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 119149280 119149280 + Missense_Mutation SNP G G T TCGA-OR-A5JB-01A-11D-A29I-10 TCGA-OR-A5JB-10A-01D-A29L-10 g.chr11:119149280G>T c.1288G>T c.(1288-1290)Gtg>Ttg p.V430L BLCA 11 119142469 119142469 + Silent SNP C C T TCGA-K4-A3WS-01A-11D-A22Z-08 TCGA-K4-A3WS-10A-01D-A22Z-08 g.chr11:119142469C>T c.468C>T c.(466-468)ctC>ctT p.L156L BLCA 11 119149279 119149279 + Silent SNP C C T TCGA-HQ-A5NE-01A-12D-A289-08 TCGA-HQ-A5NE-10A-01D-A289-08 g.chr11:119149279C>T c.1287C>T c.(1285-1287)atC>atT p.I429I BLCA 11 119149302 119149302 + Missense_Mutation SNP G G T TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr11:119149302G>T c.1310G>T c.(1309-1311)aGa>aTa p.R437I BLCA 11 119149324 119149324 + Missense_Mutation SNP G G T TCGA-XF-A9SX-01A-21D-A391-08 TCGA-XF-A9SX-10A-01D-A394-08 g.chr11:119149324G>T c.1332G>T c.(1330-1332)agG>agT p.R444S BLCA 11 119149399 119149399 + Missense_Mutation SNP G G A TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr11:119149399G>A c.1407G>A c.(1405-1407)atG>atA p.M469I BLCA 11 119167741 119167741 + Missense_Mutation SNP C C T TCGA-DK-A3IT-01A-31D-A20D-08 TCGA-DK-A3IT-10A-01D-A20D-08 g.chr11:119167741C>T c.2150C>T c.(2149-2151)tCa>tTa p.S717L BLCA 11 119169209 119169209 + Missense_Mutation SNP C C A TCGA-ZF-AA4X-01A-11D-A38G-08 TCGA-ZF-AA4X-10A-01D-A38J-08 g.chr11:119169209C>A c.2393C>A c.(2392-2394)tCc>tAc p.S798Y BLCA 11 119170254 119170254 + Silent SNP G G A TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr11:119170254G>A c.2484G>A c.(2482-2484)ccG>ccA p.P828P BLCA 11 119170312 119170312 + Missense_Mutation SNP G G A TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr11:119170312G>A c.2542G>A c.(2542-2544)Gcc>Acc p.A848T BLCA 11 119170369 119170369 + Nonsense_Mutation SNP C C T TCGA-CU-A0YR-01A-12D-A10S-08 TCGA-CU-A0YR-10A-01D-A10S-08 g.chr11:119170369C>T c.2599C>T c.(2599-2601)Cag>Tag p.Q867* BLCA 11 119170462 119170462 + Missense_Mutation SNP A A C TCGA-E7-A5KE-01A-11D-A289-08 TCGA-E7-A5KE-10A-01D-A289-08 g.chr11:119170462A>C c.2692A>C c.(2692-2694)Att>Ctt p.I898L BRCA 11 119103160 119103160 + Silent SNP G G T TCGA-AN-A0AM-01A-11W-A050-09 TCGA-AN-A0AM-10A-01W-A055-09 g.chr11:119103160G>T c.198G>T c.(196-198)gtG>gtT p.V66V BRCA 11 119103255 119103255 + Missense_Mutation SNP T T C TCGA-AR-A24S-01A-11D-A167-09 TCGA-AR-A24S-10A-01D-A167-09 g.chr11:119103255T>C c.293T>C c.(292-294)aTc>aCc p.I98T BRCA 11 119103359 119103359 + Missense_Mutation SNP T T C TCGA-AN-A0FT-01A-11W-A050-09 TCGA-AN-A0FT-10A-01W-A055-09 g.chr11:119103359T>C c.397T>C c.(397-399)Ttc>Ctc p.F133L BRCA 11 119142562 119142562 + Silent SNP G G A TCGA-B6-A0RE-01A-11W-A071-09 TCGA-B6-A0RE-10A-01W-A071-09 g.chr11:119142562G>A c.561G>A c.(559-561)gcG>gcA p.A187A BRCA 11 119148506 119148506 + Silent SNP G G A TCGA-E2-A1LG-01A-21D-A14K-09 TCGA-E2-A1LG-11A-42D-A14K-09 g.chr11:119148506G>A c.1047G>A c.(1045-1047)ctG>ctA p.L349L BRCA 11 119155748 119155748 + Missense_Mutation SNP G G C TCGA-E2-A1LG-01A-21D-A14K-09 TCGA-E2-A1LG-11A-42D-A14K-09 g.chr11:119155748G>C c.1501G>C c.(1501-1503)Gac>Cac p.D501H BRCA 11 119158602 119158602 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr11:119158602A>C c.1982A>C c.(1981-1983)cAc>cCc p.H661P BRCA 11 119170209 119170209 + Silent SNP C C A TCGA-E9-A244-01A-11D-A167-09 TCGA-E9-A244-10A-01D-A167-09 g.chr11:119170209C>A c.2439C>A c.(2437-2439)gtC>gtA p.V813V CESC 11 119149358 119149358 + Missense_Mutation SNP G G A TCGA-LP-A4AV-01A-11D-A243-09 TCGA-LP-A4AV-10A-01D-A243-09 g.chr11:119149358G>A c.1366G>A c.(1366-1368)Gat>Aat p.D456N COAD 11 119103378 119103378 + Missense_Mutation SNP G G T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:119103378G>T c.416G>T c.(415-417)aGa>aTa p.R139I COAD 11 119144604 119144604 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:119144604G>A c.617G>A c.(616-618)cGa>cAa p.R206Q COAD 11 119145620 119145620 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:119145620G>A c.826G>A c.(826-828)Gaa>Aaa p.E276K COAD 11 119145631 119145631 + Silent SNP T T G TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr11:119145631T>G c.837T>G c.(835-837)gcT>gcG p.A279A COAD 11 119145653 119145653 + Missense_Mutation SNP A A G TCGA-DM-A28E-01A-11D-A16V-10 TCGA-DM-A28E-10A-01D-A16V-10 g.chr11:119145653A>G c.859A>G c.(859-861)Aaa>Gaa p.K287E COAD 11 119145654 119145654 + Missense_Mutation SNP A A G TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr11:119145654A>G c.860A>G c.(859-861)aAa>aGa p.K287R COAD 11 119145655 119145655 + Silent SNP A A G TCGA-CK-4948-01B-11D-1650-10 TCGA-CK-4948-10A-01D-1650-10 g.chr11:119145655A>G c.861A>G c.(859-861)aaA>aaG p.K287K COAD 11 119148472 119148472 + Missense_Mutation SNP T T C TCGA-CA-6719-01A-11D-1835-10 TCGA-CA-6719-10A-01D-1835-10 g.chr11:119148472T>C c.1013T>C c.(1012-1014)tTg>tCg p.L338S COAD 11 119148472 119148472 + Missense_Mutation SNP T T C TCGA-CM-6172-01A-11D-1650-10 TCGA-CM-6172-10A-01D-1650-10 g.chr11:119148472T>C c.1013T>C c.(1012-1014)tTg>tCg p.L338S COAD 11 119148875 119148875 + Splice_Site SNP G G A TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr11:119148875G>A c.e8-1 COAD 11 119148879 119148879 + Nonsense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr11:119148879C>T c.1099C>T c.(1099-1101)Caa>Taa p.Q367* COAD 11 119148880 119148880 + Missense_Mutation SNP A A T TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr11:119148880A>T c.1100A>T c.(1099-1101)cAa>cTa p.Q367L COAD 11 119148881 119148881 + Silent SNP A A G TCGA-CA-6716-01A-11D-1835-10 TCGA-CA-6716-10A-01D-1835-10 g.chr11:119148881A>G c.1101A>G c.(1099-1101)caA>caG p.Q367Q COAD 11 119148908 119148908 + Silent SNP C C T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr11:119148908C>T c.1128C>T c.(1126-1128)tcC>tcT p.S376S COAD 11 119148908 119148908 + Silent SNP C C T TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr11:119148908C>T c.1128C>T c.(1126-1128)tcC>tcT p.S376S COAD 11 119148908 119148908 + Silent SNP C C T TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chr11:119148908C>T c.1128C>T c.(1126-1128)tcC>tcT p.S376S COAD 11 119148921 119148921 + Missense_Mutation SNP T T C TCGA-A6-5657-01A-01D-1650-10 TCGA-A6-5657-10A-01D-1650-10 g.chr11:119148921T>C c.1141T>C c.(1141-1143)Tgt>Cgt p.C381R COAD 11 119148921 119148921 + Missense_Mutation SNP T T G TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr11:119148921T>G c.1141T>G c.(1141-1143)Tgt>Ggt p.C381G COAD 11 119148922 119148922 + Missense_Mutation SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr11:119148922G>A c.1142G>A c.(1141-1143)tGt>tAt p.C381Y COAD 11 119148922 119148922 + Missense_Mutation SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr11:119148922G>A c.1142G>A c.(1141-1143)tGt>tAt p.C381Y COAD 11 119148923 119148923 + Silent SNP T T C TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr11:119148923T>C c.1143T>C c.(1141-1143)tgT>tgC p.C381C COAD 11 119148931 119148931 + Missense_Mutation SNP G G A TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr11:119148931G>A c.1151G>A c.(1150-1152)tGt>tAt p.C384Y COAD 11 119148963 119148963 + Missense_Mutation SNP C C T TCGA-AZ-5407-01A-01D-1719-10 TCGA-AZ-5407-10A-01D-1719-10 g.chr11:119148963C>T c.1183C>T c.(1183-1185)Ccc>Tcc p.P395S COAD 11 119148964 119148964 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr11:119148964C>T c.1184C>T c.(1183-1185)cCc>cTc p.P395L COAD 11 119148968 119148968 + Silent SNP T T C TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr11:119148968T>C c.1188T>C c.(1186-1188)tgT>tgC p.C396C COAD 11 119148973 119148973 + Missense_Mutation SNP A A G TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr11:119148973A>G c.1193A>G c.(1192-1194)cAc>cGc p.H398R COAD 11 119148979 119148979 + Missense_Mutation SNP T T C TCGA-A6-5662-01A-01D-1650-10 TCGA-A6-5662-10A-01D-1650-10 g.chr11:119148979T>C c.1199T>C c.(1198-1200)aTg>aCg p.M400T COAD 11 119148979 119148979 + Missense_Mutation SNP T T C TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chr11:119148979T>C c.1199T>C c.(1198-1200)aTg>aCg p.M400T COAD 11 119148981 119148981 + Missense_Mutation SNP T T C TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr11:119148981T>C c.1201T>C c.(1201-1203)Tgc>Cgc p.C401R COAD 11 119148981 119148981 + Missense_Mutation SNP T T C TCGA-CM-6164-01A-11D-1650-10 TCGA-CM-6164-10A-01D-1650-10 g.chr11:119148981T>C c.1201T>C c.(1201-1203)Tgc>Cgc p.C401R COAD 11 119148990 119148990 + Missense_Mutation SNP T T C TCGA-AA-3511-01A-21D-1835-10 TCGA-AA-3511-11A-01D-1835-10 g.chr11:119148990T>C c.1210T>C c.(1210-1212)Tgt>Cgt p.C404R COAD 11 119149000 119149000 + Missense_Mutation SNP C C T TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr11:119149000C>T c.1220C>T c.(1219-1221)tCc>tTc p.S407F COAD 11 119149003 119149003 + Missense_Mutation SNP G G C TCGA-AZ-6603-01A-11D-1835-10 TCGA-AZ-6603-11A-02D-1835-10 g.chr11:119149003G>C c.1223G>C c.(1222-1224)tGg>tCg p.W408S COAD 11 119149218 119149218 + Splice_Site SNP A A G TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr11:119149218A>G c.e9-1 COAD 11 119149237 119149237 + Silent SNP C C A TCGA-DM-A28G-01A-11D-A16V-10 TCGA-DM-A28G-10A-01D-A16V-10 g.chr11:119149237C>A c.1245C>A c.(1243-1245)ggC>ggA p.G415G COAD 11 119149242 119149242 + Missense_Mutation SNP C C T TCGA-AA-3968-01A-01W-0995-10 TCGA-AA-3968-10A-01W-0995-10 g.chr11:119149242C>T c.1250C>T c.(1249-1251)cCt>cTt p.P417L COAD 11 119149243 119149243 + Silent SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr11:119149243T>C c.1251T>C c.(1249-1251)ccT>ccC p.P417P COAD 11 119149243 119149243 + Silent SNP T T C TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr11:119149243T>C c.1251T>C c.(1249-1251)ccT>ccC p.P417P COAD 11 119149250 119149250 + Nonsense_Mutation SNP C C T TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr11:119149250C>T c.1258C>T c.(1258-1260)Cga>Tga p.R420* COAD 11 119149251 119149251 + Missense_Mutation SNP G G A TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr11:119149251G>A c.1259G>A c.(1258-1260)cGa>cAa p.R420Q COAD 11 119149291 119149291 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:119149291G>A c.1299G>A c.(1297-1299)ccG>ccA p.P433P COAD 11 119149377 119149377 + Missense_Mutation SNP G G T TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr11:119149377G>T c.1385G>T c.(1384-1386)cGa>cTa p.R462L COAD 11 119155743 119155743 + Missense_Mutation SNP G G A TCGA-D5-6923-01A-11D-1924-10 TCGA-D5-6923-10A-01D-1924-10 g.chr11:119155743G>A c.1496G>A c.(1495-1497)cGa>cAa p.R499Q COAD 11 119155973 119155973 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:119155973G>A c.1638G>A c.(1636-1638)ccG>ccA p.P546P COAD 11 119156011 119156011 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:119156011G>A c.1676G>A c.(1675-1677)cGa>cAa p.R559Q COAD 11 119156239 119156239 + Missense_Mutation SNP C C A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr11:119156239C>A c.1904C>A c.(1903-1905)cCt>cAt p.P635H COAD 11 119169130 119169130 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:119169130G>T c.2314G>T c.(2314-2316)Gat>Tat p.D772Y COAD 11 119169220 119169220 + Missense_Mutation SNP T T C TCGA-CM-6164-01A-11D-1650-10 TCGA-CM-6164-10A-01D-1650-10 g.chr11:119169220T>C c.2404T>C c.(2404-2406)Tgg>Cgg p.W802R COAD 11 119169221 119169221 + Nonsense_Mutation SNP G G A TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr11:119169221G>A c.2405G>A c.(2404-2406)tGg>tAg p.W802* COAD 11 119170313 119170313 + Missense_Mutation SNP C C T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr11:119170313C>T c.2543C>T c.(2542-2544)gCc>gTc p.A848V COAD 11 119170373 119170373 + Missense_Mutation SNP G G T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:119170373G>T c.2603G>T c.(2602-2604)gGg>gTg p.G868V COADREAD 11 119103378 119103378 + Missense_Mutation SNP G G T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:119103378G>T c.416G>T c.(415-417)aGa>aTa p.R139I COADREAD 11 119103391 119103391 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:119103391G>T c.429G>T c.(427-429)gaG>gaT p.E143D COADREAD 11 119142447 119142447 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:119142447G>A c.446G>A c.(445-447)cGa>cAa p.R149Q COADREAD 11 119144604 119144604 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr11:119144604G>A c.617G>A c.(616-618)cGa>cAa p.R206Q COADREAD 11 119144733 119144733 + Splice_Site SNP A A G TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr11:119144733A>G c.746A>G c.(745-747)cAg>cGg p.Q249R COADREAD 11 119145620 119145620 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:119145620G>A c.826G>A c.(826-828)Gaa>Aaa p.E276K COADREAD 11 119145631 119145631 + Silent SNP T T G TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr11:119145631T>G c.837T>G c.(835-837)gcT>gcG p.A279A COADREAD 11 119145653 119145653 + Missense_Mutation SNP A A G TCGA-DM-A28E-01A-11D-A16V-10 TCGA-DM-A28E-10A-01D-A16V-10 g.chr11:119145653A>G c.859A>G c.(859-861)Aaa>Gaa p.K287E COADREAD 11 119145654 119145654 + Missense_Mutation SNP A A G TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr11:119145654A>G c.860A>G c.(859-861)aAa>aGa p.K287R COADREAD 11 119145655 119145655 + Silent SNP A A G TCGA-CK-4948-01B-11D-1650-10 TCGA-CK-4948-10A-01D-1650-10 g.chr11:119145655A>G c.861A>G c.(859-861)aaA>aaG p.K287K COADREAD 11 119148472 119148472 + Missense_Mutation SNP T T C TCGA-CA-6719-01A-11D-1835-10 TCGA-CA-6719-10A-01D-1835-10 g.chr11:119148472T>C c.1013T>C c.(1012-1014)tTg>tCg p.L338S COADREAD 11 119148472 119148472 + Missense_Mutation SNP T T C TCGA-CM-6172-01A-11D-1650-10 TCGA-CM-6172-10A-01D-1650-10 g.chr11:119148472T>C c.1013T>C c.(1012-1014)tTg>tCg p.L338S COADREAD 11 119148875 119148875 + Splice_Site SNP G G A TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr11:119148875G>A c.e8-1 COADREAD 11 119148879 119148879 + Nonsense_Mutation SNP C C T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr11:119148879C>T c.1099C>T c.(1099-1101)Caa>Taa p.Q367* COADREAD 11 119148880 119148880 + Missense_Mutation SNP A A T TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr11:119148880A>T c.1100A>T c.(1099-1101)cAa>cTa p.Q367L COADREAD 11 119148881 119148881 + Silent SNP A A G TCGA-CA-6716-01A-11D-1835-10 TCGA-CA-6716-10A-01D-1835-10 g.chr11:119148881A>G c.1101A>G c.(1099-1101)caA>caG p.Q367Q COADREAD 11 119148908 119148908 + Silent SNP C C T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr11:119148908C>T c.1128C>T c.(1126-1128)tcC>tcT p.S376S COADREAD 11 119148908 119148908 + Silent SNP C C T TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr11:119148908C>T c.1128C>T c.(1126-1128)tcC>tcT p.S376S COADREAD 11 119148908 119148908 + Silent SNP C C T TCGA-CM-5860-01A-01D-1650-10 TCGA-CM-5860-10A-01D-1650-10 g.chr11:119148908C>T c.1128C>T c.(1126-1128)tcC>tcT p.S376S COADREAD 11 119148921 119148921 + Missense_Mutation SNP T T C TCGA-A6-5657-01A-01D-1650-10 TCGA-A6-5657-10A-01D-1650-10 g.chr11:119148921T>C c.1141T>C c.(1141-1143)Tgt>Cgt p.C381R COADREAD 11 119148921 119148921 + Missense_Mutation SNP T T G TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr11:119148921T>G c.1141T>G c.(1141-1143)Tgt>Ggt p.C381G COADREAD 11 119148922 119148922 + Missense_Mutation SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr11:119148922G>A c.1142G>A c.(1141-1143)tGt>tAt p.C381Y COADREAD 11 119148922 119148922 + Missense_Mutation SNP G G A TCGA-G4-6309-01A-21D-1835-10 TCGA-G4-6309-10A-01D-1835-10 g.chr11:119148922G>A c.1142G>A c.(1141-1143)tGt>tAt p.C381Y COADREAD 11 119148923 119148923 + Silent SNP T T C TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr11:119148923T>C c.1143T>C c.(1141-1143)tgT>tgC p.C381C COADREAD 11 119148923 119148923 + Silent SNP T T C TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr11:119148923T>C c.1143T>C c.(1141-1143)tgT>tgC p.C381C COADREAD 11 119148931 119148931 + Missense_Mutation SNP G G A TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr11:119148931G>A c.1151G>A c.(1150-1152)tGt>tAt p.C384Y COADREAD 11 119148963 119148963 + Missense_Mutation SNP C C T TCGA-AZ-5407-01A-01D-1719-10 TCGA-AZ-5407-10A-01D-1719-10 g.chr11:119148963C>T c.1183C>T c.(1183-1185)Ccc>Tcc p.P395S COADREAD 11 119148964 119148964 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr11:119148964C>T c.1184C>T c.(1183-1185)cCc>cTc p.P395L COADREAD 11 119148966 119148966 + Missense_Mutation SNP T T C TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr11:119148966T>C c.1186T>C c.(1186-1188)Tgt>Cgt p.C396R COADREAD 11 119148968 119148968 + Silent SNP T T C TCGA-AG-A016-01A-01W-A005-10 TCGA-AG-A016-10A-01W-A005-10 g.chr11:119148968T>C c.1188T>C c.(1186-1188)tgT>tgC p.C396C COADREAD 11 119148968 119148968 + Silent SNP T T C TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr11:119148968T>C c.1188T>C c.(1186-1188)tgT>tgC p.C396C COADREAD 11 119148973 119148973 + Missense_Mutation SNP A A G TCGA-CK-4947-01B-11D-1650-10 TCGA-CK-4947-10A-01D-1650-10 g.chr11:119148973A>G c.1193A>G c.(1192-1194)cAc>cGc p.H398R COADREAD 11 119148979 119148979 + Missense_Mutation SNP T T C TCGA-A6-5662-01A-01D-1650-10 TCGA-A6-5662-10A-01D-1650-10 g.chr11:119148979T>C c.1199T>C c.(1198-1200)aTg>aCg p.M400T COADREAD 11 119148979 119148979 + Missense_Mutation SNP T T C TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chr11:119148979T>C c.1199T>C c.(1198-1200)aTg>aCg p.M400T COADREAD 11 119148981 119148981 + Missense_Mutation SNP T T C TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr11:119148981T>C c.1201T>C c.(1201-1203)Tgc>Cgc p.C401R COADREAD 11 119148981 119148981 + Missense_Mutation SNP T T C TCGA-CM-6164-01A-11D-1650-10 TCGA-CM-6164-10A-01D-1650-10 g.chr11:119148981T>C c.1201T>C c.(1201-1203)Tgc>Cgc p.C401R COADREAD 11 119148990 119148990 + Missense_Mutation SNP T T C TCGA-AA-3511-01A-21D-1835-10 TCGA-AA-3511-11A-01D-1835-10 g.chr11:119148990T>C c.1210T>C c.(1210-1212)Tgt>Cgt p.C404R COADREAD 11 119149000 119149000 + Missense_Mutation SNP C C T TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr11:119149000C>T c.1220C>T c.(1219-1221)tCc>tTc p.S407F COADREAD 11 119149003 119149003 + Missense_Mutation SNP G G C TCGA-AZ-6603-01A-11D-1835-10 TCGA-AZ-6603-11A-02D-1835-10 g.chr11:119149003G>C c.1223G>C c.(1222-1224)tGg>tCg p.W408S COADREAD 11 119149218 119149218 + Splice_Site SNP A A G TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr11:119149218A>G c.e9-1 COADREAD 11 119149237 119149237 + Silent SNP C C A TCGA-DM-A28G-01A-11D-A16V-10 TCGA-DM-A28G-10A-01D-A16V-10 g.chr11:119149237C>A c.1245C>A c.(1243-1245)ggC>ggA p.G415G COADREAD 11 119149242 119149242 + Missense_Mutation SNP C C T TCGA-AA-3968-01A-01W-0995-10 TCGA-AA-3968-10A-01W-0995-10 g.chr11:119149242C>T c.1250C>T c.(1249-1251)cCt>cTt p.P417L COADREAD 11 119149243 119149243 + Silent SNP T T C TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr11:119149243T>C c.1251T>C c.(1249-1251)ccT>ccC p.P417P COADREAD 11 119149243 119149243 + Silent SNP T T C TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr11:119149243T>C c.1251T>C c.(1249-1251)ccT>ccC p.P417P COADREAD 11 119149245 119149245 + Missense_Mutation SNP T T C TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr11:119149245T>C c.1253T>C c.(1252-1254)tTc>tCc p.F418S COADREAD 11 119149247 119149247 + Missense_Mutation SNP T T C TCGA-AG-3742-01A-11D-1657-10 TCGA-AG-3742-11A-01D-1657-10 g.chr11:119149247T>C c.1255T>C c.(1255-1257)Tgc>Cgc p.C419R COADREAD 11 119149250 119149250 + Nonsense_Mutation SNP C C T TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr11:119149250C>T c.1258C>T c.(1258-1260)Cga>Tga p.R420* COADREAD 11 119149251 119149251 + Missense_Mutation SNP G G A TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr11:119149251G>A c.1259G>A c.(1258-1260)cGa>cAa p.R420Q COADREAD 11 119149291 119149291 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:119149291G>A c.1299G>A c.(1297-1299)ccG>ccA p.P433P COADREAD 11 119149377 119149377 + Missense_Mutation SNP G G T TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr11:119149377G>T c.1385G>T c.(1384-1386)cGa>cTa p.R462L COADREAD 11 119155743 119155743 + Missense_Mutation SNP G G A TCGA-D5-6923-01A-11D-1924-10 TCGA-D5-6923-10A-01D-1924-10 g.chr11:119155743G>A c.1496G>A c.(1495-1497)cGa>cAa p.R499Q COADREAD 11 119155973 119155973 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr11:119155973G>A c.1638G>A c.(1636-1638)ccG>ccA p.P546P COADREAD 11 119156011 119156011 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr11:119156011G>A c.1676G>A c.(1675-1677)cGa>cAa p.R559Q COADREAD 11 119156239 119156239 + Missense_Mutation SNP C C A TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chr11:119156239C>A c.1904C>A c.(1903-1905)cCt>cAt p.P635H COADREAD 11 119169130 119169130 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr11:119169130G>T c.2314G>T c.(2314-2316)Gat>Tat p.D772Y COADREAD 11 119169179 119169179 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:119169179G>A c.2363G>A c.(2362-2364)cGa>cAa p.R788Q COADREAD 11 119169220 119169220 + Missense_Mutation SNP T T C TCGA-CM-6164-01A-11D-1650-10 TCGA-CM-6164-10A-01D-1650-10 g.chr11:119169220T>C c.2404T>C c.(2404-2406)Tgg>Cgg p.W802R COADREAD 11 119169221 119169221 + Nonsense_Mutation SNP G G A TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr11:119169221G>A c.2405G>A c.(2404-2406)tGg>tAg p.W802* COADREAD 11 119170313 119170313 + Missense_Mutation SNP C C T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr11:119170313C>T c.2543C>T c.(2542-2544)gCc>gTc p.A848V COADREAD 11 119170373 119170373 + Missense_Mutation SNP G G T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr11:119170373G>T c.2603G>T c.(2602-2604)gGg>gTg p.G868V DLBC 11 119168130 119168130 + Silent SNP G G C TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr11:119168130G>C c.2190G>C c.(2188-2190)acG>acC p.T730T DLBC 11 119170362 119170362 + Silent SNP C C T TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr11:119170362C>T c.2592C>T c.(2590-2592)ctC>ctT p.L864L DLBC 11 119170480 119170480 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr11:119170480G>A c.2710G>A c.(2710-2712)Gta>Ata p.V904I ESCA 11 119077233 119077233 + Missense_Mutation SNP C C T TCGA-LN-A4A4-01A-11D-A27G-09 TCGA-LN-A4A4-10A-01D-A27G-09 g.chr11:119077233C>T c.106C>T c.(106-108)Cac>Tac p.H36Y ESCA 11 119146741 119146741 + Missense_Mutation SNP C C G TCGA-IC-A6RE-01A-11D-A33E-09 TCGA-IC-A6RE-10A-01D-A33H-09 g.chr11:119146741C>G c.904C>G c.(904-906)Cag>Gag p.Q302E ESCA 11 119149355 119149355 + Missense_Mutation SNP T T A TCGA-LN-A49R-01A-11D-A247-09 TCGA-LN-A49R-10A-01D-A247-09 g.chr11:119149355T>A c.1363T>A c.(1363-1365)Tat>Aat p.Y455N ESCA 11 119155736 119155736 + Missense_Mutation SNP C C T TCGA-R6-A6DQ-01B-11D-A31U-09 TCGA-R6-A6DQ-10A-01D-A31U-09 g.chr11:119155736C>T c.1489C>T c.(1489-1491)Cca>Tca p.P497S ESCA 11 119169165 119169165 + Silent SNP C C G TCGA-L5-A891-01A-11D-A36J-09 TCGA-L5-A891-11A-21D-A36M-09 g.chr11:119169165C>G c.2349C>G c.(2347-2349)gcC>gcG p.A783A ESCA 11 119169200 119169200 + Missense_Mutation SNP A A T TCGA-L5-A8NI-01A-11D-A37C-09 TCGA-L5-A8NI-11A-11D-A37F-09 g.chr11:119169200A>T c.2384A>T c.(2383-2385)aAt>aTt p.N795I ESCA 11 119170428 119170428 + Missense_Mutation SNP G G C TCGA-VR-AA7B-01A-31D-A403-09 TCGA-VR-AA7B-10A-01D-A403-09 g.chr11:119170428G>C c.2658G>C c.(2656-2658)gaG>gaC p.E886D GBM 11 119148932 119148932 + Missense_Mutation SNP T T G TCGA-06-2562-01A-01D-1494-08 TCGA-06-2562-10A-01D-1494-08 g.chr11:119148932T>G c.1152T>G c.(1150-1152)tgT>tgG p.C384W GBMLGG 11 119077233 119077235 + In_Frame_Del DEL CAC CAC - TCGA-S9-A6TY-01A-12D-A32B-08 TCGA-S9-A6TY-10A-01D-A329-08 g.chr11:119077233_119077235delCAC c.106_108delCAC c.(106-108)cacdel p.H42del GBMLGG 11 119103190 119103190 + Silent SNP G G A TCGA-FG-A6IZ-01A-11D-A31L-08 TCGA-FG-A6IZ-10A-01D-A31J-08 g.chr11:119103190G>A c.228G>A c.(226-228)gcG>gcA p.A76A GBMLGG 11 119148932 119148932 + Missense_Mutation SNP T T G TCGA-06-2562-01A-01D-1494-08 TCGA-06-2562-10A-01D-1494-08 g.chr11:119148932T>G c.1152T>G c.(1150-1152)tgT>tgG p.C384W HNSC 11 119103214 119103214 + Silent SNP C C T TCGA-BA-4077-01B-01D-1434-08 TCGA-BA-4077-10A-01D-1434-08 g.chr11:119103214C>T c.252C>T c.(250-252)atC>atT p.I84I HNSC 11 119144609 119144609 + Missense_Mutation SNP G G C TCGA-CR-7374-01A-11D-2012-08 TCGA-CR-7374-10A-01D-2013-08 g.chr11:119144609G>C c.622G>C c.(622-624)Gct>Cct p.A208P HNSC 11 119149355 119149356 + In_Frame_Ins INS - - ATG TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr11:119149355_119149356insATG c.1363_1364insATG c.(1363-1365)tat>tATGat p.460_461insD HNSC 11 119169109 119169109 + Missense_Mutation SNP G G A TCGA-CQ-6223-01A-11D-1912-08 TCGA-CQ-6223-10A-01D-1912-08 g.chr11:119169109G>A c.2293G>A c.(2293-2295)Gag>Aag p.E765K KIPAN 11 119168096 119168096 + Missense_Mutation SNP C C T TCGA-B0-5094-01A-01D-1421-08 TCGA-B0-5094-11A-01D-1421-08 g.chr11:119168096C>T c.2156C>T c.(2155-2157)gCa>gTa p.A719V KIRC 11 119168096 119168096 + Missense_Mutation SNP C C T TCGA-B0-5094-01A-01D-1421-08 TCGA-B0-5094-11A-01D-1421-08 g.chr11:119168096C>T c.2156C>T c.(2155-2157)gCa>gTa p.A719V LAML 11 119148875 119148875 + Splice_Site SNP G G C TCGA-AB-2914-03A-01W-0732-08 TCGA-AB-2914-11A-01W-0732-08 g.chr11:119148875G>C c.e8-1 LAML 11 119148880 119148880 + Missense_Mutation SNP A A G TCGA-AB-2989-03A-01D-0739-09 TCGA-AB-2989-11A-01D-0739-09 g.chr11:119148880A>G c.1100A>G c.(1099-1101)cAa>cGa p.Q367R LAML 11 119168130 119168130 + Silent SNP G G A TCGA-AB-2978-03A-01D-0739-09 TCGA-AB-2978-11A-01D-0739-09 g.chr11:119168130G>A c.2190G>A c.(2188-2190)acG>acA p.T730T LGG 11 119077233 119077235 + In_Frame_Del DEL CAC CAC - TCGA-S9-A6TY-01A-12D-A32B-08 TCGA-S9-A6TY-10A-01D-A329-08 g.chr11:119077233_119077235delCAC c.106_108delCAC c.(106-108)cacdel p.H42del LGG 11 119103190 119103190 + Silent SNP G G A TCGA-FG-A6IZ-01A-11D-A31L-08 TCGA-FG-A6IZ-10A-01D-A31J-08 g.chr11:119103190G>A c.228G>A c.(226-228)gcG>gcA p.A76A LIHC 11 119103248 119103248 + Missense_Mutation SNP C C T TCGA-UB-A7MF-01A-11D-A33K-10 TCGA-UB-A7MF-10A-01D-A33K-10 g.chr11:119103248C>T c.286C>T c.(286-288)Cgt>Tgt p.R96C LIHC 11 119168164 119168165 + Frame_Shift_Ins INS - - CATCTAT TCGA-ZS-A9CG-01A-11D-A36X-10 TCGA-ZS-A9CG-10A-01D-A370-10 g.chr11:119168164_119168165insCATCTAT c.2224_2225insCATCTAT c.(2224-2226)ccafs p.-744fs LIHC 11 119169140 119169140 + Missense_Mutation SNP A A T TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr11:119169140A>T c.2324A>T c.(2323-2325)gAt>gTt p.D775V LIHC 11 119170325 119170325 + Missense_Mutation SNP C C T TCGA-DD-AADG-01A-11D-A40R-10 TCGA-DD-AADG-10A-01D-A40U-10 g.chr11:119170325C>T c.2555C>T c.(2554-2556)aCc>aTc p.T852I LUAD 11 119077161 119077161 + Frame_Shift_Del DEL G G - TCGA-97-8176-01A-11D-2393-08 TCGA-97-8176-10B-01D-2393-08 g.chr11:119077161delG c.34delG c.(34-36)gggfs p.G14fs LUAD 11 119077233 119077235 + In_Frame_Del DEL CAC CAC - TCGA-62-8398-01A-11D-2323-08 TCGA-62-8398-10A-01D-2323-08 g.chr11:119077233_119077235delCAC c.106_108delCAC c.(106-108)cacdel p.H42del LUAD 11 119103165 119103165 + Missense_Mutation SNP G G T TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chr11:119103165G>T c.203G>T c.(202-204)cGg>cTg p.R68L LUAD 11 119142461 119142461 + Missense_Mutation SNP C C G TCGA-MP-A4SY-01A-21D-A24P-08 TCGA-MP-A4SY-10A-01D-A24P-08 g.chr11:119142461C>G c.460C>G c.(460-462)Ctg>Gtg p.L154V LUAD 11 119144584 119144584 + Silent SNP A A T TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr11:119144584A>T c.597A>T c.(595-597)atA>atT p.I199I LUAD 11 119145632 119145632 + Missense_Mutation SNP C C T TCGA-17-Z017-01A-01W-0746-08 TCGA-17-Z017-11A-01W-0746-08 g.chr11:119145632C>T c.838C>T c.(838-840)Cgg>Tgg p.R280W LUAD 11 119148982 119148982 + Missense_Mutation SNP G G T TCGA-97-7937-01A-11D-2167-08 TCGA-97-7937-10A-01D-2167-08 g.chr11:119148982G>T c.1202G>T c.(1201-1203)tGc>tTc p.C401F LUAD 11 119149229 119149229 + Missense_Mutation SNP G G C TCGA-50-5946-01A-11D-1753-08 TCGA-50-5946-10A-01D-1753-08 g.chr11:119149229G>C c.1237G>C c.(1237-1239)Ggt>Cgt p.G413R LUAD 11 119149277 119149288 + In_Frame_Del DEL ATCGTGGTAGAT ATCGTGGTAGAT - TCGA-78-7153-01A-11D-2036-08 TCGA-78-7153-10A-01D-2036-08 g.chr11:119149277_119149288delATCGTGGTAGAT c.1285_1296delATCGTGGTAGAT c.(1285-1296)atcgtggtagatdel p.IVVD429del LUAD 11 119169209 119169209 + Missense_Mutation SNP C C A TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chr11:119169209C>A c.2393C>A c.(2392-2394)tCc>tAc p.S798Y LUAD 11 119170450 119170450 + Nonsense_Mutation SNP G G T TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr11:119170450G>T c.2680G>T c.(2680-2682)Gaa>Taa p.E894* LUSC 11 119103223 119103223 + Silent SNP G G A TCGA-21-5786-01A-01D-1632-08 TCGA-21-5786-10A-01D-1632-08 g.chr11:119103223G>A c.261G>A c.(259-261)ctG>ctA p.L87L LUSC 11 119103295 119103295 + Silent SNP A A G TCGA-18-3412-01A-01D-0983-08 TCGA-18-3412-11A-01D-0983-08 g.chr11:119103295A>G c.333A>G c.(331-333)gaA>gaG p.E111E LUSC 11 119148970 119148970 + Missense_Mutation SNP G G T TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr11:119148970G>T c.1190G>T c.(1189-1191)gGa>gTa p.G397V LUSC 11 119149393 119149393 + Silent SNP C C A TCGA-21-5786-01A-01D-1632-08 TCGA-21-5786-10A-01D-1632-08 g.chr11:119149393C>A c.1401C>A c.(1399-1401)ctC>ctA p.L467L LUSC 11 119149399 119149399 + Missense_Mutation SNP G G A TCGA-46-6026-01A-11D-1817-08 TCGA-46-6026-10A-01D-1817-08 g.chr11:119149399G>A c.1407G>A c.(1405-1407)atG>atA p.M469I LUSC 11 119155697 119155697 + Missense_Mutation SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr11:119155697C>T c.1450C>T c.(1450-1452)Cca>Tca p.P484S LUSC 11 119155953 119155953 + Silent SNP C C A TCGA-66-2744-01A-01D-0983-08 TCGA-66-2744-11A-01D-0983-08 g.chr11:119155953C>A c.1618C>A c.(1618-1620)Cga>Aga p.R540R OV 11 119148471 119148471 + Silent SNP T T C TCGA-24-2293-01A-01W-0799-08 TCGA-24-2293-10A-01W-0799-08 g.chr11:119148471T>C c.1012T>C c.(1012-1014)Ttg>Ctg p.L338L PAAD 11 119144654 119144654 + Missense_Mutation SNP G G C TCGA-2J-AABO-01A-21D-A40W-08 TCGA-2J-AABO-10A-01D-A40W-08 g.chr11:119144654G>C c.667G>C c.(667-669)Gct>Cct p.A223P PAAD 11 119145571 119145571 + Missense_Mutation SNP C C A TCGA-FB-A78T-01A-12D-A32N-08 TCGA-FB-A78T-10A-01D-A32N-08 g.chr11:119145571C>A c.777C>A c.(775-777)aaC>aaA p.N259K PAAD 11 119148958 119148958 + Missense_Mutation SNP T T C TCGA-HV-A7OL-01A-11D-A33T-08 TCGA-HV-A7OL-10A-01D-A33W-08 g.chr11:119148958T>C c.1178T>C c.(1177-1179)aTt>aCt p.I393T PRAD 11 119169173 119169173 + Missense_Mutation SNP C C G TCGA-KK-A8IK-01A-11D-A364-08 TCGA-KK-A8IK-11A-11D-A362-08 g.chr11:119169173C>G c.2357C>G c.(2356-2358)gCc>gGc p.A786G READ 11 119103391 119103391 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:119103391G>T c.429G>T c.(427-429)gaG>gaT p.E143D READ 11 119142447 119142447 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:119142447G>A c.446G>A c.(445-447)cGa>cAa p.R149Q READ 11 119144733 119144733 + Splice_Site SNP A A G TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr11:119144733A>G c.746A>G c.(745-747)cAg>cGg p.Q249R READ 11 119148923 119148923 + Silent SNP T T C TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr11:119148923T>C c.1143T>C c.(1141-1143)tgT>tgC p.C381C READ 11 119148966 119148966 + Missense_Mutation SNP T T C TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr11:119148966T>C c.1186T>C c.(1186-1188)Tgt>Cgt p.C396R READ 11 119148968 119148968 + Silent SNP T T C TCGA-AG-A016-01A-01W-A005-10 TCGA-AG-A016-10A-01W-A005-10 g.chr11:119148968T>C c.1188T>C c.(1186-1188)tgT>tgC p.C396C READ 11 119149245 119149245 + Missense_Mutation SNP T T C TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr11:119149245T>C c.1253T>C c.(1252-1254)tTc>tCc p.F418S READ 11 119149247 119149247 + Missense_Mutation SNP T T C TCGA-AG-3742-01A-11D-1657-10 TCGA-AG-3742-11A-01D-1657-10 g.chr11:119149247T>C c.1255T>C c.(1255-1257)Tgc>Cgc p.C419R READ 11 119169179 119169179 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:119169179G>A c.2363G>A c.(2362-2364)cGa>cAa p.R788Q SKCM 11 119103163 119103163 + Silent SNP G G A TCGA-EE-A2GU-06A-11D-A196-08 TCGA-EE-A2GU-10A-01D-A198-08 g.chr11:119103163G>A c.201G>A c.(199-201)gtG>gtA p.V67V SKCM 11 119103291 119103291 + Missense_Mutation SNP G G A TCGA-EE-A2MT-06A-11D-A197-08 TCGA-EE-A2MT-10A-01D-A199-08 g.chr11:119103291G>A c.329G>A c.(328-330)gGa>gAa p.G110E SKCM 11 119142544 119142544 + Silent SNP T T C TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:119142544T>C c.543T>C c.(541-543)atT>atC p.I181I SKCM 11 119145646 119145646 + Silent SNP C C T TCGA-GN-A267-06A-21D-A196-08 TCGA-GN-A267-10A-01D-A198-08 g.chr11:119145646C>T c.852C>T c.(850-852)ttC>ttT p.F284F SKCM 11 119148871 119148874 + Splice_Site DEL CAAA CAAA - TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr11:119148871_119148874delCAAA c.e8-1 SKCM 11 119149238 119149238 + Missense_Mutation SNP T T A TCGA-EB-A44Q-06A-11D-A25O-08 TCGA-EB-A44Q-10A-01D-A25O-08 g.chr11:119149238T>A c.1246T>A c.(1246-1248)Tgt>Agt p.C416S SKCM 11 119149242 119149242 + Missense_Mutation SNP C C A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr11:119149242C>A c.1250C>A c.(1249-1251)cCt>cAt p.P417H SKCM 11 119149244 119149244 + Missense_Mutation SNP T T A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr11:119149244T>A c.1252T>A c.(1252-1254)Ttc>Atc p.F418I SKCM 11 119149279 119149279 + Silent SNP C C T TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr11:119149279C>T c.1287C>T c.(1285-1287)atC>atT p.I429I SKCM 11 119155688 119155688 + Missense_Mutation SNP C C T TCGA-EE-A3J3-06A-11D-A20D-08 TCGA-EE-A3J3-10A-01D-A20D-08 g.chr11:119155688C>T c.1441C>T c.(1441-1443)Ccg>Tcg p.P481S SKCM 11 119155689 119155689 + Missense_Mutation SNP C C T TCGA-EE-A3J3-06A-11D-A20D-08 TCGA-EE-A3J3-10A-01D-A20D-08 g.chr11:119155689C>T c.1442C>T c.(1441-1443)cCg>cTg p.P481L SKCM 11 119155775 119155775 + Missense_Mutation SNP C C T TCGA-EE-A2MN-06A-11D-A197-08 TCGA-EE-A2MN-10A-01D-A199-08 g.chr11:119155775C>T c.1528C>T c.(1528-1530)Ccc>Tcc p.P510S SKCM 11 119156009 119156009 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:119156009C>T c.1674C>T c.(1672-1674)tcC>tcT p.S558S SKCM 11 119158644 119158644 + Missense_Mutation SNP C C T TCGA-ER-A199-06A-11D-A197-08 TCGA-ER-A199-10A-01D-A199-08 g.chr11:119158644C>T c.2024C>T c.(2023-2025)tCt>tTt p.S675F SKCM 11 119170400 119170400 + Missense_Mutation SNP C C T TCGA-EE-A2GD-06A-11D-A196-08 TCGA-EE-A2GD-10A-01D-A198-08 g.chr11:119170400C>T c.2630C>T c.(2629-2631)gCt>gTt p.A877V SKCM 11 119170443 119170443 + Silent SNP C C T TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr11:119170443C>T c.2673C>T c.(2671-2673)atC>atT p.I891I

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation AML-US 11 119155746 119155746 insertion of <=200bp - TGACCTGG frameshift_variant L500LTW? BLCA-CN 11 119170265 119170265 single base substitution A T missense_variant N832I 2495A>T BLCA-US 11 119142469 119142469 single base substitution C T synonymous_variant L156L 468C>T BLCA-US 11 119149302 119149302 single base substitution G T missense_variant R437I 1310G>T BLCA-US 11 119149399 119149399 single base substitution G A missense_variant M469I 1407G>A BLCA-US 11 119167741 119167741 single base substitution C T missense_variant S717L 2150C>T BLCA-US 11 119170369 119170369 single base substitution C T stop_gained Q867* 2599C>T BLCA-US 11 119181552 119181552 single base substitution G A downstream_gene_variant BLCA-US 11 119181614 119181614 single base substitution C T downstream_gene_variant BLCA-US 11 119182861 119182861 single base substitution C T downstream_gene_variant BLCA-US 11 119183625 119183625 single base substitution C G downstream_gene_variant BRCA-EU 11 119072782 119072782 single base substitution C T upstream_gene_variant BRCA-EU 11 119072981 119072981 single base substitution C T upstream_gene_variant BRCA-EU 11 119073464 119073464 single base substitution C A upstream_gene_variant BRCA-EU 11 119076241 119076241 single base substitution C G upstream_gene_variant BRCA-EU 11 119076503 119076503 single base substitution C T upstream_gene_variant BRCA-EU 11 119076914 119076914 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 11 119077574 119077574 single base substitution G C intron_variant BRCA-EU 11 119078882 119078882 deletion of <=200bp A - intron_variant BRCA-EU 11 119079766 119079766 single base substitution C A intron_variant BRCA-EU 11 119080136 119080136 single base substitution C T intron_variant BRCA-EU 11 119080302 119080302 single base substitution G A intron_variant BRCA-EU 11 119080676 119080676 single base substitution C T intron_variant BRCA-EU 11 119082550 119082550 single base substitution A G intron_variant BRCA-EU 11 119083277 119083277 single base substitution G A intron_variant BRCA-EU 11 119083715 119083715 single base substitution A G intron_variant BRCA-EU 11 119086062 119086062 single base substitution G T intron_variant BRCA-EU 11 119090326 119090326 single base substitution C G intron_variant BRCA-EU 11 119094308 119094308 deletion of <=200bp T - intron_variant BRCA-EU 11 119094361 119094361 insertion of <=200bp - TC intron_variant BRCA-EU 11 119095655 119095655 single base substitution A G intron_variant BRCA-EU 11 119095721 119095721 single base substitution T C intron_variant BRCA-EU 11 119098395 119098395 single base substitution G T intron_variant BRCA-EU 11 119099982 119099982 single base substitution G T intron_variant BRCA-EU 11 119099983 119099983 single base substitution A T intron_variant BRCA-EU 11 119102688 119102688 single base substitution C T intron_variant BRCA-EU 11 119103277 119103277 single base substitution G A synonymous_variant K105K 315G>A BRCA-EU 11 119104307 119104307 single base substitution C T intron_variant BRCA-EU 11 119104631 119104631 single base substitution T A intron_variant BRCA-EU 11 119106592 119106592 single base substitution A C intron_variant BRCA-EU 11 119107060 119107060 single base substitution T G intron_variant BRCA-EU 11 119107726 119107726 single base substitution C T intron_variant BRCA-EU 11 119109705 119109705 single base substitution C T intron_variant BRCA-EU 11 119110086 119110086 single base substitution C G intron_variant BRCA-EU 11 119110323 119110323 single base substitution G T intron_variant BRCA-EU 11 119112153 119112153 single base substitution G C intron_variant BRCA-EU 11 119113285 119113285 single base substitution G C intron_variant BRCA-EU 11 119113712 119113712 single base substitution G A intron_variant BRCA-EU 11 119114091 119114091 single base substitution G T intron_variant BRCA-EU 11 119114505 119114505 single base substitution C T intron_variant BRCA-EU 11 119115815 119115815 single base substitution C T intron_variant BRCA-EU 11 119116353 119116353 single base substitution C T intron_variant BRCA-EU 11 119116926 119116926 single base substitution G T intron_variant BRCA-EU 11 119118396 119118396 single base substitution C T intron_variant BRCA-EU 11 119118838 119118838 single base substitution T A intron_variant BRCA-EU 11 119120538 119120538 insertion of <=200bp - T intron_variant BRCA-EU 11 119121160 119121160 single base substitution T C intron_variant BRCA-EU 11 119121849 119121849 single base substitution C G intron_variant BRCA-EU 11 119124496 119124496 single base substitution G A intron_variant BRCA-EU 11 119125659 119125659 single base substitution C T intron_variant BRCA-EU 11 119129474 119129474 deletion of <=200bp T - intron_variant BRCA-EU 11 119129903 119129903 deletion of <=200bp G - intron_variant BRCA-EU 11 119130010 119130010 single base substitution G T intron_variant BRCA-EU 11 119132025 119132025 single base substitution A G intron_variant BRCA-EU 11 119132834 119132838 deletion of <=200bp CACTT - intron_variant BRCA-EU 11 119133321 119133321 single base substitution G A intron_variant BRCA-EU 11 119133390 119133390 single base substitution C A intron_variant BRCA-EU 11 119133442 119133442 single base substitution G A intron_variant BRCA-EU 11 119136262 119136262 single base substitution A G intron_variant BRCA-EU 11 119136482 119136482 single base substitution C G intron_variant BRCA-EU 11 119137405 119137405 single base substitution A C intron_variant BRCA-EU 11 119143565 119143565 single base substitution C A intron_variant BRCA-EU 11 119146519 119146519 single base substitution C T intron_variant BRCA-EU 11 119147270 119147270 single base substitution C T intron_variant BRCA-EU 11 119147494 119147494 single base substitution A T intron_variant BRCA-EU 11 119147926 119147926 single base substitution C G intron_variant BRCA-EU 11 119151506 119151506 single base substitution G C intron_variant BRCA-EU 11 119151651 119151651 single base substitution C G intron_variant BRCA-EU 11 119151867 119151867 single base substitution C T intron_variant BRCA-EU 11 119153580 119153580 single base substitution G A intron_variant BRCA-EU 11 119153585 119153585 single base substitution G C intron_variant BRCA-EU 11 119154079 119154079 single base substitution A C intron_variant BRCA-EU 11 119154740 119154740 deletion of <=200bp A - intron_variant BRCA-EU 11 119158082 119158082 single base substitution C T intron_variant BRCA-EU 11 119159944 119159944 single base substitution C G intron_variant BRCA-EU 11 119160859 119160859 single base substitution G A intron_variant BRCA-EU 11 119162165 119162165 single base substitution C T intron_variant BRCA-EU 11 119162441 119162441 single base substitution A T intron_variant BRCA-EU 11 119162575 119162575 deletion of <=200bp T - intron_variant BRCA-EU 11 119163320 119163320 single base substitution G A intron_variant BRCA-EU 11 119164854 119164854 single base substitution A T intron_variant BRCA-EU 11 119164989 119164989 single base substitution A G intron_variant BRCA-EU 11 119165126 119165126 single base substitution C G intron_variant BRCA-EU 11 119166279 119166279 single base substitution A T intron_variant BRCA-EU 11 119166280 119166280 deletion of <=200bp T - intron_variant BRCA-EU 11 119166966 119166966 deletion of <=200bp T - intron_variant BRCA-EU 11 119171551 119171551 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 119172011 119172011 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 119172093 119172093 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 119172424 119172424 single base substitution C T 3_prime_UTR_variant BRCA-EU 11 119172492 119172492 single base substitution G T 3_prime_UTR_variant BRCA-EU 11 119172665 119172665 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 119172912 119172912 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 119172939 119172939 single base substitution C T 3_prime_UTR_variant BRCA-EU 11 119173332 119173332 single base substitution C T 3_prime_UTR_variant BRCA-EU 11 119174017 119174042 deletion of <=200bp ATGACCACTGTTCATTGAAAAATAGT - 3_prime_UTR_variant BRCA-EU 11 119175804 119175804 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 119176059 119176059 single base substitution C T 3_prime_UTR_variant BRCA-EU 11 119176310 119176310 single base substitution A G 3_prime_UTR_variant BRCA-EU 11 119177965 119177965 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 119180582 119180582 single base substitution G A downstream_gene_variant BRCA-EU 11 119180638 119180638 single base substitution A G downstream_gene_variant BRCA-EU 11 119182481 119182481 single base substitution G A downstream_gene_variant BRCA-EU 11 119182514 119182514 single base substitution T C downstream_gene_variant BRCA-EU 11 119182712 119182712 single base substitution G A downstream_gene_variant BRCA-EU 11 119183685 119183685 single base substitution A G downstream_gene_variant BRCA-FR 11 119076503 119076503 single base substitution C T upstream_gene_variant BRCA-FR 11 119088713 119088713 single base substitution T C intron_variant BRCA-FR 11 119121160 119121160 single base substitution T C intron_variant BRCA-FR 11 119143565 119143565 single base substitution C A intron_variant BRCA-FR 11 119147270 119147270 single base substitution C T intron_variant BRCA-FR 11 119153585 119153585 single base substitution G C intron_variant BRCA-FR 11 119154545 119154545 single base substitution C T intron_variant BRCA-FR 11 119159944 119159944 single base substitution C G intron_variant BRCA-FR 11 119165126 119165126 single base substitution C G intron_variant BRCA-FR 11 119173332 119173332 single base substitution C T 3_prime_UTR_variant BRCA-FR 11 119182481 119182481 single base substitution G A downstream_gene_variant BRCA-UK 11 119106072 119106072 single base substitution G A intron_variant BRCA-UK 11 119110086 119110086 single base substitution C G intron_variant BRCA-UK 11 119177702 119177702 single base substitution C G 3_prime_UTR_variant BRCA-US 11 119103160 119103160 single base substitution G T splice_region_variant BRCA-US 11 119103255 119103255 single base substitution T C missense_variant I98T 293T>C BRCA-US 11 119103359 119103359 single base substitution T C missense_variant F133L 397T>C BRCA-US 11 119142562 119142562 single base substitution G A synonymous_variant A187A 561G>A BRCA-US 11 119148506 119148506 single base substitution G A synonymous_variant L349L 1047G>A BRCA-US 11 119155748 119155748 single base substitution G C missense_variant D501H 1501G>C BRCA-US 11 119158602 119158602 single base substitution A C missense_variant H661P 1982A>C BRCA-US 11 119170209 119170209 single base substitution C A synonymous_variant V813V 2439C>A BRCA-US 11 119181151 119181151 single base substitution C T downstream_gene_variant BRCA-US 11 119181178 119181178 single base substitution T A downstream_gene_variant BRCA-US 11 119182249 119182249 single base substitution G T downstream_gene_variant BRCA-US 11 119183561 119183561 single base substitution G C downstream_gene_variant BRCA-US 11 119183643 119183643 single base substitution C T downstream_gene_variant BTCA-JP 11 119142639 119142639 single base substitution G A intron_variant BTCA-JP 11 119144685 119144685 single base substitution A G missense_variant N233S 698A>G BTCA-JP 11 119148323 119148323 deletion of <=200bp T - intron_variant BTCA-JP 11 119149127 119149127 deletion of <=200bp T - intron_variant BTCA-JP 11 119149280 119149280 single base substitution G A missense_variant V430M 1288G>A BTCA-JP 11 119158455 119158455 single base substitution G C intron_variant BTCA-JP 11 119170273 119170273 single base substitution C T missense_variant R835W 2503C>T BTCA-JP 11 119181407 119181407 single base substitution G A downstream_gene_variant CESC-US 11 119149358 119149358 single base substitution G A missense_variant D456N 1366G>A CLLE-ES 11 119085652 119085652 single base substitution T G intron_variant CLLE-ES 11 119104915 119104915 single base substitution C T intron_variant CLLE-ES 11 119120733 119120733 single base substitution C T intron_variant CLLE-ES 11 119139062 119139062 single base substitution A G intron_variant CLLE-ES 11 119149894 119149894 single base substitution T C intron_variant CLLE-ES 11 119164084 119164084 single base substitution C T intron_variant CLLE-ES 11 119174529 119174529 single base substitution A G 3_prime_UTR_variant COAD-US 11 119103378 119103378 single base substitution G T missense_variant R139I 416G>T COAD-US 11 119144604 119144604 single base substitution G A missense_variant R206Q 617G>A COAD-US 11 119145620 119145620 single base substitution G A missense_variant E276K 826G>A COAD-US 11 119149000 119149000 single base substitution C T missense_variant S407F 1220C>T COAD-US 11 119155690 119155690 single base substitution G A synonymous_variant P481P 1443G>A COAD-US 11 119169085 119169085 single base substitution G A missense_variant A757T 2269G>A COAD-US 11 119169130 119169130 single base substitution G T missense_variant D772Y 2314G>T COAD-US 11 119180610 119180610 single base substitution C T downstream_gene_variant COAD-US 11 119181151 119181151 single base substitution C T downstream_gene_variant COAD-US 11 119181170 119181170 single base substitution T C downstream_gene_variant COAD-US 11 119181807 119181807 single base substitution G T downstream_gene_variant COAD-US 11 119182270 119182270 single base substitution C T downstream_gene_variant COAD-US 11 119182271 119182271 single base substitution C T downstream_gene_variant COAD-US 11 119182285 119182285 single base substitution C T downstream_gene_variant COAD-US 11 119182825 119182825 single base substitution G A downstream_gene_variant COAD-US 11 119183067 119183067 single base substitution C T downstream_gene_variant COAD-US 11 119183068 119183068 single base substitution C T downstream_gene_variant COCA-CN 11 119077003 119077003 single base substitution C T 5_prime_UTR_variant COCA-CN 11 119103218 119103218 single base substitution G T missense_variant D86Y 256G>T COCA-CN 11 119103249 119103249 single base substitution G A missense_variant R96H 287G>A COCA-CN 11 119114032 119114032 single base substitution T C intron_variant COCA-CN 11 119135162 119135162 single base substitution C T intron_variant COCA-CN 11 119144659 119144659 single base substitution G A synonymous_variant L224L 672G>A COCA-CN 11 119145753 119145753 single base substitution T G intron_variant COCA-CN 11 119146744 119146744 single base substitution T C missense_variant W303R 907T>C COCA-CN 11 119146892 119146892 single base substitution C T intron_variant COCA-CN 11 119149449 119149449 single base substitution C A intron_variant COCA-CN 11 119155666 119155666 single base substitution T G intron_variant COCA-CN 11 119155916 119155916 single base substitution T C synonymous_variant L527L 1581T>C COCA-CN 11 119155954 119155954 single base substitution G A missense_variant R540Q 1619G>A COCA-CN 11 119168077 119168077 single base substitution C T intron_variant COCA-CN 11 119168104 119168104 single base substitution T C missense_variant C722R 2164T>C COCA-CN 11 119168250 119168250 single base substitution A C intron_variant COCA-CN 11 119180560 119180560 single base substitution G T downstream_gene_variant COCA-CN 11 119181050 119181050 single base substitution G A downstream_gene_variant COCA-CN 11 119181676 119181676 single base substitution C A downstream_gene_variant COCA-CN 11 119182979 119182979 single base substitution T C downstream_gene_variant COCA-CN 11 119183011 119183011 single base substitution G A downstream_gene_variant COCA-CN 11 119183297 119183297 single base substitution G A downstream_gene_variant COCA-CN 11 119183757 119183757 single base substitution G T downstream_gene_variant EOPC-DE 11 119160466 119160466 single base substitution A C intron_variant EOPC-DE 11 119166886 119166886 single base substitution G A intron_variant ESAD-UK 11 119074453 119074453 deletion of <=200bp A - upstream_gene_variant ESAD-UK 11 119074666 119074666 deletion of <=200bp T - upstream_gene_variant ESAD-UK 11 119076336 119076336 single base substitution T C upstream_gene_variant ESAD-UK 11 119078252 119078252 single base substitution A T intron_variant ESAD-UK 11 119078882 119078882 deletion of <=200bp A - intron_variant ESAD-UK 11 119079188 119079188 single base substitution C A intron_variant ESAD-UK 11 119082792 119082792 single base substitution G A intron_variant ESAD-UK 11 119083011 119083011 deletion of <=200bp A - intron_variant ESAD-UK 11 119083683 119083683 single base substitution A C intron_variant ESAD-UK 11 119084271 119084271 single base substitution C T intron_variant ESAD-UK 11 119084812 119084812 single base substitution A G intron_variant ESAD-UK 11 119085202 119085202 single base substitution G A intron_variant ESAD-UK 11 119085521 119085521 single base substitution A G intron_variant ESAD-UK 11 119086976 119086976 single base substitution C T intron_variant ESAD-UK 11 119089766 119089766 single base substitution A T intron_variant ESAD-UK 11 119091119 119091119 single base substitution G T intron_variant ESAD-UK 11 119094317 119094317 single base substitution A T intron_variant ESAD-UK 11 119096037 119096037 single base substitution C T intron_variant ESAD-UK 11 119097356 119097356 single base substitution C T intron_variant ESAD-UK 11 119100694 119100694 single base substitution C T intron_variant ESAD-UK 11 119102949 119102949 single base substitution C T intron_variant ESAD-UK 11 119104352 119104352 single base substitution A T intron_variant ESAD-UK 11 119104770 119104770 single base substitution G A intron_variant ESAD-UK 11 119105816 119105816 insertion of <=200bp - T intron_variant ESAD-UK 11 119106487 119106487 single base substitution C G intron_variant ESAD-UK 11 119108020 119108020 single base substitution C T intron_variant ESAD-UK 11 119108437 119108437 single base substitution C T intron_variant ESAD-UK 11 119113566 119113566 single base substitution T A intron_variant ESAD-UK 11 119119140 119119140 single base substitution T A intron_variant ESAD-UK 11 119119971 119119971 single base substitution A G intron_variant ESAD-UK 11 119122253 119122253 single base substitution A G intron_variant ESAD-UK 11 119122720 119122720 single base substitution T G intron_variant ESAD-UK 11 119122880 119122880 single base substitution C T intron_variant ESAD-UK 11 119133088 119133088 single base substitution G C intron_variant ESAD-UK 11 119134823 119134823 single base substitution A T intron_variant ESAD-UK 11 119137181 119137181 single base substitution A G intron_variant ESAD-UK 11 119137682 119137682 deletion of <=200bp T - intron_variant ESAD-UK 11 119141576 119141576 single base substitution C T intron_variant ESAD-UK 11 119141924 119141924 single base substitution C T intron_variant ESAD-UK 11 119143694 119143694 single base substitution T A intron_variant ESAD-UK 11 119143696 119143696 single base substitution T A intron_variant ESAD-UK 11 119148327 119148327 single base substitution T C intron_variant ESAD-UK 11 119149036 119149036 single base substitution G A intron_variant ESAD-UK 11 119153295 119153295 single base substitution T G intron_variant ESAD-UK 11 119153588 119153588 single base substitution G T intron_variant ESAD-UK 11 119153649 119153649 single base substitution A C intron_variant ESAD-UK 11 119153687 119153687 single base substitution C T intron_variant ESAD-UK 11 119158469 119158469 single base substitution T C intron_variant ESAD-UK 11 119158836 119158836 single base substitution G A intron_variant ESAD-UK 11 119159971 119159971 single base substitution T C intron_variant ESAD-UK 11 119164167 119164167 single base substitution C T intron_variant ESAD-UK 11 119164186 119164186 single base substitution A G intron_variant ESAD-UK 11 119164237 119164237 single base substitution T C intron_variant ESAD-UK 11 119166280 119166280 single base substitution T A intron_variant ESAD-UK 11 119168093 119168093 single base substitution G A splice_acceptor_variant ESAD-UK 11 119169134 119169134 single base substitution G A missense_variant G773E 2318G>A ESAD-UK 11 119173269 119173270 deletion of <=200bp TC - 3_prime_UTR_variant ESAD-UK 11 119177385 119177385 single base substitution T C 3_prime_UTR_variant ESAD-UK 11 119177551 119177551 single base substitution G A 3_prime_UTR_variant ESAD-UK 11 119177822 119177822 single base substitution G A 3_prime_UTR_variant ESAD-UK 11 119181170 119181170 single base substitution T C downstream_gene_variant ESAD-UK 11 119182103 119182103 single base substitution C T downstream_gene_variant ESAD-UK 11 119182195 119182195 single base substitution G A downstream_gene_variant ESAD-UK 11 119182496 119182496 single base substitution C G downstream_gene_variant ESCA-CN 11 119103029 119103029 single base substitution C T intron_variant ESCA-CN 11 119155954 119155954 single base substitution G A missense_variant R540Q 1619G>A ESCA-CN 11 119181729 119181729 insertion of <=200bp - CT downstream_gene_variant ESCA-CN 11 119183454 119183454 single base substitution A G downstream_gene_variant GBM-US 11 119148932 119148932 single base substitution T G missense_variant C384W 1152T>G KIRC-US 11 119168096 119168096 single base substitution C T missense_variant A719V 2156C>T KIRC-US 11 119182813 119182813 deletion of <=200bp G - downstream_gene_variant KIRP-US 11 119182661 119182661 single base substitution T A downstream_gene_variant KIRP-US 11 119183001 119183001 single base substitution A C downstream_gene_variant LAML-KR 11 119148966 119148966 single base substitution T C missense_variant C396R 1186T>C LICA-CN 11 119167692 119167692 single base substitution A T missense_variant M701L 2101A>T LICA-CN 11 119183273 119183273 single base substitution A T downstream_gene_variant LICA-FR 11 119077163 119077163 single base substitution G T synonymous_variant G12G 36G>T LICA-FR 11 119085518 119085538 deletion of <=200bp CCCATTAGAGCTCCTTAGGAC - intron_variant LICA-FR 11 119116282 119116282 single base substitution T C intron_variant LICA-FR 11 119120262 119120262 insertion of <=200bp - A intron_variant LICA-FR 11 119128444 119128444 single base substitution A G intron_variant LICA-FR 11 119152511 119152511 single base substitution A T intron_variant LICA-FR 11 119181552 119181552 single base substitution G T downstream_gene_variant LIHC-US 11 119103248 119103248 single base substitution C T missense_variant R96C 286C>T LINC-JP 11 119081889 119081889 single base substitution C A intron_variant LINC-JP 11 119083693 119083693 single base substitution A G intron_variant LINC-JP 11 119089241 119089241 single base substitution A G intron_variant LINC-JP 11 119097202 119097202 deletion of <=200bp T - intron_variant LINC-JP 11 119100260 119100260 single base substitution G A intron_variant LINC-JP 11 119114508 119114508 single base substitution A C intron_variant LINC-JP 11 119122227 119122227 single base substitution A G intron_variant LINC-JP 11 119123594 119123594 single base substitution G A intron_variant LINC-JP 11 119140724 119140724 single base substitution A T intron_variant LINC-JP 11 119141146 119141146 single base substitution A T intron_variant LINC-JP 11 119142304 119142304 single base substitution G T intron_variant LINC-JP 11 119142305 119142305 single base substitution G T intron_variant LINC-JP 11 119142721 119142721 single base substitution T A intron_variant LINC-JP 11 119144808 119144808 single base substitution T A intron_variant LINC-JP 11 119145880 119145880 single base substitution G A intron_variant LINC-JP 11 119156102 119156102 single base substitution A T synonymous_variant S589S 1767A>T LINC-JP 11 119165519 119165519 single base substitution G A intron_variant LINC-JP 11 119172716 119172716 single base substitution T A 3_prime_UTR_variant LINC-JP 11 119177652 119177652 deletion of <=200bp A - 3_prime_UTR_variant LINC-JP 11 119177652 119177652 insertion of <=200bp - A 3_prime_UTR_variant LINC-JP 11 119180559 119180559 single base substitution T C downstream_gene_variant LINC-JP 11 119183170 119183170 single base substitution A C downstream_gene_variant LIRI-JP 11 119073973 119073973 single base substitution C T upstream_gene_variant LIRI-JP 11 119079014 119079014 single base substitution T C intron_variant LIRI-JP 11 119080688 119080688 single base substitution A G intron_variant LIRI-JP 11 119080812 119080812 single base substitution A G intron_variant LIRI-JP 11 119083131 119083131 single base substitution T G intron_variant LIRI-JP 11 119085072 119085072 single base substitution G C intron_variant LIRI-JP 11 119087108 119087108 single base substitution A G intron_variant LIRI-JP 11 119088475 119088475 single base substitution A G intron_variant LIRI-JP 11 119088793 119088793 single base substitution A G intron_variant LIRI-JP 11 119089125 119089125 single base substitution T C intron_variant LIRI-JP 11 119089239 119089239 single base substitution A G intron_variant LIRI-JP 11 119089896 119089896 single base substitution T C intron_variant LIRI-JP 11 119092073 119092073 single base substitution G C intron_variant LIRI-JP 11 119092230 119092230 single base substitution C A intron_variant LIRI-JP 11 119092813 119092813 single base substitution C T intron_variant LIRI-JP 11 119095281 119095281 single base substitution A G intron_variant LIRI-JP 11 119096131 119096131 single base substitution C T intron_variant LIRI-JP 11 119099814 119099814 single base substitution A C intron_variant LIRI-JP 11 119102715 119102715 single base substitution A G intron_variant LIRI-JP 11 119104538 119104538 single base substitution G A intron_variant LIRI-JP 11 119104543 119104543 single base substitution C G intron_variant LIRI-JP 11 119107160 119107160 single base substitution A G intron_variant LIRI-JP 11 119111688 119111688 single base substitution C G intron_variant LIRI-JP 11 119113020 119113020 single base substitution A T intron_variant LIRI-JP 11 119113712 119113712 single base substitution G T intron_variant LIRI-JP 11 119115628 119115628 single base substitution G T intron_variant LIRI-JP 11 119118905 119118905 single base substitution A G intron_variant LIRI-JP 11 119122677 119122677 single base substitution A T intron_variant LIRI-JP 11 119126241 119126241 single base substitution T C intron_variant LIRI-JP 11 119126357 119126382 deletion of <=200bp TTGTCTCATTACGGAAGTAATCAAAA - intron_variant LIRI-JP 11 119126590 119126590 single base substitution C T intron_variant LIRI-JP 11 119126740 119126740 single base substitution T C intron_variant LIRI-JP 11 119127075 119127075 single base substitution G C intron_variant LIRI-JP 11 119127390 119127390 single base substitution T C intron_variant LIRI-JP 11 119129652 119129652 single base substitution T A intron_variant LIRI-JP 11 119137375 119137375 single base substitution A G intron_variant LIRI-JP 11 119138236 119138236 single base substitution A T intron_variant LIRI-JP 11 119139510 119139510 single base substitution T C intron_variant LIRI-JP 11 119140091 119140091 single base substitution C T intron_variant LIRI-JP 11 119140890 119140890 single base substitution T C intron_variant LIRI-JP 11 119145648 119145649 deletion of <=200bp TT - frameshift_variant I285 LIRI-JP 11 119145756 119145756 single base substitution C T intron_variant LIRI-JP 11 119146711 119146711 single base substitution A G missense_variant I292V 874A>G LIRI-JP 11 119146759 119146759 single base substitution G A missense_variant V308I 922G>A LIRI-JP 11 119151435 119151435 single base substitution T A intron_variant LIRI-JP 11 119152013 119152013 single base substitution G A intron_variant LIRI-JP 11 119153492 119153492 single base substitution G A intron_variant LIRI-JP 11 119153949 119153949 single base substitution A G intron_variant LIRI-JP 11 119154136 119154136 single base substitution T C intron_variant LIRI-JP 11 119155947 119155947 deletion of <=200bp A - frameshift_variant T538 LIRI-JP 11 119157728 119157728 single base substitution T A intron_variant LIRI-JP 11 119159857 119159857 single base substitution A G intron_variant LIRI-JP 11 119162523 119162523 single base substitution C T intron_variant LIRI-JP 11 119166911 119166911 single base substitution T G intron_variant LIRI-JP 11 119170928 119170931 deletion of <=200bp CAGG - 3_prime_UTR_variant LIRI-JP 11 119171344 119171344 single base substitution A G 3_prime_UTR_variant LIRI-JP 11 119173062 119173062 single base substitution A G 3_prime_UTR_variant LIRI-JP 11 119173370 119173370 single base substitution T A 3_prime_UTR_variant LIRI-JP 11 119175072 119175072 single base substitution G A 3_prime_UTR_variant LIRI-JP 11 119178792 119178792 single base substitution A G 3_prime_UTR_variant LIRI-JP 11 119180217 119180217 deletion of <=200bp T - downstream_gene_variant LIRI-JP 11 119183672 119183672 single base substitution G A downstream_gene_variant LUSC-KR 11 119073661 119073661 single base substitution C T upstream_gene_variant LUSC-KR 11 119074786 119074786 single base substitution C T upstream_gene_variant LUSC-KR 11 119078946 119078946 single base substitution G A intron_variant LUSC-KR 11 119079500 119079500 single base substitution A T intron_variant LUSC-KR 11 119084516 119084516 single base substitution A C intron_variant LUSC-KR 11 119106231 119106231 single base substitution G A intron_variant LUSC-KR 11 119114225 119114225 single base substitution A T intron_variant LUSC-KR 11 119114252 119114252 single base substitution A T intron_variant LUSC-KR 11 119114285 119114285 single base substitution A G intron_variant LUSC-KR 11 119118890 119118890 single base substitution C A intron_variant LUSC-KR 11 119128711 119128711 single base substitution C T intron_variant LUSC-KR 11 119130270 119130270 single base substitution G T intron_variant LUSC-KR 11 119135175 119135175 single base substitution T C intron_variant LUSC-KR 11 119135343 119135343 single base substitution C T intron_variant LUSC-KR 11 119136594 119136594 single base substitution T A intron_variant LUSC-KR 11 119146626 119146626 single base substitution G T intron_variant LUSC-KR 11 119151298 119151298 single base substitution G T intron_variant LUSC-KR 11 119153377 119153377 single base substitution G C intron_variant LUSC-KR 11 119156394 119156394 single base substitution C A intron_variant LUSC-KR 11 119159524 119159524 single base substitution G A intron_variant LUSC-KR 11 119160565 119160565 single base substitution G T intron_variant LUSC-KR 11 119172598 119172598 single base substitution G C 3_prime_UTR_variant LUSC-KR 11 119173110 119173110 single base substitution C T 3_prime_UTR_variant LUSC-KR 11 119173188 119173188 single base substitution C T 3_prime_UTR_variant LUSC-KR 11 119174345 119174345 single base substitution G A 3_prime_UTR_variant LUSC-KR 11 119175626 119175626 single base substitution C T 3_prime_UTR_variant LUSC-KR 11 119177805 119177805 single base substitution T C 3_prime_UTR_variant LUSC-KR 11 119178539 119178539 single base substitution G A 3_prime_UTR_variant LUSC-KR 11 119179678 119179678 single base substitution T C downstream_gene_variant LUSC-KR 11 119183447 119183447 single base substitution C T downstream_gene_variant LUSC-US 11 119103223 119103223 single base substitution G A synonymous_variant L87L 261G>A LUSC-US 11 119103295 119103295 single base substitution A G synonymous_variant E111E 333A>G LUSC-US 11 119148970 119148970 single base substitution G T missense_variant G397V 1190G>T LUSC-US 11 119149393 119149393 single base substitution C A synonymous_variant L467L 1401C>A LUSC-US 11 119149399 119149399 single base substitution G A missense_variant M469I 1407G>A LUSC-US 11 119155697 119155697 single base substitution C T missense_variant P484S 1450C>T LUSC-US 11 119155953 119155953 single base substitution C A synonymous_variant R540R 1618C>A MALY-DE 11 119081341 119081341 single base substitution T C intron_variant MALY-DE 11 119083021 119083021 single base substitution A G intron_variant MALY-DE 11 119085505 119085506 deletion of <=200bp TC - intron_variant MALY-DE 11 119089774 119089774 single base substitution A T intron_variant MALY-DE 11 119091989 119091989 single base substitution A T intron_variant MALY-DE 11 119093099 119093099 single base substitution A G intron_variant MALY-DE 11 119093895 119093909 deletion of <=200bp TTTTTTTTTTTTTTT - intron_variant MALY-DE 11 119095760 119095761 deletion of <=200bp GT - intron_variant MALY-DE 11 119111455 119111455 single base substitution T C intron_variant MALY-DE 11 119122364 119122364 single base substitution C G intron_variant MALY-DE 11 119129600 119129600 single base substitution T C intron_variant MALY-DE 11 119134357 119134361 deletion of <=200bp GTTTT - intron_variant MALY-DE 11 119136112 119136112 single base substitution A G intron_variant MALY-DE 11 119143544 119143544 single base substitution T A intron_variant MALY-DE 11 119143748 119143748 single base substitution T A intron_variant MALY-DE 11 119156421 119156421 single base substitution C T intron_variant MALY-DE 11 119161040 119161040 single base substitution G T intron_variant MALY-DE 11 119164503 119164503 single base substitution G A intron_variant MALY-DE 11 119171881 119171881 single base substitution G C 3_prime_UTR_variant MALY-DE 11 119177965 119177965 single base substitution G C 3_prime_UTR_variant MALY-DE 11 119178778 119178781 deletion of <=200bp AGTT - 3_prime_UTR_variant MELA-AU 11 119071753 119071753 single base substitution G A upstream_gene_variant MELA-AU 11 119072163 119072163 single base substitution G A upstream_gene_variant MELA-AU 11 119072451 119072451 single base substitution G A upstream_gene_variant MELA-AU 11 119072550 119072550 single base substitution G A upstream_gene_variant MELA-AU 11 119073228 119073228 single base substitution G A upstream_gene_variant MELA-AU 11 119073683 119073683 single base substitution T C upstream_gene_variant MELA-AU 11 119074472 119074472 single base substitution C T upstream_gene_variant MELA-AU 11 119075046 119075046 single base substitution G A upstream_gene_variant MELA-AU 11 119076044 119076044 single base substitution G A upstream_gene_variant MELA-AU 11 119076887 119076887 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 11 119076946 119076946 single base substitution C T 5_prime_UTR_variant MELA-AU 11 119078769 119078769 single base substitution C T intron_variant MELA-AU 11 119079142 119079142 single base substitution C T intron_variant MELA-AU 11 119079219 119079219 single base substitution C T intron_variant MELA-AU 11 119079768 119079768 single base substitution A T intron_variant MELA-AU 11 119079832 119079832 single base substitution T C intron_variant MELA-AU 11 119080488 119080488 single base substitution T G intron_variant MELA-AU 11 119081221 119081221 single base substitution C T intron_variant MELA-AU 11 119081666 119081666 single base substitution C T intron_variant MELA-AU 11 119083133 119083133 single base substitution C T intron_variant MELA-AU 11 119083251 119083251 single base substitution C T intron_variant MELA-AU 11 119084662 119084662 single base substitution C T intron_variant MELA-AU 11 119086074 119086074 single base substitution C T intron_variant MELA-AU 11 119086215 119086215 single base substitution A T intron_variant MELA-AU 11 119086290 119086290 single base substitution C T intron_variant MELA-AU 11 119086584 119086584 single base substitution C T intron_variant MELA-AU 11 119087050 119087065 deletion of <=200bp ATTTATTTATTTATTT - intron_variant MELA-AU 11 119087145 119087145 single base substitution A G intron_variant MELA-AU 11 119087565 119087565 single base substitution C T intron_variant MELA-AU 11 119087591 119087591 single base substitution C T intron_variant MELA-AU 11 119087639 119087639 single base substitution A G intron_variant MELA-AU 11 119088317 119088317 single base substitution A T intron_variant MELA-AU 11 119089592 119089592 single base substitution T C intron_variant MELA-AU 11 119090255 119090255 single base substitution C T intron_variant MELA-AU 11 119090487 119090488 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 11 119090952 119090952 single base substitution C T intron_variant MELA-AU 11 119091059 119091059 single base substitution C T intron_variant MELA-AU 11 119091278 119091278 single base substitution C T intron_variant MELA-AU 11 119092312 119092312 single base substitution C A intron_variant MELA-AU 11 119092362 119092362 single base substitution C T intron_variant MELA-AU 11 119093583 119093583 single base substitution C T intron_variant MELA-AU 11 119094419 119094419 single base substitution C T intron_variant MELA-AU 11 119094457 119094457 single base substitution C T intron_variant MELA-AU 11 119094657 119094657 single base substitution C T intron_variant MELA-AU 11 119095541 119095541 single base substitution G A intron_variant MELA-AU 11 119096232 119096232 single base substitution C T intron_variant MELA-AU 11 119096506 119096506 single base substitution C T intron_variant MELA-AU 11 119096643 119096643 single base substitution C T intron_variant MELA-AU 11 119096674 119096674 single base substitution G A intron_variant MELA-AU 11 119098284 119098284 single base substitution G A intron_variant MELA-AU 11 119099550 119099550 single base substitution C T intron_variant MELA-AU 11 119099653 119099653 single base substitution C T intron_variant MELA-AU 11 119100303 119100304 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 119100847 119100847 single base substitution G A intron_variant MELA-AU 11 119102514 119102514 single base substitution C T intron_variant MELA-AU 11 119102760 119102760 single base substitution C T intron_variant MELA-AU 11 119102992 119102992 single base substitution A G intron_variant MELA-AU 11 119103125 119103125 single base substitution C T intron_variant MELA-AU 11 119103804 119103804 single base substitution G A intron_variant MELA-AU 11 119104949 119104949 single base substitution C T intron_variant MELA-AU 11 119105078 119105078 single base substitution C T intron_variant MELA-AU 11 119105764 119105764 single base substitution C T intron_variant MELA-AU 11 119106545 119106545 single base substitution C T intron_variant MELA-AU 11 119106753 119106753 single base substitution C T intron_variant MELA-AU 11 119107395 119107395 single base substitution C T intron_variant MELA-AU 11 119108246 119108246 single base substitution C T intron_variant MELA-AU 11 119108878 119108879 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 119108923 119108923 single base substitution C T intron_variant MELA-AU 11 119109186 119109186 single base substitution C T intron_variant MELA-AU 11 119109559 119109559 single base substitution G A intron_variant MELA-AU 11 119110065 119110065 single base substitution C T intron_variant MELA-AU 11 119111580 119111580 single base substitution C T intron_variant MELA-AU 11 119112949 119112949 single base substitution C T intron_variant MELA-AU 11 119113599 119113599 single base substitution C T intron_variant MELA-AU 11 119115279 119115279 single base substitution C G intron_variant MELA-AU 11 119115839 119115839 single base substitution C T intron_variant MELA-AU 11 119115951 119115951 single base substitution T A intron_variant MELA-AU 11 119116353 119116353 single base substitution C T intron_variant MELA-AU 11 119117176 119117176 single base substitution T A intron_variant MELA-AU 11 119117475 119117475 single base substitution T C intron_variant MELA-AU 11 119117818 119117818 single base substitution C T intron_variant MELA-AU 11 119117825 119117825 single base substitution G A intron_variant MELA-AU 11 119118515 119118515 single base substitution C T intron_variant MELA-AU 11 119120414 119120414 single base substitution C T intron_variant MELA-AU 11 119120797 119120797 single base substitution C T intron_variant MELA-AU 11 119120881 119120881 single base substitution G A intron_variant MELA-AU 11 119120882 119120882 single base substitution G A intron_variant MELA-AU 11 119120981 119120981 single base substitution C T intron_variant MELA-AU 11 119121024 119121024 single base substitution C T intron_variant MELA-AU 11 119121247 119121247 single base substitution C T intron_variant MELA-AU 11 119121488 119121488 single base substitution C T intron_variant MELA-AU 11 119121873 119121873 single base substitution C T intron_variant MELA-AU 11 119122224 119122224 single base substitution C G intron_variant MELA-AU 11 119122874 119122874 single base substitution A G intron_variant MELA-AU 11 119123169 119123169 single base substitution C T intron_variant MELA-AU 11 119123367 119123367 single base substitution A T intron_variant MELA-AU 11 119124010 119124010 single base substitution A G intron_variant MELA-AU 11 119124330 119124330 single base substitution C T intron_variant MELA-AU 11 119124653 119124653 single base substitution C T intron_variant MELA-AU 11 119125172 119125172 single base substitution G T intron_variant MELA-AU 11 119126156 119126156 single base substitution C T intron_variant MELA-AU 11 119127362 119127362 single base substitution C T intron_variant MELA-AU 11 119127580 119127580 single base substitution C T intron_variant MELA-AU 11 119127769 119127769 single base substitution T G intron_variant MELA-AU 11 119127781 119127781 single base substitution C T intron_variant MELA-AU 11 119128089 119128089 single base substitution C T intron_variant MELA-AU 11 119128357 119128357 single base substitution C T intron_variant MELA-AU 11 119128445 119128445 single base substitution G A intron_variant MELA-AU 11 119128532 119128532 single base substitution C T intron_variant MELA-AU 11 119129378 119129378 single base substitution G A intron_variant MELA-AU 11 119129679 119129679 single base substitution A G intron_variant MELA-AU 11 119131077 119131077 single base substitution C T intron_variant MELA-AU 11 119131569 119131569 single base substitution C T intron_variant MELA-AU 11 119131623 119131623 single base substitution C G intron_variant MELA-AU 11 119131974 119131974 single base substitution C T intron_variant MELA-AU 11 119132565 119132565 single base substitution T C intron_variant MELA-AU 11 119133111 119133111 single base substitution T C intron_variant MELA-AU 11 119133591 119133591 single base substitution C T intron_variant MELA-AU 11 119134967 119134967 single base substitution T C intron_variant MELA-AU 11 119135160 119135160 single base substitution C T intron_variant MELA-AU 11 119135167 119135167 single base substitution C T intron_variant MELA-AU 11 119135182 119135182 single base substitution T C intron_variant MELA-AU 11 119135454 119135454 single base substitution A T intron_variant MELA-AU 11 119135622 119135622 single base substitution C T intron_variant MELA-AU 11 119135653 119135653 single base substitution C T intron_variant MELA-AU 11 119135671 119135671 single base substitution C T intron_variant MELA-AU 11 119136782 119136782 single base substitution C T intron_variant MELA-AU 11 119136857 119136857 single base substitution T C intron_variant MELA-AU 11 119137129 119137129 single base substitution T C intron_variant MELA-AU 11 119138158 119138158 single base substitution C T intron_variant MELA-AU 11 119140322 119140322 single base substitution C T intron_variant MELA-AU 11 119141459 119141459 single base substitution T A intron_variant MELA-AU 11 119142271 119142271 single base substitution C T intron_variant MELA-AU 11 119142860 119142860 single base substitution C T intron_variant MELA-AU 11 119142930 119142930 single base substitution C T intron_variant MELA-AU 11 119144312 119144312 single base substitution G A intron_variant MELA-AU 11 119144508 119144508 single base substitution C T intron_variant MELA-AU 11 119144691 119144691 single base substitution A G missense_variant Y235C 704A>G MELA-AU 11 119144977 119144977 single base substitution C T intron_variant MELA-AU 11 119145704 119145704 single base substitution C T intron_variant MELA-AU 11 119145756 119145756 single base substitution C T intron_variant MELA-AU 11 119148085 119148085 single base substitution C T intron_variant MELA-AU 11 119148397 119148397 single base substitution C T intron_variant MELA-AU 11 119148874 119148874 single base substitution A T splice_acceptor_variant MELA-AU 11 119148875 119148876 deletion of <=200bp GG - frameshift_variant QE366 MELA-AU 11 119148875 119148876 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant E366K 1096G>A MELA-AU 11 119148919 119148919 single base substitution T C missense_variant L380P 1139T>C MELA-AU 11 119148958 119148959 multiple base substitution (>=2bp and <=200bp) TT GA missense_variant I393R 1178TT>GA MELA-AU 11 119148973 119148973 single base substitution A C missense_variant H398P 1193A>C MELA-AU 11 119148990 119148990 single base substitution T G missense_variant C404G 1210T>G MELA-AU 11 119149180 119149180 single base substitution T C intron_variant MELA-AU 11 119149235 119149235 single base substitution G A missense_variant G415S 1243G>A MELA-AU 11 119149348 119149348 single base substitution C T synonymous_variant S452S 1356C>T MELA-AU 11 119151159 119151159 single base substitution C T intron_variant MELA-AU 11 119151161 119151161 single base substitution C T intron_variant MELA-AU 11 119151964 119151964 single base substitution C T intron_variant MELA-AU 11 119153890 119153890 single base substitution A C intron_variant MELA-AU 11 119154064 119154064 single base substitution C T intron_variant MELA-AU 11 119154872 119154872 single base substitution C T intron_variant MELA-AU 11 119154931 119154931 single base substitution T C intron_variant MELA-AU 11 119155775 119155775 single base substitution C T missense_variant P510S 1528C>T MELA-AU 11 119156176 119156176 single base substitution T C missense_variant L614S 1841T>C MELA-AU 11 119157271 119157271 single base substitution A T intron_variant MELA-AU 11 119157463 119157463 single base substitution C T intron_variant MELA-AU 11 119157711 119157711 single base substitution C T intron_variant MELA-AU 11 119158344 119158344 single base substitution C T intron_variant MELA-AU 11 119159754 119159754 single base substitution C T intron_variant MELA-AU 11 119159836 119159836 single base substitution C T intron_variant MELA-AU 11 119160523 119160523 single base substitution G A intron_variant MELA-AU 11 119160704 119160704 single base substitution C T intron_variant MELA-AU 11 119161391 119161391 single base substitution T C intron_variant MELA-AU 11 119161512 119161512 single base substitution A G intron_variant MELA-AU 11 119161522 119161522 single base substitution G A intron_variant MELA-AU 11 119161688 119161688 single base substitution C T intron_variant MELA-AU 11 119162126 119162126 single base substitution G A intron_variant MELA-AU 11 119162999 119162999 single base substitution C T intron_variant MELA-AU 11 119163097 119163097 single base substitution C T intron_variant MELA-AU 11 119163330 119163330 single base substitution C T intron_variant MELA-AU 11 119163673 119163673 single base substitution C T intron_variant MELA-AU 11 119163903 119163903 single base substitution C G intron_variant MELA-AU 11 119164024 119164024 single base substitution G T intron_variant MELA-AU 11 119164744 119164744 single base substitution C T intron_variant MELA-AU 11 119165674 119165674 single base substitution C G intron_variant MELA-AU 11 119165960 119165960 single base substitution C T intron_variant MELA-AU 11 119166051 119166051 single base substitution C A intron_variant MELA-AU 11 119166056 119166056 single base substitution C A intron_variant MELA-AU 11 119166072 119166072 single base substitution C G intron_variant MELA-AU 11 119166167 119166167 single base substitution C G intron_variant MELA-AU 11 119166314 119166314 single base substitution C G intron_variant MELA-AU 11 119166369 119166369 single base substitution C G intron_variant MELA-AU 11 119166774 119166774 single base substitution C T intron_variant MELA-AU 11 119166914 119166914 single base substitution G A intron_variant MELA-AU 11 119166943 119166943 single base substitution C T intron_variant MELA-AU 11 119166973 119166973 single base substitution C T intron_variant MELA-AU 11 119167357 119167357 single base substitution G A intron_variant MELA-AU 11 119169419 119169436 deletion of <=200bp CTTTAGGATTTTTGCAGA - intron_variant MELA-AU 11 119169568 119169568 single base substitution C T intron_variant MELA-AU 11 119170054 119170091 deletion of <=200bp TGAACCTGTAAAACCCAGCCTTGTGACTGAAGAGCACA - intron_variant MELA-AU 11 119170096 119170096 single base substitution C T intron_variant MELA-AU 11 119171105 119171105 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119171410 119171410 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119171586 119171586 single base substitution A G 3_prime_UTR_variant MELA-AU 11 119171779 119171779 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119171780 119171780 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119171859 119171859 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119171870 119171870 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119172283 119172283 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119172393 119172393 single base substitution T C 3_prime_UTR_variant MELA-AU 11 119172434 119172434 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119172635 119172635 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119172905 119172905 single base substitution G A 3_prime_UTR_variant MELA-AU 11 119173025 119173025 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119173230 119173230 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119173942 119173942 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119173995 119173995 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119175541 119175541 single base substitution G A 3_prime_UTR_variant MELA-AU 11 119175592 119175592 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119175642 119175642 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119175962 119175962 single base substitution C T 3_prime_UTR_variant MELA-AU 11 119177322 119177322 single base substitution T A 3_prime_UTR_variant MELA-AU 11 119178943 119178943 single base substitution C G downstream_gene_variant MELA-AU 11 119179182 119179182 single base substitution G T downstream_gene_variant MELA-AU 11 119179826 119179826 single base substitution T A downstream_gene_variant MELA-AU 11 119180068 119180068 single base substitution G A downstream_gene_variant MELA-AU 11 119180169 119180170 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 119182001 119182001 single base substitution A C downstream_gene_variant MELA-AU 11 119182738 119182738 single base substitution C T downstream_gene_variant MELA-AU 11 119183298 119183298 single base substitution C T downstream_gene_variant MELA-AU 11 119183714 119183714 single base substitution C T downstream_gene_variant NBL-US 11 119142561 119142561 single base substitution C T missense_variant A187V 560C>T ORCA-IN 11 119072225 119072225 single base substitution C A upstream_gene_variant ORCA-IN 11 119095759 119095759 single base substitution G T intron_variant ORCA-IN 11 119135165 119135165 single base substitution C T intron_variant ORCA-IN 11 119159192 119159192 single base substitution G C intron_variant ORCA-IN 11 119182656 119182656 single base substitution C A downstream_gene_variant OV-AU 11 119072646 119072646 single base substitution C A upstream_gene_variant OV-AU 11 119077541 119077541 single base substitution G A intron_variant OV-AU 11 119079918 119079918 single base substitution T A intron_variant OV-AU 11 119082057 119082057 single base substitution G A intron_variant OV-AU 11 119087073 119087073 single base substitution T C intron_variant OV-AU 11 119096674 119096674 single base substitution G A intron_variant OV-AU 11 119096677 119096677 single base substitution A G intron_variant OV-AU 11 119108733 119108733 single base substitution C G intron_variant OV-AU 11 119109809 119109809 single base substitution A G intron_variant OV-AU 11 119109932 119109932 single base substitution C G intron_variant OV-AU 11 119111807 119111807 single base substitution G C intron_variant OV-AU 11 119112168 119112168 single base substitution G T intron_variant OV-AU 11 119123966 119123966 single base substitution C G intron_variant OV-AU 11 119127419 119127419 single base substitution C G intron_variant OV-AU 11 119129666 119129666 single base substitution G A intron_variant OV-AU 11 119134515 119134515 single base substitution G A intron_variant OV-AU 11 119135128 119135128 single base substitution C T intron_variant OV-AU 11 119150602 119150602 single base substitution T G intron_variant OV-AU 11 119151882 119151882 single base substitution T G intron_variant OV-AU 11 119155476 119155476 single base substitution C G intron_variant OV-AU 11 119160712 119160712 single base substitution A C intron_variant OV-AU 11 119163924 119163924 single base substitution C A intron_variant OV-AU 11 119170693 119170693 single base substitution C G 3_prime_UTR_variant OV-AU 11 119171098 119171098 single base substitution G A 3_prime_UTR_variant OV-AU 11 119174210 119174210 single base substitution G T 3_prime_UTR_variant OV-US 11 119183335 119183335 single base substitution C T downstream_gene_variant PACA-AU 11 119072990 119072990 single base substitution G A upstream_gene_variant PACA-AU 11 119087050 119087053 deletion of <=200bp ATTT - intron_variant PACA-AU 11 119087050 119087065 deletion of <=200bp ATTTATTTATTTATTT - intron_variant PACA-AU 11 119090084 119090084 single base substitution C G intron_variant PACA-AU 11 119090615 119090615 single base substitution A C intron_variant PACA-AU 11 119092491 119092491 single base substitution A C intron_variant PACA-AU 11 119094316 119094316 single base substitution T A intron_variant PACA-AU 11 119096438 119096438 single base substitution T C intron_variant PACA-AU 11 119098581 119098581 single base substitution A G intron_variant PACA-AU 11 119102599 119102599 single base substitution G A intron_variant PACA-AU 11 119107974 119107976 deletion of <=200bp ATT - intron_variant PACA-AU 11 119119248 119119248 single base substitution A C intron_variant PACA-AU 11 119123798 119123798 single base substitution A G intron_variant PACA-AU 11 119128286 119128286 insertion of <=200bp - T intron_variant PACA-AU 11 119128955 119128955 insertion of <=200bp - A intron_variant PACA-AU 11 119132937 119132937 single base substitution G A intron_variant PACA-AU 11 119135113 119135113 single base substitution C T intron_variant PACA-AU 11 119141465 119141465 single base substitution T G intron_variant PACA-AU 11 119142878 119142878 single base substitution C G intron_variant PACA-AU 11 119143693 119143693 insertion of <=200bp - TA intron_variant PACA-AU 11 119144723 119144723 single base substitution C T stop_gained R246* 736C>T PACA-AU 11 119145706 119145706 insertion of <=200bp - T intron_variant PACA-AU 11 119146079 119146079 single base substitution T G intron_variant PACA-AU 11 119147948 119147949 deletion of <=200bp CG - intron_variant PACA-AU 11 119148662 119148662 single base substitution G A intron_variant PACA-AU 11 119149585 119149585 deletion of <=200bp T - intron_variant PACA-AU 11 119151100 119151100 single base substitution T C intron_variant PACA-AU 11 119151397 119151397 single base substitution C T intron_variant PACA-AU 11 119156951 119156951 single base substitution G A intron_variant PACA-AU 11 119164065 119164065 single base substitution A C intron_variant PACA-AU 11 119164792 119164792 single base substitution G C intron_variant PACA-AU 11 119166451 119166451 single base substitution C T intron_variant PACA-AU 11 119166647 119166647 single base substitution A C intron_variant PACA-AU 11 119167079 119167079 single base substitution A C intron_variant PACA-AU 11 119179521 119179521 single base substitution A T downstream_gene_variant PACA-AU 11 119181630 119181630 single base substitution C T downstream_gene_variant PACA-AU 11 119183849 119183849 single base substitution C T downstream_gene_variant PACA-CA 11 119073098 119073098 single base substitution C T upstream_gene_variant PACA-CA 11 119073378 119073378 single base substitution G A upstream_gene_variant PACA-CA 11 119074453 119074453 deletion of <=200bp A - upstream_gene_variant PACA-CA 11 119075532 119075532 single base substitution C G upstream_gene_variant PACA-CA 11 119079168 119079168 single base substitution C T intron_variant PACA-CA 11 119080041 119080041 single base substitution T G intron_variant PACA-CA 11 119082498 119082498 single base substitution G A intron_variant PACA-CA 11 119083011 119083011 deletion of <=200bp A - intron_variant PACA-CA 11 119085398 119085398 single base substitution T C intron_variant PACA-CA 11 119089765 119089765 single base substitution T A intron_variant PACA-CA 11 119091775 119091775 single base substitution G A intron_variant PACA-CA 11 119094361 119094364 deletion of <=200bp TCTC - intron_variant PACA-CA 11 119095931 119095931 single base substitution C T intron_variant PACA-CA 11 119098836 119098836 deletion of <=200bp T - intron_variant PACA-CA 11 119099118 119099118 single base substitution C T intron_variant PACA-CA 11 119105743 119105743 insertion of <=200bp - T intron_variant PACA-CA 11 119107482 119107482 deletion of <=200bp T - intron_variant PACA-CA 11 119108938 119108938 single base substitution T C intron_variant PACA-CA 11 119114055 119114055 deletion of <=200bp T - intron_variant PACA-CA 11 119116069 119116069 single base substitution C T intron_variant PACA-CA 11 119116223 119116223 single base substitution G A intron_variant PACA-CA 11 119117579 119117579 single base substitution G A intron_variant PACA-CA 11 119118471 119118471 single base substitution G A intron_variant PACA-CA 11 119118784 119118784 single base substitution C T intron_variant PACA-CA 11 119120090 119120090 single base substitution A C intron_variant PACA-CA 11 119121611 119121611 single base substitution A G intron_variant PACA-CA 11 119121694 119121694 insertion of <=200bp - T intron_variant PACA-CA 11 119122173 119122173 single base substitution G T intron_variant PACA-CA 11 119129907 119129907 deletion of <=200bp T - intron_variant PACA-CA 11 119132910 119132910 single base substitution A T intron_variant PACA-CA 11 119135177 119135177 deletion of <=200bp C - intron_variant PACA-CA 11 119143678 119143678 single base substitution T A intron_variant PACA-CA 11 119148949 119148949 single base substitution A G missense_variant D390G 1169A>G PACA-CA 11 119149009 119149009 single base substitution T C splice_donor_variant PACA-CA 11 119149435 119149435 single base substitution G A intron_variant PACA-CA 11 119150726 119150726 single base substitution G A intron_variant PACA-CA 11 119169166 119169166 single base substitution G A missense_variant V784M 2350G>A PACA-CA 11 119178832 119178832 single base substitution T A 3_prime_UTR_variant PACA-CA 11 119180729 119180729 single base substitution G T downstream_gene_variant PACA-CA 11 119180858 119180858 single base substitution A G downstream_gene_variant PAEN-AU 11 119082849 119082849 single base substitution G A intron_variant PAEN-AU 11 119087050 119087050 insertion of <=200bp - ATTT intron_variant PAEN-AU 11 119090658 119090658 single base substitution C A intron_variant PAEN-AU 11 119097769 119097769 single base substitution G A intron_variant PAEN-AU 11 119098527 119098527 single base substitution T C intron_variant PAEN-IT 11 119078120 119078120 single base substitution G C intron_variant PAEN-IT 11 119133026 119133026 single base substitution G T intron_variant PAEN-IT 11 119162259 119162259 single base substitution A G intron_variant PBCA-DE 11 119087050 119087057 deletion of <=200bp ATTTATTT - intron_variant PBCA-DE 11 119091834 119091834 single base substitution G C intron_variant PBCA-DE 11 119095760 119095761 deletion of <=200bp GT - intron_variant PBCA-DE 11 119108796 119108796 single base substitution G A intron_variant PBCA-DE 11 119111574 119111574 single base substitution G A intron_variant PBCA-DE 11 119119382 119119382 single base substitution C A intron_variant PBCA-DE 11 119124142 119124142 single base substitution T C intron_variant PBCA-DE 11 119127244 119127244 single base substitution A G intron_variant PBCA-DE 11 119135093 119135093 single base substitution T C intron_variant PBCA-DE 11 119138648 119138648 single base substitution T G intron_variant PBCA-DE 11 119140195 119140195 single base substitution G A intron_variant PBCA-DE 11 119152765 119152765 single base substitution C T intron_variant PBCA-DE 11 119183298 119183298 single base substitution C T downstream_gene_variant PRAD-CA 11 119083692 119083692 single base substitution G A intron_variant PRAD-CA 11 119083693 119083693 single base substitution A G intron_variant PRAD-CA 11 119104650 119104650 single base substitution A G intron_variant PRAD-CA 11 119121409 119121409 single base substitution C T intron_variant PRAD-CA 11 119123886 119123886 single base substitution C T intron_variant PRAD-CA 11 119135128 119135128 single base substitution C T intron_variant PRAD-CA 11 119145599 119145599 single base substitution A G missense_variant M269V 805A>G PRAD-UK 11 119080171 119080171 single base substitution A T intron_variant PRAD-UK 11 119092131 119092131 single base substitution G A intron_variant PRAD-UK 11 119096729 119096729 single base substitution G A intron_variant PRAD-UK 11 119096971 119096971 single base substitution G T intron_variant PRAD-UK 11 119101442 119101442 single base substitution G A intron_variant PRAD-UK 11 119147204 119147204 single base substitution G A intron_variant PRAD-UK 11 119149891 119149891 single base substitution T A intron_variant PRAD-UK 11 119151158 119151158 single base substitution C A intron_variant READ-US 11 119144603 119144603 single base substitution C T stop_gained R206* 616C>T READ-US 11 119144604 119144604 single base substitution G A missense_variant R206Q 617G>A READ-US 11 119145620 119145620 single base substitution G A missense_variant E276K 826G>A READ-US 11 119170451 119170451 single base substitution A G missense_variant E894G 2681A>G RECA-EU 11 119091234 119091234 single base substitution A C intron_variant RECA-EU 11 119096531 119096531 single base substitution G C intron_variant RECA-EU 11 119097540 119097540 single base substitution A G intron_variant RECA-EU 11 119113996 119113996 single base substitution G T intron_variant RECA-EU 11 119116364 119116364 single base substitution G A intron_variant RECA-EU 11 119120037 119120037 single base substitution G C intron_variant RECA-EU 11 119123719 119123719 single base substitution A G intron_variant RECA-EU 11 119140167 119140167 single base substitution G A intron_variant RECA-EU 11 119144331 119144331 single base substitution G T intron_variant RECA-EU 11 119160156 119160156 single base substitution T A intron_variant RECA-EU 11 119163326 119163326 single base substitution G A intron_variant RECA-EU 11 119167214 119167214 single base substitution A C intron_variant RECA-EU 11 119174499 119174499 single base substitution G T 3_prime_UTR_variant RECA-EU 11 119178676 119178676 single base substitution G A 3_prime_UTR_variant SKCA-BR 11 119071764 119071764 single base substitution A T upstream_gene_variant SKCA-BR 11 119072852 119072853 deletion of <=200bp GT - upstream_gene_variant SKCA-BR 11 119076743 119076743 single base substitution A G upstream_gene_variant SKCA-BR 11 119077753 119077753 single base substitution T G intron_variant SKCA-BR 11 119083682 119083682 insertion of <=200bp - CA intron_variant SKCA-BR 11 119086138 119086138 insertion of <=200bp - AT intron_variant SKCA-BR 11 119086139 119086139 insertion of <=200bp - AT intron_variant SKCA-BR 11 119090391 119090391 insertion of <=200bp - CT intron_variant SKCA-BR 11 119090753 119090753 single base substitution T G intron_variant SKCA-BR 11 119094780 119094780 single base substitution C T intron_variant SKCA-BR 11 119099093 119099093 single base substitution A G intron_variant SKCA-BR 11 119101052 119101052 single base substitution C G intron_variant SKCA-BR 11 119104910 119104910 single base substitution T G intron_variant SKCA-BR 11 119110185 119110185 single base substitution T C intron_variant SKCA-BR 11 119111759 119111759 single base substitution C T intron_variant SKCA-BR 11 119114214 119114215 deletion of <=200bp CA - intron_variant SKCA-BR 11 119115829 119115829 single base substitution A C intron_variant SKCA-BR 11 119118831 119118831 single base substitution T G intron_variant SKCA-BR 11 119121733 119121733 single base substitution C T intron_variant SKCA-BR 11 119128089 119128089 single base substitution C T intron_variant SKCA-BR 11 119130602 119130602 single base substitution C T intron_variant SKCA-BR 11 119135098 119135098 insertion of <=200bp - TTTCTCTTCTCTTCTC intron_variant SKCA-BR 11 119135098 119135098 insertion of <=200bp - TTTCTCTTCTCTTCTCTTCTC intron_variant SKCA-BR 11 119135098 119135113 deletion of <=200bp TTTCTCTTCTCTTCTC - intron_variant SKCA-BR 11 119135126 119135126 single base substitution C T intron_variant SKCA-BR 11 119135128 119135152 deletion of <=200bp CTTCTCTTCTCTTCTCTTCTCTTCT - intron_variant SKCA-BR 11 119135152 119135152 insertion of <=200bp - TC intron_variant SKCA-BR 11 119135166 119135167 deletion of <=200bp TC - intron_variant SKCA-BR 11 119139956 119139957 deletion of <=200bp CT - intron_variant SKCA-BR 11 119140507 119140507 single base substitution C T intron_variant SKCA-BR 11 119144791 119144791 insertion of <=200bp - CT intron_variant SKCA-BR 11 119144991 119144991 single base substitution A G intron_variant SKCA-BR 11 119146163 119146164 deletion of <=200bp CA - intron_variant SKCA-BR 11 119148929 119148929 single base substitution A G missense_variant I383M 1149A>G SKCA-BR 11 119155106 119155106 single base substitution C T intron_variant SKCA-BR 11 119161329 119161330 deletion of <=200bp CA - intron_variant SKCA-BR 11 119164328 119164328 single base substitution C T intron_variant SKCA-BR 11 119168688 119168688 single base substitution C T intron_variant SKCA-BR 11 119170997 119170997 single base substitution T C 3_prime_UTR_variant SKCA-BR 11 119171570 119171570 single base substitution C T 3_prime_UTR_variant SKCA-BR 11 119173366 119173366 single base substitution T G 3_prime_UTR_variant SKCA-BR 11 119175740 119175740 single base substitution C T 3_prime_UTR_variant SKCA-BR 11 119179557 119179557 single base substitution C T downstream_gene_variant SKCA-BR 11 119183644 119183644 single base substitution G A downstream_gene_variant SKCM-US 11 119103163 119103163 single base substitution G A synonymous_variant V67V 201G>A SKCM-US 11 119103291 119103291 single base substitution G A missense_variant G110E 329G>A SKCM-US 11 119142544 119142544 single base substitution T C synonymous_variant I181I 543T>C SKCM-US 11 119144732 119144732 single base substitution C T stop_gained Q249* 745C>T SKCM-US 11 119145646 119145646 single base substitution C T synonymous_variant F284F 852C>T SKCM-US 11 119148871 119148874 deletion of <=200bp CAAA - splice_acceptor_variant SKCM-US 11 119148881 119148881 single base substitution A T missense_variant Q367H 1101A>T SKCM-US 11 119148884 119148895 deletion of <=200bp TGAATTATACTG - inframe_deletion YELYC368Y SKCM-US 11 119149238 119149238 single base substitution T A missense_variant C416S 1246T>A SKCM-US 11 119149242 119149242 single base substitution C A missense_variant P417H 1250C>A SKCM-US 11 119149244 119149244 single base substitution T A missense_variant F418I 1252T>A SKCM-US 11 119149250 119149250 single base substitution C G missense_variant R420G 1258C>G SKCM-US 11 119149279 119149279 single base substitution C T synonymous_variant I429I 1287C>T SKCM-US 11 119155775 119155775 single base substitution C T missense_variant P510S 1528C>T SKCM-US 11 119156009 119156009 single base substitution C T synonymous_variant S558S 1674C>T SKCM-US 11 119158644 119158644 single base substitution C T missense_variant S675F 2024C>T SKCM-US 11 119168174 119168174 single base substitution C T missense_variant T745I 2234C>T SKCM-US 11 119170216 119170216 single base substitution G A missense_variant G816S 2446G>A SKCM-US 11 119170400 119170400 single base substitution C T missense_variant A877V 2630C>T SKCM-US 11 119170443 119170443 single base substitution C T synonymous_variant I891I 2673C>T SKCM-US 11 119181572 119181572 single base substitution C G downstream_gene_variant SKCM-US 11 119182038 119182038 single base substitution C A downstream_gene_variant SKCM-US 11 119182819 119182819 single base substitution G A downstream_gene_variant STAD-US 11 119146846 119146846 single base substitution T C splice_donor_variant STAD-US 11 119155727 119155727 deletion of <=200bp C - frameshift_variant P494 STAD-US 11 119156153 119156153 single base substitution T C synonymous_variant S606S 1818T>C STAD-US 11 119169107 119169107 single base substitution C A missense_variant P764H 2291C>A STAD-US 11 119170326 119170326 single base substitution C T synonymous_variant T852T 2556C>T STAD-US 11 119182355 119182355 insertion of <=200bp - G downstream_gene_variant STAD-US 11 119182655 119182655 single base substitution C A downstream_gene_variant STAD-US 11 119183094 119183094 single base substitution G A downstream_gene_variant STAD-US 11 119183298 119183298 single base substitution C T downstream_gene_variant STAD-US 11 119183610 119183610 single base substitution G T downstream_gene_variant THCA-SA 11 119171106 119171106 single base substitution C T 3_prime_UTR_variant THCA-SA 11 119172536 119172536 single base substitution A G 3_prime_UTR_variant THCA-SA 11 119177938 119177938 single base substitution A G 3_prime_UTR_variant THCA-SA 11 119182812 119182812 insertion of <=200bp - G downstream_gene_variant UCEC-US 11 119103241 119103241 single base substitution G A synonymous_variant Q93Q 279G>A UCEC-US 11 119142558 119142558 single base substitution C T missense_variant A186V 557C>T UCEC-US 11 119145620 119145620 single base substitution G A missense_variant E276K 826G>A UCEC-US 11 119146802 119146802 single base substitution A C missense_variant K322T 965A>C UCEC-US 11 119149250 119149250 single base substitution C T stop_gained R420* 1258C>T UCEC-US 11 119149279 119149279 single base substitution C T synonymous_variant I429I 1287C>T UCEC-US 11 119149368 119149368 single base substitution A T missense_variant D459V 1376A>T UCEC-US 11 119155929 119155929 single base substitution C T missense_variant P532S 1594C>T UCEC-US 11 119155972 119155972 single base substitution C T missense_variant P546L 1637C>T UCEC-US 11 119156200 119156200 single base substitution T G missense_variant F622C 1865T>G UCEC-US 11 119158653 119158653 single base substitution C A missense_variant A678D 2033C>A UCEC-US 11 119169186 119169186 single base substitution C T synonymous_variant L790L 2370C>T UCEC-US 11 119170234 119170234 single base substitution A G missense_variant R822G 2464A>G UCEC-US 11 119170319 119170319 single base substitution C T missense_variant A850V 2549C>T UCEC-US 11 119170373 119170373 single base substitution G A missense_variant G868E 2603G>A UCEC-US 11 119180610 119180610 single base substitution C A downstream_gene_variant UCEC-US 11 119181087 119181087 single base substitution C T downstream_gene_variant UCEC-US 11 119181830 119181830 single base substitution G A downstream_gene_variant UCEC-US 11 119182085 119182085 single base substitution T C downstream_gene_variant UCEC-US 11 119182786 119182786 single base substitution G A downstream_gene_variant UCEC-US 11 119183044 119183044 single base substitution T C downstream_gene_variant UCEC-US 11 119183299 119183299 single base substitution G A downstream_gene_variant UCEC-US 11 119183659 119183659 single base substitution C T downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 2246943 COSM4413401 c.1169A>T p.D390V Substitution - Missense 11:119278239-119278239 + PD8373a COSM5945214 c.1110A>T p.L370F Substitution - Missense 11:119278180-119278180 + 2217109 COSM4169413 c.? p.? Unknown 1275881 COSM34057 c.1150T>C p.C384R Substitution - Missense 11:119278220-119278220 + PD8076a COSM5945226 c.2614C>T p.Q872* Substitution - Nonsense 11:119299674-119299674 + 1598352 COSM133606 c.1096-10_1106>CCGGGG p.? Unknown 11:119278156-119278176 + 1234404 COSM34057 c.1150T>C p.C384R Substitution - Missense 11:119278220-119278220 + 01-P8014 COSM4574112 c.2216C>T p.S739F Substitution - Missense 11:119297446-119297446 + 1234388 COSM34080 c.1259G>T p.R420L Substitution - Missense 11:119278541-119278541 + 35 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + 1275884 COSM34059 c.1210T>C p.C404R Substitution - Missense 11:119278280-119278280 + PCSI_0083_Pa_X COSM3375687 c.1227+2T>C p.? Unknown 11:119278299-119278299 + 388 COSM3721153 c.1972G>C p.E658Q Substitution - Missense 11:119287882-119287882 + 1275886 COSM34064 c.1227+4C>T p.? Unknown 11:119278301-119278301 + S02-14875-TP COSM4990133 c.1237G>A p.G413S Substitution - Missense 11:119278519-119278519 + TCGA-18-3409-01 COSM686896 c.1450C>T p.P484S Substitution - Missense 11:119284987-119284987 + TCGA-D1-A17D-01 COSM923809 c.279G>A p.Q93Q Substitution - coding silent 11:119232531-119232531 + 1874577 COSM1234989 c.1246T>A p.C416S Substitution - Missense 11:119278528-119278528 + 5 COSM3738507 c.? p.P417S Substitution - Missense PCSI_0083_Pa_X COSM132872 c.1169A>G p.D390G Substitution - Missense 11:119278239-119278239 + AML_412 COSM34056 c.1141T>C p.C381R Substitution - Missense 11:119278211-119278211 + 1275882 COSM34058 c.1186T>C p.C396R Substitution - Missense 11:119278256-119278256 + PD6646a COSM3719949 c.1201T>A p.C401S Substitution - Missense 11:119278271-119278271 + PD7619a COSM5945223 c.1321A>T p.S441C Substitution - Missense 11:119278603-119278603 + PD11153a COSM34054 c.1112A>G p.Y371C Substitution - Missense 11:119278182-119278182 + 1275878 COSM34057 c.1150T>C p.C384R Substitution - Missense 11:119278220-119278220 + 1507682 COSM87283 c.1193A>G p.H398R Substitution - Missense 11:119278263-119278263 + PD6255a COSM4384634 c.1027C>T p.R343* Substitution - Nonsense 11:119277776-119277776 + 1633150 COSM144248 c.2033C>T p.A678V Substitution - Missense 11:119287943-119287943 + 1275879 COSM34057 c.1150T>C p.C384R Substitution - Missense 11:119278220-119278220 + 1234399 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + 1429855 COSM49107 c.1144A>G p.K382E Substitution - Missense 11:119278214-119278214 + PD11022a COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + CSCC-52-T COSM4501946 c.600C>T p.V200V Substitution - coding silent 11:119273877-119273877 + 1950467 COSM1583040 c.? p.E366Q Substitution - Missense PD7387a COSM34073 c.1142G>A p.C381Y Substitution - Missense 11:119278212-119278212 + TCGA-BR-4362-01 COSM4018515 c.1818T>C p.S606S Substitution - coding silent 11:119285443-119285443 + 1773516 COSM34117 c.? p.R420Q Substitution - Missense Case_13 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + 1610753 COSM133823 c.1112A>C p.Y371S Substitution - Missense 11:119278182-119278182 + 1281389 COSM34132 c.? p.R420G Substitution - Missense 1302755 COSM36364 c.1106_1171del66 p.E369_D390del22 Deletion - In frame 11:119278176-119278241 + 8049335 COSM4387952 c.736C>T p.R246* Substitution - Nonsense 11:119274013-119274013 + 1_RESISTANT COSM222220 c.601C>T p.P201S Substitution - Missense 11:119273878-119273878 + 1275885 COSM34060 c.1222T>C p.W408R Substitution - Missense 11:119278292-119278292 + LUAD-NYU847 COSM376592 c.747+1G>A p.? Unknown 11:119274025-119274025 + TCGA-GN-A263-01 COSM3868562 c.745C>T p.Q249* Substitution - Nonsense 11:119274022-119274022 + DM36 COSM5611243 c.1178_1179TT>GA p.I393R Substitution - Missense 11:119278248-119278249 + sysucc-311T COSM5477447 c.2164T>C p.C722R Substitution - Missense 11:119297394-119297394 + 2047210 COSM1168047 c.? p.? Unknown 2542200 COSM34117 c.? p.R420Q Substitution - Missense S01366 COSM309873 c.2266G>T p.A756S Substitution - Missense 11:119298372-119298372 + PT24_2 COSM5904602 c.1969C>A p.P657T Substitution - Missense 11:119287879-119287879 + 2538139 COSM5944176 c.841C>T p.L281F Substitution - Missense 11:119274925-119274925 + 2047170 COSM1168047 c.? p.? Unknown TCGA-D1-A17Q-01 COSM923811 c.826G>A p.E276K Substitution - Missense 11:119274910-119274910 + 2492700 COSM1351842 c.1184C>T p.P395L Substitution - Missense 11:119278254-119278254 + 1773528 COSM330637 c.? p.P417H Substitution - Missense TCGA-AN-A0FT-01 COSM428539 c.397T>C p.F133L Substitution - Missense 11:119232649-119232649 + TCGA-D1-A0ZO-01 COSM923822 c.2549C>T p.A850V Substitution - Missense 11:119299609-119299609 + PD10987a COSM5945213 c.1102T>A p.Y368N Substitution - Missense 11:119278172-119278172 + 1507669 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + Pat_65_A COSM1721168 c.1364_1366delATG p.D460delD Deletion - In frame 11:119278646-119278648 + 1234382 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + 585203 COSM319245 c.2192A>G p.Y731C Substitution - Missense 11:119297422-119297422 + TCGA-E9-A244-01 COSM1475113 c.2439C>A p.V813V Substitution - coding silent 11:119299499-119299499 + 2321366 COSM4669520 c.1363_1364insATG p.D460_E461insD Insertion - In frame 11:119278645-119278646 + 1610761 COSM133826 c.1243G>A p.G415S Substitution - Missense 11:119278525-119278525 + 20613 COSM34053 c.1111T>G p.Y371D Substitution - Missense 11:119278181-119278181 + PD11254a COSM4385831 c.1100A>C p.Q367P Substitution - Missense 11:119278170-119278170 + TCGA-08-0346-01 COSM1321865 c.1234G>A p.E412K Substitution - Missense 11:119278516-119278516 + TCGA-AB-2989-03 COSM87287 c.1100A>G p.Q367R Substitution - Missense 11:119278170-119278170 + 1317125 COSM41272 c.1171G>A p.V391I Substitution - Missense 11:119278241-119278241 + NB-1263 COSM1283936 c.560C>T p.A187V Substitution - Missense 11:119271851-119271851 + CSCC-11-T COSM4538804 c.2601G>A p.Q867Q Substitution - coding silent 11:119299661-119299661 + 1773529 COSM330638 c.? p.C396Y Substitution - Missense 1234396 COSM34073 c.1142G>A p.C381Y Substitution - Missense 11:119278212-119278212 + 1773524 COSM49099 c.? p.C381R Substitution - Missense 1610759 COSM133825 c.1195C>G p.L399V Substitution - Missense 11:119278265-119278265 + PD10801a COSM36363 c.1202G>C p.C401S Substitution - Missense 11:119278272-119278272 + 14 COSM330632 c.? p.C384Y Substitution - Missense 1773514 COSM330627 c.? p.W408C Substitution - Missense HD-0375 COSM49102 c.? p.L380P Substitution - Missense SH-3458 COSM5020009 c.513T>C p.S171S Substitution - coding silent 11:119271804-119271804 + 2492703 COSM1351842 c.1184C>T p.P395L Substitution - Missense 11:119278254-119278254 + PD6277a COSM4384638 c.1193A>C p.H398P Substitution - Missense 11:119278263-119278263 + PD11283a COSM5945224 c.2584G>A p.E862K Substitution - Missense 11:119299644-119299644 + 2217108 COSM49100 c.? p.P417L Substitution - Missense S02273 COSM5681513 c.448A>T p.N150Y Substitution - Missense 11:119271739-119271739 + S09-31237-TP COSM4990137 c.2686G>T p.V896F Substitution - Missense 11:119299746-119299746 + 1_PRE-TREATMENT COSM222220 c.601C>T p.P201S Substitution - Missense 11:119273878-119273878 + 2 COSM34117 c.? p.R420Q Substitution - Missense TCGA-AN-A0AM-01 COSM428538 c.198G>T p.V66V Substitution - coding silent 11:119232450-119232450 + 1317075 COSM41269 c.239G>A p.S80N Substitution - Missense 11:119232491-119232491 + Pat_06_B COSM5837984 c.2252G>A p.G751D Substitution - Missense 11:119298358-119298358 + T18 COSM5065003 c.1102_1103insATGCAG p.Y368_E369insAD Insertion - In frame 11:119278172-119278173 + AML_215 COSM5879358 c.1096-2A>T p.? Unknown 11:119278164-119278164 + 38 COSM3738507 c.? p.P417S Substitution - Missense B22-Tumor COSM1746083 c.2495A>T p.N832I Substitution - Missense 11:119299555-119299555 + RK032_C01 COSM1627826 c.854_855delTT p.I285fs*26 Deletion - Frameshift 11:119274938-119274939 + Pat_40_B COSM1721168 c.1364_1366delATG p.D460delD Deletion - In frame 11:119278646-119278648 + 1317076 COSM41272 c.1171G>A p.V391I Substitution - Missense 11:119278241-119278241 + HD-0263 COSM49100 c.? p.P417L Substitution - Missense HD-0547 COSM219132 c.1258C>T p.R420* Substitution - Nonsense 11:119278540-119278540 + PD6787a COSM4385658 c.638_639insA p.H213fs*17 Insertion - Frameshift 11:119273915-119273916 + 17 COSM3738513 c.? p.I383M Substitution - Missense TCGA-EJ-7123-01 COSM3670685 c.2359C>A p.R787S Substitution - Missense 11:119298465-119298465 + UPN03031 COSM34110 c.? p.S376fs*18 Unknown PD11065a COSM34058 c.1186T>C p.C396R Substitution - Missense 11:119278256-119278256 + 45 COSM1732669 c.1172_1173insGGATGT p.V391_K392insDV Insertion - In frame 11:119278242-119278243 + 1773526 COSM330635 c.? p.I423N Substitution - Missense MOLM-13 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + PD6197a COSM4384634 c.1027C>T p.R343* Substitution - Nonsense 11:119277776-119277776 + 1234386 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + 1773518 COSM34117 c.? p.R420Q Substitution - Missense 52 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + 36 COSM1732670 c.1095+1G>C p.? Unknown 11:119277845-119277845 + TCGA-UB-A7MF-01 COSM4918909 c.286C>T p.R96C Substitution - Missense 11:119232538-119232538 + 1279246 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + DM79 COSM3397468 c.1152T>G p.C384W Substitution - Missense 11:119278222-119278222 + 2047195 COSM1168047 c.? p.? Unknown 1275872 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + 1275875 COSM34054 c.1112A>G p.Y371C Substitution - Missense 11:119278182-119278182 + 2156691 COSM1168047 c.? p.? Unknown TCGA-13-0758-01 COSM1321865 c.1234G>A p.E412K Substitution - Missense 11:119278516-119278516 + YUFERY COSM5371804 c.465C>T p.S155S Substitution - coding silent 11:119271756-119271756 + 1950471 COSM34117 c.? p.R420Q Substitution - Missense MO_1263 COSM5557770 c.576A>C p.K192N Substitution - Missense 11:119271867-119271867 + 1505358 COSM87244 c.1250C>G p.P417R Substitution - Missense 11:119278532-119278532 + TCGA-AX-A0J0-01 COSM923817 c.1865T>G p.F622C Substitution - Missense 11:119285490-119285490 + 1276025 COSM34070 c.1253T>C p.F418S Substitution - Missense 11:119278535-119278535 + TCGA-EB-A3Y7-01 COSM3444160 c.1258C>G p.R420G Substitution - Missense 11:119278540-119278540 + 1998601 COSM34065 c.1228-2A>G p.? Unknown 11:119278508-119278508 + PD8210a COSM4387952 c.736C>T p.R246* Substitution - Nonsense 11:119274013-119274013 + 2217385 COSM4169640 c.? p.C396R Substitution - Missense AML_225 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + TCGA-A8-A0A6-01 COSM3808559 c.1982A>C p.H661P Substitution - Missense 11:119287892-119287892 + 14 COSM87284 c.1202G>A p.C401Y Substitution - Missense 11:119278272-119278272 + 2080310 COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + SA237 COSM212843 c.842T>A p.L281H Substitution - Missense 11:119274926-119274926 + WA40 COSM239166 c.19A>T p.K7* Substitution - Nonsense 11:119206436-119206436 + PD9327a COSM34058 c.1186T>C p.C396R Substitution - Missense 11:119278256-119278256 + YURTHE COSM1704665 c.1697C>T p.P566L Substitution - Missense 11:119285322-119285322 + CPCG0095-F1 COSM4879841 c.805A>G p.M269V Substitution - Missense 11:119274889-119274889 + 2047202 COSM1168047 c.? p.? Unknown P151 COSM5008172 c.1263T>G p.C421W Substitution - Missense 11:119278545-119278545 + TCGA-BR-4368-01 COSM4018516 c.2291C>A p.P764H Substitution - Missense 11:119298397-119298397 + PD9220a COSM34070 c.1253T>C p.F418S Substitution - Missense 11:119278535-119278535 + 1857584 COSM1178066 c.? p.W408R Substitution - Missense 1234390 COSM34065 c.1228-2A>G p.? Unknown 11:119278508-119278508 + 10 COSM3738509 c.? p.K392N Substitution - Missense 169 COSM3721152 c.1973A>T p.E658V Substitution - Missense 11:119287883-119287883 + 10 COSM34053 c.1111T>G p.Y371D Substitution - Missense 11:119278181-119278181 + 03 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + 1325657 COSM41676 c.? p.? Unknown 1234402 COSM34066 c.1151G>A p.C384Y Substitution - Missense 11:119278221-119278221 + D14 COSM5006932 c.907T>C p.W303R Substitution - Missense 11:119276034-119276034 + Pat_53_B COSM1721168 c.1364_1366delATG p.D460delD Deletion - In frame 11:119278646-119278648 + TCGA-F5-6814-01 COSM3415597 c.2681A>G p.E894G Substitution - Missense 11:119299741-119299741 + 2246965 COSM4422156 c.1643C>T p.P548L Substitution - Missense 11:119285268-119285268 + 2492701 COSM1351842 c.1184C>T p.P395L Substitution - Missense 11:119278254-119278254 + 1276021 COSM34066 c.1151G>A p.C384Y Substitution - Missense 11:119278221-119278221 + CSCC-52-T COSM4471395 c.1717C>T p.P573S Substitution - Missense 11:119285342-119285342 + PD6079a COSM34081 c.1250C>T p.P417L Substitution - Missense 11:119278532-119278532 + PD6793a COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + TCGA-24-2293-01 COSM79606 c.1012T>C p.L338L Substitution - coding silent 11:119277761-119277761 + 1633495 COSM144247 c.2024C>G p.S675C Substitution - Missense 11:119287934-119287934 + CSCC-10-T COSM4518319 c.600_601CC>TT p.P201S Substitution - Missense 11:119273877-119273878 + PD6122a COSM4384634 c.1027C>T p.R343* Substitution - Nonsense 11:119277776-119277776 + PD6543a COSM4384635 c.1139T>G p.L380R Substitution - Missense 11:119278209-119278209 + CSCC-27-T COSM4471710 c.1737C>T p.P579P Substitution - coding silent 11:119285362-119285362 + STC291 COSM5050591 c.1028G>A p.R343Q Substitution - Missense 11:119277777-119277777 + 1507714 COSM34057 c.1150T>C p.C384R Substitution - Missense 11:119278220-119278220 + TCGA-D3-A5GO-06 COSM3444166 c.2673C>T p.I891I Substitution - coding silent 11:119299733-119299733 + K347 COSM249332 c.2387C>T p.A796V Substitution - Missense 11:119298493-119298493 + 1540955 COSM97084 c.1183C>G p.P395A Substitution - Missense 11:119278253-119278253 + 1695991 COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + PD6240a COSM3415596 c.616C>T p.R206* Substitution - Nonsense 11:119273893-119273893 + TCGA-08-0373-01 COSM1321865 c.1234G>A p.E412K Substitution - Missense 11:119278516-119278516 + S02328 COSM5691763 c.2440A>C p.T814P Substitution - Missense 11:119299500-119299500 + PD6212a COSM4384637 c.1167G>T p.K389N Substitution - Missense 11:119278237-119278237 + TCGA-B0-5094-01 COSM466451 c.2156C>T p.A719V Substitution - Missense 11:119297386-119297386 + 2080600 COSM1168047 c.? p.? Unknown B22 COSM1746083 c.2495A>T p.N832I Substitution - Missense 11:119299555-119299555 + 2246979 COSM4422156 c.1643C>T p.P548L Substitution - Missense 11:119285268-119285268 + 31 COSM1732668 c.1276A>C p.T426P Substitution - Missense 11:119278558-119278558 + 1275877 COSM34056 c.1141T>C p.C381R Substitution - Missense 11:119278211-119278211 + 1317127 COSM41273 c.2489G>A p.R830K Substitution - Missense 11:119299549-119299549 + 1799757 COSM1168047 c.? p.? Unknown YUJUBE COSM1704667 c.2623C>T p.Q875* Substitution - Nonsense 11:119299683-119299683 + 12 COSM34070 c.1253T>C p.F418S Substitution - Missense 11:119278535-119278535 + Case_15 COSM1724993 c.1246T>C p.C416R Substitution - Missense 11:119278528-119278528 + ESCC_158 COSM5580531 c.1861C>T p.P621S Substitution - Missense 11:119285486-119285486 + WM3211 COSM34078 c.1254C>A p.F418L Substitution - Missense 11:119278536-119278536 + AML_164 COSM5879359 c.1096-1G>T p.? Unknown 11:119278165-119278165 + GCT92 COSM34065 c.1228-2A>G p.? Unknown 11:119278508-119278508 + 2201788 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + TCGA-33-4566-01 COSM686899 c.1190G>T p.G397V Substitution - Missense 11:119278260-119278260 + PT49 COSM5935693 c.2141C>T p.S714F Substitution - Missense 11:119297022-119297022 + VACO4S COSM168281 c.446G>A p.R149Q Substitution - Missense 11:119271737-119271737 + TARGET-20-PASHBI-09A-01D COSM5487508 c.1499_1500insTGACCTGG p.L503fs*115 Insertion - Frameshift 11:119285036-119285037 + 1275866 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + S01563 COSM309874 c.2136T>C p.D712D Substitution - coding silent 11:119297017-119297017 + 2080272 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + RK083_C01 COSM1627827 c.874A>G p.I292V Substitution - Missense 11:119276001-119276001 + MDS42 COSM1741217 c.1224G>T p.W408C Substitution - Missense 11:119278294-119278294 + S09-31237-TP COSM4990135 c.1862C>T p.P621L Substitution - Missense 11:119285487-119285487 + 1507660 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + TCGA-21-5786-01 COSM686902 c.261G>A p.L87L Substitution - coding silent 11:119232513-119232513 + PD6058a COSM34066 c.1151G>A p.C384Y Substitution - Missense 11:119278221-119278221 + TCGA-D1-A15X-01 COSM923818 c.2033C>A p.A678D Substitution - Missense 11:119287943-119287943 + 1275868 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + 1507656 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + 1278628 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + 81 COSM211606 c.1008_1431del424 p.F336fs*138 Deletion - Frameshift YUBER COSM1704664 c.1214T>C p.L405P Substitution - Missense 11:119278284-119278284 + 3844_T COSM3979179 c.2708A>T p.H903L Substitution - Missense 11:119299768-119299768 + MOLM-13 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + 1234401 COSM34081 c.1250C>T p.P417L Substitution - Missense 11:119278532-119278532 + 1950478 COSM34117 c.? p.R420Q Substitution - Missense 1507656 COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + PD8936a COSM4384645 c.1421C>T p.A474V Substitution - Missense 11:119278703-119278703 + TCGA-A3-3365-01 COSM1492439 c.1412A>G p.K471R Substitution - Missense 11:119278694-119278694 + 1598353 COSM133607 c.1096-96_1186>CGG p.? Unknown 11:119278069-119278256 + 1281388 COSM34131 c.1096-?_1431+?del1680 p.E366_K477del Deletion - In frame 11:119278166-119278713 + 1507723 COSM87287 c.1100A>G p.Q367R Substitution - Missense 11:119278170-119278170 + CMLPh-005 COSM1234989 c.1246T>A p.C416S Substitution - Missense 11:119278528-119278528 + PD7375a COSM3444159 c.1250C>A p.P417H Substitution - Missense 11:119278532-119278532 + 1279247 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + A549 COSM1193372 c.1753C>T p.R585C Substitution - Missense 11:119285378-119285378 + 1633149 COSM133827 c.1248T>G p.C416W Substitution - Missense 11:119278530-119278530 + 1998625 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + S01563 COSM309874 c.2136T>C p.D712D Substitution - coding silent 11:119297017-119297017 + 1234393 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + 1280851 COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + 2217262 COSM4169639 c.? p.P35Q Substitution - Missense 24397 COSM5031014 c.1111T>A p.Y371N Substitution - Missense 11:119278181-119278181 + TCGA-GN-A267-06 COSM3444157 c.852C>T p.F284F Substitution - coding silent 11:119274936-119274936 + TCGA-FW-A3R5-06 COSM3868563 c.1674C>T p.S558S Substitution - coding silent 11:119285299-119285299 + TCGA-AA-3510-01 COSM1351830 c.617G>A p.R206Q Substitution - Missense 11:119273894-119273894 + PD6255a COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + 1 COSM3738506 c.? p.C419S Substitution - Missense PT13 COSM5896104 c.1814C>T p.S605F Substitution - Missense 11:119285439-119285439 + 1275887 COSM34065 c.1228-2A>G p.? Unknown 11:119278508-119278508 + PD9214a COSM5945221 c.1256G>A p.C419Y Substitution - Missense 11:119278538-119278538 + SNU-175 COSM2106775 c.686A>T p.D229V Substitution - Missense 11:119273963-119273963 + 1459344 COSM52921 c.860A>G p.K287R Substitution - Missense 11:119274944-119274944 + 1507682 COSM87286 c.1285_1302del18 p.I429_F434delIVVDPF Deletion - In frame 11:119278567-119278584 + 2108195 COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + TCGA-A3-3316-01 COSM1492438 c.2641G>A p.A881T Substitution - Missense 11:119299701-119299701 + UPN02561 COSM34109 c.? p.G375P Substitution - Missense 1773515 COSM330628 c.? p.H398Q Substitution - Missense 8 COSM3738508 c.? p.D460del Deletion - In frame 1507695 COSM34070 c.1253T>C p.F418S Substitution - Missense 11:119278535-119278535 + 1573679 COSM132871 c.1120A>G p.M374V Substitution - Missense 11:119278190-119278190 + CSCC-29-T COSM4471343 c.1713C>T p.D571D Substitution - coding silent 11:119285338-119285338 + 2273963 COSM4406604 c.? p.I383T Substitution - Missense 1857577 COSM1169705 c.? p.S407P Substitution - Missense 10 COSM88178 c.870_1007del138 p.I292_Y337del46 Deletion - In frame 11:119275997-119276134 + TCGA-GN-A26C-01 COSM3444158 c.1101A>T p.Q367H Substitution - Missense 11:119278171-119278171 + PD8278a COSM5945221 c.1256G>A p.C419Y Substitution - Missense 11:119278538-119278538 + 1325673 COSM41675 c.? p.? Unknown UPN03149 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + 1459342 COSM52920 c.1095_1096insTCAAAG p.Q365_E366insSK Insertion - In frame 1234395 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + 1998581 COSM1666980 c.1103_1168del66 p.E369_D390del Deletion - In frame 11:119278173-119278238 + CSCC-11-T COSM4537790 c.2463G>A p.E821E Substitution - coding silent 11:119299523-119299523 + 1234398 COSM34064 c.1227+4C>T p.? Unknown 11:119278301-119278301 + PT32 COSM5907558 c.1564-6C>T p.? Unknown 11:119285183-119285183 + 1317162 COSM41271 c.745C>G p.Q249E Substitution - Missense 11:119274022-119274022 + LUAD-F00365 COSM391718 c.352delT p.F118fs*5 Deletion - Frameshift 11:119232604-119232604 + 1507722 COSM34053 c.1111T>G p.Y371D Substitution - Missense 11:119278181-119278181 + PD9348a COSM5945217 c.1194C>A p.H398Q Substitution - Missense 11:119278264-119278264 + 1857611 COSM1169418 c.? p.C404Y Substitution - Missense TCGA-B5-A1MY-01 COSM923819 c.2268C>T p.A756A Substitution - coding silent 11:119298374-119298374 + AML_136 COSM1351834 c.1096-1G>A p.? Unknown 11:119278165-119278165 + PD6212a COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + TCGA-EE-A2GD-06 COSM3444165 c.2630C>T p.A877V Substitution - Missense 11:119299690-119299690 + PD5773a COSM4384644 c.1319G>T p.G440V Substitution - Missense 11:119278601-119278601 + AML_14y_04_DX COSM34058 c.1186T>C p.C396R Substitution - Missense 11:119278256-119278256 + TCGA-EE-A181-06 COSM3444156 c.543T>C p.I181I Substitution - coding silent 11:119271834-119271834 + 1305434 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + TCGA-EI-6917-01 COSM3415596 c.616C>T p.R206* Substitution - Nonsense 11:119273893-119273893 + HCC108T COSM1604199 c.1767A>T p.S589S Substitution - coding silent 11:119285392-119285392 + Pat_41_A COSM1721649 c.2665delA p.N890fs*15 Deletion - Frameshift 11:119299725-119299725 + ME002T COSM222220 c.601C>T p.P201S Substitution - Missense 11:119273878-119273878 + TCGA-AM-5820-01 COSM3687123 c.1443G>A p.P481P Substitution - coding silent 11:119284980-119284980 + 10 COSM211605 c.1106_1228del123 p.E369_Q409del Deletion - In frame 11:119278176-119278510 + TCGA-AA-A010-01 COSM279594 c.1676G>A p.R559Q Substitution - Missense 11:119285301-119285301 + 1507689 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + TCGA-G4-6310-01 COSM1351845 c.1220C>T p.S407F Substitution - Missense 11:119278290-119278290 + PT45 COSM3415596 c.616C>T p.R206* Substitution - Nonsense 11:119273893-119273893 + HT115 COSM168281 c.446G>A p.R149Q Substitution - Missense 11:119271737-119271737 + DM6 COSM4387952 c.736C>T p.R246* Substitution - Nonsense 11:119274013-119274013 + 1280852 COSM34066 c.1151G>A p.C384Y Substitution - Missense 11:119278221-119278221 + 14 COSM3738512 c.? p.L370F Substitution - Missense LUAD-NYU848 COSM376989 c.1430A>T p.K477M Substitution - Missense 11:119278712-119278712 + TCGA-BS-A0UJ-01 COSM923821 c.2464A>G p.R822G Substitution - Missense 11:119299524-119299524 + P13 COSM5009611 c.1760G>C p.G587A Substitution - Missense 11:119285385-119285385 + 1276024 COSM34069 c.1249C>T p.P417S Substitution - Missense 11:119278531-119278531 + ccRCC-41 COSM1660995 c.896G>A p.R299H Substitution - Missense 11:119276023-119276023 + CSCC-42-T COSM4560222 c.835G>A p.A279T Substitution - Missense 11:119274919-119274919 + AML_364 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + 1507645 COSM87282 c.1223G>C p.W408S Substitution - Missense 11:119278293-119278293 + PCSI_0083_Pa_P COSM3375687 c.1227+2T>C p.? Unknown 11:119278299-119278299 + PD6537a COSM4384633 c.793C>T p.H265Y Substitution - Missense 11:119274877-119274877 + 1773524 COSM330632 c.? p.C384Y Substitution - Missense LUAD-S01315 COSM343952 c.468C>T p.L156L Substitution - coding silent 11:119271759-119271759 + 1633510 COSM87244 c.1250C>G p.P417R Substitution - Missense 11:119278532-119278532 + HCC058T COSM5804743 c.2101A>T p.M701L Substitution - Missense 11:119296982-119296982 + 1275865 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + TCGA-EB-A44Q-06 COSM1234989 c.1246T>A p.C416S Substitution - Missense 11:119278528-119278528 + CSCC-11-T COSM4570624 c.298T>G p.S100A Substitution - Missense 11:119232550-119232550 + 1857596 COSM1169706 c.? p.R420L Substitution - Missense 1857597 COSM1169706 c.? p.R420L Substitution - Missense 1950473 COSM1583042 c.? p.Y371N Substitution - Missense MDS30 COSM1741212 c.1340C>T p.A447V Substitution - Missense 11:119278622-119278622 + GCT51 COSM34065 c.1228-2A>G p.? Unknown 11:119278508-119278508 + EGCT1098 COSM4422156 c.1643C>T p.P548L Substitution - Missense 11:119285268-119285268 + LUAD-VUMN6 COSM347791 c.2144A>C p.Q715P Substitution - Missense 11:119297025-119297025 + CHC1055T COSM3666862 c.36G>T p.G12G Substitution - coding silent 11:119206453-119206453 + PD6780a COSM1732668 c.1276A>C p.T426P Substitution - Missense 11:119278558-119278558 + 12-P412 COSM4574111 c.1641T>C p.P547P Substitution - coding silent 11:119285266-119285266 + 1302757 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + 1275876 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + GC_302T-GC_302N COSM4772756 c.1010A>G p.Y337C Substitution - Missense 11:119277759-119277759 + TCGA-LP-A4AV-01 COSM4825409 c.1366G>A p.D456N Substitution - Missense 11:119278648-119278648 + TCGA-BR-6453-01 COSM4018517 c.2556C>T p.T852T Substitution - coding silent 11:119299616-119299616 + 1279645 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + UPN03028 COSM34108 c.? p.G375S Substitution - Missense pfg088T COSM4747807 c.1175_1228-37del229 p.? Unknown 11:119278245-119278473 + 1598351 COSM133605 c.1207_1227+1637>CTTT p.? Unknown 11:119278277-119278313 + TCGA-AZ-4315-01 COSM1351850 c.2314G>T p.D772Y Substitution - Missense 11:119298420-119298420 + 19 COSM3738514 c.? p.Q367P Substitution - Missense AML_596 COSM34063 c.1096-1G>C p.? Unknown 11:119278165-119278165 + PD10845a COSM34063 c.1096-1G>C p.? Unknown 11:119278165-119278165 + PGBM17PT COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + PD6212a COSM4384642 c.1267A>T p.I423F Substitution - Missense 11:119278549-119278549 + S06-38853-TP COSM4990138 c.2694T>C p.I898I Substitution - coding silent 11:119299754-119299754 + 1234379 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + 48 COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + PD6099a COSM4384641 c.1222T>A p.W408R Substitution - Missense 11:119278292-119278292 + EGCT1135 COSM5749140 c.1096-10_1107del22 p.? Unknown 11:119278156-119278177 + HD-0264 COSM49101 c.? p.E366K Substitution - Missense 1302758 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + 1998560 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + 1507724 COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + PD6178a COSM133823 c.1112A>C p.Y371S Substitution - Missense 11:119278182-119278182 + TCGA-D1-A103-01 COSM923810 c.557C>T p.A186V Substitution - Missense 11:119271848-119271848 + ME009T COSM223503 c.2037-1G>A p.? Unknown 11:119296917-119296917 + 1275873 COSM34053 c.1111T>G p.Y371D Substitution - Missense 11:119278181-119278181 + TCGA-D1-A103-01 COSM923815 c.1594C>T p.P532S Substitution - Missense 11:119285219-119285219 + 2406611 COSM5075573 c.1582C>T p.H528Y Substitution - Missense 11:119285207-119285207 + DM101 COSM5608010 c.844C>T p.Q282* Substitution - Nonsense 11:119274928-119274928 + GCT104 COSM4774929 c.595A>G p.I199V Substitution - Missense 11:119273872-119273872 + 13 COSM3738511 c.? p.Y371S Substitution - Missense Pat_36_B COSM1721649 c.2665delA p.N890fs*15 Deletion - Frameshift 11:119299725-119299725 + 1234387 COSM34076 c.1249C>G p.P417A Substitution - Missense 11:119278531-119278531 + 1998585 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + PD9297a COSM34070 c.1253T>C p.F418S Substitution - Missense 11:119278535-119278535 + 1857585 COSM1178066 c.? p.W408R Substitution - Missense 1507665 COSM41789 c.1247G>A p.C416Y Substitution - Missense 11:119278529-119278529 + 1773525 COSM330633 c.? p.C381Y Substitution - Missense TCGA-EE-A2GU-06 COSM3444154 c.201G>A p.V67V Substitution - coding silent 11:119232453-119232453 + PD8094a COSM5945222 c.1312G>A p.G438R Substitution - Missense 11:119278594-119278594 + PD8548a COSM4560222 c.835G>A p.A279T Substitution - Missense 11:119274919-119274919 + 1507663 COSM87285 c.1199T>G p.M400R Substitution - Missense 11:119278269-119278269 + 1610757 COSM133824 c.1111_1112insTAT p.L370_Y371insL Insertion - In frame 11:119278181-119278182 + 2024679 COSM1716173 c.1198A>G p.M400V Substitution - Missense 11:119278268-119278268 + 1680927 COSM34056 c.1141T>C p.C381R Substitution - Missense 11:119278211-119278211 + 02 COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + CSCC-31-T COSM4501946 c.600C>T p.V200V Substitution - coding silent 11:119273877-119273877 + 2492702 COSM1351842 c.1184C>T p.P395L Substitution - Missense 11:119278254-119278254 + TCGA-EE-A2MT-06 COSM3444155 c.329G>A p.G110E Substitution - Missense 11:119232581-119232581 + 1275869 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + Pat_36_B COSM1721168 c.1364_1366delATG p.D460delD Deletion - In frame 11:119278646-119278648 + 1773517 COSM330629 c.? p.H398P Substitution - Missense 1302759 COSM34065 c.1228-2A>G p.? Unknown 11:119278508-119278508 + 1276022 COSM34067 c.1187G>A p.C396Y Substitution - Missense 11:119278257-119278257 + 1773526 COSM330634 c.? p.V430M Substitution - Missense 28 COSM3738515 c.? p.C401Y Substitution - Missense TCGA-ER-A199-06 COSM3444162 c.2024C>T p.S675F Substitution - Missense 11:119287934-119287934 + HD-0304 COSM49101 c.? p.E366K Substitution - Missense 8 COSM3738507 c.? p.P417S Substitution - Missense Pat_14_B COSM1721649 c.2665delA p.N890fs*15 Deletion - Frameshift 11:119299725-119299725 + TCGA-DK-A3X1-01 COSM3791246 c.1310G>T p.R437I Substitution - Missense 11:119278592-119278592 + 2047211 COSM1168047 c.? p.? Unknown 2246982 COSM41790 c.1255T>C p.C419R Substitution - Missense 11:119278537-119278537 + 1275863 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + 1950467 COSM1583041 c.? p.E366D Substitution - Missense PD6268a COSM4384640 c.1212T>G p.C404W Substitution - Missense 11:119278282-119278282 + 1281386 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + SH-3458 COSM5019967 c.1485G>A p.P495P Substitution - coding silent 11:119285022-119285022 + PD6277a COSM4384639 c.1210T>G p.C404G Substitution - Missense 11:119278280-119278280 + 1275864 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + 2108220 COSM1721168 c.1364_1366delATG p.D460delD Deletion - In frame 11:119278646-119278648 + 1950469 COSM1583042 c.? p.Y371N Substitution - Missense 1275883 COSM34062 c.1190_1288del99 p.G397_I429del Deletion - In frame 11:119278260-119278570 + 06 COSM34057 c.1150T>C p.C384R Substitution - Missense 11:119278220-119278220 + 2538138 COSM5944175 c.761T>C p.L254S Substitution - Missense 11:119274845-119274845 + 11 COSM3738510 c.? p.C401S Substitution - Missense PD6898a COSM34073 c.1142G>A p.C381Y Substitution - Missense 11:119278212-119278212 + TCGA-06-2562-01 COSM3397468 c.1152T>G p.C384W Substitution - Missense 11:119278222-119278222 + SC_9007 COSM5556054 c.2421T>G p.G807G Substitution - coding silent 11:119298527-119298527 + 1280854 COSM34119 c.? p.C404S Substitution - Missense PCSI_0083_Pa_P_526 COSM3375687 c.1227+2T>C p.? Unknown 11:119278299-119278299 + 1280850 COSM34119 c.? p.C404S Substitution - Missense 11_FL COSM4170319 c.881G>A p.R294Q Substitution - Missense 11:119276008-119276008 + MEL-JWCI-WGS-20 COSM34057 c.1150T>C p.C384R Substitution - Missense 11:119278220-119278220 + 2217109 COSM4169412 c.? p.P707L Substitution - Missense 51 COSM34066 c.1151G>A p.C384Y Substitution - Missense 11:119278221-119278221 + 1234405 COSM34075 c.1192C>T p.H398Y Substitution - Missense 11:119278262-119278262 + YUPTER COSM34081 c.1250C>T p.P417L Substitution - Missense 11:119278532-119278532 + 1330208 COSM41790 c.1255T>C p.C419R Substitution - Missense 11:119278537-119278537 + SJDES021 COSM1721168 c.1364_1366delATG p.D460delD Deletion - In frame 11:119278646-119278648 + 1302756 COSM36363 c.1202G>C p.C401S Substitution - Missense 11:119278272-119278272 + 2201787 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + PD5789a COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + TCGA-BS-A0V8-01 COSM219132 c.1258C>T p.R420* Substitution - Nonsense 11:119278540-119278540 + 35M COSM5580531 c.1861C>T p.P621S Substitution - Missense 11:119285486-119285486 + 1330207 COSM41789 c.1247G>A p.C416Y Substitution - Missense 11:119278529-119278529 + PD11024a COSM5945216 c.1178T>A p.I393N Substitution - Missense 11:119278248-119278248 + PD8156a COSM5945211 c.469A>G p.I157V Substitution - Missense 11:119271760-119271760 + 1234384 COSM34072 c.1224G>C p.W408C Substitution - Missense 11:119278294-119278294 + 1279646 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + TCGA-EB-A41A-01 COSM3444163 c.2234C>T p.T745I Substitution - Missense 11:119297464-119297464 + 2246971 COSM4385831 c.1100A>C p.Q367P Substitution - Missense 11:119278170-119278170 + TCGA-21-5786-01 COSM686898 c.1401C>A p.L467L Substitution - coding silent 11:119278683-119278683 + T2950 COSM4669520 c.1363_1364insATG p.D460_E461insD Insertion - In frame 11:119278645-119278646 + 105307 COSM95795 c.741C>G p.L247L Substitution - coding silent 11:119274018-119274018 + 1429856 COSM49107 c.1144A>G p.K382E Substitution - Missense 11:119278214-119278214 + 1234392 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + PD8210a COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + PD6106a COSM4384641 c.1222T>A p.W408R Substitution - Missense 11:119278292-119278292 + 1325649 COSM41675 c.? p.? Unknown 1234394 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + TCGA-K4-A3WS-01 COSM343952 c.468C>T p.L156L Substitution - coding silent 11:119271759-119271759 + TCGA-18-3412-01 COSM686901 c.333A>G p.E111E Substitution - coding silent 11:119232585-119232585 + TCGA-G4-6314-01 COSM3687124 c.2269G>A p.A757T Substitution - Missense 11:119298375-119298375 + 1234381 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + 1507712 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + S03-45671-TP COSM4990136 c.2655C>T p.I885I Substitution - coding silent 11:119299715-119299715 + PD7774a COSM5879358 c.1096-2A>T p.? Unknown 11:119278164-119278164 + HCC108 COSM1604199 c.1767A>T p.S589S Substitution - coding silent 11:119285392-119285392 + S01524 COSM5669275 c.2542G>T p.A848S Substitution - Missense 11:119299602-119299602 + DM99 COSM5608012 c.1745C>T p.P582L Substitution - Missense 11:119285370-119285370 + TCGA-66-2744-01 COSM686895 c.1618C>A p.R540R Substitution - coding silent 11:119285243-119285243 + TCGA-AA-3510-01 COSM1351829 c.416G>T p.R139I Substitution - Missense 11:119232668-119232668 + 23 COSM1732670 c.1095+1G>C p.? Unknown 11:119277845-119277845 + SC-her2-046 COSM87283 c.1193A>G p.H398R Substitution - Missense 11:119278263-119278263 + YUPADI COSM34081 c.1250C>T p.P417L Substitution - Missense 11:119278532-119278532 + 1507657 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + 1610270 COSM34065 c.1228-2A>G p.? Unknown 11:119278508-119278508 + RK199_C01 COSM3738891 c.922G>A p.V308I Substitution - Missense 11:119276049-119276049 + 1325650 COSM41675 c.? p.? Unknown 2011-2263:2012-1327-T COSM4604172 c.1208C>G p.S403C Substitution - Missense 11:119278278-119278278 + TCGA-EI-6917-01 COSM923811 c.826G>A p.E276K Substitution - Missense 11:119274910-119274910 + PD9312a COSM5945212 c.734C>T p.T245I Substitution - Missense 11:119274011-119274011 + PD7937a COSM34071 c.1127C>T p.S376F Substitution - Missense 11:119278197-119278197 + ESCC_157 COSM5646200 c.714T>C p.V238V Substitution - coding silent 11:119273991-119273991 + AML_662 COSM34058 c.1186T>C p.C396R Substitution - Missense 11:119278256-119278256 + 93417 COSM5030978 c.810_811insT p.L272fs*4 Insertion - Frameshift 11:119274894-119274895 + 1633496 COSM144249 c.1204delA p.T402fs*30 Deletion - Frameshift 11:119278274-119278274 + TCGA-AX-A05S-01 COSM923823 c.2603G>A p.G868E Substitution - Missense 11:119299663-119299663 + TCGA-BS-A0UV-01 COSM923820 c.2370C>T p.L790L Substitution - coding silent 11:119298476-119298476 + TCGA-E2-A1LG-01 COSM1475111 c.1501G>C p.D501H Substitution - Missense 11:119285038-119285038 + 2246991 COSM87287 c.1100A>G p.Q367R Substitution - Missense 11:119278170-119278170 + PD7375a COSM4384647 c.1837G>T p.E613* Substitution - Nonsense 11:119285462-119285462 + 1275880 COSM34057 c.1150T>C p.C384R Substitution - Missense 11:119278220-119278220 + MOLM-14 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + TCGA-EB-A5UN-06 COSM3444164 c.2446G>A p.G816S Substitution - Missense 11:119299506-119299506 + 1275867 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + 2321325 COSM4774993 c.1786C>T p.P596S Substitution - Missense 11:119285411-119285411 + TCGA-A5-A0GI-01 COSM923814 c.1376A>T p.D459V Substitution - Missense 11:119278658-119278658 + PD10806a COSM36363 c.1202G>C p.C401S Substitution - Missense 11:119278272-119278272 + 1281387 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + PD11022a COSM34058 c.1186T>C p.C396R Substitution - Missense 11:119278256-119278256 + PD6816a COSM4385659 c.809_810insT p.L272fs*4 Insertion - Frameshift 11:119274893-119274894 + HD-0193 COSM49099 c.? p.C381R Substitution - Missense 1280848 COSM34117 c.? p.R420Q Substitution - Missense 3 COSM34117 c.? p.R420Q Substitution - Missense 2_PRE-TREATMENT COSM1721649 c.2665delA p.N890fs*15 Deletion - Frameshift 11:119299725-119299725 + YURIF COSM1704667 c.2623C>T p.Q875* Substitution - Nonsense 11:119299683-119299683 + PD9384a COSM1475109 c.293T>C p.I98T Substitution - Missense 11:119232545-119232545 + 1459343 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + PD11243a COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + PD10894a COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + CMML-01 COSM132882 c.1223G>T p.W408L Substitution - Missense 11:119278293-119278293 + LIS09PT2 COSM1732275 c.2465G>C p.R822T Substitution - Missense 11:119299525-119299525 + GCT23 COSM5749255 c.1103A>G p.Y368C Substitution - Missense 11:119278173-119278173 + 22 COSM330633 c.? p.C381Y Substitution - Missense T464 COSM4669519 c.1298C>T p.P433L Substitution - Missense 11:119278580-119278580 + 1998634 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + KYSE180 COSM2106773 c.641C>T p.P214L Substitution - Missense 11:119273918-119273918 + AML_229 COSM87285 c.1199T>G p.M400R Substitution - Missense 11:119278269-119278269 + 2439394 COSM5369884 c.? p.I383K Substitution - Missense AML_410 COSM34057 c.1150T>C p.C384R Substitution - Missense 11:119278220-119278220 + SNU-175 COSM4650214 c.152T>C p.V51A Substitution - Missense 11:119206569-119206569 + 1998562 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + YUBER COSM34081 c.1250C>T p.P417L Substitution - Missense 11:119278532-119278532 + TCGA-DK-A3X1-01 COSM686897 c.1407G>A p.M469I Substitution - Missense 11:119278689-119278689 + TCGA-02-0083-01 COSM35526 c.1283C>T p.P428L Substitution - Missense 11:119278565-119278565 + TCGA-B5-A11Y-01 COSM923816 c.1637C>T p.P546L Substitution - Missense 11:119285262-119285262 + 1234403 COSM34082 c.1360A>G p.N454D Substitution - Missense 11:119278642-119278642 + 2217253 COSM1168047 c.? p.? Unknown STC252 COSM5050593 c.2067G>T p.G689G Substitution - coding silent 11:119296948-119296948 + 1610755 COSM34070 c.1253T>C p.F418S Substitution - Missense 11:119278535-119278535 + 1857576 COSM1169705 c.? p.S407P Substitution - Missense KYSE-410 COSM4439361 c.1228-2A>T p.? Unknown 11:119278508-119278508 + 1857610 COSM1169418 c.? p.C404Y Substitution - Missense ESCC_BICR_002T COSM5440755 c.1619G>A p.R540Q Substitution - Missense 11:119285244-119285244 + 127T COSM4669520 c.1363_1364insATG p.D460_E461insD Insertion - In frame 11:119278645-119278646 + PD6787a COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + PD8936a COSM4384643 c.1319G>A p.G440D Substitution - Missense 11:119278601-119278601 + 1234385 COSM34078 c.1254C>A p.F418L Substitution - Missense 11:119278536-119278536 + 1507663 COSM34057 c.1150T>C p.C384R Substitution - Missense 11:119278220-119278220 + TCGA-EE-A2MN-06 COSM3444161 c.1528C>T p.P510S Substitution - Missense 11:119285065-119285065 + PD17951a COSM5351700 c.1263_1277del15 p.I423_E427delIKGTE Deletion - In frame 11:119278545-119278559 + YUWAND COSM1704666 c.2108C>T p.P703L Substitution - Missense 11:119296989-119296989 + 2290929 COSM4440267 c.1480delC p.P495fs*120 Deletion - Frameshift 11:119285017-119285017 + TCGA-CU-A0YR-01 COSM415310 c.2599C>T p.Q867* Substitution - Nonsense 11:119299659-119299659 + 1610760 COSM133826 c.1243G>A p.G415S Substitution - Missense 11:119278525-119278525 + ESCC_158 COSM5646614 c.1571C>G p.S524C Substitution - Missense 11:119285196-119285196 + 1275862 COSM34063 c.1096-1G>C p.? Unknown 11:119278165-119278165 + PD8735a COSM4384648 c.2032G>A p.A678T Substitution - Missense 11:119287942-119287942 + GCT36 COSM5749691 c.1247G>T p.C416F Substitution - Missense 11:119278529-119278529 + AML_392 COSM34069 c.1249C>T p.P417S Substitution - Missense 11:119278531-119278531 + 1275888 COSM34061 c.1244G>T p.G415V Substitution - Missense 11:119278526-119278526 + SJHGG042_D COSM4970793 c.1285_1286insGAACCC p.I429>RTL Complex - insertion inframe 11:119278567-119278568 + 1275871 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + GCT05 COSM87287 c.1100A>G p.Q367R Substitution - Missense 11:119278170-119278170 + 1317077 COSM41591 c.1379_1381delATG p.D460delD Deletion - In frame 11:119278661-119278663 + PD7369a COSM4384650 c.2183G>A p.S728N Substitution - Missense 11:119297413-119297413 + 1325678 COSM41675 c.? p.? Unknown TCGA-02-0083-01 COSM35588 c.1827G>A p.W609* Substitution - Nonsense 11:119285452-119285452 + PD8646a COSM4384646 c.1690C>T p.P564S Substitution - Missense 11:119285315-119285315 + 2016805 COSM1168047 c.? p.? Unknown 587234 COSM1199719 c.1804G>A p.A602T Substitution - Missense 11:119285429-119285429 + GCT22 COSM5749254 c.2569C>T p.L857F Substitution - Missense 11:119299629-119299629 + 2217109 COSM4169411 c.? p.F194L Substitution - Missense PD8056a COSM5945215 c.1149A>G p.I383M Substitution - Missense 11:119278219-119278219 + DM99 COSM5608013 c.1618C>T p.R540* Substitution - Nonsense 11:119285243-119285243 + TCGA-EI-6917-01 COSM1351830 c.617G>A p.R206Q Substitution - Missense 11:119273894-119273894 + TCGA-GF-A6C9-06 COSM4902045 c.1252T>A p.F418I Substitution - Missense 11:119278534-119278534 + AML_136 COSM5879357 c.1096-2_1099AGGAAC>12 p.? Unknown 11:119278164-119278169 + STC252 COSM5050592 c.1687C>T p.R563C Substitution - Missense 11:119285312-119285312 + HCT-15 COSM1676499 c.1208C>T p.S403F Substitution - Missense 11:119278278-119278278 + PD10897a COSM5945224 c.2584G>A p.E862K Substitution - Missense 11:119299644-119299644 + 1234389 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + TCGA-D1-A163-01 COSM923813 c.1287C>T p.I429I Substitution - coding silent 11:119278569-119278569 + TCGA-D9-A1JW-06 COSM3444159 c.1250C>A p.P417H Substitution - Missense 11:119278532-119278532 + 1773519 COSM330630 c.? p.Y371H Substitution - Missense KYSE-180 COSM2106773 c.641C>T p.P214L Substitution - Missense 11:119273918-119273918 + CHC1055T COSM3666862 c.36G>T p.G12G Substitution - coding silent 11:119206453-119206453 + HCT15 COSM1676499 c.1208C>T p.S403F Substitution - Missense 11:119278278-119278278 + TCGA-AB-2914-03 COSM34063 c.1096-1G>C p.? Unknown 11:119278165-119278165 + AML_602 COSM1234989 c.1246T>A p.C416S Substitution - Missense 11:119278528-119278528 + 1773521 COSM330631 c.? p.F418L Substitution - Missense 1507673 COSM34058 c.1186T>C p.C396R Substitution - Missense 11:119278256-119278256 + 1325681 COSM41676 c.? p.? Unknown TCGA-AB-2978-03 COSM166484 c.2190G>A p.T730T Substitution - coding silent 11:119297420-119297420 + LUAD-S01315 COSM343953 c.650C>A p.S217Y Substitution - Missense 11:119273927-119273927 + S01366 COSM309873 c.2266G>T p.A756S Substitution - Missense 11:119298372-119298372 + TCGA-B5-A11N-01 COSM923812 c.965A>C p.K322T Substitution - Missense 11:119276092-119276092 + PD9310a COSM5945227 c.2661G>A p.M887I Substitution - Missense 11:119299721-119299721 + PD9220a COSM34078 c.1254C>A p.F418L Substitution - Missense 11:119278536-119278536 + 2228002 COSM34063 c.1096-1G>C p.? Unknown 11:119278165-119278165 + TCGA-AR-A24S-01 COSM1475109 c.293T>C p.I98T Substitution - Missense 11:119232545-119232545 + 1_RESISTANT COSM1721168 c.1364_1366delATG p.D460delD Deletion - In frame 11:119278646-119278648 + 2321342 COSM4775083 c.2297A>T p.E766V Substitution - Missense 11:119298403-119298403 + PD7098a COSM4384649 c.2101A>G p.M701V Substitution - Missense 11:119296982-119296982 + 1563417 COSM34065 c.1228-2A>G p.? Unknown 11:119278508-119278508 + 1507705 COSM87284 c.1202G>A p.C401Y Substitution - Missense 11:119278272-119278272 + BD124T COSM5492878 c.1288G>A p.V430M Substitution - Missense 11:119278570-119278570 + 1234383 COSM34171 c.1227+5G>A p.? Unknown 11:119278302-119278302 + 1776389 COSM405296 c.1096-78_1108>CAGTCTTCA p.? Unknown 11:119278166-119278178 + 1234397 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + TCGA-46-6026-01 COSM686897 c.1407G>A p.M469I Substitution - Missense 11:119278689-119278689 + TCGA-BR-7703-01 COSM4018514 c.1007+2T>C p.? Unknown 11:119276136-119276136 + 112140 COSM94012 c.958C>G p.H320D Substitution - Missense 11:119276085-119276085 + PD10972a COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + TCGA-B6-A0RE-01 COSM428540 c.561G>A p.A187A Substitution - coding silent 11:119271852-119271852 + 1573680 COSM132872 c.1169A>G p.D390G Substitution - Missense 11:119278239-119278239 + TCGA-AZ-4315-01 COSM923811 c.826G>A p.E276K Substitution - Missense 11:119274910-119274910 + 1234380 COSM34076 c.1249C>G p.P417A Substitution - Missense 11:119278531-119278531 + 1280849 COSM34118 c.? p.R420P Substitution - Missense 1234378 COSM34071 c.1127C>T p.S376F Substitution - Missense 11:119278197-119278197 + 1998593 COSM1666981 c.2030C>T p.A677V Substitution - Missense 11:119287940-119287940 + 1773527 COSM330636 c.? p.G397V Substitution - Missense 1998574 COSM36363 c.1202G>C p.C401S Substitution - Missense 11:119278272-119278272 + DM28 COSM5608011 c.2396C>T p.S799F Substitution - Missense 11:119298502-119298502 + S02120 COSM5673448 c.1022A>G p.D341G Substitution - Missense 11:119277771-119277771 + PD8030a COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + YUPROST COSM1704663 c.1196T>C p.L399P Substitution - Missense 11:119278266-119278266 + pfg043T COSM4760617 c.2445A>C p.E815D Substitution - Missense 11:119299505-119299505 + 1459345 COSM52922 c.1496G>T p.R499L Substitution - Missense 11:119285033-119285033 + 1773520 COSM34117 c.? p.R420Q Substitution - Missense TCGA-E2-A1LG-01 COSM1475110 c.1047G>A p.L349L Substitution - coding silent 11:119277796-119277796 + 1507710 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + 1317128 COSM41274 c.2542G>A p.A848T Substitution - Missense 11:119299602-119299602 + 1317126 COSM41275 c.2406G>A p.W802* Substitution - Nonsense 11:119298512-119298512 + PD6848a COSM4384631 c.562G>T p.E188* Substitution - Nonsense 11:119271853-119271853 + HDC90 COSM4637254 c.1477C>T p.L493F Substitution - Missense 11:119285014-119285014 + 1633279 COSM144247 c.2024C>G p.S675C Substitution - Missense 11:119287934-119287934 + 1773522 COSM49102 c.? p.L380P Substitution - Missense 1751615 COSM307362 c.1101_1102insCAA p.Q367_Y368insQ Insertion - In frame 11:119278171-119278172 + 1998633 COSM34060 c.1222T>C p.W408R Substitution - Missense 11:119278292-119278292 + SCA37 COSM248733 c.592A>C p.T198P Substitution - Missense 11:119273869-119273869 + TCGA-AA-A010-01 COSM279593 c.1299G>A p.P433P Substitution - coding silent 11:119278581-119278581 + 37 COSM34058 c.1186T>C p.C396R Substitution - Missense 11:119278256-119278256 + BZ03 COSM1721168 c.1364_1366delATG p.D460delD Deletion - In frame 11:119278646-119278648 + LUAD-S01345 COSM396842 c.523C>T p.Q175* Substitution - Nonsense 11:119271814-119271814 + 1695990 COSM249797 c.1259G>C p.R420P Substitution - Missense 11:119278541-119278541 + TARGET-30-PAMDAL-01A-01W COSM1283936 c.560C>T p.A187V Substitution - Missense 11:119271851-119271851 + 2080287 COSM1724993 c.1246T>C p.C416R Substitution - Missense 11:119278528-119278528 + PD6876a COSM4384632 c.770A>G p.N257S Substitution - Missense 11:119274854-119274854 + HD-0180 COSM49098 c.? p.Y368* Substitution - Nonsense 1234386 COSM34079 c.1384C>T p.R462* Substitution - Nonsense 11:119278666-119278666 + TCGA-AG-A016-01 COSM290107 c.1188T>C p.C396C Substitution - coding silent 11:119278258-119278258 + PD9376a COSM5945225 c.2600A>G p.Q867R Substitution - Missense 11:119299660-119299660 + 2521260 COSM5891434 c.1941+2T>G p.? Unknown 11:119285568-119285568 + 1234400 COSM34074 c.1186T>G p.C396G Substitution - Missense 11:119278256-119278256 + RK109_C01 COSM1627828 c.1612delA p.T538fs*77 Deletion - Frameshift 11:119285237-119285237 + 2217108 COSM4169428 c.? p.F418I Substitution - Missense PD8385a COSM5945219 c.1210T>A p.C404S Substitution - Missense 11:119278280-119278280 + 1279568 COSM34143 c.1096_1227del132 p.Q367_E410del44 Deletion - In frame 11:119278166-119278297 + 1276023 COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + 2321304 COSM4774929 c.595A>G p.I199V Substitution - Missense 11:119273872-119273872 + PCSI_0083_Pa_P COSM132872 c.1169A>G p.D390G Substitution - Missense 11:119278239-119278239 + BRC7 COSM5027500 c.1054T>G p.L352V Substitution - Missense 11:119277803-119277803 + 44 COSM34066 c.1151G>A p.C384Y Substitution - Missense 11:119278221-119278221 + 1857609 COSM1169418 c.? p.C404Y Substitution - Missense 1275874 COSM34053 c.1111T>G p.Y371D Substitution - Missense 11:119278181-119278181 + 1998596 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + PD7387a COSM4384636 c.1148T>C p.I383T Substitution - Missense 11:119278218-119278218 + 1507709 COSM34058 c.1186T>C p.C396R Substitution - Missense 11:119278256-119278256 + PD8393a COSM5945218 c.1196T>A p.L399H Substitution - Missense 11:119278266-119278266 + GCT88 COSM5749966 c.1129A>G p.T377A Substitution - Missense 11:119278199-119278199 + 1998624 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + 11 COSM34055 c.1139T>C p.L380P Substitution - Missense 11:119278209-119278209 + PD8456a COSM34058 c.1186T>C p.C396R Substitution - Missense 11:119278256-119278256 + 1610763 COSM133827 c.1248T>G p.C416W Substitution - Missense 11:119278530-119278530 + Gp2D COSM4626754 c.116A>G p.H39R Substitution - Missense 11:119206533-119206533 + 1773523 COSM49099 c.? p.C381R Substitution - Missense 82 COSM250078 c.?_?del? p.? Unknown sysucc-274T COSM5475470 c.287G>A p.R96H Substitution - Missense 11:119232539-119232539 + 40 COSM34067 c.1187G>A p.C396Y Substitution - Missense 11:119278257-119278257 + 1280853 COSM34066 c.1151G>A p.C384Y Substitution - Missense 11:119278221-119278221 + TCGA-FS-A1ZA-06 COSM923813 c.1287C>T p.I429I Substitution - coding silent 11:119278569-119278569 + PD11153a COSM5945220 c.1228-1G>A p.? Unknown 11:119278509-119278509 + BD135T COSM5516594 c.2503C>T p.R835W Substitution - Missense 11:119299563-119299563 + 02 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + 19 COSM34077 c.1259G>A p.R420Q Substitution - Missense 11:119278541-119278541 + PD6500a COSM34068 c.1211G>A p.C404Y Substitution - Missense 11:119278281-119278281 + S10-24679-TP COSM4990134 c.1706C>T p.P569L Substitution - Missense 11:119285331-119285331 + CSCC-31-T COSM4479066 c.2291C>T p.P764L Substitution - Missense 11:119298397-119298397 + LUAD-FH5PJ COSM133826 c.1243G>A p.G415S Substitution - Missense 11:119278525-119278525 + MEL-JWCI-WGS-6 COSM1167626 c.1082_1095+9del23 p.? Unknown 11:119277831-119277853 + 84 COSM250077 c.964_1380del417 p.K322_D460del Unknown 1317075 COSM41270 c.280C>T p.H94Y Substitution - Missense 11:119232532-119232532 + Pat_36_B COSM5837983 c.1429A>G p.K477E Substitution - Missense 11:119278711-119278711 + TCGA-DK-A3IT-01 COSM1297722 c.2150C>T p.S717L Substitution - Missense 11:119297031-119297031 + 1330206 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 + 1275870 COSM34052 c.1111T>C p.Y371H Substitution - Missense 11:119278181-119278181 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.504096 11q23.3 165360

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - Frameshift p.T538Hfs*77 c.1611delC 11 119155946 HC A G 3-UTRSNV . c.2718+856A>G 11 119171344 HC A G Missense p.I292V c.874A>G 11 119146711 HC A G Missense p.Q367R c.1100A>G 11 119148880 AML A G Missense p.Y731C c.2192A>G 11 119168132 SCLC A G Synonymous p.E111E c.333A>G 11 119103295 LUSC A - IntronicDeletion . c.747+16delA 11 119144745 STAD A T Missense p.D459V c.1376A>T 11 119149368 UCEC A T Missense p.Q367H c.1101A>T 11 119148881 CM A T Synonymous p.I199I c.597A>T 11 119144584 LUAD CAAA - IntronicDeletion . c.1096-5_1096-2delCAAA 11 119148871 CM C A Missense p.P417H c.1250C>A 11 119149242 CM C A Missense p.P764H c.2291C>A 11 119169107 STAD C A Synonymous p.L467L c.1401C>A 11 119149393 LUSC C A Synonymous p.R540R c.1618C>A 11 119155953 LUSC C A Synonymous p.V813V c.2439C>A 11 119170209 BRCA CC TT Missense p.A756V c.2267_2268delinsTT 11 119169083 CM CC TT Missense p.P481L c.1441_1442delinsTT 11 119155688 CM C T Missense p.A187V c.560C>T 11 119142561 NB C T Missense p.A719V c.2156C>T 11 119168096 RCCC C T Missense p.A850V c.2549C>T 11 119170319 UCEC C T Missense p.A877V c.2630C>T 11 119170400 CM C T Missense p.P201S c.601C>T 11 119144588 CM C T Missense p.P510S c.1528C>T 11 119155775 CM C T Missense p.P546L c.1637C>T 11 119155972 UCEC C T Missense p.R280W c.838C>T 11 119145632 LUAD C T Missense p.S253F c.758C>T 11 119145552 CM C T Missense p.S675F c.2024C>T 11 119158644 CM C T Missense p.S717L c.2150C>T 11 119167741 BLCA C T Nonsense p.Q249* c.745C>T 11 119144732 CM C T Nonsense p.Q867* c.2599C>T 11 119170369 BLCA C T Nonsense p.R420* c.1258C>T 11 119149250 UCEC C T Nonsense p.R499* c.1495C>T 11 119155742 STAD C T Synonymous p.F284F c.852C>T 11 119145646 CM C T Synonymous p.F468F c.1404C>T 11 119149396 CM C T Synonymous p.I429I c.1287C>T 11 119149279 CM C T Synonymous p.I429I c.1287C>T 11 119149279 UCEC C T Synonymous p.I84I c.252C>T 11 119103214 HNSC C T Synonymous p.P662P c.1986C>T 11 119158606 CM C T Synonymous p.T852T c.2556C>T 11 119170326 STAD G A Missense p.A757T c.2269G>A 11 119169085 LUAD G A Missense p.E765K c.2293G>A 11 119169109 HNSC G A Missense p.G110E c.329G>A 11 119103291 CM G A Missense p.G868E c.2603G>A 11 119170373 UCEC G A Missense p.M469I c.1407G>A 11 119149399 LUSC G A Missense p.R612K c.1835G>A 11 119156170 MM G A Missense p.S512N c.1535G>A 11 119155782 HNSC G A Synonymous p.A187A c.561G>A 11 119142562 BRCA G A Synonymous p.L349L c.1047G>A 11 119148506 BRCA G A Synonymous p.L87L c.261G>A 11 119103223 LUSC G A Synonymous p.Q93Q c.279G>A 11 119103241 UCEC G A Synonymous p.T730T c.2190G>A 11 119168130 AML G A Synonymous p.V67V c.201G>A 11 119103163 CM G C Missense p.A208P c.622G>C 11 119144609 HNSC G C Missense p.D501H c.1501G>C 11 119155748 BRCA G C Missense p.R540P c.1619G>C 11 119155954 BRCA G C SpliceAcceptorSNV . c.1096-1G>C 11 119148875 AML G T Missense p.A756S c.2266G>T 11 119169082 SCLC G T Nonsense p.E768* c.2302G>T 11 119169118 LUAD G T Nonsense p.E894* c.2680G>T 11 119170450 LUAD G T Synonymous p.V66V c.198G>T 11 119103160 BRCA T A Missense p.L281H c.842T>A 11 119145636 BRCA TCAAAGTGACCCAGGTGAGTTTT - SpliceDonorDeletion . c.1082_1095+9delTCAAAGTGACCCAGGTGAGTTTT 11 119148541 CM T C Missense p.C384R c.1150T>C 11 119148930 CM T C Missense p.F133L c.397T>C 11 119103359 BRCA T C Missense p.I98T c.293T>C 11 119103255 BRCA T C Synonymous p.C396C c.1188T>C 11 119148968 COREAD T C Synonymous p.D712D c.2136T>C 11 119167727 SCLC T C Synonymous p.I181I c.543T>C 11 119142544 CM T C Synonymous p.L338L c.1012T>C 11 119148471 OV T G Missense p.C384W c.1152T>G 11 119148932 GBM T G Missense p.F418V c.1252T>G 11 119149244 CM T G Missense p.L352V c.1054T>G 11 119148513 BRCA TT - Frameshift p.I285Sfs*26 c.853_854delAT 11 119145647 HC