Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 9 140069483 140069483 + Missense_Mutation SNP C C T TCGA-2F-A9KR-01A-11D-A38G-08 TCGA-2F-A9KR-10A-01D-A38J-08 g.chr9:140069483C>T c.2380G>A c.(2380-2382)Gag>Aag p.E794K BLCA 9 140069557 140069557 + Missense_Mutation SNP G G A TCGA-DK-AA6L-01A-11D-A391-08 TCGA-DK-AA6L-10A-01D-A394-08 g.chr9:140069557G>A c.2306C>T c.(2305-2307)tCa>tTa p.S769L BLCA 9 140069557 140069557 + Missense_Mutation SNP G G A TCGA-FD-A3SN-01A-12D-A22Z-08 TCGA-FD-A3SN-10A-01D-A22Z-08 g.chr9:140069557G>A c.2306C>T c.(2305-2307)tCa>tTa p.S769L BLCA 9 140069732 140069732 + Missense_Mutation SNP G G C TCGA-DK-AA6L-01A-11D-A391-08 TCGA-DK-AA6L-10A-01D-A394-08 g.chr9:140069732G>C c.2213C>G c.(2212-2214)tCc>tGc p.S738C BLCA 9 140070222 140070222 + Missense_Mutation SNP C C T TCGA-ZF-AA4R-01A-11D-A38G-08 TCGA-ZF-AA4R-10A-01D-A38J-08 g.chr9:140070222C>T c.1958G>A c.(1957-1959)cGc>cAc p.R653H BLCA 9 140074639 140074639 + Missense_Mutation SNP C C G TCGA-K4-A3WU-01B-11D-A23M-08 TCGA-K4-A3WU-10A-01D-A23K-08 g.chr9:140074639C>G c.1884G>C c.(1882-1884)caG>caC p.Q628H BLCA 9 140074760 140074760 + Missense_Mutation SNP G G A TCGA-ZF-A9RD-01A-11D-A42E-08 TCGA-ZF-A9RD-10A-01D-A42H-08 g.chr9:140074760G>A c.1763C>T c.(1762-1764)cCg>cTg p.P588L BLCA 9 140075251 140075251 + Silent SNP G G A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr9:140075251G>A c.1599C>T c.(1597-1599)ttC>ttT p.F533F BLCA 9 140076196 140076196 + Missense_Mutation SNP C C T TCGA-K4-A3WU-01B-11D-A23M-08 TCGA-K4-A3WU-10A-01D-A23K-08 g.chr9:140076196C>T c.1405G>A c.(1405-1407)Gac>Aac p.D469N BLCA 9 140076208 140076208 + Missense_Mutation SNP C C G TCGA-XF-AAMX-01A-11D-A42E-08 TCGA-XF-AAMX-10A-01D-A42H-08 g.chr9:140076208C>G c.1393G>C c.(1393-1395)Gag>Cag p.E465Q BLCA 9 140080711 140080711 + Missense_Mutation SNP C C T TCGA-FD-A62O-01A-11D-A30E-08 TCGA-FD-A62O-10A-01D-A30H-08 g.chr9:140080711C>T c.838G>A c.(838-840)Gag>Aag p.E280K BLCA 9 140080789 140080789 + Missense_Mutation SNP C C T TCGA-XF-AAMX-01A-11D-A42E-08 TCGA-XF-AAMX-10A-01D-A42H-08 g.chr9:140080789C>T c.760G>A c.(760-762)Gag>Aag p.E254K BLCA 9 140082285 140082285 + Missense_Mutation SNP C C T TCGA-XF-AAMX-01A-11D-A42E-08 TCGA-XF-AAMX-10A-01D-A42H-08 g.chr9:140082285C>T c.388G>A c.(388-390)Gag>Aag p.E130K BLCA 9 140082487 140082487 + Silent SNP C C A TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr9:140082487C>A c.186G>T c.(184-186)ctG>ctT p.L62L BRCA 9 140082004 140082004 + Silent SNP C C T TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chr9:140082004C>T c.669G>A c.(667-669)ggG>ggA p.G223G CESC 9 140069483 140069483 + Missense_Mutation SNP C C T TCGA-LP-A7HU-01A-11D-A33O-09 TCGA-LP-A7HU-10A-01D-A33O-09 g.chr9:140069483C>T c.2380G>A c.(2380-2382)Gag>Aag p.E794K CESC 9 140082173 140082173 + Missense_Mutation SNP C C T TCGA-IR-A3LH-01A-21D-A20U-09 TCGA-IR-A3LH-10A-01D-A20U-09 g.chr9:140082173C>T c.500G>A c.(499-501)aGa>aAa p.R167K CESC 9 140082187 140082187 + Missense_Mutation SNP G G C TCGA-LP-A5U2-01A-11D-A28B-09 TCGA-LP-A5U2-10A-01D-A28E-09 g.chr9:140082187G>C c.486C>G c.(484-486)ttC>ttG p.F162L CESC 9 140082274 140082274 + Silent SNP C C T TCGA-C5-A7CO-01A-11D-A351-09 TCGA-C5-A7CO-10A-01D-A351-09 g.chr9:140082274C>T c.399G>A c.(397-399)gaG>gaA p.E133E CESC 9 140082506 140082506 + Missense_Mutation SNP C C T TCGA-EA-A5FO-01A-21D-A28B-09 TCGA-EA-A5FO-10A-01D-A28E-09 g.chr9:140082506C>T c.167G>A c.(166-168)cGg>cAg p.R56Q COAD 9 140069728 140069728 + Silent SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr9:140069728G>A c.2217C>T c.(2215-2217)ggC>ggT p.G739G COAD 9 140074650 140074650 + Missense_Mutation SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr9:140074650T>C c.1873A>G c.(1873-1875)Aag>Gag p.K625E COAD 9 140074650 140074650 + Missense_Mutation SNP T T C TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr9:140074650T>C c.1873A>G c.(1873-1875)Aag>Gag p.K625E COAD 9 140075363 140075363 + Missense_Mutation SNP C C T TCGA-AA-A03F-01A-11W-A096-10 TCGA-AA-A03F-11A-12W-A096-10 g.chr9:140075363C>T c.1487G>A c.(1486-1488)cGg>cAg p.R496Q COAD 9 140076156 140076156 + Missense_Mutation SNP G G A TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:140076156G>A c.1445C>T c.(1444-1446)cCg>cTg p.P482L COAD 9 140077641 140077641 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:140077641G>T c.1222C>A c.(1222-1224)Cgc>Agc p.R408S COAD 9 140079405 140079405 + Silent SNP G G A TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr9:140079405G>A c.1008C>T c.(1006-1008)taC>taT p.Y336Y COAD 9 140082429 140082429 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr9:140082429C>T c.244G>A c.(244-246)Gat>Aat p.D82N COADREAD 9 140069728 140069728 + Silent SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr9:140069728G>A c.2217C>T c.(2215-2217)ggC>ggT p.G739G COADREAD 9 140074650 140074650 + Missense_Mutation SNP T T C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr9:140074650T>C c.1873A>G c.(1873-1875)Aag>Gag p.K625E COADREAD 9 140074650 140074650 + Missense_Mutation SNP T T C TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr9:140074650T>C c.1873A>G c.(1873-1875)Aag>Gag p.K625E COADREAD 9 140075363 140075363 + Missense_Mutation SNP C C T TCGA-AA-A03F-01A-11W-A096-10 TCGA-AA-A03F-11A-12W-A096-10 g.chr9:140075363C>T c.1487G>A c.(1486-1488)cGg>cAg p.R496Q COADREAD 9 140076156 140076156 + Missense_Mutation SNP G G A TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:140076156G>A c.1445C>T c.(1444-1446)cCg>cTg p.P482L COADREAD 9 140077641 140077641 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:140077641G>T c.1222C>A c.(1222-1224)Cgc>Agc p.R408S COADREAD 9 140079405 140079405 + Silent SNP G G A TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr9:140079405G>A c.1008C>T c.(1006-1008)taC>taT p.Y336Y COADREAD 9 140082199 140082199 + Silent SNP G G A TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr9:140082199G>A c.474C>T c.(472-474)cgC>cgT p.R158R COADREAD 9 140082429 140082429 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr9:140082429C>T c.244G>A c.(244-246)Gat>Aat p.D82N ESCA 9 140074823 140074823 + Missense_Mutation SNP G G A TCGA-2H-A9GN-01A-11D-A37C-09 TCGA-2H-A9GN-11A-11D-A37F-09 g.chr9:140074823G>A c.1700C>T c.(1699-1701)tCc>tTc p.S567F ESCA 9 140075323 140075323 + Silent SNP G G A TCGA-V5-AASX-01A-11D-A387-09 TCGA-V5-AASX-10A-01D-A38A-09 g.chr9:140075323G>A c.1527C>T c.(1525-1527)taC>taT p.Y509Y ESCA 9 140082363 140082363 + Missense_Mutation SNP C C G TCGA-Z6-AAPN-01A-11D-A403-09 TCGA-Z6-AAPN-10A-01D-A403-09 g.chr9:140082363C>G c.310G>C c.(310-312)Gag>Cag p.E104Q GBM 9 140074735 140074735 + Silent SNP C C A TCGA-06-2569-01A-01D-1494-08 TCGA-06-2569-10A-01D-1494-08 g.chr9:140074735C>A c.1788G>T c.(1786-1788)ctG>ctT p.L596L GBMLGG 9 140074735 140074735 + Silent SNP C C A TCGA-06-2569-01A-01D-1494-08 TCGA-06-2569-10A-01D-1494-08 g.chr9:140074735C>A c.1788G>T c.(1786-1788)ctG>ctT p.L596L GBMLGG 9 140074825 140074825 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:140074825G>A c.1698C>T c.(1696-1698)gaC>gaT p.D566D GBMLGG 9 140079392 140079392 + Missense_Mutation SNP T T C TCGA-E1-5307-01A-01D-1893-08 TCGA-E1-5307-10A-01D-1893-08 g.chr9:140079392T>C c.1021A>G c.(1021-1023)Atc>Gtc p.I341V GBMLGG 9 140082371 140082371 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:140082371G>T c.302C>A c.(301-303)tCt>tAt p.S101Y HNSC 9 140078134 140078134 + Silent SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr9:140078134G>A c.1158C>T c.(1156-1158)ctC>ctT p.L386L HNSC 9 140082436 140082436 + Silent SNP C C T TCGA-P3-A6T5-01A-11D-A34J-08 TCGA-P3-A6T5-10A-01D-A34M-08 g.chr9:140082436C>T c.237G>A c.(235-237)ctG>ctA p.L79L KICH 9 140074818 140074818 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr9:140074818G>A c.1705C>T c.(1705-1707)Cgc>Tgc p.R569C KIPAN 9 140074818 140074818 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr9:140074818G>A c.1705C>T c.(1705-1707)Cgc>Tgc p.R569C KIPAN 9 140075307 140075307 + Missense_Mutation SNP A A T TCGA-CZ-4853-01A-01D-1429-08 TCGA-CZ-4853-11A-01D-1429-08 g.chr9:140075307A>T c.1543T>A c.(1543-1545)Ttc>Atc p.F515I KIRC 9 140075307 140075307 + Missense_Mutation SNP A A T TCGA-CZ-4853-01A-01D-1429-08 TCGA-CZ-4853-11A-01D-1429-08 g.chr9:140075307A>T c.1543T>A c.(1543-1545)Ttc>Atc p.F515I LGG 9 140074825 140074825 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:140074825G>A c.1698C>T c.(1696-1698)gaC>gaT p.D566D LGG 9 140079392 140079392 + Missense_Mutation SNP T T C TCGA-E1-5307-01A-01D-1893-08 TCGA-E1-5307-10A-01D-1893-08 g.chr9:140079392T>C c.1021A>G c.(1021-1023)Atc>Gtc p.I341V LGG 9 140082371 140082371 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:140082371G>T c.302C>A c.(301-303)tCt>tAt p.S101Y LIHC 9 140075299 140075299 + Silent SNP A A G TCGA-DD-AAE9-01A-11D-A40R-10 TCGA-DD-AAE9-10A-01D-A40U-10 g.chr9:140075299A>G c.1551T>C c.(1549-1551)aaT>aaC p.N517N LIHC 9 140075345 140075345 + Missense_Mutation SNP A A C TCGA-DD-AAE9-01A-11D-A40R-10 TCGA-DD-AAE9-10A-01D-A40U-10 g.chr9:140075345A>C c.1505T>G c.(1504-1506)aTc>aGc p.I502S LIHC 9 140077646 140077646 + Missense_Mutation SNP G G A TCGA-DD-AACA-01A-11D-A40R-10 TCGA-DD-AACA-10A-01D-A40U-10 g.chr9:140077646G>A c.1217C>T c.(1216-1218)gCg>gTg p.A406V LIHC 9 140077667 140077667 + Missense_Mutation SNP A A G TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr9:140077667A>G c.1196T>C c.(1195-1197)cTc>cCc p.L399P LIHC 9 140077677 140077677 + Missense_Mutation SNP T T A TCGA-DD-AACV-01A-11D-A40R-10 TCGA-DD-AACV-10A-01D-A40U-10 g.chr9:140077677T>A c.1186A>T c.(1186-1188)Atc>Ttc p.I396F LIHC 9 140082090 140082090 + Missense_Mutation SNP T T C TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr9:140082090T>C c.583A>G c.(583-585)Aca>Gca p.T195A LIHC 9 140082406 140082406 + Silent SNP A A G TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr9:140082406A>G c.267T>C c.(265-267)ccT>ccC p.P89P LUAD 9 140075363 140075363 + Missense_Mutation SNP C C A TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr9:140075363C>A c.1487G>T c.(1486-1488)cGg>cTg p.R496L LUAD 9 140075364 140075364 + Missense_Mutation SNP G G A TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr9:140075364G>A c.1486C>T c.(1486-1488)Cgg>Tgg p.R496W LUAD 9 140077638 140077638 + Missense_Mutation SNP C C A TCGA-55-8616-01A-11D-2393-08 TCGA-55-8616-10A-01D-2393-08 g.chr9:140077638C>A c.1225G>T c.(1225-1227)Gtg>Ttg p.V409L LUAD 9 140077680 140077680 + Missense_Mutation SNP C C G TCGA-55-7726-01A-11D-2167-08 TCGA-55-7726-10A-01D-2167-08 g.chr9:140077680C>G c.1183G>C c.(1183-1185)Gac>Cac p.D395H LUAD 9 140079461 140079461 + Missense_Mutation SNP C C A TCGA-55-8085-01A-11D-2238-08 TCGA-55-8085-10A-01D-2238-08 g.chr9:140079461C>A c.952G>T c.(952-954)Ggc>Tgc p.G318C LUAD 9 140080784 140080784 + Silent SNP C C A TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr9:140080784C>A c.765G>T c.(763-765)cgG>cgT p.R255R LUAD 9 140082025 140082025 + Silent SNP C C T TCGA-MP-A4TK-01A-11D-A24P-08 TCGA-MP-A4TK-10A-01D-A24P-08 g.chr9:140082025C>T c.648G>A c.(646-648)ctG>ctA p.L216L LUSC 9 140076197 140076197 + Silent SNP C C T TCGA-66-2794-01A-01D-1267-08 TCGA-66-2794-11A-01D-1267-08 g.chr9:140076197C>T c.1404G>A c.(1402-1404)caG>caA p.Q468Q OV 9 140074648 140074648 + Missense_Mutation SNP C C A TCGA-25-2401-01A-01W-0799-08 TCGA-25-2401-10A-01W-0799-08 g.chr9:140074648C>A c.1875G>T c.(1873-1875)aaG>aaT p.K625N OV 9 140081941 140081941 + Silent SNP G G A TCGA-36-2532-01A-01D-1526-09 TCGA-36-2532-10A-01D-1526-09 g.chr9:140081941G>A c.732C>T c.(730-732)agC>agT p.S244S PAAD 9 140069809 140069809 + Silent SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:140069809G>T c.2136C>A c.(2134-2136)acC>acA p.T712T PAAD 9 140069920 140069920 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:140069920G>T c.2025C>A c.(2023-2025)agC>agA p.S675R PAAD 9 140080689 140080689 + Missense_Mutation SNP C C T TCGA-2J-AABR-01A-11D-A40W-08 TCGA-2J-AABR-10A-01D-A40W-08 g.chr9:140080689C>T c.860G>A c.(859-861)cGt>cAt p.R287H PAAD 9 140082017 140082017 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:140082017G>A c.656C>T c.(655-657)cCg>cTg p.P219L PAAD 9 140082360 140082360 + Missense_Mutation SNP G G C TCGA-LB-A8F3-01A-11D-A36O-08 TCGA-LB-A8F3-10A-01D-A367-08 g.chr9:140082360G>C c.313C>G c.(313-315)Ccc>Gcc p.P105A PRAD 9 140070252 140070252 + Missense_Mutation SNP A A G TCGA-HC-8262-01A-11D-2260-08 TCGA-HC-8262-10A-01D-2260-08 g.chr9:140070252A>G c.1928T>C c.(1927-1929)cTg>cCg p.L643P PRAD 9 140074781 140074781 + Missense_Mutation SNP C C T TCGA-2A-A8W1-01A-11D-A377-08 TCGA-2A-A8W1-10A-01D-A37A-08 g.chr9:140074781C>T c.1742G>A c.(1741-1743)cGg>cAg p.R581Q PRAD 9 140074793 140074793 + Missense_Mutation SNP T T C TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:140074793T>C c.1730A>G c.(1729-1731)gAg>gGg p.E577G PRAD 9 140082419 140082419 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:140082419G>A c.254C>T c.(253-255)gCc>gTc p.A85V READ 9 140082199 140082199 + Silent SNP G G A TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr9:140082199G>A c.474C>T c.(472-474)cgC>cgT p.R158R SARC 9 140070253 140070253 + Silent SNP G G A TCGA-DX-A3UE-01A-11D-A307-09 TCGA-DX-A3UE-10A-01D-A307-09 g.chr9:140070253G>A c.1927C>T c.(1927-1929)Ctg>Ttg p.L643L SARC 9 140075277 140075277 + Missense_Mutation SNP C C T TCGA-WK-A8XT-01A-11D-A37C-09 TCGA-WK-A8XT-10A-01D-A37F-09 g.chr9:140075277C>T c.1573G>A c.(1573-1575)Gac>Aac p.D525N SARC 9 140080800 140080800 + Missense_Mutation SNP A A C TCGA-3B-A9HZ-01A-11D-A38Z-09 TCGA-3B-A9HZ-10A-01D-A38Z-09 g.chr9:140080800A>C c.749T>G c.(748-750)cTc>cGc p.L250R SKCM 9 140074636 140074636 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr9:140074636G>A c.1887C>T c.(1885-1887)ctC>ctT p.L629L SKCM 9 140074659 140074659 + Missense_Mutation SNP A A G TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr9:140074659A>G c.1864T>C c.(1864-1866)Tac>Cac p.Y622H SKCM 9 140075310 140075310 + Missense_Mutation SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr9:140075310G>A c.1540C>T c.(1540-1542)Ctc>Ttc p.L514F SKCM 9 140075311 140075311 + Silent SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr9:140075311G>A c.1539C>T c.(1537-1539)gaC>gaT p.D513D SKCM 9 140075357 140075357 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr9:140075357G>A c.1493C>T c.(1492-1494)tCa>tTa p.S498L SKCM 9 140077625 140077625 + Missense_Mutation SNP G G A TCGA-D3-A5GU-06A-11D-A27K-08 TCGA-D3-A5GU-10A-01D-A27N-08 g.chr9:140077625G>A c.1238C>T c.(1237-1239)tCc>tTc p.S413F SKCM 9 140079372 140079372 + Silent SNP G G A TCGA-ER-A19D-06A-11D-A197-08 TCGA-ER-A19D-10A-01D-A199-08 g.chr9:140079372G>A c.1041C>T c.(1039-1041)atC>atT p.I347I SKCM 9 140079372 140079372 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:140079372G>A c.1041C>T c.(1039-1041)atC>atT p.I347I SKCM 9 140079394 140079394 + Missense_Mutation SNP C C T TCGA-EE-A2GP-06A-11D-A197-08 TCGA-EE-A2GP-10A-01D-A199-08 g.chr9:140079394C>T c.1019G>A c.(1018-1020)cGc>cAc p.R340H SKCM 9 140081953 140081953 + Silent SNP G G A TCGA-GN-A4U3-06A-11D-A32N-08 TCGA-GN-A4U3-10F-01D-A32N-08 g.chr9:140081953G>A c.720C>T c.(718-720)ttC>ttT p.F240F SKCM 9 140082095 140082095 + Missense_Mutation SNP C C T TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr9:140082095C>T c.578G>A c.(577-579)gGg>gAg p.G193E SKCM 9 140082507 140082507 + Missense_Mutation SNP G G A TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr9:140082507G>A c.166C>T c.(166-168)Cgg>Tgg p.R56W BLCA 19 1453084 1453084 + Silent SNP G G A TCGA-CU-A5W6-01A-11D-A289-08 TCGA-CU-A5W6-10A-01D-A289-08 g.chr19:1453084G>A c.84G>A c.(82-84)gaG>gaA p.E28E BLCA 19 1453566 1453566 + Silent SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr19:1453566G>A c.369G>A c.(367-369)ctG>ctA p.L123L BLCA 19 1455193 1455193 + Silent SNP C C G TCGA-KQ-A41S-01A-12D-A339-08 TCGA-KQ-A41S-10C-01D-A339-08 g.chr19:1455193C>G c.459C>G c.(457-459)ctC>ctG p.L153L BLCA 19 1455391 1455391 + Silent SNP G G A TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr19:1455391G>A c.531G>A c.(529-531)tcG>tcA p.S177S BLCA 19 1456894 1456894 + Missense_Mutation SNP G G A TCGA-G2-A2EJ-01A-11D-A17V-08 TCGA-G2-A2EJ-10A-01D-A17V-08 g.chr19:1456894G>A c.859G>A c.(859-861)Gac>Aac p.D287N BLCA 19 1461114 1461114 + Missense_Mutation SNP G G T TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr19:1461114G>T c.1600G>T c.(1600-1602)Gtg>Ttg p.V534L BLCA 19 1461973 1461973 + Silent SNP G G A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr19:1461973G>A c.1650G>A c.(1648-1650)ctG>ctA p.L550L BLCA 19 1462069 1462069 + Silent SNP G G T TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr19:1462069G>T c.1746G>T c.(1744-1746)gtG>gtT p.V582V BLCA 19 1462114 1462114 + Silent SNP C C T TCGA-FD-A3N5-01A-11D-A21A-08 TCGA-FD-A3N5-10A-01D-A21A-08 g.chr19:1462114C>T c.1791C>T c.(1789-1791)atC>atT p.I597I BLCA 19 1466155 1466155 + Missense_Mutation SNP C C T TCGA-UY-A78L-01A-12D-A339-08 TCGA-UY-A78L-10A-01D-A339-08 g.chr19:1466155C>T c.2855C>T c.(2854-2856)tCg>tTg p.S952L BLCA 19 1466484 1466484 + Missense_Mutation SNP G G C TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr19:1466484G>C c.3184G>C c.(3184-3186)Gag>Cag p.E1062Q BLCA 19 1466922 1466922 + Missense_Mutation SNP C C G TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr19:1466922C>G c.3622C>G c.(3622-3624)Ccc>Gcc p.P1208A BLCA 19 1467046 1467046 + Missense_Mutation SNP G G A TCGA-4Z-AA7Y-01A-11D-A391-08 TCGA-4Z-AA7Y-10A-01D-A394-08 g.chr19:1467046G>A c.3746G>A c.(3745-3747)cGc>cAc p.R1249H BRCA 19 1456366 1456366 + Missense_Mutation SNP A A G TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr19:1456366A>G c.779A>G c.(778-780)cAc>cGc p.H260R BRCA 19 1460266 1460266 + Missense_Mutation SNP C C A TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr19:1460266C>A c.1390C>A c.(1390-1392)Cgc>Agc p.R464S BRCA 19 1465771 1465771 + Missense_Mutation SNP G G A TCGA-E2-A1IN-01A-11D-A13L-09 TCGA-E2-A1IN-10A-01D-A188-09 g.chr19:1465771G>A c.2471G>A c.(2470-2472)cGa>cAa p.R824Q BRCA 19 1465789 1465789 + Missense_Mutation SNP A A C TCGA-B6-A2IU-01A-32D-A19T-09 TCGA-B6-A2IU-10A-01D-A18P-09 g.chr19:1465789A>C c.2489A>C c.(2488-2490)gAg>gCg p.E830A BRCA 19 1468432 1468432 + Nonsense_Mutation SNP C C A TCGA-E2-A2P6-01A-11D-A19Y-09 TCGA-E2-A2P6-10B-01D-A19Y-09 g.chr19:1468432C>A c.5132C>A c.(5131-5133)tCg>tAg p.S1711* CESC 19 1456386 1456386 + Nonsense_Mutation SNP C C T TCGA-EK-A2RA-01A-11D-A18J-09 TCGA-EK-A2RA-10A-01D-A18J-09 g.chr19:1456386C>T c.799C>T c.(799-801)Cag>Tag p.Q267* CESC 19 1462028 1462028 + Missense_Mutation SNP G G A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr19:1462028G>A c.1705G>A c.(1705-1707)Gcg>Acg p.A569T CESC 19 1465202 1465202 + Silent SNP G G C TCGA-IR-A3LI-01A-11D-A20U-09 TCGA-IR-A3LI-10A-01D-A20U-09 g.chr19:1465202G>C c.1902G>C c.(1900-1902)ctG>ctC p.L634L COAD 19 1457967 1457967 + Missense_Mutation SNP C C T TCGA-AA-3941-01A-01W-0995-10 TCGA-AA-3941-10A-01W-0995-10 g.chr19:1457967C>T c.1211C>T c.(1210-1212)cCg>cTg p.P404L COAD 19 1460264 1460264 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr19:1460264G>A c.1388G>A c.(1387-1389)cGc>cAc p.R463H COAD 19 1466939 1466939 + Silent SNP G G A TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr19:1466939G>A c.3639G>A c.(3637-3639)acG>acA p.T1213T COAD 19 1466939 1466939 + Silent SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr19:1466939G>A c.3639G>A c.(3637-3639)acG>acA p.T1213T COAD 19 1466993 1466993 + Silent SNP G G A TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr19:1466993G>A c.3693G>A c.(3691-3693)ctG>ctA p.L1231L COAD 19 1468532 1468532 + Missense_Mutation SNP A A C TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr19:1468532A>C c.5232A>C c.(5230-5232)gaA>gaC p.E1744D COADREAD 19 1455453 1455453 + Missense_Mutation SNP T T C TCGA-AF-5654-01A-01D-1657-10 TCGA-AF-5654-10A-01D-1657-10 g.chr19:1455453T>C c.593T>C c.(592-594)aTg>aCg p.M198T COADREAD 19 1457967 1457967 + Missense_Mutation SNP C C T TCGA-AA-3941-01A-01W-0995-10 TCGA-AA-3941-10A-01W-0995-10 g.chr19:1457967C>T c.1211C>T c.(1210-1212)cCg>cTg p.P404L COADREAD 19 1460264 1460264 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr19:1460264G>A c.1388G>A c.(1387-1389)cGc>cAc p.R463H COADREAD 19 1462030 1462030 + Silent SNP G G A TCGA-AG-A00Y-01A-02W-A005-10 TCGA-AG-A00Y-10A-01W-A005-10 g.chr19:1462030G>A c.1707G>A c.(1705-1707)gcG>gcA p.A569A COADREAD 19 1466939 1466939 + Silent SNP G G A TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr19:1466939G>A c.3639G>A c.(3637-3639)acG>acA p.T1213T COADREAD 19 1466939 1466939 + Silent SNP G G A TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr19:1466939G>A c.3639G>A c.(3637-3639)acG>acA p.T1213T COADREAD 19 1466993 1466993 + Silent SNP G G A TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr19:1466993G>A c.3693G>A c.(3691-3693)ctG>ctA p.L1231L COADREAD 19 1468532 1468532 + Missense_Mutation SNP A A C TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr19:1468532A>C c.5232A>C c.(5230-5232)gaA>gaC p.E1744D DLBC 19 1469030 1469030 + Silent SNP A A G TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr19:1469030A>G c.5730A>G c.(5728-5730)aaA>aaG p.K1910K DLBC 19 1469078 1469078 + Silent SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr19:1469078G>A c.5778G>A c.(5776-5778)tcG>tcA p.S1926S ESCA 19 1456085 1456085 + Missense_Mutation SNP C C G TCGA-VR-A8EO-01A-11D-A36J-09 TCGA-VR-A8EO-10A-01D-A36M-09 g.chr19:1456085C>G c.650C>G c.(649-651)tCg>tGg p.S217W ESCA 19 1457140 1457140 + Missense_Mutation SNP C C G TCGA-JY-A93F-01A-21D-A37C-09 TCGA-JY-A93F-10A-01D-A37F-09 g.chr19:1457140C>G c.1105C>G c.(1105-1107)Cgc>Ggc p.R369G ESCA 19 1466955 1466955 + Missense_Mutation SNP G G A TCGA-L5-A8NE-01A-11D-A37C-09 TCGA-L5-A8NE-11A-11D-A37F-09 g.chr19:1466955G>A c.3655G>A c.(3655-3657)Gcg>Acg p.A1219T GBM 19 1465389 1465389 + Missense_Mutation SNP C C T TCGA-06-0650-01A-02D-1696-08 TCGA-06-0650-10A-01D-1696-08 g.chr19:1465389C>T c.2089C>T c.(2089-2091)Cat>Tat p.H697Y GBM 19 1466495 1466496 + Frame_Shift_Ins INS - - T TCGA-28-2514-01A-02D-1494-08 TCGA-28-2514-10A-01D-1494-08 g.chr19:1466495_1466496insT c.3195_3196insT c.(3196-3198)tcgfs p.S1066fs GBM 19 1468647 1468647 + Missense_Mutation SNP G G A TCGA-32-4208-01A-01D-1353-08 TCGA-32-4208-10A-01D-1353-08 g.chr19:1468647G>A c.5347G>A c.(5347-5349)Ggg>Agg p.G1783R GBMLGG 19 1462051 1462051 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:1462051C>T c.1728C>T c.(1726-1728)ggC>ggT p.G576G GBMLGG 19 1465389 1465389 + Missense_Mutation SNP C C T TCGA-06-0650-01A-02D-1696-08 TCGA-06-0650-10A-01D-1696-08 g.chr19:1465389C>T c.2089C>T c.(2089-2091)Cat>Tat p.H697Y GBMLGG 19 1466495 1466496 + Frame_Shift_Ins INS - - T TCGA-28-2514-01A-02D-1494-08 TCGA-28-2514-10A-01D-1494-08 g.chr19:1466495_1466496insT c.3195_3196insT c.(3196-3198)tcgfs p.S1066fs GBMLGG 19 1468647 1468647 + Missense_Mutation SNP G G A TCGA-32-4208-01A-01D-1353-08 TCGA-32-4208-10A-01D-1353-08 g.chr19:1468647G>A c.5347G>A c.(5347-5349)Ggg>Agg p.G1783R HNSC 19 1455209 1455209 + Missense_Mutation SNP C C G TCGA-CN-4727-01A-01D-1434-08 TCGA-CN-4727-10A-01D-1434-08 g.chr19:1455209C>G c.475C>G c.(475-477)Ctg>Gtg p.L159V HNSC 19 1460307 1460307 + Missense_Mutation SNP C C A TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chr19:1460307C>A c.1431C>A c.(1429-1431)gaC>gaA p.D477E HNSC 19 1462153 1462153 + Silent SNP C C T TCGA-CV-7414-01A-11D-2078-08 TCGA-CV-7414-10A-01D-2078-08 g.chr19:1462153C>T c.1830C>T c.(1828-1830)ctC>ctT p.L610L HNSC 19 1465944 1465944 + Missense_Mutation SNP G G C TCGA-P3-A5QF-01A-11D-A28R-08 TCGA-P3-A5QF-10A-01D-A28U-08 g.chr19:1465944G>C c.2644G>C c.(2644-2646)Gag>Cag p.E882Q HNSC 19 1465950 1465950 + Missense_Mutation SNP C C T TCGA-CQ-A4CG-01A-11D-A25Y-08 TCGA-CQ-A4CG-10A-01D-A25Y-08 g.chr19:1465950C>T c.2650C>T c.(2650-2652)Cca>Tca p.P884S HNSC 19 1466497 1466497 + Missense_Mutation SNP C C T TCGA-BA-6869-01A-11D-1870-08 TCGA-BA-6869-10A-01D-1870-08 g.chr19:1466497C>T c.3197C>T c.(3196-3198)tCg>tTg p.S1066L HNSC 19 1467216 1467216 + Missense_Mutation SNP G G A TCGA-CV-7250-01A-11D-2012-08 TCGA-CV-7250-10A-01D-2013-08 g.chr19:1467216G>A c.3916G>A c.(3916-3918)Ggg>Agg p.G1306R KIPAN 19 1453570 1453570 + Missense_Mutation SNP C C T TCGA-BP-4976-01A-01D-1462-08 TCGA-BP-4976-11A-01D-1462-08 g.chr19:1453570C>T c.373C>T c.(373-375)Cgg>Tgg p.R125W KIPAN 19 1456344 1456344 + Missense_Mutation SNP C C A TCGA-B0-5108-01A-01D-1421-08 TCGA-B0-5108-11A-01D-1421-08 g.chr19:1456344C>A c.757C>A c.(757-759)Ccc>Acc p.P253T KIPAN 19 1461048 1461048 + Missense_Mutation SNP A A G TCGA-BP-4782-01A-02D-1421-08 TCGA-BP-4782-11A-01D-1421-08 g.chr19:1461048A>G c.1534A>G c.(1534-1536)Atc>Gtc p.I512V KIPAN 19 1465652 1465652 + Frame_Shift_Del DEL G G - TCGA-2Z-A9JR-01A-12D-A42J-10 TCGA-2Z-A9JR-10A-01D-A42M-10 g.chr19:1465652delG c.2352delG c.(2350-2352)ccgfs p.P784fs KIPAN 19 1467881 1467881 + Missense_Mutation SNP C C G TCGA-BP-5182-01A-01D-1429-08 TCGA-BP-5182-11A-01D-1429-08 g.chr19:1467881C>G c.4581C>G c.(4579-4581)caC>caG p.H1527Q KIPAN 19 1468067 1468067 + Silent SNP C C T TCGA-A4-7288-01A-11D-2136-08 TCGA-A4-7288-11A-01D-2136-08 g.chr19:1468067C>T c.4767C>T c.(4765-4767)ccC>ccT p.P1589P KIRC 19 1453570 1453570 + Missense_Mutation SNP C C T TCGA-BP-4976-01A-01D-1462-08 TCGA-BP-4976-11A-01D-1462-08 g.chr19:1453570C>T c.373C>T c.(373-375)Cgg>Tgg p.R125W KIRC 19 1456344 1456344 + Missense_Mutation SNP C C A TCGA-B0-5108-01A-01D-1421-08 TCGA-B0-5108-11A-01D-1421-08 g.chr19:1456344C>A c.757C>A c.(757-759)Ccc>Acc p.P253T KIRC 19 1461048 1461048 + Missense_Mutation SNP A A G TCGA-BP-4782-01A-02D-1421-08 TCGA-BP-4782-11A-01D-1421-08 g.chr19:1461048A>G c.1534A>G c.(1534-1536)Atc>Gtc p.I512V KIRC 19 1467881 1467881 + Missense_Mutation SNP C C G TCGA-BP-5182-01A-01D-1429-08 TCGA-BP-5182-11A-01D-1429-08 g.chr19:1467881C>G c.4581C>G c.(4579-4581)caC>caG p.H1527Q KIRP 19 1465652 1465652 + Frame_Shift_Del DEL G G - TCGA-2Z-A9JR-01A-12D-A42J-10 TCGA-2Z-A9JR-10A-01D-A42M-10 g.chr19:1465652delG c.2352delG c.(2350-2352)ccgfs p.P784fs KIRP 19 1468067 1468067 + Silent SNP C C T TCGA-A4-7288-01A-11D-2136-08 TCGA-A4-7288-11A-01D-2136-08 g.chr19:1468067C>T c.4767C>T c.(4765-4767)ccC>ccT p.P1589P LGG 19 1462051 1462051 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:1462051C>T c.1728C>T c.(1726-1728)ggC>ggT p.G576G LIHC 19 1456316 1456316 + Silent SNP G G A TCGA-DD-A4NN-01A-11D-A28X-10 TCGA-DD-A4NN-10A-01D-A28X-10 g.chr19:1456316G>A c.729G>A c.(727-729)gcG>gcA p.A243A LIHC 19 1460853 1460853 + Missense_Mutation SNP C C G TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr19:1460853C>G c.1518C>G c.(1516-1518)caC>caG p.H506Q LIHC 19 1468353 1468354 + In_Frame_Ins INS - - AGT TCGA-RC-A6M6-01A-11D-A32G-10 TCGA-RC-A6M6-10A-01D-A32G-10 g.chr19:1468353_1468354insAGT c.5053_5054insAGT c.(5053-5055)gag>gAGTag p.1685_1686ins* LIHC 19 1469059 1469059 + Missense_Mutation SNP A A G TCGA-DD-A3A1-01A-11D-A20W-10 TCGA-DD-A3A1-11A-11D-A20W-10 g.chr19:1469059A>G c.5759A>G c.(5758-5760)cAg>cGg p.Q1920R LUAD 19 1453291 1453291 + Missense_Mutation SNP G G T TCGA-44-7670-01A-11D-2063-08 TCGA-44-7670-10A-01D-2063-08 g.chr19:1453291G>T c.187G>T c.(187-189)Gtg>Ttg p.V63L LUAD 19 1461077 1461077 + Silent SNP C C T TCGA-91-8499-01A-11D-2393-08 TCGA-91-8499-10A-01D-2393-08 g.chr19:1461077C>T c.1563C>T c.(1561-1563)gaC>gaT p.D521D LUAD 19 1462038 1462038 + Missense_Mutation SNP G G A TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr19:1462038G>A c.1715G>A c.(1714-1716)tGc>tAc p.C572Y LUAD 19 1462064 1462064 + Missense_Mutation SNP C C A TCGA-55-8507-01A-11D-2393-08 TCGA-55-8507-10A-01D-2393-08 g.chr19:1462064C>A c.1741C>A c.(1741-1743)Ctg>Atg p.L581M LUAD 19 1462091 1462091 + Nonsense_Mutation SNP C C T TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chr19:1462091C>T c.1768C>T c.(1768-1770)Cag>Tag p.Q590* LUAD 19 1465263 1465263 + Missense_Mutation SNP C C A TCGA-55-7994-01A-11D-2184-08 TCGA-55-7994-10A-01D-2184-08 g.chr19:1465263C>A c.1963C>A c.(1963-1965)Cgc>Agc p.R655S LUAD 19 1465425 1465425 + Missense_Mutation SNP G G T TCGA-55-A48Z-01A-12D-A24P-08 TCGA-55-A48Z-10A-01D-A24P-08 g.chr19:1465425G>T c.2125G>T c.(2125-2127)Gtg>Ttg p.V709L LUAD 19 1467052 1467052 + Missense_Mutation SNP G G A TCGA-55-8302-01A-11D-2323-08 TCGA-55-8302-10A-01D-2323-08 g.chr19:1467052G>A c.3752G>A c.(3751-3753)cGg>cAg p.R1251Q LUAD 19 1467098 1467098 + Silent SNP G G A TCGA-95-8494-01A-11D-2323-08 TCGA-95-8494-10A-01D-2323-08 g.chr19:1467098G>A c.3798G>A c.(3796-3798)gaG>gaA p.E1266E LUAD 19 1468918 1468918 + Missense_Mutation SNP C C T TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr19:1468918C>T c.5618C>T c.(5617-5619)tCc>tTc p.S1873F LUAD 19 1470032 1470032 + Silent SNP C C T TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr19:1470032C>T c.6732C>T c.(6730-6732)ttC>ttT p.F2244F LUSC 19 1453249 1453249 + Missense_Mutation SNP G G A TCGA-39-5022-01A-21D-1817-08 TCGA-39-5022-11A-01D-1817-08 g.chr19:1453249G>A c.145G>A c.(145-147)Gtc>Atc p.V49I LUSC 19 1468499 1468499 + Silent SNP C C G TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr19:1468499C>G c.5199C>G c.(5197-5199)ccC>ccG p.P1733P LUSC 19 1470100 1470100 + Missense_Mutation SNP C C T TCGA-21-1078-01A-01D-1521-08 TCGA-21-1078-11A-01D-1521-08 g.chr19:1470100C>T c.6800C>T c.(6799-6801)tCg>tTg p.S2267L OV 19 1467803 1467803 + Silent SNP C C T TCGA-13-2061-01A-01D-1526-09 TCGA-13-2061-10A-01D-1526-09 g.chr19:1467803C>T c.4503C>T c.(4501-4503)ccC>ccT p.P1501P PAAD 19 1465269 1465269 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:1465269G>A c.1969G>A c.(1969-1971)Gcc>Acc p.A657T PAAD 19 1466480 1466480 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:1466480G>A c.3180G>A c.(3178-3180)gcG>gcA p.A1060A PAAD 19 1466897 1466897 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:1466897C>T c.3597C>T c.(3595-3597)ccC>ccT p.P1199P PAAD 19 1467872 1467872 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:1467872G>A c.4572G>A c.(4570-4572)acG>acA p.T1524T PAAD 19 1467886 1467886 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:1467886G>A c.4586G>A c.(4585-4587)cGc>cAc p.R1529H PCPG 19 1453055 1453055 + Missense_Mutation SNP A A G TCGA-WB-A81R-01A-11D-A35I-08 TCGA-WB-A81R-10A-01D-A35G-08 g.chr19:1453055A>G c.55A>G c.(55-57)Aag>Gag p.K19E PCPG 19 1465635 1465637 + In_Frame_Del DEL GAC GAC - TCGA-S7-A7WL-01A-11D-A35I-08 TCGA-S7-A7WL-10A-01D-A35G-08 g.chr19:1465635_1465637delGAC c.2335_2337delGAC c.(2335-2337)gacdel p.D782del PRAD 19 1461079 1461079 + Missense_Mutation SNP T T C TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:1461079T>C c.1565T>C c.(1564-1566)aTc>aCc p.I522T PRAD 19 1462106 1462106 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:1462106G>A c.1783G>A c.(1783-1785)Gcc>Acc p.A595T PRAD 19 1465241 1465241 + Silent SNP C C T TCGA-YJ-A8SW-01A-11D-A377-08 TCGA-YJ-A8SW-10A-01D-A37A-08 g.chr19:1465241C>T c.1941C>T c.(1939-1941)ggC>ggT p.G647G PRAD 19 1465425 1465425 + Frame_Shift_Del DEL G G - TCGA-2A-A8VT-01A-11D-A377-08 TCGA-2A-A8VT-10A-01D-A37A-08 g.chr19:1465425delG c.2125delG c.(2125-2127)gtgfs p.V709fs PRAD 19 1465595 1465595 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:1465595C>T c.2295C>T c.(2293-2295)gaC>gaT p.D765D READ 19 1455453 1455453 + Missense_Mutation SNP T T C TCGA-AF-5654-01A-01D-1657-10 TCGA-AF-5654-10A-01D-1657-10 g.chr19:1455453T>C c.593T>C c.(592-594)aTg>aCg p.M198T READ 19 1462030 1462030 + Silent SNP G G A TCGA-AG-A00Y-01A-02W-A005-10 TCGA-AG-A00Y-10A-01W-A005-10 g.chr19:1462030G>A c.1707G>A c.(1705-1707)gcG>gcA p.A569A SARC 19 1455427 1455427 + Silent SNP C C T TCGA-DX-A1KZ-01A-11D-A24N-09 TCGA-DX-A1KZ-10A-01D-A24N-09 g.chr19:1455427C>T c.567C>T c.(565-567)ttC>ttT p.F189F SKCM 19 1453051 1453051 + Silent SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr19:1453051C>T c.51C>T c.(49-51)gcC>gcT p.A17A SKCM 19 1457134 1457134 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:1457134G>A c.1099G>A c.(1099-1101)Gag>Aag p.E367K SKCM 19 1460252 1460252 + Missense_Mutation SNP A A G TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr19:1460252A>G c.1376A>G c.(1375-1377)aAc>aGc p.N459S SKCM 19 1460850 1460850 + Silent SNP C C T TCGA-D3-A1Q6-06A-11D-A196-08 TCGA-D3-A1Q6-10A-01D-A198-08 g.chr19:1460850C>T c.1515C>T c.(1513-1515)ctC>ctT p.L505L SKCM 19 1462005 1462005 + Missense_Mutation SNP C C T TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr19:1462005C>T c.1682C>T c.(1681-1683)tCt>tTt p.S561F SKCM 19 1465272 1465272 + Missense_Mutation SNP C C T TCGA-ER-A3EV-06A-11D-A20D-08 TCGA-ER-A3EV-10A-01D-A20D-08 g.chr19:1465272C>T c.1972C>T c.(1972-1974)Cgt>Tgt p.R658C SKCM 19 1465626 1465626 + Missense_Mutation SNP G G A TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr19:1465626G>A c.2326G>A c.(2326-2328)Ggc>Agc p.G776S SKCM 19 1465736 1465736 + Silent SNP G G A TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr19:1465736G>A c.2436G>A c.(2434-2436)caG>caA p.Q812Q SKCM 19 1465837 1465837 + Missense_Mutation SNP A A C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr19:1465837A>C c.2537A>C c.(2536-2538)aAg>aCg p.K846T SKCM 19 1465875 1465875 + Missense_Mutation SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr19:1465875G>A c.2575G>A c.(2575-2577)Gag>Aag p.E859K SKCM 19 1466297 1466297 + Nonsense_Mutation SNP T T A TCGA-EB-A5UN-06A-11D-A30X-08 TCGA-EB-A5UN-10A-01D-A30X-08 g.chr19:1466297T>A c.2997T>A c.(2995-2997)taT>taA p.Y999* SKCM 19 1466377 1466377 + Missense_Mutation SNP G G A TCGA-ER-A19H-06A-12D-A196-08 TCGA-ER-A19H-10A-01D-A198-08 g.chr19:1466377G>A c.3077G>A c.(3076-3078)cGg>cAg p.R1026Q SKCM 19 1466440 1466440 + Missense_Mutation SNP C C T TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr19:1466440C>T c.3140C>T c.(3139-3141)cCg>cTg p.P1047L SKCM 19 1468579 1468579 + Missense_Mutation SNP A A C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr19:1468579A>C c.5279A>C c.(5278-5280)aAg>aCg p.K1760T SKCM 19 1468588 1468588 + Missense_Mutation SNP G G A TCGA-D3-A2JD-06A-11D-A19A-08 TCGA-D3-A2JD-10A-01D-A19A-08 g.chr19:1468588G>A c.5288G>A c.(5287-5289)gGg>gAg p.G1763E

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US 9 140087053 140087053 insertion of <=200bp - CCT upstream_gene_variant BLCA-CN 9 140084366 140084366 single base substitution A C upstream_gene_variant BLCA-US 9 140069557 140069557 single base substitution G A downstream_gene_variant BLCA-US 9 140069557 140069557 single base substitution G A exon_variant BLCA-US 9 140069557 140069557 single base substitution G A missense_variant S769L 2306C>T BLCA-US 9 140074639 140074639 single base substitution C G downstream_gene_variant BLCA-US 9 140074639 140074639 single base substitution C G exon_variant BLCA-US 9 140074639 140074639 single base substitution C G missense_variant Q628H 1884G>C BLCA-US 9 140074639 140074639 single base substitution C G upstream_gene_variant BLCA-US 9 140075251 140075251 single base substitution G A downstream_gene_variant BLCA-US 9 140075251 140075251 single base substitution G A synonymous_variant F533F 1599C>T BLCA-US 9 140075251 140075251 single base substitution G A upstream_gene_variant BLCA-US 9 140076196 140076196 single base substitution C T downstream_gene_variant BLCA-US 9 140076196 140076196 single base substitution C T exon_variant BLCA-US 9 140076196 140076196 single base substitution C T missense_variant D469N 1405G>A BLCA-US 9 140076196 140076196 single base substitution C T upstream_gene_variant BLCA-US 9 140083594 140083594 single base substitution G A upstream_gene_variant BLCA-US 9 140083657 140083657 single base substitution G A upstream_gene_variant BLCA-US 9 140086816 140086816 single base substitution G T upstream_gene_variant BRCA-EU 9 140066182 140066182 single base substitution G T downstream_gene_variant BRCA-EU 9 140067544 140067544 deletion of <=200bp G - downstream_gene_variant BRCA-EU 9 140067544 140067544 insertion of <=200bp - G downstream_gene_variant BRCA-EU 9 140068523 140068523 single base substitution G C downstream_gene_variant BRCA-EU 9 140068908 140068908 single base substitution T C downstream_gene_variant BRCA-EU 9 140069304 140069304 single base substitution C T 3_prime_UTR_variant BRCA-EU 9 140069304 140069304 single base substitution C T downstream_gene_variant BRCA-EU 9 140069304 140069304 single base substitution C T exon_variant BRCA-EU 9 140069406 140069406 single base substitution C T downstream_gene_variant BRCA-EU 9 140069406 140069406 single base substitution C T exon_variant BRCA-EU 9 140069406 140069406 single base substitution C T synonymous_variant K819K 2457G>A BRCA-EU 9 140069604 140069604 single base substitution G T downstream_gene_variant BRCA-EU 9 140069604 140069604 single base substitution G T splice_region_variant BRCA-EU 9 140070507 140070507 single base substitution G A exon_variant BRCA-EU 9 140070507 140070507 single base substitution G A intron_variant BRCA-EU 9 140070778 140070778 single base substitution G C exon_variant BRCA-EU 9 140070778 140070778 single base substitution G C intron_variant BRCA-EU 9 140070778 140070778 single base substitution G C upstream_gene_variant BRCA-EU 9 140071396 140071399 deletion of <=200bp GGGG - downstream_gene_variant BRCA-EU 9 140071396 140071399 deletion of <=200bp GGGG - exon_variant BRCA-EU 9 140071396 140071399 deletion of <=200bp GGGG - intron_variant BRCA-EU 9 140071396 140071399 deletion of <=200bp GGGG - upstream_gene_variant BRCA-EU 9 140072012 140072012 single base substitution A G downstream_gene_variant BRCA-EU 9 140072012 140072012 single base substitution A G intron_variant BRCA-EU 9 140072012 140072012 single base substitution A G upstream_gene_variant BRCA-EU 9 140073422 140073422 single base substitution C T downstream_gene_variant BRCA-EU 9 140073422 140073422 single base substitution C T intron_variant BRCA-EU 9 140073422 140073422 single base substitution C T upstream_gene_variant BRCA-EU 9 140074401 140074401 single base substitution C T downstream_gene_variant BRCA-EU 9 140074401 140074401 single base substitution C T intron_variant BRCA-EU 9 140074401 140074401 single base substitution C T upstream_gene_variant BRCA-EU 9 140079462 140079462 single base substitution G A exon_variant BRCA-EU 9 140079462 140079462 single base substitution G A synonymous_variant A317A 951C>T BRCA-EU 9 140079462 140079462 single base substitution G A upstream_gene_variant BRCA-EU 9 140081183 140081183 single base substitution G A intron_variant BRCA-EU 9 140081183 140081183 single base substitution G A upstream_gene_variant BRCA-EU 9 140084082 140084082 single base substitution G A upstream_gene_variant BRCA-EU 9 140085439 140085439 single base substitution A G upstream_gene_variant BRCA-EU 9 140085684 140085684 single base substitution G A upstream_gene_variant BRCA-FR 9 140069604 140069604 single base substitution G T downstream_gene_variant BRCA-FR 9 140069604 140069604 single base substitution G T splice_region_variant BRCA-FR 9 140070507 140070507 single base substitution G A exon_variant BRCA-FR 9 140070507 140070507 single base substitution G A intron_variant BRCA-FR 9 140070778 140070778 single base substitution G C exon_variant BRCA-FR 9 140070778 140070778 single base substitution G C intron_variant BRCA-FR 9 140070778 140070778 single base substitution G C upstream_gene_variant BRCA-FR 9 140073082 140073082 single base substitution G C downstream_gene_variant BRCA-FR 9 140073082 140073082 single base substitution G C intron_variant BRCA-FR 9 140073082 140073082 single base substitution G C upstream_gene_variant BRCA-KR 9 140074849 140074849 single base substitution C T downstream_gene_variant BRCA-KR 9 140074849 140074849 single base substitution C T intron_variant BRCA-KR 9 140074849 140074849 single base substitution C T upstream_gene_variant BRCA-KR 9 140079372 140079372 single base substitution G A exon_variant BRCA-KR 9 140079372 140079372 single base substitution G A synonymous_variant I347I 1041C>T BRCA-KR 9 140079372 140079372 single base substitution G A upstream_gene_variant BRCA-UK 9 140070281 140070281 single base substitution C T exon_variant BRCA-UK 9 140070281 140070281 single base substitution C T synonymous_variant R633R 1899G>A BRCA-UK 9 140081310 140081310 single base substitution C G intron_variant BRCA-UK 9 140081310 140081310 single base substitution C G upstream_gene_variant BRCA-UK 9 140082109 140082109 single base substitution C G missense_variant K188N 564G>C BRCA-UK 9 140082109 140082109 single base substitution C G upstream_gene_variant BRCA-US 9 140082004 140082004 single base substitution C T synonymous_variant G223G 669G>A BRCA-US 9 140082004 140082004 single base substitution C T upstream_gene_variant BRCA-US 9 140083571 140083571 single base substitution G C upstream_gene_variant BRCA-US 9 140083619 140083619 single base substitution G A upstream_gene_variant BTCA-JP 9 140065900 140065900 deletion of <=200bp G - downstream_gene_variant BTCA-JP 9 140069565 140069565 single base substitution C A downstream_gene_variant BTCA-JP 9 140069565 140069565 single base substitution C A exon_variant BTCA-JP 9 140069565 140069565 single base substitution C A missense_variant E766D 2298G>T BTCA-JP 9 140074972 140074972 single base substitution G A downstream_gene_variant BTCA-JP 9 140074972 140074972 single base substitution G A missense_variant R540C 1618C>T BTCA-JP 9 140074972 140074972 single base substitution G A upstream_gene_variant BTCA-JP 9 140076300 140076300 single base substitution G A exon_variant BTCA-JP 9 140076300 140076300 single base substitution G A missense_variant T434I 1301C>T BTCA-JP 9 140076300 140076300 single base substitution G A upstream_gene_variant BTCA-JP 9 140077638 140077638 deletion of <=200bp C - exon_variant BTCA-JP 9 140077638 140077638 deletion of <=200bp C - frameshift_variant V409 BTCA-JP 9 140077638 140077638 deletion of <=200bp C - upstream_gene_variant BTCA-JP 9 140086975 140086975 single base substitution G A upstream_gene_variant CESC-US 9 140069483 140069483 single base substitution C T downstream_gene_variant CESC-US 9 140069483 140069483 single base substitution C T exon_variant CESC-US 9 140069483 140069483 single base substitution C T missense_variant E794K 2380G>A CESC-US 9 140080858 140080858 single base substitution C G exon_variant CESC-US 9 140080858 140080858 single base substitution C G intron_variant CESC-US 9 140080858 140080858 single base substitution C G upstream_gene_variant CESC-US 9 140082173 140082173 single base substitution C T missense_variant R167K 500G>A CESC-US 9 140082173 140082173 single base substitution C T upstream_gene_variant CESC-US 9 140082187 140082187 single base substitution G C missense_variant F162L 486C>G CESC-US 9 140082187 140082187 single base substitution G C upstream_gene_variant CESC-US 9 140082274 140082274 single base substitution C T synonymous_variant E133E 399G>A CESC-US 9 140082274 140082274 single base substitution C T upstream_gene_variant CESC-US 9 140082506 140082506 single base substitution C T missense_variant R56Q 167G>A CESC-US 9 140082506 140082506 single base substitution C T upstream_gene_variant CESC-US 9 140084301 140084301 single base substitution G A upstream_gene_variant CESC-US 9 140086993 140086993 single base substitution C G upstream_gene_variant CESC-US 9 140087025 140087027 deletion of <=200bp TCC - upstream_gene_variant CLLE-ES 9 140073108 140073108 single base substitution G C downstream_gene_variant CLLE-ES 9 140073108 140073108 single base substitution G C intron_variant CLLE-ES 9 140073108 140073108 single base substitution G C upstream_gene_variant COAD-US 9 140069728 140069728 single base substitution G A downstream_gene_variant COAD-US 9 140069728 140069728 single base substitution G A exon_variant COAD-US 9 140069728 140069728 single base substitution G A synonymous_variant G739G 2217C>T COAD-US 9 140075365 140075365 single base substitution C A downstream_gene_variant COAD-US 9 140075365 140075365 single base substitution C A missense_variant K495N 1485G>T COAD-US 9 140075365 140075365 single base substitution C A upstream_gene_variant COAD-US 9 140076156 140076156 single base substitution G A downstream_gene_variant COAD-US 9 140076156 140076156 single base substitution G A exon_variant COAD-US 9 140076156 140076156 single base substitution G A missense_variant P482L 1445C>T COAD-US 9 140076156 140076156 single base substitution G A upstream_gene_variant COAD-US 9 140077641 140077641 single base substitution G T exon_variant COAD-US 9 140077641 140077641 single base substitution G T missense_variant R408S 1222C>A COAD-US 9 140077641 140077641 single base substitution G T upstream_gene_variant COAD-US 9 140079405 140079405 single base substitution G A exon_variant COAD-US 9 140079405 140079405 single base substitution G A synonymous_variant Y336Y 1008C>T COAD-US 9 140079405 140079405 single base substitution G A upstream_gene_variant COAD-US 9 140082429 140082429 single base substitution C T missense_variant D82N 244G>A COAD-US 9 140082429 140082429 single base substitution C T upstream_gene_variant COAD-US 9 140083566 140083568 deletion of <=200bp AGG - upstream_gene_variant COAD-US 9 140087009 140087009 single base substitution T C upstream_gene_variant COAD-US 9 140087025 140087027 deletion of <=200bp TCC - upstream_gene_variant COAD-US 9 140087030 140087030 single base substitution C T upstream_gene_variant COAD-US 9 140087050 140087050 single base substitution C G upstream_gene_variant COCA-CN 9 140066190 140066190 single base substitution C T downstream_gene_variant COCA-CN 9 140066196 140066196 single base substitution T C downstream_gene_variant COCA-CN 9 140066446 140066446 single base substitution G A downstream_gene_variant COCA-CN 9 140066845 140066845 single base substitution G A downstream_gene_variant COCA-CN 9 140069542 140069542 single base substitution T C downstream_gene_variant COCA-CN 9 140069542 140069542 single base substitution T C exon_variant COCA-CN 9 140069542 140069542 single base substitution T C missense_variant Y774C 2321A>G COCA-CN 9 140070138 140070138 single base substitution A T exon_variant COCA-CN 9 140070138 140070138 single base substitution A T intron_variant COCA-CN 9 140070366 140070366 single base substitution G A exon_variant COCA-CN 9 140070366 140070366 single base substitution G A intron_variant COCA-CN 9 140075291 140075291 single base substitution C T downstream_gene_variant COCA-CN 9 140075291 140075291 single base substitution C T missense_variant R520H 1559G>A COCA-CN 9 140075291 140075291 single base substitution C T upstream_gene_variant COCA-CN 9 140075466 140075466 single base substitution G A downstream_gene_variant COCA-CN 9 140075466 140075466 single base substitution G A intron_variant COCA-CN 9 140075466 140075466 single base substitution G A upstream_gene_variant COCA-CN 9 140076035 140076035 single base substitution A G downstream_gene_variant COCA-CN 9 140076035 140076035 single base substitution A G intron_variant COCA-CN 9 140076035 140076035 single base substitution A G upstream_gene_variant COCA-CN 9 140076362 140076362 single base substitution G A intron_variant COCA-CN 9 140076362 140076362 single base substitution G A upstream_gene_variant COCA-CN 9 140078227 140078227 single base substitution C T exon_variant COCA-CN 9 140078227 140078227 single base substitution C T synonymous_variant R355R 1065G>A COCA-CN 9 140078227 140078227 single base substitution C T upstream_gene_variant COCA-CN 9 140079552 140079552 single base substitution C T intron_variant COCA-CN 9 140079552 140079552 single base substitution C T upstream_gene_variant COCA-CN 9 140082017 140082017 single base substitution G T missense_variant P219Q 656C>A COCA-CN 9 140082017 140082017 single base substitution G T upstream_gene_variant COCA-CN 9 140082136 140082136 single base substitution G A synonymous_variant C179C 537C>T COCA-CN 9 140082136 140082136 single base substitution G A upstream_gene_variant COCA-CN 9 140082578 140082578 single base substitution G A intron_variant COCA-CN 9 140082578 140082578 single base substitution G A upstream_gene_variant COCA-CN 9 140086486 140086486 single base substitution G A upstream_gene_variant COCA-CN 9 140087231 140087231 single base substitution C T upstream_gene_variant EOPC-DE 9 140065206 140065206 single base substitution G A downstream_gene_variant EOPC-DE 9 140068213 140068213 single base substitution A G downstream_gene_variant ESAD-UK 9 140064298 140064298 single base substitution G A downstream_gene_variant ESAD-UK 9 140064750 140064750 single base substitution G T downstream_gene_variant ESAD-UK 9 140066040 140066040 single base substitution G A downstream_gene_variant ESAD-UK 9 140070425 140070425 single base substitution C G exon_variant ESAD-UK 9 140070425 140070425 single base substitution C G intron_variant ESAD-UK 9 140071886 140071886 single base substitution C T downstream_gene_variant ESAD-UK 9 140071886 140071886 single base substitution C T intron_variant ESAD-UK 9 140071886 140071886 single base substitution C T upstream_gene_variant ESAD-UK 9 140075361 140075361 single base substitution G A downstream_gene_variant ESAD-UK 9 140075361 140075361 single base substitution G A missense_variant R497C 1489C>T ESAD-UK 9 140075361 140075361 single base substitution G A upstream_gene_variant ESAD-UK 9 140078338 140078338 single base substitution C T intron_variant ESAD-UK 9 140078338 140078338 single base substitution C T upstream_gene_variant ESAD-UK 9 140079892 140079892 single base substitution C T intron_variant ESAD-UK 9 140079892 140079892 single base substitution C T upstream_gene_variant ESAD-UK 9 140081762 140081762 single base substitution A G intron_variant ESAD-UK 9 140081762 140081762 single base substitution A G upstream_gene_variant ESAD-UK 9 140082488 140082488 single base substitution A G missense_variant L62P 185T>C ESAD-UK 9 140082488 140082488 single base substitution A G upstream_gene_variant ESAD-UK 9 140082972 140082972 single base substitution C T missense_variant V5I 13G>A ESAD-UK 9 140082972 140082972 single base substitution C T upstream_gene_variant ESAD-UK 9 140083437 140083437 single base substitution C A upstream_gene_variant ESAD-UK 9 140084160 140084160 deletion of <=200bp C - upstream_gene_variant ESAD-UK 9 140084393 140084393 single base substitution G C upstream_gene_variant ESAD-UK 9 140086290 140086290 single base substitution G A upstream_gene_variant ESCA-CN 9 140082208 140082208 single base substitution A G synonymous_variant T155T 465T>C ESCA-CN 9 140082208 140082208 single base substitution A G upstream_gene_variant GBM-US 9 140074735 140074735 single base substitution C A downstream_gene_variant GBM-US 9 140074735 140074735 single base substitution C A exon_variant GBM-US 9 140074735 140074735 single base substitution C A synonymous_variant L596L 1788G>T GBM-US 9 140074735 140074735 single base substitution C A upstream_gene_variant GBM-US 9 140086667 140086667 single base substitution C T upstream_gene_variant GBM-US 9 140086816 140086816 single base substitution G T upstream_gene_variant KIRC-US 9 140075307 140075307 single base substitution A T downstream_gene_variant KIRC-US 9 140075307 140075307 single base substitution A T missense_variant F515I 1543T>A KIRC-US 9 140075307 140075307 single base substitution A T upstream_gene_variant KIRC-US 9 140083619 140083619 single base substitution G A upstream_gene_variant LGG-US 9 140079392 140079392 single base substitution T C exon_variant LGG-US 9 140079392 140079392 single base substitution T C missense_variant I341V 1021A>G LGG-US 9 140079392 140079392 single base substitution T C upstream_gene_variant LICA-FR 9 140069794 140069794 single base substitution C T exon_variant LICA-FR 9 140069794 140069794 single base substitution C T synonymous_variant E717E 2151G>A LICA-FR 9 140069890 140069890 single base substitution C A exon_variant LICA-FR 9 140069890 140069890 single base substitution C A synonymous_variant V685V 2055G>T LICA-FR 9 140077599 140077599 single base substitution C A exon_variant LICA-FR 9 140077599 140077599 single base substitution C A stop_gained E422* 1264G>T LICA-FR 9 140077599 140077599 single base substitution C A upstream_gene_variant LICA-FR 9 140079425 140079425 single base substitution T G exon_variant LICA-FR 9 140079425 140079425 single base substitution T G synonymous_variant R330R 988A>C LICA-FR 9 140079425 140079425 single base substitution T G upstream_gene_variant LICA-FR 9 140082975 140082975 single base substitution C T missense_variant A4T 10G>A LICA-FR 9 140082975 140082975 single base substitution C T upstream_gene_variant LIHC-US 9 140086995 140086995 single base substitution G A upstream_gene_variant LINC-JP 9 140069476 140069476 single base substitution T A downstream_gene_variant LINC-JP 9 140069476 140069476 single base substitution T A exon_variant LINC-JP 9 140069476 140069476 single base substitution T A missense_variant Q796L 2387A>T LINC-JP 9 140069906 140069906 single base substitution T A exon_variant LINC-JP 9 140069906 140069906 single base substitution T A missense_variant E680V 2039A>T LINC-JP 9 140077638 140077638 single base substitution C T exon_variant LINC-JP 9 140077638 140077638 single base substitution C T missense_variant V409M 1225G>A LINC-JP 9 140077638 140077638 single base substitution C T upstream_gene_variant LINC-JP 9 140081170 140081170 single base substitution C T intron_variant LINC-JP 9 140081170 140081170 single base substitution C T upstream_gene_variant LINC-JP 9 140083156 140083156 single base substitution T C upstream_gene_variant LINC-JP 9 140083167 140083167 single base substitution G A upstream_gene_variant LINC-JP 9 140087044 140087045 deletion of <=200bp CC - upstream_gene_variant LIRI-JP 9 140067428 140067428 single base substitution C T downstream_gene_variant LIRI-JP 9 140070660 140070660 single base substitution G C exon_variant LIRI-JP 9 140070660 140070660 single base substitution G C intron_variant LIRI-JP 9 140070660 140070660 single base substitution G C upstream_gene_variant LIRI-JP 9 140079895 140079895 deletion of <=200bp C - intron_variant LIRI-JP 9 140079895 140079895 deletion of <=200bp C - upstream_gene_variant LIRI-JP 9 140080129 140080129 single base substitution G T intron_variant LIRI-JP 9 140080129 140080129 single base substitution G T upstream_gene_variant LUSC-KR 9 140064263 140064263 single base substitution C A downstream_gene_variant LUSC-KR 9 140064531 140064531 single base substitution C A downstream_gene_variant LUSC-KR 9 140065155 140065155 single base substitution A T downstream_gene_variant LUSC-KR 9 140073298 140073298 single base substitution C A downstream_gene_variant LUSC-KR 9 140073298 140073298 single base substitution C A intron_variant LUSC-KR 9 140073298 140073298 single base substitution C A upstream_gene_variant LUSC-KR 9 140080534 140080534 single base substitution C A intron_variant LUSC-KR 9 140080534 140080534 single base substitution C A upstream_gene_variant LUSC-KR 9 140083640 140083640 single base substitution G T upstream_gene_variant LUSC-KR 9 140086333 140086333 single base substitution G T upstream_gene_variant LUSC-US 9 140076197 140076197 single base substitution C T downstream_gene_variant LUSC-US 9 140076197 140076197 single base substitution C T exon_variant LUSC-US 9 140076197 140076197 single base substitution C T synonymous_variant Q468Q 1404G>A LUSC-US 9 140076197 140076197 single base substitution C T upstream_gene_variant LUSC-US 9 140083606 140083606 single base substitution G A upstream_gene_variant LUSC-US 9 140086755 140086755 single base substitution C G upstream_gene_variant MALY-DE 9 140064630 140064630 single base substitution G T downstream_gene_variant MALY-DE 9 140064736 140064736 single base substitution C A downstream_gene_variant MALY-DE 9 140076523 140076523 single base substitution C T intron_variant MALY-DE 9 140076523 140076523 single base substitution C T upstream_gene_variant MALY-DE 9 140078761 140078761 single base substitution C G intron_variant MALY-DE 9 140078761 140078761 single base substitution C G upstream_gene_variant MALY-DE 9 140079094 140079114 deletion of <=200bp CACAGGGAGCCCAGACGCAGA - intron_variant MALY-DE 9 140079094 140079114 deletion of <=200bp CACAGGGAGCCCAGACGCAGA - upstream_gene_variant MALY-DE 9 140079440 140079440 single base substitution G A exon_variant MALY-DE 9 140079440 140079440 single base substitution G A missense_variant R325C 973C>T MALY-DE 9 140079440 140079440 single base substitution G A upstream_gene_variant MELA-AU 9 140064328 140064328 single base substitution G A downstream_gene_variant MELA-AU 9 140064397 140064397 single base substitution G A downstream_gene_variant MELA-AU 9 140064667 140064667 single base substitution C T downstream_gene_variant MELA-AU 9 140065183 140065184 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 140065287 140065287 single base substitution G A downstream_gene_variant MELA-AU 9 140065523 140065524 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 140065617 140065617 single base substitution C T downstream_gene_variant MELA-AU 9 140065791 140065791 single base substitution C T downstream_gene_variant MELA-AU 9 140066614 140066614 single base substitution G A downstream_gene_variant MELA-AU 9 140067409 140067409 single base substitution G A downstream_gene_variant MELA-AU 9 140067445 140067445 single base substitution C T downstream_gene_variant MELA-AU 9 140067546 140067546 single base substitution G A downstream_gene_variant MELA-AU 9 140067673 140067673 single base substitution C T downstream_gene_variant MELA-AU 9 140068072 140068072 single base substitution G A downstream_gene_variant MELA-AU 9 140068698 140068698 single base substitution C A downstream_gene_variant MELA-AU 9 140069563 140069563 single base substitution C T downstream_gene_variant MELA-AU 9 140069563 140069563 single base substitution C T exon_variant MELA-AU 9 140069563 140069563 single base substitution C T missense_variant S767N 2300G>A MELA-AU 9 140069814 140069814 single base substitution C T exon_variant MELA-AU 9 140069814 140069814 single base substitution C T missense_variant G711S 2131G>A MELA-AU 9 140070470 140070471 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 9 140070470 140070471 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 140071312 140071312 single base substitution G A downstream_gene_variant MELA-AU 9 140071312 140071312 single base substitution G A exon_variant MELA-AU 9 140071312 140071312 single base substitution G A intron_variant MELA-AU 9 140071312 140071312 single base substitution G A upstream_gene_variant MELA-AU 9 140071347 140071347 single base substitution G A downstream_gene_variant MELA-AU 9 140071347 140071347 single base substitution G A exon_variant MELA-AU 9 140071347 140071347 single base substitution G A intron_variant MELA-AU 9 140071347 140071347 single base substitution G A upstream_gene_variant MELA-AU 9 140071529 140071529 single base substitution G A downstream_gene_variant MELA-AU 9 140071529 140071529 single base substitution G A intron_variant MELA-AU 9 140071529 140071529 single base substitution G A upstream_gene_variant MELA-AU 9 140071796 140071796 single base substitution G A downstream_gene_variant MELA-AU 9 140071796 140071796 single base substitution G A intron_variant MELA-AU 9 140071796 140071796 single base substitution G A upstream_gene_variant MELA-AU 9 140071881 140071881 single base substitution T G downstream_gene_variant MELA-AU 9 140071881 140071881 single base substitution T G intron_variant MELA-AU 9 140071881 140071881 single base substitution T G upstream_gene_variant MELA-AU 9 140072307 140072307 single base substitution G A downstream_gene_variant MELA-AU 9 140072307 140072307 single base substitution G A intron_variant MELA-AU 9 140072307 140072307 single base substitution G A upstream_gene_variant MELA-AU 9 140072595 140072595 single base substitution G A downstream_gene_variant MELA-AU 9 140072595 140072595 single base substitution G A intron_variant MELA-AU 9 140072595 140072595 single base substitution G A upstream_gene_variant MELA-AU 9 140073027 140073027 single base substitution G A downstream_gene_variant MELA-AU 9 140073027 140073027 single base substitution G A intron_variant MELA-AU 9 140073027 140073027 single base substitution G A upstream_gene_variant MELA-AU 9 140073058 140073058 single base substitution G A downstream_gene_variant MELA-AU 9 140073058 140073058 single base substitution G A intron_variant MELA-AU 9 140073058 140073058 single base substitution G A upstream_gene_variant MELA-AU 9 140073182 140073182 single base substitution A C downstream_gene_variant MELA-AU 9 140073182 140073182 single base substitution A C intron_variant MELA-AU 9 140073182 140073182 single base substitution A C upstream_gene_variant MELA-AU 9 140073191 140073191 single base substitution G A downstream_gene_variant MELA-AU 9 140073191 140073191 single base substitution G A intron_variant MELA-AU 9 140073191 140073191 single base substitution G A upstream_gene_variant MELA-AU 9 140074371 140074371 single base substitution G A downstream_gene_variant MELA-AU 9 140074371 140074371 single base substitution G A intron_variant MELA-AU 9 140074371 140074371 single base substitution G A upstream_gene_variant MELA-AU 9 140074593 140074593 single base substitution G A downstream_gene_variant MELA-AU 9 140074593 140074593 single base substitution G A intron_variant MELA-AU 9 140074593 140074593 single base substitution G A upstream_gene_variant MELA-AU 9 140074733 140074733 single base substitution G A downstream_gene_variant MELA-AU 9 140074733 140074733 single base substitution G A exon_variant MELA-AU 9 140074733 140074733 single base substitution G A missense_variant S597F 1790C>T MELA-AU 9 140074733 140074733 single base substitution G A upstream_gene_variant MELA-AU 9 140074760 140074760 single base substitution G A downstream_gene_variant MELA-AU 9 140074760 140074760 single base substitution G A exon_variant MELA-AU 9 140074760 140074760 single base substitution G A missense_variant P588L 1763C>T MELA-AU 9 140074760 140074760 single base substitution G A upstream_gene_variant MELA-AU 9 140075119 140075119 single base substitution G A downstream_gene_variant MELA-AU 9 140075119 140075119 single base substitution G A intron_variant MELA-AU 9 140075119 140075119 single base substitution G A upstream_gene_variant MELA-AU 9 140075126 140075126 single base substitution G A downstream_gene_variant MELA-AU 9 140075126 140075126 single base substitution G A intron_variant MELA-AU 9 140075126 140075126 single base substitution G A upstream_gene_variant MELA-AU 9 140075310 140075311 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 140075310 140075311 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant DL513DF MELA-AU 9 140075310 140075311 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 9 140075501 140075501 single base substitution G A downstream_gene_variant MELA-AU 9 140075501 140075501 single base substitution G A intron_variant MELA-AU 9 140075501 140075501 single base substitution G A upstream_gene_variant MELA-AU 9 140075590 140075590 single base substitution G A downstream_gene_variant MELA-AU 9 140075590 140075590 single base substitution G A intron_variant MELA-AU 9 140075590 140075590 single base substitution G A upstream_gene_variant MELA-AU 9 140075788 140075789 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 9 140075788 140075789 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 140075788 140075789 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 9 140075937 140075937 single base substitution G A downstream_gene_variant MELA-AU 9 140075937 140075937 single base substitution G A intron_variant MELA-AU 9 140075937 140075937 single base substitution G A upstream_gene_variant MELA-AU 9 140075974 140075974 single base substitution G A downstream_gene_variant MELA-AU 9 140075974 140075974 single base substitution G A intron_variant MELA-AU 9 140075974 140075974 single base substitution G A upstream_gene_variant MELA-AU 9 140076066 140076067 multiple base substitution (>=2bp and <=200bp) CC AT downstream_gene_variant MELA-AU 9 140076066 140076067 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 9 140076066 140076067 multiple base substitution (>=2bp and <=200bp) CC AT upstream_gene_variant MELA-AU 9 140077380 140077380 single base substitution G A intron_variant MELA-AU 9 140077380 140077380 single base substitution G A upstream_gene_variant MELA-AU 9 140077508 140077508 single base substitution C T intron_variant MELA-AU 9 140077508 140077508 single base substitution C T upstream_gene_variant MELA-AU 9 140077751 140077751 single base substitution G A exon_variant MELA-AU 9 140077751 140077751 single base substitution G A intron_variant MELA-AU 9 140077751 140077751 single base substitution G A upstream_gene_variant MELA-AU 9 140077771 140077771 single base substitution G A exon_variant MELA-AU 9 140077771 140077771 single base substitution G A intron_variant MELA-AU 9 140077771 140077771 single base substitution G A upstream_gene_variant MELA-AU 9 140078109 140078109 single base substitution G A intron_variant MELA-AU 9 140078109 140078109 single base substitution G A upstream_gene_variant MELA-AU 9 140078161 140078161 single base substitution G A exon_variant MELA-AU 9 140078161 140078161 single base substitution G A synonymous_variant S377S 1131C>T MELA-AU 9 140078161 140078161 single base substitution G A upstream_gene_variant MELA-AU 9 140078330 140078330 single base substitution G A intron_variant MELA-AU 9 140078330 140078330 single base substitution G A upstream_gene_variant MELA-AU 9 140079331 140079331 single base substitution G A intron_variant MELA-AU 9 140079331 140079331 single base substitution G A upstream_gene_variant MELA-AU 9 140079372 140079372 single base substitution G A exon_variant MELA-AU 9 140079372 140079372 single base substitution G A synonymous_variant I347I 1041C>T MELA-AU 9 140079372 140079372 single base substitution G A upstream_gene_variant MELA-AU 9 140079654 140079654 single base substitution C T intron_variant MELA-AU 9 140079654 140079654 single base substitution C T upstream_gene_variant MELA-AU 9 140079899 140079899 single base substitution G A intron_variant MELA-AU 9 140079899 140079899 single base substitution G A upstream_gene_variant MELA-AU 9 140079943 140079943 single base substitution G A intron_variant MELA-AU 9 140079943 140079943 single base substitution G A upstream_gene_variant MELA-AU 9 140080147 140080147 single base substitution G A intron_variant MELA-AU 9 140080147 140080147 single base substitution G A upstream_gene_variant MELA-AU 9 140080393 140080393 single base substitution C T intron_variant MELA-AU 9 140080393 140080393 single base substitution C T upstream_gene_variant MELA-AU 9 140080423 140080423 single base substitution G A intron_variant MELA-AU 9 140080423 140080423 single base substitution G A upstream_gene_variant MELA-AU 9 140081000 140081000 single base substitution G A intron_variant MELA-AU 9 140081000 140081000 single base substitution G A upstream_gene_variant MELA-AU 9 140081218 140081218 single base substitution G A intron_variant MELA-AU 9 140081218 140081218 single base substitution G A upstream_gene_variant MELA-AU 9 140081329 140081329 single base substitution A T intron_variant MELA-AU 9 140081329 140081329 single base substitution A T upstream_gene_variant MELA-AU 9 140082720 140082720 single base substitution G A intron_variant MELA-AU 9 140082720 140082720 single base substitution G A upstream_gene_variant MELA-AU 9 140084636 140084636 single base substitution C T upstream_gene_variant MELA-AU 9 140084745 140084745 single base substitution C T upstream_gene_variant MELA-AU 9 140084905 140084905 single base substitution G A upstream_gene_variant MELA-AU 9 140085466 140085466 single base substitution G A upstream_gene_variant MELA-AU 9 140086038 140086038 single base substitution C T upstream_gene_variant MELA-AU 9 140086680 140086680 single base substitution C A upstream_gene_variant MELA-AU 9 140086682 140086682 single base substitution C G upstream_gene_variant MELA-AU 9 140087459 140087459 single base substitution C T upstream_gene_variant MELA-AU 9 140087628 140087628 single base substitution A G upstream_gene_variant ORCA-IN 9 140072671 140072671 single base substitution G A downstream_gene_variant ORCA-IN 9 140072671 140072671 single base substitution G A intron_variant ORCA-IN 9 140072671 140072671 single base substitution G A upstream_gene_variant ORCA-IN 9 140083574 140083574 single base substitution G A upstream_gene_variant OV-AU 9 140069436 140069436 single base substitution G T downstream_gene_variant OV-AU 9 140069436 140069436 single base substitution G T exon_variant OV-AU 9 140069436 140069436 single base substitution G T synonymous_variant V809V 2427C>A OV-AU 9 140074570 140074570 single base substitution G A downstream_gene_variant OV-AU 9 140074570 140074570 single base substitution G A intron_variant OV-AU 9 140074570 140074570 single base substitution G A upstream_gene_variant OV-AU 9 140074668 140074686 deletion of <=200bp GGGCTGCCCTGATATCCTC - downstream_gene_variant OV-AU 9 140074668 140074686 deletion of <=200bp GGGCTGCCCTGATATCCTC - exon_variant OV-AU 9 140074668 140074686 deletion of <=200bp GGGCTGCCCTGATATCCTC - frameshift_variant EDIRAAL613 OV-AU 9 140074668 140074686 deletion of <=200bp GGGCTGCCCTGATATCCTC - upstream_gene_variant OV-AU 9 140076442 140076442 single base substitution G C intron_variant OV-AU 9 140076442 140076442 single base substitution G C upstream_gene_variant OV-AU 9 140077345 140077345 single base substitution C A intron_variant OV-AU 9 140077345 140077345 single base substitution C A upstream_gene_variant OV-AU 9 140077615 140077615 single base substitution G T exon_variant OV-AU 9 140077615 140077615 single base substitution G T synonymous_variant I416I 1248C>A OV-AU 9 140077615 140077615 single base substitution G T upstream_gene_variant OV-AU 9 140082816 140082816 single base substitution G C intron_variant OV-AU 9 140082816 140082816 single base substitution G C upstream_gene_variant OV-AU 9 140086863 140086863 single base substitution C A upstream_gene_variant PACA-AU 9 140065760 140065760 single base substitution A G downstream_gene_variant PACA-AU 9 140065809 140065809 single base substitution C T downstream_gene_variant PACA-AU 9 140074818 140074818 single base substitution G A downstream_gene_variant PACA-AU 9 140074818 140074818 single base substitution G A exon_variant PACA-AU 9 140074818 140074818 single base substitution G A missense_variant R569C 1705C>T PACA-AU 9 140074818 140074818 single base substitution G A upstream_gene_variant PACA-AU 9 140075292 140075292 single base substitution G A downstream_gene_variant PACA-AU 9 140075292 140075292 single base substitution G A missense_variant R520C 1558C>T PACA-AU 9 140075292 140075292 single base substitution G A upstream_gene_variant PACA-AU 9 140079817 140079817 single base substitution G C intron_variant PACA-AU 9 140079817 140079817 single base substitution G C upstream_gene_variant PACA-AU 9 140079825 140079825 single base substitution C T intron_variant PACA-AU 9 140079825 140079825 single base substitution C T upstream_gene_variant PACA-AU 9 140082928 140082928 single base substitution C A missense_variant E19D 57G>T PACA-AU 9 140082928 140082928 single base substitution C A upstream_gene_variant PACA-AU 9 140086380 140086380 single base substitution G A upstream_gene_variant PACA-CA 9 140064973 140064973 deletion of <=200bp C - downstream_gene_variant PACA-CA 9 140066906 140066906 single base substitution C T downstream_gene_variant PACA-CA 9 140068006 140068006 single base substitution C T downstream_gene_variant PACA-CA 9 140074828 140074828 single base substitution C T downstream_gene_variant PACA-CA 9 140074828 140074828 single base substitution C T exon_variant PACA-CA 9 140074828 140074828 single base substitution C T synonymous_variant A565A 1695G>A PACA-CA 9 140074828 140074828 single base substitution C T upstream_gene_variant PACA-CA 9 140075182 140075182 single base substitution A G downstream_gene_variant PACA-CA 9 140075182 140075182 single base substitution A G intron_variant PACA-CA 9 140075182 140075182 single base substitution A G upstream_gene_variant PACA-CA 9 140078352 140078352 single base substitution G T intron_variant PACA-CA 9 140078352 140078352 single base substitution G T upstream_gene_variant PACA-CA 9 140085557 140085557 single base substitution G A upstream_gene_variant PAEN-AU 9 140066827 140066827 single base substitution A G downstream_gene_variant PAEN-AU 9 140076531 140076531 single base substitution C T intron_variant PAEN-AU 9 140076531 140076531 single base substitution C T upstream_gene_variant PBCA-DE 9 140073376 140073376 single base substitution G A downstream_gene_variant PBCA-DE 9 140073376 140073376 single base substitution G A intron_variant PBCA-DE 9 140073376 140073376 single base substitution G A upstream_gene_variant PBCA-DE 9 140078937 140078937 single base substitution C G intron_variant PBCA-DE 9 140078937 140078937 single base substitution C G upstream_gene_variant PBCA-DE 9 140080911 140080912 deletion of <=200bp CA - exon_variant PBCA-DE 9 140080911 140080912 deletion of <=200bp CA - intron_variant PBCA-DE 9 140080911 140080912 deletion of <=200bp CA - upstream_gene_variant PBCA-DE 9 140086243 140086243 single base substitution G C upstream_gene_variant PRAD-CA 9 140071935 140071935 single base substitution A C downstream_gene_variant PRAD-CA 9 140071935 140071935 single base substitution A C intron_variant PRAD-CA 9 140071935 140071935 single base substitution A C upstream_gene_variant PRAD-CA 9 140078645 140078645 single base substitution C A intron_variant PRAD-CA 9 140078645 140078645 single base substitution C A upstream_gene_variant PRAD-CA 9 140084376 140084376 single base substitution G A upstream_gene_variant PRAD-US 9 140070252 140070252 single base substitution A G exon_variant PRAD-US 9 140070252 140070252 single base substitution A G missense_variant L643P 1928T>C PRAD-US 9 140086590 140086590 single base substitution G A upstream_gene_variant READ-US 9 140082199 140082199 single base substitution G A synonymous_variant R158R 474C>T READ-US 9 140082199 140082199 single base substitution G A upstream_gene_variant RECA-EU 9 140068518 140068518 single base substitution G A downstream_gene_variant RECA-EU 9 140071404 140071404 single base substitution G A downstream_gene_variant RECA-EU 9 140071404 140071404 single base substitution G A exon_variant RECA-EU 9 140071404 140071404 single base substitution G A intron_variant RECA-EU 9 140071404 140071404 single base substitution G A upstream_gene_variant RECA-EU 9 140087550 140087550 single base substitution T C upstream_gene_variant SKCA-BR 9 140064666 140064666 single base substitution A C downstream_gene_variant SKCA-BR 9 140064967 140064967 single base substitution A C downstream_gene_variant SKCA-BR 9 140065769 140065769 single base substitution A C downstream_gene_variant SKCA-BR 9 140067084 140067084 single base substitution T C downstream_gene_variant SKCA-BR 9 140067543 140067543 single base substitution T G downstream_gene_variant SKCA-BR 9 140071541 140071541 single base substitution A G downstream_gene_variant SKCA-BR 9 140071541 140071541 single base substitution A G intron_variant SKCA-BR 9 140071541 140071541 single base substitution A G upstream_gene_variant SKCA-BR 9 140071764 140071765 deletion of <=200bp TG - downstream_gene_variant SKCA-BR 9 140071764 140071765 deletion of <=200bp TG - intron_variant SKCA-BR 9 140071764 140071765 deletion of <=200bp TG - upstream_gene_variant SKCA-BR 9 140071766 140071766 insertion of <=200bp - TGGGACCTGCCAA downstream_gene_variant SKCA-BR 9 140071766 140071766 insertion of <=200bp - TGGGACCTGCCAA intron_variant SKCA-BR 9 140071766 140071766 insertion of <=200bp - TGGGACCTGCCAA upstream_gene_variant SKCA-BR 9 140075200 140075200 single base substitution C A downstream_gene_variant SKCA-BR 9 140075200 140075200 single base substitution C A intron_variant SKCA-BR 9 140075200 140075200 single base substitution C A upstream_gene_variant SKCA-BR 9 140076385 140076385 single base substitution T C intron_variant SKCA-BR 9 140076385 140076385 single base substitution T C upstream_gene_variant SKCA-BR 9 140079093 140079114 deletion of <=200bp GCACAGGGAGCCCAGACGCAGA - intron_variant SKCA-BR 9 140079093 140079114 deletion of <=200bp GCACAGGGAGCCCAGACGCAGA - upstream_gene_variant SKCA-BR 9 140080499 140080499 single base substitution A G intron_variant SKCA-BR 9 140080499 140080499 single base substitution A G upstream_gene_variant SKCA-BR 9 140082090 140082090 single base substitution T C missense_variant T195A 583A>G SKCA-BR 9 140082090 140082090 single base substitution T C upstream_gene_variant SKCA-BR 9 140082562 140082562 single base substitution T G splice_region_variant SKCA-BR 9 140082562 140082562 single base substitution T G upstream_gene_variant SKCA-BR 9 140085030 140085030 single base substitution G A upstream_gene_variant SKCM-US 9 140074636 140074636 single base substitution G A downstream_gene_variant SKCM-US 9 140074636 140074636 single base substitution G A exon_variant SKCM-US 9 140074636 140074636 single base substitution G A synonymous_variant L629L 1887C>T SKCM-US 9 140074636 140074636 single base substitution G A upstream_gene_variant SKCM-US 9 140074659 140074659 single base substitution A G downstream_gene_variant SKCM-US 9 140074659 140074659 single base substitution A G exon_variant SKCM-US 9 140074659 140074659 single base substitution A G missense_variant Y622H 1864T>C SKCM-US 9 140074659 140074659 single base substitution A G upstream_gene_variant SKCM-US 9 140075357 140075357 single base substitution G A downstream_gene_variant SKCM-US 9 140075357 140075357 single base substitution G A missense_variant S498L 1493C>T SKCM-US 9 140075357 140075357 single base substitution G A upstream_gene_variant SKCM-US 9 140076234 140076234 single base substitution A G downstream_gene_variant SKCM-US 9 140076234 140076234 single base substitution A G exon_variant SKCM-US 9 140076234 140076234 single base substitution A G missense_variant L456P 1367T>C SKCM-US 9 140076234 140076234 single base substitution A G upstream_gene_variant SKCM-US 9 140077625 140077625 single base substitution G A exon_variant SKCM-US 9 140077625 140077625 single base substitution G A missense_variant S413F 1238C>T SKCM-US 9 140077625 140077625 single base substitution G A upstream_gene_variant SKCM-US 9 140079372 140079372 single base substitution G A exon_variant SKCM-US 9 140079372 140079372 single base substitution G A synonymous_variant I347I 1041C>T SKCM-US 9 140079372 140079372 single base substitution G A upstream_gene_variant SKCM-US 9 140079394 140079394 single base substitution C T exon_variant SKCM-US 9 140079394 140079394 single base substitution C T missense_variant R340H 1019G>A SKCM-US 9 140079394 140079394 single base substitution C T upstream_gene_variant SKCM-US 9 140082095 140082095 single base substitution C T missense_variant G193E 578G>A SKCM-US 9 140082095 140082095 single base substitution C T upstream_gene_variant SKCM-US 9 140082264 140082264 single base substitution G A missense_variant R137C 409C>T SKCM-US 9 140082264 140082264 single base substitution G A upstream_gene_variant SKCM-US 9 140082963 140082963 single base substitution C A missense_variant A8S 22G>T SKCM-US 9 140082963 140082963 single base substitution C A upstream_gene_variant SKCM-US 9 140083669 140083669 single base substitution C A upstream_gene_variant SKCM-US 9 140086682 140086682 single base substitution C G upstream_gene_variant STAD-US 9 140069716 140069716 single base substitution C A downstream_gene_variant STAD-US 9 140069716 140069716 single base substitution C A exon_variant STAD-US 9 140069716 140069716 single base substitution C A missense_variant Q743H 2229G>T STAD-US 9 140069815 140069815 deletion of <=200bp G - exon_variant STAD-US 9 140069815 140069815 deletion of <=200bp G - frameshift_variant P710 STAD-US 9 140074684 140074684 single base substitution C A downstream_gene_variant STAD-US 9 140074684 140074684 single base substitution C A exon_variant STAD-US 9 140074684 140074684 single base substitution C A missense_variant E613D 1839G>T STAD-US 9 140074684 140074684 single base substitution C A upstream_gene_variant STAD-US 9 140077586 140077586 single base substitution C T exon_variant STAD-US 9 140077586 140077586 single base substitution C T missense_variant R426H 1277G>A STAD-US 9 140077586 140077586 single base substitution C T upstream_gene_variant STAD-US 9 140079368 140079368 single base substitution G A exon_variant STAD-US 9 140079368 140079368 single base substitution G A stop_gained R349* 1045C>T STAD-US 9 140079368 140079368 single base substitution G A upstream_gene_variant STAD-US 9 140079432 140079432 single base substitution G A exon_variant STAD-US 9 140079432 140079432 single base substitution G A synonymous_variant H327H 981C>T STAD-US 9 140079432 140079432 single base substitution G A upstream_gene_variant STAD-US 9 140080740 140080740 single base substitution C T exon_variant STAD-US 9 140080740 140080740 single base substitution C T missense_variant R270Q 809G>A STAD-US 9 140080740 140080740 single base substitution C T upstream_gene_variant STAD-US 9 140082263 140082263 single base substitution C T missense_variant R137H 410G>A STAD-US 9 140082263 140082263 single base substitution C T upstream_gene_variant STAD-US 9 140086680 140086680 deletion of <=200bp C - upstream_gene_variant STAD-US 9 140086686 140086686 single base substitution A G upstream_gene_variant STAD-US 9 140087050 140087050 single base substitution C G upstream_gene_variant THCA-SA 9 140079404 140079404 single base substitution C T exon_variant THCA-SA 9 140079404 140079404 single base substitution C T missense_variant A337T 1009G>A THCA-SA 9 140079404 140079404 single base substitution C T upstream_gene_variant UCEC-US 9 140070239 140070239 single base substitution G A exon_variant UCEC-US 9 140070239 140070239 single base substitution G A synonymous_variant D647D 1941C>T UCEC-US 9 140075291 140075291 single base substitution C T downstream_gene_variant UCEC-US 9 140075291 140075291 single base substitution C T missense_variant R520H 1559G>A UCEC-US 9 140075291 140075291 single base substitution C T upstream_gene_variant UCEC-US 9 140075360 140075360 single base substitution C T downstream_gene_variant UCEC-US 9 140075360 140075360 single base substitution C T missense_variant R497H 1490G>A UCEC-US 9 140075360 140075360 single base substitution C T upstream_gene_variant UCEC-US 9 140076140 140076140 single base substitution G A downstream_gene_variant UCEC-US 9 140076140 140076140 single base substitution G A exon_variant UCEC-US 9 140076140 140076140 single base substitution G A synonymous_variant A487A 1461C>T UCEC-US 9 140076140 140076140 single base substitution G A upstream_gene_variant UCEC-US 9 140076259 140076259 single base substitution C T downstream_gene_variant UCEC-US 9 140076259 140076259 single base substitution C T exon_variant UCEC-US 9 140076259 140076259 single base substitution C T missense_variant G448R 1342G>A UCEC-US 9 140076259 140076259 single base substitution C T upstream_gene_variant UCEC-US 9 140076277 140076277 single base substitution G A exon_variant UCEC-US 9 140076277 140076277 single base substitution G A synonymous_variant L442L 1324C>T UCEC-US 9 140076277 140076277 single base substitution G A upstream_gene_variant UCEC-US 9 140077668 140077668 single base substitution G T exon_variant UCEC-US 9 140077668 140077668 single base substitution G T missense_variant L399I 1195C>A UCEC-US 9 140077668 140077668 single base substitution G T upstream_gene_variant UCEC-US 9 140079394 140079394 single base substitution C T exon_variant UCEC-US 9 140079394 140079394 single base substitution C T missense_variant R340H 1019G>A UCEC-US 9 140079394 140079394 single base substitution C T upstream_gene_variant UCEC-US 9 140079477 140079477 single base substitution G A exon_variant UCEC-US 9 140079477 140079477 single base substitution G A synonymous_variant P312P 936C>T UCEC-US 9 140079477 140079477 single base substitution G A upstream_gene_variant UCEC-US 9 140080712 140080712 single base substitution G A exon_variant UCEC-US 9 140080712 140080712 single base substitution G A synonymous_variant G279G 837C>T UCEC-US 9 140080712 140080712 single base substitution G A upstream_gene_variant UCEC-US 9 140082279 140082279 single base substitution G T missense_variant L132M 394C>A UCEC-US 9 140082279 140082279 single base substitution G T upstream_gene_variant UCEC-US 9 140082343 140082343 single base substitution T C synonymous_variant L110L 330A>G UCEC-US 9 140082343 140082343 single base substitution T C upstream_gene_variant UCEC-US 9 140087025 140087027 deletion of <=200bp TCC - upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand ESCC_86 COSM5636560 c.6667C>A p.L2223I Substitution - Missense 19:1469968-1469968 + TCGA-CZ-4853-01 COSM487258 c.1543T>A p.F515I Substitution - Missense 9:137180855-137180855 - PTC_448 COSM5747104 c.1009G>A p.A337T Substitution - Missense 9:137184952-137184952 - TCGA-06-2569-01 COSM3413483 c.1788G>T p.L596L Substitution - coding silent 9:137180283-137180283 - TCGA-K4-A3WU-01 COSM3779858 c.1405G>A p.D469N Substitution - Missense 9:137181744-137181744 - HCC107 COSM1611676 c.4633C>T p.R1545W Substitution - Missense 19:1467934-1467934 + SS6003111 COSM3849412 c.185T>C p.L62P Substitution - Missense 9:137188036-137188036 - MO_1012 COSM5566114 c.1363C>A p.R455R Substitution - coding silent 19:1460240-1460240 + YUKLAB COSM1701978 c.1349G>A p.G450E Substitution - Missense 9:137181800-137181800 - ESCC_35 COSM5628723 c.217G>C p.E73Q Substitution - Missense 9:137188004-137188004 - pfg034T COSM4762012 c.2046C>G p.S682R Substitution - Missense 9:137175447-137175447 - TCGA-22-5473-01 COSM709776 c.5199C>G p.P1733P Substitution - coding silent 19:1468500-1468500 + TCGA-G2-A2EJ-01 COSM1304092 c.859G>A p.D287N Substitution - Missense 19:1456895-1456895 + HCC28T COSM1611678 c.6783C>T p.H2261H Substitution - coding silent 19:1470084-1470084 + TCGA-AP-A059-01 COSM1107063 c.394C>A p.L132M Substitution - Missense 9:137187827-137187827 - TCGA-A6-6781-01 COSM1390903 c.1388G>A p.R463H Substitution - Missense 19:1460265-1460265 + HCT15 COSM4632758 c.4542G>A p.S1514S Substitution - coding silent 19:1467843-1467843 + RKO COSM4614830 c.1167_1180del14 p.D392fs*28 Deletion - Frameshift 19:1457203-1457216 + TCGA-RP-A695-06 COSM4896981 c.2436G>A p.Q812Q Substitution - coding silent 19:1465737-1465737 + 01-P1216 COSM4588655 c.2170C>T p.R724W Substitution - Missense 9:137175323-137175323 - STC232 COSM5063796 c.2116C>T p.R706C Substitution - Missense 9:137175377-137175377 - TCGA-CG-5728-01 COSM4074848 c.5167G>A p.G1723R Substitution - Missense 19:1468468-1468468 + TCGA-21-1078-01 COSM709774 c.6800C>T p.S2267L Substitution - Missense 19:1470101-1470101 + TCGA-AB-2807-03 COSM1319629 c.868C>A p.H290N Substitution - Missense 9:137186229-137186229 - CHC1725T COSM4800725 c.6230C>G p.T2077S Substitution - Missense 19:1469531-1469531 + TCGA-BR-4184-01 COSM3282178 c.1431C>T p.D477D Substitution - coding silent 19:1460308-1460308 + ESO-049 COSM1244924 c.808C>T p.R270W Substitution - Missense 9:137186289-137186289 - T3091 COSM4662413 c.1666G>A p.A556T Substitution - Missense 19:1461990-1461990 + C0055T COSM4422741 c.3334A>T p.S1112C Substitution - Missense 19:1466635-1466635 + TCGA-FU-A3HZ-01 COSM4838814 c.1705G>A p.A569T Substitution - Missense 19:1462029-1462029 + TCGA-AA-3492-01 COSM5096849 c.5670delC p.P1892fs*104 Deletion - Frameshift 19:1468971-1468971 + I2L-P6-Tumor-Biopsy COSM5359521 c.1274G>A p.R425H Substitution - Missense 9:137183137-137183137 - C086 COSM3282173 c.1316C>T p.A439V Substitution - Missense 19:1460193-1460193 + TCGA-BR-6452-01 COSM4074832 c.1838C>T p.T613I Substitution - Missense 19:1462162-1462162 + TCGA-GN-A266-06 COSM3655960 c.1864T>C p.Y622H Substitution - Missense 9:137180207-137180207 - TCGA-EE-A29V-06 COSM3529364 c.2326G>A p.G776S Substitution - Missense 19:1465627-1465627 + TCGA-EE-A2MI-06 COSM3655965 c.578G>A p.G193E Substitution - Missense 9:137187643-137187643 - TCGA-A6-6780-01 COSM5093201 c.3541C>T p.P1181S Substitution - Missense 19:1466842-1466842 + 2334199 COSM318673 c.1380C>A p.D460E Substitution - Missense 9:137181769-137181769 - CHC304T COSM4788508 c.988A>C p.R330R Substitution - coding silent 9:137184973-137184973 - GCT44 COSM5749812 c.446_448delAGA p.K150delK Deletion - In frame 19:1455181-1455183 + CSCC-35-T COSM4536784 c.2344G>A p.V782M Substitution - Missense 9:137175067-137175067 - ccRCC-99 COSM1660569 c.2632G>A p.D878N Substitution - Missense 19:1465933-1465933 + 1_PRE-TREATMENT COSM1718060 c.4825G>A p.D1609N Substitution - Missense 19:1468126-1468126 + TCGA-AA-3710-01 COSM5105746 c.906G>T p.K302N Substitution - Missense 9:137185055-137185055 - TCGA-AA-A03F-01 COSM301088 c.1487G>A p.R496Q Substitution - Missense 9:137180911-137180911 - CRC-02T COSM5455765 c.1065G>A p.R355R Substitution - coding silent 9:137183775-137183775 - CSCC-41-T COSM4528108 c.1510G>C p.E504Q Substitution - Missense 19:1460846-1460846 + TCGA-CD-A4MG-01 COSM4074847 c.5160C>T p.F1720F Substitution - coding silent 19:1468461-1468461 + 587224 COSM1182715 c.967C>T p.R323C Substitution - Missense 9:137184994-137184994 - TCGA-BR-6706-01 COSM4074837 c.2345A>G p.D782G Substitution - Missense 19:1465646-1465646 + TCGA-AA-3510-01 COSM1461337 c.244G>A p.D82N Substitution - Missense 9:137187977-137187977 - LS513 COSM3088781 c.1215G>A p.K405K Substitution - coding silent 9:137183196-137183196 - OVCAR-4 COSM1166671 c.982G>A p.V328M Substitution - Missense 9:137184979-137184979 - BN24 COSM1624777 c.2039A>T p.E680V Substitution - Missense 9:137175454-137175454 - CHC2200T COSM4952923 c.2055G>T p.V685V Substitution - coding silent 9:137175438-137175438 - T3724 COSM3088760 c.2130delC p.G711fs*52 Deletion - Frameshift 9:137175363-137175363 - TCGA-32-4208-01 COSM3403832 c.5347G>A p.G1783R Substitution - Missense 19:1468648-1468648 + TCGA-AA-3941-01 COSM296739 c.1211C>T p.P404L Substitution - Missense 19:1457968-1457968 + I2L-P19Ta-Tumor-Organoid COSM3088760 c.2130delC p.G711fs*52 Deletion - Frameshift 9:137175363-137175363 - AOCS-116-1-3 COSM4140316 c.981G>C p.A327A Substitution - coding silent 19:1457017-1457017 + 0109_CRUK_PC_0109_T1_DNA COSM5422332 c.6002C>G p.S2001W Substitution - Missense 19:1469303-1469303 + TCGA-DY-A1DD-01 COSM1569354 c.474C>T p.R158R Substitution - coding silent 9:137187747-137187747 - TCGA-E2-A1IN-01 COSM1480682 c.2471G>A p.R824Q Substitution - Missense 19:1465772-1465772 + SNU-C2B COSM4615282 c.4465delG p.D1490fs*90 Deletion - Frameshift 19:1467766-1467766 + DN14012 COSM5961253 c.3831C>T p.S1277S Substitution - coding silent 19:1467132-1467132 + 46M COSM5587169 c.1834C>T p.P612S Substitution - Missense 9:137180237-137180237 - LUAD-E00934 COSM403449 c.2220G>C p.M740I Substitution - Missense 9:137175273-137175273 - TCGA-AY-6197-01 COSM1461334 c.1445C>T p.P482L Substitution - Missense 9:137181704-137181704 - TCGA-EE-A3JD-06 COSM4395305 c.1887C>T p.L629L Substitution - coding silent 9:137180184-137180184 - TCGA-WS-AB45-01 COSM5190376 c.2971C>T p.R991C Substitution - Missense 19:1466272-1466272 + ATL053 COSM5711239 c.1048+1G>A p.? Unknown 9:137184912-137184912 - CHEWS004 COSM4580695 c.6G>A p.A2A Substitution - coding silent 19:1453007-1453007 + PTC-7C COSM4131288 c.4384A>C p.R1462R Substitution - coding silent 19:1467685-1467685 + ID46 COSM1166652 c.20T>C p.V7A Substitution - Missense 9:137188513-137188513 - HX13T COSM1624778 c.1225G>A p.V409M Substitution - Missense 9:137183186-137183186 - HCC4T COSM1624778 c.1225G>A p.V409M Substitution - Missense 9:137183186-137183186 - BD135T COSM5516508 c.1225delG p.V409fs*20 Deletion - Frameshift 9:137183186-137183186 - TCGA-BP-4976-01 COSM474238 c.373C>T p.R125W Substitution - Missense 19:1453571-1453571 + TCGA-BP-4782-01 COSM474242 c.1534A>G p.I512V Substitution - Missense 19:1461049-1461049 + sysucc-1317T COSM5450555 c.656C>A p.P219Q Substitution - Missense 9:137187565-137187565 - MO_1184 COSM5567079 c.2861G>A p.R954H Substitution - Missense 19:1466162-1466162 + AOCS-137-1-X COSM4152191 c.2427C>A p.V809V Substitution - coding silent 9:137174984-137174984 - 8035603 COSM3395690 c.1705C>T p.R569C Substitution - Missense 9:137180366-137180366 - OSCC-GB_00160111 COSM3712813 c.3205C>T p.R1069* Substitution - Nonsense 19:1466506-1466506 + TCGA-LP-A7HU-01 COSM4825717 c.2380G>A p.E794K Substitution - Missense 9:137175031-137175031 - CHC1725T COSM4800725 c.6230C>G p.T2077S Substitution - Missense 19:1469531-1469531 + HCC137T COSM1611677 c.4766C>T p.P1589L Substitution - Missense 19:1468067-1468067 + SC_9047 COSM5550477 c.2250C>T p.A750A Substitution - coding silent 19:1465551-1465551 + CSCC-44-T COSM4516304 c.1768_1769GG>AA p.G590K Substitution - Missense 9:137180302-137180303 - TCGA-BR-7703-01 COSM4074831 c.1432G>A p.V478I Substitution - Missense 19:1460309-1460309 + TCGA-AA-3672-01 COSM5102393 c.1795A>G p.S599G Substitution - Missense 19:1462119-1462119 + TCGA-EA-A5FO-01 COSM4851823 c.167G>A p.R56Q Substitution - Missense 9:137188054-137188054 - YUOMEGA COSM5410803 c.926C>T p.P309L Substitution - Missense 9:137185035-137185035 - TCGA-AA-3833-01 COSM5112368 c.1934C>T p.A645V Substitution - Missense 19:1465235-1465235 + DN12171 COSM5767635 c.6580G>T p.E2194* Substitution - Nonsense 19:1469881-1469881 + ESCC_50 COSM5630955 c.1023C>T p.I341I Substitution - coding silent 9:137184938-137184938 - HCT15 COSM4632759 c.6597C>T p.P2199P Substitution - coding silent 19:1469898-1469898 + TCGA-AZ-6605-01 COSM5143104 c.1854-1G>A p.? Unknown 19:1465154-1465154 + TCGA-ER-A3EV-06 COSM3282228 c.1972C>T p.R658C Substitution - Missense 19:1465273-1465273 + TCGA-ER-A19D-06 COSM3655964 c.1041C>T p.I347I Substitution - coding silent 9:137184920-137184920 - 8064632 COSM1733245 c.1558C>T p.R520C Substitution - Missense 9:137180840-137180840 - B104 COSM1750683 c.1628G>A p.R543Q Substitution - Missense 19:1461143-1461143 + TCGA-EE-A2GP-06 COSM1107060 c.1019G>A p.R340H Substitution - Missense 9:137184942-137184942 - CLL118 COSM1290876 c.2335_2337delGAC p.D782delD Deletion - In frame 19:1465636-1465638 + ASHPC_0009_Pa_P COSM3787562 c.12C>T p.S4S Substitution - coding silent 19:1453013-1453013 + T3151 COSM4662418 c.6724delG p.A2242fs*>62 Deletion - Frameshift 19:1470025-1470025 + YUKADI COSM1701977 c.1603_1604CC>TT p.P535F Substitution - Missense 9:137180794-137180795 - T3306 COSM4661482 c.1602C>T p.S534S Substitution - coding silent 9:137180796-137180796 - T3155 COSM4662419 c.6783delC p.H2261fs*>43 Deletion - Frameshift 19:1470084-1470084 + 37M COSM5583277 c.3542C>T p.P1181L Substitution - Missense 19:1466843-1466843 + TCGA-G4-6298-01 COSM3422466 c.5778G>A p.S1926S Substitution - coding silent 19:1469079-1469079 + ESCC_74 COSM5634737 c.2838G>A p.P946P Substitution - coding silent 19:1466139-1466139 + TCGA-EB-A5UN-06 COSM3529366 c.2997T>A p.Y999* Substitution - Nonsense 19:1466298-1466298 + CHC892T COSM4959900 c.4937G>A p.G1646D Substitution - Missense 19:1468238-1468238 + TCGA-AG-4022-01 COSM3749467 c.5730A>G p.K1910K Substitution - coding silent 19:1469031-1469031 + PD13608a COSM5767635 c.6580G>T p.E2194* Substitution - Nonsense 19:1469881-1469881 + CSCC-6-T COSM4529762 c.163G>A p.G55R Substitution - Missense 19:1453268-1453268 + T256 COSM4662416 c.4652C>T p.P1551L Substitution - Missense 19:1467953-1467953 + TCGA-D1-A176-01 COSM1107056 c.1461C>T p.A487A Substitution - coding silent 9:137181688-137181688 - 409 COSM4430683 c.3348G>T p.A1116A Substitution - coding silent 19:1466649-1466649 + TCGA-FS-A1ZA-06 COSM3529360 c.1376A>G p.N459S Substitution - Missense 19:1460253-1460253 + TCGA-E2-A2P6-01 COSM3822118 c.5132C>A p.S1711* Substitution - Nonsense 19:1468433-1468433 + pfg008T COSM1643785 c.845A>G p.E282G Substitution - Missense 9:137186252-137186252 - 66 COSM5743919 c.4291C>T p.R1431C Substitution - Missense 19:1467592-1467592 + AOCS-120-3-6 COSM4152192 c.1248C>A p.I416I Substitution - coding silent 9:137183163-137183163 - TCGA-G9-6342-01 COSM3675299 c.617G>T p.R206L Substitution - Missense 9:137187604-137187604 - RKO COSM4648203 c.1969G>A p.A657T Substitution - Missense 19:1465270-1465270 + TCGA-EB-A5SF-01 COSM3926486 c.22G>T p.A8S Substitution - Missense 9:137188511-137188511 - ATL052 COSM5706875 c.4292G>A p.R1431H Substitution - Missense 19:1467593-1467593 + ESO-708 COSM1244925 c.1897C>T p.R633W Substitution - Missense 9:137175831-137175831 - ESO-859 COSM1238202 c.2648C>T p.A883V Substitution - Missense 19:1465949-1465949 + T368 COSM3282290 c.6759delG p.G2255fs*>49 Deletion - Frameshift 19:1470060-1470060 + ESCC_BICR_018T COSM5429069 c.3940C>T p.H1314Y Substitution - Missense 19:1467241-1467241 + HCC53T COSM1624776 c.2387A>T p.Q796L Substitution - Missense 9:137175024-137175024 - 0065_CRUK_PC_0065_T1_DNA COSM4413716 c.2997T>G p.Y999* Substitution - Nonsense 19:1466298-1466298 + AOCS-137-3-7 COSM4152191 c.2427C>A p.V809V Substitution - coding silent 9:137174984-137174984 - T578 COSM4662411 c.254G>T p.S85I Substitution - Missense 19:1453452-1453452 + TCGA-FW-A3R5-06 COSM3891655 c.1099G>A p.E367K Substitution - Missense 19:1457135-1457135 + PCSI_0142_Pa_P_526 COSM4808351 c.3951G>T p.G1317G Substitution - coding silent 19:1467252-1467252 + CCK81 COSM1166671 c.982G>A p.V328M Substitution - Missense 9:137184979-137184979 - pfg059T COSM4762013 c.1042G>A p.V348I Substitution - Missense 9:137184919-137184919 - 25_tFL COSM4170982 c.1657G>A p.V553M Substitution - Missense 19:1461981-1461981 + TCGA-A6-5661-01 COSM1390922 c.3639G>A p.T1213T Substitution - coding silent 19:1466940-1466940 + TCGA-DK-A3X1-01 COSM3796709 c.3622C>G p.P1208A Substitution - Missense 19:1466923-1466923 + TCGA-HU-8602-01 COSM3282177 c.1397C>T p.A466V Substitution - Missense 19:1460274-1460274 + 474 COSM4438325 c.2205G>C p.E735D Substitution - Missense 9:137175288-137175288 - CoCM-1 COSM4621063 c.1804G>A p.G602S Substitution - Missense 19:1462128-1462128 + TCGA-WS-AB45-01 COSM5192119 c.775G>A p.E259K Substitution - Missense 9:137186322-137186322 - pfg122T COSM3282235 c.2587G>A p.A863T Substitution - Missense 19:1465888-1465888 + PCSI_0508_Pa_P_526 COSM4964630 c.4706T>C p.I1569T Substitution - Missense 19:1468007-1468007 + CHC892T COSM4798323 c.10G>A p.A4T Substitution - Missense 9:137188523-137188523 - HCT15 COSM4632760 c.6625C>G p.L2209V Substitution - Missense 19:1469926-1469926 + SNUH_G14_S1 COSM3685552 c.2080C>T p.R694W Substitution - Missense 9:137175413-137175413 - ATL009 COSM5706872 c.1067T>G p.F356C Substitution - Missense 19:1457103-1457103 + TCGA-D5-6928-01 COSM5165311 c.2520_2525delGGCCAA p.A845_K846delAK Deletion - In frame 19:1465821-1465826 + S01297 COSM5667815 c.1072A>T p.I358F Substitution - Missense 9:137183768-137183768 - T28 COSM5619171 c.891C>T p.V297V Substitution - coding silent 9:137185070-137185070 - ID39 COSM1166671 c.982G>A p.V328M Substitution - Missense 9:137184979-137184979 - T3064 COSM4662412 c.645C>T p.R215R Substitution - coding silent 19:1456081-1456081 + TCGA-RU-A8FL-01 COSM5188491 c.3444G>A p.S1148S Substitution - coding silent 19:1466745-1466745 + TCGA-IH-A3EA-01 COSM3529362 c.1536C>T p.I512I Substitution - coding silent 19:1461051-1461051 + 61 COSM5741323 c.4513G>T p.A1505S Substitution - Missense 19:1467814-1467814 + CHC304T COSM4788508 c.988A>C p.R330R Substitution - coding silent 9:137184973-137184973 - TCGA-DD-A4NN-01 COSM4935249 c.729G>A p.A243A Substitution - coding silent 19:1456317-1456317 + OSCC-GB_00730111 COSM4888916 c.3555C>A p.C1185* Substitution - Nonsense 19:1466856-1466856 + BN32T COSM1624779 c.908T>G p.V303G Substitution - Missense 9:137185053-137185053 - TCGA-IR-A3LH-01 COSM4832547 c.500G>A p.R167K Substitution - Missense 9:137187721-137187721 - TCGA-BG-A0VZ-01 COSM1107057 c.1342G>A p.G448R Substitution - Missense 9:137181807-137181807 - 19 COSM5747104 c.1009G>A p.A337T Substitution - Missense 9:137184952-137184952 - TCGA-EE-A2MJ-06 COSM3655961 c.1493C>T p.S498L Substitution - Missense 9:137180905-137180905 - T2997 COSM4661483 c.1385C>T p.A462V Substitution - Missense 9:137181764-137181764 - sysucc-1317T COSM5449194 c.1285C>T p.R429C Substitution - Missense 19:1458042-1458042 + TCGA-EB-A44O-01 COSM3655966 c.409C>T p.R137C Substitution - Missense 9:137187812-137187812 - TCGA-AP-A0LM-01 COSM1107054 c.1559G>A p.R520H Substitution - Missense 9:137180839-137180839 - TCGA-AX-A1C8-01 COSM1107061 c.936C>T p.P312P Substitution - coding silent 9:137185025-137185025 - Pat_76_B COSM5875926 c.2152G>A p.E718K Substitution - Missense 9:137175341-137175341 - Pat_76_A COSM5875929 c.1235C>T p.P412L Substitution - Missense 9:137183176-137183176 - SNU-C2B COSM4615281 c.3667delC p.E1225fs*13 Deletion - Frameshift 19:1466968-1466968 + BD124T COSM5492616 c.1618C>T p.R540C Substitution - Missense 9:137180520-137180520 - SNU-175 COSM3088775 c.1382C>T p.P461L Substitution - Missense 9:137181767-137181767 - SNU-175 COSM3282192 c.1665C>T p.S555S Substitution - coding silent 19:1461989-1461989 + BD6T COSM5499337 c.1834G>A p.A612T Substitution - Missense 19:1462158-1462158 + TCGA-CK-6748-01 COSM5155821 c.1064T>C p.V355A Substitution - Missense 19:1457100-1457100 + QC2-32-T2 COSM4074847 c.5160C>T p.F1720F Substitution - coding silent 19:1468461-1468461 + LS180 COSM4646266 c.1035G>A p.M345I Substitution - Missense 19:1457071-1457071 + TCGA-AO-A128-01 COSM3822116 c.1390C>A p.R464S Substitution - Missense 19:1460267-1460267 + TCGA-25-2401-01 COSM69631 c.1875G>T p.K625N Substitution - Missense 9:137180196-137180196 - TCGA-HU-8245-01 COSM4074838 c.2723G>A p.R908Q Substitution - Missense 19:1466024-1466024 + TCGA-G4-6320-01 COSM3692413 c.333C>T p.H111H Substitution - coding silent 19:1453531-1453531 + 169 COSM3728719 c.1770G>A p.Q590Q Substitution - coding silent 19:1462094-1462094 + AD67 COSM5966681 c.567_596del30 p.F189_E199>L Complex - deletion inframe 19:1455428-1455457 + TCGA-66-2794-01 COSM753060 c.1404G>A p.Q468Q Substitution - coding silent 9:137181745-137181745 - TCGA-AP-A054-01 COSM1107064 c.330A>G p.L110L Substitution - coding silent 9:137187891-137187891 - TCGA-A5-A0R8-01 COSM1107055 c.1490G>A p.R497H Substitution - Missense 9:137180908-137180908 - sysucc-1450T COSM5480232 c.4371C>T p.G1457G Substitution - coding silent 19:1467672-1467672 + T3724 COSM4661485 c.1126G>A p.V376M Substitution - Missense 9:137183714-137183714 - C0065T COSM4154063 c.1024G>T p.D342Y Substitution - Missense 19:1457060-1457060 + pfg008T COSM1643785 c.845A>G p.E282G Substitution - Missense 9:137186252-137186252 - TCGA-BR-6452-01 COSM3905992 c.410G>A p.R137H Substitution - Missense 9:137187811-137187811 - TCGA-HU-A4G8-01 COSM3282192 c.1665C>T p.S555S Substitution - coding silent 19:1461989-1461989 + ACINAR18 COSM1733245 c.1558C>T p.R520C Substitution - Missense 9:137180840-137180840 - HCC159T COSM5806824 c.3690C>A p.S1230R Substitution - Missense 19:1466991-1466991 + ESO-0292 COSM1240837 c.863A>C p.E288A Substitution - Missense 9:137186234-137186234 - TCGA-A4-7288-01 COSM3989750 c.4767C>T p.P1589P Substitution - coding silent 19:1468068-1468068 + TCGA-G4-6298-01 COSM3749467 c.5730A>G p.K1910K Substitution - coding silent 19:1469031-1469031 + TCGA-D3-A5GU-06 COSM3655963 c.1238C>T p.S413F Substitution - Missense 9:137183173-137183173 - BN24T COSM1624777 c.2039A>T p.E680V Substitution - Missense 9:137175454-137175454 - B104-Tumor COSM1750683 c.1628G>A p.R543Q Substitution - Missense 19:1461143-1461143 + Gp2D COSM4628857 c.920A>G p.D307G Substitution - Missense 9:137185041-137185041 - S02285 COSM5684647 c.2142C>T p.C714C Substitution - coding silent 19:1465443-1465443 + TCGA-D5-6927-01 COSM3749467 c.5730A>G p.K1910K Substitution - coding silent 19:1469031-1469031 + TCGA-BR-4292-01 COSM4074843 c.3505G>T p.G1169C Substitution - Missense 19:1466806-1466806 + TCGA-A6-A566-01 COSM5096174 c.1482C>T p.I494I Substitution - coding silent 19:1460818-1460818 + PD11760a COSM5792862 c.2753C>G p.A918G Substitution - Missense 19:1466054-1466054 + ESO15T COSM1172577 c.1363C>T p.R455W Substitution - Missense 19:1460240-1460240 + I2L-P7-Tumor-Organoid COSM5365657 c.4538A>G p.D1513G Substitution - Missense 19:1467839-1467839 + TCGA-F1-A448-01 COSM3905988 c.1277G>A p.R426H Substitution - Missense 9:137183134-137183134 - TCGA-C5-A7CO-01 COSM4856280 c.399G>A p.E133E Substitution - coding silent 9:137187822-137187822 - TCGA-DK-A2I4-01 COSM3796708 c.1746G>T p.V582V Substitution - coding silent 19:1462070-1462070 + 1946219 COSM1578301 c.822G>A p.E274E Substitution - coding silent 9:137186275-137186275 - Pat_76_A COSM5875926 c.2152G>A p.E718K Substitution - Missense 9:137175341-137175341 - BB22T COSM33564 c.1684G>T p.A562S Substitution - Missense 19:1462008-1462008 + pfg181T COSM4748504 c.1558G>A p.A520T Substitution - Missense 19:1461073-1461073 + 395 COSM4428745 c.607C>A p.L203M Substitution - Missense 9:137187614-137187614 - TCGA-CM-6677-01 COSM5161030 c.4516G>T p.V1506L Substitution - Missense 19:1467817-1467817 + TCGA-CK-5916-01 COSM5154698 c.5171T>C p.L1724P Substitution - Missense 19:1468472-1468472 + 4_RESISTANT COSM1724452 c.1333_1334insG p.D445fs*11 Insertion - Frameshift 9:137181815-137181816 - TCGA-A6-5661-01 COSM1461336 c.1008C>T p.Y336Y Substitution - coding silent 9:137184953-137184953 - TCGA-HU-A4GQ-01 COSM4074835 c.1952A>C p.N651T Substitution - Missense 19:1465253-1465253 + TCGA-A6-5661-01 COSM3692426 c.3004G>A p.V1002M Substitution - Missense 19:1466305-1466305 + CCK81 COSM4620734 c.1292T>C p.M431T Substitution - Missense 19:1458049-1458049 + sysucc-1370T COSM1107054 c.1559G>A p.R520H Substitution - Missense 9:137180839-137180839 - TCGA-DK-A1AC-01 COSM1304093 c.1600G>T p.V534L Substitution - Missense 19:1461115-1461115 + TCGA-BR-8284-01 COSM3905987 c.1839G>T p.E613D Substitution - Missense 9:137180232-137180232 - CHC892T COSM4798323 c.10G>A p.A4T Substitution - Missense 9:137188523-137188523 - YUDEDE COSM1711570 c.1495G>A p.A499T Substitution - Missense 19:1460831-1460831 + PCSI_0476_Pa_P_526 COSM5031364 c.3115G>T p.V1039F Substitution - Missense 19:1466416-1466416 + Pat_50_A COSM5875927 c.1450C>T p.P484S Substitution - Missense 9:137181699-137181699 - ME029T COSM226814 c.856C>T p.R286C Substitution - Missense 19:1456892-1456892 + STC246 COSM3282193 c.1729G>A p.A577T Substitution - Missense 19:1462053-1462053 + 2293782 COSM4609439 c.1747G>T p.A583S Substitution - Missense 9:137180324-137180324 - PD4120a COSM159047 c.1899G>A p.R633R Substitution - coding silent 9:137175829-137175829 - sysucc-1247T COSM4770830 c.985G>A p.G329R Substitution - Missense 19:1457021-1457021 + CSCC-37-T COSM4565505 c.2169_2170CC>TT p.R724W Substitution - Missense 9:137175323-137175324 - HT115 COSM1304092 c.859G>A p.D287N Substitution - Missense 19:1456895-1456895 + 16T COSM3712813 c.3205C>T p.R1069* Substitution - Nonsense 19:1466506-1466506 + RKO COSM4649310 c.1956C>T p.D652D Substitution - coding silent 9:137175772-137175772 - SNU-175 COSM3282184 c.1525G>A p.V509M Substitution - Missense 19:1461040-1461040 + LIM2551 COSM1750683 c.1628G>A p.R543Q Substitution - Missense 19:1461143-1461143 + ME043T COSM228519 c.1892C>T p.A631V Substitution - Missense 9:137175836-137175836 - TCGA-EE-A3J7-06 COSM3891660 c.1682C>T p.S561F Substitution - Missense 19:1462006-1462006 + TCGA-AP-A059-01 COSM1107058 c.1324C>T p.L442L Substitution - coding silent 9:137181825-137181825 - TCGA-06-0650-01 COSM3403831 c.2089C>T p.H697Y Substitution - Missense 19:1465390-1465390 + TCGA-EE-A3AE-06 COSM3529368 c.3140C>T p.P1047L Substitution - Missense 19:1466441-1466441 + TCGA-CK-4951-01 COSM5153368 c.944C>A p.P315H Substitution - Missense 9:137185017-137185017 - S00838 COSM5661518 c.5781C>G p.P1927P Substitution - coding silent 19:1469082-1469082 + RKO COSM4649309 c.2068G>T p.A690S Substitution - Missense 9:137175425-137175425 - S01297 COSM5667526 c.4725C>G p.P1575P Substitution - coding silent 19:1468026-1468026 + TCGA-AP-A059-01 COSM1107060 c.1019G>A p.R340H Substitution - Missense 9:137184942-137184942 - 587342 COSM1183198 c.5050G>A p.V1684M Substitution - Missense 19:1468351-1468351 + TCGA-BP-5182-01 COSM474244 c.4581C>G p.H1527Q Substitution - Missense 19:1467882-1467882 + T3091 COSM4662414 c.2370C>T p.A790A Substitution - coding silent 19:1465671-1465671 + TCGA-CG-4469-01 COSM3905990 c.981C>T p.H327H Substitution - coding silent 9:137184980-137184980 - PD4120a COSM159046 c.564G>C p.K188N Substitution - Missense 9:137187657-137187657 - TCGA-BR-4292-01 COSM3905989 c.1045C>T p.R349* Substitution - Nonsense 9:137184916-137184916 - HCC28 COSM1611678 c.6783C>T p.H2261H Substitution - coding silent 19:1470084-1470084 + TCGA-D3-A1Q6-06 COSM3529361 c.1515C>T p.L505L Substitution - coding silent 19:1460851-1460851 + HCC53 COSM1624776 c.2387A>T p.Q796L Substitution - Missense 9:137175024-137175024 - PTC-70C COSM4163622 c.1224C>T p.R408R Substitution - coding silent 9:137183187-137183187 - BD124T COSM5492615 c.2298G>T p.E766D Substitution - Missense 9:137175113-137175113 - TCGA-ER-A19H-06 COSM3529367 c.3077G>A p.R1026Q Substitution - Missense 19:1466378-1466378 + HCC4 COSM1624778 c.1225G>A p.V409M Substitution - Missense 9:137183186-137183186 - TCGA-CD-A4MG-01 COSM4074836 c.2319C>T p.S773S Substitution - coding silent 19:1465620-1465620 + TCGA-36-2532-01 COSM1330634 c.732C>T p.S244S Substitution - coding silent 9:137187489-137187489 - Pat_60_B COSM5875930 c.575A>G p.E192G Substitution - Missense 9:137187646-137187646 - CHC892T COSM4960124 c.2151G>A p.E717E Substitution - coding silent 9:137175342-137175342 - 19 COSM5747103 c.1966T>C p.S656P Substitution - Missense 9:137175762-137175762 - Pa14C COSM84462 c.2823T>G p.H941Q Substitution - Missense 19:1466124-1466124 + BCB231T COSM4955752 c.1264G>T p.E422* Substitution - Nonsense 9:137183147-137183147 - TCGA-CI-6620-01 COSM3749467 c.5730A>G p.K1910K Substitution - coding silent 19:1469031-1469031 + TCGA-D1-A17Q-01 COSM1107062 c.837C>T p.G279G Substitution - coding silent 9:137186260-137186260 - TCGA-D9-A6EC-06 COSM4401390 c.2537A>C p.K846T Substitution - Missense 19:1465838-1465838 + TCGA-CK-4951-01 COSM5149763 c.608G>A p.G203D Substitution - Missense 19:1455469-1455469 + HCC137 COSM1611677 c.4766C>T p.P1589L Substitution - Missense 19:1468067-1468067 + TCGA-13-2061-01 COSM1325461 c.4503C>T p.P1501P Substitution - coding silent 19:1467804-1467804 + Pat_16_B COSM5875931 c.97C>T p.P33S Substitution - Missense 9:137188436-137188436 - TCGA-BR-7703-01 COSM4074842 c.3130G>A p.A1044T Substitution - Missense 19:1466431-1466431 + TCGA-FD-A3SN-01 COSM3779855 c.2306C>T p.S769L Substitution - Missense 9:137175105-137175105 - TCGA-DK-A2I4-01 COSM3796707 c.1650G>A p.L550L Substitution - coding silent 19:1461974-1461974 + MO_1012 COSM5562001 c.773C>A p.P258H Substitution - Missense 19:1456361-1456361 + 587336 COSM1183196 c.286C>A p.L96M Substitution - Missense 19:1453484-1453484 + TCGA-UB-A7MB-01 COSM1711571 c.1518C>G p.H506Q Substitution - Missense 19:1460854-1460854 + NYU929 COSM4770830 c.985G>A p.G329R Substitution - Missense 19:1457021-1457021 + SNU-C2B COSM4651674 c.2002C>T p.L668L Substitution - coding silent 9:137175726-137175726 - TCGA-IR-A3LI-01 COSM4846243 c.1902G>C p.L634L Substitution - coding silent 19:1465203-1465203 + CHC1035T COSM3668186 c.564G>A p.E188E Substitution - coding silent 19:1455425-1455425 + PD4826a COSM5795917 c.1297G>C p.E433Q Substitution - Missense 19:1458054-1458054 + TCGA-DK-A1AC-01 COSM1304091 c.369G>A p.L123L Substitution - coding silent 19:1453567-1453567 + AOCS-116-1-3 COSM4140315 c.980C>A p.A327E Substitution - Missense 19:1457016-1457016 + LUAD-RT-S01777 COSM382610 c.1805C>T p.P602L Substitution - Missense 9:137180266-137180266 - pfg143T COSM4748507 c.5266G>A p.A1756T Substitution - Missense 19:1468567-1468567 + 8036161 COSM3395691 c.57G>T p.E19D Substitution - Missense 9:137188476-137188476 - Pat_76_B COSM5875929 c.1235C>T p.P412L Substitution - Missense 9:137183176-137183176 - TCGA-AA-3697-01 COSM3756372 c.687G>A p.A229A Substitution - coding silent 19:1456123-1456123 + I2L-P19Tb-Tumor-Organoid COSM5364727 c.6811delC p.F2273fs*>31 Deletion - Frameshift 19:1470112-1470112 + TCGA-D5-6540-01 COSM1390923 c.3693G>A p.L1231L Substitution - coding silent 19:1466994-1466994 + 585208 COSM324700 c.154G>T p.E52* Substitution - Nonsense 9:137188067-137188067 - HCC2157 COSM33348 c.6007G>A p.G2003S Substitution - Missense 19:1469308-1469308 + TCGA-QL-A97D-01 COSM5188205 c.5687C>A p.A1896D Substitution - Missense 19:1468988-1468988 + NB-1243 COSM1283403 c.1692G>C p.M564I Substitution - Missense 9:137180379-137180379 - BD9T COSM5502112 c.2740C>T p.R914W Substitution - Missense 19:1466041-1466041 + TCGA-CK-4951-01 COSM5153369 c.558G>A p.Q186Q Substitution - coding silent 9:137187663-137187663 - TCGA-K4-A3WU-01 COSM3779856 c.1884G>C p.Q628H Substitution - Missense 9:137180187-137180187 - SE9PT COSM1580240 c.964C>T p.R322C Substitution - Missense 9:137184997-137184997 - SKNEP1 COSM4580696 c.334G>T p.G112C Substitution - Missense 19:1453532-1453532 + TCGA-AY-6197-01 COSM3692420 c.885G>T p.L295L Substitution - coding silent 19:1456921-1456921 + TCGA-AP-A059-01 COSM1107059 c.1195C>A p.L399I Substitution - Missense 9:137183216-137183216 - CSCC-27-T COSM4499480 c.5439C>T p.A1813A Substitution - coding silent 19:1468740-1468740 + TCGA-AZ-6601-01 COSM5142457 c.1443+6C>T p.? Unknown 19:1460326-1460326 + HX35T COSM1611678 c.6783C>T p.H2261H Substitution - coding silent 19:1470084-1470084 + 8062308 COSM84462 c.2823T>G p.H941Q Substitution - Missense 19:1466124-1466124 + NCI-H720 COSM5368147 c.6466C>G p.H2156D Substitution - Missense 19:1469767-1469767 + TCGA-LP-A5U2-01 COSM4833827 c.486C>G p.F162L Substitution - Missense 9:137187735-137187735 - DLD1 COSM4623839 c.1723G>A p.D575N Substitution - Missense 19:1462047-1462047 + I2L-P6-Tumor-Organoid COSM5359521 c.1274G>A p.R425H Substitution - Missense 9:137183137-137183137 - TCGA-AA-3864-01 COSM5114722 c.728C>T p.A243V Substitution - Missense 19:1456316-1456316 + BCM275T COSM4951801 c.4093G>A p.G1365S Substitution - Missense 19:1467394-1467394 + KM12 COSM3282280 c.5176G>A p.V1726M Substitution - Missense 19:1468477-1468477 + TCGA-A6-3809-01 COSM5086443 c.440_442delAGG p.E149delE Deletion - In frame 19:1455175-1455177 + LP6007504-DNA_A01 COSM4408806 c.650C>T p.S217L Substitution - Missense 19:1456086-1456086 + TCGA-D5-6928-01 COSM1461332 c.2217C>T p.G739G Substitution - coding silent 9:137175276-137175276 - CHC2200T COSM4952923 c.2055G>T p.V685V Substitution - coding silent 9:137175438-137175438 - TCGA-CG-4306-01 COSM4074809 c.602G>A p.R201H Substitution - Missense 19:1455463-1455463 + H1155 COSM1195463 c.1627C>T p.R543W Substitution - Missense 19:1461142-1461142 + TCGA-B0-5108-01 COSM474240 c.757C>A p.P253T Substitution - Missense 19:1456345-1456345 + T2939 COSM4662415 c.4570delA p.T1524fs*56 Deletion - Frameshift 19:1467871-1467871 + A673 COSM4588656 c.1992G>A p.A664A Substitution - coding silent 9:137175736-137175736 - TCGA-BR-8680-01 COSM4074840 c.2816G>A p.R939H Substitution - Missense 19:1466117-1466117 + TCGA-EK-A2RA-01 COSM4848247 c.799C>T p.Q267* Substitution - Nonsense 19:1456387-1456387 + SC_9047 COSM5572309 c.3452A>C p.Y1151S Substitution - Missense 19:1466753-1466753 + BD124T COSM5492617 c.1301C>T p.T434I Substitution - Missense 9:137181848-137181848 - C135 COSM4617883 c.3309C>T p.A1103A Substitution - coding silent 19:1466610-1466610 + HCC107T COSM1611676 c.4633C>T p.R1545W Substitution - Missense 19:1467934-1467934 + S00936 COSM309203 c.2050G>A p.A684T Substitution - Missense 19:1465351-1465351 + CHC1035T COSM3668186 c.564G>A p.E188E Substitution - coding silent 19:1455425-1455425 + 304_T COSM3952543 c.1852G>T p.A618S Substitution - Missense 9:137180219-137180219 - BD123T COSM5521118 c.2284C>T p.R762* Substitution - Nonsense 19:1465585-1465585 + TCGA-D5-6530-01 COSM5163199 c.1001G>A p.R334H Substitution - Missense 9:137184960-137184960 - ESCC_5 COSM5623170 c.744G>A p.P248P Substitution - coding silent 19:1456332-1456332 + TCGA-A6-6781-01 COSM5094388 c.6895G>A p.A2299T Substitution - Missense 19:1470196-1470196 + TCGA-NH-A5IV-01 COSM5183029 c.793A>G p.T265A Substitution - Missense 19:1456381-1456381 + 2521260 COSM5891527 c.6496G>A p.A2166T Substitution - Missense 19:1469797-1469797 + TCGA-G4-6298-01 COSM3692425 c.2952C>A p.T984T Substitution - coding silent 19:1466253-1466253 + DN14066 COSM5962876 c.1353C>T p.H451H Substitution - coding silent 19:1460230-1460230 + TCGA-FD-A3N5-01 COSM1304094 c.1791C>T p.I597I Substitution - coding silent 19:1462115-1462115 + TCGA-BR-7707-01 COSM3905986 c.2229G>T p.Q743H Substitution - Missense 9:137175264-137175264 - Patient3_Tu COSM1235723 c.1724G>A p.R575Q Substitution - Missense 9:137180347-137180347 - HCC098T COSM5806824 c.3690C>A p.S1230R Substitution - Missense 19:1466991-1466991 + TCGA-QG-A5Z2-01 COSM5187986 c.802G>A p.V268M Substitution - Missense 9:137186295-137186295 - 44 COSM5734201 c.1143C>A p.C381* Substitution - Nonsense 19:1457179-1457179 + KPOPBR-19-T COSM3655964 c.1041C>T p.I347I Substitution - coding silent 9:137184920-137184920 - PTC-28C COSM4163622 c.1224C>T p.R408R Substitution - coding silent 9:137183187-137183187 - TCGA-AA-3510-01 COSM1390924 c.5232A>C p.E1744D Substitution - Missense 19:1468533-1468533 + HCC017T COSM5815116 c.3067C>A p.P1023T Substitution - Missense 19:1466368-1466368 + T1154 COSM4661481 c.2210A>C p.D737A Substitution - Missense 9:137175283-137175283 - 234 COSM3731235 c.2752G>A p.A918T Substitution - Missense 19:1466053-1466053 + 47_tFL COSM4170983 c.3913G>A p.G1305S Substitution - Missense 19:1467214-1467214 + ME011T COSM224546 c.727G>A p.A243T Substitution - Missense 19:1456315-1456315 + BCM275T COSM4951801 c.4093G>A p.G1365S Substitution - Missense 19:1467394-1467394 + T3064 COSM4662417 c.5006G>A p.G1669D Substitution - Missense 19:1468307-1468307 + TCGA-D9-A6EC-06 COSM4404810 c.5279A>C p.K1760T Substitution - Missense 19:1468580-1468580 + CHC892T COSM4959900 c.4937G>A p.G1646D Substitution - Missense 19:1468238-1468238 + Gp5D COSM4628857 c.920A>G p.D307G Substitution - Missense 9:137185041-137185041 - TCGA-CK-5916-01 COSM3699289 c.1485G>T p.K495N Substitution - Missense 9:137180913-137180913 - TCGA-B6-A2IU-01 COSM3822117 c.2489A>C p.E830A Substitution - Missense 19:1465790-1465790 + Pat_41_B COSM5875928 c.1255G>A p.V419M Substitution - Missense 9:137183156-137183156 - PCSI_0185_Pa_P COSM3378625 c.1993G>A p.D665N Substitution - Missense 19:1465294-1465294 + PCSI_0357_Pa_P_526 COSM4964548 c.1706C>T p.A569V Substitution - Missense 19:1462030-1462030 + TCGA-D8-A1XQ-01 COSM3848111 c.669G>A p.G223G Substitution - coding silent 9:137187552-137187552 - BD72T COSM5513420 c.1522-10delC p.? Unknown 19:1461027-1461027 + ESCC_BICR_068T COSM5437275 c.465T>C p.T155T Substitution - coding silent 9:137187756-137187756 - BCB231T COSM4955752 c.1264G>T p.E422* Substitution - Nonsense 9:137183147-137183147 - S02255 COSM5681011 c.532G>A p.G178R Substitution - Missense 9:137187689-137187689 - OSCC-GB_01370111 COSM5955816 c.667G>C p.D223H Substitution - Missense 19:1456103-1456103 + TCGA-FP-A4BE-01 COSM4074839 c.2778C>T p.S926S Substitution - coding silent 19:1466079-1466079 + sysucc-1163T COSM5458080 c.3305A>C p.E1102A Substitution - Missense 19:1466606-1466606 + BD6T COSM5499336 c.857G>A p.R286H Substitution - Missense 19:1456893-1456893 + PD18283a COSM3770494 c.6519G>A p.T2173T Substitution - coding silent 19:1469820-1469820 + pfg173T COSM4748506 c.3805G>C p.D1269H Substitution - Missense 19:1467106-1467106 + 61 COSM5741322 c.4376G>A p.G1459D Substitution - Missense 19:1467677-1467677 + TCGA-AG-A00Y-01 COSM289908 c.1707G>A p.A569A Substitution - coding silent 19:1462031-1462031 + TCGA-AZ-4315-01 COSM1461335 c.1222C>A p.R408S Substitution - Missense 9:137183189-137183189 - 8031133 COSM3388645 c.6801G>A p.S2267S Substitution - coding silent 19:1470102-1470102 + HCC128T COSM1611674 c.4275G>T p.R1425S Substitution - Missense 19:1467576-1467576 + TCGA-G4-6299-01 COSM5174306 c.49G>A p.G17R Substitution - Missense 9:137188484-137188484 - TCGA-G4-6320-01 COSM3692427 c.3691C>T p.L1231L Substitution - coding silent 19:1466992-1466992 + TCGA-CL-4957-01 COSM3422466 c.5778G>A p.S1926S Substitution - coding silent 19:1469079-1469079 + BD57T COSM5510980 c.2097C>T p.P699P Substitution - coding silent 19:1465398-1465398 + TCGA-AZ-6600-01 COSM3692428 c.5793G>A p.P1931P Substitution - coding silent 19:1469094-1469094 + PDA_004 COSM4997975 c.1372C>A p.L458M Substitution - Missense 19:1460249-1460249 + 529 COSM5612294 c.609C>T p.G203G Substitution - coding silent 19:1455470-1455470 + TCGA-EB-A3Y7-01 COSM3655962 c.1367T>C p.L456P Substitution - Missense 9:137181782-137181782 - LUAD-B00915 COSM332730 c.1763A>G p.K588R Substitution - Missense 19:1462087-1462087 + CSCC-17-T COSM4472148 c.1763C>T p.P588L Substitution - Missense 9:137180308-137180308 - YUKAT COSM5388802 c.1109T>C p.V370A Substitution - Missense 19:1457145-1457145 + ESCC_158 COSM5646720 c.164G>C p.G55A Substitution - Missense 19:1453269-1453269 + Case3 COSM5711833 c.2815C>T p.R939C Substitution - Missense 19:1466116-1466116 + SNUH_G16_S1 COSM3282279 c.5165C>G p.S1722C Substitution - Missense 19:1468466-1468466 + TCGA-D3-A2JD-06 COSM3529374 c.5288G>A p.G1763E Substitution - Missense 19:1468589-1468589 + NCI-H835 COSM5368376 c.1301T>A p.L434Q Substitution - Missense 19:1458058-1458058 + TCGA-HC-8262-01 COSM4392634 c.1928T>C p.L643P Substitution - Missense 9:137175800-137175800 - HCC086T COSM5813121 c.2795C>T p.A932V Substitution - Missense 19:1466096-1466096 + sysucc-731T COSM5460209 c.6655G>A p.A2219T Substitution - Missense 19:1469956-1469956 + TCGA-D1-A15Z-01 COSM1107053 c.1941C>T p.D647D Substitution - coding silent 9:137175787-137175787 - SNUH_G26_S1 COSM3685553 c.780T>C p.A260A Substitution - coding silent 9:137186317-137186317 - 587284 COSM1183197 c.5384A>G p.Y1795C Substitution - Missense 19:1468685-1468685 + LP6005409-DNA_E02 COSM4411606 c.1371G>A p.P457P Substitution - coding silent 19:1460248-1460248 + TCGA-D7-A4YV-01 COSM4074830 c.1395C>T p.Y465Y Substitution - coding silent 19:1460272-1460272 + TCGA-39-5022-01 COSM709794 c.145G>A p.V49I Substitution - Missense 19:1453250-1453250 + TCGA-E1-5307-01 COSM3929960 c.1021A>G p.I341V Substitution - Missense 9:137184940-137184940 - PTC-10C COSM4131286 c.2845G>A p.A949T Substitution - Missense 19:1466146-1466146 + TCGA-DK-A3WW-01 COSM3779857 c.1599C>T p.F533F Substitution - coding silent 9:137180799-137180799 - I2L-P7-Tumor-Organoid COSM5365572 c.2212G>A p.A738T Substitution - Missense 19:1465513-1465513 + 2_tFL COSM4170981 c.1639-1G>A p.? Unknown 19:1461962-1461962 + T368 COSM4661484 c.1265A>G p.E422G Substitution - Missense 9:137183146-137183146 - YUKLAB COSM1711571 c.1518C>G p.H506Q Substitution - Missense 19:1460854-1460854 + I2L-P19Ta-Tumor-Biopsy COSM3088760 c.2130delC p.G711fs*52 Deletion - Frameshift 9:137175363-137175363 - HCT8 COSM4632759 c.6597C>T p.P2199P Substitution - coding silent 19:1469898-1469898 + KM12 COSM4639026 c.693C>T p.D231D Substitution - coding silent 19:1456129-1456129 + HCC2998 COSM4631655 c.1150T>C p.C384R Substitution - Missense 19:1457186-1457186 + TCGA-BH-A18G-01 COSM3822111 c.779A>G p.H260R Substitution - Missense 19:1456367-1456367 + TCGA-F4-6856-01 COSM1390922 c.3639G>A p.T1213T Substitution - coding silent 19:1466940-1466940 + TCGA-A6-5659-01 COSM5088353 c.3733G>T p.D1245Y Substitution - Missense 19:1467034-1467034 + DLD1 COSM4623840 c.3839C>T p.A1280V Substitution - Missense 19:1467140-1467140 + PTC_327 COSM5960321 c.2185G>C p.E729Q Substitution - Missense 19:1465486-1465486 + tumor_4131095 COSM5948688 c.973C>T p.R325C Substitution - Missense 9:137184988-137184988 - 1_RESISTANT COSM1718060 c.4825G>A p.D1609N Substitution - Missense 19:1468126-1468126 + CHC892T COSM4960124 c.2151G>A p.E717E Substitution - coding silent 9:137175342-137175342 - TP_2034 COSM5555322 c.1017C>A p.G339G Substitution - coding silent 19:1457053-1457053 + TCGA-CG-5723-01 COSM4074841 c.3076C>T p.R1026W Substitution - Missense 19:1466377-1466377 + CHC2113T COSM4788411 c.4319G>A p.G1440E Substitution - Missense 19:1467620-1467620 + HCT15 COSM3282174 c.1370C>T p.P457L Substitution - Missense 19:1460247-1460247 + PCSI_0103_Pa_P COSM3382479 c.1695G>A p.A565A Substitution - coding silent 9:137180376-137180376 - YUVAIL COSM1711572 c.1588G>A p.E530K Substitution - Missense 19:1461103-1461103 + TCGA-HU-A4GX-01 COSM4074844 c.3691C>A p.L1231M Substitution - Missense 19:1466992-1466992 + PTC-10C COSM1325461 c.4503C>T p.P1501P Substitution - coding silent 19:1467804-1467804 + TCGA-EE-A29E-06 COSM3529365 c.2575G>A p.E859K Substitution - Missense 19:1465876-1465876 + YUKAT COSM5410802 c.2394C>T p.Y798Y Substitution - coding silent 9:137175017-137175017 - CHC2113T COSM4788411 c.4319G>A p.G1440E Substitution - Missense 19:1467620-1467620 + TCGA-BR-8680-01 COSM4074804 c.357C>A p.S119R Substitution - Missense 19:1453555-1453555 + TCGA-HU-A4G8-01 COSM3905991 c.809G>A p.R270Q Substitution - Missense 9:137186288-137186288 - HCC2218 COSM26556 c.1131C>G p.I377M Substitution - Missense 19:1457167-1457167 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.446376 19p13.3 612034 Hs.533262 9q34.3 606946

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.L643P c.1928T>C 9 140070252 PRAD A T Missense p.F515I c.1543T>A 9 140075307 RCCC C A Missense p.K625N c.1875G>T 9 140074648 OV C A Nonsense p.E52* c.154G>T 9 140082519 SCLC C A Synonymous p.L596L c.1788G>T 9 140074735 GBM CG AA Missense p.R496L c.1486_1487delinsTT 9 140075363 LUAD C G Missense p.E610D c.1830G>C 9 140074693 HNSC C G Missense p.K188N c.564G>C 9 140082109 BRCA C G Missense p.M564I c.1692G>C 9 140074831 NB C T Missense p.G193E c.578G>A 9 140082095 CM C T Missense p.G448R c.1342G>A 9 140076259 UCEC C T Missense p.R340H c.1019G>A 9 140079394 CM C T Missense p.R496Q c.1487G>A 9 140075363 COREAD C T Missense p.R497H c.1490G>A 9 140075360 UCEC C T Synonymous p.L751L c.2253G>A 9 140069692 CM C T Synonymous p.Q468Q c.1404G>A 9 140076197 LUSC C T Synonymous p.Q663Q c.1989G>A 9 140070191 CM C T Synonymous p.R633R c.1899G>A 9 140070281 BRCA G A Missense p.A631V c.1892C>T 9 140070288 CM G A Missense p.P461L c.1382C>T 9 140076219 CM G A Missense p.R633W c.1897C>T 9 140070283 ESCA G A Nonsense p.R349* c.1045C>T 9 140079368 STAD G A Synonymous p.A23A c.69C>T 9 140082916 CM G A Synonymous p.A487A c.1461C>T 9 140076140 UCEC G A Synonymous p.D647D c.1941C>T 9 140070239 UCEC G A Synonymous p.F285F c.855C>T 9 140080694 CM G A Synonymous p.H327H c.981C>T 9 140079432 STAD G A Synonymous p.I347I c.1041C>T 9 140079372 CM G A Synonymous p.L629L c.1887C>T 9 140074636 CM G A Synonymous p.S88S c.264C>T 9 140082409 CM GC AT Missense p.P587S c.1758_1759delinsAT 9 140074764 THCA G C IntronicSNV . c.1890+1525C>G 9 140073108 CLL GG AA Missense p.L514F c.1539_1540delinsTT 9 140075310 CM G T Missense p.D460E c.1380C>A 9 140076221 SCLC T A Missense p.Y213F c.638A>T 9 140082035 STAD T C Missense p.E282G c.845A>G 9 140080704 STAD T C Missense p.I341V c.1021A>G 9 140079392 LGG T C Synonymous p.L110L c.330A>G 9 140082343 UCEC A G Missense p.D782G c.2345A>G 19 1465645 STAD A G Missense p.I512V c.1534A>G 19 1461048 RCCC A G Missense p.N459S c.1376A>G 19 1460252 CM C A 3-UTRSNV . c.6909+1917C>A 19 1472126 HC C A Missense p.P1519Q c.4556C>A 19 1467856 CM C A Missense p.P253T c.757C>A 19 1456344 RCCC C G Missense p.H1527Q c.4581C>G 19 1467881 RCCC C G Missense p.L159V c.475C>G 19 1455209 HNSC C G Synonymous p.P1733P c.5199C>G 19 1468499 LUSC C T Missense p.A883V c.2648C>T 19 1465948 ESCA C T Missense p.H697Y c.2089C>T 19 1465389 GBM C T Missense p.P1047L c.3140C>T 19 1466440 CM C T Missense p.P404L c.1211C>T 19 1457967 COREAD C T Missense p.R125W c.373C>T 19 1453570 RCCC C T Missense p.R658C c.1972C>T 19 1465272 CM C T Missense p.S1066L c.3197C>T 19 1466497 HNSC C T Missense p.S2267L c.6800C>T 19 1470100 LUSC C T Missense p.S561F c.1682C>T 19 1462005 CM C T Nonsense p.Q590* c.1768C>T 19 1462091 LUAD C T Synonymous p.I512I c.1536C>T 19 1461050 CM C T Synonymous p.I597I c.1791C>T 19 1462114 BLCA C T Synonymous p.L505L c.1515C>T 19 1460850 CM C T Synonymous p.L610L c.1830C>T 19 1462153 HNSC GAC - InFrameDeletion p.D782delD c.2334_2336delTGA 19 1465634 CLL G A Missense p.A684T c.2050G>A 19 1465350 SCLC G A Missense p.A792T c.2374G>A 19 1465674 CM G A Missense p.D287N c.859G>A 19 1456894 BLCA G A Missense p.G1306R c.3916G>A 19 1467216 HNSC G A Missense p.G1723R c.5167G>A 19 1468467 STAD G A Missense p.G1763E c.5288G>A 19 1468588 CM G A Missense p.G1783R c.5347G>A 19 1468647 GBM G A Missense p.G2003S c.6007G>A 19 1469307 BRCA G A Missense p.G776S c.2326G>A 19 1465626 CM G A Missense p.R1026Q c.3077G>A 19 1466377 CM G A Missense p.R201H c.602G>A 19 1455462 STAD G A Missense p.R824Q c.2471G>A 19 1465771 BRCA G A Missense p.V49I c.145G>A 19 1453249 LUSC G A Synonymous p.A569A c.1707G>A 19 1462030 COREAD G A Synonymous p.L550L c.1650G>A 19 1461973 BLCA G A Synonymous p.R622R c.1866G>A 19 1465166 CM G T Missense p.A562S c.1684G>T 19 1462007 BRCA G T Missense p.G1169C c.3505G>T 19 1466805 STAD G T Synonymous p.V582V c.1746G>T 19 1462069 BLCA - T Frameshift p.S1066Ffs*24 c.3196dupT 19 1466496 GBM T G Missense p.H941Q c.2823T>G 19 1466123 PAAD