>A c.(994-996)Cta>Ata p.L332I LUAD 11 103908684 103908684 + Missense_Mutation SNP G G T TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr11:103908684G>T c.1134G>T c.(1132-1134)gaG>gaT p.E378D LUSC 11 103907666 103907666 + Missense_Mutation SNP G G A TCGA-60-2726-01A-01D-1522-08 TCGA-60-2726-11A-01D-1522-08 g.chr11:103907666G>A c.116G>A c.(115-117)aGa>aAa p.R39K LUSC 11 103907805 103907805 + Silent SNP A A G TCGA-37-4135-01A-01D-1352-08 TCGA-37-4135-10A-01D-1352-08 g.chr11:103907805A>G c.255A>G c.(253-255)ccA>ccG p.P85P LUSC 11 103908027 103908027 + Silent SNP G G A TCGA-18-4083-01A-01D-1352-08 TCGA-18-4083-11A-01D-1352-08 g.chr11:103908027G>A c.477G>A c.(475-477)ctG>ctA p.L159L LUSC 11 103908335 103908335 + Missense_Mutation SNP G G T TCGA-43-2578-01A-01D-1522-08 TCGA-43-2578-11A-01D-1522-08 g.chr11:103908335G>T c.785G>T c.(784-786)gGc>gTc p.G262V LUSC 11 103908395 103908395 + Missense_Mutation SNP T T G TCGA-22-5491-01A-01D-1632-08 TCGA-22-5491-11A-01D-1632-08 g.chr11:103908395T>G c.845T>G c.(844-846)gTg>gGg p.V282G LUSC 11 103908634 103908634 + Missense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr11:103908634C>T c.1084C>T c.(1084-1086)Cct>Tct p.P362S LUSC 11 103908673 103908673 + Missense_Mutation SNP G G A TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr11:103908673G>A c.1123G>A c.(1123-1125)Ggg>Agg p.G375R PAAD 11 103907738 103907738 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:103907738C>T c.188C>T c.(187-189)tCc>tTc p.S63F PAAD 11 103908400 103908400 + Nonsense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:103908400C>T c.850C>T c.(850-852)Cga>Tga p.R284* PRAD 11 103907873 103907873 + Missense_Mutation SNP G G A TCGA-HC-8265-01A-11D-2260-08 TCGA-HC-8265-10A-01D-2260-08 g.chr11:103907873G>A c.323G>A c.(322-324)cGt>cAt p.R108H PRAD 11 103908337 103908337 + Missense_Mutation SNP G G A TCGA-EJ-A7NN-01A-11D-A33T-08 TCGA-EJ-A7NN-10A-01D-A33W-08 g.chr11:103908337G>A c.787G>A c.(787-789)Gcc>Acc p.A263T PRAD 11 103908404 103908404 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:103908404G>A c.854G>A c.(853-855)cGg>cAg p.R285Q READ 11 103908679 103908679 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:103908679G>A c.1129G>A c.(1129-1131)Gat>Aat p.D377N SARC 11 103908223 103908223 + Missense_Mutation SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr11:103908223G>A c.673G>A c.(673-675)Gaa>Aaa p.E225K SARC 11 103908420 103908420 + Silent SNP T T C TCGA-DX-AB2H-01A-11D-A38Z-09 TCGA-DX-AB2H-10A-01D-A38Z-09 g.chr11:103908420T>C c.870T>C c.(868-870)gcT>gcC p.A290A SKCM 11 103907685 103907685 + Silent SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr11:103907685C>T c.135C>T c.(133-135)atC>atT p.I45I SKCM 11 103907691 103907691 + Silent SNP C C T TCGA-DA-A1HW-06A-11D-A19A-08 TCGA-DA-A1HW-10A-01D-A19A-08 g.chr11:103907691C>T c.141C>T c.(139-141)atC>atT p.I47I SKCM 11 103907695 103907695 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr11:103907695C>T c.145C>T c.(145-147)Cac>Tac p.H49Y SKCM 11 103907782 103907782 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr11:103907782G>A c.232G>A c.(232-234)Gac>Aac p.D78N SKCM 11 103907792 103907792 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr11:103907792G>A c.242G>A c.(241-243)gGa>gAa p.G81E SKCM 11 103907797 103907797 + Missense_Mutation SNP C C T TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr11:103907797C>T c.247C>T c.(247-249)Cgg>Tgg p.R83W SKCM 11 103907887 103907887 + Missense_Mutation SNP G G A TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr11:103907887G>A c.337G>A c.(337-339)Gga>Aga p.G113R SKCM 11 103907979 103907979 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:103907979C>T c.429C>T c.(427-429)ccC>ccT p.P143P SKCM 11 103908010 103908010 + Missense_Mutation SNP C C T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr11:103908010C>T c.460C>T c.(460-462)Ccc>Tcc p.P154S SKCM 11 103908033 103908033 + Silent SNP G G A TCGA-FW-A3TU-06A-11D-A23B-08 TCGA-FW-A3TU-10A-01D-A23B-08 g.chr11:103908033G>A c.483G>A c.(481-483)aaG>aaA p.K161K SKCM 11 103908034 103908034 + Missense_Mutation SNP G G A TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chr11:103908034G>A c.484G>A c.(484-486)Gaa>Aaa p.E162K SKCM 11 103908034 103908034 + Missense_Mutation SNP G G A TCGA-FW-A3TU-06A-11D-A23B-08 TCGA-FW-A3TU-10A-01D-A23B-08 g.chr11:103908034G>A c.484G>A c.(484-486)Gaa>Aaa p.E162K SKCM 11 103908105 103908105 + Silent SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr11:103908105G>A c.555G>A c.(553-555)gaG>gaA p.E185E SKCM 11 103908115 103908115 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:103908115G>A c.565G>A c.(565-567)Gaa>Aaa p.E189K SKCM 11 103908168 103908168 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:103908168G>A c.618G>A c.(616-618)ctG>ctA p.L206L SKCM 11 103908172 103908172 + Missense_Mutation SNP C C T TCGA-EE-A3J4-06A-11D-A20D-08 TCGA-EE-A3J4-10A-01D-A20D-08 g.chr11:103908172C>T c.622C>T c.(622-624)Cgg>Tgg p.R208W SKCM 11 103908174 103908174 + Silent SNP G G A TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chr11:103908174G>A c.624G>A c.(622-624)cgG>cgA p.R208R SKCM 11 103908196 103908196 + Missense_Mutation SNP G G A TCGA-EE-A3JH-06A-11D-A21A-08 TCGA-EE-A3JH-10A-01D-A21A-08 g.chr11:103908196G>A c.646G>A c.(646-648)Gag>Aag p.E216K SKCM 11 103908311 103908311 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr11:103908311C>T c.761C>T c.(760-762)cCt>cTt p.P254L SKCM 11 103908370 103908370 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:103908370G>A c.820G>A c.(820-822)Gag>Aag p.E274K SKCM 11 103908478 103908478 + Missense_Mutation SNP G G A TCGA-D3-A2JN-06A-11D-A196-08 TCGA-D3-A2JN-10A-01D-A198-08 g.chr11:103908478G>A c.928G>A c.(928-930)Gaa>Aaa p.E310K SKCM 11 103908641 103908641 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:103908641G>A c.1091G>A c.(1090-1092)gGa>gAa p.G364E SKCM 11 103908686 103908686 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:103908686C>T c.1136C>T c.(1135-1137)tCt>tTt p.S379F SKCM 11 103908697 103908697 + Missense_Mutation SNP G G A TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr11:103908697G>A c.1147G>A c.(1147-1149)Gaa>Aaa p.E383K SKCM 11 103908728 103908728 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:103908728G>A c.1178G>A c.(1177-1179)cGa>cAa p.R393Q

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 103908079 103908079 single base substitution G C missense_variant E177Q 529G>C BLCA-US 11 103908030 103908030 single base substitution C G synonymous_variant L160L 480C>G BLCA-US 11 103908506 103908506 single base substitution C G missense_variant S319C 956C>G BLCA-US 11 103908520 103908520 single base substitution C A missense_variant Q324K 970C>A BRCA-EU 11 103902687 103902687 single base substitution C T upstream_gene_variant BRCA-EU 11 103902969 103902969 single base substitution A G upstream_gene_variant BRCA-EU 11 103903315 103903315 single base substitution A C upstream_gene_variant BRCA-EU 11 103903442 103903442 single base substitution A T upstream_gene_variant BRCA-EU 11 103906439 103906439 single base substitution T A upstream_gene_variant BRCA-EU 11 103907169 103907169 single base substitution C A upstream_gene_variant BRCA-EU 11 103907363 103907363 single base substitution C A 5_prime_UTR_variant BRCA-EU 11 103907409 103907409 single base substitution G A 5_prime_UTR_variant BRCA-EU 11 103908054 103908054 single base substitution G A synonymous_variant A168A 504G>A BRCA-EU 11 103908733 103908733 single base substitution G A missense_variant E395K 1183G>A BRCA-EU 11 103908817 103908817 single base substitution A G 3_prime_UTR_variant BRCA-EU 11 103909832 103909832 single base substitution A G 3_prime_UTR_variant BRCA-EU 11 103909947 103909947 single base substitution T A downstream_gene_variant BRCA-EU 11 103910485 103910485 single base substitution T A downstream_gene_variant BRCA-EU 11 103910503 103910503 single base substitution C T downstream_gene_variant BRCA-EU 11 103911684 103911684 single base substitution C A downstream_gene_variant BRCA-EU 11 103911785 103911785 single base substitution T C downstream_gene_variant BRCA-EU 11 103911880 103911880 single base substitution G A downstream_gene_variant BRCA-EU 11 103912194 103912194 single base substitution C A downstream_gene_variant BRCA-EU 11 103912216 103912216 single base substitution T C downstream_gene_variant BRCA-EU 11 103912784 103912784 single base substitution G C downstream_gene_variant BRCA-EU 11 103912997 103912997 single base substitution T A downstream_gene_variant BRCA-EU 11 103913362 103913362 single base substitution T G downstream_gene_variant BRCA-EU 11 103914015 103914015 single base substitution C T downstream_gene_variant BRCA-EU 11 103914100 103914100 single base substitution A G downstream_gene_variant BRCA-EU 11 103914161 103914161 single base substitution C A downstream_gene_variant BRCA-FR 11 103907169 103907169 single base substitution C A upstream_gene_variant BRCA-FR 11 103907363 103907363 single base substitution C A 5_prime_UTR_variant BRCA-FR 11 103910539 103910539 single base substitution G C downstream_gene_variant BRCA-UK 11 103914100 103914100 single base substitution A G downstream_gene_variant BRCA-US 11 103907556 103907556 single base substitution G A synonymous_variant L2L 6G>A BRCA-US 11 103907921 103907921 single base substitution G A missense_variant R124Q 371G>A BRCA-US 11 103908037 103908037 single base substitution C T missense_variant R163C 487C>T BRCA-US 11 103908260 103908260 single base substitution G T missense_variant S237I 710G>T BRCA-US 11 103908332 103908332 single base substitution C T missense_variant S261L 782C>T BRCA-US 11 103908577 103908577 single base substitution G A missense_variant D343N 1027G>A BTCA-JP 11 103907529 103907529 single base substitution C G 5_prime_UTR_variant BTCA-JP 11 103908146 103908146 single base substitution G T missense_variant R199L 596G>T CESC-US 11 103908011 103908011 single base substitution C T missense_variant P154L 461C>T CESC-US 11 103908368 103908368 single base substitution C T missense_variant A273V 818C>T CLLE-ES 11 103913087 103913087 single base substitution A G downstream_gene_variant COAD-US 11 103907586 103907586 single base substitution C T synonymous_variant L12L 36C>T COAD-US 11 103907676 103907676 single base substitution C T synonymous_variant V42V 126C>T COAD-US 11 103907742 103907742 single base substitution C T synonymous_variant Y64Y 192C>T COAD-US 11 103907781 103907781 single base substitution G T missense_variant K77N 231G>T COAD-US 11 103907882 103907882 single base substitution A T missense_variant H111L 332A>T COAD-US 11 103908038 103908038 single base substitution G A missense_variant R163H 488G>A COAD-US 11 103908404 103908404 single base substitution G A missense_variant R285Q 854G>A COAD-US 11 103908452 103908452 single base substitution G A missense_variant R301H 902G>A COAD-US 11 103908728 103908728 single base substitution G A missense_variant R393Q 1178G>A COCA-CN 11 103907677 103907677 single base substitution G A missense_variant E43K 127G>A COCA-CN 11 103907704 103907704 single base substitution C T stop_gained R52* 154C>T COCA-CN 11 103907758 103907758 single base substitution G A missense_variant D70N 208G>A COCA-CN 11 103907817 103907817 single base substitution G A synonymous_variant P89P 267G>A COCA-CN 11 103908038 103908038 single base substitution G A missense_variant R163H 488G>A COCA-CN 11 103908068 103908068 single base substitution G A missense_variant S173N 518G>A COCA-CN 11 103908081 103908081 single base substitution G T missense_variant E177D 531G>T COCA-CN 11 103908244 103908244 single base substitution G T stop_gained E232* 694G>T COCA-CN 11 103908373 103908373 single base substitution C T stop_gained R275* 823C>T COCA-CN 11 103908443 103908443 single base substitution T G missense_variant I298S 893T>G COCA-CN 11 103908577 103908577 single base substitution G A missense_variant D343N 1027G>A EOPC-DE 11 103905591 103905591 single base substitution C T upstream_gene_variant ESAD-UK 11 103902349 103902349 single base substitution G T upstream_gene_variant ESAD-UK 11 103902546 103902546 single base substitution A C upstream_gene_variant ESAD-UK 11 103903009 103903009 single base substitution T C upstream_gene_variant ESAD-UK 11 103903442 103903442 deletion of <=200bp A - upstream_gene_variant ESAD-UK 11 103903547 103903547 single base substitution T C upstream_gene_variant ESAD-UK 11 103903671 103903671 single base substitution G C upstream_gene_variant ESAD-UK 11 103904233 103904233 single base substitution A C upstream_gene_variant ESAD-UK 11 103904314 103904314 single base substitution A C upstream_gene_variant ESAD-UK 11 103904639 103904639 single base substitution C A upstream_gene_variant ESAD-UK 11 103904689 103904689 single base substitution C G upstream_gene_variant ESAD-UK 11 103905038 103905038 single base substitution T G upstream_gene_variant ESAD-UK 11 103905132 103905132 single base substitution C A upstream_gene_variant ESAD-UK 11 103905495 103905495 single base substitution C T upstream_gene_variant ESAD-UK 11 103905526 103905526 single base substitution A T upstream_gene_variant ESAD-UK 11 103905613 103905613 single base substitution G A upstream_gene_variant ESAD-UK 11 103905629 103905629 single base substitution C A upstream_gene_variant ESAD-UK 11 103905814 103905814 single base substitution T C upstream_gene_variant ESAD-UK 11 103905867 103905867 single base substitution T C upstream_gene_variant ESAD-UK 11 103905886 103905886 single base substitution A C upstream_gene_variant ESAD-UK 11 103905992 103905992 single base substitution T C upstream_gene_variant ESAD-UK 11 103906467 103906467 single base substitution T C upstream_gene_variant ESAD-UK 11 103906729 103906729 single base substitution C A upstream_gene_variant ESAD-UK 11 103906935 103906935 single base substitution A C upstream_gene_variant ESAD-UK 11 103907092 103907092 single base substitution A T upstream_gene_variant ESAD-UK 11 103907170 103907170 single base substitution T A upstream_gene_variant ESAD-UK 11 103907596 103907596 single base substitution A T missense_variant T16S 46A>T ESAD-UK 11 103907836 103907836 single base substitution T G missense_variant F96V 286T>G ESAD-UK 11 103908057 103908057 single base substitution A C missense_variant E169D 507A>C ESAD-UK 11 103908213 103908213 single base substitution A C missense_variant Q221H 663A>C ESAD-UK 11 103908337 103908337 single base substitution G A missense_variant A263T 787G>A ESAD-UK 11 103908587 103908587 single base substitution A C missense_variant K346T 1037A>C ESAD-UK 11 103908641 103908641 single base substitution G A missense_variant G364E 1091G>A ESAD-UK 11 103908679 103908679 single base substitution G C missense_variant D377H 1129G>C ESAD-UK 11 103908701 103908701 single base substitution T G missense_variant I384S 1151T>G ESAD-UK 11 103908798 103908798 single base substitution A C 3_prime_UTR_variant ESAD-UK 11 103908822 103908822 single base substitution A C 3_prime_UTR_variant ESAD-UK 11 103908829 103908829 single base substitution A C 3_prime_UTR_variant ESAD-UK 11 103909387 103909387 single base substitution A T 3_prime_UTR_variant ESAD-UK 11 103909832 103909832 single base substitution A C 3_prime_UTR_variant ESAD-UK 11 103909832 103909832 single base substitution A G 3_prime_UTR_variant ESAD-UK 11 103909832 103909832 single base substitution A T 3_prime_UTR_variant ESAD-UK 11 103909834 103909834 single base substitution T G 3_prime_UTR_variant ESAD-UK 11 103909954 103909954 single base substitution C T downstream_gene_variant ESAD-UK 11 103910080 103910080 single base substitution A C downstream_gene_variant ESAD-UK 11 103910256 103910256 single base substitution C T downstream_gene_variant ESAD-UK 11 103910368 103910368 single base substitution C A downstream_gene_variant ESAD-UK 11 103910427 103910427 single base substitution A G downstream_gene_variant ESAD-UK 11 103910867 103910867 single base substitution T C downstream_gene_variant ESAD-UK 11 103911363 103911363 single base substitution T C downstream_gene_variant ESAD-UK 11 103911742 103911742 single base substitution T C downstream_gene_variant ESAD-UK 11 103911908 103911908 single base substitution G T downstream_gene_variant ESAD-UK 11 103912128 103912128 single base substitution T A downstream_gene_variant ESAD-UK 11 103912438 103912438 single base substitution A T downstream_gene_variant ESAD-UK 11 103912669 103912669 single base substitution A G downstream_gene_variant ESAD-UK 11 103912815 103912815 single base substitution G A downstream_gene_variant ESAD-UK 11 103912868 103912868 single base substitution A G downstream_gene_variant ESAD-UK 11 103913058 103913058 single base substitution C A downstream_gene_variant ESAD-UK 11 103913121 103913121 single base substitution T A downstream_gene_variant ESAD-UK 11 103913798 103913798 single base substitution T A downstream_gene_variant ESAD-UK 11 103914030 103914030 single base substitution T C downstream_gene_variant ESAD-UK 11 103914419 103914419 single base substitution G A downstream_gene_variant ESAD-UK 11 103914524 103914524 single base substitution A G downstream_gene_variant ESAD-UK 11 103914565 103914565 single base substitution A C downstream_gene_variant ESCA-CN 11 103907653 103907653 single base substitution G A missense_variant E35K 103G>A ESCA-CN 11 103908538 103908538 single base substitution C G missense_variant L330V 988C>G ESCA-CN 11 103908618 103908618 single base substitution G A synonymous_variant T356T 1068G>A GBM-US 11 103908056 103908056 single base substitution A C missense_variant E169A 506A>C GBM-US 11 103908142 103908142 single base substitution C G missense_variant L198V 592C>G GBM-US 11 103908618 103908618 single base substitution G A synonymous_variant T356T 1068G>A KIRC-US 11 103908554 103908554 single base substitution T C missense_variant L335P 1004T>C KIRC-US 11 103908556 103908556 single base substitution C T missense_variant R336W 1006C>T LGG-US 11 103907873 103907873 single base substitution G A missense_variant R108H 323G>A LGG-US 11 103908169 103908169 single base substitution G C missense_variant D207H 619G>C LIAD-FR 11 103908255 103908255 single base substitution C T synonymous_variant P235P 705C>T LICA-FR 11 103905357 103905357 single base substitution T C upstream_gene_variant LICA-FR 11 103908358 103908358 single base substitution C A missense_variant Q270K 808C>A LICA-FR 11 103908435 103908435 single base substitution A T synonymous_variant T295T 885A>T LICA-FR 11 103908639 103908639 single base substitution G T missense_variant E363D 1089G>T LIHC-US 11 103908038 103908038 single base substitution G A missense_variant R163H 488G>A LIHC-US 11 103908140 103908140 single base substitution G T missense_variant R197M 590G>T LIHC-US 11 103908253 103908253 single base substitution C A missense_variant P235T 703C>A LINC-JP 11 103902372 103902372 single base substitution T C upstream_gene_variant LINC-JP 11 103906627 103906627 single base substitution A C upstream_gene_variant LINC-JP 11 103907541 103907541 single base substitution G T 5_prime_UTR_variant LINC-JP 11 103907560 103907560 single base substitution A G missense_variant T4A 10A>G LINC-JP 11 103907652 103907652 single base substitution C T synonymous_variant C34C 102C>T LINC-JP 11 103907682 103907682 single base substitution G T missense_variant E44D 132G>T LINC-JP 11 103908256 103908256 single base substitution G T stop_gained E236* 706G>T LINC-JP 11 103908796 103908796 single base substitution T C 3_prime_UTR_variant LIRI-JP 11 103902656 103902656 single base substitution G A upstream_gene_variant LIRI-JP 11 103902923 103902923 deletion of <=200bp C - upstream_gene_variant LIRI-JP 11 103903675 103903675 single base substitution A T upstream_gene_variant LIRI-JP 11 103903748 103903748 single base substitution T C upstream_gene_variant LIRI-JP 11 103903766 103903766 single base substitution T A upstream_gene_variant LIRI-JP 11 103904504 103904504 single base substitution G T upstream_gene_variant LIRI-JP 11 103905057 103905057 single base substitution C A upstream_gene_variant LIRI-JP 11 103905431 103905431 single base substitution C T upstream_gene_variant LIRI-JP 11 103905613 103905613 single base substitution G A upstream_gene_variant LIRI-JP 11 103905763 103905763 single base substitution G A upstream_gene_variant LIRI-JP 11 103906930 103906930 single base substitution G T upstream_gene_variant LIRI-JP 11 103907873 103907873 single base substitution G T missense_variant R108L 323G>T LIRI-JP 11 103908037 103908037 single base substitution C T missense_variant R163C 487C>T LIRI-JP 11 103909235 103909235 single base substitution C T 3_prime_UTR_variant LIRI-JP 11 103909498 103909498 single base substitution G T 3_prime_UTR_variant LIRI-JP 11 103911434 103911434 single base substitution C A downstream_gene_variant LIRI-JP 11 103911493 103911493 single base substitution A T downstream_gene_variant LIRI-JP 11 103911625 103911625 single base substitution T G downstream_gene_variant LIRI-JP 11 103912213 103912213 deletion of <=200bp A - downstream_gene_variant LIRI-JP 11 103912300 103912300 single base substitution C T downstream_gene_variant LIRI-JP 11 103913151 103913151 single base substitution C G downstream_gene_variant LIRI-JP 11 103913432 103913432 single base substitution T A downstream_gene_variant LIRI-JP 11 103914071 103914071 single base substitution A G downstream_gene_variant LIRI-JP 11 103914156 103914156 single base substitution A G downstream_gene_variant LIRI-JP 11 103914195 103914195 single base substitution G A downstream_gene_variant LIRI-JP 11 103914290 103914290 single base substitution A G downstream_gene_variant LIRI-JP 11 103914533 103914533 single base substitution A C downstream_gene_variant LUSC-KR 11 103905823 103905823 single base substitution C A upstream_gene_variant LUSC-KR 11 103906385 103906385 single base substitution G C upstream_gene_variant LUSC-KR 11 103908128 103908128 single base substitution G T missense_variant R193I 578G>T LUSC-KR 11 103908412 103908412 single base substitution G T missense_variant G288W 862G>T LUSC-KR 11 103909890 103909890 single base substitution C G 3_prime_UTR_variant LUSC-KR 11 103912412 103912412 single base substitution C A downstream_gene_variant LUSC-KR 11 103914748 103914748 single base substitution C T downstream_gene_variant LUSC-US 11 103907666 103907666 single base substitution G A missense_variant R39K 116G>A LUSC-US 11 103907805 103907805 single base substitution A G synonymous_variant P85P 255A>G LUSC-US 11 103908027 103908027 single base substitution G A synonymous_variant L159L 477G>A LUSC-US 11 103908335 103908335 single base substitution G T missense_variant G262V 785G>T LUSC-US 11 103908395 103908395 single base substitution T G missense_variant V282G 845T>G LUSC-US 11 103908634 103908634 single base substitution C T missense_variant P362S 1084C>T LUSC-US 11 103908673 103908673 single base substitution G A missense_variant G375R 1123G>A MALY-DE 11 103903515 103903515 single base substitution A C upstream_gene_variant MALY-DE 11 103903625 103903625 single base substitution A G upstream_gene_variant MALY-DE 11 103903778 103903779 deletion of <=200bp GT - upstream_gene_variant MALY-DE 11 103905215 103905215 single base substitution C T upstream_gene_variant MALY-DE 11 103910146 103910146 single base substitution T C downstream_gene_variant MALY-DE 11 103911650 103911650 single base substitution A T downstream_gene_variant MELA-AU 11 103902325 103902325 single base substitution G A upstream_gene_variant MELA-AU 11 103902469 103902469 single base substitution C T upstream_gene_variant MELA-AU 11 103902546 103902546 single base substitution A G upstream_gene_variant MELA-AU 11 103902564 103902564 single base substitution C T upstream_gene_variant MELA-AU 11 103902601 103902601 single base substitution C T upstream_gene_variant MELA-AU 11 103902836 103902836 single base substitution G A upstream_gene_variant MELA-AU 11 103903248 103903248 single base substitution T G upstream_gene_variant MELA-AU 11 103903484 103903484 single base substitution C T upstream_gene_variant MELA-AU 11 103903847 103903847 single base substitution C T upstream_gene_variant MELA-AU 11 103904708 103904708 single base substitution C T upstream_gene_variant MELA-AU 11 103904899 103904899 single base substitution A C upstream_gene_variant MELA-AU 11 103905029 103905029 single base substitution C T upstream_gene_variant MELA-AU 11 103905217 103905217 single base substitution C T upstream_gene_variant MELA-AU 11 103905291 103905291 single base substitution G A upstream_gene_variant MELA-AU 11 103905864 103905864 single base substitution C T upstream_gene_variant MELA-AU 11 103905871 103905871 single base substitution G A upstream_gene_variant MELA-AU 11 103906026 103906026 single base substitution C T upstream_gene_variant MELA-AU 11 103906209 103906209 single base substitution C T upstream_gene_variant MELA-AU 11 103906210 103906210 single base substitution C T upstream_gene_variant MELA-AU 11 103906261 103906261 single base substitution C T upstream_gene_variant MELA-AU 11 103906382 103906382 single base substitution T C upstream_gene_variant MELA-AU 11 103906498 103906498 single base substitution C T upstream_gene_variant MELA-AU 11 103906586 103906586 single base substitution C T upstream_gene_variant MELA-AU 11 103906589 103906589 single base substitution C A upstream_gene_variant MELA-AU 11 103906595 103906595 single base substitution G A upstream_gene_variant MELA-AU 11 103906933 103906933 single base substitution G A upstream_gene_variant MELA-AU 11 103906977 103906977 single base substitution G A upstream_gene_variant MELA-AU 11 103907691 103907691 single base substitution C T synonymous_variant I47I 141C>T MELA-AU 11 103907763 103907763 single base substitution C T synonymous_variant I71I 213C>T MELA-AU 11 103907792 103907792 single base substitution G A missense_variant G81E 242G>A MELA-AU 11 103907804 103907804 single base substitution C T missense_variant P85L 254C>T MELA-AU 11 103907887 103907887 single base substitution G A missense_variant G113R 337G>A MELA-AU 11 103907908 103907908 single base substitution C T missense_variant P120S 358C>T MELA-AU 11 103907921 103907921 single base substitution G A missense_variant R124Q 371G>A MELA-AU 11 103907942 103907942 single base substitution G A missense_variant G131E 392G>A MELA-AU 11 103907982 103907982 single base substitution C T synonymous_variant A144A 432C>T MELA-AU 11 103908010 103908010 single base substitution C T missense_variant P154S 460C>T MELA-AU 11 103908047 103908047 single base substitution C T missense_variant P166L 497C>T MELA-AU 11 103908105 103908105 single base substitution G A synonymous_variant E185E 555G>A MELA-AU 11 103908162 103908162 single base substitution C A missense_variant D204E 612C>A MELA-AU 11 103908199 103908199 single base substitution G A missense_variant E217K 649G>A MELA-AU 11 103908457 103908457 single base substitution C T missense_variant H303Y 907C>T MELA-AU 11 103908538 103908538 single base substitution C T synonymous_variant L330L 988C>T MELA-AU 11 103908631 103908631 single base substitution C T missense_variant L361F 1081C>T MELA-AU 11 103908667 103908667 single base substitution G A missense_variant V373I 1117G>A MELA-AU 11 103908697 103908697 single base substitution G A missense_variant E383K 1147G>A MELA-AU 11 103908722 103908722 single base substitution C T missense_variant S391L 1172C>T MELA-AU 11 103908785 103908785 single base substitution C T 3_prime_UTR_variant MELA-AU 11 103908928 103908928 single base substitution C T 3_prime_UTR_variant MELA-AU 11 103909001 103909001 single base substitution G A 3_prime_UTR_variant MELA-AU 11 103909322 103909322 single base substitution C T 3_prime_UTR_variant MELA-AU 11 103909505 103909505 single base substitution C T 3_prime_UTR_variant MELA-AU 11 103909911 103909911 single base substitution G A 3_prime_UTR_variant MELA-AU 11 103910151 103910151 single base substitution C T downstream_gene_variant MELA-AU 11 103910195 103910195 single base substitution T C downstream_gene_variant MELA-AU 11 103910230 103910230 single base substitution C T downstream_gene_variant MELA-AU 11 103911141 103911141 single base substitution A T downstream_gene_variant MELA-AU 11 103911161 103911161 single base substitution A G downstream_gene_variant MELA-AU 11 103911352 103911352 single base substitution A T downstream_gene_variant MELA-AU 11 103912129 103912129 single base substitution C T downstream_gene_variant MELA-AU 11 103912203 103912203 single base substitution G A downstream_gene_variant MELA-AU 11 103912217 103912217 single base substitution G A downstream_gene_variant MELA-AU 11 103912519 103912519 single base substitution C T downstream_gene_variant MELA-AU 11 103912533 103912533 single base substitution G A downstream_gene_variant MELA-AU 11 103912586 103912586 single base substitution C T downstream_gene_variant MELA-AU 11 103912626 103912626 single base substitution G A downstream_gene_variant MELA-AU 11 103912641 103912641 single base substitution C T downstream_gene_variant MELA-AU 11 103912725 103912725 single base substitution C T downstream_gene_variant MELA-AU 11 103912960 103912960 single base substitution T A downstream_gene_variant MELA-AU 11 103912966 103912966 single base substitution C T downstream_gene_variant MELA-AU 11 103913007 103913007 single base substitution A T downstream_gene_variant MELA-AU 11 103913531 103913531 single base substitution G A downstream_gene_variant MELA-AU 11 103913566 103913566 single base substitution C T downstream_gene_variant MELA-AU 11 103913609 103913609 single base substitution C T downstream_gene_variant MELA-AU 11 103913646 103913646 single base substitution G A downstream_gene_variant MELA-AU 11 103913723 103913723 single base substitution C T downstream_gene_variant MELA-AU 11 103914006 103914006 single base substitution G A downstream_gene_variant MELA-AU 11 103914249 103914249 single base substitution G A downstream_gene_variant MELA-AU 11 103914309 103914309 single base substitution G A downstream_gene_variant MELA-AU 11 103914613 103914613 single base substitution G A downstream_gene_variant MELA-AU 11 103914720 103914720 single base substitution G A downstream_gene_variant MELA-AU 11 103914774 103914774 single base substitution G A downstream_gene_variant MELA-AU 11 103914849 103914849 single base substitution G A downstream_gene_variant MELA-AU 11 103914851 103914851 single base substitution A T downstream_gene_variant ORCA-IN 11 103907862 103907862 single base substitution G A synonymous_variant T104T 312G>A ORCA-IN 11 103908336 103908336 single base substitution C T synonymous_variant G262G 786C>T ORCA-IN 11 103908557 103908557 single base substitution G A missense_variant R336Q 1007G>A ORCA-IN 11 103910537 103910537 single base substitution C T downstream_gene_variant OV-AU 11 103903046 103903046 single base substitution T C upstream_gene_variant OV-AU 11 103906253 103906253 single base substitution A T upstream_gene_variant OV-AU 11 103914810 103914810 single base substitution A C downstream_gene_variant PACA-AU 11 103905174 103905174 single base substitution G A upstream_gene_variant PACA-AU 11 103905764 103905764 single base substitution C A upstream_gene_variant PACA-AU 11 103905857 103905857 single base substitution G T upstream_gene_variant PACA-AU 11 103906893 103906893 single base substitution A G upstream_gene_variant PACA-AU 11 103908161 103908161 single base substitution A T missense_variant D204V 611A>T PACA-AU 11 103908804 103908804 single base substitution G T 3_prime_UTR_variant PACA-AU 11 103913559 103913559 single base substitution T C downstream_gene_variant PACA-AU 11 103913569 103913569 single base substitution T C downstream_gene_variant PACA-CA 11 103903751 103903751 single base substitution C T upstream_gene_variant PACA-CA 11 103904032 103904032 single base substitution G C upstream_gene_variant PACA-CA 11 103905832 103905833 deletion of <=200bp AG - upstream_gene_variant PACA-CA 11 103908404 103908404 single base substitution G A missense_variant R285Q 854G>A PACA-CA 11 103908451 103908451 single base substitution C T missense_variant R301C 901C>T PACA-CA 11 103908612 103908612 single base substitution T A synonymous_variant T354T 1062T>A PACA-CA 11 103910058 103910058 single base substitution A C downstream_gene_variant PACA-CA 11 103910969 103910969 single base substitution C A downstream_gene_variant PACA-CA 11 103913711 103913711 single base substitution A C downstream_gene_variant PBCA-DE 11 103907006 103907006 insertion of <=200bp - A upstream_gene_variant PBCA-DE 11 103907172 103907172 insertion of <=200bp - A upstream_gene_variant PBCA-DE 11 103907477 103907477 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant PBCA-DE 11 103910008 103910008 single base substitution T A downstream_gene_variant PRAD-CA 11 103902927 103902927 single base substitution A C upstream_gene_variant PRAD-CA 11 103903420 103903420 single base substitution C T upstream_gene_variant PRAD-CA 11 103904531 103904531 single base substitution A G upstream_gene_variant PRAD-CA 11 103908350 103908350 single base substitution T C missense_variant I267T 800T>C PRAD-CA 11 103909398 103909398 single base substitution C T 3_prime_UTR_variant PRAD-CA 11 103909541 103909541 single base substitution G A 3_prime_UTR_variant PRAD-CA 11 103912716 103912716 single base substitution T C downstream_gene_variant PRAD-CA 11 103914176 103914176 single base substitution A T downstream_gene_variant PRAD-UK 11 103905190 103905190 single base substitution A G upstream_gene_variant PRAD-US 11 103907873 103907873 single base substitution G A missense_variant R108H 323G>A READ-US 11 103908279 103908279 single base substitution G A missense_variant M243I 729G>A READ-US 11 103908633 103908633 single base substitution T C synonymous_variant L361L 1083T>C RECA-EU 11 103905140 103905140 single base substitution A G upstream_gene_variant RECA-EU 11 103907576 103907576 single base substitution G A missense_variant R9Q 26G>A SKCA-BR 11 103904594 103904594 single base substitution T A upstream_gene_variant SKCA-BR 11 103905570 103905570 single base substitution C T upstream_gene_variant SKCA-BR 11 103906793 103906793 single base substitution C T upstream_gene_variant SKCA-BR 11 103907171 103907171 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 11 103907763 103907763 single base substitution C T synonymous_variant I71I 213C>T SKCA-BR 11 103908034 103908034 single base substitution G A missense_variant E162K 484G>A SKCA-BR 11 103908158 103908158 single base substitution C T missense_variant A203V 608C>T SKCA-BR 11 103910153 103910153 single base substitution C T downstream_gene_variant SKCA-BR 11 103913494 103913494 single base substitution C T downstream_gene_variant SKCM-US 11 103907685 103907685 single base substitution C T synonymous_variant I45I 135C>T SKCM-US 11 103907691 103907691 single base substitution C T synonymous_variant I47I 141C>T SKCM-US 11 103907695 103907695 single base substitution C T missense_variant H49Y 145C>T SKCM-US 11 103907782 103907782 single base substitution G A missense_variant D78N 232G>A SKCM-US 11 103907792 103907792 single base substitution G A missense_variant G81E 242G>A SKCM-US 11 103907797 103907797 single base substitution C T missense_variant R83W 247C>T SKCM-US 11 103907887 103907887 single base substitution G A missense_variant G113R 337G>A SKCM-US 11 103907979 103907979 single base substitution C T synonymous_variant P143P 429C>T SKCM-US 11 103908010 103908010 single base substitution C T missense_variant P154S 460C>T SKCM-US 11 103908034 103908034 single base substitution G A missense_variant E162K 484G>A SKCM-US 11 103908037 103908037 single base substitution C T missense_variant R163C 487C>T SKCM-US 11 103908105 103908105 single base substitution G A synonymous_variant E185E 555G>A SKCM-US 11 103908115 103908115 single base substitution G A missense_variant E189K 565G>A SKCM-US 11 103908168 103908168 single base substitution G A synonymous_variant L206L 618G>A SKCM-US 11 103908172 103908172 single base substitution C T missense_variant R208W 622C>T SKCM-US 11 103908174 103908174 single base substitution G A synonymous_variant R208R 624G>A SKCM-US 11 103908196 103908196 single base substitution G A missense_variant E216K 646G>A SKCM-US 11 103908310 103908310 single base substitution C T missense_variant P254S 760C>T SKCM-US 11 103908311 103908311 single base substitution C T missense_variant P254L 761C>T SKCM-US 11 103908354 103908354 single base substitution G A missense_variant M268I 804G>A SKCM-US 11 103908370 103908370 single base substitution G A missense_variant E274K 820G>A SKCM-US 11 103908505 103908505 single base substitution T C missense_variant S319P 955T>C SKCM-US 11 103908522 103908522 single base substitution A G synonymous_variant Q324Q 972A>G SKCM-US 11 103908533 103908533 single base substitution T G missense_variant M328R 983T>G SKCM-US 11 103908641 103908641 single base substitution G A missense_variant G364E 1091G>A SKCM-US 11 103908686 103908686 single base substitution C T missense_variant S379F 1136C>T SKCM-US 11 103908697 103908697 single base substitution G A missense_variant E383K 1147G>A SKCM-US 11 103908728 103908728 single base substitution G A missense_variant R393Q 1178G>A STAD-US 11 103907607 103907607 single base substitution C G synonymous_variant L19L 57C>G STAD-US 11 103907617 103907617 single base substitution C A missense_variant P23T 67C>A STAD-US 11 103907643 103907643 single base substitution G T missense_variant K31N 93G>T STAD-US 11 103907674 103907674 single base substitution G A missense_variant V42I 124G>A STAD-US 11 103907674 103907674 single base substitution G T missense_variant V42F 124G>T STAD-US 11 103907697 103907697 single base substitution C T synonymous_variant H49H 147C>T STAD-US 11 103907764 103907764 single base substitution G A missense_variant V72M 214G>A STAD-US 11 103907793 103907793 single base substitution A T synonymous_variant G81G 243A>T STAD-US 11 103907841 103907841 single base substitution T C synonymous_variant S97S 291T>C STAD-US 11 103907911 103907911 single base substitution G A missense_variant A121T 361G>A STAD-US 11 103907980 103907980 single base substitution G A missense_variant A144T 430G>A STAD-US 11 103907993 103907993 single base substitution G A missense_variant S148N 443G>A STAD-US 11 103908053 103908053 single base substitution C T missense_variant A168V 503C>T STAD-US 11 103908214 103908214 single base substitution A T missense_variant N222Y 664A>T STAD-US 11 103908222 103908222 single base substitution A G synonymous_variant E224E 672A>G STAD-US 11 103908242 103908242 single base substitution T C missense_variant I231T 692T>C STAD-US 11 103908380 103908380 single base substitution A C missense_variant N277T 830A>C STAD-US 11 103908451 103908451 single base substitution C A missense_variant R301S 901C>A STAD-US 11 103908557 103908557 single base substitution G A missense_variant R336Q 1007G>A STAD-US 11 103908603 103908603 single base substitution C T synonymous_variant I351I 1053C>T STAD-US 11 103908618 103908618 single base substitution G A synonymous_variant T356T 1068G>A STAD-US 11 103908639 103908639 single base substitution G T missense_variant E363D 1089G>T STAD-US 11 103908678 103908678 single base substitution A C missense_variant Q376H 1128A>C STAD-US 11 103908681 103908681 single base substitution T C synonymous_variant D377D 1131T>C STAD-US 11 103908695 103908695 single base substitution A C missense_variant K382T 1145A>C THCA-SA 11 103907956 103907956 single base substitution G A missense_variant G136S 406G>A THCA-SA 11 103909166 103909166 single base substitution C A 3_prime_UTR_variant UCEC-US 11 103907653 103907653 single base substitution G A missense_variant E35K 103G>A UCEC-US 11 103907763 103907763 single base substitution C T synonymous_variant I71I 213C>T UCEC-US 11 103907774 103907774 single base substitution T C missense_variant L75P 224T>C UCEC-US 11 103907910 103907910 single base substitution C T synonymous_variant P120P 360C>T UCEC-US 11 103907980 103907980 single base substitution G A missense_variant A144T 430G>A UCEC-US 11 103908053 103908053 single base substitution C T missense_variant A168V 503C>T UCEC-US 11 103908146 103908146 single base substitution G A missense_variant R199H 596G>A UCEC-US 11 103908438 103908438 single base substitution G T missense_variant Q296H 888G>T UCEC-US 11 103908440 103908440 single base substitution G T missense_variant R297I 890G>T UCEC-US 11 103908489 103908489 single base substitution C G missense_variant F313L 939C>G UCEC-US 11 103908618 103908618 single base substitution G A synonymous_variant T356T 1068G>A UCEC-US 11 103908727 103908727 single base substitution C T stop_gained R393* 1177C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand CSCC-6-T COSM231264 c.649G>A p.E217K Substitution - Missense 11:104037471-104037471 + TCGA-RP-A693-06 COSM4895438 c.1147G>A p.E383K Substitution - Missense 11:104037969-104037969 + ESCC-246T COSM922418 c.1068G>A p.T356T Substitution - coding silent 11:104037890-104037890 + C0037T COSM4165619 c.26G>A p.R9Q Substitution - Missense 11:104036848-104036848 + CSCC-27-T COSM3868313 c.618G>A p.L206L Substitution - coding silent 11:104037440-104037440 + TCGA-AP-A056-01 COSM922414 c.890G>T p.R297I Substitution - Missense 11:104037712-104037712 + PD11342a COSM1249852 c.504G>A p.A168A Substitution - coding silent 11:104037326-104037326 + ESO-171 COSM1249861 c.88T>G p.F30V Substitution - Missense 11:104036910-104036910 + BCM759T COSM4017392 c.1089G>T p.E363D Substitution - Missense 11:104037911-104037911 + 587376 COSM1203198 c.1027G>A p.D343N Substitution - Missense 11:104037849-104037849 + TCGA-CA-6717-01 COSM1350496 c.1178G>A p.R393Q Substitution - Missense 11:104038000-104038000 + PT23_2 COSM5903779 c.320C>G p.S107C Substitution - Missense 11:104037142-104037142 + ESCC_BICR_023T COSM5436288 c.988C>G p.L330V Substitution - Missense 11:104037810-104037810 + ESO-250 COSM1249863 c.1151T>G p.I384S Substitution - Missense 11:104037973-104037973 + OSCC-GB_00740111 COSM4017388 c.1007G>A p.R336Q Substitution - Missense 11:104037829-104037829 + Au2 COSM3808202 c.371G>A p.R124Q Substitution - Missense 11:104037193-104037193 + HCC4T COSM1603970 c.102C>T p.C34C Substitution - coding silent 11:104036924-104036924 + B86 COSM1746011 c.529G>C p.E177Q Substitution - Missense 11:104037351-104037351 + TCGA-GF-A6C9-06 COSM4899897 c.232G>A p.D78N Substitution - Missense 11:104037054-104037054 + TCGA-MI-A75G-01 COSM4939930 c.703C>A p.P235T Substitution - Missense 11:104037525-104037525 + TCGA-BR-8591-01 COSM4017397 c.1131T>C p.D377D Substitution - coding silent 11:104037953-104037953 + CRC-29T COSM5452190 c.823C>T p.R275* Substitution - Nonsense 11:104037645-104037645 + PCSI_0083_Pa_X COSM3375619 c.901C>T p.R301C Substitution - Missense 11:104037723-104037723 + TCGA-DI-A0WH-01 COSM922420 c.1177C>T p.R393* Substitution - Nonsense 11:104037999-104037999 + TCGA-CD-8536-01 COSM1350479 c.124G>A p.V42I Substitution - Missense 11:104036946-104036946 + ME100L COSM231265 c.649G>A p.E217K Substitution - Missense 11:104037471-104037471 + TCGA-BR-8686-01 COSM4017369 c.147C>T p.H49H Substitution - coding silent 11:104036969-104036969 + HX13T COSM1603970 c.102C>T p.C34C Substitution - coding silent 11:104036924-104036924 + TCGA-A5-A0GA-01 COSM922418 c.1068G>A p.T356T Substitution - coding silent 11:104037890-104037890 + TCGA-DU-7012-01 COSM3670647 c.323G>A p.R108H Substitution - Missense 11:104037145-104037145 + YURAY COSM4676679 c.127G>A p.E43K Substitution - Missense 11:104036949-104036949 + HCC142 COSM1603973 c.132G>T p.E44D Substitution - Missense 11:104036954-104036954 + SNUH_G76_S1 COSM4419792 c.1185G>A p.E395E Substitution - coding silent 11:104038007-104038007 + I2L-P7-Tumor-Organoid COSM5361087 c.342G>T p.Q114H Substitution - Missense 11:104037164-104037164 + BD119T COSM5520900 c.596G>T p.R199L Substitution - Missense 11:104037418-104037418 + CRC-02T COSM1350490 c.488G>A p.R163H Substitution - Missense 11:104037310-104037310 + TCGA-EE-A181-06 COSM2108975 c.565G>A p.E189K Substitution - Missense 11:104037387-104037387 + 2492701 COSM3808202 c.371G>A p.R124Q Substitution - Missense 11:104037193-104037193 + J13_T COSM3979031 c.862G>T p.G288W Substitution - Missense 11:104037684-104037684 + C086 COSM5529623 c.392G>A p.G131E Substitution - Missense 11:104037214-104037214 + SC_9023 COSM5555060 c.754G>A p.G252R Substitution - Missense 11:104037576-104037576 + T20 COSM4676690 c.609C>T p.A203A Substitution - coding silent 11:104037431-104037431 + TCGA-FW-A3R5-06 COSM3868313 c.618G>A p.L206L Substitution - coding silent 11:104037440-104037440 + HN_62432 COSM127787 c.1053C>A p.I351I Substitution - coding silent 11:104037875-104037875 + SC_9109 COSM2108927 c.22G>A p.V8M Substitution - Missense 11:104036844-104036844 + TCGA-37-4135-01 COSM685742 c.255A>G p.P85P Substitution - coding silent 11:104037077-104037077 + TCGA-BR-6452-01 COSM4017382 c.692T>C p.I231T Substitution - Missense 11:104037514-104037514 + S02277 COSM5683006 c.300G>A p.A100A Substitution - coding silent 11:104037122-104037122 + TCGA-BR-6452-01 COSM4017370 c.243A>T p.G81G Substitution - coding silent 11:104037065-104037065 + S01861 COSM5670967 c.314delC p.S106fs*40 Deletion - Frameshift 11:104037136-104037136 + 2492703 COSM3808202 c.371G>A p.R124Q Substitution - Missense 11:104037193-104037193 + SNU-C4 COSM922408 c.430G>A p.A144T Substitution - Missense 11:104037252-104037252 + ESO-043 COSM1249853 c.1128A>T p.Q376H Substitution - Missense 11:104037950-104037950 + OSCC-GB_00530111 COSM4676694 c.786C>T p.G262G Substitution - coding silent 11:104037608-104037608 + CRC-29T COSM5452191 c.823C>T p.R275* Substitution - Nonsense 11:104037645-104037645 + 587342 COSM1203197 c.632A>G p.Q211R Substitution - Missense 11:104037454-104037454 + TCGA-F5-6814-01 COSM3415448 c.1083T>C p.L361L Substitution - coding silent 11:104037905-104037905 + T10 COSM5341371 c.107C>T p.A36V Substitution - Missense 11:104036929-104036929 + 36 COSM87751 c.232G>A p.D78N Substitution - Missense 11:104037054-104037054 + LUAD-S01409 COSM346287 c.902G>A p.R301H Substitution - Missense 11:104037724-104037724 + Pat_04_A COSM4895439 c.1147G>A p.E383K Substitution - Missense 11:104037969-104037969 + TCGA-EE-A2MR-06 COSM3442815 c.145C>T p.H49Y Substitution - Missense 11:104036967-104036967 + SS6003117 COSM3442844 c.1091G>A p.G364E Substitution - Missense 11:104037913-104037913 + CSCC-55-T COSM4531934 c.183G>A p.L61L Substitution - coding silent 11:104037005-104037005 + TCGA-B7-5816-01 COSM4017385 c.830A>C p.N277T Substitution - Missense 11:104037652-104037652 + OSCC-GB_00740111 COSM4017389 c.1007G>A p.R336Q Substitution - Missense 11:104037829-104037829 + T2272 COSM4676692 c.661C>A p.Q221K Substitution - Missense 11:104037483-104037483 + CSCC-52-T COSM4542522 c.31G>A p.D11N Substitution - Missense 11:104036853-104036853 + TCGA-CG-4437-01 COSM4017386 c.901C>A p.R301S Substitution - Missense 11:104037723-104037723 + TCGA-AP-A056-01 COSM922415 c.890G>T p.R297I Substitution - Missense 11:104037712-104037712 + B86 COSM1746010 c.529G>C p.E177Q Substitution - Missense 11:104037351-104037351 + TCGA-D3-A3C7-06 COSM3442829 c.624G>A p.R208R Substitution - coding silent 11:104037446-104037446 + 990515 COSM1582070 c.1120A>C p.S374R Substitution - Missense 11:104037942-104037942 + TCGA-D3-A3C8-06 COSM3442824 c.484G>A p.E162K Substitution - Missense 11:104037306-104037306 + TCGA-AG-A002-01 COSM260374 c.1129G>A p.D377N Substitution - Missense 11:104037951-104037951 + TCGA-CG-4436-01 COSM4017395 c.1128A>C p.Q376H Substitution - Missense 11:104037950-104037950 + HCC137T COSM1603968 c.10A>G p.T4A Substitution - Missense 11:104036832-104036832 + HCC142 COSM1603972 c.132G>T p.E44D Substitution - Missense 11:104036954-104036954 + 3N09-VS-3T09 COSM4979162 c.465C>T p.H155H Substitution - coding silent 11:104037287-104037287 + PCSI_0083_Pa_P_526 COSM3375618 c.901C>T p.R301C Substitution - Missense 11:104037723-104037723 + HCC137 COSM1603969 c.10A>G p.T4A Substitution - Missense 11:104036832-104036832 + TCGA-AP-A056-01 COSM922403 c.213C>T p.I71I Substitution - coding silent 11:104037035-104037035 + CSCC-55-T COSM685731 c.1123G>A p.G375R Substitution - Missense 11:104037945-104037945 + TCGA-G2-A2EJ-01 COSM1297578 c.956C>G p.S319C Substitution - Missense 11:104037778-104037778 + CHEWS031 COSM4519933 c.1035G>A p.K345K Substitution - coding silent 11:104037857-104037857 + TCGA-CD-5800-01 COSM4017363 c.67C>A p.P23T Substitution - Missense 11:104036889-104036889 + CSCC-62-T COSM4522008 c.1140G>T p.S380S Substitution - coding silent 11:104037962-104037962 + TCGA-B7-5816-01 COSM4017384 c.830A>C p.N277T Substitution - Missense 11:104037652-104037652 + 347 COSM98360 c.922C>G p.Q308E Substitution - Missense 11:104037744-104037744 + TCGA-AX-A060-01 COSM922407 c.360C>T p.P120P Substitution - coding silent 11:104037182-104037182 + 12 COSM922421 c.1177C>T p.R393* Substitution - Nonsense 11:104037999-104037999 + CSCC-27-T COSM4559177 c.795G>A p.M265I Substitution - Missense 11:104037617-104037617 + CSCC-18-T COSM3868315 c.622C>T p.R208W Substitution - Missense 11:104037444-104037444 + 2492701 COSM3808203 c.371G>A p.R124Q Substitution - Missense 11:104037193-104037193 + TCGA-C5-A1BI-01 COSM4841593 c.818C>T p.A273V Substitution - Missense 11:104037640-104037640 + CSCC-6-T COSM4552579 c.563G>A p.R188K Substitution - Missense 11:104037385-104037385 + MO_1084 COSM5565390 c.853C>T p.R285W Substitution - Missense 11:104037675-104037675 + TCGA-ER-A19K-01 COSM3442838 c.955T>C p.S319P Substitution - Missense 11:104037777-104037777 + S02065 COSM5672534 c.427C>A p.P143T Substitution - Missense 11:104037249-104037249 + TCGA-AA-A010-01 COSM280326 c.166G>A p.E56K Substitution - Missense 11:104036988-104036988 + 587332 COSM1203194 c.878T>C p.V293A Substitution - Missense 11:104037700-104037700 + TCGA-AN-A046-01 COSM1203198 c.1027G>A p.D343N Substitution - Missense 11:104037849-104037849 + OSCC-GB_00840111 COSM4676684 c.312G>A p.T104T Substitution - coding silent 11:104037134-104037134 + PD6730b COSM5791789 c.1183G>A p.E395K Substitution - Missense 11:104038005-104038005 + 2318491 COSM4776902 c.1183G>C p.E395Q Substitution - Missense 11:104038005-104038005 + TCGA-A5-A0GP-01 COSM922400 c.103G>A p.E35K Substitution - Missense 11:104036925-104036925 + CSCC-16-T COSM4571201 c.401T>C p.V134A Substitution - Missense 11:104037223-104037223 + LUAD-S01409 COSM346288 c.902G>A p.R301H Substitution - Missense 11:104037724-104037724 + TCGA-IH-A3EA-01 COSM3442841 c.972A>G p.Q324Q Substitution - coding silent 11:104037794-104037794 + TCGA-CC-A5UE-01 COSM1350490 c.488G>A p.R163H Substitution - Missense 11:104037310-104037310 + T3064 COSM4676687 c.418C>A p.L140M Substitution - Missense 11:104037240-104037240 + 2521243 COSM200190 c.824G>A p.R275Q Substitution - Missense 11:104037646-104037646 + LUAD-RT-S01813 COSM383078 c.597T>C p.R199R Substitution - coding silent 11:104037419-104037419 + C70 COSM4619380 c.732C>T p.L244L Substitution - coding silent 11:104037554-104037554 + HCC2998 COSM1676398 c.202G>T p.D68Y Substitution - Missense 11:104037024-104037024 + TCGA-CD-A4MG-01 COSM4017365 c.93G>T p.K31N Substitution - Missense 11:104036915-104036915 + TCGA-60-2726-01 COSM685744 c.116G>A p.R39K Substitution - Missense 11:104036938-104036938 + TCGA-BR-8686-01 COSM4017368 c.147C>T p.H49H Substitution - coding silent 11:104036969-104036969 + TCGA-FW-A3R5-06 COSM3868317 c.1136C>T p.S379F Substitution - Missense 11:104037958-104037958 + TCGA-BR-4257-01 COSM4017374 c.361G>A p.A121T Substitution - Missense 11:104037183-104037183 + TCGA-FW-A3R5-06 COSM3730192 c.820G>A p.E274K Substitution - Missense 11:104037642-104037642 + TCGA-C5-A1BI-01 COSM4841594 c.818C>T p.A273V Substitution - Missense 11:104037640-104037640 + C135 COSM4617065 c.850C>T p.R284* Substitution - Nonsense 11:104037672-104037672 + LUAD-LIP77 COSM342096 c.322_323CG>AA p.R108>? Complex 11:104037144-104037145 + TCGA-CD-A4MG-01 COSM4017364 c.93G>T p.K31N Substitution - Missense 11:104036915-104036915 + 436 COSM4433967 c.571G>A p.A191T Substitution - Missense 11:104037393-104037393 + TCGA-AZ-6601-01 COSM346288 c.902G>A p.R301H Substitution - Missense 11:104037724-104037724 + CSCC-55-T COSM922402 c.213C>T p.I71I Substitution - coding silent 11:104037035-104037035 + PT48 COSM4017389 c.1007G>A p.R336Q Substitution - Missense 11:104037829-104037829 + TCGA-HU-A4G3-01 COSM1284434 c.214G>A p.V72M Substitution - Missense 11:104037036-104037036 + STC246 COSM5050474 c.59A>G p.Q20R Substitution - Missense 11:104036881-104036881 + T3610 COSM4676684 c.312G>A p.T104T Substitution - coding silent 11:104037134-104037134 + LUAD-NYU1026 COSM368287 c.265C>A p.P89T Substitution - Missense 11:104037087-104037087 + CSCC-38-T COSM4549828 c.483G>A p.K161K Substitution - coding silent 11:104037305-104037305 + ESCC_61 COSM4183589 c.27G>A p.R9R Substitution - coding silent 11:104036849-104036849 + TCGA-BH-A204-01 COSM1474955 c.782C>T p.S261L Substitution - Missense 11:104037604-104037604 + S02292 COSM5687263 c.1047G>C p.L349L Substitution - coding silent 11:104037869-104037869 + TCGA-A5-A0VP-01 COSM922409 c.430G>A p.A144T Substitution - Missense 11:104037252-104037252 + 2492700 COSM3808202 c.371G>A p.R124Q Substitution - Missense 11:104037193-104037193 + TCGA-18-3409-01 COSM685733 c.1084C>T p.P362S Substitution - Missense 11:104037906-104037906 + TCGA-D3-A3C8-06 COSM3442825 c.484G>A p.E162K Substitution - Missense 11:104037306-104037306 + ESO-043 COSM1249854 c.1128A>T p.Q376H Substitution - Missense 11:104037950-104037950 + KYSE-150 COSM2108952 c.278G>A p.R93H Substitution - Missense 11:104037100-104037100 + TCGA-D7-A4Z0-01 COSM4017398 c.1145A>C p.K382T Substitution - Missense 11:104037967-104037967 + ME100L COSM231264 c.649G>A p.E217K Substitution - Missense 11:104037471-104037471 + ESCC_61 COSM4183588 c.27G>A p.R9R Substitution - coding silent 11:104036849-104036849 + SJHGG060_A COSM200183 c.322C>T p.R108C Substitution - Missense 11:104037144-104037144 + TCGA-EE-A29L-06 COSM3442827 c.555G>A p.E185E Substitution - coding silent 11:104037377-104037377 + 5 COSM922421 c.1177C>T p.R393* Substitution - Nonsense 11:104037999-104037999 + LUAD-E01317 COSM403649 c.1140G>A p.S380S Substitution - coding silent 11:104037962-104037962 + TCGA-AN-A046-01 COSM3808205 c.710G>T p.S237I Substitution - Missense 11:104037532-104037532 + TCGA-06-0192-01 COSM2150640 c.506A>C p.E169A Substitution - Missense 11:104037328-104037328 + TCGA-G4-6306-01 COSM1350477 c.36C>T p.L12L Substitution - coding silent 11:104036858-104036858 + 262LT COSM1284433 c.214G>A p.V72M Substitution - Missense 11:104037036-104037036 + ATL055 COSM428309 c.487C>T p.R163C Substitution - Missense 11:104037309-104037309 + TCGA-CG-5721-01 COSM4017372 c.291T>C p.S97S Substitution - coding silent 11:104037113-104037113 + CRC-03T COSM5451116 c.518G>A p.S173N Substitution - Missense 11:104037340-104037340 + TCGA-EE-A3JH-06 COSM3442830 c.646G>A p.E216K Substitution - Missense 11:104037468-104037468 + ESO-118 COSM237282 c.387G>A p.A129A Substitution - coding silent 11:104037209-104037209 + T3064 COSM4676686 c.418C>A p.L140M Substitution - Missense 11:104037240-104037240 + ESO-122 COSM1249860 c.838A>T p.R280W Substitution - Missense 11:104037660-104037660 + LS174T COSM4645753 c.212T>C p.I71T Substitution - Missense 11:104037034-104037034 + 66 COSM5743506 c.311C>T p.T104M Substitution - Missense 11:104037133-104037133 + RK021_C01 COSM428309 c.487C>T p.R163C Substitution - Missense 11:104037309-104037309 + Mx41 COSM50373 c.1151T>G p.I384S Substitution - Missense 11:104037973-104037973 + ESO-250 COSM50373 c.1151T>G p.I384S Substitution - Missense 11:104037973-104037973 + CHC121T COSM216935 c.808C>A p.Q270K Substitution - Missense 11:104037630-104037630 + 587278 COSM1203192 c.248G>A p.R83Q Substitution - Missense 11:104037070-104037070 + 587342 COSM1203196 c.632A>G p.Q211R Substitution - Missense 11:104037454-104037454 + MO_1084 COSM5565389 c.853C>T p.R285W Substitution - Missense 11:104037675-104037675 + ESCC-246T COSM922419 c.1068G>A p.T356T Substitution - coding silent 11:104037890-104037890 + TCGA-EB-A4IS-01 COSM3442837 c.804G>A p.M268I Substitution - Missense 11:104037626-104037626 + HCC4 COSM1603970 c.102C>T p.C34C Substitution - coding silent 11:104036924-104036924 + TCGA-AZ-4615-01 COSM3687064 c.231G>T p.K77N Substitution - Missense 11:104037053-104037053 + SC_9008 COSM3687064 c.231G>T p.K77N Substitution - Missense 11:104037053-104037053 + CSCC-38-T COSM4549827 c.483G>A p.K161K Substitution - coding silent 11:104037305-104037305 + TCGA-P5-A5EV-01 COSM4420487 c.619G>C p.D207H Substitution - Missense 11:104037441-104037441 + S01022 COSM5665619 c.496C>A p.P166T Substitution - Missense 11:104037318-104037318 + HCC2998 COSM2108962 c.456C>A p.S152S Substitution - coding silent 11:104037278-104037278 + YUDIVI COSM2108963 c.466G>A p.D156N Substitution - Missense 11:104037288-104037288 + CSCC-18-T COSM3868316 c.622C>T p.R208W Substitution - Missense 11:104037444-104037444 + Au2 COSM3808203 c.371G>A p.R124Q Substitution - Missense 11:104037193-104037193 + TCGA-FW-A3R5-06 COSM3730191 c.820G>A p.E274K Substitution - Missense 11:104037642-104037642 + TCGA-FW-A3R5-06 COSM1350497 c.1178G>A p.R393Q Substitution - Missense 11:104038000-104038000 + LUAD-LIP77 COSM342095 c.322_323CG>AA p.R108>? Complex 11:104037144-104037145 + C086 COSM5529624 c.392G>A p.G131E Substitution - Missense 11:104037214-104037214 + CHC121T COSM216936 c.808C>A p.Q270K Substitution - Missense 11:104037630-104037630 + Au1 COSM5596571 c.900C>T p.G300G Substitution - coding silent 11:104037722-104037722 + TCGA-EE-A29L-06 COSM3442826 c.555G>A p.E185E Substitution - coding silent 11:104037377-104037377 + HCC2998 COSM1676398 c.202G>T p.D68Y Substitution - Missense 11:104037024-104037024 + Gp2D COSM4626730 c.317G>T p.S106I Substitution - Missense 11:104037139-104037139 + S02299 COSM5690012 c.614C>A p.P205Q Substitution - Missense 11:104037436-104037436 + TCGA-BR-8284-01 COSM4017378 c.664A>T p.N222Y Substitution - Missense 11:104037486-104037486 + 462 COSM4436686 c.451C>G p.L151V Substitution - Missense 11:104037273-104037273 + TCGA-CK-4947-01 COSM1350482 c.192C>T p.Y64Y Substitution - coding silent 11:104037014-104037014 + J13_T COSM3979030 c.862G>T p.G288W Substitution - Missense 11:104037684-104037684 + NB-3211 COSM1284434 c.214G>A p.V72M Substitution - Missense 11:104037036-104037036 + I2L-P7-Tumor-Organoid COSM5361088 c.342G>T p.Q114H Substitution - Missense 11:104037164-104037164 + TCGA-RP-A693-06 COSM4895439 c.1147G>A p.E383K Substitution - Missense 11:104037969-104037969 + cSCCP1 COSM136030 c.978G>A p.M326I Substitution - Missense 11:104037800-104037800 + TCGA-DA-A1HW-06 COSM3442813 c.141C>T p.I47I Substitution - coding silent 11:104036963-104036963 + TCGA-FW-A3R5-06 COSM3868318 c.1136C>T p.S379F Substitution - Missense 11:104037958-104037958 + C135 COSM4617064 c.850C>T p.R284* Substitution - Nonsense 11:104037672-104037672 + LUAD-RT-S01813 COSM383077 c.597T>C p.R199R Substitution - coding silent 11:104037419-104037419 + 8035823 COSM3769171 c.611A>T p.D204V Substitution - Missense 11:104037433-104037433 + CSCC-6-T COSM4552580 c.563G>A p.R188K Substitution - Missense 11:104037385-104037385 + LUAD-YINHD COSM348324 c.429C>T p.P143P Substitution - coding silent 11:104037251-104037251 + TCGA-HU-A4G9-01 COSM4017391 c.1053C>T p.I351I Substitution - coding silent 11:104037875-104037875 + TCGA-CD-8535-01 COSM4017380 c.672A>G p.E224E Substitution - coding silent 11:104037494-104037494 + TCGA-BS-A0UV-01 COSM922411 c.503C>T p.A168V Substitution - Missense 11:104037325-104037325 + CSCC-55-T COSM922403 c.213C>T p.I71I Substitution - coding silent 11:104037035-104037035 + TCGA-BS-A0UV-01 COSM922410 c.503C>T p.A168V Substitution - Missense 11:104037325-104037325 + CRC-03T COSM5451115 c.518G>A p.S173N Substitution - Missense 11:104037340-104037340 + TCGA-BR-4362-01 COSM4017393 c.1089G>T p.E363D Substitution - Missense 11:104037911-104037911 + 2521243 COSM200189 c.824G>A p.R275Q Substitution - Missense 11:104037646-104037646 + TCGA-22-5491-01 COSM685736 c.845T>G p.V282G Substitution - Missense 11:104037667-104037667 + TCGA-MI-A75G-01 COSM4939931 c.703C>A p.P235T Substitution - Missense 11:104037525-104037525 + TCGA-CD-8536-01 COSM4017377 c.443G>A p.S148N Substitution - Missense 11:104037265-104037265 + ESO-122 COSM1249857 c.88T>C p.F30L Substitution - Missense 11:104036910-104036910 + CHC2206T COSM4956925 c.885A>T p.T295T Substitution - coding silent 11:104037707-104037707 + TCGA-ER-A19K-01 COSM3442843 c.983T>G p.M328R Substitution - Missense 11:104037805-104037805 + S02292 COSM5687262 c.1047G>C p.L349L Substitution - coding silent 11:104037869-104037869 + TCGA-B0-5121-01 COSM466238 c.974C>T p.P325L Substitution - Missense 11:104037796-104037796 + LUAD-NYU160 COSM370409 c.958A>G p.I320V Substitution - Missense 11:104037780-104037780 + TCGA-AX-A060-01 COSM922406 c.360C>T p.P120P Substitution - coding silent 11:104037182-104037182 + TCGA-BR-6452-01 COSM4017383 c.692T>C p.I231T Substitution - Missense 11:104037514-104037514 + TCGA-BH-A204-01 COSM1474956 c.782C>T p.S261L Substitution - Missense 11:104037604-104037604 + ESO-118 COSM237281 c.387G>A p.A129A Substitution - coding silent 11:104037209-104037209 + ccRCC-84 COSM1661406 c.897T>G p.I299M Substitution - Missense 11:104037719-104037719 + TCGA-EK-A2RJ-01 COSM4831950 c.461C>T p.P154L Substitution - Missense 11:104037283-104037283 + PT23_1 COSM4676682 c.208G>A p.D70N Substitution - Missense 11:104037030-104037030 + 6115219 COSM5558749 c.516C>A p.L172L Substitution - coding silent 11:104037338-104037338 + TCGA-FW-A3R5-06 COSM348324 c.429C>T p.P143P Substitution - coding silent 11:104037251-104037251 + HCC82T COSM1603974 c.706G>T p.E236* Substitution - Nonsense 11:104037528-104037528 + LUAD-E01317 COSM403648 c.1140G>A p.S380S Substitution - coding silent 11:104037962-104037962 + HCC4T COSM1603971 c.102C>T p.C34C Substitution - coding silent 11:104036924-104036924 + TCGA-AP-A059-01 COSM922412 c.888G>T p.Q296H Substitution - Missense 11:104037710-104037710 + TCGA-GN-A263-01 COSM428309 c.487C>T p.R163C Substitution - Missense 11:104037309-104037309 + PD11342a COSM1249851 c.504G>A p.A168A Substitution - coding silent 11:104037326-104037326 + TCGA-18-4083-01 COSM685739 c.477G>A p.L159L Substitution - coding silent 11:104037299-104037299 + TCGA-AZ-4615-01 COSM3687063 c.231G>T p.K77N Substitution - Missense 11:104037053-104037053 + PCSI_0083_Pa_P COSM3375619 c.901C>T p.R301C Substitution - Missense 11:104037723-104037723 + HCC4 COSM1603971 c.102C>T p.C34C Substitution - coding silent 11:104036924-104036924 + BCM759T COSM4017393 c.1089G>T p.E363D Substitution - Missense 11:104037911-104037911 + TCGA-AZ-4615-01 COSM3687066 c.854G>A p.R285Q Substitution - Missense 11:104037676-104037676 + T2269 COSM4676678 c.127G>A p.E43K Substitution - Missense 11:104036949-104036949 + T3610 COSM4676685 c.312G>A p.T104T Substitution - coding silent 11:104037134-104037134 + TCGA-AZ-6598-01 COSM1350486 c.332A>T p.H111L Substitution - Missense 11:104037154-104037154 + ESCC_32 COSM348323 c.429C>T p.P143P Substitution - coding silent 11:104037251-104037251 + CSCC-4-T COSM4560530 c.847G>A p.D283N Substitution - Missense 11:104037669-104037669 + TCGA-74-6584-01 COSM922419 c.1068G>A p.T356T Substitution - coding silent 11:104037890-104037890 + 462 COSM4436685 c.451C>G p.L151V Substitution - Missense 11:104037273-104037273 + T10 COSM5341370 c.107C>T p.A36V Substitution - Missense 11:104036929-104036929 + SS6003314 COSM4091242 c.1037A>C p.K346T Substitution - Missense 11:104037859-104037859 + TCGA-AN-A046-01 COSM1203199 c.1027G>A p.D343N Substitution - Missense 11:104037849-104037849 + 587278 COSM1203193 c.248G>A p.R83Q Substitution - Missense 11:104037070-104037070 + HCC137T COSM1603969 c.10A>G p.T4A Substitution - Missense 11:104036832-104036832 + PT35 COSM3868316 c.622C>T p.R208W Substitution - Missense 11:104037444-104037444 + TCGA-DU-7012-01 COSM3670646 c.323G>A p.R108H Substitution - Missense 11:104037145-104037145 + CHC2206T COSM4956925 c.885A>T p.T295T Substitution - coding silent 11:104037707-104037707 + HCC82T COSM1603975 c.706G>T p.E236* Substitution - Nonsense 11:104037528-104037528 + SNUH_G76_S1 COSM4419791 c.1185G>A p.E395E Substitution - coding silent 11:104038007-104038007 + Pat_76_A COSM3670647 c.323G>A p.R108H Substitution - Missense 11:104037145-104037145 + TCGA-FW-A3R5-06 COSM3868314 c.618G>A p.L206L Substitution - coding silent 11:104037440-104037440 + TCGA-C8-A12T-01 COSM428308 c.487C>T p.R163C Substitution - Missense 11:104037309-104037309 + HCC142T COSM1603973 c.132G>T p.E44D Substitution - Missense 11:104036954-104036954 + ESO-0459 COSM1249855 c.724A>G p.T242A Substitution - Missense 11:104037546-104037546 + TCGA-AP-A0LF-01 COSM922416 c.939C>G p.F313L Substitution - Missense 11:104037761-104037761 + TCGA-AA-3492-01 COSM1350480 c.126C>T p.V42V Substitution - coding silent 11:104036948-104036948 + TCGA-GF-A6C9-06 COSM87751 c.232G>A p.D78N Substitution - Missense 11:104037054-104037054 + TCGA-CC-A5UE-01 COSM1350491 c.488G>A p.R163H Substitution - Missense 11:104037310-104037310 + PT23_1 COSM4676683 c.208G>A p.D70N Substitution - Missense 11:104037030-104037030 + Pat_76_A COSM3670646 c.323G>A p.R108H Substitution - Missense 11:104037145-104037145 + LUAD-NYU1026 COSM368286 c.265C>A p.P89T Substitution - Missense 11:104037087-104037087 + TCGA-AP-A056-01 COSM922402 c.213C>T p.I71I Substitution - coding silent 11:104037035-104037035 + TCGA-FW-A3R5-06 COSM1350496 c.1178G>A p.R393Q Substitution - Missense 11:104038000-104038000 + YUBER COSM1704502 c.193G>A p.G65S Substitution - Missense 11:104037015-104037015 + CSCC-27-T COSM4519893 c.1032G>A p.L344L Substitution - coding silent 11:104037854-104037854 + BCM759T COSM4017392 c.1089G>T p.E363D Substitution - Missense 11:104037911-104037911 + TCGA-CG-4436-01 COSM4017394 c.1128A>C p.Q376H Substitution - Missense 11:104037950-104037950 + TCGA-BR-8382-01 COSM922410 c.503C>T p.A168V Substitution - Missense 11:104037325-104037325 + TCGA-B0-5812-01 COSM466237 c.53C>G p.S18C Substitution - Missense 11:104036875-104036875 + CSCC-62-T COSM4487633 c.320C>T p.S107F Substitution - Missense 11:104037142-104037142 + TCGA-BP-4975-01 COSM466241 c.1004T>C p.L335P Substitution - Missense 11:104037826-104037826 + C70 COSM4619381 c.732C>T p.L244L Substitution - coding silent 11:104037554-104037554 + TCGA-CG-4305-01 COSM4017361 c.57C>G p.L19L Substitution - coding silent 11:104036879-104036879 + TCGA-CC-A7IK-01 COSM4925037 c.590G>T p.R197M Substitution - Missense 11:104037412-104037412 + CSCC-16-T COSM3442818 c.247C>T p.R83W Substitution - Missense 11:104037069-104037069 + TCGA-EI-6917-01 COSM3415446 c.729G>A p.M243I Substitution - Missense 11:104037551-104037551 + CSCC-55-T COSM685732 c.1123G>A p.G375R Substitution - Missense 11:104037945-104037945 + ESCC_BICR_020T COSM922401 c.103G>A p.E35K Substitution - Missense 11:104036925-104036925 + T3535 COSM4676689 c.543G>T p.Q181H Substitution - Missense 11:104037365-104037365 + PCSI_0087_Pa_X COSM3375621 c.1062T>A p.T354T Substitution - coding silent 11:104037884-104037884 + CSCC-55-T COSM4531935 c.183G>A p.L61L Substitution - coding silent 11:104037005-104037005 + T231 COSM4676695 c.786C>T p.G262G Substitution - coding silent 11:104037608-104037608 + OSCC-GB_00840111 COSM4676685 c.312G>A p.T104T Substitution - coding silent 11:104037134-104037134 + CSCC-16-T COSM4571200 c.401T>C p.V134A Substitution - Missense 11:104037223-104037223 + TCGA-EK-A2RJ-01 COSM4831951 c.461C>T p.P154L Substitution - Missense 11:104037283-104037283 + S01022 COSM5665618 c.496C>A p.P166T Substitution - Missense 11:104037318-104037318 + ESO-0067 COSM1249851 c.504G>A p.A168A Substitution - coding silent 11:104037326-104037326 + TCGA-E7-A3Y1-01 COSM3791118 c.970C>A p.Q324K Substitution - Missense 11:104037792-104037792 + TCGA-EE-A2MR-06 COSM3442814 c.145C>T p.H49Y Substitution - Missense 11:104036967-104036967 + PTC-7C COSM4145190 c.406G>A p.G136S Substitution - Missense 11:104037228-104037228 + 12 COSM922420 c.1177C>T p.R393* Substitution - Nonsense 11:104037999-104037999 + TCGA-G4-6628-01 COSM1350491 c.488G>A p.R163H Substitution - Missense 11:104037310-104037310 + PD6730b COSM5791788 c.1183G>A p.E395K Substitution - Missense 11:104038005-104038005 + TCGA-BP-4975-01 COSM466240 c.1004T>C p.L335P Substitution - Missense 11:104037826-104037826 + T20 COSM4676691 c.609C>T p.A203A Substitution - coding silent 11:104037431-104037431 + TCGA-AZ-6601-01 COSM346287 c.902G>A p.R301H Substitution - Missense 11:104037724-104037724 + 381_T COSM3979028 c.266C>A p.P89Q Substitution - Missense 11:104037088-104037088 + NB-3211 COSM1284433 c.214G>A p.V72M Substitution - Missense 11:104037036-104037036 + SS6003117 COSM3442845 c.1091G>A p.G364E Substitution - Missense 11:104037913-104037913 + TCGA-EW-A1PB-01 COSM3808203 c.371G>A p.R124Q Substitution - Missense 11:104037193-104037193 + ESO-171 COSM1249862 c.88T>G p.F30V Substitution - Missense 11:104036910-104036910 + T3187 COSM1249862 c.88T>G p.F30V Substitution - Missense 11:104036910-104036910 + TCGA-EW-A1PB-01 COSM3808202 c.371G>A p.R124Q Substitution - Missense 11:104037193-104037193 + TCGA-IH-A3EA-01 COSM3442840 c.972A>G p.Q324Q Substitution - coding silent 11:104037794-104037794 + TCGA-BR-4257-01 COSM4017375 c.361G>A p.A121T Substitution - Missense 11:104037183-104037183 + TCGA-18-3409-01 COSM685734 c.1084C>T p.P362S Substitution - Missense 11:104037906-104037906 + LAU50_2 COSM232141 c.244C>A p.P82T Substitution - Missense 11:104037066-104037066 + 7996 COSM5613294 c.741C>G p.N247K Substitution - Missense 11:104037563-104037563 + CHC2206T COSM4956926 c.885A>T p.T295T Substitution - coding silent 11:104037707-104037707 + CSCC-4-T COSM4560529 c.847G>A p.D283N Substitution - Missense 11:104037669-104037669 + TCGA-BR-8382-01 COSM922411 c.503C>T p.A168V Substitution - Missense 11:104037325-104037325 + BD119T COSM5520899 c.596G>T p.R199L Substitution - Missense 11:104037418-104037418 + B86-Tumor COSM1746010 c.529G>C p.E177Q Substitution - Missense 11:104037351-104037351 + 2492702 COSM3808202 c.371G>A p.R124Q Substitution - Missense 11:104037193-104037193 + TCGA-06-0192-01 COSM2150641 c.506A>C p.E169A Substitution - Missense 11:104037328-104037328 + SJHGG060_A COSM200184 c.322C>T p.R108C Substitution - Missense 11:104037144-104037144 + TCGA-EE-A181-06 COSM3442845 c.1091G>A p.G364E Substitution - Missense 11:104037913-104037913 + TCGA-CG-4437-01 COSM4017387 c.901C>A p.R301S Substitution - Missense 11:104037723-104037723 + TCGA-CD-A4MG-01 COSM922418 c.1068G>A p.T356T Substitution - coding silent 11:104037890-104037890 + 262LT COSM1284434 c.214G>A p.V72M Substitution - Missense 11:104037036-104037036 + PCSI_0329_Pa_P_526 COSM3687065 c.854G>A p.R285Q Substitution - Missense 11:104037676-104037676 + ESO-0067 COSM1249852 c.504G>A p.A168A Substitution - coding silent 11:104037326-104037326 + T3058 COSM4676680 c.207C>T p.G69G Substitution - coding silent 11:104037029-104037029 + TCGA-EE-A2MS-06 COSM3442834 c.761C>T p.P254L Substitution - Missense 11:104037583-104037583 + 226 COSM3730191 c.820G>A p.E274K Substitution - Missense 11:104037642-104037642 + CSCC-27-T COSM3868314 c.618G>A p.L206L Substitution - coding silent 11:104037440-104037440 + TCGA-CK-4947-01 COSM1350483 c.192C>T p.Y64Y Substitution - coding silent 11:104037014-104037014 + CSCC-16-T COSM3442819 c.247C>T p.R83W Substitution - Missense 11:104037069-104037069 + 436 COSM4433968 c.571G>A p.A191T Substitution - Missense 11:104037393-104037393 + TCGA-AA-3492-01 COSM1350481 c.126C>T p.V42V Substitution - coding silent 11:104036948-104036948 + CRC-02T COSM1350491 c.488G>A p.R163H Substitution - Missense 11:104037310-104037310 + CHC1854T COSM3666838 c.705C>T p.P235P Substitution - coding silent 11:104037527-104037527 + SS6003314 COSM4091241 c.1037A>C p.K346T Substitution - Missense 11:104037859-104037859 + BCM759T COSM4017393 c.1089G>T p.E363D Substitution - Missense 11:104037911-104037911 + TCGA-A5-A0GP-01 COSM922401 c.103G>A p.E35K Substitution - Missense 11:104036925-104036925 + TCGA-EE-A2MS-06 COSM3442835 c.761C>T p.P254L Substitution - Missense 11:104037583-104037583 + TCGA-BR-8078-01 COSM4017389 c.1007G>A p.R336Q Substitution - Missense 11:104037829-104037829 + CSCC-55-T COSM4165620 c.26G>A p.R9Q Substitution - Missense 11:104036848-104036848 + TCGA-G4-6306-01 COSM1350476 c.36C>T p.L12L Substitution - coding silent 11:104036858-104036858 + TCGA-AZ-6598-01 COSM1350487 c.332A>T p.H111L Substitution - Missense 11:104037154-104037154 + TCGA-FS-A1ZK-06 COSM3442819 c.247C>T p.R83W Substitution - Missense 11:104037069-104037069 + PT48 COSM4017388 c.1007G>A p.R336Q Substitution - Missense 11:104037829-104037829 + TCGA-BR-4362-01 COSM4017392 c.1089G>T p.E363D Substitution - Missense 11:104037911-104037911 + TCGA-BP-4164-01 COSM1135087 c.1006C>T p.R336W Substitution - Missense 11:104037828-104037828 + TCGA-BR-8284-01 COSM4017379 c.664A>T p.N222Y Substitution - Missense 11:104037486-104037486 + TCGA-FW-A3R5-06 COSM348323 c.429C>T p.P143P Substitution - coding silent 11:104037251-104037251 + TCGA-P5-A5EV-01 COSM4420488 c.619G>C p.D207H Substitution - Missense 11:104037441-104037441 + TCGA-28-2513-01 COSM3397369 c.592C>G p.L198V Substitution - Missense 11:104037414-104037414 + TCGA-ER-A194-01 COSM3442832 c.760C>T p.P254S Substitution - Missense 11:104037582-104037582 + TCGA-E2-A1LB-01 COSM1474953 c.6G>A p.L2L Substitution - coding silent 11:104036828-104036828 + 3N09-VS-3T09 COSM4979161 c.465C>T p.H155H Substitution - coding silent 11:104037287-104037287 + TCGA-60-2726-01 COSM685743 c.116G>A p.R39K Substitution - Missense 11:104036938-104036938 + B86-Tumor COSM1746011 c.529G>C p.E177Q Substitution - Missense 11:104037351-104037351 + 381_T COSM3979029 c.266C>A p.P89Q Substitution - Missense 11:104037088-104037088 + TCGA-F5-6814-01 COSM3415447 c.1083T>C p.L361L Substitution - coding silent 11:104037905-104037905 + TCGA-CA-6717-01 COSM1350497 c.1178G>A p.R393Q Substitution - Missense 11:104038000-104038000 + T3058 COSM4676681 c.207C>T p.G69G Substitution - coding silent 11:104037029-104037029 + TCGA-EI-6917-01 COSM3415445 c.729G>A p.M243I Substitution - Missense 11:104037551-104037551 + TCGA-CD-8535-01 COSM4017381 c.672A>G p.E224E Substitution - coding silent 11:104037494-104037494 + TCGA-A5-A0GA-01 COSM922419 c.1068G>A p.T356T Substitution - coding silent 11:104037890-104037890 + pfg181T COSM4759663 c.428C>A p.P143H Substitution - Missense 11:104037250-104037250 + ccRCC-84 COSM1661405 c.897T>G p.I299M Substitution - Missense 11:104037719-104037719 + 6115219 COSM5558748 c.516C>A p.L172L Substitution - coding silent 11:104037338-104037338 + CSCC-6-T COSM231265 c.649G>A p.E217K Substitution - Missense 11:104037471-104037471 + TCGA-CD-8536-01 COSM4017376 c.443G>A p.S148N Substitution - Missense 11:104037265-104037265 + TCGA-B0-5121-01 COSM466239 c.974C>T p.P325L Substitution - Missense 11:104037796-104037796 + T2269 COSM4676679 c.127G>A p.E43K Substitution - Missense 11:104036949-104036949 + ATL055 COSM428308 c.487C>T p.R163C Substitution - Missense 11:104037309-104037309 + 990515 COSM1582069 c.1120A>C p.S374R Substitution - Missense 11:104037942-104037942 + T3062 COSM4017374 c.361G>A p.A121T Substitution - Missense 11:104037183-104037183 + TCGA-74-6584-01 COSM922418 c.1068G>A p.T356T Substitution - coding silent 11:104037890-104037890 + TCGA-D7-A4Z0-01 COSM4017399 c.1145A>C p.K382T Substitution - Missense 11:104037967-104037967 + TCGA-A5-A0VP-01 COSM922408 c.430G>A p.A144T Substitution - Missense 11:104037252-104037252 + 66 COSM5743507 c.311C>T p.T104M Substitution - Missense 11:104037133-104037133 + TCGA-06-0192 COSM2150640 c.506A>C p.E169A Substitution - Missense 11:104037328-104037328 + CSCC-35-T COSM4456894 c.1026C>T p.I342I Substitution - coding silent 11:104037848-104037848 + YUDIVI COSM2108964 c.466G>A p.D156N Substitution - Missense 11:104037288-104037288 + 347 COSM99209 c.922C>G p.Q308E Substitution - Missense 11:104037744-104037744 + TCGA-28-2513-01 COSM3397368 c.592C>G p.L198V Substitution - Missense 11:104037414-104037414 + TCGA-CD-5800-01 COSM4017362 c.67C>A p.P23T Substitution - Missense 11:104036889-104036889 + TCGA-BR-6452-01 COSM4017371 c.243A>T p.G81G Substitution - coding silent 11:104037065-104037065 + CSCC-55-T COSM4165619 c.26G>A p.R9Q Substitution - Missense 11:104036848-104036848 + PCSI_0083_Pa_X COSM3375618 c.901C>T p.R301C Substitution - Missense 11:104037723-104037723 + CSCC-62-T COSM4522007 c.1140G>T p.S380S Substitution - coding silent 11:104037962-104037962 + T2269 COSM4676683 c.208G>A p.D70N Substitution - Missense 11:104037030-104037030 + TCGA-BR-8591-01 COSM4017396 c.1131T>C p.D377D Substitution - coding silent 11:104037953-104037953 + TCGA-G2-A2EJ-01 COSM1297579 c.956C>G p.S319C Substitution - Missense 11:104037778-104037778 + TCGA-ER-A194-01 COSM3442833 c.760C>T p.P254S Substitution - Missense 11:104037582-104037582 + CHC121T COSM216935 c.808C>A p.Q270K Substitution - Missense 11:104037630-104037630 + YUWAND COSM1704504 c.241G>A p.G81R Substitution - Missense 11:104037063-104037063 + TCGA-FS-A1ZK-06 COSM3442818 c.247C>T p.R83W Substitution - Missense 11:104037069-104037069 + 8035823 COSM3769170 c.611A>T p.D204V Substitution - Missense 11:104037433-104037433 + TCGA-D1-A17Q-01 COSM922404 c.224T>C p.L75P Substitution - Missense 11:104037046-104037046 + TCGA-EE-A20C-06 COSM3442823 c.460C>T p.P154S Substitution - Missense 11:104037282-104037282 + 5 COSM922420 c.1177C>T p.R393* Substitution - Nonsense 11:104037999-104037999 + TCGA-ER-A19K-01 COSM3442842 c.983T>G p.M328R Substitution - Missense 11:104037805-104037805 + T2269 COSM4676682 c.208G>A p.D70N Substitution - Missense 11:104037030-104037030 + TCGA-BR-4369-01 COSM4017367 c.124G>T p.V42F Substitution - Missense 11:104036946-104036946 + TCGA-E7-A3Y1-01 COSM3791117 c.970C>A p.Q324K Substitution - Missense 11:104037792-104037792 + TCGA-33-4566-01 COSM685731 c.1123G>A p.G375R Substitution - Missense 11:104037945-104037945 + RK021_C01 COSM428308 c.487C>T p.R163C Substitution - Missense 11:104037309-104037309 + MD-340 COSM302032 c.783G>A p.S261S Substitution - coding silent 11:104037605-104037605 + NCHP_DIPG105 COSM4746070 c.457A>G p.N153D Substitution - Missense 11:104037279-104037279 + TCGA-DI-A0WH-01 COSM922421 c.1177C>T p.R393* Substitution - Nonsense 11:104037999-104037999 + TCGA-C4-A0F6-01 COSM415375 c.480C>G p.L160L Substitution - coding silent 11:104037302-104037302 + SC_9017 COSM2108959 c.440G>A p.R147H Substitution - Missense 11:104037262-104037262 + Au1 COSM5596572 c.900C>T p.G300G Substitution - coding silent 11:104037722-104037722 + C086 COSM231265 c.649G>A p.E217K Substitution - Missense 11:104037471-104037471 + HN_62432 COSM127786 c.1053C>A p.I351I Substitution - coding silent 11:104037875-104037875 + S02065 COSM5672535 c.427C>A p.P143T Substitution - Missense 11:104037249-104037249 + Gp2D COSM4626733 c.821A>G p.E274G Substitution - Missense 11:104037643-104037643 + TCGA-HC-8265-01 COSM3670647 c.323G>A p.R108H Substitution - Missense 11:104037145-104037145 + TCGA-AA-A010-01 COSM280327 c.166G>A p.E56K Substitution - Missense 11:104036988-104036988 + TCGA-D9-A6EC-06 COSM4401953 c.135C>T p.I45I Substitution - coding silent 11:104036957-104036957 + 7313 COSM5613292 c.253C>A p.P85T Substitution - Missense 11:104037075-104037075 + 6115122 COSM1350490 c.488G>A p.R163H Substitution - Missense 11:104037310-104037310 + STC252 COSM3442820 c.337G>A p.G113R Substitution - Missense 11:104037159-104037159 + SNU-C4 COSM922409 c.430G>A p.A144T Substitution - Missense 11:104037252-104037252 + LUAD-YINHD COSM348323 c.429C>T p.P143P Substitution - coding silent 11:104037251-104037251 + TCGA-AP-A0LM-01 COSM200186 c.596G>A p.R199H Substitution - Missense 11:104037418-104037418 + CHC121T COSM216935 c.808C>A p.Q270K Substitution - Missense 11:104037630-104037630 + HCC2998 COSM1676397 c.202G>T p.D68Y Substitution - Missense 11:104037024-104037024 + TCGA-BR-8078-01 COSM4017388 c.1007G>A p.R336Q Substitution - Missense 11:104037829-104037829 + TCGA-AG-A002-01 COSM260373 c.1129G>A p.D377N Substitution - Missense 11:104037951-104037951 + T94 COSM237282 c.387G>A p.A129A Substitution - coding silent 11:104037209-104037209 + T94 COSM237281 c.387G>A p.A129A Substitution - coding silent 11:104037209-104037209 + PCSI_0087_Pa_X COSM3375620 c.1062T>A p.T354T Substitution - coding silent 11:104037884-104037884 + TCGA-B0-5812-01 COSM466236 c.53C>G p.S18C Substitution - Missense 11:104036875-104036875 + T231 COSM4676694 c.786C>T p.G262G Substitution - coding silent 11:104037608-104037608 + 2318491 COSM4776901 c.1183G>C p.E395Q Substitution - Missense 11:104038005-104038005 + pfg181T COSM4759662 c.428C>A p.P143H Substitution - Missense 11:104037250-104037250 + MD-340 COSM302033 c.783G>A p.S261S Substitution - coding silent 11:104037605-104037605 + PCSI_0329_Pa_P_526 COSM3687066 c.854G>A p.R285Q Substitution - Missense 11:104037676-104037676 + ESCC_BICR_023T COSM5436289 c.988C>G p.L330V Substitution - Missense 11:104037810-104037810 + TCGA-G4-6628-01 COSM1350490 c.488G>A p.R163H Substitution - Missense 11:104037310-104037310 + SC_9109 COSM2108928 c.22G>A p.V8M Substitution - Missense 11:104036844-104036844 + YUBER COSM1704501 c.193G>A p.G65S Substitution - Missense 11:104037015-104037015 + HCC137 COSM1603968 c.10A>G p.T4A Substitution - Missense 11:104036832-104036832 + YUWAND COSM1704503 c.241G>A p.G81R Substitution - Missense 11:104037063-104037063 + Gp2D COSM4626732 c.821A>G p.E274G Substitution - Missense 11:104037643-104037643 + PCSI_0083_Pa_P COSM3375618 c.901C>T p.R301C Substitution - Missense 11:104037723-104037723 + TCGA-CG-4305-01 COSM4017360 c.57C>G p.L19L Substitution - coding silent 11:104036879-104036879 + 6115122 COSM1350491 c.488G>A p.R163H Substitution - Missense 11:104037310-104037310 + TCGA-BR-4369-01 COSM4017366 c.124G>T p.V42F Substitution - Missense 11:104036946-104036946 + 587332 COSM1203195 c.878T>C p.V293A Substitution - Missense 11:104037700-104037700 + cSCCP1 COSM136031 c.978G>A p.M326I Substitution - Missense 11:104037800-104037800 + RK150_C01 COSM3738829 c.323G>T p.R108L Substitution - Missense 11:104037145-104037145 + TCGA-18-4083-01 COSM685740 c.477G>A p.L159L Substitution - coding silent 11:104037299-104037299 + HCC2998 COSM1676397 c.202G>T p.D68Y Substitution - Missense 11:104037024-104037024 + TCGA-EE-A3AA-06 COSM3442821 c.337G>A p.G113R Substitution - Missense 11:104037159-104037159 + CHC121T COSM216936 c.808C>A p.Q270K Substitution - Missense 11:104037630-104037630 + CSCC-27-T COSM4519894 c.1032G>A p.L344L Substitution - coding silent 11:104037854-104037854 + TCGA-EE-A3JH-06 COSM3442831 c.646G>A p.E216K Substitution - Missense 11:104037468-104037468 + CSCC-27-T COSM4519932 c.1035G>A p.K345K Substitution - coding silent 11:104037857-104037857 + 587376 COSM1203199 c.1027G>A p.D343N Substitution - Missense 11:104037849-104037849 + TCGA-HU-A4G3-01 COSM1284433 c.214G>A p.V72M Substitution - Missense 11:104037036-104037036 + TCGA-C8-A12T-01 COSM428309 c.487C>T p.R163C Substitution - Missense 11:104037309-104037309 + CHC2206T COSM4956926 c.885A>T p.T295T Substitution - coding silent 11:104037707-104037707 + S02277 COSM5683005 c.300G>A p.A100A Substitution - coding silent 11:104037122-104037122 + TCGA-D3-A3C7-06 COSM3442828 c.624G>A p.R208R Substitution - coding silent 11:104037446-104037446 + TCGA-AP-A0LF-01 COSM922417 c.939C>G p.F313L Substitution - Missense 11:104037761-104037761 + ESCC_BICR_020T COSM922400 c.103G>A p.E35K Substitution - Missense 11:104036925-104036925 + TCGA-EE-A2MS-06 COSM3442817 c.242G>A p.G81E Substitution - Missense 11:104037064-104037064 + S02299 COSM5690013 c.614C>A p.P205Q Substitution - Missense 11:104037436-104037436 + TCGA-GN-A263-01 COSM428308 c.487C>T p.R163C Substitution - Missense 11:104037309-104037309 + PCSI_0083_Pa_P_526 COSM3375619 c.901C>T p.R301C Substitution - Missense 11:104037723-104037723 + TCGA-43-2578-01 COSM685737 c.785G>T p.G262V Substitution - Missense 11:104037607-104037607 + TCGA-33-4566-01 COSM685732 c.1123G>A p.G375R Substitution - Missense 11:104037945-104037945 + TCGA-06-0192 COSM2150641 c.506A>C p.E169A Substitution - Missense 11:104037328-104037328 + ESO-122 COSM1249859 c.838A>T p.R280W Substitution - Missense 11:104037660-104037660 + Mx38 COSM51162 c.267G>A p.P89P Substitution - coding silent 11:104037089-104037089 + ESO-122 COSM1249858 c.88T>C p.F30L Substitution - Missense 11:104036910-104036910 + KYSE-150 COSM2108951 c.278G>A p.R93H Substitution - Missense 11:104037100-104037100 + SS6003314 COSM4091239 c.663A>C p.Q221H Substitution - Missense 11:104037485-104037485 + 347 COSM98360 c.922C>G p.Q308E Substitution - Missense 11:104037744-104037744 + HCC142T COSM1603972 c.132G>T p.E44D Substitution - Missense 11:104036954-104036954 + 18 COSM922411 c.503C>T p.A168V Substitution - Missense 11:104037325-104037325 + TCGA-D9-A6EC-06 COSM4401952 c.135C>T p.I45I Substitution - coding silent 11:104036957-104036957 + TCGA-AP-A0LM-01 COSM200185 c.596G>A p.R199H Substitution - Missense 11:104037418-104037418 + TCGA-EE-A181-06 COSM2108976 c.565G>A p.E189K Substitution - Missense 11:104037387-104037387 + CHEWS031 COSM4519932 c.1035G>A p.K345K Substitution - coding silent 11:104037857-104037857 + T3062 COSM4017375 c.361G>A p.A121T Substitution - Missense 11:104037183-104037183 + TCGA-ER-A19K-01 COSM3442839 c.955T>C p.S319P Substitution - Missense 11:104037777-104037777 + ESO-0459 COSM1249856 c.724A>G p.T242A Substitution - Missense 11:104037546-104037546 + RK150_C01 COSM3738830 c.323G>T p.R108L Substitution - Missense 11:104037145-104037145 + 7313 COSM5613291 c.253C>A p.P85T Substitution - Missense 11:104037075-104037075 + TCGA-22-5491-01 COSM685735 c.845T>G p.V282G Substitution - Missense 11:104037667-104037667 + TCGA-AP-A059-01 COSM922413 c.888G>T p.Q296H Substitution - Missense 11:104037710-104037710 + TCGA-EE-A3AA-06 COSM3442820 c.337G>A p.G113R Substitution - Missense 11:104037159-104037159 + 347 COSM99209 c.922C>G p.Q308E Substitution - Missense 11:104037744-104037744 + 2492702 COSM3808203 c.371G>A p.R124Q Substitution - Missense 11:104037193-104037193 + CSCC-52-T COSM4542521 c.31G>A p.D11N Substitution - Missense 11:104036853-104036853 + C0037T COSM4165620 c.26G>A p.R9Q Substitution - Missense 11:104036848-104036848 + Pat_04_A COSM4895438 c.1147G>A p.E383K Substitution - Missense 11:104037969-104037969 + 7996 COSM5613293 c.741C>G p.N247K Substitution - Missense 11:104037563-104037563 + C086 COSM231264 c.649G>A p.E217K Substitution - Missense 11:104037471-104037471 + TCGA-CD-A4MG-01 COSM922419 c.1068G>A p.T356T Substitution - coding silent 11:104037890-104037890 + 18 COSM922410 c.503C>T p.A168V Substitution - Missense 11:104037325-104037325 + SC_9017 COSM2108960 c.440G>A p.R147H Substitution - Missense 11:104037262-104037262 + TCGA-BR-4361-01 COSM922408 c.430G>A p.A144T Substitution - Missense 11:104037252-104037252 + T3187 COSM1249861 c.88T>G p.F30V Substitution - Missense 11:104036910-104036910 + TCGA-EE-A3J4-06 COSM3868316 c.622C>T p.R208W Substitution - Missense 11:104037444-104037444 + YURAY COSM4676678 c.127G>A p.E43K Substitution - Missense 11:104036949-104036949 + TCGA-37-4135-01 COSM685741 c.255A>G p.P85P Substitution - coding silent 11:104037077-104037077 + TCGA-D1-A17Q-01 COSM922405 c.224T>C p.L75P Substitution - Missense 11:104037046-104037046 + TCGA-E2-A1LB-01 COSM1474954 c.6G>A p.L2L Substitution - coding silent 11:104036828-104036828 + TCGA-EE-A2MS-06 COSM3442816 c.242G>A p.G81E Substitution - Missense 11:104037064-104037064 + CHC1854T COSM3666839 c.705C>T p.P235P Substitution - coding silent 11:104037527-104037527 + SC_9008 COSM3687063 c.231G>T p.K77N Substitution - Missense 11:104037053-104037053 + HCC82 COSM1603974 c.706G>T p.E236* Substitution - Nonsense 11:104037528-104037528 + 2492703 COSM3808203 c.371G>A p.R124Q Substitution - Missense 11:104037193-104037193 + TCGA-C4-A0F6-01 COSM415376 c.480C>G p.L160L Substitution - coding silent 11:104037302-104037302 + STC246 COSM5050475 c.59A>G p.Q20R Substitution - Missense 11:104036881-104036881 + 226 COSM3730192 c.820G>A p.E274K Substitution - Missense 11:104037642-104037642 + CHC121T COSM216936 c.808C>A p.Q270K Substitution - Missense 11:104037630-104037630 + TCGA-EE-A3J4-06 COSM3868315 c.622C>T p.R208W Substitution - Missense 11:104037444-104037444 + TCGA-43-2578-01 COSM685738 c.785G>T p.G262V Substitution - Missense 11:104037607-104037607 + TCGA-CC-A7IK-01 COSM4925038 c.590G>T p.R197M Substitution - Missense 11:104037412-104037412 + LAU50_2 COSM232142 c.244C>A p.P82T Substitution - Missense 11:104037066-104037066 + TCGA-EB-A4IS-01 COSM3442836 c.804G>A p.M268I Substitution - Missense 11:104037626-104037626 + TCGA-AZ-4615-01 COSM3687065 c.854G>A p.R285Q Substitution - Missense 11:104037676-104037676 + PT35 COSM3868315 c.622C>T p.R208W Substitution - Missense 11:104037444-104037444 + TCGA-HU-A4G9-01 COSM4017390 c.1053C>T p.I351I Substitution - coding silent 11:104037875-104037875 + CSCC-27-T COSM4559178 c.795G>A p.M265I Substitution - Missense 11:104037617-104037617 + PT23_2 COSM5903780 c.320C>G p.S107C Substitution - Missense 11:104037142-104037142 + HCC82 COSM1603975 c.706G>T p.E236* Substitution - Nonsense 11:104037528-104037528 + HCC2998 COSM2108961 c.456C>A p.S152S Substitution - coding silent 11:104037278-104037278 + TCGA-EE-A181-06 COSM3442844 c.1091G>A p.G364E Substitution - Missense 11:104037913-104037913 + NCHP_DIPG105 COSM4746071 c.457A>G p.N153D Substitution - Missense 11:104037279-104037279 + TCGA-EE-A20C-06 COSM3442822 c.460C>T p.P154S Substitution - Missense 11:104037282-104037282 + TCGA-CD-8536-01 COSM1350478 c.124G>A p.V42I Substitution - Missense 11:104036946-104036946 + T3535 COSM4676688 c.543G>T p.Q181H Substitution - Missense 11:104037365-104037365 + TCGA-BR-4361-01 COSM922409 c.430G>A p.A144T Substitution - Missense 11:104037252-104037252 + CSCC-62-T COSM4487632 c.320C>T p.S107F Substitution - Missense 11:104037142-104037142 + TCGA-AN-A046-01 COSM3808204 c.710G>T p.S237I Substitution - Missense 11:104037532-104037532 + HX13T COSM1603971 c.102C>T p.C34C Substitution - coding silent 11:104036924-104036924 + SC_9023 COSM5555061 c.754G>A p.G252R Substitution - Missense 11:104037576-104037576 + LS174T COSM4645754 c.212T>C p.I71T Substitution - Missense 11:104037034-104037034 + ESCC_32 COSM348324 c.429C>T p.P143P Substitution - coding silent 11:104037251-104037251 + 2492700 COSM3808203 c.371G>A p.R124Q Substitution - Missense 11:104037193-104037193 + Gp2D COSM4626731 c.317G>T p.S106I Substitution - Missense 11:104037139-104037139 + CSCC-35-T COSM4456893 c.1026C>T p.I342I Substitution - coding silent 11:104037848-104037848 + S01861 COSM5670966 c.314delC p.S106fs*40 Deletion - Frameshift 11:104037136-104037136 + TCGA-BP-4164-01 COSM1135086 c.1006C>T p.R336W Substitution - Missense 11:104037828-104037828 + OSCC-GB_00530111 COSM4676695 c.786C>T p.G262G Substitution - coding silent 11:104037608-104037608 + CSCC-27-T COSM4519933 c.1035G>A p.K345K Substitution - coding silent 11:104037857-104037857 + SS6003314 COSM4091240 c.663A>C p.Q221H Substitution - Missense 11:104037485-104037485 + TCGA-HC-8265-01 COSM3670646 c.323G>A p.R108H Substitution - Missense 11:104037145-104037145 + TCGA-DA-A1HW-06 COSM3442812 c.141C>T p.I47I Substitution - coding silent 11:104036963-104036963 + PTC-7C COSM4145191 c.406G>A p.G136S Substitution - Missense 11:104037228-104037228 + T2272 COSM4676693 c.661C>A p.Q221K Substitution - Missense 11:104037483-104037483 + Hx206 COSM51163 c.21C>T p.C7C Substitution - coding silent 11:104036843-104036843 + TCGA-CG-5721-01 COSM4017373 c.291T>C p.S97S Substitution - coding silent 11:104037113-104037113 + STC252 COSM3442821 c.337G>A p.G113R Substitution - Missense 11:104037159-104037159 + LUAD-NYU160 COSM370410 c.958A>G p.I320V Substitution - Missense 11:104037780-104037780 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.591937;Hs.591941 11q22.3

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.E169A c.506A>C 11 103908056 GBM A C Missense p.E169D c.507A>C 11 103908057 LUAD A C Missense p.N277T c.830A>C 11 103908380 STAD A C Missense p.Q376H c.1128A>C 11 103908678 STAD A G Missense p.E185G c.554A>G 11 103908104 LUAD A G Missense p.T242A c.724A>G 11 103908274 ESCA A T Missense p.Q376H c.1128A>T 11 103908678 ESCA A T Missense p.R280W c.838A>T 11 103908388 ESCA C A Missense p.A263D c.788C>A 11 103908338 LUAD C A Missense p.L332I c.994C>A 11 103908544 LUAD C A Missense p.P23T c.67C>A 11 103907617 STAD C A Missense p.P85T c.253C>A 11 103907803 NSCLC C A Missense p.Q240K c.718C>A 11 103908268 HNSC C A Missense p.Q270K c.808C>A 11 103908358 HC C A Missense p.R301S c.901C>A 11 103908451 STAD CC TT Missense p.P89L c.265_266delinsTT 11 103907815 CM C G Missense p.F313L c.939C>G 11 103908489 UCEC C G Missense p.L198V c.592C>G 11 103908142 GBM C G Missense p.N247K c.741C>G 11 103908291 NSCLC C G Missense p.S319C c.956C>G 11 103908506 BLCA C T Missense p.P154S c.460C>T 11 103908010 CM C T Missense p.P254L c.761C>T 11 103908311 CM C T Missense p.P254S c.760C>T 11 103908310 CM C T Missense p.P362S c.1084C>T 11 103908634 CM C T Missense p.R163C c.487C>T 11 103908037 BRCA C T Missense p.R163C c.487C>T 11 103908037 CM C T Missense p.R163C c.487C>T 11 103908037 HC C T Missense p.R208W c.622C>T 11 103908172 CM C T Missense p.R219W c.655C>T 11 103908205 CM C T Missense p.R336W c.1006C>T 11 103908556 RCCC C T Missense p.R83W c.247C>T 11 103907797 CM C T Missense p.S13F c.38C>T 11 103907588 CM C T Missense p.S261L c.782C>T 11 103908332 BRCA C T Nonsense p.R393* c.1177C>T 11 103908727 UCEC G A Missense p.A121T c.361G>A 11 103907911 STAD G A Missense p.A144T c.430G>A 11 103907980 UCEC G A Missense p.E162K c.484G>A 11 103908034 CM G A Missense p.E189K c.565G>A 11 103908115 CM G A Missense p.E216K c.646G>A 11 103908196 CM G A Missense p.E217K c.649G>A 11 103908199 CM G A Missense p.E310K c.928G>A 11 103908478 CM G A Missense p.E35K c.103G>A 11 103907653 UCEC G A Missense p.G113R c.337G>A 11 103907887 CM G A Missense p.G292E c.875G>A 11 103908425 HNSC G A Missense p.G364E c.1091G>A 11 103908641 CM G A Missense p.G81E c.242G>A 11 103907792 CM G A Missense p.R108H c.323G>A 11 103907873 PRAD G A Missense p.R199H c.596G>A 11 103908146 COREAD G A Missense p.R39K c.116G>A 11 103907666 LUSC G A Missense p.V72M c.214G>A 11 103907764 NB G T Missense p.E378D c.1134G>T 11 103908684 LUAD G T Missense p.G262V c.785G>T 11 103908335 LUSC G T Missense p.R163L c.488G>T 11 103908038 LUAD G T Missense p.V42F c.124G>T 11 103907674 STAD T C Missense p.F30L c.88T>C 11 103907638 ESCA T C Missense p.L335P c.1004T>C 11 103908554 RCCC T C Missense p.S319P c.955T>C 11 103908505 CM T G Missense p.F30V c.88T>G 11 103907638 ESCA T G Missense p.I384S c.1151T>G 11 103908701 ESCA T G Missense p.M328R c.983T>G 11 103908533 CM T G Missense p.V282G c.845T>G 11 103908395 LUSC