Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 11 77920580 77920580 + Missense_Mutation SNP C C A TCGA-OR-A5JA-01A-11D-A29I-10 TCGA-OR-A5JA-10A-01D-A29L-10 g.chr11:77920580C>A c.1679C>A c.(1678-1680)gCc>gAc p.A560D ACC 11 77920714 77920714 + Missense_Mutation SNP C C T TCGA-OR-A5LA-01A-11D-A29I-10 TCGA-OR-A5LA-10A-01D-A29L-10 g.chr11:77920714C>T c.1813C>T c.(1813-1815)Cgc>Tgc p.R605C BLCA 11 77907438 77907438 + Silent SNP C C T TCGA-DK-A1A6-01A-11D-A13W-08 TCGA-DK-A1A6-10A-01D-A13W-08 g.chr11:77907438C>T c.147C>T c.(145-147)taC>taT p.Y49Y BLCA 11 77909064 77909064 + Silent SNP C C T TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr11:77909064C>T c.756C>T c.(754-756)ctC>ctT p.L252L BLCA 11 77911274 77911274 + Missense_Mutation SNP C C A TCGA-4Z-AA7Q-01A-11D-A391-08 TCGA-4Z-AA7Q-10A-01D-A394-08 g.chr11:77911274C>A c.1032C>A c.(1030-1032)ttC>ttA p.F344L BLCA 11 77911809 77911809 + Silent SNP C C T TCGA-FD-A3B3-01A-12D-A202-08 TCGA-FD-A3B3-10A-01D-A202-08 g.chr11:77911809C>T c.1152C>T c.(1150-1152)ttC>ttT p.F384F BLCA 11 77911851 77911851 + Missense_Mutation SNP C C G TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr11:77911851C>G c.1194C>G c.(1192-1194)atC>atG p.I398M BLCA 11 77916913 77916913 + Missense_Mutation SNP G G A TCGA-DK-AA76-01A-11D-A391-08 TCGA-DK-AA76-10A-01D-A394-08 g.chr11:77916913G>A c.1223G>A c.(1222-1224)cGc>cAc p.R408H BLCA 11 77917004 77917004 + Silent SNP G G A TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr11:77917004G>A c.1314G>A c.(1312-1314)acG>acA p.T438T BLCA 11 77918604 77918604 + Missense_Mutation SNP G G A TCGA-KQ-A41S-01A-12D-A339-08 TCGA-KQ-A41S-10C-01D-A339-08 g.chr11:77918604G>A c.1420G>A c.(1420-1422)Gag>Aag p.E474K BLCA 11 77919932 77919932 + Silent SNP C C G TCGA-DK-A2I1-01A-11D-A17V-08 TCGA-DK-A2I1-10A-01D-A17V-08 g.chr11:77919932C>G c.1515C>G c.(1513-1515)ctC>ctG p.L505L BLCA 11 77921045 77921045 + Missense_Mutation SNP A A G TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr11:77921045A>G c.2144A>G c.(2143-2145)gAa>gGa p.E715G BLCA 11 77921098 77921098 + Missense_Mutation SNP G G A TCGA-G2-A2EF-01A-12D-A18F-08 TCGA-G2-A2EF-10A-01D-A18F-08 g.chr11:77921098G>A c.2197G>A c.(2197-2199)Gaa>Aaa p.E733K BLCA 11 77921319 77921319 + Silent SNP C C T TCGA-G2-A2EL-01A-12D-A18F-08 TCGA-G2-A2EL-10A-01D-A18F-08 g.chr11:77921319C>T c.2418C>T c.(2416-2418)ctC>ctT p.L806L BLCA 11 77921514 77921514 + Silent SNP T T A TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr11:77921514T>A c.2613T>A c.(2611-2613)gcT>gcA p.A871A BLCA 11 77924751 77924751 + Silent SNP G G T TCGA-BT-A0S7-01A-11D-A10S-08 TCGA-BT-A0S7-10A-01D-A10S-08 g.chr11:77924751G>T c.2949G>T c.(2947-2949)ccG>ccT p.P983P BLCA 11 77924770 77924770 + Missense_Mutation SNP G G A TCGA-2F-A9KO-01A-11D-A38G-08 TCGA-2F-A9KO-11A-12D-A38J-08 g.chr11:77924770G>A c.2968G>A c.(2968-2970)Gat>Aat p.D990N BLCA 11 77924859 77924859 + Silent SNP A A G TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr11:77924859A>G c.3057A>G c.(3055-3057)taA>taG p.*1019* BRCA 11 77921402 77921402 + Missense_Mutation SNP G G A TCGA-E9-A2JS-01A-11D-A17W-09 TCGA-E9-A2JS-10A-01D-A17W-09 g.chr11:77921402G>A c.2501G>A c.(2500-2502)cGc>cAc p.R834H CESC 11 77911809 77911809 + Silent SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr11:77911809C>T c.1152C>T c.(1150-1152)ttC>ttT p.F384F CESC 11 77917022 77917022 + Missense_Mutation SNP C C G TCGA-C5-A2LZ-01A-11D-A20U-09 TCGA-C5-A2LZ-10B-01D-A20U-09 g.chr11:77917022C>G c.1332C>G c.(1330-1332)atC>atG p.I444M CESC 11 77921400 77921400 + Silent SNP C C A TCGA-Q1-A5R2-01A-11D-A28B-09 TCGA-Q1-A5R2-10A-01D-A28E-09 g.chr11:77921400C>A c.2499C>A c.(2497-2499)ctC>ctA p.L833L CESC 11 77924696 77924698 + In_Frame_Del DEL AGG AGG - TCGA-EK-A2R8-01A-21D-A18J-09 TCGA-EK-A2R8-10A-01D-A18J-09 g.chr11:77924696_77924698delAGG c.2894_2896delAGG c.(2893-2898)caggag>cag p.E966del CHOL 11 77921399 77921399 + Missense_Mutation SNP T T C TCGA-W5-AA2T-01A-12D-A417-09 TCGA-W5-AA2T-10A-01D-A41A-09 g.chr11:77921399T>C c.2498T>C c.(2497-2499)cTc>cCc p.L833P COAD 11 77909004 77909004 + Silent SNP C C A TCGA-AA-3819-01A-01W-0900-09 TCGA-AA-3819-10A-01W-0900-09 g.chr11:77909004C>A c.696C>A c.(694-696)gcC>gcA p.A232A COAD 11 77911215 77911215 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:77911215G>A c.973G>A c.(973-975)Gct>Act p.A325T COAD 11 77911266 77911266 + Missense_Mutation SNP G G A TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr11:77911266G>A c.1024G>A c.(1024-1026)Gaa>Aaa p.E342K COAD 11 77911710 77911710 + Frame_Shift_Del DEL C C - TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr11:77911710delC c.1053delC c.(1051-1053)atcfs p.I351fs COAD 11 77916968 77916968 + Silent SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:77916968G>A c.1278G>A c.(1276-1278)gcG>gcA p.A426A COAD 11 77917029 77917029 + Missense_Mutation SNP G G T TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr11:77917029G>T c.1339G>T c.(1339-1341)Ggc>Tgc p.G447C COAD 11 77917031 77917031 + Silent SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:77917031C>T c.1341C>T c.(1339-1341)ggC>ggT p.G447G COAD 11 77918660 77918660 + Silent SNP A A G TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr11:77918660A>G c.1476A>G c.(1474-1476)gaA>gaG p.E492E COAD 11 77919923 77919923 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:77919923G>T c.1506G>T c.(1504-1506)gaG>gaT p.E502D COAD 11 77920714 77920714 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:77920714C>T c.1813C>T c.(1813-1815)Cgc>Tgc p.R605C COAD 11 77920730 77920730 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:77920730G>A c.1829G>A c.(1828-1830)cGc>cAc p.R610H COAD 11 77920768 77920768 + Missense_Mutation SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr11:77920768G>A c.1867G>A c.(1867-1869)Gcc>Acc p.A623T COAD 11 77921275 77921275 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:77921275G>A c.2374G>A c.(2374-2376)Gag>Aag p.E792K COAD 11 77921590 77921590 + Missense_Mutation SNP C C T TCGA-F4-6569-01A-11D-1771-10 TCGA-F4-6569-10A-01D-1771-10 g.chr11:77921590C>T c.2689C>T c.(2689-2691)Cgg>Tgg p.R897W COAD 11 77924839 77924839 + Missense_Mutation SNP T T G TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr11:77924839T>G c.3037T>G c.(3037-3039)Ttc>Gtc p.F1013V COADREAD 11 77909004 77909004 + Silent SNP C C A TCGA-AA-3819-01A-01W-0900-09 TCGA-AA-3819-10A-01W-0900-09 g.chr11:77909004C>A c.696C>A c.(694-696)gcC>gcA p.A232A COADREAD 11 77911215 77911215 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:77911215G>A c.973G>A c.(973-975)Gct>Act p.A325T COADREAD 11 77911266 77911266 + Missense_Mutation SNP G G A TCGA-CM-4746-01A-01D-1408-10 TCGA-CM-4746-10A-01D-1408-10 g.chr11:77911266G>A c.1024G>A c.(1024-1026)Gaa>Aaa p.E342K COADREAD 11 77911710 77911710 + Frame_Shift_Del DEL C C - TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr11:77911710delC c.1053delC c.(1051-1053)atcfs p.I351fs COADREAD 11 77911746 77911746 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:77911746G>A c.1089G>A c.(1087-1089)tcG>tcA p.S363S COADREAD 11 77916968 77916968 + Silent SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:77916968G>A c.1278G>A c.(1276-1278)gcG>gcA p.A426A COADREAD 11 77917029 77917029 + Missense_Mutation SNP G G T TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr11:77917029G>T c.1339G>T c.(1339-1341)Ggc>Tgc p.G447C COADREAD 11 77917031 77917031 + Silent SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:77917031C>T c.1341C>T c.(1339-1341)ggC>ggT p.G447G COADREAD 11 77918660 77918660 + Silent SNP A A G TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr11:77918660A>G c.1476A>G c.(1474-1476)gaA>gaG p.E492E COADREAD 11 77919923 77919923 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:77919923G>T c.1506G>T c.(1504-1506)gaG>gaT p.E502D COADREAD 11 77920714 77920714 + Missense_Mutation SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:77920714C>T c.1813C>T c.(1813-1815)Cgc>Tgc p.R605C COADREAD 11 77920730 77920730 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:77920730G>A c.1829G>A c.(1828-1830)cGc>cAc p.R610H COADREAD 11 77920768 77920768 + Missense_Mutation SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr11:77920768G>A c.1867G>A c.(1867-1869)Gcc>Acc p.A623T COADREAD 11 77921074 77921074 + Nonsense_Mutation SNP A A T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:77921074A>T c.2173A>T c.(2173-2175)Aag>Tag p.K725* COADREAD 11 77921275 77921275 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:77921275G>A c.2374G>A c.(2374-2376)Gag>Aag p.E792K COADREAD 11 77921590 77921590 + Missense_Mutation SNP C C T TCGA-F4-6569-01A-11D-1771-10 TCGA-F4-6569-10A-01D-1771-10 g.chr11:77921590C>T c.2689C>T c.(2689-2691)Cgg>Tgg p.R897W COADREAD 11 77924839 77924839 + Missense_Mutation SNP T T G TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr11:77924839T>G c.3037T>G c.(3037-3039)Ttc>Gtc p.F1013V DLBC 11 77911224 77911224 + Missense_Mutation SNP T T C TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr11:77911224T>C c.982T>C c.(982-984)Tct>Cct p.S328P DLBC 11 77911745 77911745 + Missense_Mutation SNP C C T TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr11:77911745C>T c.1088C>T c.(1087-1089)tCg>tTg p.S363L DLBC 11 77911745 77911745 + Missense_Mutation SNP C C T TCGA-GR-7351-01A-11D-2210-10 TCGA-GR-7351-10A-01D-2210-10 g.chr11:77911745C>T c.1088C>T c.(1087-1089)tCg>tTg p.S363L DLBC 11 77921013 77921013 + Silent SNP A A G TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr11:77921013A>G c.2112A>G c.(2110-2112)ggA>ggG p.G704G ESCA 11 77907300 77907300 + Silent SNP G G A TCGA-IG-A3Y9-01A-12D-A247-09 TCGA-IG-A3Y9-10A-01D-A247-09 g.chr11:77907300G>A c.9G>A c.(7-9)aaG>aaA p.K3K ESCA 11 77911710 77911710 + Frame_Shift_Del DEL C C - TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr11:77911710delC c.1053delC c.(1051-1053)atcfs p.I351fs ESCA 11 77920009 77920009 + Splice_Site SNP G G A TCGA-RE-A7BO-01A-11D-A33E-09 TCGA-RE-A7BO-10A-01D-A33H-09 g.chr11:77920009G>A c.1592G>A c.(1591-1593)cGg>cAg p.R531Q ESCA 11 77924691 77924691 + Splice_Site SNP G G T TCGA-Z6-AAPN-01A-11D-A403-09 TCGA-Z6-AAPN-10A-01D-A403-09 g.chr11:77924691G>T c.e11-1 ESCA 11 77924720 77924720 + Missense_Mutation SNP C C T TCGA-L5-A43I-01A-11D-A247-09 TCGA-L5-A43I-11A-11D-A247-09 g.chr11:77924720C>T c.2918C>T c.(2917-2919)gCg>gTg p.A973V GBM 11 77920718 77920718 + Missense_Mutation SNP G G A TCGA-28-5216-01A-01D-1486-08 TCGA-28-5216-10A-01D-1486-08 g.chr11:77920718G>A c.1817G>A c.(1816-1818)tGt>tAt p.C606Y GBM 11 77921629 77921629 + Missense_Mutation SNP A A C TCGA-76-4925-01A-01D-1486-08 TCGA-76-4925-10A-01D-1486-08 g.chr11:77921629A>C c.2728A>C c.(2728-2730)Acc>Ccc p.T910P GBMLGG 11 77907849 77907849 + Frame_Shift_Del DEL G G - TCGA-DB-A64W-01A-11D-A29Q-08 TCGA-DB-A64W-10A-01D-A29Q-08 g.chr11:77907849delG c.558delG c.(556-558)gtgfs p.V186fs GBMLGG 11 77916930 77916930 + Missense_Mutation SNP G G A TCGA-HT-7475-01A-11D-2024-08 TCGA-HT-7475-10A-01D-2024-08 g.chr11:77916930G>A c.1240G>A c.(1240-1242)Ggg>Agg p.G414R GBMLGG 11 77918633 77918633 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:77918633G>T c.1449G>T c.(1447-1449)aaG>aaT p.K483N GBMLGG 11 77919936 77919936 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:77919936G>A c.1519G>A c.(1519-1521)Gca>Aca p.A507T GBMLGG 11 77920718 77920718 + Missense_Mutation SNP G G A TCGA-28-5216-01A-01D-1486-08 TCGA-28-5216-10A-01D-1486-08 g.chr11:77920718G>A c.1817G>A c.(1816-1818)tGt>tAt p.C606Y GBMLGG 11 77921330 77921330 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:77921330G>A c.2429G>A c.(2428-2430)cGc>cAc p.R810H GBMLGG 11 77921496 77921496 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:77921496C>A c.2595C>A c.(2593-2595)tgC>tgA p.C865* GBMLGG 11 77921629 77921629 + Missense_Mutation SNP A A C TCGA-76-4925-01A-01D-1486-08 TCGA-76-4925-10A-01D-1486-08 g.chr11:77921629A>C c.2728A>C c.(2728-2730)Acc>Ccc p.T910P HNSC 11 77907430 77907430 + Missense_Mutation SNP C C T TCGA-UF-A7JS-01A-11D-A34J-08 TCGA-UF-A7JS-10A-01D-A34M-08 g.chr11:77907430C>T c.139C>T c.(139-141)Cgc>Tgc p.R47C HNSC 11 77909074 77909074 + Missense_Mutation SNP G G T TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chr11:77909074G>T c.766G>T c.(766-768)Gac>Tac p.D256Y HNSC 11 77911809 77911809 + Silent SNP C C T TCGA-DQ-5625-01A-01D-1870-08 TCGA-DQ-5625-10A-01D-1870-08 g.chr11:77911809C>T c.1152C>T c.(1150-1152)ttC>ttT p.F384F HNSC 11 77911847 77911847 + Missense_Mutation SNP C C T TCGA-DQ-5631-01A-01D-1870-08 TCGA-DQ-5631-10A-01D-1870-08 g.chr11:77911847C>T c.1190C>T c.(1189-1191)gCc>gTc p.A397V HNSC 11 77916981 77916981 + Missense_Mutation SNP C C T TCGA-CV-A6JO-01B-11D-A34J-08 TCGA-CV-A6JO-10A-01D-A34M-08 g.chr11:77916981C>T c.1291C>T c.(1291-1293)Cgg>Tgg p.R431W HNSC 11 77920009 77920009 + Splice_Site SNP G G T TCGA-CV-7254-01A-11D-2012-08 TCGA-CV-7254-10A-01D-2013-08 g.chr11:77920009G>T c.1592G>T c.(1591-1593)cGg>cTg p.R531L HNSC 11 77920693 77920693 + Missense_Mutation SNP C C G TCGA-CV-6961-01A-21D-1912-08 TCGA-CV-6961-10A-01D-1912-08 g.chr11:77920693C>G c.1792C>G c.(1792-1794)Ctc>Gtc p.L598V HNSC 11 77921098 77921098 + Missense_Mutation SNP G G A TCGA-CR-5250-01A-01D-1512-08 TCGA-CR-5250-10A-01D-1512-08 g.chr11:77921098G>A c.2197G>A c.(2197-2199)Gaa>Aaa p.E733K HNSC 11 77921127 77921127 + Silent SNP G G A TCGA-UF-A71D-01A-12D-A34J-08 TCGA-UF-A71D-10B-01D-A34M-08 g.chr11:77921127G>A c.2226G>A c.(2224-2226)ccG>ccA p.P742P HNSC 11 77921356 77921356 + Missense_Mutation SNP C C T TCGA-DQ-5631-01A-01D-1870-08 TCGA-DQ-5631-10A-01D-1870-08 g.chr11:77921356C>T c.2455C>T c.(2455-2457)Cgg>Tgg p.R819W HNSC 11 77921387 77921388 + Frame_Shift_Ins INS - - C TCGA-CN-5355-01A-01D-1434-08 TCGA-CN-5355-10A-01D-1434-08 g.chr11:77921387_77921388insC c.2486_2487insC c.(2485-2490)atccccfs p.IP829fs HNSC 11 77924730 77924730 + Silent SNP C C A TCGA-D6-6823-01A-11D-1912-08 TCGA-D6-6823-10A-01D-1912-08 g.chr11:77924730C>A c.2928C>A c.(2926-2928)atC>atA p.I976I HNSC 11 77924770 77924770 + Missense_Mutation SNP G G C TCGA-DQ-5624-01A-01D-1870-08 TCGA-DQ-5624-10A-01D-1870-08 g.chr11:77924770G>C c.2968G>C c.(2968-2970)Gat>Cat p.D990H KIPAN 11 77919916 77919916 + Missense_Mutation SNP C C A TCGA-CJ-4902-01A-01D-1429-08 TCGA-CJ-4902-11A-01D-1429-08 g.chr11:77919916C>A c.1499C>A c.(1498-1500)tCc>tAc p.S500Y KIPAN 11 77921086 77921086 + Nonsense_Mutation SNP C C T TCGA-B8-5550-01A-01D-1534-10 TCGA-B8-5550-10A-01D-1535-10 g.chr11:77921086C>T c.2185C>T c.(2185-2187)Cag>Tag p.Q729* KIPAN 11 77921303 77921303 + Missense_Mutation SNP C C T TCGA-DZ-6134-01A-11D-1961-08 TCGA-DZ-6134-10A-01D-1962-08 g.chr11:77921303C>T c.2402C>T c.(2401-2403)cCg>cTg p.P801L KIPAN 11 77921393 77921402 + Frame_Shift_Del DEL TGCTGCTCCG TGCTGCTCCG - TCGA-B8-4620-01A-01D-1553-08 TCGA-B8-4620-11A-01D-1553-08 g.chr11:77921393_77921402delTGCTGCTCCG c.2492_2501delTGCTGCTCCG c.(2491-2502)ctgctgctccgcfs p.LLLR831fs KIRC 11 77919916 77919916 + Missense_Mutation SNP C C A TCGA-CJ-4902-01A-01D-1429-08 TCGA-CJ-4902-11A-01D-1429-08 g.chr11:77919916C>A c.1499C>A c.(1498-1500)tCc>tAc p.S500Y KIRC 11 77921086 77921086 + Nonsense_Mutation SNP C C T TCGA-B8-5550-01A-01D-1534-10 TCGA-B8-5550-10A-01D-1535-10 g.chr11:77921086C>T c.2185C>T c.(2185-2187)Cag>Tag p.Q729* KIRC 11 77921393 77921402 + Frame_Shift_Del DEL TGCTGCTCCG TGCTGCTCCG - TCGA-B8-4620-01A-01D-1553-08 TCGA-B8-4620-11A-01D-1553-08 g.chr11:77921393_77921402delTGCTGCTCCG c.2492_2501delTGCTGCTCCG c.(2491-2502)ctgctgctccgcfs p.LLLR831fs KIRP 11 77921303 77921303 + Missense_Mutation SNP C C T TCGA-DZ-6134-01A-11D-1961-08 TCGA-DZ-6134-10A-01D-1962-08 g.chr11:77921303C>T c.2402C>T c.(2401-2403)cCg>cTg p.P801L LGG 11 77907849 77907849 + Frame_Shift_Del DEL G G - TCGA-DB-A64W-01A-11D-A29Q-08 TCGA-DB-A64W-10A-01D-A29Q-08 g.chr11:77907849delG c.558delG c.(556-558)gtgfs p.V186fs LGG 11 77916930 77916930 + Missense_Mutation SNP G G A TCGA-HT-7475-01A-11D-2024-08 TCGA-HT-7475-10A-01D-2024-08 g.chr11:77916930G>A c.1240G>A c.(1240-1242)Ggg>Agg p.G414R LGG 11 77918633 77918633 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:77918633G>T c.1449G>T c.(1447-1449)aaG>aaT p.K483N LGG 11 77919936 77919936 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:77919936G>A c.1519G>A c.(1519-1521)Gca>Aca p.A507T LGG 11 77921330 77921330 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:77921330G>A c.2429G>A c.(2428-2430)cGc>cAc p.R810H LGG 11 77921496 77921496 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:77921496C>A c.2595C>A c.(2593-2595)tgC>tgA p.C865* LIHC 11 77920573 77920573 + Missense_Mutation SNP C C A TCGA-DD-A3A7-01A-11D-A22F-10 TCGA-DD-A3A7-11A-11D-A22F-10 g.chr11:77920573C>A c.1672C>A c.(1672-1674)Ccc>Acc p.P558T LIHC 11 77920940 77920940 + Missense_Mutation SNP A A G TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr11:77920940A>G c.2039A>G c.(2038-2040)gAg>gGg p.E680G LUAD 11 77907295 77907295 + Missense_Mutation SNP G G T TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr11:77907295G>T c.4G>T c.(4-6)Gac>Tac p.D2Y LUAD 11 77907333 77907333 + Silent SNP G G T TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr11:77907333G>T c.42G>T c.(40-42)ccG>ccT p.P14P LUAD 11 77907354 77907354 + Silent SNP G G T TCGA-17-Z016-01A-01W-0746-08 TCGA-17-Z016-11A-01W-0746-08 g.chr11:77907354G>T c.63G>T c.(61-63)ctG>ctT p.L21L LUAD 11 77909055 77909055 + Silent SNP C C T TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr11:77909055C>T c.747C>T c.(745-747)gtC>gtT p.V249V LUAD 11 77911202 77911202 + Silent SNP C C T TCGA-78-7161-01A-11D-2036-08 TCGA-78-7161-10A-01D-2036-08 g.chr11:77911202C>T c.960C>T c.(958-960)ccC>ccT p.P320P LUAD 11 77916913 77916913 + Missense_Mutation SNP G G A TCGA-05-4390-01A-02D-1753-08 TCGA-05-4390-10A-01D-1753-08 g.chr11:77916913G>A c.1223G>A c.(1222-1224)cGc>cAc p.R408H LUAD 11 77918630 77918630 + Silent SNP C C T TCGA-93-7348-01A-21D-2036-08 TCGA-93-7348-10A-01D-2036-08 g.chr11:77918630C>T c.1446C>T c.(1444-1446)acC>acT p.T482T LUAD 11 77919914 77919914 + Missense_Mutation SNP T T G TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr11:77919914T>G c.1497T>G c.(1495-1497)atT>atG p.I499M LUAD 11 77920933 77920933 + Missense_Mutation SNP G G C TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr11:77920933G>C c.2032G>C c.(2032-2034)Gag>Cag p.E678Q LUAD 11 77921420 77921420 + Missense_Mutation SNP G G T TCGA-73-4670-01A-01D-1265-08 TCGA-73-4670-11A-01D-1265-08 g.chr11:77921420G>T c.2519G>T c.(2518-2520)gGc>gTc p.G840V LUAD 11 77921493 77921493 + Silent SNP C C T TCGA-49-4487-01A-21D-1855-08 TCGA-49-4487-11A-01D-1855-08 g.chr11:77921493C>T c.2592C>T c.(2590-2592)taC>taT p.Y864Y LUSC 11 77907956 77907956 + Missense_Mutation SNP C C T TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr11:77907956C>T c.665C>T c.(664-666)tCc>tTc p.S222F LUSC 11 77920699 77920699 + Missense_Mutation SNP T T G TCGA-18-4086-01A-01D-1352-08 TCGA-18-4086-11A-01D-1352-08 g.chr11:77920699T>G c.1798T>G c.(1798-1800)Ttc>Gtc p.F600V LUSC 11 77921353 77921353 + Missense_Mutation SNP A A T TCGA-46-3765-01A-01D-0983-08 TCGA-46-3765-10A-01D-0983-08 g.chr11:77921353A>T c.2452A>T c.(2452-2454)Atg>Ttg p.M818L OV 11 77907406 77907406 + Silent SNP C C T TCGA-24-1551-01A-01W-0551-08 TCGA-24-1551-10A-01W-0551-08 g.chr11:77907406C>T c.115C>T c.(115-117)Ctg>Ttg p.L39L OV 11 77917031 77917031 + Silent SNP C C G TCGA-13-0726-01A-01W-0372-09 TCGA-13-0726-10B-01W-0977-09 g.chr11:77917031C>G c.1341C>G c.(1339-1341)ggC>ggG p.G447G OV 11 77921373 77921373 + Silent SNP G G T TCGA-29-1761-01A-01W-0633-09 TCGA-29-1761-10A-01W-0633-09 g.chr11:77921373G>T c.2472G>T c.(2470-2472)ctG>ctT p.L824L PAAD 11 77907359 77907359 + Missense_Mutation SNP G G A TCGA-2L-AAQJ-01A-12D-A397-08 TCGA-2L-AAQJ-11A-11D-A39A-08 g.chr11:77907359G>A c.68G>A c.(67-69)cGg>cAg p.R23Q PAAD 11 77919947 77919947 + Silent SNP G G A TCGA-FB-AAPQ-01A-11D-A40W-08 TCGA-FB-AAPQ-11A-11D-A40W-08 g.chr11:77919947G>A c.1530G>A c.(1528-1530)acG>acA p.T510T PAAD 11 77920696 77920696 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:77920696G>A c.1795G>A c.(1795-1797)Gcc>Acc p.A599T PAAD 11 77921647 77921647 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:77921647G>T c.2746G>T c.(2746-2748)Gac>Tac p.D916Y PAAD 11 77924851 77924851 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr11:77924851G>A c.3049G>A c.(3049-3051)Gtc>Atc p.V1017I PRAD 11 77911274 77911274 + Silent SNP C C T TCGA-CH-5762-01A-11D-1576-08 TCGA-CH-5762-11A-01D-1576-08 g.chr11:77911274C>T c.1032C>T c.(1030-1032)ttC>ttT p.F344F PRAD 11 77917055 77917055 + Silent SNP C C T TCGA-2A-A8W3-01A-11D-A377-08 TCGA-2A-A8W3-10A-01D-A37A-08 g.chr11:77917055C>T c.1365C>T c.(1363-1365)atC>atT p.I455I PRAD 11 77918623 77918623 + Missense_Mutation SNP T T G TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:77918623T>G c.1439T>G c.(1438-1440)cTg>cGg p.L480R PRAD 11 77924826 77924826 + Silent SNP C C T TCGA-HC-7745-01A-11D-2114-08 TCGA-HC-7745-10A-01D-2115-08 g.chr11:77924826C>T c.3024C>T c.(3022-3024)ggC>ggT p.G1008G PRAD 11 77924841 77924841 + Missense_Mutation SNP C C G TCGA-J9-A52C-01A-11D-A26M-08 TCGA-J9-A52C-10A-01D-A26K-08 g.chr11:77924841C>G c.3039C>G c.(3037-3039)ttC>ttG p.F1013L READ 11 77911746 77911746 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:77911746G>A c.1089G>A c.(1087-1089)tcG>tcA p.S363S READ 11 77921074 77921074 + Nonsense_Mutation SNP A A T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:77921074A>T c.2173A>T c.(2173-2175)Aag>Tag p.K725* SARC 11 77921522 77921522 + Missense_Mutation SNP C C A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr11:77921522C>A c.2621C>A c.(2620-2622)cCt>cAt p.P874H SKCM 11 77910659 77910659 + Silent SNP C C T TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr11:77910659C>T c.825C>T c.(823-825)tcC>tcT p.S275S SKCM 11 77917004 77917004 + Silent SNP G G T TCGA-GN-A26D-06A-11D-A19A-08 TCGA-GN-A26D-10A-01D-A19A-08 g.chr11:77917004G>T c.1314G>T c.(1312-1314)acG>acT p.T438T SKCM 11 77917056 77917056 + Missense_Mutation SNP C C T TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr11:77917056C>T c.1366C>T c.(1366-1368)Ctt>Ttt p.L456F SKCM 11 77920580 77920580 + Missense_Mutation SNP C C T TCGA-EE-A29P-06A-11D-A197-08 TCGA-EE-A29P-10A-01D-A199-08 g.chr11:77920580C>T c.1679C>T c.(1678-1680)gCc>gTc p.A560V SKCM 11 77921051 77921053 + In_Frame_Del DEL AGA AGA - TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr11:77921051_77921053delAGA c.2150_2152delAGA c.(2149-2154)gagaag>gag p.K718del

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 77921418 77921418 single base substitution T G 3_prime_UTR_variant BLCA-CN 11 77921418 77921418 single base substitution T G downstream_gene_variant BLCA-CN 11 77921418 77921418 single base substitution T G exon_variant BLCA-CN 11 77921418 77921418 single base substitution T G synonymous_variant G407G 1221T>G BLCA-CN 11 77921418 77921418 single base substitution T G synonymous_variant G425G 1275T>G BLCA-CN 11 77921418 77921418 single base substitution T G synonymous_variant G570G 1710T>G BLCA-CN 11 77921418 77921418 single base substitution T G synonymous_variant G839G 2517T>G BLCA-US 11 77907438 77907438 single base substitution C T intron_variant BLCA-US 11 77907438 77907438 single base substitution C T synonymous_variant Y49Y 147C>T BLCA-US 11 77907438 77907438 single base substitution C T upstream_gene_variant BLCA-US 11 77911809 77911809 single base substitution C T 3_prime_UTR_variant BLCA-US 11 77911809 77911809 single base substitution C T 5_prime_UTR_variant BLCA-US 11 77911809 77911809 single base substitution C T intron_variant BLCA-US 11 77911809 77911809 single base substitution C T synonymous_variant F115F 345C>T BLCA-US 11 77911809 77911809 single base substitution C T synonymous_variant F140F 420C>T BLCA-US 11 77911809 77911809 single base substitution C T synonymous_variant F384F 1152C>T BLCA-US 11 77919932 77919932 single base substitution C G 3_prime_UTR_variant BLCA-US 11 77919932 77919932 single base substitution C G exon_variant BLCA-US 11 77919932 77919932 single base substitution C G intron_variant BLCA-US 11 77919932 77919932 single base substitution C G synonymous_variant L236L 708C>G BLCA-US 11 77919932 77919932 single base substitution C G synonymous_variant L261L 783C>G BLCA-US 11 77919932 77919932 single base substitution C G synonymous_variant L505L 1515C>G BLCA-US 11 77919932 77919932 single base substitution C G synonymous_variant L73L 219C>G BLCA-US 11 77919932 77919932 single base substitution C G synonymous_variant L91L 273C>G BLCA-US 11 77921098 77921098 single base substitution G A 3_prime_UTR_variant BLCA-US 11 77921098 77921098 single base substitution G A downstream_gene_variant BLCA-US 11 77921098 77921098 single base substitution G A exon_variant BLCA-US 11 77921098 77921098 single base substitution G A missense_variant E301K 901G>A BLCA-US 11 77921098 77921098 single base substitution G A missense_variant E319K 955G>A BLCA-US 11 77921098 77921098 single base substitution G A missense_variant E464K 1390G>A BLCA-US 11 77921098 77921098 single base substitution G A missense_variant E733K 2197G>A BLCA-US 11 77924751 77924751 single base substitution G T 3_prime_UTR_variant BLCA-US 11 77924751 77924751 single base substitution G T downstream_gene_variant BLCA-US 11 77924751 77924751 single base substitution G T exon_variant BLCA-US 11 77924751 77924751 single base substitution G T synonymous_variant P551P 1653G>T BLCA-US 11 77924751 77924751 single base substitution G T synonymous_variant P569P 1707G>T BLCA-US 11 77924751 77924751 single base substitution G T synonymous_variant P714P 2142G>T BLCA-US 11 77924751 77924751 single base substitution G T synonymous_variant P983P 2949G>T BRCA-EU 11 77895231 77895231 single base substitution C G upstream_gene_variant BRCA-EU 11 77895250 77895250 single base substitution T C upstream_gene_variant BRCA-EU 11 77899787 77899787 single base substitution C A upstream_gene_variant BRCA-EU 11 77899964 77899964 single base substitution C G 5_prime_UTR_variant BRCA-EU 11 77899964 77899964 single base substitution C G exon_variant BRCA-EU 11 77899965 77899965 single base substitution A G 5_prime_UTR_variant BRCA-EU 11 77899965 77899965 single base substitution A G exon_variant BRCA-EU 11 77899990 77900014 deletion of <=200bp GGGCTTCCTGGATACATAGAGGCTT - 5_prime_UTR_variant BRCA-EU 11 77899990 77900014 deletion of <=200bp GGGCTTCCTGGATACATAGAGGCTT - exon_variant BRCA-EU 11 77900006 77900006 single base substitution T C 5_prime_UTR_variant BRCA-EU 11 77900006 77900006 single base substitution T C exon_variant BRCA-EU 11 77901552 77901552 single base substitution C G intron_variant BRCA-EU 11 77902932 77902932 single base substitution C T intron_variant BRCA-EU 11 77902932 77902932 single base substitution C T upstream_gene_variant BRCA-EU 11 77903772 77903772 single base substitution A G intron_variant BRCA-EU 11 77903772 77903772 single base substitution A G upstream_gene_variant BRCA-EU 11 77904057 77904057 single base substitution T G intron_variant BRCA-EU 11 77904057 77904057 single base substitution T G upstream_gene_variant BRCA-EU 11 77905151 77905151 single base substitution A C intron_variant BRCA-EU 11 77905151 77905151 single base substitution A C upstream_gene_variant BRCA-EU 11 77905639 77905639 single base substitution G A intron_variant BRCA-EU 11 77905639 77905639 single base substitution G A upstream_gene_variant BRCA-EU 11 77905821 77905821 single base substitution C G intron_variant BRCA-EU 11 77905821 77905821 single base substitution C G upstream_gene_variant BRCA-EU 11 77907460 77907460 single base substitution C T intron_variant BRCA-EU 11 77907460 77907460 single base substitution C T missense_variant P57S 169C>T BRCA-EU 11 77907460 77907460 single base substitution C T upstream_gene_variant BRCA-EU 11 77908296 77908296 deletion of <=200bp T - intron_variant BRCA-EU 11 77908296 77908296 deletion of <=200bp T - upstream_gene_variant BRCA-EU 11 77908426 77908426 single base substitution G A intron_variant BRCA-EU 11 77908426 77908426 single base substitution G A upstream_gene_variant BRCA-EU 11 77909493 77909493 single base substitution A C intron_variant BRCA-EU 11 77909493 77909493 single base substitution A C upstream_gene_variant BRCA-EU 11 77909989 77909989 single base substitution C G intron_variant BRCA-EU 11 77909989 77909989 single base substitution C G upstream_gene_variant BRCA-EU 11 77910073 77910073 single base substitution C T 5_prime_UTR_variant BRCA-EU 11 77910073 77910073 single base substitution C T intron_variant BRCA-EU 11 77913420 77913420 deletion of <=200bp A - intron_variant BRCA-EU 11 77913420 77913420 deletion of <=200bp A - upstream_gene_variant BRCA-EU 11 77914245 77914245 single base substitution C A intron_variant BRCA-EU 11 77914245 77914245 single base substitution C A upstream_gene_variant BRCA-EU 11 77914570 77914570 single base substitution C T intron_variant BRCA-EU 11 77914570 77914570 single base substitution C T upstream_gene_variant BRCA-EU 11 77914594 77914594 single base substitution G A intron_variant BRCA-EU 11 77914594 77914594 single base substitution G A upstream_gene_variant BRCA-EU 11 77916253 77916253 single base substitution C T intron_variant BRCA-EU 11 77916253 77916253 single base substitution C T upstream_gene_variant BRCA-EU 11 77917059 77917059 single base substitution C T 3_prime_UTR_variant BRCA-EU 11 77917059 77917059 single base substitution C T intron_variant BRCA-EU 11 77917059 77917059 single base substitution C T stop_gained Q188* 562C>T BRCA-EU 11 77917059 77917059 single base substitution C T stop_gained Q213* 637C>T BRCA-EU 11 77917059 77917059 single base substitution C T stop_gained Q25* 73C>T BRCA-EU 11 77917059 77917059 single base substitution C T stop_gained Q457* 1369C>T BRCA-EU 11 77917059 77917059 single base substitution C T synonymous_variant F41F 123C>T BRCA-EU 11 77917059 77917059 single base substitution C T upstream_gene_variant BRCA-EU 11 77917725 77917725 single base substitution T C intron_variant BRCA-EU 11 77917725 77917725 single base substitution T C upstream_gene_variant BRCA-EU 11 77917917 77917917 single base substitution G T intron_variant BRCA-EU 11 77917917 77917917 single base substitution G T upstream_gene_variant BRCA-EU 11 77920856 77920856 deletion of <=200bp C - 3_prime_UTR_variant BRCA-EU 11 77920856 77920856 deletion of <=200bp C - downstream_gene_variant BRCA-EU 11 77920856 77920856 deletion of <=200bp C - exon_variant BRCA-EU 11 77920856 77920856 deletion of <=200bp C - frameshift_variant T220 BRCA-EU 11 77920856 77920856 deletion of <=200bp C - frameshift_variant T238 BRCA-EU 11 77920856 77920856 deletion of <=200bp C - frameshift_variant T383 BRCA-EU 11 77920856 77920856 deletion of <=200bp C - frameshift_variant T652 BRCA-EU 11 77921304 77921304 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 77921304 77921304 single base substitution G A downstream_gene_variant BRCA-EU 11 77921304 77921304 single base substitution G A exon_variant BRCA-EU 11 77921304 77921304 single base substitution G A synonymous_variant P369P 1107G>A BRCA-EU 11 77921304 77921304 single base substitution G A synonymous_variant P387P 1161G>A BRCA-EU 11 77921304 77921304 single base substitution G A synonymous_variant P532P 1596G>A BRCA-EU 11 77921304 77921304 single base substitution G A synonymous_variant P801P 2403G>A BRCA-EU 11 77921601 77921601 single base substitution C G 3_prime_UTR_variant BRCA-EU 11 77921601 77921601 single base substitution C G downstream_gene_variant BRCA-EU 11 77921601 77921601 single base substitution C G exon_variant BRCA-EU 11 77921601 77921601 single base substitution C G missense_variant F468L 1404C>G BRCA-EU 11 77921601 77921601 single base substitution C G missense_variant F486L 1458C>G BRCA-EU 11 77921601 77921601 single base substitution C G missense_variant F631L 1893C>G BRCA-EU 11 77921601 77921601 single base substitution C G missense_variant F900L 2700C>G BRCA-EU 11 77922144 77922144 single base substitution G C downstream_gene_variant BRCA-EU 11 77922144 77922144 single base substitution G C intron_variant BRCA-EU 11 77922569 77922569 single base substitution T C downstream_gene_variant BRCA-EU 11 77922569 77922569 single base substitution T C intron_variant BRCA-EU 11 77922732 77922732 single base substitution C G downstream_gene_variant BRCA-EU 11 77922732 77922732 single base substitution C G intron_variant BRCA-EU 11 77924426 77924426 single base substitution G A downstream_gene_variant BRCA-EU 11 77924426 77924426 single base substitution G A intron_variant BRCA-EU 11 77924444 77924444 single base substitution T C downstream_gene_variant BRCA-EU 11 77924444 77924444 single base substitution T C intron_variant BRCA-EU 11 77926844 77926844 single base substitution G A downstream_gene_variant BRCA-EU 11 77928225 77928225 single base substitution C T downstream_gene_variant BRCA-EU 11 77929943 77929943 single base substitution G T downstream_gene_variant BRCA-FR 11 77900006 77900006 single base substitution T C 5_prime_UTR_variant BRCA-FR 11 77900006 77900006 single base substitution T C exon_variant BRCA-FR 11 77905821 77905821 single base substitution C G intron_variant BRCA-FR 11 77905821 77905821 single base substitution C G upstream_gene_variant BRCA-FR 11 77916253 77916253 single base substitution C T intron_variant BRCA-FR 11 77916253 77916253 single base substitution C T upstream_gene_variant BRCA-FR 11 77917059 77917059 single base substitution C T 3_prime_UTR_variant BRCA-FR 11 77917059 77917059 single base substitution C T intron_variant BRCA-FR 11 77917059 77917059 single base substitution C T stop_gained Q188* 562C>T BRCA-FR 11 77917059 77917059 single base substitution C T stop_gained Q213* 637C>T BRCA-FR 11 77917059 77917059 single base substitution C T stop_gained Q25* 73C>T BRCA-FR 11 77917059 77917059 single base substitution C T stop_gained Q457* 1369C>T BRCA-FR 11 77917059 77917059 single base substitution C T synonymous_variant F41F 123C>T BRCA-FR 11 77917059 77917059 single base substitution C T upstream_gene_variant BRCA-FR 11 77921601 77921601 single base substitution C G 3_prime_UTR_variant BRCA-FR 11 77921601 77921601 single base substitution C G downstream_gene_variant BRCA-FR 11 77921601 77921601 single base substitution C G exon_variant BRCA-FR 11 77921601 77921601 single base substitution C G missense_variant F468L 1404C>G BRCA-FR 11 77921601 77921601 single base substitution C G missense_variant F486L 1458C>G BRCA-FR 11 77921601 77921601 single base substitution C G missense_variant F631L 1893C>G BRCA-FR 11 77921601 77921601 single base substitution C G missense_variant F900L 2700C>G BRCA-FR 11 77928225 77928225 single base substitution C T downstream_gene_variant BRCA-UK 11 77908426 77908426 single base substitution G A intron_variant BRCA-UK 11 77908426 77908426 single base substitution G A upstream_gene_variant BRCA-UK 11 77924978 77924978 single base substitution C T 3_prime_UTR_variant BRCA-UK 11 77924978 77924978 single base substitution C T downstream_gene_variant BRCA-UK 11 77924978 77924978 single base substitution C T exon_variant BRCA-US 11 77920855 77920855 insertion of <=200bp - C 3_prime_UTR_variant BRCA-US 11 77920855 77920855 insertion of <=200bp - C downstream_gene_variant BRCA-US 11 77920855 77920855 insertion of <=200bp - C exon_variant BRCA-US 11 77920855 77920855 insertion of <=200bp - C frameshift_variant T220H? BRCA-US 11 77920855 77920855 insertion of <=200bp - C frameshift_variant T238H? BRCA-US 11 77920855 77920855 insertion of <=200bp - C frameshift_variant T383H? BRCA-US 11 77920855 77920855 insertion of <=200bp - C frameshift_variant T652H? BRCA-US 11 77920856 77920856 deletion of <=200bp C - 3_prime_UTR_variant BRCA-US 11 77920856 77920856 deletion of <=200bp C - downstream_gene_variant BRCA-US 11 77920856 77920856 deletion of <=200bp C - exon_variant BRCA-US 11 77920856 77920856 deletion of <=200bp C - frameshift_variant T220 BRCA-US 11 77920856 77920856 deletion of <=200bp C - frameshift_variant T238 BRCA-US 11 77920856 77920856 deletion of <=200bp C - frameshift_variant T383 BRCA-US 11 77920856 77920856 deletion of <=200bp C - frameshift_variant T652 BRCA-US 11 77921402 77921402 single base substitution G A 3_prime_UTR_variant BRCA-US 11 77921402 77921402 single base substitution G A downstream_gene_variant BRCA-US 11 77921402 77921402 single base substitution G A exon_variant BRCA-US 11 77921402 77921402 single base substitution G A missense_variant R402H 1205G>A BRCA-US 11 77921402 77921402 single base substitution G A missense_variant R420H 1259G>A BRCA-US 11 77921402 77921402 single base substitution G A missense_variant R565H 1694G>A BRCA-US 11 77921402 77921402 single base substitution G A missense_variant R834H 2501G>A BRCA-US 11 77930333 77930333 single base substitution C G downstream_gene_variant BRCA-US 11 77930371 77930371 single base substitution C G downstream_gene_variant BTCA-JP 11 77911773 77911773 single base substitution G A 3_prime_UTR_variant BTCA-JP 11 77911773 77911773 single base substitution G A 5_prime_UTR_variant BTCA-JP 11 77911773 77911773 single base substitution G A intron_variant BTCA-JP 11 77911773 77911773 single base substitution G A synonymous_variant Q103Q 309G>A BTCA-JP 11 77911773 77911773 single base substitution G A synonymous_variant Q128Q 384G>A BTCA-JP 11 77911773 77911773 single base substitution G A synonymous_variant Q372Q 1116G>A BTCA-JP 11 77920687 77920688 deletion of <=200bp CT - 3_prime_UTR_variant BTCA-JP 11 77920687 77920688 deletion of <=200bp CT - downstream_gene_variant BTCA-JP 11 77920687 77920688 deletion of <=200bp CT - exon_variant BTCA-JP 11 77920687 77920688 deletion of <=200bp CT - frameshift_variant L164 BTCA-JP 11 77920687 77920688 deletion of <=200bp CT - frameshift_variant L182 BTCA-JP 11 77920687 77920688 deletion of <=200bp CT - frameshift_variant L327 BTCA-JP 11 77920687 77920688 deletion of <=200bp CT - frameshift_variant L596 CESC-US 11 77911809 77911809 single base substitution C T 3_prime_UTR_variant CESC-US 11 77911809 77911809 single base substitution C T 5_prime_UTR_variant CESC-US 11 77911809 77911809 single base substitution C T intron_variant CESC-US 11 77911809 77911809 single base substitution C T synonymous_variant F115F 345C>T CESC-US 11 77911809 77911809 single base substitution C T synonymous_variant F140F 420C>T CESC-US 11 77911809 77911809 single base substitution C T synonymous_variant F384F 1152C>T CESC-US 11 77917022 77917022 single base substitution C G 3_prime_UTR_variant CESC-US 11 77917022 77917022 single base substitution C G intron_variant CESC-US 11 77917022 77917022 single base substitution C G missense_variant I12M 36C>G CESC-US 11 77917022 77917022 single base substitution C G missense_variant I175M 525C>G CESC-US 11 77917022 77917022 single base substitution C G missense_variant I200M 600C>G CESC-US 11 77917022 77917022 single base substitution C G missense_variant I444M 1332C>G CESC-US 11 77917022 77917022 single base substitution C G stop_gained S29* 86C>G CESC-US 11 77917022 77917022 single base substitution C G upstream_gene_variant CESC-US 11 77921400 77921400 single base substitution C A 3_prime_UTR_variant CESC-US 11 77921400 77921400 single base substitution C A downstream_gene_variant CESC-US 11 77921400 77921400 single base substitution C A exon_variant CESC-US 11 77921400 77921400 single base substitution C A synonymous_variant L401L 1203C>A CESC-US 11 77921400 77921400 single base substitution C A synonymous_variant L419L 1257C>A CESC-US 11 77921400 77921400 single base substitution C A synonymous_variant L564L 1692C>A CESC-US 11 77921400 77921400 single base substitution C A synonymous_variant L833L 2499C>A CESC-US 11 77924696 77924698 deletion of <=200bp AGG - 3_prime_UTR_variant CESC-US 11 77924696 77924698 deletion of <=200bp AGG - downstream_gene_variant CESC-US 11 77924696 77924698 deletion of <=200bp AGG - exon_variant CESC-US 11 77924696 77924698 deletion of <=200bp AGG - inframe_deletion QE533Q CESC-US 11 77924696 77924698 deletion of <=200bp AGG - inframe_deletion QE551Q CESC-US 11 77924696 77924698 deletion of <=200bp AGG - inframe_deletion QE696Q CESC-US 11 77924696 77924698 deletion of <=200bp AGG - inframe_deletion QE965Q CLLE-ES 11 77897418 77897437 deletion of <=200bp AAAAAAAAAAAAAAAAAAAA - upstream_gene_variant CLLE-ES 11 77918028 77918028 single base substitution T A intron_variant CLLE-ES 11 77918028 77918028 single base substitution T A upstream_gene_variant COAD-US 11 77911215 77911215 single base substitution G A 5_prime_UTR_variant COAD-US 11 77911215 77911215 single base substitution G A exon_variant COAD-US 11 77911215 77911215 single base substitution G A intron_variant COAD-US 11 77911215 77911215 single base substitution G A missense_variant A325T 973G>A COAD-US 11 77911215 77911215 single base substitution G A missense_variant A56T 166G>A COAD-US 11 77911215 77911215 single base substitution G A missense_variant A81T 241G>A COAD-US 11 77911266 77911266 single base substitution G A 3_prime_UTR_variant COAD-US 11 77911266 77911266 single base substitution G A 5_prime_UTR_variant COAD-US 11 77911266 77911266 single base substitution G A intron_variant COAD-US 11 77911266 77911266 single base substitution G A missense_variant E342K 1024G>A COAD-US 11 77911266 77911266 single base substitution G A missense_variant E73K 217G>A COAD-US 11 77911266 77911266 single base substitution G A missense_variant E98K 292G>A COAD-US 11 77911779 77911779 single base substitution G A 3_prime_UTR_variant COAD-US 11 77911779 77911779 single base substitution G A 5_prime_UTR_variant COAD-US 11 77911779 77911779 single base substitution G A intron_variant COAD-US 11 77911779 77911779 single base substitution G A synonymous_variant A105A 315G>A COAD-US 11 77911779 77911779 single base substitution G A synonymous_variant A130A 390G>A COAD-US 11 77911779 77911779 single base substitution G A synonymous_variant A374A 1122G>A COAD-US 11 77916968 77916968 single base substitution G A 3_prime_UTR_variant COAD-US 11 77916968 77916968 single base substitution G A 5_prime_UTR_variant COAD-US 11 77916968 77916968 single base substitution G A intron_variant COAD-US 11 77916968 77916968 single base substitution G A missense_variant R11Q 32G>A COAD-US 11 77916968 77916968 single base substitution G A synonymous_variant A157A 471G>A COAD-US 11 77916968 77916968 single base substitution G A synonymous_variant A182A 546G>A COAD-US 11 77916968 77916968 single base substitution G A synonymous_variant A426A 1278G>A COAD-US 11 77916968 77916968 single base substitution G A upstream_gene_variant COAD-US 11 77917064 77917064 single base substitution C T 3_prime_UTR_variant COAD-US 11 77917064 77917064 single base substitution C T intron_variant COAD-US 11 77917064 77917064 single base substitution C T missense_variant P43L 128C>T COAD-US 11 77917064 77917064 single base substitution C T synonymous_variant A189A 567C>T COAD-US 11 77917064 77917064 single base substitution C T synonymous_variant A214A 642C>T COAD-US 11 77917064 77917064 single base substitution C T synonymous_variant A26A 78C>T COAD-US 11 77917064 77917064 single base substitution C T synonymous_variant A458A 1374C>T COAD-US 11 77917064 77917064 single base substitution C T upstream_gene_variant COAD-US 11 77918660 77918660 single base substitution A G 3_prime_UTR_variant COAD-US 11 77918660 77918660 single base substitution A G exon_variant COAD-US 11 77918660 77918660 single base substitution A G intron_variant COAD-US 11 77918660 77918660 single base substitution A G synonymous_variant E223E 669A>G COAD-US 11 77918660 77918660 single base substitution A G synonymous_variant E248E 744A>G COAD-US 11 77918660 77918660 single base substitution A G synonymous_variant E492E 1476A>G COAD-US 11 77918660 77918660 single base substitution A G synonymous_variant E60E 180A>G COAD-US 11 77918660 77918660 single base substitution A G synonymous_variant E78E 234A>G COAD-US 11 77919923 77919923 single base substitution G T 3_prime_UTR_variant COAD-US 11 77919923 77919923 single base substitution G T exon_variant COAD-US 11 77919923 77919923 single base substitution G T intron_variant COAD-US 11 77919923 77919923 single base substitution G T missense_variant E233D 699G>T COAD-US 11 77919923 77919923 single base substitution G T missense_variant E258D 774G>T COAD-US 11 77919923 77919923 single base substitution G T missense_variant E502D 1506G>T COAD-US 11 77919923 77919923 single base substitution G T missense_variant E70D 210G>T COAD-US 11 77919923 77919923 single base substitution G T missense_variant E88D 264G>T COAD-US 11 77920714 77920714 single base substitution C T 3_prime_UTR_variant COAD-US 11 77920714 77920714 single base substitution C T downstream_gene_variant COAD-US 11 77920714 77920714 single base substitution C T exon_variant COAD-US 11 77920714 77920714 single base substitution C T missense_variant R173C 517C>T COAD-US 11 77920714 77920714 single base substitution C T missense_variant R191C 571C>T COAD-US 11 77920714 77920714 single base substitution C T missense_variant R336C 1006C>T COAD-US 11 77920714 77920714 single base substitution C T missense_variant R605C 1813C>T COAD-US 11 77920730 77920730 single base substitution G A 3_prime_UTR_variant COAD-US 11 77920730 77920730 single base substitution G A downstream_gene_variant COAD-US 11 77920730 77920730 single base substitution G A exon_variant COAD-US 11 77920730 77920730 single base substitution G A missense_variant R178H 533G>A COAD-US 11 77920730 77920730 single base substitution G A missense_variant R196H 587G>A COAD-US 11 77920730 77920730 single base substitution G A missense_variant R341H 1022G>A COAD-US 11 77920730 77920730 single base substitution G A missense_variant R610H 1829G>A COAD-US 11 77920768 77920768 single base substitution G A 3_prime_UTR_variant COAD-US 11 77920768 77920768 single base substitution G A downstream_gene_variant COAD-US 11 77920768 77920768 single base substitution G A exon_variant COAD-US 11 77920768 77920768 single base substitution G A missense_variant A191T 571G>A COAD-US 11 77920768 77920768 single base substitution G A missense_variant A209T 625G>A COAD-US 11 77920768 77920768 single base substitution G A missense_variant A354T 1060G>A COAD-US 11 77920768 77920768 single base substitution G A missense_variant A623T 1867G>A COAD-US 11 77920855 77920855 insertion of <=200bp - C 3_prime_UTR_variant COAD-US 11 77920855 77920855 insertion of <=200bp - C downstream_gene_variant COAD-US 11 77920855 77920855 insertion of <=200bp - C exon_variant COAD-US 11 77920855 77920855 insertion of <=200bp - C frameshift_variant T220H? COAD-US 11 77920855 77920855 insertion of <=200bp - C frameshift_variant T238H? COAD-US 11 77920855 77920855 insertion of <=200bp - C frameshift_variant T383H? COAD-US 11 77920855 77920855 insertion of <=200bp - C frameshift_variant T652H? COAD-US 11 77920856 77920856 deletion of <=200bp C - 3_prime_UTR_variant COAD-US 11 77920856 77920856 deletion of <=200bp C - downstream_gene_variant COAD-US 11 77920856 77920856 deletion of <=200bp C - exon_variant COAD-US 11 77920856 77920856 deletion of <=200bp C - frameshift_variant T220 COAD-US 11 77920856 77920856 deletion of <=200bp C - frameshift_variant T238 COAD-US 11 77920856 77920856 deletion of <=200bp C - frameshift_variant T383 COAD-US 11 77920856 77920856 deletion of <=200bp C - frameshift_variant T652 COAD-US 11 77920930 77920930 single base substitution A G 3_prime_UTR_variant COAD-US 11 77920930 77920930 single base substitution A G downstream_gene_variant COAD-US 11 77920930 77920930 single base substitution A G exon_variant COAD-US 11 77920930 77920930 single base substitution A G missense_variant I245V 733A>G COAD-US 11 77920930 77920930 single base substitution A G missense_variant I263V 787A>G COAD-US 11 77920930 77920930 single base substitution A G missense_variant I408V 1222A>G COAD-US 11 77920930 77920930 single base substitution A G missense_variant I677V 2029A>G COAD-US 11 77920964 77920964 single base substitution C T 3_prime_UTR_variant COAD-US 11 77920964 77920964 single base substitution C T downstream_gene_variant COAD-US 11 77920964 77920964 single base substitution C T exon_variant COAD-US 11 77920964 77920964 single base substitution C T missense_variant T256M 767C>T COAD-US 11 77920964 77920964 single base substitution C T missense_variant T274M 821C>T COAD-US 11 77920964 77920964 single base substitution C T missense_variant T419M 1256C>T COAD-US 11 77920964 77920964 single base substitution C T missense_variant T688M 2063C>T COAD-US 11 77921275 77921275 single base substitution G A 3_prime_UTR_variant COAD-US 11 77921275 77921275 single base substitution G A downstream_gene_variant COAD-US 11 77921275 77921275 single base substitution G A exon_variant COAD-US 11 77921275 77921275 single base substitution G A missense_variant E360K 1078G>A COAD-US 11 77921275 77921275 single base substitution G A missense_variant E378K 1132G>A COAD-US 11 77921275 77921275 single base substitution G A missense_variant E523K 1567G>A COAD-US 11 77921275 77921275 single base substitution G A missense_variant E792K 2374G>A COAD-US 11 77921590 77921590 single base substitution C T 3_prime_UTR_variant COAD-US 11 77921590 77921590 single base substitution C T downstream_gene_variant COAD-US 11 77921590 77921590 single base substitution C T exon_variant COAD-US 11 77921590 77921590 single base substitution C T missense_variant R465W 1393C>T COAD-US 11 77921590 77921590 single base substitution C T missense_variant R483W 1447C>T COAD-US 11 77921590 77921590 single base substitution C T missense_variant R628W 1882C>T COAD-US 11 77921590 77921590 single base substitution C T missense_variant R897W 2689C>T COAD-US 11 77930345 77930345 single base substitution T C downstream_gene_variant COCA-CN 11 77907446 77907446 single base substitution G T intron_variant COCA-CN 11 77907446 77907446 single base substitution G T missense_variant G52V 155G>T COCA-CN 11 77907446 77907446 single base substitution G T upstream_gene_variant COCA-CN 11 77907543 77907543 single base substitution C T intron_variant COCA-CN 11 77907543 77907543 single base substitution C T synonymous_variant R84R 252C>T COCA-CN 11 77907543 77907543 single base substitution C T upstream_gene_variant COCA-CN 11 77907890 77907890 single base substitution C T 5_prime_UTR_variant COCA-CN 11 77907890 77907890 single base substitution C T exon_variant COCA-CN 11 77907890 77907890 single base substitution C T intron_variant COCA-CN 11 77907890 77907890 single base substitution C T missense_variant A200V 599C>T COCA-CN 11 77907890 77907890 single base substitution C T upstream_gene_variant COCA-CN 11 77911231 77911231 single base substitution T A 5_prime_UTR_variant COCA-CN 11 77911231 77911231 single base substitution T A exon_variant COCA-CN 11 77911231 77911231 single base substitution T A intron_variant COCA-CN 11 77911231 77911231 single base substitution T A missense_variant L330H 989T>A COCA-CN 11 77911231 77911231 single base substitution T A missense_variant L61H 182T>A COCA-CN 11 77911231 77911231 single base substitution T A missense_variant L86H 257T>A COCA-CN 11 77921031 77921031 single base substitution G A 3_prime_UTR_variant COCA-CN 11 77921031 77921031 single base substitution G A downstream_gene_variant COCA-CN 11 77921031 77921031 single base substitution G A exon_variant COCA-CN 11 77921031 77921031 single base substitution G A synonymous_variant E278E 834G>A COCA-CN 11 77921031 77921031 single base substitution G A synonymous_variant E296E 888G>A COCA-CN 11 77921031 77921031 single base substitution G A synonymous_variant E441E 1323G>A COCA-CN 11 77921031 77921031 single base substitution G A synonymous_variant E710E 2130G>A COCA-CN 11 77924544 77924544 single base substitution G A downstream_gene_variant COCA-CN 11 77924544 77924544 single base substitution G A intron_variant COCA-CN 11 77930272 77930272 single base substitution C T downstream_gene_variant EOPC-DE 11 77904819 77904819 single base substitution A C intron_variant EOPC-DE 11 77904819 77904819 single base substitution A C upstream_gene_variant EOPC-DE 11 77919051 77919051 single base substitution C T intron_variant ESAD-UK 11 77895666 77895666 single base substitution A T upstream_gene_variant ESAD-UK 11 77899461 77899461 deletion of <=200bp C - upstream_gene_variant ESAD-UK 11 77900748 77900748 single base substitution C T intron_variant ESAD-UK 11 77901372 77901372 single base substitution C T intron_variant ESAD-UK 11 77902023 77902023 single base substitution T C intron_variant ESAD-UK 11 77902608 77902608 single base substitution T A intron_variant ESAD-UK 11 77906939 77906939 single base substitution G A intron_variant ESAD-UK 11 77906939 77906939 single base substitution G A upstream_gene_variant ESAD-UK 11 77907594 77907594 single base substitution C T intron_variant ESAD-UK 11 77907594 77907594 single base substitution C T synonymous_variant L101L 303C>T ESAD-UK 11 77907594 77907594 single base substitution C T upstream_gene_variant ESAD-UK 11 77909157 77909157 single base substitution C T intron_variant ESAD-UK 11 77909157 77909157 single base substitution C T upstream_gene_variant ESAD-UK 11 77911805 77911805 single base substitution G A 3_prime_UTR_variant ESAD-UK 11 77911805 77911805 single base substitution G A 5_prime_UTR_variant ESAD-UK 11 77911805 77911805 single base substitution G A intron_variant ESAD-UK 11 77911805 77911805 single base substitution G A missense_variant R114Q 341G>A ESAD-UK 11 77911805 77911805 single base substitution G A missense_variant R139Q 416G>A ESAD-UK 11 77911805 77911805 single base substitution G A missense_variant R383Q 1148G>A ESAD-UK 11 77911922 77911922 single base substitution G A intron_variant ESAD-UK 11 77912559 77912559 single base substitution A G intron_variant ESAD-UK 11 77912933 77912933 single base substitution C T intron_variant ESAD-UK 11 77915558 77915558 single base substitution G A intron_variant ESAD-UK 11 77915558 77915558 single base substitution G A upstream_gene_variant ESAD-UK 11 77915956 77915956 single base substitution T C intron_variant ESAD-UK 11 77915956 77915956 single base substitution T C upstream_gene_variant ESAD-UK 11 77918479 77918479 single base substitution C T exon_variant ESAD-UK 11 77918479 77918479 single base substitution C T intron_variant ESAD-UK 11 77920530 77920530 single base substitution C A 3_prime_UTR_variant ESAD-UK 11 77920530 77920530 single base substitution C A downstream_gene_variant ESAD-UK 11 77920530 77920530 single base substitution C A exon_variant ESAD-UK 11 77920530 77920530 single base substitution C A stop_gained C111* 333C>A ESAD-UK 11 77920530 77920530 single base substitution C A stop_gained C129* 387C>A ESAD-UK 11 77920530 77920530 single base substitution C A stop_gained C274* 822C>A ESAD-UK 11 77920530 77920530 single base substitution C A stop_gained C543* 1629C>A ESAD-UK 11 77925640 77925640 single base substitution C A 3_prime_UTR_variant ESAD-UK 11 77925640 77925640 single base substitution C A downstream_gene_variant ESAD-UK 11 77925652 77925652 single base substitution G T 3_prime_UTR_variant ESAD-UK 11 77925652 77925652 single base substitution G T downstream_gene_variant ESAD-UK 11 77925966 77925966 single base substitution C A downstream_gene_variant ESAD-UK 11 77930299 77930299 single base substitution C A downstream_gene_variant ESCA-CN 11 77921580 77921580 single base substitution C G 3_prime_UTR_variant ESCA-CN 11 77921580 77921580 single base substitution C G downstream_gene_variant ESCA-CN 11 77921580 77921580 single base substitution C G exon_variant ESCA-CN 11 77921580 77921580 single base substitution C G missense_variant F461L 1383C>G ESCA-CN 11 77921580 77921580 single base substitution C G missense_variant F479L 1437C>G ESCA-CN 11 77921580 77921580 single base substitution C G missense_variant F624L 1872C>G ESCA-CN 11 77921580 77921580 single base substitution C G missense_variant F893L 2679C>G GBM-US 11 77920718 77920718 single base substitution G A 3_prime_UTR_variant GBM-US 11 77920718 77920718 single base substitution G A downstream_gene_variant GBM-US 11 77920718 77920718 single base substitution G A exon_variant GBM-US 11 77920718 77920718 single base substitution G A missense_variant C174Y 521G>A GBM-US 11 77920718 77920718 single base substitution G A missense_variant C192Y 575G>A GBM-US 11 77920718 77920718 single base substitution G A missense_variant C337Y 1010G>A GBM-US 11 77920718 77920718 single base substitution G A missense_variant C606Y 1817G>A GBM-US 11 77921415 77921415 insertion of <=200bp - G 3_prime_UTR_variant GBM-US 11 77921415 77921415 insertion of <=200bp - G downstream_gene_variant GBM-US 11 77921415 77921415 insertion of <=200bp - G exon_variant GBM-US 11 77921415 77921415 insertion of <=200bp - G frameshift_variant A406A? GBM-US 11 77921415 77921415 insertion of <=200bp - G frameshift_variant A424A? GBM-US 11 77921415 77921415 insertion of <=200bp - G frameshift_variant A569A? GBM-US 11 77921415 77921415 insertion of <=200bp - G frameshift_variant A838A? GBM-US 11 77921629 77921629 single base substitution A C 3_prime_UTR_variant GBM-US 11 77921629 77921629 single base substitution A C downstream_gene_variant GBM-US 11 77921629 77921629 single base substitution A C exon_variant GBM-US 11 77921629 77921629 single base substitution A C missense_variant T478P 1432A>C GBM-US 11 77921629 77921629 single base substitution A C missense_variant T496P 1486A>C GBM-US 11 77921629 77921629 single base substitution A C missense_variant T641P 1921A>C GBM-US 11 77921629 77921629 single base substitution A C missense_variant T910P 2728A>C KIRC-US 11 77919916 77919916 single base substitution C A 3_prime_UTR_variant KIRC-US 11 77919916 77919916 single base substitution C A exon_variant KIRC-US 11 77919916 77919916 single base substitution C A intron_variant KIRC-US 11 77919916 77919916 single base substitution C A missense_variant S231Y 692C>A KIRC-US 11 77919916 77919916 single base substitution C A missense_variant S256Y 767C>A KIRC-US 11 77919916 77919916 single base substitution C A missense_variant S500Y 1499C>A KIRC-US 11 77919916 77919916 single base substitution C A missense_variant S68Y 203C>A KIRC-US 11 77919916 77919916 single base substitution C A missense_variant S86Y 257C>A KIRC-US 11 77921086 77921086 single base substitution C T 3_prime_UTR_variant KIRC-US 11 77921086 77921086 single base substitution C T downstream_gene_variant KIRC-US 11 77921086 77921086 single base substitution C T exon_variant KIRC-US 11 77921086 77921086 single base substitution C T stop_gained Q297* 889C>T KIRC-US 11 77921086 77921086 single base substitution C T stop_gained Q315* 943C>T KIRC-US 11 77921086 77921086 single base substitution C T stop_gained Q460* 1378C>T KIRC-US 11 77921086 77921086 single base substitution C T stop_gained Q729* 2185C>T KIRP-US 11 77921303 77921303 single base substitution C T 3_prime_UTR_variant KIRP-US 11 77921303 77921303 single base substitution C T downstream_gene_variant KIRP-US 11 77921303 77921303 single base substitution C T exon_variant KIRP-US 11 77921303 77921303 single base substitution C T missense_variant P369L 1106C>T KIRP-US 11 77921303 77921303 single base substitution C T missense_variant P387L 1160C>T KIRP-US 11 77921303 77921303 single base substitution C T missense_variant P532L 1595C>T KIRP-US 11 77921303 77921303 single base substitution C T missense_variant P801L 2402C>T LAML-KR 11 77924870 77924870 single base substitution C T 3_prime_UTR_variant LAML-KR 11 77924870 77924870 single base substitution C T downstream_gene_variant LAML-KR 11 77924870 77924870 single base substitution C T exon_variant LGG-US 11 77907849 77907849 deletion of <=200bp G - 5_prime_UTR_variant LGG-US 11 77907849 77907849 deletion of <=200bp G - exon_variant LGG-US 11 77907849 77907849 deletion of <=200bp G - frameshift_variant V186 LGG-US 11 77907849 77907849 deletion of <=200bp G - intron_variant LGG-US 11 77907849 77907849 deletion of <=200bp G - upstream_gene_variant LGG-US 11 77916930 77916930 single base substitution G A 3_prime_UTR_variant LGG-US 11 77916930 77916930 single base substitution G A 5_prime_UTR_variant LGG-US 11 77916930 77916930 single base substitution G A intron_variant LGG-US 11 77916930 77916930 single base substitution G A missense_variant G145R 433G>A LGG-US 11 77916930 77916930 single base substitution G A missense_variant G170R 508G>A LGG-US 11 77916930 77916930 single base substitution G A missense_variant G414R 1240G>A LGG-US 11 77916930 77916930 single base substitution G A upstream_gene_variant LIAD-FR 11 77907744 77907744 single base substitution C T intron_variant LIAD-FR 11 77907744 77907744 single base substitution C T synonymous_variant H151H 453C>T LIAD-FR 11 77907744 77907744 single base substitution C T upstream_gene_variant LICA-FR 11 77897773 77897773 single base substitution C A upstream_gene_variant LICA-FR 11 77905328 77905328 single base substitution C G intron_variant LICA-FR 11 77905328 77905328 single base substitution C G upstream_gene_variant LICA-FR 11 77909178 77909178 single base substitution C T intron_variant LICA-FR 11 77909178 77909178 single base substitution C T upstream_gene_variant LICA-FR 11 77921586 77921586 single base substitution C T 3_prime_UTR_variant LICA-FR 11 77921586 77921586 single base substitution C T downstream_gene_variant LICA-FR 11 77921586 77921586 single base substitution C T exon_variant LICA-FR 11 77921586 77921586 single base substitution C T synonymous_variant D463D 1389C>T LICA-FR 11 77921586 77921586 single base substitution C T synonymous_variant D481D 1443C>T LICA-FR 11 77921586 77921586 single base substitution C T synonymous_variant D626D 1878C>T LICA-FR 11 77921586 77921586 single base substitution C T synonymous_variant D895D 2685C>T LICA-FR 11 77923747 77923747 single base substitution T A downstream_gene_variant LICA-FR 11 77923747 77923747 single base substitution T A intron_variant LICA-FR 11 77923866 77923866 single base substitution C A downstream_gene_variant LICA-FR 11 77923866 77923866 single base substitution C A intron_variant LIHC-US 11 77920573 77920573 single base substitution C A 3_prime_UTR_variant LIHC-US 11 77920573 77920573 single base substitution C A downstream_gene_variant LIHC-US 11 77920573 77920573 single base substitution C A exon_variant LIHC-US 11 77920573 77920573 single base substitution C A missense_variant P126T 376C>A LIHC-US 11 77920573 77920573 single base substitution C A missense_variant P144T 430C>A LIHC-US 11 77920573 77920573 single base substitution C A missense_variant P289T 865C>A LIHC-US 11 77920573 77920573 single base substitution C A missense_variant P558T 1672C>A LINC-JP 11 77900490 77900490 single base substitution G A intron_variant LINC-JP 11 77901457 77901457 single base substitution G T intron_variant LINC-JP 11 77907191 77907191 single base substitution C T intron_variant LINC-JP 11 77907191 77907191 single base substitution C T upstream_gene_variant LINC-JP 11 77910908 77910908 single base substitution C G intron_variant LINC-JP 11 77914933 77914933 single base substitution C T intron_variant LINC-JP 11 77914933 77914933 single base substitution C T upstream_gene_variant LINC-JP 11 77918371 77918371 single base substitution T A exon_variant LINC-JP 11 77918371 77918371 single base substitution T A intron_variant LINC-JP 11 77920855 77920855 single base substitution A G 3_prime_UTR_variant LINC-JP 11 77920855 77920855 single base substitution A G downstream_gene_variant LINC-JP 11 77920855 77920855 single base substitution A G exon_variant LINC-JP 11 77920855 77920855 single base substitution A G missense_variant T220A 658A>G LINC-JP 11 77920855 77920855 single base substitution A G missense_variant T238A 712A>G LINC-JP 11 77920855 77920855 single base substitution A G missense_variant T383A 1147A>G LINC-JP 11 77920855 77920855 single base substitution A G missense_variant T652A 1954A>G LINC-JP 11 77925273 77925273 single base substitution T G 3_prime_UTR_variant LINC-JP 11 77925273 77925273 single base substitution T G downstream_gene_variant LINC-JP 11 77925284 77925285 deletion of <=200bp GT - 3_prime_UTR_variant LINC-JP 11 77925284 77925285 deletion of <=200bp GT - downstream_gene_variant LINC-JP 11 77927315 77927315 single base substitution G T downstream_gene_variant LIRI-JP 11 77899101 77899101 insertion of <=200bp - TA upstream_gene_variant LIRI-JP 11 77902010 77902010 single base substitution G A intron_variant LIRI-JP 11 77903435 77903435 single base substitution T C intron_variant LIRI-JP 11 77903435 77903435 single base substitution T C upstream_gene_variant LIRI-JP 11 77905141 77905141 single base substitution A T intron_variant LIRI-JP 11 77905141 77905141 single base substitution A T upstream_gene_variant LIRI-JP 11 77905921 77905921 single base substitution T G intron_variant LIRI-JP 11 77905921 77905921 single base substitution T G upstream_gene_variant LIRI-JP 11 77911098 77911098 single base substitution T A intron_variant LIRI-JP 11 77913938 77913938 single base substitution G A intron_variant LIRI-JP 11 77913938 77913938 single base substitution G A upstream_gene_variant LIRI-JP 11 77915595 77915595 single base substitution G A intron_variant LIRI-JP 11 77915595 77915595 single base substitution G A upstream_gene_variant LIRI-JP 11 77915718 77915718 single base substitution A G intron_variant LIRI-JP 11 77915718 77915718 single base substitution A G upstream_gene_variant LIRI-JP 11 77917493 77917493 single base substitution A G intron_variant LIRI-JP 11 77917493 77917493 single base substitution A G upstream_gene_variant LIRI-JP 11 77918552 77918552 single base substitution G C exon_variant LIRI-JP 11 77918552 77918552 single base substitution G C intron_variant LIRI-JP 11 77922391 77922391 single base substitution G T downstream_gene_variant LIRI-JP 11 77922391 77922391 single base substitution G T intron_variant LIRI-JP 11 77923183 77923183 single base substitution G A downstream_gene_variant LIRI-JP 11 77923183 77923183 single base substitution G A intron_variant LIRI-JP 11 77923390 77923390 single base substitution A G downstream_gene_variant LIRI-JP 11 77923390 77923390 single base substitution A G intron_variant LIRI-JP 11 77925759 77925759 single base substitution A C downstream_gene_variant LIRI-JP 11 77925930 77925933 deletion of <=200bp ACTT - downstream_gene_variant LIRI-JP 11 77926094 77926094 single base substitution G C downstream_gene_variant LIRI-JP 11 77926401 77926401 single base substitution T C downstream_gene_variant LIRI-JP 11 77927829 77927829 single base substitution A G downstream_gene_variant LUSC-KR 11 77902468 77902468 single base substitution G T intron_variant LUSC-KR 11 77908586 77908586 single base substitution G A intron_variant LUSC-KR 11 77908586 77908586 single base substitution G A upstream_gene_variant LUSC-KR 11 77909235 77909235 single base substitution T A intron_variant LUSC-KR 11 77909235 77909235 single base substitution T A upstream_gene_variant LUSC-KR 11 77909759 77909759 single base substitution C G intron_variant LUSC-KR 11 77909759 77909759 single base substitution C G upstream_gene_variant LUSC-KR 11 77915083 77915083 single base substitution C T intron_variant LUSC-KR 11 77915083 77915083 single base substitution C T upstream_gene_variant LUSC-KR 11 77916293 77916293 single base substitution G T intron_variant LUSC-KR 11 77916293 77916293 single base substitution G T upstream_gene_variant LUSC-KR 11 77920895 77920895 single base substitution A T 3_prime_UTR_variant LUSC-KR 11 77920895 77920895 single base substitution A T downstream_gene_variant LUSC-KR 11 77920895 77920895 single base substitution A T exon_variant LUSC-KR 11 77920895 77920895 single base substitution A T missense_variant K233M 698A>T LUSC-KR 11 77920895 77920895 single base substitution A T missense_variant K251M 752A>T LUSC-KR 11 77920895 77920895 single base substitution A T missense_variant K396M 1187A>T LUSC-KR 11 77920895 77920895 single base substitution A T missense_variant K665M 1994A>T LUSC-KR 11 77927121 77927121 single base substitution C A downstream_gene_variant LUSC-KR 11 77930345 77930345 single base substitution T C downstream_gene_variant LUSC-US 11 77907956 77907956 single base substitution C T 5_prime_UTR_variant LUSC-US 11 77907956 77907956 single base substitution C T exon_variant LUSC-US 11 77907956 77907956 single base substitution C T intron_variant LUSC-US 11 77907956 77907956 single base substitution C T missense_variant S222F 665C>T LUSC-US 11 77907956 77907956 single base substitution C T upstream_gene_variant LUSC-US 11 77920699 77920699 single base substitution T G 3_prime_UTR_variant LUSC-US 11 77920699 77920699 single base substitution T G downstream_gene_variant LUSC-US 11 77920699 77920699 single base substitution T G exon_variant LUSC-US 11 77920699 77920699 single base substitution T G missense_variant F168V 502T>G LUSC-US 11 77920699 77920699 single base substitution T G missense_variant F186V 556T>G LUSC-US 11 77920699 77920699 single base substitution T G missense_variant F331V 991T>G LUSC-US 11 77920699 77920699 single base substitution T G missense_variant F600V 1798T>G LUSC-US 11 77921353 77921353 single base substitution A T 3_prime_UTR_variant LUSC-US 11 77921353 77921353 single base substitution A T downstream_gene_variant LUSC-US 11 77921353 77921353 single base substitution A T exon_variant LUSC-US 11 77921353 77921353 single base substitution A T missense_variant M386L 1156A>T LUSC-US 11 77921353 77921353 single base substitution A T missense_variant M404L 1210A>T LUSC-US 11 77921353 77921353 single base substitution A T missense_variant M549L 1645A>T LUSC-US 11 77921353 77921353 single base substitution A T missense_variant M818L 2452A>T MALY-DE 11 77911362 77911362 single base substitution G T intron_variant MALY-DE 11 77911812 77911812 single base substitution G C 3_prime_UTR_variant MALY-DE 11 77911812 77911812 single base substitution G C 5_prime_UTR_variant MALY-DE 11 77911812 77911812 single base substitution G C intron_variant MALY-DE 11 77911812 77911812 single base substitution G C synonymous_variant P116P 348G>C MALY-DE 11 77911812 77911812 single base substitution G C synonymous_variant P141P 423G>C MALY-DE 11 77911812 77911812 single base substitution G C synonymous_variant P385P 1155G>C MALY-DE 11 77919580 77919580 single base substitution G A intron_variant MALY-DE 11 77924284 77924284 single base substitution G A downstream_gene_variant MALY-DE 11 77924284 77924284 single base substitution G A intron_variant MALY-DE 11 77928426 77928426 single base substitution G A downstream_gene_variant MELA-AU 11 77894931 77894931 single base substitution T G upstream_gene_variant MELA-AU 11 77895319 77895319 single base substitution A G upstream_gene_variant MELA-AU 11 77895807 77895807 single base substitution T C upstream_gene_variant MELA-AU 11 77895811 77895811 single base substitution C T upstream_gene_variant MELA-AU 11 77895906 77895906 single base substitution C T upstream_gene_variant MELA-AU 11 77896591 77896591 single base substitution G A upstream_gene_variant MELA-AU 11 77896994 77896994 single base substitution C T upstream_gene_variant MELA-AU 11 77897565 77897565 single base substitution G A upstream_gene_variant MELA-AU 11 77897581 77897581 single base substitution G T upstream_gene_variant MELA-AU 11 77898021 77898021 single base substitution C T upstream_gene_variant MELA-AU 11 77898521 77898521 single base substitution A G upstream_gene_variant MELA-AU 11 77898615 77898615 single base substitution G A upstream_gene_variant MELA-AU 11 77898798 77898799 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 77898804 77898804 single base substitution G A upstream_gene_variant MELA-AU 11 77899508 77899508 single base substitution G A upstream_gene_variant MELA-AU 11 77899521 77899521 single base substitution G A upstream_gene_variant MELA-AU 11 77899788 77899788 single base substitution G A upstream_gene_variant MELA-AU 11 77899804 77899804 single base substitution G A upstream_gene_variant MELA-AU 11 77899838 77899838 single base substitution C T upstream_gene_variant MELA-AU 11 77899908 77899908 single base substitution C T 5_prime_UTR_variant MELA-AU 11 77899908 77899908 single base substitution C T exon_variant MELA-AU 11 77899908 77899908 single base substitution C T upstream_gene_variant MELA-AU 11 77900238 77900239 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 77900897 77900912 deletion of <=200bp TGGCCCAGACATGGGC - intron_variant MELA-AU 11 77901574 77901575 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 77901930 77901930 single base substitution G A intron_variant MELA-AU 11 77901949 77901949 single base substitution C T intron_variant MELA-AU 11 77902212 77902212 single base substitution T C intron_variant MELA-AU 11 77902416 77902416 single base substitution G C intron_variant MELA-AU 11 77902688 77902688 single base substitution C T intron_variant MELA-AU 11 77903264 77903264 single base substitution C T intron_variant MELA-AU 11 77903264 77903264 single base substitution C T upstream_gene_variant MELA-AU 11 77903320 77903320 single base substitution C T intron_variant MELA-AU 11 77903320 77903320 single base substitution C T upstream_gene_variant MELA-AU 11 77903327 77903327 single base substitution C T intron_variant MELA-AU 11 77903327 77903327 single base substitution C T upstream_gene_variant MELA-AU 11 77903379 77903379 single base substitution C T intron_variant MELA-AU 11 77903379 77903379 single base substitution C T upstream_gene_variant MELA-AU 11 77903465 77903465 single base substitution C T intron_variant MELA-AU 11 77903465 77903465 single base substitution C T upstream_gene_variant MELA-AU 11 77904142 77904143 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 11 77904142 77904143 multiple base substitution (>=2bp and <=200bp) GG AT upstream_gene_variant MELA-AU 11 77904240 77904240 single base substitution T G intron_variant MELA-AU 11 77904240 77904240 single base substitution T G upstream_gene_variant MELA-AU 11 77904254 77904254 single base substitution T A intron_variant MELA-AU 11 77904254 77904254 single base substitution T A upstream_gene_variant MELA-AU 11 77904300 77904300 single base substitution C G intron_variant MELA-AU 11 77904300 77904300 single base substitution C G upstream_gene_variant MELA-AU 11 77904817 77904817 single base substitution G A intron_variant MELA-AU 11 77904817 77904817 single base substitution G A upstream_gene_variant MELA-AU 11 77906936 77906936 single base substitution C T intron_variant MELA-AU 11 77906936 77906936 single base substitution C T upstream_gene_variant MELA-AU 11 77907925 77907925 single base substitution C T 5_prime_UTR_variant MELA-AU 11 77907925 77907925 single base substitution C T exon_variant MELA-AU 11 77907925 77907925 single base substitution C T intron_variant MELA-AU 11 77907925 77907925 single base substitution C T missense_variant P212S 634C>T MELA-AU 11 77907925 77907925 single base substitution C T upstream_gene_variant MELA-AU 11 77907996 77907996 single base substitution A G intron_variant MELA-AU 11 77907996 77907996 single base substitution A G upstream_gene_variant MELA-AU 11 77908049 77908049 single base substitution G A intron_variant MELA-AU 11 77908049 77908049 single base substitution G A upstream_gene_variant MELA-AU 11 77908502 77908502 single base substitution G A intron_variant MELA-AU 11 77908502 77908502 single base substitution G A upstream_gene_variant MELA-AU 11 77908712 77908712 single base substitution C T intron_variant MELA-AU 11 77908712 77908712 single base substitution C T upstream_gene_variant MELA-AU 11 77908805 77908805 single base substitution T A intron_variant MELA-AU 11 77908805 77908805 single base substitution T A upstream_gene_variant MELA-AU 11 77908949 77908950 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 77908949 77908950 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 77909418 77909418 single base substitution G T intron_variant MELA-AU 11 77909418 77909418 single base substitution G T upstream_gene_variant MELA-AU 11 77909597 77909597 single base substitution C T intron_variant MELA-AU 11 77909597 77909597 single base substitution C T upstream_gene_variant MELA-AU 11 77909613 77909613 single base substitution C T intron_variant MELA-AU 11 77909613 77909613 single base substitution C T upstream_gene_variant MELA-AU 11 77910224 77910224 single base substitution C T 5_prime_UTR_variant MELA-AU 11 77910224 77910224 single base substitution C T intron_variant MELA-AU 11 77910423 77910423 single base substitution C T 5_prime_UTR_variant MELA-AU 11 77910423 77910423 single base substitution C T intron_variant MELA-AU 11 77910876 77910876 single base substitution C T intron_variant MELA-AU 11 77911033 77911033 single base substitution C T intron_variant MELA-AU 11 77911347 77911347 single base substitution A G intron_variant MELA-AU 11 77911803 77911803 single base substitution C T 3_prime_UTR_variant MELA-AU 11 77911803 77911803 single base substitution C T 5_prime_UTR_variant MELA-AU 11 77911803 77911803 single base substitution C T intron_variant MELA-AU 11 77911803 77911803 single base substitution C T synonymous_variant F113F 339C>T MELA-AU 11 77911803 77911803 single base substitution C T synonymous_variant F138F 414C>T MELA-AU 11 77911803 77911803 single base substitution C T synonymous_variant F382F 1146C>T MELA-AU 11 77913542 77913542 single base substitution C T intron_variant MELA-AU 11 77913542 77913542 single base substitution C T upstream_gene_variant MELA-AU 11 77913713 77913713 single base substitution A T intron_variant MELA-AU 11 77913713 77913713 single base substitution A T upstream_gene_variant MELA-AU 11 77913832 77913832 single base substitution T C intron_variant MELA-AU 11 77913832 77913832 single base substitution T C upstream_gene_variant MELA-AU 11 77914797 77914797 single base substitution C T intron_variant MELA-AU 11 77914797 77914797 single base substitution C T upstream_gene_variant MELA-AU 11 77915276 77915276 single base substitution T C intron_variant MELA-AU 11 77915276 77915276 single base substitution T C upstream_gene_variant MELA-AU 11 77915455 77915455 single base substitution G A intron_variant MELA-AU 11 77915455 77915455 single base substitution G A upstream_gene_variant MELA-AU 11 77915700 77915700 single base substitution G A intron_variant MELA-AU 11 77915700 77915700 single base substitution G A upstream_gene_variant MELA-AU 11 77916082 77916082 single base substitution G A intron_variant MELA-AU 11 77916082 77916082 single base substitution G A upstream_gene_variant MELA-AU 11 77918066 77918066 single base substitution C T intron_variant MELA-AU 11 77918066 77918066 single base substitution C T upstream_gene_variant MELA-AU 11 77918258 77918258 single base substitution C T intron_variant MELA-AU 11 77918258 77918258 single base substitution C T upstream_gene_variant MELA-AU 11 77918471 77918471 single base substitution T A exon_variant MELA-AU 11 77918471 77918471 single base substitution T A intron_variant MELA-AU 11 77918872 77918872 single base substitution C T intron_variant MELA-AU 11 77918941 77918941 single base substitution C T intron_variant MELA-AU 11 77919292 77919293 deletion of <=200bp TA - intron_variant MELA-AU 11 77919513 77919513 single base substitution C T intron_variant MELA-AU 11 77919704 77919704 single base substitution C T intron_variant MELA-AU 11 77920567 77920567 deletion of <=200bp G - 3_prime_UTR_variant MELA-AU 11 77920567 77920567 deletion of <=200bp G - downstream_gene_variant MELA-AU 11 77920567 77920567 deletion of <=200bp G - exon_variant MELA-AU 11 77920567 77920567 deletion of <=200bp G - frameshift_variant E124 MELA-AU 11 77920567 77920567 deletion of <=200bp G - frameshift_variant E142 MELA-AU 11 77920567 77920567 deletion of <=200bp G - frameshift_variant E287 MELA-AU 11 77920567 77920567 deletion of <=200bp G - frameshift_variant E556 MELA-AU 11 77921475 77921476 multiple base substitution (>=2bp and <=200bp) GG AT 3_prime_UTR_variant MELA-AU 11 77921475 77921476 multiple base substitution (>=2bp and <=200bp) GG AT downstream_gene_variant MELA-AU 11 77921475 77921476 multiple base substitution (>=2bp and <=200bp) GG AT exon_variant MELA-AU 11 77921475 77921476 multiple base substitution (>=2bp and <=200bp) GG AT stop_gained SE426S* MELA-AU 11 77921475 77921476 multiple base substitution (>=2bp and <=200bp) GG AT stop_gained SE444S* MELA-AU 11 77921475 77921476 multiple base substitution (>=2bp and <=200bp) GG AT stop_gained SE589S* MELA-AU 11 77921475 77921476 multiple base substitution (>=2bp and <=200bp) GG AT stop_gained SE858S* MELA-AU 11 77922300 77922301 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 77922300 77922301 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 77922609 77922609 single base substitution C T downstream_gene_variant MELA-AU 11 77922609 77922609 single base substitution C T intron_variant MELA-AU 11 77924441 77924442 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 77924441 77924442 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 77924815 77924815 single base substitution C T 3_prime_UTR_variant MELA-AU 11 77924815 77924815 single base substitution C T downstream_gene_variant MELA-AU 11 77924815 77924815 single base substitution C T exon_variant MELA-AU 11 77924815 77924815 single base substitution C T missense_variant P1005S 3013C>T MELA-AU 11 77924815 77924815 single base substitution C T missense_variant P573S 1717C>T MELA-AU 11 77924815 77924815 single base substitution C T missense_variant P591S 1771C>T MELA-AU 11 77924815 77924815 single base substitution C T missense_variant P736S 2206C>T MELA-AU 11 77927241 77927241 single base substitution C A downstream_gene_variant MELA-AU 11 77930161 77930161 single base substitution G A downstream_gene_variant MELA-AU 11 77930379 77930379 single base substitution G A downstream_gene_variant MELA-AU 11 77930729 77930729 single base substitution C T downstream_gene_variant ORCA-IN 11 77907303 77907303 single base substitution C T intron_variant ORCA-IN 11 77907303 77907303 single base substitution C T synonymous_variant I4I 12C>T ORCA-IN 11 77907303 77907303 single base substitution C T upstream_gene_variant ORCA-IN 11 77911968 77911968 single base substitution C A intron_variant ORCA-IN 11 77920724 77920724 single base substitution G A 3_prime_UTR_variant ORCA-IN 11 77920724 77920724 single base substitution G A downstream_gene_variant ORCA-IN 11 77920724 77920724 single base substitution G A exon_variant ORCA-IN 11 77920724 77920724 single base substitution G A missense_variant R176H 527G>A ORCA-IN 11 77920724 77920724 single base substitution G A missense_variant R194H 581G>A ORCA-IN 11 77920724 77920724 single base substitution G A missense_variant R339H 1016G>A ORCA-IN 11 77920724 77920724 single base substitution G A missense_variant R608H 1823G>A ORCA-IN 11 77930004 77930005 deletion of <=200bp AG - downstream_gene_variant OV-AU 11 77897735 77897735 single base substitution C T upstream_gene_variant OV-AU 11 77902215 77902215 single base substitution A C intron_variant OV-AU 11 77905137 77905137 single base substitution G C intron_variant OV-AU 11 77905137 77905137 single base substitution G C upstream_gene_variant OV-AU 11 77905321 77905321 single base substitution C T intron_variant OV-AU 11 77905321 77905321 single base substitution C T upstream_gene_variant OV-AU 11 77906525 77906525 single base substitution C A intron_variant OV-AU 11 77906525 77906525 single base substitution C A upstream_gene_variant OV-AU 11 77918004 77918004 single base substitution G T intron_variant OV-AU 11 77918004 77918004 single base substitution G T upstream_gene_variant OV-AU 11 77919747 77919747 single base substitution G A intron_variant OV-AU 11 77921771 77921773 deletion of <=200bp ACA - 3_prime_UTR_variant OV-AU 11 77921771 77921773 deletion of <=200bp ACA - downstream_gene_variant OV-AU 11 77921771 77921773 deletion of <=200bp ACA - exon_variant OV-AU 11 77921771 77921773 deletion of <=200bp ACA - inframe_deletion DN525D OV-AU 11 77921771 77921773 deletion of <=200bp ACA - inframe_deletion DN543D OV-AU 11 77921771 77921773 deletion of <=200bp ACA - inframe_deletion DN688D OV-AU 11 77921771 77921773 deletion of <=200bp ACA - inframe_deletion DN957D OV-AU 11 77924124 77924124 single base substitution G A downstream_gene_variant OV-AU 11 77924124 77924124 single base substitution G A intron_variant OV-AU 11 77928925 77928925 single base substitution G T downstream_gene_variant OV-US 11 77917031 77917031 single base substitution C G 3_prime_UTR_variant OV-US 11 77917031 77917031 single base substitution C G intron_variant OV-US 11 77917031 77917031 single base substitution C G missense_variant A32G 95C>G OV-US 11 77917031 77917031 single base substitution C G synonymous_variant G15G 45C>G OV-US 11 77917031 77917031 single base substitution C G synonymous_variant G178G 534C>G OV-US 11 77917031 77917031 single base substitution C G synonymous_variant G203G 609C>G OV-US 11 77917031 77917031 single base substitution C G synonymous_variant G447G 1341C>G OV-US 11 77917031 77917031 single base substitution C G upstream_gene_variant PACA-AU 11 77895826 77895826 single base substitution C T upstream_gene_variant PACA-AU 11 77899957 77899957 single base substitution C T 5_prime_UTR_variant PACA-AU 11 77899957 77899957 single base substitution C T exon_variant PACA-AU 11 77901061 77901061 single base substitution C T intron_variant PACA-AU 11 77905179 77905179 single base substitution C G intron_variant PACA-AU 11 77905179 77905179 single base substitution C G upstream_gene_variant PACA-AU 11 77906850 77906850 single base substitution C T intron_variant PACA-AU 11 77906850 77906850 single base substitution C T upstream_gene_variant PACA-AU 11 77907007 77907007 single base substitution C G intron_variant PACA-AU 11 77907007 77907007 single base substitution C G upstream_gene_variant PACA-AU 11 77907241 77907241 single base substitution C T intron_variant PACA-AU 11 77907241 77907241 single base substitution C T upstream_gene_variant PACA-AU 11 77925340 77925340 single base substitution T G 3_prime_UTR_variant PACA-AU 11 77925340 77925340 single base substitution T G downstream_gene_variant PACA-AU 11 77928787 77928787 deletion of <=200bp G - downstream_gene_variant PACA-CA 11 77896666 77896666 single base substitution C A upstream_gene_variant PACA-CA 11 77898926 77898926 single base substitution T C upstream_gene_variant PACA-CA 11 77899793 77899793 single base substitution C T upstream_gene_variant PACA-CA 11 77900644 77900644 single base substitution C T intron_variant PACA-CA 11 77906504 77906504 single base substitution G A intron_variant PACA-CA 11 77906504 77906504 single base substitution G A upstream_gene_variant PACA-CA 11 77907520 77907520 single base substitution G A intron_variant PACA-CA 11 77907520 77907520 single base substitution G A missense_variant A77T 229G>A PACA-CA 11 77907520 77907520 single base substitution G A upstream_gene_variant PACA-CA 11 77908218 77908218 single base substitution C T intron_variant PACA-CA 11 77908218 77908218 single base substitution C T upstream_gene_variant PACA-CA 11 77909891 77909891 single base substitution G C intron_variant PACA-CA 11 77909891 77909891 single base substitution G C upstream_gene_variant PACA-CA 11 77916912 77916912 single base substitution C T 3_prime_UTR_variant PACA-CA 11 77916912 77916912 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant PACA-CA 11 77916912 77916912 single base substitution C T intron_variant PACA-CA 11 77916912 77916912 single base substitution C T missense_variant R139C 415C>T PACA-CA 11 77916912 77916912 single base substitution C T missense_variant R164C 490C>T PACA-CA 11 77916912 77916912 single base substitution C T missense_variant R408C 1222C>T PACA-CA 11 77916912 77916912 single base substitution C T upstream_gene_variant PACA-CA 11 77918390 77918390 single base substitution T C exon_variant PACA-CA 11 77918390 77918390 single base substitution T C intron_variant PACA-CA 11 77919517 77919517 single base substitution G A intron_variant PACA-CA 11 77922043 77922043 single base substitution C G downstream_gene_variant PACA-CA 11 77922043 77922043 single base substitution C G intron_variant PACA-CA 11 77925285 77925285 insertion of <=200bp - G 3_prime_UTR_variant PACA-CA 11 77925285 77925285 insertion of <=200bp - G downstream_gene_variant PACA-CA 11 77927084 77927084 single base substitution T C downstream_gene_variant PACA-CA 11 77927443 77927443 deletion of <=200bp T - downstream_gene_variant PACA-CA 11 77928118 77928118 single base substitution A G downstream_gene_variant PACA-CA 11 77928280 77928280 single base substitution C T downstream_gene_variant PACA-CA 11 77929715 77929715 single base substitution C A downstream_gene_variant PAEN-IT 11 77906116 77906116 single base substitution C G intron_variant PAEN-IT 11 77906116 77906116 single base substitution C G upstream_gene_variant PBCA-DE 11 77895376 77895379 deletion of <=200bp TATT - upstream_gene_variant PBCA-DE 11 77897376 77897376 insertion of <=200bp - CC upstream_gene_variant PBCA-DE 11 77901048 77901048 single base substitution G A intron_variant PBCA-DE 11 77916764 77916764 insertion of <=200bp - G intron_variant PBCA-DE 11 77916764 77916764 insertion of <=200bp - G upstream_gene_variant PBCA-DE 11 77919657 77919661 deletion of <=200bp GAAGA - intron_variant PRAD-CA 11 77896448 77896448 single base substitution G A upstream_gene_variant PRAD-CA 11 77899805 77899805 single base substitution A T upstream_gene_variant PRAD-UK 11 77908296 77908296 deletion of <=200bp T - intron_variant PRAD-UK 11 77908296 77908296 deletion of <=200bp T - upstream_gene_variant PRAD-UK 11 77918345 77918345 single base substitution G T exon_variant PRAD-UK 11 77918345 77918345 single base substitution G T intron_variant PRAD-UK 11 77918921 77918921 single base substitution C T intron_variant PRAD-US 11 77911274 77911274 single base substitution C T 3_prime_UTR_variant PRAD-US 11 77911274 77911274 single base substitution C T 5_prime_UTR_variant PRAD-US 11 77911274 77911274 single base substitution C T intron_variant PRAD-US 11 77911274 77911274 single base substitution C T synonymous_variant F100F 300C>T PRAD-US 11 77911274 77911274 single base substitution C T synonymous_variant F344F 1032C>T PRAD-US 11 77911274 77911274 single base substitution C T synonymous_variant F75F 225C>T PRAD-US 11 77924826 77924826 single base substitution C T 3_prime_UTR_variant PRAD-US 11 77924826 77924826 single base substitution C T downstream_gene_variant PRAD-US 11 77924826 77924826 single base substitution C T exon_variant PRAD-US 11 77924826 77924826 single base substitution C T synonymous_variant G1008G 3024C>T PRAD-US 11 77924826 77924826 single base substitution C T synonymous_variant G576G 1728C>T PRAD-US 11 77924826 77924826 single base substitution C T synonymous_variant G594G 1782C>T PRAD-US 11 77924826 77924826 single base substitution C T synonymous_variant G739G 2217C>T PRAD-US 11 77924841 77924841 single base substitution C G 3_prime_UTR_variant PRAD-US 11 77924841 77924841 single base substitution C G downstream_gene_variant PRAD-US 11 77924841 77924841 single base substitution C G exon_variant PRAD-US 11 77924841 77924841 single base substitution C G missense_variant F1013L 3039C>G PRAD-US 11 77924841 77924841 single base substitution C G missense_variant F581L 1743C>G PRAD-US 11 77924841 77924841 single base substitution C G missense_variant F599L 1797C>G PRAD-US 11 77924841 77924841 single base substitution C G missense_variant F744L 2232C>G PRAD-US 11 77930359 77930359 single base substitution C T downstream_gene_variant READ-US 11 77919947 77919947 single base substitution G A 3_prime_UTR_variant READ-US 11 77919947 77919947 single base substitution G A exon_variant READ-US 11 77919947 77919947 single base substitution G A intron_variant READ-US 11 77919947 77919947 single base substitution G A synonymous_variant T241T 723G>A READ-US 11 77919947 77919947 single base substitution G A synonymous_variant T266T 798G>A READ-US 11 77919947 77919947 single base substitution G A synonymous_variant T510T 1530G>A READ-US 11 77919947 77919947 single base substitution G A synonymous_variant T78T 234G>A READ-US 11 77919947 77919947 single base substitution G A synonymous_variant T96T 288G>A RECA-EU 11 77898977 77898977 single base substitution C T upstream_gene_variant RECA-EU 11 77904559 77904559 single base substitution A C intron_variant RECA-EU 11 77904559 77904559 single base substitution A C upstream_gene_variant RECA-EU 11 77906574 77906574 single base substitution T G intron_variant RECA-EU 11 77906574 77906574 single base substitution T G upstream_gene_variant RECA-EU 11 77917587 77917587 single base substitution G A intron_variant RECA-EU 11 77917587 77917587 single base substitution G A upstream_gene_variant RECA-EU 11 77921842 77921842 single base substitution G A downstream_gene_variant RECA-EU 11 77921842 77921842 single base substitution G A intron_variant RECA-EU 11 77929805 77929805 single base substitution G A downstream_gene_variant SKCA-BR 11 77897338 77897338 single base substitution G A upstream_gene_variant SKCA-BR 11 77899722 77899722 single base substitution T G upstream_gene_variant SKCA-BR 11 77899903 77899903 single base substitution T G 5_prime_UTR_variant SKCA-BR 11 77899903 77899903 single base substitution T G exon_variant SKCA-BR 11 77899903 77899903 single base substitution T G upstream_gene_variant SKCA-BR 11 77899927 77899927 single base substitution A C 5_prime_UTR_variant SKCA-BR 11 77899927 77899927 single base substitution A C exon_variant SKCA-BR 11 77899927 77899927 single base substitution A C upstream_gene_variant SKCA-BR 11 77900028 77900028 single base substitution T G 5_prime_UTR_variant SKCA-BR 11 77900028 77900028 single base substitution T G exon_variant SKCA-BR 11 77903996 77903996 single base substitution C T intron_variant SKCA-BR 11 77903996 77903996 single base substitution C T upstream_gene_variant SKCA-BR 11 77907153 77907153 single base substitution C T intron_variant SKCA-BR 11 77907153 77907153 single base substitution C T upstream_gene_variant SKCA-BR 11 77908275 77908275 single base substitution C G intron_variant SKCA-BR 11 77908275 77908275 single base substitution C G upstream_gene_variant SKCA-BR 11 77916553 77916553 single base substitution C T intron_variant SKCA-BR 11 77916553 77916553 single base substitution C T upstream_gene_variant SKCA-BR 11 77916860 77916860 single base substitution C T intron_variant SKCA-BR 11 77916860 77916860 single base substitution C T upstream_gene_variant SKCA-BR 11 77916861 77916861 single base substitution C T intron_variant SKCA-BR 11 77916861 77916861 single base substitution C T upstream_gene_variant SKCA-BR 11 77920822 77920822 single base substitution C G 3_prime_UTR_variant SKCA-BR 11 77920822 77920822 single base substitution C G downstream_gene_variant SKCA-BR 11 77920822 77920822 single base substitution C G exon_variant SKCA-BR 11 77920822 77920822 single base substitution C G missense_variant R209G 625C>G SKCA-BR 11 77920822 77920822 single base substitution C G missense_variant R227G 679C>G SKCA-BR 11 77920822 77920822 single base substitution C G missense_variant R372G 1114C>G SKCA-BR 11 77920822 77920822 single base substitution C G missense_variant R641G 1921C>G SKCA-BR 11 77921387 77921387 single base substitution T C 3_prime_UTR_variant SKCA-BR 11 77921387 77921387 single base substitution T C downstream_gene_variant SKCA-BR 11 77921387 77921387 single base substitution T C exon_variant SKCA-BR 11 77921387 77921387 single base substitution T C missense_variant I397T 1190T>C SKCA-BR 11 77921387 77921387 single base substitution T C missense_variant I415T 1244T>C SKCA-BR 11 77921387 77921387 single base substitution T C missense_variant I560T 1679T>C SKCA-BR 11 77921387 77921387 single base substitution T C missense_variant I829T 2486T>C SKCA-BR 11 77922154 77922154 single base substitution A C downstream_gene_variant SKCA-BR 11 77922154 77922154 single base substitution A C intron_variant SKCA-BR 11 77923367 77923367 single base substitution A T downstream_gene_variant SKCA-BR 11 77923367 77923367 single base substitution A T intron_variant SKCA-BR 11 77925285 77925285 single base substitution T G 3_prime_UTR_variant SKCA-BR 11 77925285 77925285 single base substitution T G downstream_gene_variant SKCA-BR 11 77925436 77925436 single base substitution C G 3_prime_UTR_variant SKCA-BR 11 77925436 77925436 single base substitution C G downstream_gene_variant SKCM-US 11 77910659 77910659 single base substitution C T intron_variant SKCM-US 11 77910659 77910659 single base substitution C T synonymous_variant S275S 825C>T SKCM-US 11 77910659 77910659 single base substitution C T synonymous_variant S31S 93C>T SKCM-US 11 77910659 77910659 single base substitution C T synonymous_variant S6S 18C>T SKCM-US 11 77920580 77920580 single base substitution C T 3_prime_UTR_variant SKCM-US 11 77920580 77920580 single base substitution C T downstream_gene_variant SKCM-US 11 77920580 77920580 single base substitution C T exon_variant SKCM-US 11 77920580 77920580 single base substitution C T missense_variant A128V 383C>T SKCM-US 11 77920580 77920580 single base substitution C T missense_variant A146V 437C>T SKCM-US 11 77920580 77920580 single base substitution C T missense_variant A291V 872C>T SKCM-US 11 77920580 77920580 single base substitution C T missense_variant A560V 1679C>T SKCM-US 11 77921051 77921053 deletion of <=200bp AGA - 3_prime_UTR_variant SKCM-US 11 77921051 77921053 deletion of <=200bp AGA - downstream_gene_variant SKCM-US 11 77921051 77921053 deletion of <=200bp AGA - exon_variant SKCM-US 11 77921051 77921053 deletion of <=200bp AGA - inframe_deletion EK285E SKCM-US 11 77921051 77921053 deletion of <=200bp AGA - inframe_deletion EK303E SKCM-US 11 77921051 77921053 deletion of <=200bp AGA - inframe_deletion EK448E SKCM-US 11 77921051 77921053 deletion of <=200bp AGA - inframe_deletion EK717E STAD-US 11 77907363 77907363 single base substitution C T intron_variant STAD-US 11 77907363 77907363 single base substitution C T synonymous_variant R24R 72C>T STAD-US 11 77907363 77907363 single base substitution C T upstream_gene_variant STAD-US 11 77907439 77907439 single base substitution G A intron_variant STAD-US 11 77907439 77907439 single base substitution G A missense_variant V50M 148G>A STAD-US 11 77907439 77907439 single base substitution G A upstream_gene_variant STAD-US 11 77911746 77911746 single base substitution G A 3_prime_UTR_variant STAD-US 11 77911746 77911746 single base substitution G A 5_prime_UTR_variant STAD-US 11 77911746 77911746 single base substitution G A intron_variant STAD-US 11 77911746 77911746 single base substitution G A synonymous_variant S119S 357G>A STAD-US 11 77911746 77911746 single base substitution G A synonymous_variant S363S 1089G>A STAD-US 11 77911746 77911746 single base substitution G A synonymous_variant S94S 282G>A STAD-US 11 77916960 77916960 single base substitution G A 3_prime_UTR_variant STAD-US 11 77916960 77916960 single base substitution G A 5_prime_UTR_variant STAD-US 11 77916960 77916960 single base substitution G A intron_variant STAD-US 11 77916960 77916960 single base substitution G A missense_variant E155K 463G>A STAD-US 11 77916960 77916960 single base substitution G A missense_variant E180K 538G>A STAD-US 11 77916960 77916960 single base substitution G A missense_variant E424K 1270G>A STAD-US 11 77916960 77916960 single base substitution G A synonymous_variant A8A 24G>A STAD-US 11 77916960 77916960 single base substitution G A upstream_gene_variant STAD-US 11 77920554 77920554 single base substitution G A 3_prime_UTR_variant STAD-US 11 77920554 77920554 single base substitution G A downstream_gene_variant STAD-US 11 77920554 77920554 single base substitution G A exon_variant STAD-US 11 77920554 77920554 single base substitution G A synonymous_variant S119S 357G>A STAD-US 11 77920554 77920554 single base substitution G A synonymous_variant S137S 411G>A STAD-US 11 77920554 77920554 single base substitution G A synonymous_variant S282S 846G>A STAD-US 11 77920554 77920554 single base substitution G A synonymous_variant S551S 1653G>A STAD-US 11 77920763 77920763 single base substitution T C 3_prime_UTR_variant STAD-US 11 77920763 77920763 single base substitution T C downstream_gene_variant STAD-US 11 77920763 77920763 single base substitution T C exon_variant STAD-US 11 77920763 77920763 single base substitution T C missense_variant I189T 566T>C STAD-US 11 77920763 77920763 single base substitution T C missense_variant I207T 620T>C STAD-US 11 77920763 77920763 single base substitution T C missense_variant I352T 1055T>C STAD-US 11 77920763 77920763 single base substitution T C missense_variant I621T 1862T>C STAD-US 11 77920856 77920856 insertion of <=200bp - C 3_prime_UTR_variant STAD-US 11 77920856 77920856 insertion of <=200bp - C downstream_gene_variant STAD-US 11 77920856 77920856 insertion of <=200bp - C exon_variant STAD-US 11 77920856 77920856 insertion of <=200bp - C frameshift_variant T220T? STAD-US 11 77920856 77920856 insertion of <=200bp - C frameshift_variant T238T? STAD-US 11 77920856 77920856 insertion of <=200bp - C frameshift_variant T383T? STAD-US 11 77920856 77920856 insertion of <=200bp - C frameshift_variant T652T? STAD-US 11 77921035 77921035 single base substitution G A 3_prime_UTR_variant STAD-US 11 77921035 77921035 single base substitution G A downstream_gene_variant STAD-US 11 77921035 77921035 single base substitution G A exon_variant STAD-US 11 77921035 77921035 single base substitution G A missense_variant V280M 838G>A STAD-US 11 77921035 77921035 single base substitution G A missense_variant V298M 892G>A STAD-US 11 77921035 77921035 single base substitution G A missense_variant V443M 1327G>A STAD-US 11 77921035 77921035 single base substitution G A missense_variant V712M 2134G>A STAD-US 11 77921181 77921181 single base substitution C T 3_prime_UTR_variant STAD-US 11 77921181 77921181 single base substitution C T downstream_gene_variant STAD-US 11 77921181 77921181 single base substitution C T exon_variant STAD-US 11 77921181 77921181 single base substitution C T synonymous_variant S328S 984C>T STAD-US 11 77921181 77921181 single base substitution C T synonymous_variant S346S 1038C>T STAD-US 11 77921181 77921181 single base substitution C T synonymous_variant S491S 1473C>T STAD-US 11 77921181 77921181 single base substitution C T synonymous_variant S760S 2280C>T STAD-US 11 77921303 77921303 single base substitution C A 3_prime_UTR_variant STAD-US 11 77921303 77921303 single base substitution C A downstream_gene_variant STAD-US 11 77921303 77921303 single base substitution C A exon_variant STAD-US 11 77921303 77921303 single base substitution C A missense_variant P369Q 1106C>A STAD-US 11 77921303 77921303 single base substitution C A missense_variant P387Q 1160C>A STAD-US 11 77921303 77921303 single base substitution C A missense_variant P532Q 1595C>A STAD-US 11 77921303 77921303 single base substitution C A missense_variant P801Q 2402C>A STAD-US 11 77921697 77921697 single base substitution G A 3_prime_UTR_variant STAD-US 11 77921697 77921697 single base substitution G A downstream_gene_variant STAD-US 11 77921697 77921697 single base substitution G A exon_variant STAD-US 11 77921697 77921697 single base substitution G A synonymous_variant E500E 1500G>A STAD-US 11 77921697 77921697 single base substitution G A synonymous_variant E518E 1554G>A STAD-US 11 77921697 77921697 single base substitution G A synonymous_variant E663E 1989G>A STAD-US 11 77921697 77921697 single base substitution G A synonymous_variant E932E 2796G>A STAD-US 11 77930333 77930333 single base substitution C A downstream_gene_variant THCA-SA 11 77917064 77917064 single base substitution C T 3_prime_UTR_variant THCA-SA 11 77917064 77917064 single base substitution C T intron_variant THCA-SA 11 77917064 77917064 single base substitution C T missense_variant P43L 128C>T THCA-SA 11 77917064 77917064 single base substitution C T synonymous_variant A189A 567C>T THCA-SA 11 77917064 77917064 single base substitution C T synonymous_variant A214A 642C>T THCA-SA 11 77917064 77917064 single base substitution C T synonymous_variant A26A 78C>T THCA-SA 11 77917064 77917064 single base substitution C T synonymous_variant A458A 1374C>T THCA-SA 11 77917064 77917064 single base substitution C T upstream_gene_variant UCEC-US 11 77907300 77907300 single base substitution G T intron_variant UCEC-US 11 77907300 77907300 single base substitution G T missense_variant K3N 9G>T UCEC-US 11 77907300 77907300 single base substitution G T upstream_gene_variant UCEC-US 11 77911266 77911266 single base substitution G A 3_prime_UTR_variant UCEC-US 11 77911266 77911266 single base substitution G A 5_prime_UTR_variant UCEC-US 11 77911266 77911266 single base substitution G A intron_variant UCEC-US 11 77911266 77911266 single base substitution G A missense_variant E342K 1024G>A UCEC-US 11 77911266 77911266 single base substitution G A missense_variant E73K 217G>A UCEC-US 11 77911266 77911266 single base substitution G A missense_variant E98K 292G>A UCEC-US 11 77911784 77911784 single base substitution T C 3_prime_UTR_variant UCEC-US 11 77911784 77911784 single base substitution T C 5_prime_UTR_variant UCEC-US 11 77911784 77911784 single base substitution T C intron_variant UCEC-US 11 77911784 77911784 single base substitution T C missense_variant L107P 320T>C UCEC-US 11 77911784 77911784 single base substitution T C missense_variant L132P 395T>C UCEC-US 11 77911784 77911784 single base substitution T C missense_variant L376P 1127T>C UCEC-US 11 77917010 77917010 single base substitution G T 3_prime_UTR_variant UCEC-US 11 77917010 77917010 single base substitution G T intron_variant UCEC-US 11 77917010 77917010 single base substitution G T missense_variant K171N 513G>T UCEC-US 11 77917010 77917010 single base substitution G T missense_variant K196N 588G>T UCEC-US 11 77917010 77917010 single base substitution G T missense_variant K440N 1320G>T UCEC-US 11 77917010 77917010 single base substitution G T missense_variant K8N 24G>T UCEC-US 11 77917010 77917010 single base substitution G T missense_variant R25I 74G>T UCEC-US 11 77917010 77917010 single base substitution G T upstream_gene_variant UCEC-US 11 77919935 77919935 single base substitution C T 3_prime_UTR_variant UCEC-US 11 77919935 77919935 single base substitution C T exon_variant UCEC-US 11 77919935 77919935 single base substitution C T intron_variant UCEC-US 11 77919935 77919935 single base substitution C T synonymous_variant S237S 711C>T UCEC-US 11 77919935 77919935 single base substitution C T synonymous_variant S262S 786C>T UCEC-US 11 77919935 77919935 single base substitution C T synonymous_variant S506S 1518C>T UCEC-US 11 77919935 77919935 single base substitution C T synonymous_variant S74S 222C>T UCEC-US 11 77919935 77919935 single base substitution C T synonymous_variant S92S 276C>T UCEC-US 11 77921047 77921047 single base substitution G A 3_prime_UTR_variant UCEC-US 11 77921047 77921047 single base substitution G A downstream_gene_variant UCEC-US 11 77921047 77921047 single base substitution G A exon_variant UCEC-US 11 77921047 77921047 single base substitution G A missense_variant E284K 850G>A UCEC-US 11 77921047 77921047 single base substitution G A missense_variant E302K 904G>A UCEC-US 11 77921047 77921047 single base substitution G A missense_variant E447K 1339G>A UCEC-US 11 77921047 77921047 single base substitution G A missense_variant E716K 2146G>A UCEC-US 11 77921120 77921120 single base substitution C T 3_prime_UTR_variant UCEC-US 11 77921120 77921120 single base substitution C T downstream_gene_variant UCEC-US 11 77921120 77921120 single base substitution C T exon_variant UCEC-US 11 77921120 77921120 single base substitution C T missense_variant T308I 923C>T UCEC-US 11 77921120 77921120 single base substitution C T missense_variant T326I 977C>T UCEC-US 11 77921120 77921120 single base substitution C T missense_variant T471I 1412C>T UCEC-US 11 77921120 77921120 single base substitution C T missense_variant T740I 2219C>T UCEC-US 11 77921488 77921488 single base substitution T C 3_prime_UTR_variant UCEC-US 11 77921488 77921488 single base substitution T C downstream_gene_variant UCEC-US 11 77921488 77921488 single base substitution T C exon_variant UCEC-US 11 77921488 77921488 single base substitution T C missense_variant Y431H 1291T>C UCEC-US 11 77921488 77921488 single base substitution T C missense_variant Y449H 1345T>C UCEC-US 11 77921488 77921488 single base substitution T C missense_variant Y594H 1780T>C UCEC-US 11 77921488 77921488 single base substitution T C missense_variant Y863H 2587T>C UCEC-US 11 77921626 77921626 single base substitution G C 3_prime_UTR_variant UCEC-US 11 77921626 77921626 single base substitution G C downstream_gene_variant UCEC-US 11 77921626 77921626 single base substitution G C exon_variant UCEC-US 11 77921626 77921626 single base substitution G C missense_variant V477L 1429G>C UCEC-US 11 77921626 77921626 single base substitution G C missense_variant V495L 1483G>C UCEC-US 11 77921626 77921626 single base substitution G C missense_variant V640L 1918G>C UCEC-US 11 77921626 77921626 single base substitution G C missense_variant V909L 2725G>C UCEC-US 11 77924770 77924770 single base substitution G T 3_prime_UTR_variant UCEC-US 11 77924770 77924770 single base substitution G T downstream_gene_variant UCEC-US 11 77924770 77924770 single base substitution G T exon_variant UCEC-US 11 77924770 77924770 single base substitution G T missense_variant D558Y 1672G>T UCEC-US 11 77924770 77924770 single base substitution G T missense_variant D576Y 1726G>T UCEC-US 11 77924770 77924770 single base substitution G T missense_variant D721Y 2161G>T UCEC-US 11 77924770 77924770 single base substitution G T missense_variant D990Y 2968G>T UCEC-US 11 77924787 77924787 single base substitution G T 3_prime_UTR_variant UCEC-US 11 77924787 77924787 single base substitution G T downstream_gene_variant UCEC-US 11 77924787 77924787 single base substitution G T exon_variant UCEC-US 11 77924787 77924787 single base substitution G T missense_variant E563D 1689G>T UCEC-US 11 77924787 77924787 single base substitution G T missense_variant E581D 1743G>T UCEC-US 11 77924787 77924787 single base substitution G T missense_variant E726D 2178G>T UCEC-US 11 77924787 77924787 single base substitution G T missense_variant E995D 2985G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 585270 COSM324222 c.1075G>T p.V359F Substitution - Missense 11:78200686-78200686 + SNU-C4 COSM1357161 c.1053delC p.M354fs*119 Deletion - Frameshift 11:78200664-78200664 + TCGA-AU-6004-01 COSM1357180 c.1222_1223insC p.T411fs*74 Insertion - Frameshift 11:78209809-78209810 + PDA_004 COSM3752757 c.1297A>G p.I433V Substitution - Missense 11:78209884-78209884 + Gp5D COSM4611889 c.1222_1223insCC p.T411fs*24 Insertion - Frameshift 11:78209809-78209810 + TCGA-E9-A2JS-01 COSM3810490 c.2501G>A p.R834H Substitution - Missense 11:78210356-78210356 + TCGA-DD-A3A7-01 COSM4916170 c.940C>A p.P314T Substitution - Missense 11:78209527-78209527 + TCGA-AA-3821-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-AU-6004-01 COSM1357169 c.1476A>G p.E492E Substitution - coding silent 11:78207614-78207614 + sysucc-882T COSM5446968 c.155G>T p.G52V Substitution - Missense 11:78196400-78196400 + TCGA-D7-8575-01 COSM4036923 c.2064G>A p.E688E Substitution - coding silent 11:78210651-78210651 + 3N09-VS-3T09 COSM4979160 c.2045G>A p.R682Q Substitution - Missense 11:78210632-78210632 + PAPNNX COSM5004840 c.2059C>T p.P687S Substitution - Missense 11:78210646-78210646 + 2492730 COSM5728848 c.1605C>T p.R535R Substitution - coding silent 11:78210192-78210192 + B66-Tumor COSM3931449 c.1785T>G p.G595G Substitution - coding silent 11:78210372-78210372 + Pat_30_A COSM5839656 c.1087_1089delCGC p.R366delR Deletion - In frame 11:78209674-78209676 + 671204 COSM1645115 c.828G>A p.W276* Substitution - Nonsense 11:78199616-78199616 + DLD1 COSM2019380 c.2439C>T p.F813F Substitution - coding silent 11:78210294-78210294 + CSCC-38-T COSM4469287 c.1591C>T p.R531W Substitution - Missense 11:78208962-78208962 + CAL27 COSM2019304 c.552C>T p.F184F Substitution - coding silent 11:78205928-78205928 + SC_9096 COSM5566916 c.2462G>A p.R821H Substitution - Missense 11:78210317-78210317 + TCGA-E9-A2JS-01 COSM3810491 c.1769G>A p.R590H Substitution - Missense 11:78210356-78210356 + Pat_40_A COSM5839657 c.2627C>T p.A876V Substitution - Missense 11:78210482-78210482 + TCGA-BR-6452-01 COSM4036921 c.1670C>A p.P557Q Substitution - Missense 11:78210257-78210257 + TCGA-BR-8680-01 COSM4036912 c.1653G>A p.S551S Substitution - coding silent 11:78209508-78209508 + TCGA-76-4925 COSM2157518 c.2728A>C p.T910P Substitution - Missense 11:78210583-78210583 + TCGA-BH-A18G-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + PT49 COSM5935819 c.1148C>T p.P383L Substitution - Missense 11:78209735-78209735 + T2197 COSM4739792 c.35A>T p.D12V Substitution - Missense 11:78198029-78198029 + LS411 COSM2019383 c.1780G>A p.A594T Substitution - Missense 11:78210367-78210367 + 671204 COSM1645116 c.96G>A p.W32* Substitution - Nonsense 11:78199616-78199616 + TCGA-BK-A0CB-01 COSM932261 c.786C>T p.S262S Substitution - coding silent 11:78208889-78208889 + H23 COSM1196397 c.1630C>G p.Q544E Substitution - Missense 11:78209485-78209485 + TCGA-D5-6530-01 COSM5162185 c.738T>C p.D246D Substitution - coding silent 11:78198000-78198000 + CSCC-29-T COSM4517063 c.2000_2001CC>TT p.S667F Substitution - Missense 11:78210587-78210588 + TCGA-HT-7475-01 COSM3967853 c.1240G>A p.G414R Substitution - Missense 11:78205884-78205884 + CSCC-31-T COSM4472170 c.1764C>T p.S588S Substitution - coding silent 11:78209619-78209619 + TCGA-AD-6964-01 COSM1357179 c.1954_1955insC p.T655fs*74 Insertion - Frameshift 11:78209809-78209810 + TCGA-AG-A002-01 COSM264616 c.1441A>T p.K481* Substitution - Nonsense 11:78210028-78210028 + TCGA-AP-A056-01 COSM932263 c.1414G>A p.E472K Substitution - Missense 11:78210001-78210001 + TCGA-EJ-5505-01 COSM1127629 c.1963A>C p.T655P Substitution - Missense 11:78209818-78209818 + ESCC_BICR_053T COSM5442061 c.1947C>G p.F649L Substitution - Missense 11:78210534-78210534 + CSCC-18-T COSM4472170 c.1764C>T p.S588S Substitution - coding silent 11:78209619-78209619 + PT35 COSM5913308 c.767C>T p.S256F Substitution - Missense 11:78208870-78208870 + PT37 COSM5920311 c.754-4C>T p.? Unknown 11:78208853-78208853 + TCGA-29-1761-01 COSM1322136 c.2472G>T p.L824L Substitution - coding silent 11:78210327-78210327 + TCGA-F4-6461-01 COSM5171314 c.595C>A p.L199M Substitution - Missense 11:78196840-78196840 + TCGA-D5-6930-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + SNUH_G76_S1 COSM4418550 c.1662G>T p.P554P Substitution - coding silent 11:78209517-78209517 + ESCC_BICR_053T COSM5442060 c.2679C>G p.F893L Substitution - Missense 11:78210534-78210534 + CSCC-11-T COSM4452571 c.1975A>T p.I659F Substitution - Missense 11:78209830-78209830 + TCGA-AN-A0AK-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-CK-5916-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-BT-A0S7-01 COSM415727 c.2217G>T p.P739P Substitution - coding silent 11:78213705-78213705 + TCGA-DK-A1A6-01 COSM1298649 c.147C>T p.Y49Y Substitution - coding silent 11:78196392-78196392 + TCGA-AG-A002-01 COSM264617 c.2173A>T p.K725* Substitution - Nonsense 11:78210028-78210028 + GCT01 COSM4413588 c.923C>T p.P308L Substitution - Missense 11:78209510-78209510 + SNU-C1 COSM2019399 c.2062G>C p.E688Q Substitution - Missense 11:78210649-78210649 + ESO06T COSM1171843 c.2458C>T p.R820C Substitution - Missense 11:78210313-78210313 + LUAD-B00416 COSM330846 c.390G>A p.A130A Substitution - coding silent 11:78200733-78200733 + SNU-175 COSM2019320 c.1530G>A p.T510T Substitution - coding silent 11:78208901-78208901 + PT52 COSM5940216 c.313C>T p.P105S Substitution - Missense 11:78200656-78200656 + TCGA-AM-5820-01 COSM3687661 c.1374C>T p.A458A Substitution - coding silent 11:78206018-78206018 + SNU-C2B COSM4651114 c.481C>T p.R161C Substitution - Missense 11:78196726-78196726 + SNUH_G15_S1 COSM3676322 c.550T>G p.F184V Substitution - Missense 11:78205926-78205926 + PTC-1C COSM3752756 c.2029A>G p.I677V Substitution - Missense 11:78209884-78209884 + S02256 COSM5681208 c.1150C>T p.P384S Substitution - Missense 11:78209737-78209737 + TCGA-AP-A0LG-01 COSM932264 c.2219C>T p.T740I Substitution - Missense 11:78210074-78210074 + SNUH_G15_S1 COSM3676321 c.1282T>G p.F428V Substitution - Missense 11:78205926-78205926 + TCGA-G4-6309-01 COSM1357187 c.3037T>G p.F1013V Substitution - Missense 11:78213793-78213793 + TCGA-BR-6452-01 COSM4036920 c.2402C>A p.P801Q Substitution - Missense 11:78210257-78210257 + TCGA-76-4925 COSM2157519 c.1996A>C p.T666P Substitution - Missense 11:78210583-78210583 + T3202 COSM4739794 c.320_321insC p.M110fs*39 Insertion - Frameshift 11:78200663-78200664 + TCGA-AZ-6601-01 COSM1357160 c.241G>A p.A81T Substitution - Missense 11:78200169-78200169 + KM12 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + C135 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-29-1761-01 COSM1322137 c.1740G>T p.L580L Substitution - coding silent 11:78210327-78210327 + Pat_41_B COSM5839651 c.1120G>A p.A374T Substitution - Missense 11:78200731-78200731 + TCGA-AM-5820-01 COSM330845 c.1122G>A p.A374A Substitution - coding silent 11:78200733-78200733 + CSCC-11-T COSM4532296 c.1871G>A p.R624Q Substitution - Missense 11:78209726-78209726 + TCGA-AG-A02N-01 COSM5074565 c.2157+1G>A p.? Unknown 11:78210745-78210745 + CSCC-31-T COSM4485424 c.2198C>T p.S733F Substitution - Missense 11:78213686-78213686 + sysucc-1163T COSM5458293 c.2130G>A p.E710E Substitution - coding silent 11:78209985-78209985 + HCC2998 COSM1676327 c.665G>A p.R222K Substitution - Missense 11:78207535-78207535 + GC_302T-GC_302N COSM4772755 c.83C>T p.A28V Substitution - Missense 11:78196328-78196328 + TCGA-24-1551-01 COSM80729 c.115C>T p.L39L Substitution - coding silent 11:78196360-78196360 + TCGA-J9-A52C-01 COSM4877122 c.3039C>G p.F1013L Substitution - Missense 11:78213795-78213795 + 1_RESISTANT COSM1720948 c.1775C>T p.A592V Substitution - Missense 11:78209630-78209630 + pfg122T COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + 80 COSM5012388 c.1261A>C p.K421Q Substitution - Missense 11:78209848-78209848 + CSCC-38-T COSM4469288 c.859C>T p.R287W Substitution - Missense 11:78208962-78208962 + TCGA-F4-6569-01 COSM1357185 c.2689C>T p.R897W Substitution - Missense 11:78210544-78210544 + 4_RESISTANT COSM1724693 c.1766_1767insC p.R590fs*13 Insertion - Frameshift 11:78210353-78210354 + TCGA-AZ-6598-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + pfg122T COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + CSCC-41-T COSM4516735 c.1506_1507CC>TT p.P503S Substitution - Missense 11:78210093-78210094 + TCGA-A2-A0T2-01 COSM1357179 c.1954_1955insC p.T655fs*74 Insertion - Frameshift 11:78209809-78209810 + 587338 COSM1232049 c.1072C>A p.P358T Substitution - Missense 11:78209659-78209659 + 587284 COSM1232052 c.2335C>T p.R779C Substitution - Missense 11:78210190-78210190 + SNUH_G76_S1 COSM4417721 c.2626G>C p.A876P Substitution - Missense 11:78210481-78210481 + TCGA-BR-8680-01 COSM264615 c.1089G>A p.S363S Substitution - coding silent 11:78200700-78200700 + TCGA-CH-5762-01 COSM1127631 c.1032C>T p.F344F Substitution - coding silent 11:78200228-78200228 + sysucc-1163T COSM5458294 c.1398G>A p.E466E Substitution - coding silent 11:78209985-78209985 + TCGA-CD-8535-01 COSM4036916 c.2134G>A p.V712M Substitution - Missense 11:78209989-78209989 + TCGA-76-4925-01 COSM2157519 c.1996A>C p.T666P Substitution - Missense 11:78210583-78210583 + TCGA-G2-A2EL-01 COSM1298656 c.2418C>T p.L806L Substitution - coding silent 11:78210273-78210273 + 587224 COSM1232044 c.2312C>A p.P771H Substitution - Missense 11:78210167-78210167 + 587278 COSM1232046 c.1847G>A p.R616H Substitution - Missense 11:78209702-78209702 + TCGA-AA-3663-01 COSM1357178 c.1135G>A p.A379T Substitution - Missense 11:78209722-78209722 + RKO COSM2019360 c.2154G>T p.K718N Substitution - Missense 11:78210009-78210009 + TCGA-AG-3726-01 COSM4739793 c.1052_1053insC p.M354fs*39 Insertion - Frameshift 11:78200663-78200664 + HCT116 COSM1357162 c.321delC p.M110fs*119 Deletion - Frameshift 11:78200664-78200664 + SNU-C2B COSM2019398 c.2794G>C p.E932Q Substitution - Missense 11:78210649-78210649 + TCGA-D1-A17D-01 COSM932270 c.2725G>C p.V909L Substitution - Missense 11:78210580-78210580 + TCGA-G4-6309-01 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + EGC15 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + S02256 COSM5681207 c.1882C>T p.P628S Substitution - Missense 11:78209737-78209737 + 3N38-VS-3T38 COSM2019287 c.963C>T p.I321I Substitution - coding silent 11:78200159-78200159 + TCGA-D1-A17D-01 COSM932271 c.1993G>C p.V665L Substitution - Missense 11:78210580-78210580 + SNU-C2B COSM2019339 c.1054_1055delCT p.L354fs*6 Deletion - Frameshift 11:78209641-78209642 + TCGA-EE-A2A2-06 COSM3453581 c.825C>T p.S275S Substitution - coding silent 11:78199613-78199613 + CSCC-7-T COSM4466483 c.1437C>T p.P479P Substitution - coding silent 11:78207575-78207575 + 587284 COSM1232053 c.1603C>T p.R535C Substitution - Missense 11:78210190-78210190 + HCT116 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + HCT8 COSM2019380 c.2439C>T p.F813F Substitution - coding silent 11:78210294-78210294 + SW48 COSM2019389 c.1895C>A p.A632D Substitution - Missense 11:78210482-78210482 + TCGA-HC-7745-01 COSM4392982 c.3024C>T p.G1008G Substitution - coding silent 11:78213780-78213780 + 587386 COSM1232054 c.1277C>T p.A426V Substitution - Missense 11:78205921-78205921 + SNUH_G15_S1 COSM3676323 c.1322T>A p.I441N Substitution - Missense 11:78205966-78205966 + TCGA-DK-A2I1-01 COSM1298653 c.783C>G p.L261L Substitution - coding silent 11:78208886-78208886 + SNUH_G76_S1 COSM4418551 c.930G>T p.P310P Substitution - coding silent 11:78209517-78209517 + TCGA-F4-6569-01 COSM1357186 c.1957C>T p.R653W Substitution - Missense 11:78210544-78210544 + NCI-H23 COSM1196397 c.1630C>G p.Q544E Substitution - Missense 11:78209485-78209485 + TCGA-76-4925-01 COSM2157518 c.2728A>C p.T910P Substitution - Missense 11:78210583-78210583 + PAPNNX COSM5004839 c.2791C>T p.P931S Substitution - Missense 11:78210646-78210646 + 587278 COSM1232047 c.1115G>A p.R372H Substitution - Missense 11:78209702-78209702 + TCGA-BH-A18G-01 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + 2246951 COSM4413588 c.923C>T p.P308L Substitution - Missense 11:78209510-78209510 + SNUH_G76_S1 COSM4417722 c.1894G>C p.A632P Substitution - Missense 11:78210481-78210481 + PTC-1C COSM3752757 c.1297A>G p.I433V Substitution - Missense 11:78209884-78209884 + RKO COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + SW620 COSM2019290 c.239G>T p.G80V Substitution - Missense 11:78200167-78200167 + Pat_30_A COSM5839655 c.1819_1821delCGC p.R610delR Deletion - In frame 11:78209674-78209676 + PT49 COSM5935818 c.1880C>T p.P627L Substitution - Missense 11:78209735-78209735 + SNU-C2B COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + LS180 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + PT52 COSM5940215 c.1045C>T p.P349S Substitution - Missense 11:78200656-78200656 + TCGA-13-0727-01 COSM112061 c.1230_1231insA p.T411fs*74 Insertion - Frameshift 11:78209817-78209818 + TCGA-F4-6856-01 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + I2L-P19Tb-Tumor-Biopsy COSM5360726 c.157G>A p.A53T Substitution - Missense 11:78196402-78196402 + TCGA-AP-A059-01 COSM932254 c.1024G>A p.E342K Substitution - Missense 11:78200220-78200220 + SNUH_G15_S1 COSM3676326 c.605T>C p.L202P Substitution - Missense 11:78205981-78205981 + TCGA-HU-A4GQ-01 COSM4036914 c.1862T>C p.I621T Substitution - Missense 11:78209717-78209717 + HCT116 COSM1357161 c.1053delC p.M354fs*119 Deletion - Frameshift 11:78200664-78200664 + 101692 COSM95468 c.400C>T p.H134Y Substitution - Missense 11:78200743-78200743 + TCGA-AZ-6601-01 COSM1357159 c.973G>A p.A325T Substitution - Missense 11:78200169-78200169 + TCGA-AZ-4313-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + pfg212T COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + ESO-130 COSM932269 c.1927G>A p.E643K Substitution - Missense 11:78210514-78210514 + TCGA-46-3765-01 COSM690560 c.2452A>T p.M818L Substitution - Missense 11:78210307-78210307 + Pat_06_A COSM5839655 c.1819_1821delCGC p.R610delR Deletion - In frame 11:78209674-78209676 + HCC2998 COSM1676326 c.1397G>A p.R466K Substitution - Missense 11:78207535-78207535 + TCGA-AZ-6601-01 COSM1357163 c.1278G>A p.A426A Substitution - coding silent 11:78205922-78205922 + SNU-175 COSM2019323 c.809G>T p.S270I Substitution - Missense 11:78208912-78208912 + TCGA-B8-5550-01 COSM3359412 c.2185C>T p.Q729* Substitution - Nonsense 11:78210040-78210040 + sysucc-1370T COSM5469779 c.252C>T p.R84R Substitution - coding silent 11:78196497-78196497 + Pat_41_B COSM5839652 c.388G>A p.A130T Substitution - Missense 11:78200731-78200731 + CSCC-7-T COSM4466484 c.705C>T p.P235P Substitution - coding silent 11:78207575-78207575 + TCGA-AG-A002-01 COSM264615 c.1089G>A p.S363S Substitution - coding silent 11:78200700-78200700 + CSCC-29-T COSM4517062 c.2732_2733CC>TT p.S911F Substitution - Missense 11:78210587-78210588 + PT37 COSM5920310 c.1486-4C>T p.? Unknown 11:78208853-78208853 + EGC15 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + RKO COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + CSCC-60-T COSM4510278 c.99C>T p.P33P Substitution - coding silent 11:78199619-78199619 + 169 COSM932260 c.1518C>T p.S506S Substitution - coding silent 11:78208889-78208889 + TCGA-AA-3811-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-AZ-4315-01 COSM1357183 c.2374G>A p.E792K Substitution - Missense 11:78210229-78210229 + LS180 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + LIM2405 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + pfg212T COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + 9227_T COSM5039520 c.1372G>A p.A458T Substitution - Missense 11:78206016-78206016 + HCT15 COSM2019380 c.2439C>T p.F813F Substitution - coding silent 11:78210294-78210294 + 169 COSM932261 c.786C>T p.S262S Substitution - coding silent 11:78208889-78208889 + ESCC_40 COSM5629303 c.1220_1221insC p.T408fs*77 Insertion - Frameshift 11:78209807-78209808 + TCGA-BR-8680-01 COSM264614 c.357G>A p.S119S Substitution - coding silent 11:78200700-78200700 + CSCC-31-T COSM4472171 c.1032C>T p.S344S Substitution - coding silent 11:78209619-78209619 + NPC15F COSM4995049 c.389C>T p.A130V Substitution - Missense 11:78200732-78200732 + 3N38-VS-3T38 COSM2019288 c.231C>T p.I77I Substitution - coding silent 11:78200159-78200159 + SNUH_G76_S1 COSM4419531 c.706G>A p.V236M Substitution - Missense 11:78197968-78197968 + TCGA-G4-6588-01 COSM1357179 c.1954_1955insC p.T655fs*74 Insertion - Frameshift 11:78209809-78209810 + 80 COSM5012387 c.1993A>C p.K665Q Substitution - Missense 11:78209848-78209848 + HN_62854 COSM130115 c.163G>A p.E55K Substitution - Missense 11:78196408-78196408 + TCGA-CH-5762-01 COSM1127632 c.300C>T p.F100F Substitution - coding silent 11:78200228-78200228 + LOVO COSM1357179 c.1954_1955insC p.T655fs*74 Insertion - Frameshift 11:78209809-78209810 + TCGA-HU-A4GQ-01 COSM4036915 c.1130T>C p.I377T Substitution - Missense 11:78209717-78209717 + LOVO COSM1357180 c.1222_1223insC p.T411fs*74 Insertion - Frameshift 11:78209809-78209810 + TCGA-DZ-6134-01 COSM3986488 c.2402C>T p.P801L Substitution - Missense 11:78210257-78210257 + TCGA-AA-3811-01 COSM5108613 c.806+7C>T p.? Unknown 11:78198075-78198075 + ESO-0292 COSM1241882 c.1878C>T p.G626G Substitution - coding silent 11:78210465-78210465 + TCGA-AP-A0LM-01 COSM932258 c.1320G>T p.K440N Substitution - Missense 11:78205964-78205964 + TCGA-13-0727-01 COSM112060 c.1962_1963insA p.T655fs*74 Insertion - Frameshift 11:78209817-78209818 + LS411 COSM2019382 c.2512G>A p.A838T Substitution - Missense 11:78210367-78210367 + PD6730b COSM5791724 c.169C>T p.P57S Substitution - Missense 11:78196414-78196414 + KM12 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-B8-5550-01 COSM3359413 c.1453C>T p.Q485* Substitution - Nonsense 11:78210040-78210040 + TCGA-Q1-A5R2-01 COSM4850222 c.1767C>A p.L589L Substitution - coding silent 11:78210354-78210354 + Gp2D COSM1357180 c.1222_1223insC p.T411fs*74 Insertion - Frameshift 11:78209809-78209810 + TCGA-DK-A2I1-01 COSM1298652 c.1515C>G p.L505L Substitution - coding silent 11:78208886-78208886 + TCGA-AX-A0J1-01 COSM932274 c.2985G>T p.E995D Substitution - Missense 11:78213741-78213741 + CSCC-31-T COSM4522299 c.1155G>A p.P385P Substitution - coding silent 11:78200766-78200766 + TCGA-A6-2672-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-AU-6004-01 COSM1357170 c.744A>G p.E248E Substitution - coding silent 11:78207614-78207614 + 66 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-DZ-6134-01 COSM3986489 c.1670C>T p.P557L Substitution - Missense 11:78210257-78210257 + Pat_40_B COSM5839658 c.1895C>T p.A632V Substitution - Missense 11:78210482-78210482 + 1115156 COSM5550798 c.2186C>T p.A729V Substitution - Missense 11:78213674-78213674 + TCGA-AX-A0J0-01 COSM932273 c.2236G>T p.D746Y Substitution - Missense 11:78213724-78213724 + PD6047a COSM2019379 c.1671G>A p.P557P Substitution - coding silent 11:78210258-78210258 + TCGA-CK-6746-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + Gp5D COSM4611888 c.1954_1955insCC p.T655fs*24 Insertion - Frameshift 11:78209809-78209810 + TCGA-EI-6917-01 COSM2019321 c.798G>A p.T266T Substitution - coding silent 11:78208901-78208901 + B66-Tumor COSM3931448 c.2517T>G p.G839G Substitution - coding silent 11:78210372-78210372 + TCGA-A2-A0T2-01 COSM1357180 c.1222_1223insC p.T411fs*74 Insertion - Frameshift 11:78209809-78209810 + 3N09-VS-3T09 COSM4979159 c.2777G>A p.R926Q Substitution - Missense 11:78210632-78210632 + SNU-C1 COSM2019398 c.2794G>C p.E932Q Substitution - Missense 11:78210649-78210649 + HCT8 COSM2019381 c.1707C>T p.F569F Substitution - coding silent 11:78210294-78210294 + NCI-H23 COSM1196398 c.898C>G p.Q300E Substitution - Missense 11:78209485-78209485 + T2944 COSM4739788 c.73G>A p.V25M Substitution - Missense 11:78196318-78196318 + sysucc-783T COSM5483662 c.599C>T p.A200V Substitution - Missense 11:78196844-78196844 + TCGA-AZ-6601-01 COSM1357164 c.546G>A p.A182A Substitution - coding silent 11:78205922-78205922 + TCGA-CJ-4902-01 COSM467458 c.1499C>A p.S500Y Substitution - Missense 11:78208870-78208870 + TCGA-28-5216-01 COSM3398149 c.1817G>A p.C606Y Substitution - Missense 11:78209672-78209672 + BCM275T COSM4951852 c.2685C>T p.D895D Substitution - coding silent 11:78210540-78210540 + TCGA-AG-A02N-01 COSM5074564 c.2889+1G>A p.? Unknown 11:78210745-78210745 + 587350 COSM1232050 c.1268G>A p.S423N Substitution - Missense 11:78205912-78205912 + 1N53-VS-1T53 COSM4466484 c.705C>T p.P235P Substitution - coding silent 11:78207575-78207575 + SNU-175 COSM2019322 c.1541G>T p.S514I Substitution - Missense 11:78208912-78208912 + OSCC-GB_00560111 COSM4883795 c.1091G>A p.R364H Substitution - Missense 11:78209678-78209678 + TCGA-AZ-4315-01 COSM1357172 c.774G>T p.E258D Substitution - Missense 11:78208877-78208877 + TCGA-AG-3902-01 COSM112060 c.1962_1963insA p.T655fs*74 Insertion - Frameshift 11:78209817-78209818 + WA16 COSM242203 c.1729C>T p.R577W Substitution - Missense 11:78209584-78209584 + ESO-0292 COSM1241883 c.3001delG p.G1002fs*>17 Deletion - Frameshift 11:78213757-78213757 + I2L-P7-Tumor-Organoid COSM5361010 c.1095G>A p.S365S Substitution - coding silent 11:78200706-78200706 + LC_C32 COSM1188357 c.1519C>T p.R507W Substitution - Missense 11:78210106-78210106 + SNU-C2B COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + CSCC-41-T COSM4516734 c.2238_2239CC>TT p.P747S Substitution - Missense 11:78210093-78210094 + TCGA-CG-4306-01 COSM4036919 c.1548C>T p.S516S Substitution - coding silent 11:78210135-78210135 + TCGA-AU-6004-01 COSM1357179 c.1954_1955insC p.T655fs*74 Insertion - Frameshift 11:78209809-78209810 + DLD1 COSM4622309 c.9G>A p.K3K Substitution - coding silent 11:78196254-78196254 + T3090 COSM4532297 c.1139G>A p.R380Q Substitution - Missense 11:78209726-78209726 + TCGA-G2-A2EF-01 COSM1298655 c.1465G>A p.E489K Substitution - Missense 11:78210052-78210052 + NPC15F COSM4995048 c.1121C>T p.A374V Substitution - Missense 11:78200732-78200732 + PCSI_0310_Pa_P_526 COSM4965235 c.490C>T p.R164C Substitution - Missense 11:78205866-78205866 + TCGA-AM-5820-01 COSM330846 c.390G>A p.A130A Substitution - coding silent 11:78200733-78200733 + S00501 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-CD-A48C-01 COSM4036909 c.148G>A p.V50M Substitution - Missense 11:78196393-78196393 + TCGA-Q1-A5R2-01 COSM4850221 c.2499C>A p.L833L Substitution - coding silent 11:78210354-78210354 + J80_T COSM3953829 c.1994A>T p.K665M Substitution - Missense 11:78209849-78209849 + TCGA-AZ-4315-01 COSM1357176 c.1097G>A p.R366H Substitution - Missense 11:78209684-78209684 + 587338 COSM1232048 c.1804C>A p.P602T Substitution - Missense 11:78209659-78209659 + TCGA-AN-A0AK-01 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + ESO-0292 COSM1241884 c.2269delG p.G758fs*>17 Deletion - Frameshift 11:78213757-78213757 + TCGA-AP-A052-01 COSM932268 c.2659G>A p.E887K Substitution - Missense 11:78210514-78210514 + TCGA-AZ-6598-01 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + PT36 COSM5916139 c.1588G>T p.D530Y Substitution - Missense 11:78208959-78208959 + TCGA-AA-3672-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + CSCC-11-T COSM4452572 c.1243A>T p.I415F Substitution - Missense 11:78209830-78209830 + ESO-0292 COSM1241881 c.2610C>T p.G870G Substitution - coding silent 11:78210465-78210465 + pfg143T COSM4757848 c.2573C>T p.S858L Substitution - Missense 11:78210428-78210428 + LS174T COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-A6-3809-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-EE-A29P-06 COSM3453584 c.947C>T p.A316V Substitution - Missense 11:78209534-78209534 + TCGA-BR-8361-01 COSM4036915 c.1130T>C p.I377T Substitution - Missense 11:78209717-78209717 + SNU-C2B COSM2019338 c.1786_1787delCT p.L598fs*6 Deletion - Frameshift 11:78209641-78209642 + TCGA-46-3765-01 COSM690561 c.1720A>T p.M574L Substitution - Missense 11:78210307-78210307 + TCGA-BR-8680-01 COSM4036913 c.921G>A p.S307S Substitution - coding silent 11:78209508-78209508 + T3024 COSM4739795 c.2617C>T p.R873C Substitution - Missense 11:78210472-78210472 + CAL27 COSM2019303 c.1284C>T p.F428F Substitution - coding silent 11:78205928-78205928 + TCGA-AD-6889-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + OSCC-GB_01070111 COSM4883282 c.12C>T p.I4I Substitution - coding silent 11:78196257-78196257 + TCGA-AP-A0LG-01 COSM932265 c.1487C>T p.T496I Substitution - Missense 11:78210074-78210074 + 35M COSM1357180 c.1222_1223insC p.T411fs*74 Insertion - Frameshift 11:78209809-78209810 + T3202 COSM4739793 c.1052_1053insC p.M354fs*39 Insertion - Frameshift 11:78200663-78200664 + pfg008T COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + HCC17T COSM3746260 c.1222A>G p.T408A Substitution - Missense 11:78209809-78209809 + TCGA-18-4086-01 COSM690563 c.1066T>G p.F356V Substitution - Missense 11:78209653-78209653 + LS513 COSM2019329 c.920C>T p.S307L Substitution - Missense 11:78209507-78209507 + 587350 COSM1232051 c.536G>A p.S179N Substitution - Missense 11:78205912-78205912 + TCGA-AA-3973-01 COSM4739793 c.1052_1053insC p.M354fs*39 Insertion - Frameshift 11:78200663-78200664 + TCGA-A6-2680-01 COSM5082532 c.673+5G>A p.? Unknown 11:78196923-78196923 + LS174T COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-HC-7745-01 COSM4392983 c.2292C>T p.G764G Substitution - coding silent 11:78213780-78213780 + TCGA-AP-A0LM-01 COSM932259 c.588G>T p.K196N Substitution - Missense 11:78205964-78205964 + TCGA-AZ-4315-01 COSM1357184 c.1642G>A p.E548K Substitution - Missense 11:78210229-78210229 + BCM275T COSM4951853 c.1953C>T p.D651D Substitution - coding silent 11:78210540-78210540 + TCGA-02-0033 COSM2148959 c.89_90delGG p.R30fs*6 Deletion - Frameshift 11:78196334-78196335 + TCGA-AM-5821-01 COSM3752757 c.1297A>G p.I433V Substitution - Missense 11:78209884-78209884 + PT35 COSM5913307 c.1499C>T p.S500F Substitution - Missense 11:78208870-78208870 + TCGA-CD-8535-01 COSM4036917 c.1402G>A p.V468M Substitution - Missense 11:78209989-78209989 + H23 COSM1196398 c.898C>G p.Q300E Substitution - Missense 11:78209485-78209485 + HCC17T COSM3746259 c.1954A>G p.T652A Substitution - Missense 11:78209809-78209809 + DU-145 COSM1676324 c.890A>T p.K297M Substitution - Missense 11:78199678-78199678 + TCGA-FD-A3B3-01 COSM1298651 c.420C>T p.F140F Substitution - coding silent 11:78200763-78200763 + TCGA-G2-A2EF-01 COSM1298654 c.2197G>A p.E733K Substitution - Missense 11:78210052-78210052 + TCGA-18-4086-01 COSM690562 c.1798T>G p.F600V Substitution - Missense 11:78209653-78209653 + LC_C32 COSM1188356 c.2251C>T p.R751W Substitution - Missense 11:78210106-78210106 + CHC1124T COSM3765604 c.453C>T p.H151H Substitution - coding silent 11:78196698-78196698 + SW620 COSM2019289 c.971G>T p.G324V Substitution - Missense 11:78200167-78200167 + SNU-C2B COSM2019399 c.2062G>C p.E688Q Substitution - Missense 11:78210649-78210649 + TCGA-D5-6930-01 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + ORL-48 COSM4596696 c.2351C>T p.S784L Substitution - Missense 11:78210206-78210206 + SNUH_G15_S1 COSM3676325 c.1337T>C p.L446P Substitution - Missense 11:78205981-78205981 + ESCC_123 COSM1357164 c.546G>A p.A182A Substitution - coding silent 11:78205922-78205922 + TCGA-AM-5820-01 COSM3752759 c.1331C>T p.T444M Substitution - Missense 11:78209918-78209918 + BD72T COSM5512835 c.384G>A p.Q128Q Substitution - coding silent 11:78200727-78200727 + 585270 COSM324221 c.343G>T p.V115F Substitution - Missense 11:78200686-78200686 + TCGA-AZ-4315-01 COSM1357171 c.1506G>T p.E502D Substitution - Missense 11:78208877-78208877 + sysucc-918T COSM5453441 c.257T>A p.L86H Substitution - Missense 11:78200185-78200185 + LIM2405 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + CSCC-45-T COSM4530090 c.934G>A p.E312K Substitution - Missense 11:78209521-78209521 + 4_RESISTANT COSM1724692 c.2498_2499insC p.R834fs*13 Insertion - Frameshift 11:78210353-78210354 + 39 COSM5733800 c.250C>T p.R84C Substitution - Missense 11:78196495-78196495 + TCGA-G4-6628-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + CSCC-31-T COSM4522300 c.423G>A p.P141P Substitution - coding silent 11:78200766-78200766 + 101692 COSM95469 c.1132C>T p.H378Y Substitution - Missense 11:78200743-78200743 + PDA_004 COSM3752756 c.2029A>G p.I677V Substitution - Missense 11:78209884-78209884 + TCGA-AG-A02N-01 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-CJ-4902-01 COSM467459 c.767C>A p.S256Y Substitution - Missense 11:78208870-78208870 + TCGA-EK-A3GK-01 COSM1298651 c.420C>T p.F140F Substitution - coding silent 11:78200763-78200763 + SNUH_G22_S1 COSM3931448 c.2517T>G p.G839G Substitution - coding silent 11:78210372-78210372 + TCGA-AZ-6601-01 COSM1357174 c.1081C>T p.R361C Substitution - Missense 11:78209668-78209668 + RKO COSM2019361 c.1422G>T p.K474N Substitution - Missense 11:78210009-78210009 + TCGA-AX-A0J1-01 COSM932275 c.2253G>T p.E751D Substitution - Missense 11:78213741-78213741 + TCGA-J9-A52C-01 COSM4877123 c.2307C>G p.F769L Substitution - Missense 11:78213795-78213795 + Pat_40_B COSM5839657 c.2627C>T p.A876V Substitution - Missense 11:78210482-78210482 + DU-145 COSM1676325 c.158A>T p.K53M Substitution - Missense 11:78199678-78199678 + TCGA-EK-A3GK-01 COSM1298650 c.1152C>T p.F384F Substitution - coding silent 11:78200763-78200763 + 66 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-AM-5821-01 COSM3752756 c.2029A>G p.I677V Substitution - Missense 11:78209884-78209884 + ESO-130 COSM932268 c.2659G>A p.E887K Substitution - Missense 11:78210514-78210514 + I2L-P7-Tumor-Organoid COSM5361011 c.363G>A p.S121S Substitution - coding silent 11:78200706-78200706 + TCGA-13-0726-01 COSM81898 c.1341C>G p.G447G Substitution - coding silent 11:78205985-78205985 + T2197 COSM4739791 c.767A>T p.D256V Substitution - Missense 11:78198029-78198029 + CSCC-45-T COSM4530089 c.1666G>A p.E556K Substitution - Missense 11:78209521-78209521 + PT17_1 COSM5899058 c.2489C>T p.P830L Substitution - Missense 11:78210344-78210344 + SNU-C4 COSM1357162 c.321delC p.M110fs*119 Deletion - Frameshift 11:78200664-78200664 + TCGA-G4-6304-01 COSM5175252 c.2375_2377delAGA p.K793delK Deletion - In frame 11:78210230-78210232 + pfg008T COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + CHEWS030 COSM4574822 c.36C>T p.D12D Substitution - coding silent 11:78198030-78198030 + CSCC-60-T COSM4510277 c.831C>T p.P277P Substitution - coding silent 11:78199619-78199619 + TCGA-AM-5821-01 COSM330845 c.1122G>A p.A374A Substitution - coding silent 11:78200733-78200733 + SW48 COSM2019388 c.2627C>A p.A876D Substitution - Missense 11:78210482-78210482 + SNU-175 COSM2019321 c.798G>A p.T266T Substitution - coding silent 11:78208901-78208901 + TCGA-BK-A0CB-01 COSM932260 c.1518C>T p.S506S Substitution - coding silent 11:78208889-78208889 + CHEWS030 COSM4574821 c.768C>T p.D256D Substitution - coding silent 11:78198030-78198030 + CSCC-15-T COSM4556726 c.700G>A p.A234T Substitution - Missense 11:78197962-78197962 + 1_PRE-TREATMENT COSM1720949 c.1043C>T p.A348V Substitution - Missense 11:78209630-78209630 + ESO06T COSM1171844 c.1726C>T p.R576C Substitution - Missense 11:78210313-78210313 + T3116 COSM4739789 c.103C>T p.R35C Substitution - Missense 11:78196348-78196348 + PT49 COSM5935820 c.2890-5C>T p.? Unknown 11:78213641-78213641 + TCGA-G4-6309-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-AA-3833-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + CSCC-18-T COSM4472171 c.1032C>T p.S344S Substitution - coding silent 11:78209619-78209619 + ESCC_40 COSM1357179 c.1954_1955insC p.T655fs*74 Insertion - Frameshift 11:78209809-78209810 + 9227_T COSM5039521 c.640G>A p.A214T Substitution - Missense 11:78206016-78206016 + S00501 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + OSCC-GB_00560111 COSM4883794 c.1823G>A p.R608H Substitution - Missense 11:78209678-78209678 + TCGA-EJ-5505-01 COSM1127630 c.1231A>C p.T411P Substitution - Missense 11:78209818-78209818 + TC71 COSM2019344 c.1819C>T p.R607C Substitution - Missense 11:78209674-78209674 + TCGA-BR-6566-01 COSM4036910 c.1270G>A p.E424K Substitution - Missense 11:78205914-78205914 + TCGA-BR-6566-01 COSM4036911 c.538G>A p.E180K Substitution - Missense 11:78205914-78205914 + T3090 COSM4532296 c.1871G>A p.R624Q Substitution - Missense 11:78209726-78209726 + 1N53-VS-1T53 COSM4466483 c.1437C>T p.P479P Substitution - coding silent 11:78207575-78207575 + 2246951 COSM4413587 c.1655C>T p.P552L Substitution - Missense 11:78209510-78209510 + Gp2D COSM1357179 c.1954_1955insC p.T655fs*74 Insertion - Frameshift 11:78209809-78209810 + TCGA-G4-6586-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TC71 COSM2019345 c.1087C>T p.R363C Substitution - Missense 11:78209674-78209674 + T3024 COSM4739796 c.1885C>T p.R629C Substitution - Missense 11:78210472-78210472 + TCGA-AZ-6601-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + 2492730 COSM5728847 c.2337C>T p.R779R Substitution - coding silent 11:78210192-78210192 + TCGA-D1-A17H-01 COSM932256 c.1127T>C p.L376P Substitution - Missense 11:78200738-78200738 + TCGA-A5-A0GH-01 COSM932267 c.1855T>C p.Y619H Substitution - Missense 11:78210442-78210442 + TCGA-AP-A052-01 COSM932269 c.1927G>A p.E643K Substitution - Missense 11:78210514-78210514 + SNUH_G15_S1 COSM3676324 c.590T>A p.I197N Substitution - Missense 11:78205966-78205966 + TCGA-AD-6964-01 COSM1357180 c.1222_1223insC p.T411fs*74 Insertion - Frameshift 11:78209809-78209810 + TCGA-CM-4746-01 COSM932255 c.292G>A p.E98K Substitution - Missense 11:78200220-78200220 + TCGA-EE-A29P-06 COSM3453583 c.1679C>T p.A560V Substitution - Missense 11:78209534-78209534 + TCGA-D7-8575-01 COSM4036922 c.2796G>A p.E932E Substitution - coding silent 11:78210651-78210651 + TCGA-AM-5820-01 COSM3752758 c.2063C>T p.T688M Substitution - Missense 11:78209918-78209918 + Pat_06_A COSM5839656 c.1087_1089delCGC p.R366delR Deletion - In frame 11:78209674-78209676 + TCGA-DD-A3A7-01 COSM4916169 c.1672C>A p.P558T Substitution - Missense 11:78209527-78209527 + TCGA-AD-6889-01 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-CG-4306-01 COSM4036918 c.2280C>T p.S760S Substitution - coding silent 11:78210135-78210135 + PCSI_0310_Pa_P_526 COSM4965234 c.1222C>T p.R408C Substitution - Missense 11:78205866-78205866 + PT17_1 COSM5899059 c.1757C>T p.P586L Substitution - Missense 11:78210344-78210344 + CSCC-7-T COSM4530831 c.999G>T p.R333R Substitution - coding silent 11:78209586-78209586 + DLD1 COSM2019381 c.1707C>T p.F569F Substitution - coding silent 11:78210294-78210294 + STC297 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + PT36 COSM5916140 c.856G>T p.D286Y Substitution - Missense 11:78208959-78208959 + TCGA-AA-3819-01 COSM294073 c.696C>A p.A232A Substitution - coding silent 11:78197958-78197958 + WA16 COSM242202 c.997C>T p.R333W Substitution - Missense 11:78209584-78209584 + C135 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + SC_9096 COSM5566917 c.1730G>A p.R577H Substitution - Missense 11:78210317-78210317 + SNUH_G22_S1 COSM3931449 c.1785T>G p.G595G Substitution - coding silent 11:78210372-78210372 + TCGA-AG-A002-01 COSM264614 c.357G>A p.S119S Substitution - coding silent 11:78200700-78200700 + 587386 COSM1232055 c.545C>T p.A182V Substitution - Missense 11:78205921-78205921 + TCGA-G4-6628-01 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + pfg143T COSM4757849 c.1841C>T p.S614L Substitution - Missense 11:78210428-78210428 + TCGA-AA-3663-01 COSM1357177 c.1867G>A p.A623T Substitution - Missense 11:78209722-78209722 + NCI-H1770 COSM24331 c.781C>T p.L261F Substitution - Missense 11:78208884-78208884 + TCGA-G2-A2EL-01 COSM1298657 c.1686C>T p.L562L Substitution - coding silent 11:78210273-78210273 + TCGA-60-2698-01 COSM690564 c.665C>T p.S222F Substitution - Missense 11:78196910-78196910 + TCGA-13-0726-01 COSM81897 c.609C>G p.G203G Substitution - coding silent 11:78205985-78205985 + ORL-48 COSM4596697 c.1619C>T p.S540L Substitution - Missense 11:78210206-78210206 + TCGA-AZ-6601-01 COSM1357173 c.1813C>T p.R605C Substitution - Missense 11:78209668-78209668 + TCGA-FD-A3B3-01 COSM1298650 c.1152C>T p.F384F Substitution - coding silent 11:78200763-78200763 + TCGA-HT-7475-01 COSM3967854 c.508G>A p.G170R Substitution - Missense 11:78205884-78205884 + ESCC_123 COSM1357163 c.1278G>A p.A426A Substitution - coding silent 11:78205922-78205922 + LP6007409-DNA_A01 COSM5953369 c.1148G>A p.R383Q Substitution - Missense 11:78200759-78200759 + TCGA-QG-A5Z2-01 COSM1357179 c.1954_1955insC p.T655fs*74 Insertion - Frameshift 11:78209809-78209810 + TCGA-A5-A0GH-01 COSM932266 c.2587T>C p.Y863H Substitution - Missense 11:78210442-78210442 + LP6007409-DNA_A01 COSM5953370 c.416G>A p.R139Q Substitution - Missense 11:78200759-78200759 + LUAD-B00416 COSM330845 c.1122G>A p.A374A Substitution - coding silent 11:78200733-78200733 + Pat_40_A COSM5839658 c.1895C>T p.A632V Substitution - Missense 11:78210482-78210482 + 1115156 COSM5550797 c.2918C>T p.A973V Substitution - Missense 11:78213674-78213674 + TCGA-BR-8361-01 COSM4036914 c.1862T>C p.I621T Substitution - Missense 11:78209717-78209717 + TCGA-28-5216-01 COSM3398150 c.1085G>A p.C362Y Substitution - Missense 11:78209672-78209672 + T3262 COSM4739790 c.655G>A p.A219T Substitution - Missense 11:78196900-78196900 + BCM275T COSM4951853 c.1953C>T p.D651D Substitution - coding silent 11:78210540-78210540 + CSCC-7-T COSM4530830 c.1731G>T p.R577R Substitution - coding silent 11:78209586-78209586 + Pat_34_A COSM5839653 c.1669G>A p.E557K Substitution - Missense 11:78209524-78209524 + J80_T COSM3953830 c.1262A>T p.K421M Substitution - Missense 11:78209849-78209849 + HCT116 COSM1357182 c.1223delC p.T411fs*23 Deletion - Frameshift 11:78209810-78209810 + I2L-P17-Tumor-Organoid COSM5360556 c.12C>G p.I4M Substitution - Missense 11:78196257-78196257 + PD6047a COSM2019378 c.2403G>A p.P801P Substitution - coding silent 11:78210258-78210258 + GCT01 COSM4413587 c.1655C>T p.P552L Substitution - Missense 11:78209510-78209510 + PCSI_0337_Pa_P_526 COSM4807892 c.229G>A p.A77T Substitution - Missense 11:78196474-78196474 + TCGA-AZ-4315-01 COSM1357175 c.1829G>A p.R610H Substitution - Missense 11:78209684-78209684 + Pat_14_B COSM5839659 c.2740C>T p.P914S Substitution - Missense 11:78210595-78210595 + TCGA-AP-A056-01 COSM932262 c.2146G>A p.E716K Substitution - Missense 11:78210001-78210001 + CSCC-31-T COSM4485423 c.2930C>T p.S977F Substitution - Missense 11:78213686-78213686 + I2L-P19Tb-Tumor-Organoid COSM5360726 c.157G>A p.A53T Substitution - Missense 11:78196402-78196402 + HCC2998 COSM1676326 c.1397G>A p.R466K Substitution - Missense 11:78207535-78207535 + TCGA-D1-A17H-01 COSM932257 c.395T>C p.L132P Substitution - Missense 11:78200738-78200738 + TCGA-CM-5861-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + sysucc-918T COSM5453440 c.989T>A p.L330H Substitution - Missense 11:78200185-78200185 + TCGA-CM-4746-01 COSM932254 c.1024G>A p.E342K Substitution - Missense 11:78200220-78200220 + BCM275T COSM4951852 c.2685C>T p.D895D Substitution - coding silent 11:78210540-78210540 + HCC2998 COSM1676327 c.665G>A p.R222K Substitution - Missense 11:78207535-78207535 + HCT15 COSM2019381 c.1707C>T p.F569F Substitution - coding silent 11:78210294-78210294 + Pat_14_B COSM5839660 c.2008C>T p.P670S Substitution - Missense 11:78210595-78210595 + STC297 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-AG-3902-01 COSM112061 c.1230_1231insA p.T411fs*74 Insertion - Frameshift 11:78209817-78209818 + TCGA-EI-6917-01 COSM2019320 c.1530G>A p.T510T Substitution - coding silent 11:78208901-78208901 + TCGA-AM-5820-01 COSM3687662 c.642C>T p.A214A Substitution - coding silent 11:78206018-78206018 + TCGA-AG-3726-01 COSM4739794 c.320_321insC p.M110fs*39 Insertion - Frameshift 11:78200663-78200664 + SNU-C2B COSM2019331 c.933C>T p.P311P Substitution - coding silent 11:78209520-78209520 + 1_RESISTANT COSM1720949 c.1043C>T p.A348V Substitution - Missense 11:78209630-78209630 + TCGA-AG-A02N-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + 587224 COSM1232045 c.1580C>A p.P527H Substitution - Missense 11:78210167-78210167 + TCGA-AP-A059-01 COSM932255 c.292G>A p.E98K Substitution - Missense 11:78200220-78200220 + Pat_34_A COSM5839654 c.937G>A p.E313K Substitution - Missense 11:78209524-78209524 + 35M COSM1357179 c.1954_1955insC p.T655fs*74 Insertion - Frameshift 11:78209809-78209810 + TCGA-EE-A2A2-06 COSM3453582 c.93C>T p.S31S Substitution - coding silent 11:78199613-78199613 + TCGA-F4-6856-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-BT-A0S7-01 COSM415726 c.2949G>T p.P983P Substitution - coding silent 11:78213705-78213705 + ESCC_40 COSM1357180 c.1222_1223insC p.T411fs*74 Insertion - Frameshift 11:78209809-78209810 + LS513 COSM2019328 c.1652C>T p.S551L Substitution - Missense 11:78209507-78209507 + 1_PRE-TREATMENT COSM1720948 c.1775C>T p.A592V Substitution - Missense 11:78209630-78209630 + TCGA-CM-6171-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-B5-A0JY-01 COSM932253 c.9G>T p.K3N Substitution - Missense 11:78196254-78196254 + TCGA-AX-A0J0-01 COSM932272 c.2968G>T p.D990Y Substitution - Missense 11:78213724-78213724 + TCGA-CG-5721-01 COSM4036908 c.72C>T p.R24R Substitution - coding silent 11:78196317-78196317 + SNU-C2B COSM2019330 c.1665C>T p.P555P Substitution - coding silent 11:78209520-78209520 + TCGA-QG-A5Z2-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + TCGA-NH-A5IV-01 COSM1357181 c.1955delC p.T655fs*23 Deletion - Frameshift 11:78209810-78209810 + CSCC-11-T COSM4532297 c.1139G>A p.R380Q Substitution - Missense 11:78209726-78209726 + PT49 COSM5935821 c.2158-5C>T p.? Unknown 11:78213641-78213641 + BD72T COSM5512834 c.1116G>A p.Q372Q Substitution - coding silent 11:78200727-78200727 + ESCC_40 COSM5629302 c.1952_1953insC p.T652fs*77 Insertion - Frameshift 11:78209807-78209808 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.531249 11q14.1

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.T910P c.2728A>C 11 77921629 GBM - A Frameshift p.T655Nfs*74 c.1963dupA 11 77920864 OV AGA - InFrameDeletion p.K718delK c.2152_2154delAAG 11 77921051 CM AGGCCCCTGCCTGCTGCCCCTGGTA - IntronicDeletion . c.1038+33_1038+57delCCCCTGCCTGCTGCCCCTGGTAAGG 11 77911310 CM A T 3-UTRSNV . c.3054+84A>T 11 77924940 CM A T Missense p.M818L c.2452A>T 11 77921353 LUSC C A Missense p.S500Y c.1499C>A 11 77919916 RCCC C A Synonymous p.A232A c.696C>A 11 77909004 COREAD C A Synonymous p.I976I c.2928C>A 11 77924730 HNSC - C Frameshift p.L831Pfs*16 c.2491dupC 11 77921388 HNSC C G Missense p.L598V c.1792C>G 11 77920693 HNSC C G Synonymous p.G447G c.1341C>G 11 77917031 OV C G Synonymous p.L505L c.1515C>G 11 77919932 BLCA C T Missense p.A397V c.1190C>T 11 77911847 HNSC C T Missense p.A560V c.1679C>T 11 77920580 CM C T Missense p.R819W c.2455C>T 11 77921356 HNSC C T Missense p.T740I c.2219C>T 11 77921120 UCEC C T Nonsense p.Q729* c.2185C>T 11 77921086 RCCC C T Synonymous p.A872A c.2616C>T 11 77921517 CM C T Synonymous p.F344F c.1032C>T 11 77911274 PRAD C T Synonymous p.F384F c.1152C>T 11 77911809 BLCA C T Synonymous p.F384F c.1152C>T 11 77911809 HNSC C T Synonymous p.G1008G c.3024C>T 11 77924826 PRAD C T Synonymous p.L39L c.115C>T 11 77907406 OV C T Synonymous p.L806L c.2418C>T 11 77921319 BLCA C T Synonymous p.S275S c.825C>T 11 77910659 CM C T Synonymous p.S748S c.2244C>T 11 77921145 CM C T Synonymous p.S760S c.2280C>T 11 77921181 STAD C T Synonymous p.Y49Y c.147C>T 11 77907438 BLCA C T Synonymous p.Y864Y c.2592C>T 11 77921493 LUAD G A Missense p.C606Y c.1817G>A 11 77920718 GBM G A Missense p.E55K c.163G>A 11 77907454 HNSC G A Missense p.E733K c.2197G>A 11 77921098 BLCA G A Missense p.E733K c.2197G>A 11 77921098 HNSC G A Missense p.G414R c.1240G>A 11 77916930 LGG G A Missense p.R408H c.1223G>A 11 77916913 LUAD G A Missense p.V761I c.2281G>A 11 77921182 BRCA G C Missense p.D990H c.2968G>C 11 77924770 HNSC G C Missense p.V909L c.2725G>C 11 77921626 UCEC - G Frameshift p.G840Wfs*7 c.2516dupG 11 77921416 GBM GG TT Missense p.G366W c.1095_1096delinsTT 11 77911752 CM G T IntronicSNV . c.2890-30G>T 11 77924662 NSCLC G T Missense p.G840V c.2519G>T 11 77921420 LUAD G T Missense p.R531L c.1592G>T 11 77920009 HNSC G T Missense p.V359F c.1075G>T 11 77911732 SCLC G T Synonymous p.L21L c.63G>T 11 77907354 LUAD G T Synonymous p.P983P c.2949G>T 11 77924751 BLCA G T Synonymous p.T438T c.1314G>T 11 77917004 STAD T C Missense p.L376P c.1127T>C 11 77911784 UCEC T C Missense p.Y863H c.2587T>C 11 77921488 UCEC TGCTGCTCCG - Frameshift p.L831Pfs*117 c.2492_2501delTGCTGCTCCG 11 77921393 RCCC T G Missense p.F600V c.1798T>G 11 77920699 LUSC