Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 3 10091153 10091153 + Silent SNP C C T TCGA-OR-A5KW-01A-11D-A29I-10 TCGA-OR-A5KW-10A-01D-A29L-10 g.chr3:10091153C>T c.1509C>T c.(1507-1509)aaC>aaT p.N503N BLCA 3 10070355 10070355 + Missense_Mutation SNP G G C TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr3:10070355G>C c.14G>C c.(13-15)aGa>aCa p.R5T BLCA 3 10070396 10070396 + Missense_Mutation SNP G G T TCGA-UY-A9PH-01A-11D-A38G-08 TCGA-UY-A9PH-10A-01D-A38J-08 g.chr3:10070396G>T c.55G>T c.(55-57)Gat>Tat p.D19Y BLCA 3 10078013 10078013 + Missense_Mutation SNP T T G TCGA-DK-A1A5-01A-11D-A13W-08 TCGA-DK-A1A5-10A-01D-A13W-08 g.chr3:10078013T>G c.481T>G c.(481-483)Ttt>Gtt p.F161V BLCA 3 10084255 10084255 + Missense_Mutation SNP G G C TCGA-E7-A7PW-01A-11D-A34U-08 TCGA-E7-A7PW-10A-01D-A34X-08 g.chr3:10084255G>C c.796G>C c.(796-798)Gtg>Ctg p.V266L BLCA 3 10084780 10084780 + Missense_Mutation SNP T T G TCGA-FD-A3SS-01A-12D-A22Z-08 TCGA-FD-A3SS-10A-01D-A22Z-08 g.chr3:10084780T>G c.935T>G c.(934-936)tTg>tGg p.L312W BLCA 3 10089620 10089620 + Missense_Mutation SNP C C T TCGA-BT-A0YX-01A-11D-A10S-08 TCGA-BT-A0YX-10A-01D-A10S-08 g.chr3:10089620C>T c.1298C>T c.(1297-1299)tCa>tTa p.S433L BLCA 3 10089628 10089628 + Missense_Mutation SNP C C A TCGA-K4-A3WU-01B-11D-A23M-08 TCGA-K4-A3WU-10A-01D-A23K-08 g.chr3:10089628C>A c.1306C>A c.(1306-1308)Ctg>Atg p.L436M BLCA 3 10089677 10089677 + Missense_Mutation SNP C C T TCGA-FD-A6TA-01A-12D-A339-08 TCGA-FD-A6TA-10A-21D-A339-08 g.chr3:10089677C>T c.1355C>T c.(1354-1356)tCa>tTa p.S452L BLCA 3 10091133 10091133 + Missense_Mutation SNP C C G TCGA-BT-A0YX-01A-11D-A10S-08 TCGA-BT-A0YX-10A-01D-A10S-08 g.chr3:10091133C>G c.1489C>G c.(1489-1491)Cta>Gta p.L497V BLCA 3 10094121 10094121 + Silent SNP C C G TCGA-FD-A3B6-01A-21D-A20D-08 TCGA-FD-A3B6-10A-01D-A20D-08 g.chr3:10094121C>G c.1596C>G c.(1594-1596)ctC>ctG p.L532L BLCA 3 10106108 10106108 + Silent SNP G G A TCGA-ZF-A9R5-01A-12D-A42E-08 TCGA-ZF-A9R5-10A-01D-A42H-08 g.chr3:10106108G>A c.2016G>A c.(2014-2016)ccG>ccA p.P672P BLCA 3 10106445 10106445 + Missense_Mutation SNP G G C TCGA-GC-A3RC-01A-11D-A22Z-08 TCGA-GC-A3RC-10B-01D-A22Z-08 g.chr3:10106445G>C c.2054G>C c.(2053-2055)gGa>gCa p.G685A BLCA 3 10107147 10107147 + Missense_Mutation SNP C C A TCGA-GC-A3RC-01A-11D-A22Z-08 TCGA-GC-A3RC-10B-01D-A22Z-08 g.chr3:10107147C>A c.2238C>A c.(2236-2238)aaC>aaA p.N746K BLCA 3 10107166 10107166 + Missense_Mutation SNP G G A TCGA-DK-A3IV-01A-22D-A21A-08 TCGA-DK-A3IV-10A-01D-A21A-08 g.chr3:10107166G>A c.2257G>A c.(2257-2259)Gat>Aat p.D753N BLCA 3 10116277 10116277 + Missense_Mutation SNP G G C TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chr3:10116277G>C c.2779G>C c.(2779-2781)Gag>Cag p.E927Q BLCA 3 10119795 10119795 + Missense_Mutation SNP G G A TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chr3:10119795G>A c.2890G>A c.(2890-2892)Gag>Aag p.E964K BLCA 3 10122810 10122810 + Missense_Mutation SNP C C G TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr3:10122810C>G c.3003C>G c.(3001-3003)ttC>ttG p.F1001L BLCA 3 10127604 10127604 + Silent SNP C C T TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr3:10127604C>T c.3333C>T c.(3331-3333)ctC>ctT p.L1111L BLCA 3 10130183 10130183 + Missense_Mutation SNP G G C TCGA-2F-A9KT-01A-11D-A38G-08 TCGA-2F-A9KT-10A-01D-A38J-08 g.chr3:10130183G>C c.3517G>C c.(3517-3519)Gag>Cag p.E1173Q BLCA 3 10131998 10131998 + Missense_Mutation SNP C C T TCGA-CF-A47X-01A-31D-A23U-08 TCGA-CF-A47X-10A-01D-A23U-08 g.chr3:10131998C>T c.3706C>T c.(3706-3708)Cgt>Tgt p.R1236C BLCA 3 10133873 10133873 + Missense_Mutation SNP A A C TCGA-BT-A3PK-01A-21D-A21Z-08 TCGA-BT-A3PK-10A-01D-A21Z-08 g.chr3:10133873A>C c.3786A>C c.(3784-3786)gaA>gaC p.E1262D BLCA 3 10136015 10136015 + Missense_Mutation SNP C C T TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr3:10136015C>T c.3931C>T c.(3931-3933)Ccg>Tcg p.P1311S BLCA 3 10138051 10138051 + Silent SNP C C G TCGA-BT-A3PJ-01A-21D-A21Z-08 TCGA-BT-A3PJ-10A-01D-A21Z-08 g.chr3:10138051C>G c.4080C>G c.(4078-4080)ctC>ctG p.L1360L BRCA 3 10089628 10089628 + Silent SNP C C T TCGA-C8-A3M7-01A-12D-A21Q-09 TCGA-C8-A3M7-10A-01D-A21Q-09 g.chr3:10089628C>T c.1306C>T c.(1306-1308)Ctg>Ttg p.L436L BRCA 3 10089640 10089640 + Nonsense_Mutation SNP C C T TCGA-C8-A274-01A-11D-A16D-09 TCGA-C8-A274-10A-01D-A16D-09 g.chr3:10089640C>T c.1318C>T c.(1318-1320)Cag>Tag p.Q440* BRCA 3 10106486 10106486 + Missense_Mutation SNP C C T TCGA-E2-A15T-01A-11D-A10Y-09 TCGA-E2-A15T-10A-01D-A110-09 g.chr3:10106486C>T c.2095C>T c.(2095-2097)Ctc>Ttc p.L699F BRCA 3 10107101 10107101 + Missense_Mutation SNP C C T TCGA-B6-A0RE-01A-11W-A071-09 TCGA-B6-A0RE-10A-01W-A071-09 g.chr3:10107101C>T c.2192C>T c.(2191-2193)gCt>gTt p.A731V BRCA 3 10107574 10107574 + Nonsense_Mutation SNP G G T TCGA-E2-A10C-01A-21D-A10M-09 TCGA-E2-A10C-10A-01D-A10M-09 g.chr3:10107574G>T c.2296G>T c.(2296-2298)Gag>Tag p.E766* BRCA 3 10114587 10114587 + Missense_Mutation SNP T T A TCGA-B6-A0I1-01A-11D-A21Q-09 TCGA-B6-A0I1-10A-01D-A21Q-09 g.chr3:10114587T>A c.2527T>A c.(2527-2529)Ttt>Att p.F843I BRCA 3 10114941 10114941 + Missense_Mutation SNP G G T TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr3:10114941G>T c.2610G>T c.(2608-2610)agG>agT p.R870S BRCA 3 10119819 10119819 + Missense_Mutation SNP C C T TCGA-A7-A13E-01A-11D-A272-09 TCGA-A7-A13E-10A-02D-A272-09 g.chr3:10119819C>T c.2914C>T c.(2914-2916)Ctc>Ttc p.L972F BRCA 3 10128882 10128882 + Missense_Mutation SNP C C G TCGA-E2-A1LH-01A-11D-A14G-09 TCGA-E2-A1LH-11A-22D-A14G-09 g.chr3:10128882C>G c.3400C>G c.(3400-3402)Ctc>Gtc p.L1134V BRCA 3 10130560 10130560 + Silent SNP T T C TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr3:10130560T>C c.3609T>C c.(3607-3609)atT>atC p.I1203I BRCA 3 10138113 10138113 + Missense_Mutation SNP G G C TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-11A-13D-A29N-09 g.chr3:10138113G>C c.4142G>C c.(4141-4143)aGa>aCa p.R1381T CESC 3 10074515 10074515 + Splice_Site SNP G G C TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr3:10074515G>C c.e3-1 CESC 3 10107104 10107104 + Missense_Mutation SNP C C T TCGA-JW-A852-01A-11D-A351-09 TCGA-JW-A852-10A-01D-A351-09 g.chr3:10107104C>T c.2195C>T c.(2194-2196)cCg>cTg p.P732L CESC 3 10142946 10142946 + Nonstop_Mutation SNP G G C TCGA-DS-A0VM-01A-11D-A10S-08 TCGA-DS-A0VM-10A-01D-A10S-08 g.chr3:10142946G>C c.4356G>C c.(4354-4356)taG>taC p.*1452Y COAD 3 10076460 10076460 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr3:10076460C>T c.355C>T c.(355-357)Cgt>Tgt p.R119C COAD 3 10076915 10076915 + Nonsense_Mutation SNP C C T TCGA-AA-A02F-01A-01W-A00E-09 TCGA-AA-A02F-10A-01W-A00E-09 g.chr3:10076915C>T c.436C>T c.(436-438)Cag>Tag p.Q146* COAD 3 10081417 10081417 + Missense_Mutation SNP A A G TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr3:10081417A>G c.583A>G c.(583-585)Aag>Gag p.K195E COAD 3 10084751 10084751 + Silent SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr3:10084751G>A c.906G>A c.(904-906)cgG>cgA p.R302R COAD 3 10085543 10085543 + Missense_Mutation SNP C C T TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr3:10085543C>T c.1129C>T c.(1129-1131)Cac>Tac p.H377Y COAD 3 10102080 10102080 + Missense_Mutation SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr3:10102080G>A c.1759G>A c.(1759-1761)Gca>Aca p.A587T COAD 3 10103846 10103846 + Missense_Mutation SNP C C T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr3:10103846C>T c.1778C>T c.(1777-1779)cCt>cTt p.P593L COAD 3 10106040 10106040 + Splice_Site SNP G G T TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr3:10106040G>T c.1948G>T c.(1948-1950)Gaa>Taa p.E650* COAD 3 10106041 10106041 + Splice_Site SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr3:10106041A>G c.1949A>G c.(1948-1950)gAa>gGa p.E650G COAD 3 10106444 10106444 + Missense_Mutation SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr3:10106444G>A c.2053G>A c.(2053-2055)Gga>Aga p.G685R COAD 3 10114996 10114996 + Frame_Shift_Del DEL A A - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr3:10114996delA c.2665delA c.(2665-2667)aaafs p.K889fs COAD 3 10128850 10128850 + Missense_Mutation SNP A A G TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr3:10128850A>G c.3368A>G c.(3367-3369)cAa>cGa p.Q1123R COAD 3 10128850 10128850 + Missense_Mutation SNP A A G TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr3:10128850A>G c.3368A>G c.(3367-3369)cAa>cGa p.Q1123R COAD 3 10128851 10128851 + Silent SNP A A G TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr3:10128851A>G c.3369A>G c.(3367-3369)caA>caG p.Q1123Q COAD 3 10128851 10128851 + Silent SNP A A G TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr3:10128851A>G c.3369A>G c.(3367-3369)caA>caG p.Q1123Q COAD 3 10132030 10132031 + Frame_Shift_Ins INS - - A TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr3:10132030_10132031insA c.3738_3739insA c.(3739-3741)aaafs p.K1247fs COAD 3 10133904 10133904 + Nonsense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr3:10133904C>T c.3817C>T c.(3817-3819)Cga>Tga p.R1273* COAD 3 10134979 10134979 + Missense_Mutation SNP G G T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr3:10134979G>T c.3860G>T c.(3859-3861)aGt>aTt p.S1287I COAD 3 10135979 10135979 + Missense_Mutation SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr3:10135979C>T c.3895C>T c.(3895-3897)Cgt>Tgt p.R1299C COADREAD 3 10076388 10076388 + Nonsense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr3:10076388G>T c.283G>T c.(283-285)Gaa>Taa p.E95* COADREAD 3 10076460 10076460 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr3:10076460C>T c.355C>T c.(355-357)Cgt>Tgt p.R119C COADREAD 3 10076915 10076915 + Nonsense_Mutation SNP C C T TCGA-AA-A02F-01A-01W-A00E-09 TCGA-AA-A02F-10A-01W-A00E-09 g.chr3:10076915C>T c.436C>T c.(436-438)Cag>Tag p.Q146* COADREAD 3 10081417 10081417 + Missense_Mutation SNP A A G TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr3:10081417A>G c.583A>G c.(583-585)Aag>Gag p.K195E COADREAD 3 10084272 10084272 + Silent SNP G G T TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr3:10084272G>T c.813G>T c.(811-813)tcG>tcT p.S271S COADREAD 3 10084751 10084751 + Silent SNP G G A TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr3:10084751G>A c.906G>A c.(904-906)cgG>cgA p.R302R COADREAD 3 10085543 10085543 + Missense_Mutation SNP C C T TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr3:10085543C>T c.1129C>T c.(1129-1131)Cac>Tac p.H377Y COADREAD 3 10094090 10094090 + Missense_Mutation SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:10094090A>G c.1565A>G c.(1564-1566)gAt>gGt p.D522G COADREAD 3 10102080 10102080 + Missense_Mutation SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr3:10102080G>A c.1759G>A c.(1759-1761)Gca>Aca p.A587T COADREAD 3 10103846 10103846 + Missense_Mutation SNP C C T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr3:10103846C>T c.1778C>T c.(1777-1779)cCt>cTt p.P593L COADREAD 3 10106040 10106040 + Splice_Site SNP G G T TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr3:10106040G>T c.1948G>T c.(1948-1950)Gaa>Taa p.E650* COADREAD 3 10106041 10106041 + Splice_Site SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr3:10106041A>G c.1949A>G c.(1948-1950)gAa>gGa p.E650G COADREAD 3 10106444 10106444 + Missense_Mutation SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr3:10106444G>A c.2053G>A c.(2053-2055)Gga>Aga p.G685R COADREAD 3 10106487 10106487 + Missense_Mutation SNP T T C TCGA-DC-6160-01A-11D-1657-10 TCGA-DC-6160-10A-01D-1657-10 g.chr3:10106487T>C c.2096T>C c.(2095-2097)cTc>cCc p.L699P COADREAD 3 10114996 10114996 + Frame_Shift_Del DEL A A - TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr3:10114996delA c.2665delA c.(2665-2667)aaafs p.K889fs COADREAD 3 10115024 10115024 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:10115024C>A c.2693C>A c.(2692-2694)tCt>tAt p.S898Y COADREAD 3 10122847 10122847 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:10122847C>A c.3040C>A c.(3040-3042)Cat>Aat p.H1014N COADREAD 3 10128850 10128850 + Missense_Mutation SNP A A G TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr3:10128850A>G c.3368A>G c.(3367-3369)cAa>cGa p.Q1123R COADREAD 3 10128850 10128850 + Missense_Mutation SNP A A G TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr3:10128850A>G c.3368A>G c.(3367-3369)cAa>cGa p.Q1123R COADREAD 3 10128851 10128851 + Silent SNP A A G TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr3:10128851A>G c.3369A>G c.(3367-3369)caA>caG p.Q1123Q COADREAD 3 10128851 10128851 + Silent SNP A A G TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr3:10128851A>G c.3369A>G c.(3367-3369)caA>caG p.Q1123Q COADREAD 3 10132030 10132031 + Frame_Shift_Ins INS - - A TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr3:10132030_10132031insA c.3738_3739insA c.(3739-3741)aaafs p.K1247fs COADREAD 3 10133904 10133904 + Nonsense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr3:10133904C>T c.3817C>T c.(3817-3819)Cga>Tga p.R1273* COADREAD 3 10134979 10134979 + Missense_Mutation SNP G G T TCGA-AA-3845-01A-01W-0995-10 TCGA-AA-3845-10A-01W-0995-10 g.chr3:10134979G>T c.3860G>T c.(3859-3861)aGt>aTt p.S1287I COADREAD 3 10135979 10135979 + Missense_Mutation SNP C C T TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr3:10135979C>T c.3895C>T c.(3895-3897)Cgt>Tgt p.R1299C DLBC 3 10080992 10080992 + Missense_Mutation SNP G G A TCGA-GS-A9TT-01A-11D-A382-10 TCGA-GS-A9TT-10A-01D-A385-10 g.chr3:10080992G>A c.521G>A c.(520-522)cGa>cAa p.R174Q DLBC 3 10094085 10094085 + Nonsense_Mutation SNP T T G TCGA-GS-A9TQ-01A-11D-A382-10 TCGA-GS-A9TQ-10A-01D-A385-10 g.chr3:10094085T>G c.1560T>G c.(1558-1560)taT>taG p.Y520* ESCA 3 10107133 10107133 + Nonsense_Mutation SNP G G T TCGA-Q9-A6FW-01A-31D-A31U-09 TCGA-Q9-A6FW-10A-01D-A31U-09 g.chr3:10107133G>T c.2224G>T c.(2224-2226)Gag>Tag p.E742* ESCA 3 10108990 10108990 + Missense_Mutation SNP A A C TCGA-2H-A9GO-01A-11D-A37C-09 TCGA-2H-A9GO-11A-11D-A37F-09 g.chr3:10108990A>C c.2483A>C c.(2482-2484)aAg>aCg p.K828T ESCA 3 10114581 10114581 + Frame_Shift_Del DEL G G - TCGA-2H-A9GQ-01A-11D-A37C-09 TCGA-2H-A9GQ-11A-11D-A37F-09 g.chr3:10114581delG c.2521delG c.(2521-2523)ggafs p.G841fs ESCA 3 10127509 10127509 + Missense_Mutation SNP C C G TCGA-2H-A9GI-01A-11D-A37C-09 TCGA-2H-A9GI-11A-11D-A37F-09 g.chr3:10127509C>G c.3238C>G c.(3238-3240)Caa>Gaa p.Q1080E ESCA 3 10131997 10131997 + Silent SNP C C T TCGA-Z6-AAPN-01A-11D-A403-09 TCGA-Z6-AAPN-10A-01D-A403-09 g.chr3:10131997C>T c.3705C>T c.(3703-3705)ttC>ttT p.F1235F GBM 3 10084272 10084272 + Silent SNP G G A TCGA-06-0237-01A-02D-1491-08 TCGA-06-0237-10A-01D-1491-08 g.chr3:10084272G>A c.813G>A c.(811-813)tcG>tcA p.S271S GBM 3 10107617 10107617 + Missense_Mutation SNP C C T TCGA-06-2561-01A-02D-1494-08 TCGA-06-2561-10A-01D-1494-08 g.chr3:10107617C>T c.2339C>T c.(2338-2340)tCa>tTa p.S780L GBM 3 10108908 10108908 + Missense_Mutation SNP T T C TCGA-27-2527-01A-01D-1494-08 TCGA-27-2527-10A-01D-1494-08 g.chr3:10108908T>C c.2401T>C c.(2401-2403)Tgc>Cgc p.C801R GBMLGG 3 10083383 10083383 + Missense_Mutation SNP T T G TCGA-FG-A4MY-01A-11D-A26M-08 TCGA-FG-A4MY-10A-01D-A26K-08 g.chr3:10083383T>G c.772T>G c.(772-774)Ttc>Gtc p.F258V GBMLGG 3 10084272 10084272 + Silent SNP G G A TCGA-06-0237-01A-02D-1491-08 TCGA-06-0237-10A-01D-1491-08 g.chr3:10084272G>A c.813G>A c.(811-813)tcG>tcA p.S271S GBMLGG 3 10085520 10085520 + Missense_Mutation SNP A A G TCGA-DB-A64O-01A-11D-A29Q-08 TCGA-DB-A64O-10A-01D-A29Q-08 g.chr3:10085520A>G c.1106A>G c.(1105-1107)gAa>gGa p.E369G GBMLGG 3 10105596 10105596 + Splice_Site SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:10105596G>T c.e21+1 GBMLGG 3 10107141 10107141 + Silent SNP G G A TCGA-P5-A5F4-01A-11D-A289-08 TCGA-P5-A5F4-10A-01D-A289-08 g.chr3:10107141G>A c.2232G>A c.(2230-2232)caG>caA p.Q744Q GBMLGG 3 10107617 10107617 + Missense_Mutation SNP C C T TCGA-06-2561-01A-02D-1494-08 TCGA-06-2561-10A-01D-1494-08 g.chr3:10107617C>T c.2339C>T c.(2338-2340)tCa>tTa p.S780L GBMLGG 3 10108908 10108908 + Missense_Mutation SNP T T C TCGA-27-2527-01A-01D-1494-08 TCGA-27-2527-10A-01D-1494-08 g.chr3:10108908T>C c.2401T>C c.(2401-2403)Tgc>Cgc p.C801R GBMLGG 3 10122797 10122797 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:10122797G>A c.2990G>A c.(2989-2991)cGg>cAg p.R997Q GBMLGG 3 10123119 10123119 + Silent SNP G G A TCGA-DB-A64X-01A-11D-A29Q-08 TCGA-DB-A64X-10A-01D-A29Q-08 g.chr3:10123119G>A c.3195G>A c.(3193-3195)ctG>ctA p.L1065L GBMLGG 3 10128939 10128939 + Missense_Mutation SNP G G A TCGA-FG-A713-01A-11D-A32B-08 TCGA-FG-A713-10A-01D-A329-08 g.chr3:10128939G>A c.3457G>A c.(3457-3459)Gaa>Aaa p.E1153K GBMLGG 3 10134979 10134979 + Missense_Mutation SNP G G A TCGA-RY-A83Z-01A-11D-A36O-08 TCGA-RY-A83Z-10A-01D-A367-08 g.chr3:10134979G>A c.3860G>A c.(3859-3861)aGt>aAt p.S1287N GBMLGG 3 10136015 10136015 + Missense_Mutation SNP C C T TCGA-FG-5964-01A-11D-1705-08 TCGA-FG-5964-10A-01D-1705-08 g.chr3:10136015C>T c.3931C>T c.(3931-3933)Ccg>Tcg p.P1311S GBMLGG 3 10136015 10136015 + Missense_Mutation SNP C C T TCGA-P5-A72W-01A-11D-A32B-08 TCGA-P5-A72W-10A-01D-A329-08 g.chr3:10136015C>T c.3931C>T c.(3931-3933)Ccg>Tcg p.P1311S HNSC 3 10081025 10081025 + Missense_Mutation SNP G G C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr3:10081025G>C c.554G>C c.(553-555)aGa>aCa p.R185T HNSC 3 10083359 10083359 + Missense_Mutation SNP T T A TCGA-CN-6021-01A-11D-1683-08 TCGA-CN-6021-10A-01D-1683-08 g.chr3:10083359T>A c.748T>A c.(748-750)Tca>Aca p.S250T HNSC 3 10084814 10084814 + Silent SNP G G A TCGA-CN-A63Y-01A-11D-A30E-08 TCGA-CN-A63Y-10A-01D-A30H-08 g.chr3:10084814G>A c.969G>A c.(967-969)ttG>ttA p.L323L HNSC 3 10085242 10085242 + Missense_Mutation SNP G G A TCGA-CN-A63Y-01A-11D-A30E-08 TCGA-CN-A63Y-10A-01D-A30H-08 g.chr3:10085242G>A c.1064G>A c.(1063-1065)aGa>aAa p.R355K HNSC 3 10085540 10085540 + Missense_Mutation SNP G G A TCGA-CN-A63Y-01A-11D-A30E-08 TCGA-CN-A63Y-10A-01D-A30H-08 g.chr3:10085540G>A c.1126G>A c.(1126-1128)Gaa>Aaa p.E376K HNSC 3 10088287 10088287 + Silent SNP C C T TCGA-DQ-5624-01A-01D-1870-08 TCGA-DQ-5624-10A-01D-1870-08 g.chr3:10088287C>T c.1158C>T c.(1156-1158)ttC>ttT p.F386F HNSC 3 10089632 10089632 + Missense_Mutation SNP C C T TCGA-IQ-A61E-01A-22D-A30E-08 TCGA-IQ-A61E-10A-01D-A30H-08 g.chr3:10089632C>T c.1310C>T c.(1309-1311)tCg>tTg p.S437L HNSC 3 10089666 10089666 + Silent SNP G G A TCGA-CV-A6JM-01A-11D-A31L-08 TCGA-CV-A6JM-10A-01D-A31J-08 g.chr3:10089666G>A c.1344G>A c.(1342-1344)caG>caA p.Q448Q HNSC 3 10094157 10094157 + Missense_Mutation SNP G G C TCGA-CN-A6V1-01A-12D-A34J-08 TCGA-CN-A6V1-10B-01D-A34M-08 g.chr3:10094157G>C c.1632G>C c.(1630-1632)caG>caC p.Q544H HNSC 3 10105521 10105521 + Missense_Mutation SNP C C T TCGA-CV-7568-01A-11D-2229-08 TCGA-CV-7568-10A-01D-2229-08 g.chr3:10105521C>T c.1873C>T c.(1873-1875)Cct>Tct p.P625S HNSC 3 10122836 10122836 + Missense_Mutation SNP A A G TCGA-BA-7269-01A-11D-2012-08 TCGA-BA-7269-10A-01D-2013-08 g.chr3:10122836A>G c.3029A>G c.(3028-3030)cAa>cGa p.Q1010R HNSC 3 10136015 10136015 + Missense_Mutation SNP C C T TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr3:10136015C>T c.3931C>T c.(3931-3933)Ccg>Tcg p.P1311S KICH 3 10107113 10107113 + Missense_Mutation SNP G G A TCGA-KN-8430-01A-11D-2310-10 TCGA-KN-8430-11A-01D-2311-10 g.chr3:10107113G>A c.2204G>A c.(2203-2205)cGg>cAg p.R735Q KIPAN 3 10089633 10089633 + Silent SNP G G A TCGA-IA-A40Y-01A-11D-A25F-10 TCGA-IA-A40Y-10A-01D-A25F-10 g.chr3:10089633G>A c.1311G>A c.(1309-1311)tcG>tcA p.S437S KIPAN 3 10107113 10107113 + Missense_Mutation SNP G G A TCGA-KN-8430-01A-11D-2310-10 TCGA-KN-8430-11A-01D-2311-10 g.chr3:10107113G>A c.2204G>A c.(2203-2205)cGg>cAg p.R735Q KIRP 3 10089633 10089633 + Silent SNP G G A TCGA-IA-A40Y-01A-11D-A25F-10 TCGA-IA-A40Y-10A-01D-A25F-10 g.chr3:10089633G>A c.1311G>A c.(1309-1311)tcG>tcA p.S437S LGG 3 10083383 10083383 + Missense_Mutation SNP T T G TCGA-FG-A4MY-01A-11D-A26M-08 TCGA-FG-A4MY-10A-01D-A26K-08 g.chr3:10083383T>G c.772T>G c.(772-774)Ttc>Gtc p.F258V LGG 3 10085520 10085520 + Missense_Mutation SNP A A G TCGA-DB-A64O-01A-11D-A29Q-08 TCGA-DB-A64O-10A-01D-A29Q-08 g.chr3:10085520A>G c.1106A>G c.(1105-1107)gAa>gGa p.E369G LGG 3 10105596 10105596 + Splice_Site SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:10105596G>T c.e21+1 LGG 3 10107141 10107141 + Silent SNP G G A TCGA-P5-A5F4-01A-11D-A289-08 TCGA-P5-A5F4-10A-01D-A289-08 g.chr3:10107141G>A c.2232G>A c.(2230-2232)caG>caA p.Q744Q LGG 3 10122797 10122797 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr3:10122797G>A c.2990G>A c.(2989-2991)cGg>cAg p.R997Q LGG 3 10123119 10123119 + Silent SNP G G A TCGA-DB-A64X-01A-11D-A29Q-08 TCGA-DB-A64X-10A-01D-A29Q-08 g.chr3:10123119G>A c.3195G>A c.(3193-3195)ctG>ctA p.L1065L LGG 3 10128939 10128939 + Missense_Mutation SNP G G A TCGA-FG-A713-01A-11D-A32B-08 TCGA-FG-A713-10A-01D-A329-08 g.chr3:10128939G>A c.3457G>A c.(3457-3459)Gaa>Aaa p.E1153K LGG 3 10134979 10134979 + Missense_Mutation SNP G G A TCGA-RY-A83Z-01A-11D-A36O-08 TCGA-RY-A83Z-10A-01D-A367-08 g.chr3:10134979G>A c.3860G>A c.(3859-3861)aGt>aAt p.S1287N LGG 3 10136015 10136015 + Missense_Mutation SNP C C T TCGA-FG-5964-01A-11D-1705-08 TCGA-FG-5964-10A-01D-1705-08 g.chr3:10136015C>T c.3931C>T c.(3931-3933)Ccg>Tcg p.P1311S LGG 3 10136015 10136015 + Missense_Mutation SNP C C T TCGA-P5-A72W-01A-11D-A32B-08 TCGA-P5-A72W-10A-01D-A329-08 g.chr3:10136015C>T c.3931C>T c.(3931-3933)Ccg>Tcg p.P1311S LIHC 3 10074603 10074603 + Missense_Mutation SNP T T G TCGA-DD-AADV-01A-11D-A38X-10 TCGA-DD-AADV-10A-01D-A38X-10 g.chr3:10074603T>G c.152T>G c.(151-153)cTt>cGt p.L51R LIHC 3 10076196 10076196 + Silent SNP G G C TCGA-O8-A75V-01A-11D-A32G-10 TCGA-O8-A75V-10A-01D-A32G-10 g.chr3:10076196G>C c.249G>C c.(247-249)ctG>ctC p.L83L LIHC 3 10083389 10083389 + Silent SNP T T C TCGA-2Y-A9GZ-01A-11D-A38X-10 TCGA-2Y-A9GZ-10A-01D-A38X-10 g.chr3:10083389T>C c.778T>C c.(778-780)Ttg>Ctg p.L260L LIHC 3 10084812 10084812 + Silent SNP T T C TCGA-DD-AAE7-01A-11D-A40R-10 TCGA-DD-AAE7-10A-01D-A40U-10 g.chr3:10084812T>C c.967T>C c.(967-969)Ttg>Ctg p.L323L LIHC 3 10102063 10102063 + Missense_Mutation SNP T T C TCGA-MI-A75H-01A-11D-A32G-10 TCGA-MI-A75H-10A-01D-A32G-10 g.chr3:10102063T>C c.1742T>C c.(1741-1743)aTg>aCg p.M581T LIHC 3 10108949 10108949 + Silent SNP T T C TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr3:10108949T>C c.2442T>C c.(2440-2442)acT>acC p.T814T LIHC 3 10128833 10128833 + Silent SNP C C T TCGA-CC-A3MC-01A-11D-A22F-10 TCGA-CC-A3MC-10A-01D-A22F-10 g.chr3:10128833C>T c.3351C>T c.(3349-3351)taC>taT p.Y1117Y LIHC 3 10136948 10136948 + Missense_Mutation SNP G G A TCGA-G3-A6UC-01A-21D-A33K-10 TCGA-G3-A6UC-10A-01D-A33K-10 g.chr3:10136948G>A c.4028G>A c.(4027-4029)gGg>gAg p.G1343E LUAD 3 10084739 10084739 + Silent SNP T T C TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr3:10084739T>C c.894T>C c.(892-894)atT>atC p.I298I LUAD 3 10103867 10103867 + Missense_Mutation SNP C C G TCGA-64-1681-01A-11D-2063-08 TCGA-64-1681-10A-01D-2063-08 g.chr3:10103867C>G c.1799C>G c.(1798-1800)gCc>gGc p.A600G LUAD 3 10105580 10105580 + Silent SNP G G T TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr3:10105580G>T c.1932G>T c.(1930-1932)ctG>ctT p.L644L LUAD 3 10106488 10106488 + Silent SNP C C T TCGA-73-4677-01A-01D-1265-08 TCGA-73-4677-11A-01D-1265-08 g.chr3:10106488C>T c.2097C>T c.(2095-2097)ctC>ctT p.L699L LUAD 3 10107090 10107090 + Silent SNP G G T TCGA-50-5941-01A-11D-1753-08 TCGA-50-5941-10A-01D-1753-08 g.chr3:10107090G>T c.2181G>T c.(2179-2181)ccG>ccT p.P727P LUAD 3 10130142 10130142 + Missense_Mutation SNP C C T TCGA-55-A4DG-01A-11D-A24D-08 TCGA-55-A4DG-10A-01D-A24F-08 g.chr3:10130142C>T c.3476C>T c.(3475-3477)gCc>gTc p.A1159V LUAD 3 10132062 10132062 + Missense_Mutation SNP C C G TCGA-69-8255-01A-11D-2284-08 TCGA-69-8255-10A-01D-2284-08 g.chr3:10132062C>G c.3770C>G c.(3769-3771)tCg>tGg p.S1257W LUAD 3 10136010 10136010 + Missense_Mutation SNP G G T TCGA-78-7154-01A-11D-2036-08 TCGA-78-7154-10A-01D-2036-08 g.chr3:10136010G>T c.3926G>T c.(3925-3927)tGt>tTt p.C1309F LUAD 3 10140527 10140527 + Intron SNP G G T TCGA-53-7626-01A-12D-2063-08 TCGA-53-7626-10A-01D-2063-08 g.chr3:10140527G>T OV 3 10106040 10106040 + Splice_Site SNP G G T TCGA-23-1123-01A-01W-0488-09 TCGA-23-1123-10A-01W-0488-09 g.chr3:10106040G>T c.1948G>T c.(1948-1950)Gaa>Taa p.E650* PAAD 3 10106107 10106107 + Missense_Mutation SNP C C T TCGA-HZ-A49I-01A-12D-A26I-08 TCGA-HZ-A49I-10A-01D-A26I-08 g.chr3:10106107C>T c.2015C>T c.(2014-2016)cCg>cTg p.P672L PAAD 3 10107141 10107141 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:10107141G>A c.2232G>A c.(2230-2232)caG>caA p.Q744Q PAAD 3 10107621 10107621 + Silent SNP C C T TCGA-2L-AAQA-01A-21D-A38G-08 TCGA-2L-AAQA-11A-11D-A38J-08 g.chr3:10107621C>T c.2343C>T c.(2341-2343)ttC>ttT p.F781F PAAD 3 10108928 10108928 + Missense_Mutation SNP G G T TCGA-XD-AAUG-01A-61D-A40W-08 TCGA-XD-AAUG-10A-01D-A40W-08 g.chr3:10108928G>T c.2421G>T c.(2419-2421)gaG>gaT p.E807D PAAD 3 10108928 10108928 + Missense_Mutation SNP G G T TCGA-YB-A89D-01A-12D-A36O-08 TCGA-YB-A89D-10A-01D-A367-08 g.chr3:10108928G>T c.2421G>T c.(2419-2421)gaG>gaT p.E807D PAAD 3 10115018 10115018 + Missense_Mutation SNP C C T TCGA-HZ-8637-01A-11D-2396-08 TCGA-HZ-8637-10A-01D-2396-08 g.chr3:10115018C>T c.2687C>T c.(2686-2688)aCg>aTg p.T896M PAAD 3 10116274 10116274 + Nonsense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr3:10116274C>T c.2776C>T c.(2776-2778)Cga>Tga p.R926* PAAD 3 10123132 10123132 + Missense_Mutation SNP C C A TCGA-HZ-A77Q-01A-11D-A36O-08 TCGA-HZ-A77Q-10A-01D-A367-08 g.chr3:10123132C>A c.3208C>A c.(3208-3210)Cat>Aat p.H1070N PAAD 3 10136015 10136015 + Missense_Mutation SNP C C T TCGA-3A-A9IB-01A-21D-A397-08 TCGA-3A-A9IB-10A-01D-A39A-08 g.chr3:10136015C>T c.3931C>T c.(3931-3933)Ccg>Tcg p.P1311S PRAD 3 10107082 10107082 + Missense_Mutation SNP G G A TCGA-EJ-7325-01B-11D-A32B-08 TCGA-EJ-7325-10A-01D-A329-08 g.chr3:10107082G>A c.2173G>A c.(2173-2175)Gtg>Atg p.V725M PRAD 3 10128872 10128872 + Nonsense_Mutation SNP T T A TCGA-YL-A8S8-01A-11D-A377-08 TCGA-YL-A8S8-10A-01D-A37A-08 g.chr3:10128872T>A c.3390T>A c.(3388-3390)tgT>tgA p.C1130* READ 3 10076388 10076388 + Nonsense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr3:10076388G>T c.283G>T c.(283-285)Gaa>Taa p.E95* READ 3 10084272 10084272 + Silent SNP G G T TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr3:10084272G>T c.813G>T c.(811-813)tcG>tcT p.S271S READ 3 10094090 10094090 + Missense_Mutation SNP A A G TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:10094090A>G c.1565A>G c.(1564-1566)gAt>gGt p.D522G READ 3 10106487 10106487 + Missense_Mutation SNP T T C TCGA-DC-6160-01A-11D-1657-10 TCGA-DC-6160-10A-01D-1657-10 g.chr3:10106487T>C c.2096T>C c.(2095-2097)cTc>cCc p.L699P READ 3 10115024 10115024 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:10115024C>A c.2693C>A c.(2692-2694)tCt>tAt p.S898Y READ 3 10122847 10122847 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr3:10122847C>A c.3040C>A c.(3040-3042)Cat>Aat p.H1014N SKCM 3 10081425 10081425 + Missense_Mutation SNP G G C TCGA-D3-A1Q1-06A-21D-A196-08 TCGA-D3-A1Q1-10A-01D-A198-08 g.chr3:10081425G>C c.591G>C c.(589-591)atG>atC p.M197I SKCM 3 10081488 10081488 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:10081488C>T c.654C>T c.(652-654)atC>atT p.I218I SKCM 3 10081489 10081489 + Silent SNP C C T TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr3:10081489C>T c.655C>T c.(655-657)Cta>Tta p.L219L SKCM 3 10084758 10084758 + Silent SNP T T C TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr3:10084758T>C c.913T>C c.(913-915)Ttg>Ctg p.L305L SKCM 3 10088351 10088351 + Nonsense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:10088351C>T c.1222C>T c.(1222-1224)Cga>Tga p.R408* SKCM 3 10089602 10089602 + Splice_Site SNP T T C TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr3:10089602T>C c.1280T>C c.(1279-1281)gTt>gCt p.V427A SKCM 3 10089604 10089604 + Missense_Mutation SNP C C T TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr3:10089604C>T c.1282C>T c.(1282-1284)Ctt>Ttt p.L428F SKCM 3 10089610 10089610 + Missense_Mutation SNP G G A TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr3:10089610G>A c.1288G>A c.(1288-1290)Gat>Aat p.D430N SKCM 3 10089677 10089677 + Missense_Mutation SNP C C T TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr3:10089677C>T c.1355C>T c.(1354-1356)tCa>tTa p.S452L SKCM 3 10089677 10089677 + Missense_Mutation SNP C C T TCGA-EE-A29X-06A-11D-A196-08 TCGA-EE-A29X-10A-01D-A198-08 g.chr3:10089677C>T c.1355C>T c.(1354-1356)tCa>tTa p.S452L SKCM 3 10089688 10089688 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:10089688C>T c.1366C>T c.(1366-1368)Ctc>Ttc p.L456F SKCM 3 10091094 10091094 + Missense_Mutation SNP G G A TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr3:10091094G>A c.1450G>A c.(1450-1452)Ggg>Agg p.G484R SKCM 3 10101995 10101995 + Silent SNP G G A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr3:10101995G>A c.1674G>A c.(1672-1674)gtG>gtA p.V558V SKCM 3 10105572 10105572 + Missense_Mutation SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr3:10105572G>A c.1924G>A c.(1924-1926)Gaa>Aaa p.E642K SKCM 3 10106090 10106090 + Silent SNP G G A TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr3:10106090G>A c.1998G>A c.(1996-1998)gtG>gtA p.V666V SKCM 3 10106108 10106108 + Silent SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr3:10106108G>A c.2016G>A c.(2014-2016)ccG>ccA p.P672P SKCM 3 10127572 10127572 + Missense_Mutation SNP G G A TCGA-D3-A2JC-06A-11D-A19A-08 TCGA-D3-A2JC-10A-01D-A19A-08 g.chr3:10127572G>A c.3301G>A c.(3301-3303)Gga>Aga p.G1101R SKCM 3 10128860 10128860 + Silent SNP C C A TCGA-EE-A184-06A-11D-A196-08 TCGA-EE-A184-10B-01D-A198-08 g.chr3:10128860C>A c.3378C>A c.(3376-3378)ccC>ccA p.P1126P SKCM 3 10130136 10130136 + Missense_Mutation SNP C C T TCGA-OD-A75X-06A-12D-A32N-08 TCGA-OD-A75X-10A-01D-A32N-08 g.chr3:10130136C>T c.3470C>T c.(3469-3471)tCc>tTc p.S1157F SKCM 3 10136044 10136044 + Silent SNP C C T TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chr3:10136044C>T c.3960C>T c.(3958-3960)caC>caT p.H1320H SKCM 3 10136910 10136910 + Silent SNP C C T TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr3:10136910C>T c.3990C>T c.(3988-3990)acC>acT p.T1330T SKCM 3 10140429 10140429 + Missense_Mutation SNP C C T TCGA-GF-A6C8-06A-12D-A30X-08 TCGA-GF-A6C8-10A-01D-A30X-08 g.chr3:10140429C>T c.4211C>T c.(4210-4212)tCc>tTc p.S1404F SKCM 3 10140504 10140504 + Intron SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr3:10140504C>T SKCM 3 10140621 10140621 + Intron SNP C C T TCGA-FS-A1ZM-06A-12D-A197-08 TCGA-FS-A1ZM-10A-01D-A199-08 g.chr3:10140621C>T SKCM 3 10142871 10142871 + Splice_Site SNP G G T TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr3:10142871G>T c.e44-1

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 3 10070355 10070355 single base substitution G C exon_variant BLCA-US 3 10070355 10070355 single base substitution G C missense_variant R5T 14G>C BLCA-US 3 10078013 10078013 single base substitution T G downstream_gene_variant BLCA-US 3 10078013 10078013 single base substitution T G exon_variant BLCA-US 3 10078013 10078013 single base substitution T G missense_variant F161V 481T>G BLCA-US 3 10084780 10084780 single base substitution T G downstream_gene_variant BLCA-US 3 10084780 10084780 single base substitution T G missense_variant L312W 935T>G BLCA-US 3 10084780 10084780 single base substitution T G upstream_gene_variant BLCA-US 3 10089620 10089620 single base substitution C T exon_variant BLCA-US 3 10089620 10089620 single base substitution C T missense_variant S433L 1298C>T BLCA-US 3 10089620 10089620 single base substitution C T upstream_gene_variant BLCA-US 3 10089628 10089628 single base substitution C A exon_variant BLCA-US 3 10089628 10089628 single base substitution C A missense_variant L436M 1306C>A BLCA-US 3 10089628 10089628 single base substitution C A upstream_gene_variant BLCA-US 3 10091133 10091133 single base substitution C G downstream_gene_variant BLCA-US 3 10091133 10091133 single base substitution C G exon_variant BLCA-US 3 10091133 10091133 single base substitution C G missense_variant L497V 1489C>G BLCA-US 3 10091133 10091133 single base substitution C G upstream_gene_variant BLCA-US 3 10094121 10094121 single base substitution C G downstream_gene_variant BLCA-US 3 10094121 10094121 single base substitution C G exon_variant BLCA-US 3 10094121 10094121 single base substitution C G synonymous_variant L532L 1596C>G BLCA-US 3 10106445 10106445 single base substitution G C exon_variant BLCA-US 3 10106445 10106445 single base substitution G C missense_variant G685A 2054G>C BLCA-US 3 10107147 10107147 single base substitution C A exon_variant BLCA-US 3 10107147 10107147 single base substitution C A missense_variant N746K 2238C>A BLCA-US 3 10107166 10107166 single base substitution G A exon_variant BLCA-US 3 10107166 10107166 single base substitution G A missense_variant D753N 2257G>A BLCA-US 3 10127604 10127604 single base substitution C T splice_region_variant BLCA-US 3 10133873 10133873 single base substitution A C exon_variant BLCA-US 3 10133873 10133873 single base substitution A C missense_variant E1262D 3786A>C BLCA-US 3 10133873 10133873 single base substitution A C missense_variant K1231T 3692A>C BLCA-US 3 10133873 10133873 single base substitution A C upstream_gene_variant BLCA-US 3 10138051 10138051 single base substitution C G 3_prime_UTR_variant BLCA-US 3 10138051 10138051 single base substitution C G exon_variant BLCA-US 3 10138051 10138051 single base substitution C G synonymous_variant L1360L 4080C>G BLCA-US 3 10146088 10146088 single base substitution G A downstream_gene_variant BLCA-US 3 10146259 10146259 single base substitution C T downstream_gene_variant BRCA-EU 3 10063787 10063787 single base substitution C T upstream_gene_variant BRCA-EU 3 10067288 10067288 single base substitution C T upstream_gene_variant BRCA-EU 3 10067913 10067913 single base substitution C T upstream_gene_variant BRCA-EU 3 10071628 10071628 single base substitution C T intron_variant BRCA-EU 3 10071628 10071628 single base substitution C T upstream_gene_variant BRCA-EU 3 10071991 10071991 single base substitution G C intron_variant BRCA-EU 3 10071991 10071991 single base substitution G C upstream_gene_variant BRCA-EU 3 10072457 10072457 single base substitution G A intron_variant BRCA-EU 3 10072457 10072457 single base substitution G A upstream_gene_variant BRCA-EU 3 10072582 10072582 single base substitution C G intron_variant BRCA-EU 3 10072582 10072582 single base substitution C G upstream_gene_variant BRCA-EU 3 10073014 10073014 single base substitution C A intron_variant BRCA-EU 3 10073014 10073014 single base substitution C A upstream_gene_variant BRCA-EU 3 10073219 10073219 single base substitution T C intron_variant BRCA-EU 3 10073219 10073219 single base substitution T C upstream_gene_variant BRCA-EU 3 10075869 10075869 deletion of <=200bp A - intron_variant BRCA-EU 3 10075869 10075869 deletion of <=200bp A - upstream_gene_variant BRCA-EU 3 10076250 10076250 single base substitution T C downstream_gene_variant BRCA-EU 3 10076250 10076250 single base substitution T C intron_variant BRCA-EU 3 10076250 10076250 single base substitution T C upstream_gene_variant BRCA-EU 3 10076568 10076568 deletion of <=200bp C - downstream_gene_variant BRCA-EU 3 10076568 10076568 deletion of <=200bp C - intron_variant BRCA-EU 3 10077351 10077351 single base substitution A G downstream_gene_variant BRCA-EU 3 10077351 10077351 single base substitution A G intron_variant BRCA-EU 3 10078791 10078791 single base substitution A C downstream_gene_variant BRCA-EU 3 10078791 10078791 single base substitution A C intron_variant BRCA-EU 3 10079111 10079111 single base substitution C T downstream_gene_variant BRCA-EU 3 10079111 10079111 single base substitution C T intron_variant BRCA-EU 3 10079293 10079293 single base substitution C T downstream_gene_variant BRCA-EU 3 10079293 10079293 single base substitution C T intron_variant BRCA-EU 3 10080381 10080381 single base substitution C T downstream_gene_variant BRCA-EU 3 10080381 10080381 single base substitution C T intron_variant BRCA-EU 3 10081495 10081495 single base substitution G T exon_variant BRCA-EU 3 10081495 10081495 single base substitution G T missense_variant D221Y 661G>T BRCA-EU 3 10082161 10082161 single base substitution G A 3_prime_UTR_variant BRCA-EU 3 10082161 10082161 single base substitution G A intron_variant BRCA-EU 3 10084953 10084953 single base substitution T C downstream_gene_variant BRCA-EU 3 10084953 10084953 single base substitution T C intron_variant BRCA-EU 3 10084953 10084953 single base substitution T C upstream_gene_variant BRCA-EU 3 10086053 10086053 single base substitution C A downstream_gene_variant BRCA-EU 3 10086053 10086053 single base substitution C A intron_variant BRCA-EU 3 10086053 10086053 single base substitution C A upstream_gene_variant BRCA-EU 3 10086389 10086389 single base substitution G A downstream_gene_variant BRCA-EU 3 10086389 10086389 single base substitution G A intron_variant BRCA-EU 3 10086389 10086389 single base substitution G A upstream_gene_variant BRCA-EU 3 10086898 10086898 single base substitution G C downstream_gene_variant BRCA-EU 3 10086898 10086898 single base substitution G C intron_variant BRCA-EU 3 10086898 10086898 single base substitution G C upstream_gene_variant BRCA-EU 3 10088392 10088392 single base substitution C T exon_variant BRCA-EU 3 10088392 10088392 single base substitution C T synonymous_variant F421F 1263C>T BRCA-EU 3 10088392 10088392 single base substitution C T upstream_gene_variant BRCA-EU 3 10088788 10088788 single base substitution G A intron_variant BRCA-EU 3 10088788 10088788 single base substitution G A upstream_gene_variant BRCA-EU 3 10088834 10088834 single base substitution C G intron_variant BRCA-EU 3 10088834 10088834 single base substitution C G upstream_gene_variant BRCA-EU 3 10089497 10089497 single base substitution C G intron_variant BRCA-EU 3 10089497 10089497 single base substitution C G upstream_gene_variant BRCA-EU 3 10092010 10092010 single base substitution G T downstream_gene_variant BRCA-EU 3 10092010 10092010 single base substitution G T intron_variant BRCA-EU 3 10093274 10093274 single base substitution G T downstream_gene_variant BRCA-EU 3 10093274 10093274 single base substitution G T intron_variant BRCA-EU 3 10093833 10093833 single base substitution C T downstream_gene_variant BRCA-EU 3 10093833 10093833 single base substitution C T intron_variant BRCA-EU 3 10094291 10094291 single base substitution C T downstream_gene_variant BRCA-EU 3 10094291 10094291 single base substitution C T intron_variant BRCA-EU 3 10094649 10094649 single base substitution T C downstream_gene_variant BRCA-EU 3 10094649 10094649 single base substitution T C intron_variant BRCA-EU 3 10095728 10095728 single base substitution C T downstream_gene_variant BRCA-EU 3 10095728 10095728 single base substitution C T intron_variant BRCA-EU 3 10095988 10095988 single base substitution A T downstream_gene_variant BRCA-EU 3 10095988 10095988 single base substitution A T intron_variant BRCA-EU 3 10097174 10097174 single base substitution C G intron_variant BRCA-EU 3 10097292 10097292 single base substitution C T intron_variant BRCA-EU 3 10098557 10098557 single base substitution G A intron_variant BRCA-EU 3 10098617 10098617 single base substitution C T intron_variant BRCA-EU 3 10099074 10099074 single base substitution G A intron_variant BRCA-EU 3 10099475 10099475 insertion of <=200bp - A intron_variant BRCA-EU 3 10099672 10099672 deletion of <=200bp T - intron_variant BRCA-EU 3 10100093 10100093 single base substitution C T intron_variant BRCA-EU 3 10101377 10101377 single base substitution C G intron_variant BRCA-EU 3 10101377 10101377 single base substitution C G upstream_gene_variant BRCA-EU 3 10103994 10103994 single base substitution G A intron_variant BRCA-EU 3 10103994 10103994 single base substitution G A upstream_gene_variant BRCA-EU 3 10104032 10104032 single base substitution C T intron_variant BRCA-EU 3 10104032 10104032 single base substitution C T upstream_gene_variant BRCA-EU 3 10105504 10105504 single base substitution C T exon_variant BRCA-EU 3 10105504 10105504 single base substitution C T missense_variant S619F 1856C>T BRCA-EU 3 10105504 10105504 single base substitution C T upstream_gene_variant BRCA-EU 3 10106301 10106301 single base substitution C G intron_variant BRCA-EU 3 10106301 10106301 single base substitution C G upstream_gene_variant BRCA-EU 3 10106313 10106313 single base substitution C T intron_variant BRCA-EU 3 10106313 10106313 single base substitution C T upstream_gene_variant BRCA-EU 3 10106543 10106543 single base substitution C G exon_variant BRCA-EU 3 10106543 10106543 single base substitution C G missense_variant Q718E 2152C>G BRCA-EU 3 10107260 10107260 single base substitution T C intron_variant BRCA-EU 3 10108495 10108495 single base substitution G A intron_variant BRCA-EU 3 10109414 10109414 single base substitution G A intron_variant BRCA-EU 3 10111387 10111387 single base substitution A T intron_variant BRCA-EU 3 10111914 10111914 single base substitution C T intron_variant BRCA-EU 3 10112236 10112236 single base substitution G A intron_variant BRCA-EU 3 10113818 10113818 single base substitution A G intron_variant BRCA-EU 3 10115134 10115134 deletion of <=200bp A - downstream_gene_variant BRCA-EU 3 10115134 10115134 deletion of <=200bp A - intron_variant BRCA-EU 3 10116377 10116377 single base substitution C T downstream_gene_variant BRCA-EU 3 10116377 10116377 single base substitution C T intron_variant BRCA-EU 3 10117707 10117707 single base substitution G A downstream_gene_variant BRCA-EU 3 10117707 10117707 single base substitution G A intron_variant BRCA-EU 3 10119140 10119140 single base substitution G A downstream_gene_variant BRCA-EU 3 10119140 10119140 single base substitution G A intron_variant BRCA-EU 3 10121313 10121313 single base substitution A G intron_variant BRCA-EU 3 10123572 10123572 single base substitution G T intron_variant BRCA-EU 3 10123918 10123918 single base substitution G A intron_variant BRCA-EU 3 10123956 10123956 single base substitution T G intron_variant BRCA-EU 3 10124089 10124089 single base substitution C T intron_variant BRCA-EU 3 10124683 10124683 single base substitution G C intron_variant BRCA-EU 3 10125024 10125024 single base substitution C T intron_variant BRCA-EU 3 10125444 10125444 single base substitution C T intron_variant BRCA-EU 3 10126455 10126455 single base substitution C T intron_variant BRCA-EU 3 10127743 10127743 single base substitution G A intron_variant BRCA-EU 3 10128727 10128727 single base substitution G A intron_variant BRCA-EU 3 10129893 10129893 single base substitution T G intron_variant BRCA-EU 3 10130830 10130830 single base substitution G A intron_variant BRCA-EU 3 10130830 10130830 single base substitution G A upstream_gene_variant BRCA-EU 3 10130937 10130937 single base substitution C G intron_variant BRCA-EU 3 10130937 10130937 single base substitution C G upstream_gene_variant BRCA-EU 3 10132061 10132061 single base substitution T G intron_variant BRCA-EU 3 10132061 10132061 single base substitution T G missense_variant S1257A 3769T>G BRCA-EU 3 10132061 10132061 single base substitution T G upstream_gene_variant BRCA-EU 3 10133294 10133294 single base substitution C A intron_variant BRCA-EU 3 10133294 10133294 single base substitution C A upstream_gene_variant BRCA-EU 3 10133537 10133537 single base substitution G C intron_variant BRCA-EU 3 10133537 10133537 single base substitution G C upstream_gene_variant BRCA-EU 3 10134305 10134305 single base substitution C A intron_variant BRCA-EU 3 10134305 10134305 single base substitution C A upstream_gene_variant BRCA-EU 3 10135941 10135941 single base substitution G C intron_variant BRCA-EU 3 10136390 10136392 deletion of <=200bp TAA - intron_variant BRCA-EU 3 10136654 10136654 single base substitution A G intron_variant BRCA-EU 3 10138516 10138516 deletion of <=200bp T - intron_variant BRCA-EU 3 10138913 10138913 single base substitution G A intron_variant BRCA-EU 3 10139939 10139939 single base substitution C G intron_variant BRCA-EU 3 10141463 10141463 single base substitution A G downstream_gene_variant BRCA-EU 3 10141463 10141463 single base substitution A G intron_variant BRCA-EU 3 10141510 10141510 single base substitution G C downstream_gene_variant BRCA-EU 3 10141510 10141510 single base substitution G C intron_variant BRCA-EU 3 10142677 10142677 single base substitution C T downstream_gene_variant BRCA-EU 3 10142677 10142677 single base substitution C T intron_variant BRCA-EU 3 10143010 10143010 single base substitution T G 3_prime_UTR_variant BRCA-EU 3 10143010 10143010 single base substitution T G downstream_gene_variant BRCA-EU 3 10143288 10143288 single base substitution C G 3_prime_UTR_variant BRCA-EU 3 10143288 10143288 single base substitution C G downstream_gene_variant BRCA-EU 3 10143361 10143361 single base substitution C T 3_prime_UTR_variant BRCA-EU 3 10143361 10143361 single base substitution C T downstream_gene_variant BRCA-EU 3 10144020 10144020 single base substitution G A downstream_gene_variant BRCA-EU 3 10144219 10144219 deletion of <=200bp A - downstream_gene_variant BRCA-EU 3 10145188 10145188 single base substitution G A downstream_gene_variant BRCA-EU 3 10145342 10145342 single base substitution A G downstream_gene_variant BRCA-EU 3 10145357 10145357 single base substitution A G downstream_gene_variant BRCA-EU 3 10146063 10146063 single base substitution C T downstream_gene_variant BRCA-EU 3 10146783 10146783 single base substitution G A downstream_gene_variant BRCA-EU 3 10146934 10146934 single base substitution C G downstream_gene_variant BRCA-EU 3 10148162 10148162 single base substitution C G downstream_gene_variant BRCA-FR 3 10072010 10072010 single base substitution A C intron_variant BRCA-FR 3 10072010 10072010 single base substitution A C upstream_gene_variant BRCA-FR 3 10072582 10072582 single base substitution C G intron_variant BRCA-FR 3 10072582 10072582 single base substitution C G upstream_gene_variant BRCA-FR 3 10086898 10086898 single base substitution G C downstream_gene_variant BRCA-FR 3 10086898 10086898 single base substitution G C intron_variant BRCA-FR 3 10086898 10086898 single base substitution G C upstream_gene_variant BRCA-FR 3 10088392 10088392 single base substitution C T exon_variant BRCA-FR 3 10088392 10088392 single base substitution C T synonymous_variant F421F 1263C>T BRCA-FR 3 10088392 10088392 single base substitution C T upstream_gene_variant BRCA-FR 3 10088834 10088834 single base substitution C G intron_variant BRCA-FR 3 10088834 10088834 single base substitution C G upstream_gene_variant BRCA-FR 3 10095728 10095728 single base substitution C T downstream_gene_variant BRCA-FR 3 10095728 10095728 single base substitution C T intron_variant BRCA-FR 3 10097174 10097174 single base substitution C G intron_variant BRCA-FR 3 10098557 10098557 single base substitution G A intron_variant BRCA-FR 3 10099074 10099074 single base substitution G A intron_variant BRCA-FR 3 10104032 10104032 single base substitution C T intron_variant BRCA-FR 3 10104032 10104032 single base substitution C T upstream_gene_variant BRCA-FR 3 10105143 10105143 single base substitution T G intron_variant BRCA-FR 3 10105143 10105143 single base substitution T G upstream_gene_variant BRCA-FR 3 10105255 10105255 single base substitution T C intron_variant BRCA-FR 3 10105255 10105255 single base substitution T C upstream_gene_variant BRCA-FR 3 10106623 10106623 single base substitution C T intron_variant BRCA-FR 3 10108495 10108495 single base substitution G A intron_variant BRCA-FR 3 10113198 10113198 single base substitution C G intron_variant BRCA-FR 3 10127743 10127743 single base substitution G A intron_variant BRCA-FR 3 10128727 10128727 single base substitution G A intron_variant BRCA-FR 3 10130937 10130937 single base substitution C G intron_variant BRCA-FR 3 10130937 10130937 single base substitution C G upstream_gene_variant BRCA-FR 3 10141510 10141510 single base substitution G C downstream_gene_variant BRCA-FR 3 10141510 10141510 single base substitution G C intron_variant BRCA-FR 3 10142677 10142677 single base substitution C T downstream_gene_variant BRCA-FR 3 10142677 10142677 single base substitution C T intron_variant BRCA-KR 3 10132074 10132074 single base substitution G C intron_variant BRCA-KR 3 10132074 10132074 single base substitution G C splice_region_variant BRCA-KR 3 10132074 10132074 single base substitution G C upstream_gene_variant BRCA-UK 3 10071560 10071560 single base substitution C G intron_variant BRCA-UK 3 10071560 10071560 single base substitution C G upstream_gene_variant BRCA-UK 3 10072256 10072256 single base substitution C A intron_variant BRCA-UK 3 10072256 10072256 single base substitution C A upstream_gene_variant BRCA-UK 3 10072257 10072257 single base substitution C T intron_variant BRCA-UK 3 10072257 10072257 single base substitution C T upstream_gene_variant BRCA-UK 3 10103838 10103838 single base substitution T G exon_variant BRCA-UK 3 10103838 10103838 single base substitution T G missense_variant S590R 1770T>G BRCA-UK 3 10103838 10103838 single base substitution T G upstream_gene_variant BRCA-UK 3 10107292 10107292 single base substitution G A intron_variant BRCA-UK 3 10123048 10123048 single base substitution C T exon_variant BRCA-UK 3 10123048 10123048 single base substitution C T missense_variant H1042Y 3124C>T BRCA-UK 3 10127523 10127523 single base substitution G A exon_variant BRCA-UK 3 10127523 10127523 single base substitution G A synonymous_variant Q1084Q 3252G>A BRCA-UK 3 10148162 10148162 single base substitution C G downstream_gene_variant BRCA-US 3 10065390 10065390 single base substitution C T upstream_gene_variant BRCA-US 3 10089628 10089628 single base substitution C T exon_variant BRCA-US 3 10089628 10089628 single base substitution C T synonymous_variant L436L 1306C>T BRCA-US 3 10089628 10089628 single base substitution C T upstream_gene_variant BRCA-US 3 10089640 10089640 single base substitution C T exon_variant BRCA-US 3 10089640 10089640 single base substitution C T stop_gained Q440* 1318C>T BRCA-US 3 10089640 10089640 single base substitution C T upstream_gene_variant BRCA-US 3 10106486 10106486 single base substitution C T exon_variant BRCA-US 3 10106486 10106486 single base substitution C T missense_variant L699F 2095C>T BRCA-US 3 10107101 10107101 single base substitution C T exon_variant BRCA-US 3 10107101 10107101 single base substitution C T missense_variant A731V 2192C>T BRCA-US 3 10107574 10107574 single base substitution G T exon_variant BRCA-US 3 10107574 10107574 single base substitution G T stop_gained E766* 2296G>T BRCA-US 3 10108898 10108898 single base substitution A G exon_variant BRCA-US 3 10108898 10108898 single base substitution A G intron_variant BRCA-US 3 10108898 10108898 single base substitution A G synonymous_variant V797V 2391A>G BRCA-US 3 10108913 10108913 single base substitution G T exon_variant BRCA-US 3 10108913 10108913 single base substitution G T intron_variant BRCA-US 3 10108913 10108913 single base substitution G T missense_variant Q802H 2406G>T BRCA-US 3 10114587 10114587 single base substitution T A exon_variant BRCA-US 3 10114587 10114587 single base substitution T A missense_variant F843I 2527T>A BRCA-US 3 10114941 10114941 single base substitution G T downstream_gene_variant BRCA-US 3 10114941 10114941 single base substitution G T exon_variant BRCA-US 3 10114941 10114941 single base substitution G T missense_variant R870S 2610G>T BRCA-US 3 10119819 10119819 single base substitution C T exon_variant BRCA-US 3 10119819 10119819 single base substitution C T missense_variant L972F 2914C>T BRCA-US 3 10123020 10123020 single base substitution T G intron_variant BRCA-US 3 10130185 10130185 single base substitution G C exon_variant BRCA-US 3 10130185 10130185 single base substitution G C missense_variant E1173D 3519G>C BRCA-US 3 10130185 10130185 single base substitution G C upstream_gene_variant BRCA-US 3 10130560 10130560 single base substitution T C exon_variant BRCA-US 3 10130560 10130560 single base substitution T C synonymous_variant I1203I 3609T>C BRCA-US 3 10130560 10130560 single base substitution T C upstream_gene_variant BRCA-US 3 10138113 10138113 single base substitution G C 3_prime_UTR_variant BRCA-US 3 10138113 10138113 single base substitution G C exon_variant BRCA-US 3 10138113 10138113 single base substitution G C missense_variant R1381T 4142G>C BRCA-US 3 10146113 10146113 single base substitution C T downstream_gene_variant BRCA-US 3 10146177 10146177 single base substitution G C downstream_gene_variant BRCA-US 3 10146188 10146188 single base substitution G A downstream_gene_variant BTCA-JP 3 10070236 10070236 single base substitution C T intron_variant BTCA-JP 3 10070236 10070236 single base substitution C T upstream_gene_variant BTCA-JP 3 10070260 10070260 single base substitution C T intron_variant BTCA-JP 3 10070260 10070260 single base substitution C T upstream_gene_variant BTCA-JP 3 10074644 10074644 single base substitution C T 3_prime_UTR_variant BTCA-JP 3 10074644 10074644 single base substitution C T stop_gained Q65* 193C>T BTCA-JP 3 10074644 10074644 single base substitution C T upstream_gene_variant BTCA-JP 3 10074670 10074670 single base substitution C G intron_variant BTCA-JP 3 10074670 10074670 single base substitution C G upstream_gene_variant BTCA-JP 3 10076115 10076115 single base substitution T C intron_variant BTCA-JP 3 10076115 10076115 single base substitution T C upstream_gene_variant BTCA-JP 3 10076352 10076352 single base substitution C G downstream_gene_variant BTCA-JP 3 10076352 10076352 single base substitution C G intron_variant BTCA-JP 3 10076352 10076352 single base substitution C G upstream_gene_variant BTCA-JP 3 10084393 10084393 single base substitution C T downstream_gene_variant BTCA-JP 3 10084393 10084393 single base substitution C T intron_variant BTCA-JP 3 10084393 10084393 single base substitution C T upstream_gene_variant BTCA-JP 3 10088223 10088223 single base substitution T G downstream_gene_variant BTCA-JP 3 10088223 10088223 single base substitution T G exon_variant BTCA-JP 3 10088223 10088223 single base substitution T G intron_variant BTCA-JP 3 10088223 10088223 single base substitution T G upstream_gene_variant BTCA-JP 3 10088239 10088239 single base substitution G A downstream_gene_variant BTCA-JP 3 10088239 10088239 single base substitution G A exon_variant BTCA-JP 3 10088239 10088239 single base substitution G A intron_variant BTCA-JP 3 10088239 10088239 single base substitution G A upstream_gene_variant BTCA-JP 3 10088242 10088242 single base substitution G A downstream_gene_variant BTCA-JP 3 10088242 10088242 single base substitution G A exon_variant BTCA-JP 3 10088242 10088242 single base substitution G A intron_variant BTCA-JP 3 10088242 10088242 single base substitution G A upstream_gene_variant BTCA-JP 3 10089723 10089723 single base substitution G A exon_variant BTCA-JP 3 10089723 10089723 single base substitution G A synonymous_variant T467T 1401G>A BTCA-JP 3 10089723 10089723 single base substitution G A upstream_gene_variant BTCA-JP 3 10089738 10089738 single base substitution A G exon_variant BTCA-JP 3 10089738 10089738 single base substitution A G splice_region_variant BTCA-JP 3 10089738 10089738 single base substitution A G upstream_gene_variant BTCA-JP 3 10091153 10091153 single base substitution C T downstream_gene_variant BTCA-JP 3 10091153 10091153 single base substitution C T exon_variant BTCA-JP 3 10091153 10091153 single base substitution C T synonymous_variant N503N 1509C>T BTCA-JP 3 10103946 10103946 single base substitution A T intron_variant BTCA-JP 3 10103946 10103946 single base substitution A T upstream_gene_variant BTCA-JP 3 10105439 10105439 single base substitution A C intron_variant BTCA-JP 3 10105439 10105439 single base substitution A C upstream_gene_variant BTCA-JP 3 10106623 10106623 single base substitution C T intron_variant BTCA-JP 3 10140424 10140424 single base substitution A C 3_prime_UTR_variant BTCA-JP 3 10140424 10140424 single base substitution A C exon_variant BTCA-JP 3 10140424 10140424 single base substitution A C missense_variant Q1402H 4206A>C BTCA-JP 3 10144590 10144590 single base substitution A T downstream_gene_variant BTCA-JP 3 10146175 10146175 single base substitution C T downstream_gene_variant CESC-US 3 10074515 10074515 single base substitution G C splice_acceptor_variant CESC-US 3 10074515 10074515 single base substitution G C upstream_gene_variant CESC-US 3 10107104 10107104 single base substitution C T exon_variant CESC-US 3 10107104 10107104 single base substitution C T missense_variant P732L 2195C>T CESC-US 3 10142946 10142946 single base substitution G C 3_prime_UTR_variant CESC-US 3 10142946 10142946 single base substitution G C downstream_gene_variant CESC-US 3 10142946 10142946 single base substitution G C exon_variant CESC-US 3 10142946 10142946 single base substitution G C stop_lost *1452Y 4356G>C CESC-US 3 10146175 10146175 single base substitution C T downstream_gene_variant CLLE-ES 3 10087850 10087850 single base substitution G A downstream_gene_variant CLLE-ES 3 10087850 10087850 single base substitution G A intron_variant CLLE-ES 3 10087850 10087850 single base substitution G A upstream_gene_variant CLLE-ES 3 10106560 10106560 single base substitution G T splice_donor_variant CLLE-ES 3 10114905 10114905 single base substitution C T downstream_gene_variant CLLE-ES 3 10114905 10114905 single base substitution C T intron_variant CLLE-ES 3 10123557 10123557 single base substitution G A intron_variant CLLE-ES 3 10137477 10137477 single base substitution C A intron_variant CLLE-ES 3 10141032 10141032 single base substitution C G 3_prime_UTR_variant CLLE-ES 3 10141032 10141032 single base substitution C G intron_variant COAD-US 3 10081417 10081417 single base substitution A G exon_variant COAD-US 3 10081417 10081417 single base substitution A G missense_variant K195E 583A>G COAD-US 3 10084751 10084751 single base substitution G A downstream_gene_variant COAD-US 3 10084751 10084751 single base substitution G A synonymous_variant R302R 906G>A COAD-US 3 10084751 10084751 single base substitution G A upstream_gene_variant COAD-US 3 10085536 10085536 single base substitution A G downstream_gene_variant COAD-US 3 10085536 10085536 single base substitution A G synonymous_variant V374V 1122A>G COAD-US 3 10085536 10085536 single base substitution A G upstream_gene_variant COAD-US 3 10102080 10102080 single base substitution G A exon_variant COAD-US 3 10102080 10102080 single base substitution G A missense_variant A587T 1759G>A COAD-US 3 10102080 10102080 single base substitution G A upstream_gene_variant COAD-US 3 10114996 10114996 deletion of <=200bp A - downstream_gene_variant COAD-US 3 10114996 10114996 deletion of <=200bp A - exon_variant COAD-US 3 10114996 10114996 deletion of <=200bp A - frameshift_variant K889 COAD-US 3 10132030 10132030 insertion of <=200bp - A frameshift_variant V1246V? COAD-US 3 10132030 10132030 insertion of <=200bp - A intron_variant COAD-US 3 10132030 10132030 insertion of <=200bp - A upstream_gene_variant COAD-US 3 10138069 10138069 single base substitution T G 3_prime_UTR_variant COAD-US 3 10138069 10138069 single base substitution T G exon_variant COAD-US 3 10138069 10138069 single base substitution T G synonymous_variant L1366L 4098T>G COAD-US 3 10146443 10146443 single base substitution G T downstream_gene_variant COCA-CN 3 10070553 10070553 single base substitution G A intron_variant COCA-CN 3 10074036 10074036 single base substitution C G 3_prime_UTR_variant COCA-CN 3 10074036 10074036 single base substitution C G intron_variant COCA-CN 3 10074036 10074036 single base substitution C G upstream_gene_variant COCA-CN 3 10076030 10076030 single base substitution G A intron_variant COCA-CN 3 10076030 10076030 single base substitution G A upstream_gene_variant COCA-CN 3 10076052 10076052 single base substitution G T intron_variant COCA-CN 3 10076052 10076052 single base substitution G T upstream_gene_variant COCA-CN 3 10076064 10076064 single base substitution A T intron_variant COCA-CN 3 10076064 10076064 single base substitution A T upstream_gene_variant COCA-CN 3 10085624 10085624 single base substitution G T downstream_gene_variant COCA-CN 3 10085624 10085624 single base substitution G T intron_variant COCA-CN 3 10085624 10085624 single base substitution G T upstream_gene_variant COCA-CN 3 10088223 10088223 single base substitution T G downstream_gene_variant COCA-CN 3 10088223 10088223 single base substitution T G exon_variant COCA-CN 3 10088223 10088223 single base substitution T G intron_variant COCA-CN 3 10088223 10088223 single base substitution T G upstream_gene_variant COCA-CN 3 10088239 10088239 single base substitution G A downstream_gene_variant COCA-CN 3 10088239 10088239 single base substitution G A exon_variant COCA-CN 3 10088239 10088239 single base substitution G A intron_variant COCA-CN 3 10088239 10088239 single base substitution G A upstream_gene_variant COCA-CN 3 10088242 10088242 single base substitution G A downstream_gene_variant COCA-CN 3 10088242 10088242 single base substitution G A exon_variant COCA-CN 3 10088242 10088242 single base substitution G A intron_variant COCA-CN 3 10088242 10088242 single base substitution G A upstream_gene_variant COCA-CN 3 10088266 10088266 single base substitution G T exon_variant COCA-CN 3 10088266 10088266 single base substitution G T splice_region_variant COCA-CN 3 10088266 10088266 single base substitution G T upstream_gene_variant COCA-CN 3 10088299 10088299 single base substitution C T exon_variant COCA-CN 3 10088299 10088299 single base substitution C T synonymous_variant S390S 1170C>T COCA-CN 3 10088299 10088299 single base substitution C T upstream_gene_variant COCA-CN 3 10088308 10088308 single base substitution T C exon_variant COCA-CN 3 10088308 10088308 single base substitution T C synonymous_variant T393T 1179T>C COCA-CN 3 10088308 10088308 single base substitution T C upstream_gene_variant COCA-CN 3 10088343 10088343 single base substitution A G exon_variant COCA-CN 3 10088343 10088343 single base substitution A G missense_variant N405S 1214A>G COCA-CN 3 10088343 10088343 single base substitution A G upstream_gene_variant COCA-CN 3 10088404 10088404 single base substitution C T exon_variant COCA-CN 3 10088404 10088404 single base substitution C T synonymous_variant Y425Y 1275C>T COCA-CN 3 10088404 10088404 single base substitution C T upstream_gene_variant COCA-CN 3 10088422 10088422 single base substitution C T intron_variant COCA-CN 3 10088422 10088422 single base substitution C T upstream_gene_variant COCA-CN 3 10088443 10088443 single base substitution C A intron_variant COCA-CN 3 10088443 10088443 single base substitution C A upstream_gene_variant COCA-CN 3 10088444 10088444 single base substitution A G intron_variant COCA-CN 3 10088444 10088444 single base substitution A G upstream_gene_variant COCA-CN 3 10088461 10088461 single base substitution T C intron_variant COCA-CN 3 10088461 10088461 single base substitution T C upstream_gene_variant COCA-CN 3 10089278 10089278 single base substitution A G intron_variant COCA-CN 3 10089278 10089278 single base substitution A G upstream_gene_variant COCA-CN 3 10089723 10089723 single base substitution G A exon_variant COCA-CN 3 10089723 10089723 single base substitution G A synonymous_variant T467T 1401G>A COCA-CN 3 10089723 10089723 single base substitution G A upstream_gene_variant COCA-CN 3 10089738 10089738 single base substitution A G exon_variant COCA-CN 3 10089738 10089738 single base substitution A G splice_region_variant COCA-CN 3 10089738 10089738 single base substitution A G upstream_gene_variant COCA-CN 3 10089749 10089749 single base substitution T C downstream_gene_variant COCA-CN 3 10089749 10089749 single base substitution T C intron_variant COCA-CN 3 10089749 10089749 single base substitution T C upstream_gene_variant COCA-CN 3 10089772 10089772 single base substitution C G downstream_gene_variant COCA-CN 3 10089772 10089772 single base substitution C G intron_variant COCA-CN 3 10089772 10089772 single base substitution C G upstream_gene_variant COCA-CN 3 10089773 10089773 single base substitution A G downstream_gene_variant COCA-CN 3 10089773 10089773 single base substitution A G intron_variant COCA-CN 3 10089773 10089773 single base substitution A G upstream_gene_variant COCA-CN 3 10089775 10089775 single base substitution A G downstream_gene_variant COCA-CN 3 10089775 10089775 single base substitution A G intron_variant COCA-CN 3 10089775 10089775 single base substitution A G upstream_gene_variant COCA-CN 3 10089818 10089818 single base substitution C T downstream_gene_variant COCA-CN 3 10089818 10089818 single base substitution C T intron_variant COCA-CN 3 10089818 10089818 single base substitution C T upstream_gene_variant COCA-CN 3 10089852 10089852 single base substitution A G downstream_gene_variant COCA-CN 3 10089852 10089852 single base substitution A G intron_variant COCA-CN 3 10089852 10089852 single base substitution A G upstream_gene_variant COCA-CN 3 10090948 10090948 single base substitution T C downstream_gene_variant COCA-CN 3 10090948 10090948 single base substitution T C intron_variant COCA-CN 3 10090948 10090948 single base substitution T C upstream_gene_variant COCA-CN 3 10091035 10091035 single base substitution T C downstream_gene_variant COCA-CN 3 10091035 10091035 single base substitution T C intron_variant COCA-CN 3 10091035 10091035 single base substitution T C upstream_gene_variant COCA-CN 3 10091049 10091049 single base substitution C T downstream_gene_variant COCA-CN 3 10091049 10091049 single base substitution C T intron_variant COCA-CN 3 10091049 10091049 single base substitution C T upstream_gene_variant COCA-CN 3 10091252 10091252 single base substitution A C downstream_gene_variant COCA-CN 3 10091252 10091252 single base substitution A C intron_variant COCA-CN 3 10091261 10091261 single base substitution G A downstream_gene_variant COCA-CN 3 10091261 10091261 single base substitution G A intron_variant COCA-CN 3 10099913 10099913 single base substitution G A intron_variant COCA-CN 3 10102069 10102069 single base substitution G A exon_variant COCA-CN 3 10102069 10102069 single base substitution G A missense_variant G583D 1748G>A COCA-CN 3 10102069 10102069 single base substitution G A upstream_gene_variant COCA-CN 3 10105439 10105439 single base substitution A C intron_variant COCA-CN 3 10105439 10105439 single base substitution A C upstream_gene_variant COCA-CN 3 10106144 10106144 single base substitution C T intron_variant COCA-CN 3 10106144 10106144 single base substitution C T upstream_gene_variant COCA-CN 3 10106408 10106408 single base substitution C T exon_variant COCA-CN 3 10106408 10106408 single base substitution C T splice_region_variant COCA-CN 3 10106495 10106495 single base substitution C T exon_variant COCA-CN 3 10106495 10106495 single base substitution C T synonymous_variant L702L 2104C>T COCA-CN 3 10106533 10106533 single base substitution G T exon_variant COCA-CN 3 10106533 10106533 single base substitution G T synonymous_variant P714P 2142G>T COCA-CN 3 10106608 10106608 single base substitution T C intron_variant COCA-CN 3 10107448 10107448 single base substitution A G intron_variant COCA-CN 3 10114610 10114610 single base substitution A G exon_variant COCA-CN 3 10114610 10114610 single base substitution A G missense_variant I850M 2550A>G COCA-CN 3 10114802 10114802 single base substitution T C downstream_gene_variant COCA-CN 3 10114802 10114802 single base substitution T C intron_variant COCA-CN 3 10119932 10119932 single base substitution A C intron_variant COCA-CN 3 10123252 10123252 single base substitution T G intron_variant COCA-CN 3 10143055 10143055 single base substitution G T 3_prime_UTR_variant COCA-CN 3 10143055 10143055 single base substitution G T downstream_gene_variant COCA-CN 3 10143061 10143061 single base substitution C T 3_prime_UTR_variant COCA-CN 3 10143061 10143061 single base substitution C T downstream_gene_variant COCA-CN 3 10146210 10146210 single base substitution G A downstream_gene_variant ESAD-UK 3 10065431 10065431 single base substitution C T upstream_gene_variant ESAD-UK 3 10075087 10075087 insertion of <=200bp - A intron_variant ESAD-UK 3 10075087 10075087 insertion of <=200bp - A upstream_gene_variant ESAD-UK 3 10081621 10081621 single base substitution T C 3_prime_UTR_variant ESAD-UK 3 10081621 10081621 single base substitution T C intron_variant ESAD-UK 3 10086921 10086921 single base substitution C T downstream_gene_variant ESAD-UK 3 10086921 10086921 single base substitution C T intron_variant ESAD-UK 3 10086921 10086921 single base substitution C T upstream_gene_variant ESAD-UK 3 10092588 10092588 single base substitution G A downstream_gene_variant ESAD-UK 3 10092588 10092588 single base substitution G A intron_variant ESAD-UK 3 10094306 10094306 single base substitution G T downstream_gene_variant ESAD-UK 3 10094306 10094306 single base substitution G T intron_variant ESAD-UK 3 10100079 10100079 single base substitution C T intron_variant ESAD-UK 3 10100142 10100142 single base substitution G C intron_variant ESAD-UK 3 10100461 10100461 single base substitution G A intron_variant ESAD-UK 3 10101249 10101249 single base substitution G A intron_variant ESAD-UK 3 10101249 10101249 single base substitution G A upstream_gene_variant ESAD-UK 3 10102259 10102259 single base substitution A C intron_variant ESAD-UK 3 10102259 10102259 single base substitution A C upstream_gene_variant ESAD-UK 3 10104473 10104473 single base substitution A C intron_variant ESAD-UK 3 10104473 10104473 single base substitution A C upstream_gene_variant ESAD-UK 3 10105887 10105887 single base substitution C T intron_variant ESAD-UK 3 10105887 10105887 single base substitution C T upstream_gene_variant ESAD-UK 3 10109234 10109234 single base substitution C G intron_variant ESAD-UK 3 10109253 10109253 single base substitution G T intron_variant ESAD-UK 3 10110732 10110732 single base substitution C A intron_variant ESAD-UK 3 10110842 10110842 single base substitution A G intron_variant ESAD-UK 3 10110843 10110843 single base substitution A C intron_variant ESAD-UK 3 10113380 10113380 single base substitution G T intron_variant ESAD-UK 3 10114845 10114845 single base substitution C A downstream_gene_variant ESAD-UK 3 10114845 10114845 single base substitution C A intron_variant ESAD-UK 3 10115214 10115214 single base substitution T G downstream_gene_variant ESAD-UK 3 10115214 10115214 single base substitution T G intron_variant ESAD-UK 3 10115621 10115627 deletion of <=200bp GTTTTTT - downstream_gene_variant ESAD-UK 3 10115621 10115627 deletion of <=200bp GTTTTTT - intron_variant ESAD-UK 3 10119169 10119169 single base substitution G A downstream_gene_variant ESAD-UK 3 10119169 10119169 single base substitution G A intron_variant ESAD-UK 3 10120002 10120002 single base substitution C A intron_variant ESAD-UK 3 10122200 10122200 single base substitution A C intron_variant ESAD-UK 3 10123547 10123547 single base substitution G T intron_variant ESAD-UK 3 10124531 10124531 single base substitution G A intron_variant ESAD-UK 3 10125343 10125343 single base substitution C A intron_variant ESAD-UK 3 10126157 10126157 single base substitution T C intron_variant ESAD-UK 3 10128673 10128673 single base substitution T C intron_variant ESAD-UK 3 10129690 10129690 single base substitution G C intron_variant ESAD-UK 3 10129907 10129907 single base substitution G A intron_variant ESAD-UK 3 10130367 10130367 single base substitution C T intron_variant ESAD-UK 3 10130367 10130367 single base substitution C T upstream_gene_variant ESAD-UK 3 10133791 10133791 single base substitution A G intron_variant ESAD-UK 3 10133791 10133791 single base substitution A G upstream_gene_variant ESAD-UK 3 10133813 10133813 single base substitution A G intron_variant ESAD-UK 3 10133813 10133813 single base substitution A G upstream_gene_variant ESAD-UK 3 10136298 10136298 single base substitution T C intron_variant ESAD-UK 3 10137680 10137680 single base substitution G A intron_variant ESAD-UK 3 10139788 10139788 single base substitution T C intron_variant ESAD-UK 3 10140166 10140166 single base substitution G A intron_variant ESAD-UK 3 10145238 10145238 single base substitution G A downstream_gene_variant ESAD-UK 3 10145590 10145590 deletion of <=200bp C - downstream_gene_variant ESAD-UK 3 10146628 10146628 single base substitution T C downstream_gene_variant ESCA-CN 3 10089773 10089773 single base substitution A G downstream_gene_variant ESCA-CN 3 10089773 10089773 single base substitution A G intron_variant ESCA-CN 3 10089773 10089773 single base substitution A G upstream_gene_variant ESCA-CN 3 10089775 10089775 single base substitution A G downstream_gene_variant ESCA-CN 3 10089775 10089775 single base substitution A G intron_variant ESCA-CN 3 10089775 10089775 single base substitution A G upstream_gene_variant ESCA-CN 3 10089852 10089852 single base substitution A G downstream_gene_variant ESCA-CN 3 10089852 10089852 single base substitution A G intron_variant ESCA-CN 3 10089852 10089852 single base substitution A G upstream_gene_variant GACA-CN 3 10133915 10133915 single base substitution T G exon_variant GACA-CN 3 10133915 10133915 single base substitution T G missense_variant S1276R 3828T>G GACA-CN 3 10133915 10133915 single base substitution T G missense_variant V1245G 3734T>G GACA-CN 3 10133915 10133915 single base substitution T G upstream_gene_variant GBM-US 3 10084272 10084272 single base substitution G A downstream_gene_variant GBM-US 3 10084272 10084272 single base substitution G A synonymous_variant S271S 813G>A GBM-US 3 10084272 10084272 single base substitution G A upstream_gene_variant GBM-US 3 10107617 10107617 single base substitution C T exon_variant GBM-US 3 10107617 10107617 single base substitution C T missense_variant S780L 2339C>T GBM-US 3 10108908 10108908 single base substitution T C exon_variant GBM-US 3 10108908 10108908 single base substitution T C intron_variant GBM-US 3 10108908 10108908 single base substitution T C missense_variant C801R 2401T>C KIRC-US 3 10088404 10088404 single base substitution C T exon_variant KIRC-US 3 10088404 10088404 single base substitution C T synonymous_variant Y425Y 1275C>T KIRC-US 3 10088404 10088404 single base substitution C T upstream_gene_variant KIRC-US 3 10108913 10108913 single base substitution G T exon_variant KIRC-US 3 10108913 10108913 single base substitution G T intron_variant KIRC-US 3 10108913 10108913 single base substitution G T missense_variant Q802H 2406G>T KIRP-US 3 10089633 10089633 single base substitution G A exon_variant KIRP-US 3 10089633 10089633 single base substitution G A synonymous_variant S437S 1311G>A KIRP-US 3 10089633 10089633 single base substitution G A upstream_gene_variant LAML-KR 3 10069417 10069417 single base substitution G A intron_variant LAML-KR 3 10069417 10069417 single base substitution G A upstream_gene_variant LAML-KR 3 10069618 10069618 single base substitution T C intron_variant LAML-KR 3 10069618 10069618 single base substitution T C upstream_gene_variant LAML-KR 3 10069635 10069635 single base substitution A G intron_variant LAML-KR 3 10069635 10069635 single base substitution A G upstream_gene_variant LAML-KR 3 10088239 10088239 single base substitution G A downstream_gene_variant LAML-KR 3 10088239 10088239 single base substitution G A exon_variant LAML-KR 3 10088239 10088239 single base substitution G A intron_variant LAML-KR 3 10088239 10088239 single base substitution G A upstream_gene_variant LAML-KR 3 10088266 10088266 single base substitution G T exon_variant LAML-KR 3 10088266 10088266 single base substitution G T splice_region_variant LAML-KR 3 10088266 10088266 single base substitution G T upstream_gene_variant LAML-KR 3 10088343 10088343 single base substitution A G exon_variant LAML-KR 3 10088343 10088343 single base substitution A G missense_variant N405S 1214A>G LAML-KR 3 10088343 10088343 single base substitution A G upstream_gene_variant LAML-KR 3 10088514 10088514 single base substitution T C intron_variant LAML-KR 3 10088514 10088514 single base substitution T C upstream_gene_variant LAML-KR 3 10089402 10089402 single base substitution C T intron_variant LAML-KR 3 10089402 10089402 single base substitution C T upstream_gene_variant LAML-KR 3 10089408 10089408 single base substitution A C intron_variant LAML-KR 3 10089408 10089408 single base substitution A C upstream_gene_variant LAML-KR 3 10089414 10089414 single base substitution T C intron_variant LAML-KR 3 10089414 10089414 single base substitution T C upstream_gene_variant LAML-KR 3 10089419 10089419 single base substitution G C intron_variant LAML-KR 3 10089419 10089419 single base substitution G C upstream_gene_variant LAML-KR 3 10089426 10089426 single base substitution G A intron_variant LAML-KR 3 10089426 10089426 single base substitution G A upstream_gene_variant LAML-KR 3 10089427 10089427 single base substitution T A intron_variant LAML-KR 3 10089427 10089427 single base substitution T A upstream_gene_variant LAML-KR 3 10089430 10089430 single base substitution T A intron_variant LAML-KR 3 10089430 10089430 single base substitution T A upstream_gene_variant LAML-KR 3 10089440 10089440 single base substitution A G intron_variant LAML-KR 3 10089440 10089440 single base substitution A G upstream_gene_variant LAML-KR 3 10089509 10089509 single base substitution A G intron_variant LAML-KR 3 10089509 10089509 single base substitution A G upstream_gene_variant LAML-KR 3 10089841 10089841 single base substitution C A downstream_gene_variant LAML-KR 3 10089841 10089841 single base substitution C A intron_variant LAML-KR 3 10089841 10089841 single base substitution C A upstream_gene_variant LAML-KR 3 10089852 10089852 single base substitution A G downstream_gene_variant LAML-KR 3 10089852 10089852 single base substitution A G intron_variant LAML-KR 3 10089852 10089852 single base substitution A G upstream_gene_variant LAML-KR 3 10090357 10090357 single base substitution A G downstream_gene_variant LAML-KR 3 10090357 10090357 single base substitution A G intron_variant LAML-KR 3 10090357 10090357 single base substitution A G upstream_gene_variant LAML-KR 3 10090747 10090747 single base substitution C T downstream_gene_variant LAML-KR 3 10090747 10090747 single base substitution C T intron_variant LAML-KR 3 10090747 10090747 single base substitution C T upstream_gene_variant LAML-KR 3 10090799 10090799 single base substitution A C downstream_gene_variant LAML-KR 3 10090799 10090799 single base substitution A C intron_variant LAML-KR 3 10090799 10090799 single base substitution A C upstream_gene_variant LAML-KR 3 10090862 10090862 single base substitution T C downstream_gene_variant LAML-KR 3 10090862 10090862 single base substitution T C intron_variant LAML-KR 3 10090862 10090862 single base substitution T C upstream_gene_variant LAML-KR 3 10090941 10090941 single base substitution T A downstream_gene_variant LAML-KR 3 10090941 10090941 single base substitution T A intron_variant LAML-KR 3 10090941 10090941 single base substitution T A upstream_gene_variant LAML-KR 3 10091153 10091153 single base substitution C T downstream_gene_variant LAML-KR 3 10091153 10091153 single base substitution C T exon_variant LAML-KR 3 10091153 10091153 single base substitution C T synonymous_variant N503N 1509C>T LAML-KR 3 10095669 10095669 single base substitution C A downstream_gene_variant LAML-KR 3 10095669 10095669 single base substitution C A intron_variant LAML-KR 3 10105319 10105319 single base substitution G A intron_variant LAML-KR 3 10105319 10105319 single base substitution G A upstream_gene_variant LAML-KR 3 10105409 10105409 single base substitution A T intron_variant LAML-KR 3 10105409 10105409 single base substitution A T upstream_gene_variant LAML-KR 3 10105439 10105439 single base substitution A C intron_variant LAML-KR 3 10105439 10105439 single base substitution A C upstream_gene_variant LAML-KR 3 10105879 10105879 single base substitution T C intron_variant LAML-KR 3 10105879 10105879 single base substitution T C upstream_gene_variant LAML-KR 3 10105880 10105880 single base substitution A G intron_variant LAML-KR 3 10105880 10105880 single base substitution A G upstream_gene_variant LAML-KR 3 10106213 10106213 single base substitution A G intron_variant LAML-KR 3 10106213 10106213 single base substitution A G upstream_gene_variant LAML-KR 3 10106623 10106623 single base substitution C T intron_variant LAML-KR 3 10112737 10112737 single base substitution C T intron_variant LAML-KR 3 10115273 10115273 single base substitution G A downstream_gene_variant LAML-KR 3 10115273 10115273 single base substitution G A intron_variant LAML-KR 3 10115404 10115404 single base substitution G A downstream_gene_variant LAML-KR 3 10115404 10115404 single base substitution G A intron_variant LGG-US 3 10083383 10083383 single base substitution T G downstream_gene_variant LGG-US 3 10083383 10083383 single base substitution T G missense_variant F258V 772T>G LGG-US 3 10083383 10083383 single base substitution T G upstream_gene_variant LGG-US 3 10085520 10085520 single base substitution A G downstream_gene_variant LGG-US 3 10085520 10085520 single base substitution A G missense_variant E369G 1106A>G LGG-US 3 10085520 10085520 single base substitution A G upstream_gene_variant LGG-US 3 10123119 10123119 single base substitution G A exon_variant LGG-US 3 10123119 10123119 single base substitution G A synonymous_variant L1065L 3195G>A LGG-US 3 10146220 10146220 single base substitution C T downstream_gene_variant LICA-CN 3 10081030 10081030 single base substitution G A downstream_gene_variant LICA-CN 3 10081030 10081030 single base substitution G A exon_variant LICA-CN 3 10081030 10081030 single base substitution G A missense_variant V187M 559G>A LICA-CN 3 10085511 10085511 single base substitution A T downstream_gene_variant LICA-CN 3 10085511 10085511 single base substitution A T splice_acceptor_variant LICA-CN 3 10085511 10085511 single base substitution A T upstream_gene_variant LICA-CN 3 10128851 10128851 single base substitution A T exon_variant LICA-CN 3 10128851 10128851 single base substitution A T missense_variant Q1123H 3369A>T LICA-FR 3 10071334 10071334 single base substitution T C intron_variant LICA-FR 3 10073186 10073186 deletion of <=200bp A - intron_variant LICA-FR 3 10073186 10073186 deletion of <=200bp A - upstream_gene_variant LICA-FR 3 10085406 10085406 single base substitution G T downstream_gene_variant LICA-FR 3 10085406 10085406 single base substitution G T intron_variant LICA-FR 3 10085406 10085406 single base substitution G T upstream_gene_variant LICA-FR 3 10087286 10087286 insertion of <=200bp - T downstream_gene_variant LICA-FR 3 10087286 10087286 insertion of <=200bp - T exon_variant LICA-FR 3 10087286 10087286 insertion of <=200bp - T intron_variant LICA-FR 3 10087286 10087286 insertion of <=200bp - T upstream_gene_variant LICA-FR 3 10106352 10106352 single base substitution T A intron_variant LICA-FR 3 10106352 10106352 single base substitution T A upstream_gene_variant LICA-FR 3 10106408 10106408 single base substitution C T exon_variant LICA-FR 3 10106408 10106408 single base substitution C T splice_region_variant LICA-FR 3 10115175 10115175 single base substitution G C downstream_gene_variant LICA-FR 3 10115175 10115175 single base substitution G C intron_variant LICA-FR 3 10115371 10115371 single base substitution T C downstream_gene_variant LICA-FR 3 10115371 10115371 single base substitution T C intron_variant LICA-FR 3 10115429 10115429 single base substitution T C downstream_gene_variant LICA-FR 3 10115429 10115429 single base substitution T C intron_variant LICA-FR 3 10115500 10115500 single base substitution C T downstream_gene_variant LICA-FR 3 10115500 10115500 single base substitution C T intron_variant LICA-FR 3 10125968 10125968 single base substitution A G intron_variant LICA-FR 3 10129363 10129363 single base substitution G T intron_variant LICA-FR 3 10145954 10145968 deletion of <=200bp ACTTTTTGTAAGTTG - downstream_gene_variant LICA-FR 3 10146176 10146176 single base substitution G A downstream_gene_variant LIHC-US 3 10076196 10076196 single base substitution G C 3_prime_UTR_variant LIHC-US 3 10076196 10076196 single base substitution G C synonymous_variant L83L 249G>C LIHC-US 3 10076196 10076196 single base substitution G C upstream_gene_variant LIHC-US 3 10102063 10102063 single base substitution T C exon_variant LIHC-US 3 10102063 10102063 single base substitution T C missense_variant M581T 1742T>C LIHC-US 3 10102063 10102063 single base substitution T C upstream_gene_variant LIHC-US 3 10108898 10108898 single base substitution A G exon_variant LIHC-US 3 10108898 10108898 single base substitution A G intron_variant LIHC-US 3 10108898 10108898 single base substitution A G synonymous_variant V797V 2391A>G LIHC-US 3 10108913 10108913 single base substitution G T exon_variant LIHC-US 3 10108913 10108913 single base substitution G T intron_variant LIHC-US 3 10108913 10108913 single base substitution G T missense_variant Q802H 2406G>T LIHC-US 3 10108949 10108949 single base substitution T C exon_variant LIHC-US 3 10108949 10108949 single base substitution T C intron_variant LIHC-US 3 10108949 10108949 single base substitution T C synonymous_variant T814T 2442T>C LIHC-US 3 10128833 10128833 single base substitution C T exon_variant LIHC-US 3 10128833 10128833 single base substitution C T synonymous_variant Y1117Y 3351C>T LIHC-US 3 10136948 10136948 single base substitution G A 3_prime_UTR_variant LIHC-US 3 10136948 10136948 single base substitution G A exon_variant LIHC-US 3 10136948 10136948 single base substitution G A missense_variant G1343E 4028G>A LINC-JP 3 10068068 10068068 single base substitution T C upstream_gene_variant LINC-JP 3 10075338 10075338 single base substitution T G intron_variant LINC-JP 3 10075338 10075338 single base substitution T G upstream_gene_variant LINC-JP 3 10075837 10075837 single base substitution C A intron_variant LINC-JP 3 10075837 10075837 single base substitution C A upstream_gene_variant LINC-JP 3 10076316 10076316 single base substitution A G downstream_gene_variant LINC-JP 3 10076316 10076316 single base substitution A G intron_variant LINC-JP 3 10076316 10076316 single base substitution A G upstream_gene_variant LINC-JP 3 10077770 10077770 single base substitution C T downstream_gene_variant LINC-JP 3 10077770 10077770 single base substitution C T intron_variant LINC-JP 3 10078214 10078214 single base substitution G T downstream_gene_variant LINC-JP 3 10078214 10078214 single base substitution G T intron_variant LINC-JP 3 10088239 10088239 single base substitution G A downstream_gene_variant LINC-JP 3 10088239 10088239 single base substitution G A exon_variant LINC-JP 3 10088239 10088239 single base substitution G A intron_variant LINC-JP 3 10088239 10088239 single base substitution G A upstream_gene_variant LINC-JP 3 10088242 10088242 single base substitution G A downstream_gene_variant LINC-JP 3 10088242 10088242 single base substitution G A exon_variant LINC-JP 3 10088242 10088242 single base substitution G A intron_variant LINC-JP 3 10088242 10088242 single base substitution G A upstream_gene_variant LINC-JP 3 10088514 10088514 single base substitution T C intron_variant LINC-JP 3 10088514 10088514 single base substitution T C upstream_gene_variant LINC-JP 3 10088648 10088648 single base substitution T C intron_variant LINC-JP 3 10088648 10088648 single base substitution T C upstream_gene_variant LINC-JP 3 10088730 10088730 single base substitution A G intron_variant LINC-JP 3 10088730 10088730 single base substitution A G upstream_gene_variant LINC-JP 3 10088930 10088930 single base substitution T C intron_variant LINC-JP 3 10088930 10088930 single base substitution T C upstream_gene_variant LINC-JP 3 10088934 10088934 single base substitution G A intron_variant LINC-JP 3 10088934 10088934 single base substitution G A upstream_gene_variant LINC-JP 3 10088958 10088958 single base substitution G A intron_variant LINC-JP 3 10088958 10088958 single base substitution G A upstream_gene_variant LINC-JP 3 10088994 10088994 insertion of <=200bp - G intron_variant LINC-JP 3 10088994 10088994 insertion of <=200bp - G upstream_gene_variant LINC-JP 3 10089451 10089451 deletion of <=200bp T - intron_variant LINC-JP 3 10089451 10089451 deletion of <=200bp T - upstream_gene_variant LINC-JP 3 10089480 10089480 single base substitution C T intron_variant LINC-JP 3 10089480 10089480 single base substitution C T upstream_gene_variant LINC-JP 3 10089497 10089497 single base substitution C T intron_variant LINC-JP 3 10089497 10089497 single base substitution C T upstream_gene_variant LINC-JP 3 10089499 10089499 single base substitution A G intron_variant LINC-JP 3 10089499 10089499 single base substitution A G upstream_gene_variant LINC-JP 3 10089509 10089509 single base substitution A G intron_variant LINC-JP 3 10089509 10089509 single base substitution A G upstream_gene_variant LINC-JP 3 10089556 10089556 single base substitution T C intron_variant LINC-JP 3 10089556 10089556 single base substitution T C upstream_gene_variant LINC-JP 3 10089841 10089841 single base substitution C A downstream_gene_variant LINC-JP 3 10089841 10089841 single base substitution C A intron_variant LINC-JP 3 10089841 10089841 single base substitution C A upstream_gene_variant LINC-JP 3 10089925 10089925 single base substitution G A downstream_gene_variant LINC-JP 3 10089925 10089925 single base substitution G A intron_variant LINC-JP 3 10089925 10089925 single base substitution G A upstream_gene_variant LINC-JP 3 10091334 10091334 single base substitution T C downstream_gene_variant LINC-JP 3 10091334 10091334 single base substitution T C intron_variant LINC-JP 3 10092164 10092164 single base substitution G T downstream_gene_variant LINC-JP 3 10092164 10092164 single base substitution G T intron_variant LINC-JP 3 10093903 10093903 single base substitution G C downstream_gene_variant LINC-JP 3 10093903 10093903 single base substitution G C intron_variant LINC-JP 3 10100369 10100369 single base substitution A G intron_variant LINC-JP 3 10105319 10105319 single base substitution G A intron_variant LINC-JP 3 10105319 10105319 single base substitution G A upstream_gene_variant LINC-JP 3 10105396 10105396 single base substitution A G intron_variant LINC-JP 3 10105396 10105396 single base substitution A G upstream_gene_variant LINC-JP 3 10106524 10106524 single base substitution T G exon_variant LINC-JP 3 10106524 10106524 single base substitution T G missense_variant D711E 2133T>G LINC-JP 3 10109887 10109887 single base substitution A G intron_variant LINC-JP 3 10116198 10116198 single base substitution T A downstream_gene_variant LINC-JP 3 10116198 10116198 single base substitution T A intron_variant LINC-JP 3 10119843 10119843 single base substitution C G exon_variant LINC-JP 3 10119843 10119843 single base substitution C G missense_variant L980V 2938C>G LINC-JP 3 10138766 10138766 single base substitution A T intron_variant LINC-JP 3 10142750 10142750 single base substitution A T downstream_gene_variant LINC-JP 3 10142750 10142750 single base substitution A T intron_variant LINC-JP 3 10144646 10144646 single base substitution A G downstream_gene_variant LINC-JP 3 10145832 10145832 single base substitution G A downstream_gene_variant LINC-JP 3 10147890 10147890 single base substitution T C downstream_gene_variant LIRI-JP 3 10063314 10063314 single base substitution C T upstream_gene_variant LIRI-JP 3 10069350 10069350 single base substitution G A intron_variant LIRI-JP 3 10069350 10069350 single base substitution G A upstream_gene_variant LIRI-JP 3 10072491 10072491 single base substitution G A intron_variant LIRI-JP 3 10072491 10072491 single base substitution G A upstream_gene_variant LIRI-JP 3 10075938 10075938 single base substitution G A intron_variant LIRI-JP 3 10075938 10075938 single base substitution G A upstream_gene_variant LIRI-JP 3 10075939 10075939 single base substitution G C intron_variant LIRI-JP 3 10075939 10075939 single base substitution G C upstream_gene_variant LIRI-JP 3 10077371 10077371 single base substitution C T downstream_gene_variant LIRI-JP 3 10077371 10077371 single base substitution C T intron_variant LIRI-JP 3 10079284 10079284 single base substitution T C downstream_gene_variant LIRI-JP 3 10079284 10079284 single base substitution T C intron_variant LIRI-JP 3 10084219 10084219 single base substitution A C downstream_gene_variant LIRI-JP 3 10084219 10084219 single base substitution A C intron_variant LIRI-JP 3 10084219 10084219 single base substitution A C upstream_gene_variant LIRI-JP 3 10084802 10084802 single base substitution C T downstream_gene_variant LIRI-JP 3 10084802 10084802 single base substitution C T synonymous_variant S319S 957C>T LIRI-JP 3 10084802 10084802 single base substitution C T upstream_gene_variant LIRI-JP 3 10085646 10085646 single base substitution G A downstream_gene_variant LIRI-JP 3 10085646 10085646 single base substitution G A intron_variant LIRI-JP 3 10085646 10085646 single base substitution G A upstream_gene_variant LIRI-JP 3 10086693 10086693 single base substitution A T downstream_gene_variant LIRI-JP 3 10086693 10086693 single base substitution A T intron_variant LIRI-JP 3 10086693 10086693 single base substitution A T upstream_gene_variant LIRI-JP 3 10087380 10087380 single base substitution G T downstream_gene_variant LIRI-JP 3 10087380 10087380 single base substitution G T exon_variant LIRI-JP 3 10087380 10087380 single base substitution G T intron_variant LIRI-JP 3 10087380 10087380 single base substitution G T upstream_gene_variant LIRI-JP 3 10087478 10087478 single base substitution G T downstream_gene_variant LIRI-JP 3 10087478 10087478 single base substitution G T intron_variant LIRI-JP 3 10087478 10087478 single base substitution G T upstream_gene_variant LIRI-JP 3 10090422 10090422 single base substitution C T downstream_gene_variant LIRI-JP 3 10090422 10090422 single base substitution C T intron_variant LIRI-JP 3 10090422 10090422 single base substitution C T upstream_gene_variant LIRI-JP 3 10091035 10091035 single base substitution T C downstream_gene_variant LIRI-JP 3 10091035 10091035 single base substitution T C intron_variant LIRI-JP 3 10091035 10091035 single base substitution T C upstream_gene_variant LIRI-JP 3 10092286 10092286 single base substitution G A downstream_gene_variant LIRI-JP 3 10092286 10092286 single base substitution G A intron_variant LIRI-JP 3 10097705 10097705 single base substitution G T intron_variant LIRI-JP 3 10097722 10097722 single base substitution C T intron_variant LIRI-JP 3 10101399 10101399 single base substitution A G intron_variant LIRI-JP 3 10101399 10101399 single base substitution A G upstream_gene_variant LIRI-JP 3 10104856 10104856 single base substitution C T intron_variant LIRI-JP 3 10104856 10104856 single base substitution C T upstream_gene_variant LIRI-JP 3 10105235 10105235 single base substitution G C intron_variant LIRI-JP 3 10105235 10105235 single base substitution G C upstream_gene_variant LIRI-JP 3 10108340 10108340 single base substitution G A intron_variant LIRI-JP 3 10110915 10110915 single base substitution C T intron_variant LIRI-JP 3 10113918 10113918 single base substitution G T intron_variant LIRI-JP 3 10114078 10114078 single base substitution A C intron_variant LIRI-JP 3 10114944 10114944 single base substitution A C downstream_gene_variant LIRI-JP 3 10114944 10114944 single base substitution A C exon_variant LIRI-JP 3 10114944 10114944 single base substitution A C missense_variant K871N 2613A>C LIRI-JP 3 10115216 10115216 single base substitution C T downstream_gene_variant LIRI-JP 3 10115216 10115216 single base substitution C T intron_variant LIRI-JP 3 10115293 10115293 single base substitution C T downstream_gene_variant LIRI-JP 3 10115293 10115293 single base substitution C T intron_variant LIRI-JP 3 10115527 10115527 single base substitution T C downstream_gene_variant LIRI-JP 3 10115527 10115527 single base substitution T C intron_variant LIRI-JP 3 10116948 10116948 single base substitution A T downstream_gene_variant LIRI-JP 3 10116948 10116948 single base substitution A T intron_variant LIRI-JP 3 10117500 10117500 single base substitution C T downstream_gene_variant LIRI-JP 3 10117500 10117500 single base substitution C T intron_variant LIRI-JP 3 10119168 10119168 single base substitution C T downstream_gene_variant LIRI-JP 3 10119168 10119168 single base substitution C T intron_variant LIRI-JP 3 10119942 10119942 single base substitution A G intron_variant LIRI-JP 3 10124376 10124376 single base substitution G T intron_variant LIRI-JP 3 10124708 10124708 single base substitution C T intron_variant LIRI-JP 3 10125950 10125950 single base substitution A G intron_variant LIRI-JP 3 10126428 10126428 single base substitution G A intron_variant LIRI-JP 3 10127058 10127064 deletion of <=200bp TTCTTTT - intron_variant LIRI-JP 3 10136371 10136371 single base substitution A G intron_variant LIRI-JP 3 10136659 10136659 single base substitution G T intron_variant LIRI-JP 3 10136735 10136735 single base substitution C T intron_variant LIRI-JP 3 10138455 10138455 single base substitution G A intron_variant LIRI-JP 3 10141776 10141776 single base substitution G T downstream_gene_variant LIRI-JP 3 10141776 10141776 single base substitution G T intron_variant LIRI-JP 3 10142772 10142772 single base substitution A G downstream_gene_variant LIRI-JP 3 10142772 10142772 single base substitution A G intron_variant LIRI-JP 3 10143102 10143102 single base substitution C T 3_prime_UTR_variant LIRI-JP 3 10143102 10143102 single base substitution C T downstream_gene_variant LIRI-JP 3 10145235 10145235 single base substitution G T downstream_gene_variant LIRI-JP 3 10146636 10146636 single base substitution T C downstream_gene_variant LIRI-JP 3 10148018 10148018 single base substitution T G downstream_gene_variant LIRI-JP 3 10148498 10148498 single base substitution C T downstream_gene_variant LUSC-KR 3 10064228 10064228 single base substitution G A upstream_gene_variant LUSC-KR 3 10068498 10068498 single base substitution A C intron_variant LUSC-KR 3 10068498 10068498 single base substitution A C upstream_gene_variant LUSC-KR 3 10069728 10069728 single base substitution C T intron_variant LUSC-KR 3 10069728 10069728 single base substitution C T upstream_gene_variant LUSC-KR 3 10071104 10071104 single base substitution G C intron_variant LUSC-KR 3 10072182 10072182 single base substitution G C intron_variant LUSC-KR 3 10072182 10072182 single base substitution G C upstream_gene_variant LUSC-KR 3 10085406 10085406 single base substitution G T downstream_gene_variant LUSC-KR 3 10085406 10085406 single base substitution G T intron_variant LUSC-KR 3 10085406 10085406 single base substitution G T upstream_gene_variant LUSC-KR 3 10088223 10088223 single base substitution T G downstream_gene_variant LUSC-KR 3 10088223 10088223 single base substitution T G exon_variant LUSC-KR 3 10088223 10088223 single base substitution T G intron_variant LUSC-KR 3 10088223 10088223 single base substitution T G upstream_gene_variant LUSC-KR 3 10088239 10088239 single base substitution G A downstream_gene_variant LUSC-KR 3 10088239 10088239 single base substitution G A exon_variant LUSC-KR 3 10088239 10088239 single base substitution G A intron_variant LUSC-KR 3 10088239 10088239 single base substitution G A upstream_gene_variant LUSC-KR 3 10088242 10088242 single base substitution G A downstream_gene_variant LUSC-KR 3 10088242 10088242 single base substitution G A exon_variant LUSC-KR 3 10088242 10088242 single base substitution G A intron_variant LUSC-KR 3 10088242 10088242 single base substitution G A upstream_gene_variant LUSC-KR 3 10088299 10088299 single base substitution C T exon_variant LUSC-KR 3 10088299 10088299 single base substitution C T synonymous_variant S390S 1170C>T LUSC-KR 3 10088299 10088299 single base substitution C T upstream_gene_variant LUSC-KR 3 10088308 10088308 single base substitution T C exon_variant LUSC-KR 3 10088308 10088308 single base substitution T C synonymous_variant T393T 1179T>C LUSC-KR 3 10088308 10088308 single base substitution T C upstream_gene_variant LUSC-KR 3 10088343 10088343 single base substitution A G exon_variant LUSC-KR 3 10088343 10088343 single base substitution A G missense_variant N405S 1214A>G LUSC-KR 3 10088343 10088343 single base substitution A G upstream_gene_variant LUSC-KR 3 10088461 10088461 single base substitution T C intron_variant LUSC-KR 3 10088461 10088461 single base substitution T C upstream_gene_variant LUSC-KR 3 10088514 10088514 single base substitution T C intron_variant LUSC-KR 3 10088514 10088514 single base substitution T C upstream_gene_variant LUSC-KR 3 10088522 10088522 single base substitution G A intron_variant LUSC-KR 3 10088522 10088522 single base substitution G A upstream_gene_variant LUSC-KR 3 10089497 10089497 single base substitution C T intron_variant LUSC-KR 3 10089497 10089497 single base substitution C T upstream_gene_variant LUSC-KR 3 10089499 10089499 single base substitution A G intron_variant LUSC-KR 3 10089499 10089499 single base substitution A G upstream_gene_variant LUSC-KR 3 10089749 10089749 single base substitution T C downstream_gene_variant LUSC-KR 3 10089749 10089749 single base substitution T C intron_variant LUSC-KR 3 10089749 10089749 single base substitution T C upstream_gene_variant LUSC-KR 3 10089772 10089772 single base substitution C G downstream_gene_variant LUSC-KR 3 10089772 10089772 single base substitution C G intron_variant LUSC-KR 3 10089772 10089772 single base substitution C G upstream_gene_variant LUSC-KR 3 10089773 10089773 single base substitution A G downstream_gene_variant LUSC-KR 3 10089773 10089773 single base substitution A G intron_variant LUSC-KR 3 10089773 10089773 single base substitution A G upstream_gene_variant LUSC-KR 3 10089775 10089775 single base substitution A G downstream_gene_variant LUSC-KR 3 10089775 10089775 single base substitution A G intron_variant LUSC-KR 3 10089775 10089775 single base substitution A G upstream_gene_variant LUSC-KR 3 10089815 10089815 single base substitution A C downstream_gene_variant LUSC-KR 3 10089815 10089815 single base substitution A C intron_variant LUSC-KR 3 10089815 10089815 single base substitution A C upstream_gene_variant LUSC-KR 3 10089818 10089818 single base substitution C T downstream_gene_variant LUSC-KR 3 10089818 10089818 single base substitution C T intron_variant LUSC-KR 3 10089818 10089818 single base substitution C T upstream_gene_variant LUSC-KR 3 10089828 10089828 single base substitution G A downstream_gene_variant LUSC-KR 3 10089828 10089828 single base substitution G A intron_variant LUSC-KR 3 10089828 10089828 single base substitution G A upstream_gene_variant LUSC-KR 3 10089834 10089834 single base substitution A T downstream_gene_variant LUSC-KR 3 10089834 10089834 single base substitution A T intron_variant LUSC-KR 3 10089834 10089834 single base substitution A T upstream_gene_variant LUSC-KR 3 10089841 10089841 single base substitution C A downstream_gene_variant LUSC-KR 3 10089841 10089841 single base substitution C A intron_variant LUSC-KR 3 10089841 10089841 single base substitution C A upstream_gene_variant LUSC-KR 3 10090933 10090933 single base substitution G A downstream_gene_variant LUSC-KR 3 10090933 10090933 single base substitution G A intron_variant LUSC-KR 3 10090933 10090933 single base substitution G A upstream_gene_variant LUSC-KR 3 10090941 10090941 single base substitution T A downstream_gene_variant LUSC-KR 3 10090941 10090941 single base substitution T A intron_variant LUSC-KR 3 10090941 10090941 single base substitution T A upstream_gene_variant LUSC-KR 3 10091035 10091035 single base substitution T C downstream_gene_variant LUSC-KR 3 10091035 10091035 single base substitution T C intron_variant LUSC-KR 3 10091035 10091035 single base substitution T C upstream_gene_variant LUSC-KR 3 10091153 10091153 single base substitution C T downstream_gene_variant LUSC-KR 3 10091153 10091153 single base substitution C T exon_variant LUSC-KR 3 10091153 10091153 single base substitution C T synonymous_variant N503N 1509C>T LUSC-KR 3 10091252 10091252 single base substitution A C downstream_gene_variant LUSC-KR 3 10091252 10091252 single base substitution A C intron_variant LUSC-KR 3 10091261 10091261 single base substitution G A downstream_gene_variant LUSC-KR 3 10091261 10091261 single base substitution G A intron_variant LUSC-KR 3 10091315 10091315 single base substitution C G downstream_gene_variant LUSC-KR 3 10091315 10091315 single base substitution C G intron_variant LUSC-KR 3 10092170 10092170 single base substitution C T downstream_gene_variant LUSC-KR 3 10092170 10092170 single base substitution C T intron_variant LUSC-KR 3 10094851 10094851 single base substitution G C downstream_gene_variant LUSC-KR 3 10094851 10094851 single base substitution G C intron_variant LUSC-KR 3 10098140 10098140 single base substitution A C intron_variant LUSC-KR 3 10098809 10098809 single base substitution G T intron_variant LUSC-KR 3 10100896 10100896 single base substitution C G intron_variant LUSC-KR 3 10105215 10105215 single base substitution C G intron_variant LUSC-KR 3 10105215 10105215 single base substitution C G upstream_gene_variant LUSC-KR 3 10105409 10105409 single base substitution A T intron_variant LUSC-KR 3 10105409 10105409 single base substitution A T upstream_gene_variant LUSC-KR 3 10105439 10105439 single base substitution A C intron_variant LUSC-KR 3 10105439 10105439 single base substitution A C upstream_gene_variant LUSC-KR 3 10105742 10105742 single base substitution T C intron_variant LUSC-KR 3 10105742 10105742 single base substitution T C upstream_gene_variant LUSC-KR 3 10106345 10106345 single base substitution C T intron_variant LUSC-KR 3 10106345 10106345 single base substitution C T upstream_gene_variant LUSC-KR 3 10106352 10106352 single base substitution T A intron_variant LUSC-KR 3 10106352 10106352 single base substitution T A upstream_gene_variant LUSC-KR 3 10106366 10106366 single base substitution T C intron_variant LUSC-KR 3 10106366 10106366 single base substitution T C upstream_gene_variant LUSC-KR 3 10106386 10106386 single base substitution A G exon_variant LUSC-KR 3 10106386 10106386 single base substitution A G intron_variant LUSC-KR 3 10106408 10106408 single base substitution C T exon_variant LUSC-KR 3 10106408 10106408 single base substitution C T splice_region_variant LUSC-KR 3 10106608 10106608 single base substitution T C intron_variant LUSC-KR 3 10106623 10106623 single base substitution C T intron_variant LUSC-KR 3 10110297 10110297 single base substitution T A intron_variant LUSC-KR 3 10111883 10111883 single base substitution T C intron_variant LUSC-KR 3 10112334 10112334 single base substitution A G intron_variant LUSC-KR 3 10112348 10112348 single base substitution A G intron_variant LUSC-KR 3 10112414 10112414 single base substitution G A intron_variant LUSC-KR 3 10114944 10114944 single base substitution A C downstream_gene_variant LUSC-KR 3 10114944 10114944 single base substitution A C exon_variant LUSC-KR 3 10114944 10114944 single base substitution A C missense_variant K871N 2613A>C LUSC-KR 3 10115175 10115175 single base substitution G C downstream_gene_variant LUSC-KR 3 10115175 10115175 single base substitution G C intron_variant LUSC-KR 3 10115371 10115371 single base substitution T C downstream_gene_variant LUSC-KR 3 10115371 10115371 single base substitution T C intron_variant LUSC-KR 3 10115500 10115500 single base substitution C T downstream_gene_variant LUSC-KR 3 10115500 10115500 single base substitution C T intron_variant LUSC-KR 3 10115527 10115527 single base substitution T C downstream_gene_variant LUSC-KR 3 10115527 10115527 single base substitution T C intron_variant LUSC-KR 3 10122520 10122520 single base substitution A T intron_variant LUSC-KR 3 10129211 10129211 single base substitution C A intron_variant LUSC-KR 3 10129211 10129211 single base substitution C G intron_variant LUSC-KR 3 10131890 10131890 single base substitution G T intron_variant LUSC-KR 3 10131890 10131890 single base substitution G T upstream_gene_variant LUSC-KR 3 10136103 10136103 single base substitution T C intron_variant LUSC-KR 3 10143087 10143087 single base substitution A T 3_prime_UTR_variant LUSC-KR 3 10143087 10143087 single base substitution A T downstream_gene_variant LUSC-KR 3 10147041 10147041 single base substitution A G downstream_gene_variant LUSC-US 3 10146192 10146192 single base substitution C T downstream_gene_variant MALY-DE 3 10064382 10064383 deletion of <=200bp TC - upstream_gene_variant MALY-DE 3 10065573 10065573 single base substitution T G upstream_gene_variant MALY-DE 3 10068344 10068344 single base substitution G A intron_variant MALY-DE 3 10068344 10068344 single base substitution G A upstream_gene_variant MALY-DE 3 10071847 10071847 single base substitution C G intron_variant MALY-DE 3 10071847 10071847 single base substitution C G upstream_gene_variant MALY-DE 3 10073270 10073270 single base substitution A T intron_variant MALY-DE 3 10073270 10073270 single base substitution A T upstream_gene_variant MALY-DE 3 10075160 10075160 single base substitution C T intron_variant MALY-DE 3 10075160 10075160 single base substitution C T upstream_gene_variant MALY-DE 3 10076894 10076894 single base substitution C T downstream_gene_variant MALY-DE 3 10076894 10076894 single base substitution C T exon_variant MALY-DE 3 10076894 10076894 single base substitution C T missense_variant L139F 415C>T MALY-DE 3 10082739 10082739 single base substitution G A 3_prime_UTR_variant MALY-DE 3 10082739 10082739 single base substitution G A downstream_gene_variant MALY-DE 3 10082739 10082739 single base substitution G A intron_variant MALY-DE 3 10082739 10082739 single base substitution G A upstream_gene_variant MALY-DE 3 10090747 10090747 single base substitution C T downstream_gene_variant MALY-DE 3 10090747 10090747 single base substitution C T intron_variant MALY-DE 3 10090747 10090747 single base substitution C T upstream_gene_variant MALY-DE 3 10095174 10095174 single base substitution C A downstream_gene_variant MALY-DE 3 10095174 10095174 single base substitution C A intron_variant MALY-DE 3 10096038 10096039 deletion of <=200bp TA - downstream_gene_variant MALY-DE 3 10096038 10096039 deletion of <=200bp TA - intron_variant MALY-DE 3 10112072 10112072 insertion of <=200bp - C intron_variant MALY-DE 3 10123373 10123373 single base substitution T C intron_variant MALY-DE 3 10133659 10133659 single base substitution A C intron_variant MALY-DE 3 10133659 10133659 single base substitution A C upstream_gene_variant MALY-DE 3 10143166 10143166 single base substitution T A 3_prime_UTR_variant MALY-DE 3 10143166 10143166 single base substitution T A downstream_gene_variant MALY-DE 3 10143461 10143461 single base substitution A T 3_prime_UTR_variant MALY-DE 3 10143461 10143461 single base substitution A T downstream_gene_variant MALY-DE 3 10146882 10146882 single base substitution T C downstream_gene_variant MALY-DE 3 10147978 10147978 single base substitution T C downstream_gene_variant MELA-AU 3 10063414 10063414 single base substitution G A upstream_gene_variant MELA-AU 3 10063515 10063515 single base substitution G A upstream_gene_variant MELA-AU 3 10063615 10063615 single base substitution G A upstream_gene_variant MELA-AU 3 10063961 10063961 single base substitution G A upstream_gene_variant MELA-AU 3 10064224 10064224 single base substitution G A upstream_gene_variant MELA-AU 3 10064483 10064483 single base substitution G A upstream_gene_variant MELA-AU 3 10064605 10064605 single base substitution G A upstream_gene_variant MELA-AU 3 10065288 10065288 single base substitution G A upstream_gene_variant MELA-AU 3 10065606 10065606 single base substitution G A upstream_gene_variant MELA-AU 3 10066444 10066444 single base substitution A G upstream_gene_variant MELA-AU 3 10066882 10066882 single base substitution C T upstream_gene_variant MELA-AU 3 10066917 10066917 single base substitution G A upstream_gene_variant MELA-AU 3 10067102 10067102 single base substitution G A upstream_gene_variant MELA-AU 3 10067108 10067108 single base substitution C G upstream_gene_variant MELA-AU 3 10067356 10067356 single base substitution A G upstream_gene_variant MELA-AU 3 10067610 10067610 single base substitution G T upstream_gene_variant MELA-AU 3 10068091 10068091 single base substitution C T upstream_gene_variant MELA-AU 3 10069117 10069117 single base substitution G A intron_variant MELA-AU 3 10069117 10069117 single base substitution G A upstream_gene_variant MELA-AU 3 10069462 10069462 single base substitution G A intron_variant MELA-AU 3 10069462 10069462 single base substitution G A upstream_gene_variant MELA-AU 3 10069756 10069756 single base substitution C T intron_variant MELA-AU 3 10069756 10069756 single base substitution C T upstream_gene_variant MELA-AU 3 10069760 10069760 single base substitution G A intron_variant MELA-AU 3 10069760 10069760 single base substitution G A upstream_gene_variant MELA-AU 3 10069852 10069852 single base substitution C T intron_variant MELA-AU 3 10069852 10069852 single base substitution C T upstream_gene_variant MELA-AU 3 10069979 10069979 single base substitution C T intron_variant MELA-AU 3 10069979 10069979 single base substitution C T upstream_gene_variant MELA-AU 3 10070294 10070294 single base substitution C T intron_variant MELA-AU 3 10070294 10070294 single base substitution C T upstream_gene_variant MELA-AU 3 10070348 10070348 single base substitution T A exon_variant MELA-AU 3 10070348 10070348 single base substitution T A missense_variant S3T 7T>A MELA-AU 3 10071189 10071189 single base substitution C T intron_variant MELA-AU 3 10071830 10071830 single base substitution G A intron_variant MELA-AU 3 10071830 10071830 single base substitution G A upstream_gene_variant MELA-AU 3 10072331 10072332 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 10072331 10072332 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 3 10073489 10073489 single base substitution C T intron_variant MELA-AU 3 10073489 10073489 single base substitution C T upstream_gene_variant MELA-AU 3 10073544 10073544 single base substitution C T intron_variant MELA-AU 3 10073544 10073544 single base substitution C T upstream_gene_variant MELA-AU 3 10074465 10074465 single base substitution T A intron_variant MELA-AU 3 10074465 10074465 single base substitution T A upstream_gene_variant MELA-AU 3 10074486 10074486 single base substitution C T intron_variant MELA-AU 3 10074486 10074486 single base substitution C T upstream_gene_variant MELA-AU 3 10075008 10075008 single base substitution C T intron_variant MELA-AU 3 10075008 10075008 single base substitution C T upstream_gene_variant MELA-AU 3 10075515 10075515 single base substitution G A intron_variant MELA-AU 3 10075515 10075515 single base substitution G A upstream_gene_variant MELA-AU 3 10075636 10075636 single base substitution C T intron_variant MELA-AU 3 10075636 10075636 single base substitution C T upstream_gene_variant MELA-AU 3 10076233 10076233 single base substitution C T downstream_gene_variant MELA-AU 3 10076233 10076233 single base substitution C T intron_variant MELA-AU 3 10076233 10076233 single base substitution C T upstream_gene_variant MELA-AU 3 10076372 10076372 single base substitution C T downstream_gene_variant MELA-AU 3 10076372 10076372 single base substitution C T splice_region_variant MELA-AU 3 10076372 10076372 single base substitution C T upstream_gene_variant MELA-AU 3 10076858 10076858 single base substitution A T downstream_gene_variant MELA-AU 3 10076858 10076858 single base substitution A T missense_variant M127L 379A>T MELA-AU 3 10076858 10076858 single base substitution A T splice_region_variant MELA-AU 3 10077149 10077149 single base substitution G A downstream_gene_variant MELA-AU 3 10077149 10077149 single base substitution G A intron_variant MELA-AU 3 10077395 10077395 single base substitution C T downstream_gene_variant MELA-AU 3 10077395 10077395 single base substitution C T intron_variant MELA-AU 3 10077645 10077645 single base substitution C T downstream_gene_variant MELA-AU 3 10077645 10077645 single base substitution C T intron_variant MELA-AU 3 10077698 10077698 single base substitution C T downstream_gene_variant MELA-AU 3 10077698 10077698 single base substitution C T intron_variant MELA-AU 3 10077882 10077882 single base substitution C T downstream_gene_variant MELA-AU 3 10077882 10077882 single base substitution C T intron_variant MELA-AU 3 10079701 10079701 single base substitution A G downstream_gene_variant MELA-AU 3 10079701 10079701 single base substitution A G intron_variant MELA-AU 3 10079798 10079798 single base substitution C T downstream_gene_variant MELA-AU 3 10079798 10079798 single base substitution C T intron_variant MELA-AU 3 10080243 10080243 single base substitution C T downstream_gene_variant MELA-AU 3 10080243 10080243 single base substitution C T intron_variant MELA-AU 3 10080374 10080374 single base substitution C T downstream_gene_variant MELA-AU 3 10080374 10080374 single base substitution C T intron_variant MELA-AU 3 10080413 10080413 single base substitution C T downstream_gene_variant MELA-AU 3 10080413 10080413 single base substitution C T intron_variant MELA-AU 3 10081918 10081918 single base substitution C T 3_prime_UTR_variant MELA-AU 3 10081918 10081918 single base substitution C T intron_variant MELA-AU 3 10082159 10082159 single base substitution C T 3_prime_UTR_variant MELA-AU 3 10082159 10082159 single base substitution C T intron_variant MELA-AU 3 10082420 10082420 single base substitution C T 3_prime_UTR_variant MELA-AU 3 10082420 10082420 single base substitution C T downstream_gene_variant MELA-AU 3 10082420 10082420 single base substitution C T intron_variant MELA-AU 3 10082420 10082420 single base substitution C T upstream_gene_variant MELA-AU 3 10083828 10083828 single base substitution C T downstream_gene_variant MELA-AU 3 10083828 10083828 single base substitution C T intron_variant MELA-AU 3 10083828 10083828 single base substitution C T upstream_gene_variant MELA-AU 3 10084364 10084364 single base substitution C T downstream_gene_variant MELA-AU 3 10084364 10084364 single base substitution C T intron_variant MELA-AU 3 10084364 10084364 single base substitution C T upstream_gene_variant MELA-AU 3 10084483 10084483 single base substitution C T downstream_gene_variant MELA-AU 3 10084483 10084483 single base substitution C T intron_variant MELA-AU 3 10084483 10084483 single base substitution C T upstream_gene_variant MELA-AU 3 10084752 10084752 single base substitution G A downstream_gene_variant MELA-AU 3 10084752 10084752 single base substitution G A missense_variant E303K 907G>A MELA-AU 3 10084752 10084752 single base substitution G A upstream_gene_variant MELA-AU 3 10084764 10084764 single base substitution C T downstream_gene_variant MELA-AU 3 10084764 10084764 single base substitution C T synonymous_variant L307L 919C>T MELA-AU 3 10084764 10084764 single base substitution C T upstream_gene_variant MELA-AU 3 10085105 10085105 single base substitution C T downstream_gene_variant MELA-AU 3 10085105 10085105 single base substitution C T intron_variant MELA-AU 3 10085105 10085105 single base substitution C T upstream_gene_variant MELA-AU 3 10085939 10085939 single base substitution C T downstream_gene_variant MELA-AU 3 10085939 10085939 single base substitution C T intron_variant MELA-AU 3 10085939 10085939 single base substitution C T upstream_gene_variant MELA-AU 3 10086240 10086240 single base substitution C T downstream_gene_variant MELA-AU 3 10086240 10086240 single base substitution C T intron_variant MELA-AU 3 10086240 10086240 single base substitution C T upstream_gene_variant MELA-AU 3 10086796 10086796 single base substitution T G downstream_gene_variant MELA-AU 3 10086796 10086796 single base substitution T G intron_variant MELA-AU 3 10086796 10086796 single base substitution T G upstream_gene_variant MELA-AU 3 10087206 10087206 single base substitution C T downstream_gene_variant MELA-AU 3 10087206 10087206 single base substitution C T intron_variant MELA-AU 3 10087206 10087206 single base substitution C T upstream_gene_variant MELA-AU 3 10087264 10087264 single base substitution A G downstream_gene_variant MELA-AU 3 10087264 10087264 single base substitution A G exon_variant MELA-AU 3 10087264 10087264 single base substitution A G intron_variant MELA-AU 3 10087264 10087264 single base substitution A G upstream_gene_variant MELA-AU 3 10087634 10087634 single base substitution T A downstream_gene_variant MELA-AU 3 10087634 10087634 single base substitution T A intron_variant MELA-AU 3 10087634 10087634 single base substitution T A upstream_gene_variant MELA-AU 3 10087694 10087694 single base substitution G C downstream_gene_variant MELA-AU 3 10087694 10087694 single base substitution G C intron_variant MELA-AU 3 10087694 10087694 single base substitution G C upstream_gene_variant MELA-AU 3 10088091 10088091 single base substitution C T downstream_gene_variant MELA-AU 3 10088091 10088091 single base substitution C T intron_variant MELA-AU 3 10088091 10088091 single base substitution C T upstream_gene_variant MELA-AU 3 10088582 10088582 single base substitution G A intron_variant MELA-AU 3 10088582 10088582 single base substitution G A upstream_gene_variant MELA-AU 3 10088589 10088589 single base substitution G A intron_variant MELA-AU 3 10088589 10088589 single base substitution G A upstream_gene_variant MELA-AU 3 10088636 10088636 single base substitution G A intron_variant MELA-AU 3 10088636 10088636 single base substitution G A upstream_gene_variant MELA-AU 3 10088717 10088717 single base substitution T C intron_variant MELA-AU 3 10088717 10088717 single base substitution T C upstream_gene_variant MELA-AU 3 10088876 10088876 single base substitution C T intron_variant MELA-AU 3 10088876 10088876 single base substitution C T upstream_gene_variant MELA-AU 3 10088878 10088878 single base substitution C T intron_variant MELA-AU 3 10088878 10088878 single base substitution C T upstream_gene_variant MELA-AU 3 10088994 10088994 single base substitution T G intron_variant MELA-AU 3 10088994 10088994 single base substitution T G upstream_gene_variant MELA-AU 3 10089017 10089017 single base substitution C T intron_variant MELA-AU 3 10089017 10089017 single base substitution C T upstream_gene_variant MELA-AU 3 10089028 10089028 single base substitution C T intron_variant MELA-AU 3 10089028 10089028 single base substitution C T upstream_gene_variant MELA-AU 3 10089448 10089448 single base substitution T A intron_variant MELA-AU 3 10089448 10089448 single base substitution T A upstream_gene_variant MELA-AU 3 10089479 10089479 single base substitution C T intron_variant MELA-AU 3 10089479 10089479 single base substitution C T upstream_gene_variant MELA-AU 3 10089561 10089561 single base substitution C T intron_variant MELA-AU 3 10089561 10089561 single base substitution C T upstream_gene_variant MELA-AU 3 10089590 10089590 single base substitution C T intron_variant MELA-AU 3 10089590 10089590 single base substitution C T upstream_gene_variant MELA-AU 3 10089677 10089677 single base substitution C T exon_variant MELA-AU 3 10089677 10089677 single base substitution C T missense_variant S452L 1355C>T MELA-AU 3 10089677 10089677 single base substitution C T upstream_gene_variant MELA-AU 3 10090557 10090558 multiple base substitution (>=2bp and <=200bp) CA TG downstream_gene_variant MELA-AU 3 10090557 10090558 multiple base substitution (>=2bp and <=200bp) CA TG intron_variant MELA-AU 3 10090557 10090558 multiple base substitution (>=2bp and <=200bp) CA TG upstream_gene_variant MELA-AU 3 10090670 10090670 single base substitution G A downstream_gene_variant MELA-AU 3 10090670 10090670 single base substitution G A intron_variant MELA-AU 3 10090670 10090670 single base substitution G A upstream_gene_variant MELA-AU 3 10090897 10090897 single base substitution C T downstream_gene_variant MELA-AU 3 10090897 10090897 single base substitution C T intron_variant MELA-AU 3 10090897 10090897 single base substitution C T upstream_gene_variant MELA-AU 3 10093604 10093604 single base substitution C T downstream_gene_variant MELA-AU 3 10093604 10093604 single base substitution C T intron_variant MELA-AU 3 10093717 10093717 single base substitution C T downstream_gene_variant MELA-AU 3 10093717 10093717 single base substitution C T intron_variant MELA-AU 3 10093813 10093813 single base substitution C T downstream_gene_variant MELA-AU 3 10093813 10093813 single base substitution C T intron_variant MELA-AU 3 10094382 10094382 single base substitution C T downstream_gene_variant MELA-AU 3 10094382 10094382 single base substitution C T intron_variant MELA-AU 3 10094959 10094959 single base substitution A G downstream_gene_variant MELA-AU 3 10094959 10094959 single base substitution A G intron_variant MELA-AU 3 10095220 10095220 single base substitution A T downstream_gene_variant MELA-AU 3 10095220 10095220 single base substitution A T intron_variant MELA-AU 3 10095296 10095296 single base substitution G C downstream_gene_variant MELA-AU 3 10095296 10095296 single base substitution G C intron_variant MELA-AU 3 10095371 10095371 single base substitution C A downstream_gene_variant MELA-AU 3 10095371 10095371 single base substitution C A intron_variant MELA-AU 3 10095654 10095654 single base substitution G A downstream_gene_variant MELA-AU 3 10095654 10095654 single base substitution G A intron_variant MELA-AU 3 10095846 10095846 single base substitution T C downstream_gene_variant MELA-AU 3 10095846 10095846 single base substitution T C intron_variant MELA-AU 3 10096198 10096198 single base substitution C T intron_variant MELA-AU 3 10096365 10096365 single base substitution C T intron_variant MELA-AU 3 10097108 10097108 single base substitution C T intron_variant MELA-AU 3 10097226 10097226 single base substitution G A intron_variant MELA-AU 3 10097292 10097292 single base substitution C T intron_variant MELA-AU 3 10097476 10097500 deletion of <=200bp ACAGAGCGAGACTCTGTCTCAAAAA - intron_variant MELA-AU 3 10097518 10097518 single base substitution A T intron_variant MELA-AU 3 10097534 10097534 single base substitution A G intron_variant MELA-AU 3 10098010 10098010 single base substitution G A intron_variant MELA-AU 3 10098374 10098374 single base substitution C T intron_variant MELA-AU 3 10098492 10098492 single base substitution C A intron_variant MELA-AU 3 10098534 10098534 single base substitution C T intron_variant MELA-AU 3 10098869 10098869 single base substitution C T intron_variant MELA-AU 3 10099080 10099080 single base substitution C T intron_variant MELA-AU 3 10099172 10099173 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 10099209 10099209 single base substitution C A intron_variant MELA-AU 3 10099229 10099229 single base substitution A G intron_variant MELA-AU 3 10099614 10099614 single base substitution C T intron_variant MELA-AU 3 10099988 10099988 single base substitution C T intron_variant MELA-AU 3 10100295 10100295 single base substitution C T intron_variant MELA-AU 3 10100662 10100662 single base substitution C T intron_variant MELA-AU 3 10100702 10100702 single base substitution T A intron_variant MELA-AU 3 10100901 10100901 single base substitution T C intron_variant MELA-AU 3 10100923 10100923 single base substitution C T intron_variant MELA-AU 3 10101266 10101266 single base substitution C T intron_variant MELA-AU 3 10101266 10101266 single base substitution C T upstream_gene_variant MELA-AU 3 10101342 10101342 single base substitution C T intron_variant MELA-AU 3 10101342 10101342 single base substitution C T upstream_gene_variant MELA-AU 3 10101937 10101937 single base substitution C T intron_variant MELA-AU 3 10101937 10101937 single base substitution C T upstream_gene_variant MELA-AU 3 10102219 10102219 single base substitution C T intron_variant MELA-AU 3 10102219 10102219 single base substitution C T upstream_gene_variant MELA-AU 3 10102226 10102226 single base substitution C T intron_variant MELA-AU 3 10102226 10102226 single base substitution C T upstream_gene_variant MELA-AU 3 10102507 10102507 single base substitution C T intron_variant MELA-AU 3 10102507 10102507 single base substitution C T upstream_gene_variant MELA-AU 3 10102508 10102508 single base substitution C T intron_variant MELA-AU 3 10102508 10102508 single base substitution C T upstream_gene_variant MELA-AU 3 10102551 10102552 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 3 10102551 10102552 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 3 10102603 10102603 single base substitution C T intron_variant MELA-AU 3 10102603 10102603 single base substitution C T upstream_gene_variant MELA-AU 3 10103411 10103411 single base substitution C T intron_variant MELA-AU 3 10103411 10103411 single base substitution C T upstream_gene_variant MELA-AU 3 10103900 10103900 single base substitution G A splice_region_variant MELA-AU 3 10103900 10103900 single base substitution G A upstream_gene_variant MELA-AU 3 10103911 10103911 single base substitution C T intron_variant MELA-AU 3 10103911 10103911 single base substitution C T upstream_gene_variant MELA-AU 3 10104096 10104096 single base substitution T C intron_variant MELA-AU 3 10104096 10104096 single base substitution T C upstream_gene_variant MELA-AU 3 10105060 10105060 single base substitution G A intron_variant MELA-AU 3 10105060 10105060 single base substitution G A upstream_gene_variant MELA-AU 3 10106199 10106199 single base substitution T G intron_variant MELA-AU 3 10106199 10106199 single base substitution T G upstream_gene_variant MELA-AU 3 10106279 10106279 single base substitution C T intron_variant MELA-AU 3 10106279 10106279 single base substitution C T upstream_gene_variant MELA-AU 3 10106488 10106488 single base substitution C T exon_variant MELA-AU 3 10106488 10106488 single base substitution C T synonymous_variant L699L 2097C>T MELA-AU 3 10106550 10106550 single base substitution C T exon_variant MELA-AU 3 10106550 10106550 single base substitution C T missense_variant S720L 2159C>T MELA-AU 3 10106617 10106617 single base substitution C T intron_variant MELA-AU 3 10106692 10106692 single base substitution A T intron_variant MELA-AU 3 10106862 10106862 single base substitution A T intron_variant MELA-AU 3 10106927 10106927 single base substitution C T intron_variant MELA-AU 3 10107499 10107499 single base substitution T G intron_variant MELA-AU 3 10107615 10107615 single base substitution T C exon_variant MELA-AU 3 10107615 10107615 single base substitution T C synonymous_variant R779R 2337T>C MELA-AU 3 10108532 10108532 single base substitution C T intron_variant MELA-AU 3 10108691 10108691 single base substitution G A intron_variant MELA-AU 3 10110091 10110091 single base substitution T C intron_variant MELA-AU 3 10110349 10110349 single base substitution C T intron_variant MELA-AU 3 10110860 10110860 single base substitution C T intron_variant MELA-AU 3 10110865 10110865 single base substitution C T intron_variant MELA-AU 3 10111183 10111183 single base substitution C T intron_variant MELA-AU 3 10111502 10111502 single base substitution C T intron_variant MELA-AU 3 10111862 10111862 single base substitution C T intron_variant MELA-AU 3 10112082 10112082 single base substitution G A intron_variant MELA-AU 3 10112857 10112857 single base substitution C T intron_variant MELA-AU 3 10112908 10112908 single base substitution C T intron_variant MELA-AU 3 10113207 10113207 single base substitution C T intron_variant MELA-AU 3 10113667 10113667 single base substitution C G intron_variant MELA-AU 3 10114895 10114895 single base substitution T A downstream_gene_variant MELA-AU 3 10114895 10114895 single base substitution T A intron_variant MELA-AU 3 10114898 10114898 single base substitution T A downstream_gene_variant MELA-AU 3 10114898 10114898 single base substitution T A intron_variant MELA-AU 3 10115594 10115594 single base substitution C T downstream_gene_variant MELA-AU 3 10115594 10115594 single base substitution C T intron_variant MELA-AU 3 10115893 10115893 single base substitution C T downstream_gene_variant MELA-AU 3 10115893 10115893 single base substitution C T intron_variant MELA-AU 3 10115922 10115922 single base substitution C G downstream_gene_variant MELA-AU 3 10115922 10115922 single base substitution C G intron_variant MELA-AU 3 10116905 10116905 single base substitution C T downstream_gene_variant MELA-AU 3 10116905 10116905 single base substitution C T intron_variant MELA-AU 3 10116964 10116964 single base substitution T C downstream_gene_variant MELA-AU 3 10116964 10116964 single base substitution T C intron_variant MELA-AU 3 10117900 10117900 single base substitution A T downstream_gene_variant MELA-AU 3 10117900 10117900 single base substitution A T intron_variant MELA-AU 3 10118056 10118056 single base substitution A T downstream_gene_variant MELA-AU 3 10118056 10118056 single base substitution A T intron_variant MELA-AU 3 10118341 10118341 single base substitution C T downstream_gene_variant MELA-AU 3 10118341 10118341 single base substitution C T intron_variant MELA-AU 3 10118500 10118500 single base substitution C T downstream_gene_variant MELA-AU 3 10118500 10118500 single base substitution C T intron_variant MELA-AU 3 10119250 10119250 single base substitution T A downstream_gene_variant MELA-AU 3 10119250 10119250 single base substitution T A intron_variant MELA-AU 3 10119400 10119400 single base substitution C T downstream_gene_variant MELA-AU 3 10119400 10119400 single base substitution C T intron_variant MELA-AU 3 10119427 10119427 single base substitution G A downstream_gene_variant MELA-AU 3 10119427 10119427 single base substitution G A intron_variant MELA-AU 3 10119581 10119581 single base substitution G A downstream_gene_variant MELA-AU 3 10119581 10119581 single base substitution G A intron_variant MELA-AU 3 10119852 10119852 deletion of <=200bp C - exon_variant MELA-AU 3 10119852 10119852 deletion of <=200bp C - frameshift_variant P983 MELA-AU 3 10120532 10120532 single base substitution C T intron_variant MELA-AU 3 10120621 10120621 single base substitution C T intron_variant MELA-AU 3 10121209 10121209 single base substitution C T intron_variant MELA-AU 3 10121240 10121240 single base substitution G A intron_variant MELA-AU 3 10121483 10121483 single base substitution C T intron_variant MELA-AU 3 10121724 10121724 single base substitution G A intron_variant MELA-AU 3 10122684 10122684 single base substitution C T intron_variant MELA-AU 3 10123015 10123015 single base substitution C T intron_variant MELA-AU 3 10123422 10123422 single base substitution C T intron_variant MELA-AU 3 10124014 10124014 single base substitution C T intron_variant MELA-AU 3 10124118 10124118 single base substitution C T intron_variant MELA-AU 3 10124343 10124343 single base substitution C T intron_variant MELA-AU 3 10124462 10124462 single base substitution C T intron_variant MELA-AU 3 10125566 10125566 single base substitution C T intron_variant MELA-AU 3 10126669 10126669 single base substitution C T intron_variant MELA-AU 3 10127082 10127082 single base substitution T G intron_variant MELA-AU 3 10127389 10127389 single base substitution C T intron_variant MELA-AU 3 10127431 10127431 single base substitution C T intron_variant MELA-AU 3 10127513 10127513 single base substitution C T exon_variant MELA-AU 3 10127513 10127513 single base substitution C T missense_variant P1081L 3242C>T MELA-AU 3 10128387 10128387 single base substitution C T intron_variant MELA-AU 3 10129259 10129259 single base substitution C T intron_variant MELA-AU 3 10129362 10129362 single base substitution C T intron_variant MELA-AU 3 10129933 10129933 single base substitution G A intron_variant MELA-AU 3 10130058 10130058 single base substitution A T intron_variant MELA-AU 3 10130058 10130058 single base substitution A T upstream_gene_variant MELA-AU 3 10130639 10130639 single base substitution G A splice_region_variant MELA-AU 3 10130639 10130639 single base substitution G A upstream_gene_variant MELA-AU 3 10130662 10130662 single base substitution C T intron_variant MELA-AU 3 10130662 10130662 single base substitution C T upstream_gene_variant MELA-AU 3 10131071 10131071 single base substitution C T intron_variant MELA-AU 3 10131071 10131071 single base substitution C T upstream_gene_variant MELA-AU 3 10132021 10132021 single base substitution G A intron_variant MELA-AU 3 10132021 10132021 single base substitution G A synonymous_variant E1243E 3729G>A MELA-AU 3 10132021 10132021 single base substitution G A upstream_gene_variant MELA-AU 3 10132370 10132370 single base substitution C T intron_variant MELA-AU 3 10132370 10132370 single base substitution C T upstream_gene_variant MELA-AU 3 10132693 10132693 single base substitution G A intron_variant MELA-AU 3 10132693 10132693 single base substitution G A upstream_gene_variant MELA-AU 3 10132937 10132937 single base substitution C T intron_variant MELA-AU 3 10132937 10132937 single base substitution C T upstream_gene_variant MELA-AU 3 10133240 10133240 single base substitution C T intron_variant MELA-AU 3 10133240 10133240 single base substitution C T upstream_gene_variant MELA-AU 3 10133667 10133667 single base substitution C T intron_variant MELA-AU 3 10133667 10133667 single base substitution C T upstream_gene_variant MELA-AU 3 10133795 10133795 single base substitution C T intron_variant MELA-AU 3 10133795 10133795 single base substitution C T upstream_gene_variant MELA-AU 3 10134027 10134027 single base substitution C T intron_variant MELA-AU 3 10134027 10134027 single base substitution C T upstream_gene_variant MELA-AU 3 10134036 10134036 single base substitution C T intron_variant MELA-AU 3 10134036 10134036 single base substitution C T upstream_gene_variant MELA-AU 3 10134092 10134092 single base substitution G A intron_variant MELA-AU 3 10134092 10134092 single base substitution G A upstream_gene_variant MELA-AU 3 10135029 10135029 single base substitution G A intron_variant MELA-AU 3 10136217 10136219 deletion of <=200bp CTC - intron_variant MELA-AU 3 10136424 10136424 single base substitution C T intron_variant MELA-AU 3 10136978 10136978 single base substitution C A intron_variant MELA-AU 3 10137144 10137144 single base substitution C T intron_variant MELA-AU 3 10137183 10137183 single base substitution C T intron_variant MELA-AU 3 10137250 10137250 single base substitution G A intron_variant MELA-AU 3 10138524 10138524 single base substitution C T intron_variant MELA-AU 3 10139125 10139125 single base substitution C T intron_variant MELA-AU 3 10140182 10140182 single base substitution C T intron_variant MELA-AU 3 10140665 10140666 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 3 10140665 10140666 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 3 10141204 10141204 single base substitution G A 3_prime_UTR_variant MELA-AU 3 10141204 10141204 single base substitution G A intron_variant MELA-AU 3 10141542 10141542 single base substitution C T downstream_gene_variant MELA-AU 3 10141542 10141542 single base substitution C T intron_variant MELA-AU 3 10141978 10141978 single base substitution C T downstream_gene_variant MELA-AU 3 10141978 10141978 single base substitution C T intron_variant MELA-AU 3 10142081 10142081 single base substitution G A downstream_gene_variant MELA-AU 3 10142081 10142081 single base substitution G A intron_variant MELA-AU 3 10142797 10142797 single base substitution C T downstream_gene_variant MELA-AU 3 10142797 10142797 single base substitution C T intron_variant MELA-AU 3 10142941 10142941 single base substitution G A 3_prime_UTR_variant MELA-AU 3 10142941 10142941 single base substitution G A downstream_gene_variant MELA-AU 3 10142941 10142941 single base substitution G A exon_variant MELA-AU 3 10142941 10142941 single base substitution G A missense_variant D1451N 4351G>A MELA-AU 3 10143410 10143410 single base substitution C T 3_prime_UTR_variant MELA-AU 3 10143410 10143410 single base substitution C T downstream_gene_variant MELA-AU 3 10144027 10144027 single base substitution C T downstream_gene_variant MELA-AU 3 10144138 10144138 single base substitution C T downstream_gene_variant MELA-AU 3 10144322 10144322 single base substitution C T downstream_gene_variant MELA-AU 3 10144410 10144410 single base substitution C T downstream_gene_variant MELA-AU 3 10144527 10144539 deletion of <=200bp AAAAAAAAAAAAA - downstream_gene_variant MELA-AU 3 10144876 10144876 single base substitution C T downstream_gene_variant MELA-AU 3 10144877 10144877 single base substitution G A downstream_gene_variant MELA-AU 3 10144914 10144914 single base substitution C T downstream_gene_variant MELA-AU 3 10145561 10145561 single base substitution C T downstream_gene_variant MELA-AU 3 10145592 10145592 single base substitution C T downstream_gene_variant MELA-AU 3 10146202 10146202 single base substitution C T downstream_gene_variant MELA-AU 3 10146326 10146326 single base substitution C T downstream_gene_variant MELA-AU 3 10146467 10146467 single base substitution C T downstream_gene_variant MELA-AU 3 10146536 10146536 single base substitution C T downstream_gene_variant MELA-AU 3 10146634 10146634 single base substitution A T downstream_gene_variant MELA-AU 3 10146782 10146782 single base substitution C T downstream_gene_variant MELA-AU 3 10146829 10146829 single base substitution C T downstream_gene_variant MELA-AU 3 10147182 10147182 single base substitution C T downstream_gene_variant MELA-AU 3 10147231 10147231 single base substitution C T downstream_gene_variant MELA-AU 3 10147316 10147316 single base substitution C T downstream_gene_variant MELA-AU 3 10147716 10147716 single base substitution C T downstream_gene_variant MELA-AU 3 10148049 10148049 single base substitution C T downstream_gene_variant MELA-AU 3 10148295 10148295 single base substitution C T downstream_gene_variant MELA-AU 3 10148426 10148426 single base substitution C T downstream_gene_variant MELA-AU 3 10148481 10148481 single base substitution C T downstream_gene_variant NBL-US 3 10084803 10084803 single base substitution C A downstream_gene_variant NBL-US 3 10084803 10084803 single base substitution C A missense_variant Q320K 958C>A NBL-US 3 10084803 10084803 single base substitution C A upstream_gene_variant ORCA-IN 3 10063483 10063483 single base substitution T A upstream_gene_variant ORCA-IN 3 10073045 10073045 single base substitution G T intron_variant ORCA-IN 3 10073045 10073045 single base substitution G T upstream_gene_variant OV-AU 3 10064224 10064224 single base substitution G A upstream_gene_variant OV-AU 3 10066821 10066821 single base substitution T C upstream_gene_variant OV-AU 3 10071157 10071157 single base substitution G C intron_variant OV-AU 3 10072515 10072515 single base substitution T G intron_variant OV-AU 3 10072515 10072515 single base substitution T G upstream_gene_variant OV-AU 3 10078564 10078564 single base substitution G A downstream_gene_variant OV-AU 3 10078564 10078564 single base substitution G A intron_variant OV-AU 3 10078726 10078726 single base substitution G A downstream_gene_variant OV-AU 3 10078726 10078726 single base substitution G A intron_variant OV-AU 3 10082447 10082447 single base substitution C T 3_prime_UTR_variant OV-AU 3 10082447 10082447 single base substitution C T downstream_gene_variant OV-AU 3 10082447 10082447 single base substitution C T intron_variant OV-AU 3 10082447 10082447 single base substitution C T upstream_gene_variant OV-AU 3 10086595 10086595 single base substitution C T downstream_gene_variant OV-AU 3 10086595 10086595 single base substitution C T intron_variant OV-AU 3 10086595 10086595 single base substitution C T upstream_gene_variant OV-AU 3 10086909 10086909 single base substitution C T downstream_gene_variant OV-AU 3 10086909 10086909 single base substitution C T intron_variant OV-AU 3 10086909 10086909 single base substitution C T upstream_gene_variant OV-AU 3 10098563 10098563 single base substitution G T intron_variant OV-AU 3 10103580 10103580 single base substitution C G intron_variant OV-AU 3 10103580 10103580 single base substitution C G upstream_gene_variant OV-AU 3 10108198 10108198 single base substitution A G intron_variant OV-AU 3 10109908 10109908 single base substitution G C intron_variant OV-AU 3 10110550 10110550 single base substitution C A intron_variant OV-AU 3 10115213 10115213 single base substitution C T downstream_gene_variant OV-AU 3 10115213 10115213 single base substitution C T intron_variant OV-AU 3 10125445 10125445 single base substitution G A intron_variant OV-AU 3 10125677 10125677 single base substitution T G intron_variant OV-AU 3 10139558 10139558 single base substitution T G intron_variant OV-AU 3 10146617 10146617 single base substitution T C downstream_gene_variant OV-US 3 10106040 10106040 single base substitution G T exon_variant OV-US 3 10106040 10106040 single base substitution G T splice_region_variant OV-US 3 10106040 10106040 single base substitution G T stop_gained E650* 1948G>T OV-US 3 10106040 10106040 single base substitution G T upstream_gene_variant PACA-AU 3 10066051 10066051 single base substitution T C upstream_gene_variant PACA-AU 3 10067815 10067815 single base substitution G C upstream_gene_variant PACA-AU 3 10074951 10074951 single base substitution G T intron_variant PACA-AU 3 10074951 10074951 single base substitution G T upstream_gene_variant PACA-AU 3 10083378 10083378 single base substitution C T downstream_gene_variant PACA-AU 3 10083378 10083378 single base substitution C T missense_variant P256L 767C>T PACA-AU 3 10083378 10083378 single base substitution C T upstream_gene_variant PACA-AU 3 10086835 10086835 single base substitution C T downstream_gene_variant PACA-AU 3 10086835 10086835 single base substitution C T intron_variant PACA-AU 3 10086835 10086835 single base substitution C T upstream_gene_variant PACA-AU 3 10089623 10089623 single base substitution C T exon_variant PACA-AU 3 10089623 10089623 single base substitution C T missense_variant S434F 1301C>T PACA-AU 3 10089623 10089623 single base substitution C T upstream_gene_variant PACA-AU 3 10101866 10101866 single base substitution A G intron_variant PACA-AU 3 10101866 10101866 single base substitution A G upstream_gene_variant PACA-AU 3 10107613 10107613 single base substitution C T exon_variant PACA-AU 3 10107613 10107613 single base substitution C T missense_variant R779C 2335C>T PACA-AU 3 10115876 10115876 single base substitution C A downstream_gene_variant PACA-AU 3 10115876 10115876 single base substitution C A intron_variant PACA-AU 3 10117586 10117586 single base substitution T G downstream_gene_variant PACA-AU 3 10117586 10117586 single base substitution T G intron_variant PACA-AU 3 10120033 10120036 deletion of <=200bp TTTA - intron_variant PACA-AU 3 10120863 10120863 single base substitution C T intron_variant PACA-AU 3 10124239 10124239 single base substitution T C intron_variant PACA-AU 3 10135088 10135088 single base substitution C G intron_variant PACA-AU 3 10135501 10135501 single base substitution G T intron_variant PACA-AU 3 10138148 10138148 single base substitution G T 3_prime_UTR_variant PACA-AU 3 10138148 10138148 single base substitution G T exon_variant PACA-AU 3 10138148 10138148 single base substitution G T missense_variant D1393Y 4177G>T PACA-AU 3 10146761 10146761 single base substitution T C downstream_gene_variant PACA-AU 3 10147303 10147303 single base substitution G A downstream_gene_variant PACA-AU 3 10148132 10148132 single base substitution G C downstream_gene_variant PACA-CA 3 10063761 10063761 single base substitution G A upstream_gene_variant PACA-CA 3 10065294 10065294 single base substitution C T upstream_gene_variant PACA-CA 3 10068470 10068470 single base substitution G A intron_variant PACA-CA 3 10068470 10068470 single base substitution G A upstream_gene_variant PACA-CA 3 10074624 10074624 single base substitution T C 3_prime_UTR_variant PACA-CA 3 10074624 10074624 single base substitution T C missense_variant I58T 173T>C PACA-CA 3 10074624 10074624 single base substitution T C upstream_gene_variant PACA-CA 3 10078668 10078668 single base substitution C T downstream_gene_variant PACA-CA 3 10078668 10078668 single base substitution C T intron_variant PACA-CA 3 10081422 10081422 single base substitution C T exon_variant PACA-CA 3 10081422 10081422 single base substitution C T synonymous_variant I196I 588C>T PACA-CA 3 10081643 10081643 deletion of <=200bp C - 3_prime_UTR_variant PACA-CA 3 10081643 10081643 deletion of <=200bp C - intron_variant PACA-CA 3 10083201 10083201 single base substitution G A 3_prime_UTR_variant PACA-CA 3 10083201 10083201 single base substitution G A downstream_gene_variant PACA-CA 3 10083201 10083201 single base substitution G A intron_variant PACA-CA 3 10083201 10083201 single base substitution G A upstream_gene_variant PACA-CA 3 10083355 10083355 single base substitution C A downstream_gene_variant PACA-CA 3 10083355 10083355 single base substitution C A synonymous_variant V248V 744C>A PACA-CA 3 10083355 10083355 single base substitution C A upstream_gene_variant PACA-CA 3 10088587 10088587 single base substitution C T intron_variant PACA-CA 3 10088587 10088587 single base substitution C T upstream_gene_variant PACA-CA 3 10089723 10089723 single base substitution G A exon_variant PACA-CA 3 10089723 10089723 single base substitution G A synonymous_variant T467T 1401G>A PACA-CA 3 10089723 10089723 single base substitution G A upstream_gene_variant PACA-CA 3 10093684 10093684 insertion of <=200bp - A downstream_gene_variant PACA-CA 3 10093684 10093684 insertion of <=200bp - A intron_variant PACA-CA 3 10100647 10100647 single base substitution A G intron_variant PACA-CA 3 10106264 10106264 single base substitution C T intron_variant PACA-CA 3 10106264 10106264 single base substitution C T upstream_gene_variant PACA-CA 3 10107285 10107285 single base substitution T A intron_variant PACA-CA 3 10108898 10108898 single base substitution A G exon_variant PACA-CA 3 10108898 10108898 single base substitution A G intron_variant PACA-CA 3 10108898 10108898 single base substitution A G synonymous_variant V797V 2391A>G PACA-CA 3 10108913 10108913 single base substitution G T exon_variant PACA-CA 3 10108913 10108913 single base substitution G T intron_variant PACA-CA 3 10108913 10108913 single base substitution G T missense_variant Q802H 2406G>T PACA-CA 3 10114137 10114137 single base substitution A T intron_variant PACA-CA 3 10125867 10125867 single base substitution G A intron_variant PACA-CA 3 10127169 10127169 single base substitution G A intron_variant PACA-CA 3 10132912 10132912 single base substitution A G intron_variant PACA-CA 3 10132912 10132912 single base substitution A G upstream_gene_variant PACA-CA 3 10135930 10135930 single base substitution G A intron_variant PACA-CA 3 10141376 10141376 single base substitution A C downstream_gene_variant PACA-CA 3 10141376 10141376 single base substitution A C intron_variant PACA-CA 3 10145267 10145267 deletion of <=200bp A - downstream_gene_variant PAEN-AU 3 10074113 10074113 single base substitution C T intron_variant PAEN-AU 3 10074113 10074113 single base substitution C T splice_region_variant PAEN-AU 3 10074113 10074113 single base substitution C T upstream_gene_variant PAEN-AU 3 10079607 10079607 single base substitution A G downstream_gene_variant PAEN-AU 3 10079607 10079607 single base substitution A G intron_variant PAEN-AU 3 10107412 10107412 single base substitution A T intron_variant PAEN-AU 3 10112371 10112371 deletion of <=200bp G - intron_variant PAEN-IT 3 10081651 10081651 single base substitution C A 3_prime_UTR_variant PAEN-IT 3 10081651 10081651 single base substitution C A intron_variant PBCA-DE 3 10064382 10064383 deletion of <=200bp TC - upstream_gene_variant PBCA-DE 3 10071462 10071462 insertion of <=200bp - TTGTTG intron_variant PBCA-DE 3 10071462 10071462 insertion of <=200bp - TTGTTG upstream_gene_variant PBCA-DE 3 10073032 10073032 deletion of <=200bp A - intron_variant PBCA-DE 3 10073032 10073032 deletion of <=200bp A - upstream_gene_variant PBCA-DE 3 10088845 10088845 insertion of <=200bp - GGTTT intron_variant PBCA-DE 3 10088845 10088845 insertion of <=200bp - GGTTT upstream_gene_variant PBCA-DE 3 10089550 10089553 deletion of <=200bp ACTA - intron_variant PBCA-DE 3 10089550 10089553 deletion of <=200bp ACTA - upstream_gene_variant PBCA-DE 3 10089935 10089936 deletion of <=200bp TC - downstream_gene_variant PBCA-DE 3 10089935 10089936 deletion of <=200bp TC - intron_variant PBCA-DE 3 10089935 10089936 deletion of <=200bp TC - upstream_gene_variant PBCA-DE 3 10096021 10096022 deletion of <=200bp AT - downstream_gene_variant PBCA-DE 3 10096021 10096022 deletion of <=200bp AT - intron_variant PBCA-DE 3 10096038 10096039 deletion of <=200bp TA - downstream_gene_variant PBCA-DE 3 10096038 10096039 deletion of <=200bp TA - intron_variant PBCA-DE 3 10098297 10098297 single base substitution C T intron_variant PBCA-DE 3 10111864 10111864 single base substitution G A intron_variant PBCA-DE 3 10115429 10115429 single base substitution T C downstream_gene_variant PBCA-DE 3 10115429 10115429 single base substitution T C intron_variant PBCA-DE 3 10136046 10136046 single base substitution G A intron_variant PBCA-DE 3 10136046 10136046 single base substitution G A missense_variant R1321Q 3962G>A PBCA-DE 3 10136046 10136046 single base substitution G A splice_region_variant PBCA-DE 3 10141144 10141144 insertion of <=200bp - A 3_prime_UTR_variant PBCA-DE 3 10141144 10141144 insertion of <=200bp - A intron_variant PBCA-DE 3 10143864 10143864 single base substitution A G downstream_gene_variant PRAD-CA 3 10064226 10064226 single base substitution A G upstream_gene_variant PRAD-CA 3 10065938 10065938 single base substitution A T upstream_gene_variant PRAD-CA 3 10083541 10083541 single base substitution T C downstream_gene_variant PRAD-CA 3 10083541 10083541 single base substitution T C intron_variant PRAD-CA 3 10083541 10083541 single base substitution T C upstream_gene_variant PRAD-CA 3 10091304 10091304 single base substitution A G downstream_gene_variant PRAD-CA 3 10091304 10091304 single base substitution A G intron_variant PRAD-CA 3 10125465 10125465 single base substitution A G intron_variant PRAD-CA 3 10125466 10125466 single base substitution A G intron_variant PRAD-UK 3 10064382 10064383 deletion of <=200bp TC - upstream_gene_variant PRAD-UK 3 10082010 10082010 single base substitution G A 3_prime_UTR_variant PRAD-UK 3 10082010 10082010 single base substitution G A intron_variant PRAD-UK 3 10084405 10084405 single base substitution C G downstream_gene_variant PRAD-UK 3 10084405 10084405 single base substitution C G intron_variant PRAD-UK 3 10084405 10084405 single base substitution C G upstream_gene_variant PRAD-UK 3 10087446 10087446 single base substitution C T downstream_gene_variant PRAD-UK 3 10087446 10087446 single base substitution C T intron_variant PRAD-UK 3 10087446 10087446 single base substitution C T upstream_gene_variant PRAD-UK 3 10088104 10088104 single base substitution C T downstream_gene_variant PRAD-UK 3 10088104 10088104 single base substitution C T intron_variant PRAD-UK 3 10088104 10088104 single base substitution C T upstream_gene_variant PRAD-UK 3 10106366 10106366 single base substitution T C intron_variant PRAD-UK 3 10106366 10106366 single base substitution T C upstream_gene_variant PRAD-UK 3 10124559 10124559 single base substitution G A intron_variant PRAD-UK 3 10129233 10129233 single base substitution G C intron_variant PRAD-US 3 10145972 10145972 single base substitution A G downstream_gene_variant READ-US 3 10084272 10084272 single base substitution G T downstream_gene_variant READ-US 3 10084272 10084272 single base substitution G T synonymous_variant S271S 813G>T READ-US 3 10084272 10084272 single base substitution G T upstream_gene_variant RECA-EU 3 10081286 10081286 single base substitution T C intron_variant RECA-EU 3 10088299 10088299 single base substitution C T exon_variant RECA-EU 3 10088299 10088299 single base substitution C T synonymous_variant S390S 1170C>T RECA-EU 3 10088299 10088299 single base substitution C T upstream_gene_variant RECA-EU 3 10088308 10088308 single base substitution T C exon_variant RECA-EU 3 10088308 10088308 single base substitution T C synonymous_variant T393T 1179T>C RECA-EU 3 10088308 10088308 single base substitution T C upstream_gene_variant RECA-EU 3 10088693 10088693 single base substitution C A intron_variant RECA-EU 3 10088693 10088693 single base substitution C A upstream_gene_variant RECA-EU 3 10103895 10103895 single base substitution G T missense_variant Q609H 1827G>T RECA-EU 3 10103895 10103895 single base substitution G T splice_region_variant RECA-EU 3 10103895 10103895 single base substitution G T upstream_gene_variant RECA-EU 3 10107975 10107975 single base substitution G A intron_variant RECA-EU 3 10115216 10115216 single base substitution C T downstream_gene_variant RECA-EU 3 10115216 10115216 single base substitution C T intron_variant RECA-EU 3 10116184 10116184 single base substitution A T downstream_gene_variant RECA-EU 3 10116184 10116184 single base substitution A T intron_variant RECA-EU 3 10116930 10116930 single base substitution G A downstream_gene_variant RECA-EU 3 10116930 10116930 single base substitution G A intron_variant RECA-EU 3 10120949 10120949 single base substitution G T intron_variant SKCA-BR 3 10063689 10063689 single base substitution G A upstream_gene_variant SKCA-BR 3 10066031 10066031 single base substitution G A upstream_gene_variant SKCA-BR 3 10066207 10066207 single base substitution G A upstream_gene_variant SKCA-BR 3 10067821 10067821 single base substitution T G upstream_gene_variant SKCA-BR 3 10069661 10069661 single base substitution C T intron_variant SKCA-BR 3 10069661 10069661 single base substitution C T upstream_gene_variant SKCA-BR 3 10070738 10070738 single base substitution C T intron_variant SKCA-BR 3 10073417 10073417 single base substitution G A intron_variant SKCA-BR 3 10073417 10073417 single base substitution G A upstream_gene_variant SKCA-BR 3 10076850 10076850 single base substitution T A downstream_gene_variant SKCA-BR 3 10076850 10076850 single base substitution T A splice_region_variant SKCA-BR 3 10077633 10077633 single base substitution G A downstream_gene_variant SKCA-BR 3 10077633 10077633 single base substitution G A intron_variant SKCA-BR 3 10078694 10078694 insertion of <=200bp - GT downstream_gene_variant SKCA-BR 3 10078694 10078694 insertion of <=200bp - GT intron_variant SKCA-BR 3 10081180 10081180 single base substitution G A downstream_gene_variant SKCA-BR 3 10081180 10081180 single base substitution G A intron_variant SKCA-BR 3 10081696 10081696 single base substitution T C 3_prime_UTR_variant SKCA-BR 3 10081696 10081696 single base substitution T C intron_variant SKCA-BR 3 10081947 10081947 single base substitution C T 3_prime_UTR_variant SKCA-BR 3 10081947 10081947 single base substitution C T intron_variant SKCA-BR 3 10082591 10082591 single base substitution C T 3_prime_UTR_variant SKCA-BR 3 10082591 10082591 single base substitution C T downstream_gene_variant SKCA-BR 3 10082591 10082591 single base substitution C T intron_variant SKCA-BR 3 10082591 10082591 single base substitution C T upstream_gene_variant SKCA-BR 3 10082626 10082626 single base substitution C T 3_prime_UTR_variant SKCA-BR 3 10082626 10082626 single base substitution C T downstream_gene_variant SKCA-BR 3 10082626 10082626 single base substitution C T intron_variant SKCA-BR 3 10082626 10082626 single base substitution C T upstream_gene_variant SKCA-BR 3 10085130 10085130 single base substitution C G downstream_gene_variant SKCA-BR 3 10085130 10085130 single base substitution C G intron_variant SKCA-BR 3 10085130 10085130 single base substitution C G upstream_gene_variant SKCA-BR 3 10086848 10086848 insertion of <=200bp - GTTTTGTTTTTGT downstream_gene_variant SKCA-BR 3 10086848 10086848 insertion of <=200bp - GTTTTGTTTTTGT intron_variant SKCA-BR 3 10086848 10086848 insertion of <=200bp - GTTTTGTTTTTGT upstream_gene_variant SKCA-BR 3 10087772 10087772 single base substitution C T downstream_gene_variant SKCA-BR 3 10087772 10087772 single base substitution C T intron_variant SKCA-BR 3 10087772 10087772 single base substitution C T upstream_gene_variant SKCA-BR 3 10089265 10089265 single base substitution C T intron_variant SKCA-BR 3 10089265 10089265 single base substitution C T upstream_gene_variant SKCA-BR 3 10090543 10090545 deletion of <=200bp CTA - downstream_gene_variant SKCA-BR 3 10090543 10090545 deletion of <=200bp CTA - intron_variant SKCA-BR 3 10090543 10090545 deletion of <=200bp CTA - upstream_gene_variant SKCA-BR 3 10090557 10090557 single base substitution C T downstream_gene_variant SKCA-BR 3 10090557 10090557 single base substitution C T intron_variant SKCA-BR 3 10090557 10090557 single base substitution C T upstream_gene_variant SKCA-BR 3 10090558 10090558 single base substitution A G downstream_gene_variant SKCA-BR 3 10090558 10090558 single base substitution A G intron_variant SKCA-BR 3 10090558 10090558 single base substitution A G upstream_gene_variant SKCA-BR 3 10090717 10090717 single base substitution G A downstream_gene_variant SKCA-BR 3 10090717 10090717 single base substitution G A intron_variant SKCA-BR 3 10090717 10090717 single base substitution G A upstream_gene_variant SKCA-BR 3 10090821 10090821 single base substitution T C downstream_gene_variant SKCA-BR 3 10090821 10090821 single base substitution T C intron_variant SKCA-BR 3 10090821 10090821 single base substitution T C upstream_gene_variant SKCA-BR 3 10090862 10090862 single base substitution T C downstream_gene_variant SKCA-BR 3 10090862 10090862 single base substitution T C intron_variant SKCA-BR 3 10090862 10090862 single base substitution T C upstream_gene_variant SKCA-BR 3 10090933 10090933 single base substitution G A downstream_gene_variant SKCA-BR 3 10090933 10090933 single base substitution G A intron_variant SKCA-BR 3 10090933 10090933 single base substitution G A upstream_gene_variant SKCA-BR 3 10091035 10091035 single base substitution T C downstream_gene_variant SKCA-BR 3 10091035 10091035 single base substitution T C intron_variant SKCA-BR 3 10091035 10091035 single base substitution T C upstream_gene_variant SKCA-BR 3 10091049 10091049 single base substitution C T downstream_gene_variant SKCA-BR 3 10091049 10091049 single base substitution C T intron_variant SKCA-BR 3 10091049 10091049 single base substitution C T upstream_gene_variant SKCA-BR 3 10091252 10091252 single base substitution A C downstream_gene_variant SKCA-BR 3 10091252 10091252 single base substitution A C intron_variant SKCA-BR 3 10091261 10091261 single base substitution G A downstream_gene_variant SKCA-BR 3 10091261 10091261 single base substitution G A intron_variant SKCA-BR 3 10091742 10091742 single base substitution C T downstream_gene_variant SKCA-BR 3 10091742 10091742 single base substitution C T intron_variant SKCA-BR 3 10092537 10092537 single base substitution G A downstream_gene_variant SKCA-BR 3 10092537 10092537 single base substitution G A intron_variant SKCA-BR 3 10094610 10094610 single base substitution G T downstream_gene_variant SKCA-BR 3 10094610 10094610 single base substitution G T intron_variant SKCA-BR 3 10094735 10094735 single base substitution T A downstream_gene_variant SKCA-BR 3 10094735 10094735 single base substitution T A intron_variant SKCA-BR 3 10094851 10094851 single base substitution G C downstream_gene_variant SKCA-BR 3 10094851 10094851 single base substitution G C intron_variant SKCA-BR 3 10096159 10096159 single base substitution T A downstream_gene_variant SKCA-BR 3 10096159 10096159 single base substitution T A intron_variant SKCA-BR 3 10096731 10096731 single base substitution C T intron_variant SKCA-BR 3 10099945 10099945 single base substitution C T intron_variant SKCA-BR 3 10107202 10107202 single base substitution C T intron_variant SKCA-BR 3 10107453 10107453 single base substitution G A intron_variant SKCA-BR 3 10109861 10109861 single base substitution C T intron_variant SKCA-BR 3 10110244 10110244 single base substitution C T intron_variant SKCA-BR 3 10111143 10111143 insertion of <=200bp - GGCTC intron_variant SKCA-BR 3 10111177 10111177 single base substitution C G intron_variant SKCA-BR 3 10111569 10111569 single base substitution C T intron_variant SKCA-BR 3 10111998 10111998 single base substitution C T intron_variant SKCA-BR 3 10112786 10112786 single base substitution G A intron_variant SKCA-BR 3 10113568 10113568 single base substitution T C intron_variant SKCA-BR 3 10113569 10113569 single base substitution G C intron_variant SKCA-BR 3 10115166 10115166 single base substitution C T downstream_gene_variant SKCA-BR 3 10115166 10115166 single base substitution C T intron_variant SKCA-BR 3 10115528 10115528 single base substitution C T downstream_gene_variant SKCA-BR 3 10115528 10115528 single base substitution C T intron_variant SKCA-BR 3 10120114 10120114 single base substitution C T intron_variant SKCA-BR 3 10127067 10127067 single base substitution C T intron_variant SKCA-BR 3 10128065 10128065 single base substitution C T intron_variant SKCA-BR 3 10128925 10128925 single base substitution C T exon_variant SKCA-BR 3 10128925 10128925 single base substitution C T missense_variant S1148F 3443C>T SKCA-BR 3 10129362 10129362 single base substitution C T intron_variant SKCA-BR 3 10132958 10132958 single base substitution T G intron_variant SKCA-BR 3 10132958 10132958 single base substitution T G upstream_gene_variant SKCA-BR 3 10138727 10138727 single base substitution C A intron_variant SKCA-BR 3 10139291 10139291 single base substitution C T intron_variant SKCA-BR 3 10141082 10141082 single base substitution G A 3_prime_UTR_variant SKCA-BR 3 10141082 10141082 single base substitution G A intron_variant SKCA-BR 3 10143086 10143086 insertion of <=200bp - TA 3_prime_UTR_variant SKCA-BR 3 10143086 10143086 insertion of <=200bp - TA downstream_gene_variant SKCA-BR 3 10143451 10143451 single base substitution C T 3_prime_UTR_variant SKCA-BR 3 10143451 10143451 single base substitution C T downstream_gene_variant SKCA-BR 3 10143671 10143671 single base substitution G T downstream_gene_variant SKCA-BR 3 10144138 10144138 single base substitution C T downstream_gene_variant SKCA-BR 3 10146616 10146621 deletion of <=200bp ATTATT - downstream_gene_variant SKCA-BR 3 10147433 10147434 deletion of <=200bp TA - downstream_gene_variant SKCA-BR 3 10147506 10147506 single base substitution T A downstream_gene_variant SKCA-BR 3 10147516 10147516 single base substitution G A downstream_gene_variant SKCM-US 3 10081425 10081425 single base substitution G C exon_variant SKCM-US 3 10081425 10081425 single base substitution G C missense_variant M197I 591G>C SKCM-US 3 10081488 10081488 single base substitution C T exon_variant SKCM-US 3 10081488 10081488 single base substitution C T synonymous_variant I218I 654C>T SKCM-US 3 10081489 10081489 single base substitution C T exon_variant SKCM-US 3 10081489 10081489 single base substitution C T synonymous_variant L219L 655C>T SKCM-US 3 10084758 10084758 single base substitution T C downstream_gene_variant SKCM-US 3 10084758 10084758 single base substitution T C synonymous_variant L305L 913T>C SKCM-US 3 10084758 10084758 single base substitution T C upstream_gene_variant SKCM-US 3 10088351 10088351 single base substitution C T exon_variant SKCM-US 3 10088351 10088351 single base substitution C T stop_gained R408* 1222C>T SKCM-US 3 10088351 10088351 single base substitution C T upstream_gene_variant SKCM-US 3 10089602 10089602 single base substitution T C missense_variant V427A 1280T>C SKCM-US 3 10089602 10089602 single base substitution T C splice_region_variant SKCM-US 3 10089602 10089602 single base substitution T C upstream_gene_variant SKCM-US 3 10089604 10089604 single base substitution C T exon_variant SKCM-US 3 10089604 10089604 single base substitution C T missense_variant L428F 1282C>T SKCM-US 3 10089604 10089604 single base substitution C T upstream_gene_variant SKCM-US 3 10089610 10089610 single base substitution G A exon_variant SKCM-US 3 10089610 10089610 single base substitution G A missense_variant D430N 1288G>A SKCM-US 3 10089610 10089610 single base substitution G A upstream_gene_variant SKCM-US 3 10089677 10089677 single base substitution C T exon_variant SKCM-US 3 10089677 10089677 single base substitution C T missense_variant S452L 1355C>T SKCM-US 3 10089677 10089677 single base substitution C T upstream_gene_variant SKCM-US 3 10089688 10089688 single base substitution C T exon_variant SKCM-US 3 10089688 10089688 single base substitution C T missense_variant L456F 1366C>T SKCM-US 3 10089688 10089688 single base substitution C T upstream_gene_variant SKCM-US 3 10091094 10091094 single base substitution G A downstream_gene_variant SKCM-US 3 10091094 10091094 single base substitution G A exon_variant SKCM-US 3 10091094 10091094 single base substitution G A missense_variant G484R 1450G>A SKCM-US 3 10091094 10091094 single base substitution G A upstream_gene_variant SKCM-US 3 10101995 10101995 single base substitution G A exon_variant SKCM-US 3 10101995 10101995 single base substitution G A synonymous_variant V558V 1674G>A SKCM-US 3 10101995 10101995 single base substitution G A upstream_gene_variant SKCM-US 3 10105572 10105572 single base substitution G A exon_variant SKCM-US 3 10105572 10105572 single base substitution G A missense_variant E642K 1924G>A SKCM-US 3 10105572 10105572 single base substitution G A upstream_gene_variant SKCM-US 3 10106090 10106090 single base substitution G A exon_variant SKCM-US 3 10106090 10106090 single base substitution G A synonymous_variant V666V 1998G>A SKCM-US 3 10106090 10106090 single base substitution G A upstream_gene_variant SKCM-US 3 10106108 10106108 single base substitution G A exon_variant SKCM-US 3 10106108 10106108 single base substitution G A synonymous_variant P672P 2016G>A SKCM-US 3 10106108 10106108 single base substitution G A upstream_gene_variant SKCM-US 3 10128860 10128860 single base substitution C A exon_variant SKCM-US 3 10128860 10128860 single base substitution C A synonymous_variant P1126P 3378C>A SKCM-US 3 10130575 10130575 single base substitution C T exon_variant SKCM-US 3 10130575 10130575 single base substitution C T synonymous_variant V1208V 3624C>T SKCM-US 3 10130575 10130575 single base substitution C T upstream_gene_variant SKCM-US 3 10130618 10130618 single base substitution T C exon_variant SKCM-US 3 10130618 10130618 single base substitution T C missense_variant F1223L 3667T>C SKCM-US 3 10130618 10130618 single base substitution T C upstream_gene_variant SKCM-US 3 10136044 10136044 single base substitution C T 3_prime_UTR_variant SKCM-US 3 10136044 10136044 single base substitution C T intron_variant SKCM-US 3 10136044 10136044 single base substitution C T synonymous_variant H1320H 3960C>T SKCM-US 3 10136910 10136910 single base substitution C T 3_prime_UTR_variant SKCM-US 3 10136910 10136910 single base substitution C T exon_variant SKCM-US 3 10136910 10136910 single base substitution C T synonymous_variant T1330T 3990C>T SKCM-US 3 10140504 10140504 single base substitution C T missense_variant S1429F 4286C>T SKCM-US 3 10140504 10140504 single base substitution C T splice_region_variant SKCM-US 3 10140621 10140621 single base substitution C T intron_variant SKCM-US 3 10140621 10140621 single base substitution C T missense_variant P1468L 4403C>T SKCM-US 3 10146064 10146064 single base substitution C T downstream_gene_variant SKCM-US 3 10146202 10146202 single base substitution C T downstream_gene_variant SKCM-US 3 10146260 10146260 single base substitution C T downstream_gene_variant SKCM-US 3 10146326 10146326 single base substitution C T downstream_gene_variant SKCM-US 3 10146351 10146351 single base substitution G T downstream_gene_variant SKCM-US 3 10146467 10146467 single base substitution C T downstream_gene_variant STAD-US 3 10074520 10074520 single base substitution C T 3_prime_UTR_variant STAD-US 3 10074520 10074520 single base substitution C T synonymous_variant T23T 69C>T STAD-US 3 10074520 10074520 single base substitution C T upstream_gene_variant STAD-US 3 10076903 10076903 single base substitution A T downstream_gene_variant STAD-US 3 10076903 10076903 single base substitution A T exon_variant STAD-US 3 10076903 10076903 single base substitution A T missense_variant I142F 424A>T STAD-US 3 10078012 10078012 deletion of <=200bp T - downstream_gene_variant STAD-US 3 10078012 10078012 deletion of <=200bp T - exon_variant STAD-US 3 10078012 10078012 deletion of <=200bp T - frameshift_variant Y160 STAD-US 3 10081483 10081483 single base substitution G A exon_variant STAD-US 3 10081483 10081483 single base substitution G A missense_variant E217K 649G>A STAD-US 3 10084268 10084268 single base substitution T C downstream_gene_variant STAD-US 3 10084268 10084268 single base substitution T C missense_variant L270S 809T>C STAD-US 3 10084268 10084268 single base substitution T C upstream_gene_variant STAD-US 3 10084330 10084330 single base substitution G A downstream_gene_variant STAD-US 3 10084330 10084330 single base substitution G A missense_variant A291T 871G>A STAD-US 3 10084330 10084330 single base substitution G A upstream_gene_variant STAD-US 3 10091175 10091175 single base substitution G A downstream_gene_variant STAD-US 3 10091175 10091175 single base substitution G A exon_variant STAD-US 3 10091175 10091175 single base substitution G A missense_variant A511T 1531G>A STAD-US 3 10106458 10106458 single base substitution C T exon_variant STAD-US 3 10106458 10106458 single base substitution C T synonymous_variant Y689Y 2067C>T STAD-US 3 10106464 10106464 single base substitution T C exon_variant STAD-US 3 10106464 10106464 single base substitution T C synonymous_variant T691T 2073T>C STAD-US 3 10114936 10114936 single base substitution G T downstream_gene_variant STAD-US 3 10114936 10114936 single base substitution G T splice_acceptor_variant STAD-US 3 10119789 10119789 deletion of <=200bp C - exon_variant STAD-US 3 10119789 10119789 deletion of <=200bp C - frameshift_variant P962 STAD-US 3 10130195 10130195 single base substitution A G exon_variant STAD-US 3 10130195 10130195 single base substitution A G missense_variant I1177V 3529A>G STAD-US 3 10130195 10130195 single base substitution A G upstream_gene_variant STAD-US 3 10130535 10130535 single base substitution G A exon_variant STAD-US 3 10130535 10130535 single base substitution G A missense_variant S1195N 3584G>A STAD-US 3 10130535 10130535 single base substitution G A upstream_gene_variant STAD-US 3 10133927 10133927 single base substitution C G exon_variant STAD-US 3 10133927 10133927 single base substitution C G missense_variant N1280K 3840C>G STAD-US 3 10133927 10133927 single base substitution C G missense_variant T1249S 3746C>G STAD-US 3 10133927 10133927 single base substitution C G upstream_gene_variant STAD-US 3 10138154 10138154 single base substitution C T splice_region_variant STAD-US 3 10138154 10138154 single base substitution C T stop_gained Q1395* 4183C>T STAD-US 3 10140588 10140588 single base substitution A G intron_variant STAD-US 3 10140588 10140588 single base substitution A G missense_variant Y1457C 4370A>G STAD-US 3 10146117 10146117 single base substitution C T downstream_gene_variant THCA-SA 3 10088343 10088343 single base substitution A G exon_variant THCA-SA 3 10088343 10088343 single base substitution A G missense_variant N405S 1214A>G THCA-SA 3 10088343 10088343 single base substitution A G upstream_gene_variant THCA-SA 3 10088394 10088394 single base substitution C G exon_variant THCA-SA 3 10088394 10088394 single base substitution C G missense_variant S422C 1265C>G THCA-SA 3 10088394 10088394 single base substitution C G upstream_gene_variant THCA-US 3 10091163 10091163 single base substitution A G downstream_gene_variant THCA-US 3 10091163 10091163 single base substitution A G exon_variant THCA-US 3 10091163 10091163 single base substitution A G missense_variant M507V 1519A>G THCA-US 3 10106101 10106101 single base substitution T C exon_variant THCA-US 3 10106101 10106101 single base substitution T C missense_variant V670A 2009T>C THCA-US 3 10106101 10106101 single base substitution T C upstream_gene_variant THCA-US 3 10106529 10106529 single base substitution G A exon_variant THCA-US 3 10106529 10106529 single base substitution G A missense_variant G713D 2138G>A UCEC-US 3 10081522 10081522 single base substitution G T exon_variant UCEC-US 3 10081522 10081522 single base substitution G T stop_gained E230* 688G>T UCEC-US 3 10084272 10084272 single base substitution G A downstream_gene_variant UCEC-US 3 10084272 10084272 single base substitution G A synonymous_variant S271S 813G>A UCEC-US 3 10084272 10084272 single base substitution G A upstream_gene_variant UCEC-US 3 10085213 10085213 single base substitution C T downstream_gene_variant UCEC-US 3 10085213 10085213 single base substitution C T synonymous_variant L345L 1035C>T UCEC-US 3 10085213 10085213 single base substitution C T upstream_gene_variant UCEC-US 3 10088317 10088317 single base substitution G T exon_variant UCEC-US 3 10088317 10088317 single base substitution G T missense_variant K396N 1188G>T UCEC-US 3 10088317 10088317 single base substitution G T upstream_gene_variant UCEC-US 3 10089616 10089616 single base substitution T C exon_variant UCEC-US 3 10089616 10089616 single base substitution T C missense_variant C432R 1294T>C UCEC-US 3 10089616 10089616 single base substitution T C upstream_gene_variant UCEC-US 3 10094113 10094113 single base substitution C T downstream_gene_variant UCEC-US 3 10094113 10094113 single base substitution C T exon_variant UCEC-US 3 10094113 10094113 single base substitution C T stop_gained R530* 1588C>T UCEC-US 3 10106495 10106495 single base substitution C T exon_variant UCEC-US 3 10106495 10106495 single base substitution C T synonymous_variant L702L 2104C>T UCEC-US 3 10107112 10107112 single base substitution C T exon_variant UCEC-US 3 10107112 10107112 single base substitution C T missense_variant R735W 2203C>T UCEC-US 3 10108961 10108961 single base substitution C T exon_variant UCEC-US 3 10108961 10108961 single base substitution C T intron_variant UCEC-US 3 10108961 10108961 single base substitution C T synonymous_variant H818H 2454C>T UCEC-US 3 10114940 10114940 single base substitution G A downstream_gene_variant UCEC-US 3 10114940 10114940 single base substitution G A exon_variant UCEC-US 3 10114940 10114940 single base substitution G A missense_variant R870K 2609G>A UCEC-US 3 10116324 10116324 single base substitution G A downstream_gene_variant UCEC-US 3 10116324 10116324 single base substitution G A exon_variant UCEC-US 3 10116324 10116324 single base substitution G A synonymous_variant T942T 2826G>A UCEC-US 3 10123089 10123089 single base substitution C T exon_variant UCEC-US 3 10123089 10123089 single base substitution C T synonymous_variant Y1055Y 3165C>T UCEC-US 3 10130579 10130579 single base substitution G T exon_variant UCEC-US 3 10130579 10130579 single base substitution G T stop_gained E1210* 3628G>T UCEC-US 3 10130579 10130579 single base substitution G T upstream_gene_variant UCEC-US 3 10134990 10134990 single base substitution C A 3_prime_UTR_variant UCEC-US 3 10134990 10134990 single base substitution C A exon_variant UCEC-US 3 10134990 10134990 single base substitution C A missense_variant L1291M 3871C>A UCEC-US 3 10136907 10136907 single base substitution A G 3_prime_UTR_variant UCEC-US 3 10136907 10136907 single base substitution A G exon_variant UCEC-US 3 10136907 10136907 single base substitution A G synonymous_variant E1329E 3987A>G UCEC-US 3 10138023 10138023 single base substitution C T 3_prime_UTR_variant UCEC-US 3 10138023 10138023 single base substitution C T exon_variant UCEC-US 3 10138023 10138023 single base substitution C T missense_variant T1351M 4052C>T UCEC-US 3 10138089 10138089 single base substitution C A 3_prime_UTR_variant UCEC-US 3 10138089 10138089 single base substitution C A exon_variant UCEC-US 3 10138089 10138089 single base substitution C A missense_variant A1373D 4118C>A UCEC-US 3 10142924 10142924 single base substitution A C 3_prime_UTR_variant UCEC-US 3 10142924 10142924 single base substitution A C downstream_gene_variant UCEC-US 3 10142924 10142924 single base substitution A C exon_variant UCEC-US 3 10142924 10142924 single base substitution A C missense_variant E1445A 4334A>C UCEC-US 3 10145989 10145989 single base substitution C T downstream_gene_variant UCEC-US 3 10146027 10146027 single base substitution C T downstream_gene_variant UCEC-US 3 10146326 10146326 single base substitution C T downstream_gene_variant UCEC-US 3 10146332 10146333 deletion of <=200bp GT - downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand SCC-25 COSM4593246 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + TCGA-BT-A0YX-01 COSM419481 c.1489C>G p.L497V Substitution - Missense 3:10049449-10049449 + TCGA-B6-A0RE-01 COSM445216 c.2192C>T p.A731V Substitution - Missense 3:10065417-10065417 + TCGA-DA-A3F8-06 COSM3584584 c.1355C>T p.S452L Substitution - Missense 3:10047993-10047993 + TCGA-DI-A0WH-01 COSM1035745 c.429C>T p.D143D Substitution - coding silent 3:10035224-10035224 + Detroit_562 COSM4157094 c.1137G>T p.V379V Substitution - coding silent 3:10046582-10046582 + sysucc-1240T COSM4157098 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + UPCI:SCC090 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + S01733 COSM4386858 c.1278+3_1278+5delAAG p.? Unknown 3:10046726-10046728 + SCC-15 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + C0034T COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + CN-AML-CR-29-Dx COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + GC_337T-GC_337N COSM4591323 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + 1N45-VS-1T45 COSM4975869 c.3470C>T p.S1157F Substitution - Missense 3:10088452-10088452 + TCGA-B7-5816-01 COSM4111910 c.4370A>G p.Y1457C Substitution - Missense 3:10098904-10098904 + sysucc-1640T COSM4152593 c.1179T>C p.T393T Substitution - coding silent 3:10046624-10046624 + TCGA-K4-A3WU-01 COSM3800823 c.1306C>A p.L436M Substitution - Missense 3:10047944-10047944 + HCT15 COSM2915752 c.4335G>A p.E1445E Substitution - coding silent 3:10101241-10101241 + ESO-021 COSM1251994 c.4129C>T p.L1377F Substitution - Missense 3:10096416-10096416 + PD4100a COSM160981 c.1770T>G p.S590R Substitution - Missense 3:10062154-10062154 + TCGA-FW-A3R5-06 COSM3914398 c.1366C>T p.L456F Substitution - Missense 3:10048004-10048004 + UPCI:SCC090 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + 3N31-VS-3T31 COSM4980668 c.838G>A p.V280M Substitution - Missense 3:10042613-10042613 + TCGA-GN-A269-01 COSM3584653 c.3667T>C p.F1223L Substitution - Missense 3:10088934-10088934 + TCGA-FW-A3R5-06 COSM1241156 c.1222C>T p.R408* Substitution - Nonsense 3:10046667-10046667 + sysucc-1878T COSM5766105 c.1413+3A>G p.? Unknown 3:10048054-10048054 + LUAD-B01811 COSM334482 c.1618G>C p.A540P Substitution - Missense 3:10052459-10052459 + TCGA-EE-A29D-06 COSM3584621 c.1924G>A p.E642K Substitution - Missense 3:10063888-10063888 + SH-0348 COSM5019051 c.1440T>C p.H480H Substitution - coding silent 3:10049400-10049400 + PCSI_0090_Pa_X COSM3380314 c.173T>C p.I58T Substitution - Missense 3:10032940-10032940 + PT35 COSM4157094 c.1137G>T p.V379V Substitution - coding silent 3:10046582-10046582 + C135 COSM4618274 c.2886C>G p.P962P Substitution - coding silent 3:10078107-10078107 + p2_VI-2 COSM1738294 c.427G>C p.D143H Substitution - Missense 3:10035222-10035222 + sysucc-1038T COSM4422613 c.1170C>T p.S390S Substitution - coding silent 3:10046615-10046615 + TCGA-AC-A2QJ-01 COSM3845666 c.2391A>G p.V797V Substitution - coding silent 3:10067214-10067214 + PT26 COSM3766820 c.2613A>C p.K871N Substitution - Missense 3:10073260-10073260 + YUSEL COSM1692356 c.2516C>T p.P839L Substitution - Missense 3:10072892-10072892 + TCGA-B0-4827-01 COSM1130392 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + p2_VI-1 COSM1738294 c.427G>C p.D143H Substitution - Missense 3:10035222-10035222 + TCGA-A7-A13E-01 COSM3845672 c.2914C>T p.L972F Substitution - Missense 3:10078135-10078135 + SCC-25 COSM4591323 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + Detroit_562 COSM4593246 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + 116 COSM1741463 c.812C>T p.S271L Substitution - Missense 3:10042587-10042587 + ESO-837 COSM1251997 c.3223T>C p.W1075R Substitution - Missense 3:10081463-10081463 + TCGA-GN-A269-01 COSM3584654 c.3667T>C p.F1223L Substitution - Missense 3:10088934-10088934 + HCC90T COSM1616666 c.2938C>G p.L980V Substitution - Missense 3:10078159-10078159 + 8067216 COSM3780605 c.767C>T p.P256L Substitution - Missense 3:10041694-10041694 + 1261_T COSM3944605 c.2866G>C p.E956Q Substitution - Missense 3:10078087-10078087 + LUAD_E01047 COSM390204 c.1161C>A p.I387I Substitution - coding silent 3:10046606-10046606 + sysucc-1365T COSM5766105 c.1413+3A>G p.? Unknown 3:10048054-10048054 + TCGA-06-0237 COSM1154050 c.813G>A p.S271S Substitution - coding silent 3:10042588-10042588 + SH-3133 COSM5019051 c.1440T>C p.H480H Substitution - coding silent 3:10049400-10049400 + TCGA-B5-A11E-01 COSM1593207 c.1035C>T p.L345L Substitution - coding silent 3:10043529-10043529 + UM-SCC-11B COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + CAL27 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + PTC-77C COSM4157099 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + NOKSI COSM4591323 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + 2011-2370:2012-1299-T COSM4606114 c.916G>C p.D306H Substitution - Missense 3:10043077-10043077 + TCGA-27-2527-01 COSM3408075 c.2401T>C p.C801R Substitution - Missense 3:10067224-10067224 + PD4120a COSM160982 c.3124C>T p.H1042Y Substitution - Missense 3:10081364-10081364 + TCGA-D3-A51T-06 COSM3584604 c.1674G>A p.V558V Substitution - coding silent 3:10060311-10060311 + SCC-25 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-GC-A3RC-01 COSM3800831 c.2238C>A p.N746K Substitution - Missense 3:10065463-10065463 + TCGA-FW-A3R5-06 COSM3914397 c.654C>T p.I218I Substitution - coding silent 3:10039804-10039804 + TCGA-BC-A112-01 COSM1130393 c.2391A>G p.V797V Substitution - coding silent 3:10067214-10067214 + TCGA-AC-A2QJ-01 COSM3364905 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + PTC_435 COSM5957042 c.1265C>G p.S422C Substitution - Missense 3:10046710-10046710 + TCGA-AP-A059-01 COSM1593179 c.4334A>C p.E1445A Substitution - Missense 3:10101240-10101240 + TCGA-B5-A0JY-01 COSM1035750 c.1188G>T p.K396N Substitution - Missense 3:10046633-10046633 + TCGA-DI-A0WH-01 COSM1154049 c.429C>T p.D143D Substitution - coding silent 3:10035224-10035224 + TCGA-AP-A059-01 COSM1593183 c.3871C>A p.L1291M Substitution - Missense 3:10093306-10093306 + TCGA-FG-A4MY-01 COSM3974040 c.772T>G p.F258V Substitution - Missense 3:10041699-10041699 + TCGA-CG-4465-01 COSM4111825 c.69C>T p.T23T Substitution - coding silent 3:10032836-10032836 + TCGA-BR-4184-01 COSM4111832 c.871G>A p.A291T Substitution - Missense 3:10042646-10042646 + SH-9771 COSM5021023 c.4186-5T>C p.? Unknown 3:10098715-10098715 + TCGA-AA-A00N-01 COSM275089 c.3817C>T p.R1273* Substitution - Nonsense 3:10092220-10092220 + UPCI:SCC090 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + HCC061T COSM5805919 c.559G>A p.V187M Substitution - Missense 3:10039346-10039346 + sysucc-1247T COSM5037547 c.1414-9C>T p.? Unknown 3:10049365-10049365 + C0034T COSM4152593 c.1179T>C p.T393T Substitution - coding silent 3:10046624-10046624 + TCGA-O8-A75V-01 COSM4930570 c.249G>C p.L83L Substitution - coding silent 3:10034512-10034512 + CSCC-15-T COSM4482814 c.2642C>T p.S881F Substitution - Missense 3:10073289-10073289 + HCC061T COSM5805920 c.559G>A p.V187M Substitution - Missense 3:10039346-10039346 + TCGA-EE-A184-06 COSM3584647 c.3378C>A p.P1126P Substitution - coding silent 3:10087176-10087176 + TCGA-FW-A3R5-06 COSM3914411 c.4281+5C>T p.? Unknown 3:10098820-10098820 + SH-3327 COSM5019433 c.2702G>T p.G901V Substitution - Missense 3:10073349-10073349 + 1N45-VS-1T45 COSM4975871 c.3707G>T p.R1236L Substitution - Missense 3:10090315-10090315 + TCGA-C8-A3M7-01 COSM3845650 c.1306C>T p.L436L Substitution - coding silent 3:10047944-10047944 + 47T COSM5575767 c.3092A>G p.H1031R Substitution - Missense 3:10081215-10081215 + 9227_T COSM5040201 c.1202G>A p.R401K Substitution - Missense 3:10046647-10046647 + TCGA-HU-A4G8-01 COSM4111902 c.4183C>T p.Q1395* Substitution - Nonsense 3:10096470-10096470 + TCGA-F1-A448-01 COSM2915480 c.2067C>T p.Y689Y Substitution - coding silent 3:10064774-10064774 + UM-SCC-2 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + C086 COSM3584585 c.1355C>T p.S452L Substitution - Missense 3:10047993-10047993 + sysucc-1038T COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + NOKSI COSM4593246 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + Pat_06_A COSM5863107 c.2775_2776delCC p.F925fs*6 Deletion - Frameshift 3:10074589-10074590 + PT37 COSM5918083 c.86C>T p.S29F Substitution - Missense 3:10032853-10032853 + HCT15 COSM1669962 c.3818G>A p.R1273Q Substitution - Missense 3:10092221-10092221 + T3116 COSM4683350 c.2102C>T p.P701L Substitution - Missense 3:10064809-10064809 + 440 COSM4434456 c.1183A>T p.T395S Substitution - Missense 3:10046628-10046628 + RK121_C01 COSM3766820 c.2613A>C p.K871N Substitution - Missense 3:10073260-10073260 + Pat_28_B COSM3584583 c.1288G>A p.D430N Substitution - Missense 3:10047926-10047926 + Detroit_562 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + PTC-70C COSM4157094 c.1137G>T p.V379V Substitution - coding silent 3:10046582-10046582 + PCSI_0194_Pa_P COSM4157099 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + S09-31237-TP COSM4991802 c.1598T>G p.F533C Substitution - Missense 3:10052439-10052439 + TCGA-BS-A0UV-01 COSM1593182 c.3987A>G p.E1329E Substitution - coding silent 3:10095223-10095223 + TCGA-BG-A0MQ-01 COSM1035747 c.813G>A p.S271S Substitution - coding silent 3:10042588-10042588 + C99 COSM4620440 c.3436A>G p.T1146A Substitution - Missense 3:10087234-10087234 + TCGA-AP-A056-01 COSM1593185 c.3165C>T p.Y1055Y Substitution - coding silent 3:10081405-10081405 + SW48 COSM2915697 c.4048G>A p.D1350N Substitution - Missense 3:10096335-10096335 + sysucc-1317T COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + HCC90 COSM1616666 c.2938C>G p.L980V Substitution - Missense 3:10078159-10078159 + RK046_C02 COSM1632669 c.957C>T p.S319S Substitution - coding silent 3:10043118-10043118 + TCGA-EE-A3JA-06 COSM3584581 c.1282C>T p.L428F Substitution - Missense 3:10047920-10047920 + TCGA-FS-A1ZW-06 COSM3584582 c.1288G>A p.D430N Substitution - Missense 3:10047926-10047926 + sysucc-1640T COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + SCC-15 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + SH-5693 COSM5020235 c.1367T>G p.L456R Substitution - Missense 3:10048005-10048005 + HCT-15 COSM1669961 c.3818G>A p.R1273Q Substitution - Missense 3:10092221-10092221 + BHY COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-AP-A056-01 COSM1035786 c.3165C>T p.Y1055Y Substitution - coding silent 3:10081405-10081405 + Br02X COSM39696 c.2774_2775insT p.R926fs*6 Insertion - Frameshift 3:10074588-10074589 + SUDHL7 COSM1580877 c.2180C>T p.P727L Substitution - Missense 3:10065405-10065405 + 4472_T COSM3944599 c.1528A>C p.N510H Substitution - Missense 3:10049488-10049488 + TCGA-EE-A184-06 COSM3584648 c.3378C>A p.P1126P Substitution - coding silent 3:10087176-10087176 + STC263 COSM5059159 c.1092G>A p.W364* Substitution - Nonsense 3:10043586-10043586 + TCGA-DK-A1AC-01 COSM1308326 c.3333C>T p.L1111L Substitution - coding silent 3:10085920-10085920 + TCGA-DV-5574-01 COSM1417229 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + 2318494 COSM4777223 c.3298C>G p.Q1100E Substitution - Missense 3:10085885-10085885 + ESCC_74 COSM5634764 c.4235G>A p.S1412N Substitution - Missense 3:10098769-10098769 + TCGA-DK-A1AC-01 COSM1308312 c.14G>C p.R5T Substitution - Missense 3:10028671-10028671 + TCGA-B5-A0JY-01 COSM1035785 c.2826G>A p.T942T Substitution - coding silent 3:10074640-10074640 + sysucc-1240T COSM5766105 c.1413+3A>G p.? Unknown 3:10048054-10048054 + TCGA-BG-A0MQ-01 COSM1154050 c.813G>A p.S271S Substitution - coding silent 3:10042588-10042588 + 131T COSM1725655 c.3581A>G p.E1194G Substitution - Missense 3:10088848-10088848 + UD-SCC-2 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-EE-A29X-06 COSM3584585 c.1355C>T p.S452L Substitution - Missense 3:10047993-10047993 + SCC-9 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + TCGA-B6-A0RE-01 COSM1484373 c.2192C>T p.A731V Substitution - Missense 3:10065417-10065417 + YUPAT COSM1692353 c.1153C>T p.L385F Substitution - Missense 3:10046598-10046598 + TCGA-BS-A0UF-01 COSM1035800 c.3628G>T p.E1210* Substitution - Nonsense 3:10088895-10088895 + sysucc-1577T COSM1417230 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + DLD1 COSM1669962 c.3818G>A p.R1273Q Substitution - Missense 3:10092221-10092221 + DN11190 COSM5789087 c.1263C>T p.F421F Substitution - coding silent 3:10046708-10046708 + SJRHB003_D COSM3364905 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + WSU-HN30 COSM4593247 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + p2_VI-1 COSM1738296 c.438+5G>C p.? Unknown 3:10035238-10035238 + sysucc-1038T COSM4152593 c.1179T>C p.T393T Substitution - coding silent 3:10046624-10046624 + CSCC-32-T COSM4484163 c.2776C>T p.R926* Substitution - Nonsense 3:10074590-10074590 + 186T COSM5576143 c.1390T>G p.F464V Substitution - Missense 3:10048028-10048028 + TARGET-30-PASWYR COSM1284877 c.958C>A p.Q320K Substitution - Missense 3:10043119-10043119 + TCGA-C8-A274-01 COSM1484369 c.1318C>T p.Q440* Substitution - Nonsense 3:10047956-10047956 + Detroit_562 COSM1417229 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + RK046_C02 COSM1632670 c.957C>T p.S319S Substitution - coding silent 3:10043118-10043118 + TCGA-FW-A3R5-06 COSM1241157 c.1222C>T p.R408* Substitution - Nonsense 3:10046667-10046667 + 3N31-VS-3T31 COSM4980667 c.838G>A p.V280M Substitution - Missense 3:10042613-10042613 + BD171T COSM5494740 c.193C>T p.Q65* Substitution - Nonsense 3:10032960-10032960 + C008 COSM5522652 c.2597G>A p.G866E Substitution - Missense 3:10072973-10072973 + TCGA-C8-A3M7-01 COSM3845649 c.1306C>T p.L436L Substitution - coding silent 3:10047944-10047944 + TCGA-BS-A0UV-01 COSM1035784 c.2609G>A p.R870K Substitution - Missense 3:10073256-10073256 + SCC-25 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + sysucc-966T COSM4157098 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + KPOPBR-35-T COSM5963290 c.3777+5G>C p.? Unknown 3:10090390-10090390 + 587376 COSM1206498 c.1263C>A p.F421L Substitution - Missense 3:10046708-10046708 + Case1 COSM1579136 c.167G>T p.G56V Substitution - Missense 3:10032934-10032934 + TCGA-CG-4305-01 COSM4111892 c.3584G>A p.S1195N Substitution - Missense 3:10088851-10088851 + sysucc-1878T COSM4157098 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + sysucc-809T COSM4157099 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + SJDES006 COSM4583739 c.2442T>C p.T814T Substitution - coding silent 3:10067265-10067265 + LN18 COSM1417230 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + TCGA-BR-8372-01 COSM4111831 c.809T>C p.L270S Substitution - Missense 3:10042584-10042584 + CSCC-31-T COSM4485881 c.2989C>G p.R997G Substitution - Missense 3:10081112-10081112 + 186T COSM5576144 c.1390T>G p.F464V Substitution - Missense 3:10048028-10048028 + BD171T COSM5494739 c.193C>T p.Q65* Substitution - Nonsense 3:10032960-10032960 + HCC90T COSM1616665 c.2938C>G p.L980V Substitution - Missense 3:10078159-10078159 + S01733 COSM1417231 c.1278+1delG p.? Unknown 3:10046724-10046724 + TCGA-06-0237-01 COSM1035747 c.813G>A p.S271S Substitution - coding silent 3:10042588-10042588 + CSCC-32-T COSM4484164 c.2776C>T p.R926* Substitution - Nonsense 3:10074590-10074590 + HCC152 COSM3660058 c.2133T>G p.D711E Substitution - Missense 3:10064840-10064840 + PD7307a COSM5789087 c.1263C>T p.F421F Substitution - coding silent 3:10046708-10046708 + Detroit_562 COSM3759563 c.1122A>G p.V374V Substitution - coding silent 3:10043852-10043852 + TCGA-O8-A75V-01 COSM4930569 c.249G>C p.L83L Substitution - coding silent 3:10034512-10034512 + U373 COSM1417229 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + TCGA-BR-6452-01 COSM4111835 c.1531G>A p.A511T Substitution - Missense 3:10049491-10049491 + DLBCL781 COSM1580884 c.3446C>T p.A1149V Substitution - Missense 3:10087244-10087244 + TCGA-BT-A3PK-01 COSM3800832 c.3786A>C p.E1262D Substitution - Missense 3:10092189-10092189 + sysucc-783T COSM1035774 c.2104C>T p.L702L Substitution - coding silent 3:10064811-10064811 + CSCC-16-T COSM4477897 c.2194C>T p.P732S Substitution - Missense 3:10065419-10065419 + 2318494 COSM4777222 c.3298C>G p.Q1100E Substitution - Missense 3:10085885-10085885 + WSU-HN13 COSM4591322 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + UM-SCC-4 COSM4591322 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + HCT15 COSM1669961 c.3818G>A p.R1273Q Substitution - Missense 3:10092221-10092221 + TCGA-DK-A1AC-01 COSM1308325 c.3333C>T p.L1111L Substitution - coding silent 3:10085920-10085920 + PTC-70C COSM4157095 c.1137G>T p.V379V Substitution - coding silent 3:10046582-10046582 + TCGA-BT-A0YX-01 COSM1133669 c.1298C>T p.S433L Substitution - Missense 3:10047936-10047936 + ESO-021 COSM1251995 c.4129C>T p.L1377F Substitution - Missense 3:10096416-10096416 + T98G COSM1417229 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + 8 COSM4166890 c.3706C>T p.R1236C Substitution - Missense 3:10090314-10090314 + ML_07_T_01 COSM5037547 c.1414-9C>T p.? Unknown 3:10049365-10049365 + SH-9771 COSM5021022 c.4186-5T>C p.? Unknown 3:10098715-10098715 + DLD1 COSM2915752 c.4335G>A p.E1445E Substitution - coding silent 3:10101241-10101241 + 1N45-VS-1T45 COSM4975870 c.3470C>T p.S1157F Substitution - Missense 3:10088452-10088452 + TCGA-AC-A5XS-01 COSM4390881 c.4142G>C p.R1381T Substitution - Missense 3:10096429-10096429 + 168-02-2TD COSM1317109 c.2168+1G>T p.? Unknown 3:10064876-10064876 + XHDG39 COSM4769962 c.2022-5C>T p.? Unknown 3:10064724-10064724 + TCGA-AP-A051-01 COSM1593204 c.1588C>T p.R530* Substitution - Nonsense 3:10052429-10052429 + C0034T COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + sysucc-1397T COSM4422613 c.1170C>T p.S390S Substitution - coding silent 3:10046615-10046615 + sysucc-867T COSM4152593 c.1179T>C p.T393T Substitution - coding silent 3:10046624-10046624 + TCGA-BR-4368-01 COSM4111896 c.3840C>G p.N1280K Substitution - Missense 3:10092243-10092243 + CAL27 COSM4591323 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + C0034T COSM4422613 c.1170C>T p.S390S Substitution - coding silent 3:10046615-10046615 + T3658 COSM4683355 c.4160G>C p.G1387A Substitution - Missense 3:10096447-10096447 + TCGA-RP-A695-06 COSM4897045 c.913T>C p.L305L Substitution - coding silent 3:10043074-10043074 + TCGA-AN-A046-01 COSM3845673 c.3106-10T>G p.? Unknown 3:10081336-10081336 + C658 COSM4443453 c.3760G>T p.A1254S Substitution - Missense 3:10090368-10090368 + 2233440 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + TCGA-B6-A0I1-01 COSM3845668 c.2527T>A p.F843I Substitution - Missense 3:10072903-10072903 + T3064 COSM4683344 c.617A>G p.N206S Substitution - Missense 3:10039767-10039767 + T55 COSM4683353 c.3215delT p.F1073fs*26 Deletion - Frameshift 3:10081455-10081455 + Detroit_562 COSM4594709 c.1509C>T p.N503N Substitution - coding silent 3:10049469-10049469 + ESO-005 COSM1251993 c.3895C>T p.R1299C Substitution - Missense 3:10094295-10094295 + S07-16280-TP COSM4991809 c.3756C>A p.G1252G Substitution - coding silent 3:10090364-10090364 + YUCHIME COSM1692357 c.3376C>T p.P1126S Substitution - Missense 3:10087174-10087174 + RK121_C01 COSM3766819 c.2613A>C p.K871N Substitution - Missense 3:10073260-10073260 + NOKSI COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + sysucc-1365T COSM5766106 c.1413+3A>G p.? Unknown 3:10048054-10048054 + 587376 COSM1206501 c.3373A>G p.I1125V Substitution - Missense 3:10087171-10087171 + CLL158 COSM1291563 c.1368C>G p.L456L Substitution - coding silent 3:10048006-10048006 + 169 COSM2915471 c.2015C>T p.P672L Substitution - Missense 3:10064423-10064423 + DLBCL783 COSM1580883 c.2942C>T p.T981I Substitution - Missense 3:10078163-10078163 + LUAD-YINHD COSM350687 c.3834C>T p.L1278L Substitution - coding silent 3:10092237-10092237 + PTC-7C COSM4157096 c.1348A>G p.I450V Substitution - Missense 3:10047986-10047986 + I2L-P31-Tumor-Organoid COSM5355499 c.1890T>A p.L630L Substitution - coding silent 3:10063854-10063854 + 587222 COSM1206494 c.2592G>T p.K864N Substitution - Missense 3:10072968-10072968 + sysucc-1038T COSM4422612 c.1170C>T p.S390S Substitution - coding silent 3:10046615-10046615 + SCC-15 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + SH-4435 COSM5019433 c.2702G>T p.G901V Substitution - Missense 3:10073349-10073349 + SH-1641 COSM5019434 c.2702G>T p.G901V Substitution - Missense 3:10073349-10073349 + 1604875 COSM141034 c.2035C>T p.P679S Substitution - Missense 3:10064742-10064742 + TCGA-DB-A64O-01 COSM3974042 c.1106A>G p.E369G Substitution - Missense 3:10043836-10043836 + RK152_C01 COSM3766820 c.2613A>C p.K871N Substitution - Missense 3:10073260-10073260 + ACINAR03 COSM1732714 c.2769_2770insT p.R926fs*6 Insertion - Frameshift 3:10074583-10074584 + CAL33 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + TCGA-BT-A3PK-01 COSM3800833 c.3786A>C p.E1262D Substitution - Missense 3:10092189-10092189 + 587376 COSM1206499 c.1263C>A p.F421L Substitution - Missense 3:10046708-10046708 + WSU-HN8 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + C086 COSM5531025 c.4397C>T p.P1466L Substitution - Missense 3:10098931-10098931 + TCGA-AD-6964-01 COSM1417224 c.583A>G p.K195E Substitution - Missense 3:10039733-10039733 + TCGA-EE-A3AG-06 COSM3584658 c.3990C>T p.T1330T Substitution - coding silent 3:10095226-10095226 + 440 COSM4434455 c.1183A>T p.T395S Substitution - Missense 3:10046628-10046628 + T263 COSM4683346 c.943C>T p.R315W Substitution - Missense 3:10043104-10043104 + TCGA-AM-5820-01 COSM3759563 c.1122A>G p.V374V Substitution - coding silent 3:10043852-10043852 + TCGA-EE-A3JA-06 COSM3584580 c.1282C>T p.L428F Substitution - Missense 3:10047920-10047920 + TCGA-06-2561 COSM2152757 c.2339C>T p.S780L Substitution - Missense 3:10065933-10065933 + SJDES007-R2 COSM4583732 c.1142A>G p.D381G Substitution - Missense 3:10046587-10046587 + TCGA-G4-6588-01 COSM1417239 c.2665delA p.N890fs*14 Deletion - Frameshift 3:10073312-10073312 + PT52 COSM5939100 c.904C>T p.R302W Substitution - Missense 3:10043065-10043065 + DLD1 COSM1669961 c.3818G>A p.R1273Q Substitution - Missense 3:10092221-10092221 + ME009T COSM222774 c.2623G>A p.D875N Substitution - Missense 3:10073270-10073270 + 8031704 COSM1168974 c.2335C>T p.R779C Substitution - Missense 3:10065929-10065929 + 7 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-G3-A6UC-01 COSM4929758 c.4028G>A p.G1343E Substitution - Missense 3:10095264-10095264 + ESO-0292 COSM1241157 c.1222C>T p.R408* Substitution - Nonsense 3:10046667-10046667 + MPCC_0032_Pa_C COSM3380317 c.744C>A p.V248V Substitution - coding silent 3:10041671-10041671 + ML_07_T_01 COSM5037546 c.1414-9C>T p.? Unknown 3:10049365-10049365 + Detroit_562 COSM4157095 c.1137G>T p.V379V Substitution - coding silent 3:10046582-10046582 + Pat_26_A COSM5863112 c.3963+2delT p.? Unknown 3:10094365-10094365 + TCGA-B0-5691-01 COSM1136903 c.2761T>C p.S921P Substitution - Missense 3:10074575-10074575 + DLBCL891 COSM1580872 c.311T>C p.I104T Substitution - Missense 3:10034732-10034732 + TCGA-DD-A39Y-01 COSM4583740 c.2442T>C p.T814T Substitution - coding silent 3:10067265-10067265 + TCGA-E2-A15T-01 COSM445215 c.2095C>T p.L699F Substitution - Missense 3:10064802-10064802 + p2_VI-1 COSM1738298 c.475G>T p.E159* Substitution - Nonsense 3:10036323-10036323 + PT42 COSM5925044 c.787C>T p.R263C Substitution - Missense 3:10042562-10042562 + ESCC_74 COSM5634763 c.4234A>G p.S1412G Substitution - Missense 3:10098768-10098768 + Case1 COSM1579137 c.167G>T p.G56V Substitution - Missense 3:10032934-10032934 + 8034048 COSM3391931 c.4177G>T p.D1393Y Substitution - Missense 3:10096464-10096464 + RK152_C01 COSM3766819 c.2613A>C p.K871N Substitution - Missense 3:10073260-10073260 + UM-SCC-2 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + PTC_441 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + 2_FL COSM4171189 c.2914C>A p.L972I Substitution - Missense 3:10078135-10078135 + CSCC-31-T COSM4485880 c.2989C>G p.R997G Substitution - Missense 3:10081112-10081112 + YUKAT COSM5397674 c.435G>A p.L145L Substitution - coding silent 3:10035230-10035230 + sysucc-1640T COSM1417229 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + TCGA-A8-A09Z-01 COSM3845679 c.3609T>C p.I1203I Substitution - coding silent 3:10088876-10088876 + ESCC_18 COSM4157098 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + Detroit_562 COSM4593247 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + T3091 COSM4683357 c.4342A>G p.S1448G Substitution - Missense 3:10098876-10098876 + SJDES006 COSM4583740 c.2442T>C p.T814T Substitution - coding silent 3:10067265-10067265 + TCGA-BP-4971-01 COSM1130392 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + S06-38853-TP COSM4991807 c.3434C>G p.S1145* Substitution - Nonsense 3:10087232-10087232 + 116 COSM1741464 c.812C>T p.S271L Substitution - Missense 3:10042587-10042587 + PCSI_0044_Pa_P COSM3364905 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + TCGA-BR-6452-01 COSM4111834 c.1531G>A p.A511T Substitution - Missense 3:10049491-10049491 + UM-SCC-4 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + XHDG39 COSM4769961 c.2022-5C>T p.? Unknown 3:10064724-10064724 + TCGA-BR-4361-01 COSM4111876 c.2073T>C p.T691T Substitution - coding silent 3:10064780-10064780 + HCT8 COSM1669962 c.3818G>A p.R1273Q Substitution - Missense 3:10092221-10092221 + ESO-005 COSM180509 c.3895C>T p.R1299C Substitution - Missense 3:10094295-10094295 + TCGA-FD-A3B6-01 COSM1308313 c.1596C>G p.L532L Substitution - coding silent 3:10052437-10052437 + T3116 COSM4683349 c.2102C>T p.P701L Substitution - Missense 3:10064809-10064809 + HCT-15 COSM1669962 c.3818G>A p.R1273Q Substitution - Missense 3:10092221-10092221 + YUCHIME COSM1692358 c.3376C>T p.P1126S Substitution - Missense 3:10087174-10087174 + 2012-705:2012-1310-T COSM4605102 c.3187C>T p.Q1063* Substitution - Nonsense 3:10081427-10081427 + TCGA-FD-A3SS-01 COSM3800821 c.935T>G p.L312W Substitution - Missense 3:10043096-10043096 + HCC152T COSM3660058 c.2133T>G p.D711E Substitution - Missense 3:10064840-10064840 + Detroit_562 COSM1417230 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + TCGA-AN-A046-01 COSM3845674 c.3106-10T>G p.? Unknown 3:10081336-10081336 + SNU-C4 COSM4653581 c.352G>A p.E118K Substitution - Missense 3:10034773-10034773 + Detroit_562 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + UM-SCC-17B COSM4593247 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + WSU-HN13 COSM4593247 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + T55 COSM4683354 c.3215delT p.F1073fs*26 Deletion - Frameshift 3:10081455-10081455 + BZ09 COSM5758092 c.3859A>T p.S1287C Substitution - Missense 3:10093294-10093294 + SCC-15 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-AA-3663-01 COSM1417234 c.1759G>A p.A587T Substitution - Missense 3:10060396-10060396 + TCGA-CG-5726-01 COSM4111886 c.2606-1G>T p.? Unknown 3:10073252-10073252 + DLBCL895 COSM1580881 c.2801C>G p.S934C Substitution - Missense 3:10074615-10074615 + TCGA-06-2561 COSM2152756 c.2339C>T p.S780L Substitution - Missense 3:10065933-10065933 + 278LT COSM4381594 c.4376A>G p.Y1459C Substitution - Missense 3:10098910-10098910 + TCGA-G4-6299-01 COSM1417256 c.3738_3739insA p.I1249fs*2 Insertion - Frameshift 3:10090346-10090347 + BHY COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + PT13 COSM5895678 c.3225-6C>T p.? Unknown 3:10085806-10085806 + p2_VI-1 COSM1738293 c.463G>A p.E155K Substitution - Missense 3:10036311-10036311 + SJRHB003_D COSM1130392 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + 93VU147T COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + SCC-9 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + 8067216 COSM3780604 c.767C>T p.P256L Substitution - Missense 3:10041694-10041694 + 587222 COSM1206497 c.3031G>T p.E1011* Substitution - Nonsense 3:10081154-10081154 + 169 COSM2915470 c.2015C>T p.P672L Substitution - Missense 3:10064423-10064423 + TCGA-BS-A0UV-01 COSM1593187 c.2609G>A p.R870K Substitution - Missense 3:10073256-10073256 + CAL27 COSM4591322 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + NOKSI COSM4591322 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + SCC-9 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + MZ7-mel COSM13875 c.3367C>T p.Q1123* Substitution - Nonsense 3:10087165-10087165 + WSU-HN6 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + WSU-HN8 COSM4593246 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + HT COSM1580874 c.1696A>G p.T566A Substitution - Missense 3:10060333-10060333 + ESCC_168 COSM5648775 c.2381G>T p.R794L Substitution - Missense 3:10065975-10065975 + 131T COSM1725656 c.3581A>G p.E1194G Substitution - Missense 3:10088848-10088848 + p2_VI-2 COSM1738299 c.475G>T p.E159* Substitution - Nonsense 3:10036323-10036323 + SCC-9 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + STC263 COSM5059158 c.1092G>A p.W364* Substitution - Nonsense 3:10043586-10043586 + Farage COSM1580879 c.2725G>T p.G909W Substitution - Missense 3:10074539-10074539 + WSU-HN8 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-D3-A1Q1-06 COSM3584574 c.591G>C p.M197I Substitution - Missense 3:10039741-10039741 + 587222 COSM1206495 c.2592G>T p.K864N Substitution - Missense 3:10072968-10072968 + H1703 COSM1196592 c.289G>A p.V97I Substitution - Missense 3:10034710-10034710 + LS411 COSM2915666 c.3715A>G p.M1239V Substitution - Missense 3:10090323-10090323 + TCGA-K4-A3WU-01 COSM3800822 c.1306C>A p.L436M Substitution - Missense 3:10047944-10047944 + CN-AML-CR-42-Dx COSM4594708 c.1509C>T p.N503N Substitution - coding silent 3:10049469-10049469 + sysucc-1640T COSM1417230 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + TCGA-AG-3892-01 COSM256924 c.283G>T p.E95* Substitution - Nonsense 3:10034704-10034704 + C99 COSM4620441 c.3436A>G p.T1146A Substitution - Missense 3:10087234-10087234 + HCT8 COSM1669961 c.3818G>A p.R1273Q Substitution - Missense 3:10092221-10092221 + TCGA-D1-A160-01 COSM1593194 c.2203C>T p.R735W Substitution - Missense 3:10065428-10065428 + TCGA-AD-6889-01 COSM1417226 c.906G>A p.R302R Substitution - coding silent 3:10043067-10043067 + TCGA-J8-A3O0-01 COSM3372928 c.2009T>C p.V670A Substitution - Missense 3:10064417-10064417 + TCGA-BR-4361-01 COSM4111875 c.2073T>C p.T691T Substitution - coding silent 3:10064780-10064780 + sysucc-826T COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + WSU-HN13 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + sysucc-809T COSM4157098 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + YUPAT COSM1692354 c.1153C>T p.L385F Substitution - Missense 3:10046598-10046598 + TCGA-AP-A0LM-01 COSM1035812 c.4118C>A p.A1373D Substitution - Missense 3:10096405-10096405 + TCGA-A7-A13E-01 COSM3845671 c.2914C>T p.L972F Substitution - Missense 3:10078135-10078135 + 7 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + PD23570a COSM5768150 c.1856C>T p.S619F Substitution - Missense 3:10063820-10063820 + Pat_26_A COSM5863113 c.3963+2delT p.? Unknown 3:10094365-10094365 + p2_VI-2 COSM1738293 c.463G>A p.E155K Substitution - Missense 3:10036311-10036311 + C0091T COSM4152598 c.1827G>T p.Q609H Substitution - Missense 3:10062211-10062211 + BICR_22 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + sysucc-1878T COSM5766106 c.1413+3A>G p.? Unknown 3:10048054-10048054 + SH-3327 COSM5019434 c.2702G>T p.G901V Substitution - Missense 3:10073349-10073349 + S01733 COSM4386859 c.1278+3_1278+5delAAG p.? Unknown 3:10046726-10046728 + SJDES007-R2 COSM4583731 c.1142A>G p.D381G Substitution - Missense 3:10046587-10046587 + LUAD-YINHD COSM350685 c.42G>C p.E14D Substitution - Missense 3:10028699-10028699 + CN-AML-CR-29-Dx COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + PDA_055 COSM4593247 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + TCGA-AP-A059-01 COSM1035801 c.3871C>A p.L1291M Substitution - Missense 3:10093306-10093306 + PTC_435 COSM5957043 c.1265C>G p.S422C Substitution - Missense 3:10046710-10046710 + LUAD-NYU689 COSM375979 c.157A>C p.K53Q Substitution - Missense 3:10032924-10032924 + TCGA-G4-6299-01 COSM1417257 c.3738_3739insA p.I1249fs*2 Insertion - Frameshift 3:10090346-10090347 + TCGA-BT-A3PJ-01 COSM3800835 c.4080C>G p.L1360L Substitution - coding silent 3:10096367-10096367 + sysucc-1397T COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + ORL-48 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + T3658 COSM4683356 c.4160G>C p.G1387A Substitution - Missense 3:10096447-10096447 + CAL27 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + T3080 COSM4683352 c.2884delC p.P963fs*18 Deletion - Frameshift 3:10078105-10078105 + TCGA-06-0237 COSM1035747 c.813G>A p.S271S Substitution - coding silent 3:10042588-10042588 + TCGA-CG-5721-01 COSM4111826 c.424A>T p.I142F Substitution - Missense 3:10035219-10035219 + C086 COSM5531027 c.3208C>T p.H1070Y Substitution - Missense 3:10081448-10081448 + CRC-02T COSM5455109 c.2550A>G p.I850M Substitution - Missense 3:10072926-10072926 + TCGA-IA-A40Y-01 COSM3992609 c.1311G>A p.S437S Substitution - coding silent 3:10047949-10047949 + TCGA-AC-A2QJ-01 COSM1130393 c.2391A>G p.V797V Substitution - coding silent 3:10067214-10067214 + WSU-HN8 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + ORL-48 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + TCGA-DD-A39Y-01 COSM4583739 c.2442T>C p.T814T Substitution - coding silent 3:10067265-10067265 + PDA_011 COSM4593247 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + GC_337T-GC_337N COSM4591322 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + TCGA-E2-A10C-01 COSM1484374 c.2296G>T p.E766* Substitution - Nonsense 3:10065890-10065890 + TCGA-AM-5820-01 COSM3759562 c.1122A>G p.V374V Substitution - coding silent 3:10043852-10043852 + SCC-25 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + UM-SCC-2 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + CAL33 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + SCC-25 COSM4593247 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + 4472_T COSM3944600 c.1528A>C p.N510H Substitution - Missense 3:10049488-10049488 + WSU-HN13 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-AH-6544-01 COSM1566380 c.813G>T p.S271S Substitution - coding silent 3:10042588-10042588 + sysucc-1038T COSM4152592 c.1179T>C p.T393T Substitution - coding silent 3:10046624-10046624 + PT37 COSM5918084 c.86C>T p.S29F Substitution - Missense 3:10032853-10032853 + p2_VI-1 COSM1738295 c.427G>C p.D143H Substitution - Missense 3:10035222-10035222 + TCGA-CD-5803-01 COSM4111828 c.649G>A p.E217K Substitution - Missense 3:10039799-10039799 + TCGA-BH-A18V-06 COSM3845677 c.3519G>C p.E1173D Substitution - Missense 3:10088501-10088501 + TCGA-IM-A3U2-01 COSM3372929 c.2138G>A p.G713D Substitution - Missense 3:10064845-10064845 + TCGA-GC-A3RC-01 COSM3800828 c.2054G>C p.G685A Substitution - Missense 3:10064761-10064761 + sysucc-867T COSM4152592 c.1179T>C p.T393T Substitution - coding silent 3:10046624-10046624 + TCGA-JW-A852-01 COSM4823754 c.2195C>T p.P732L Substitution - Missense 3:10065420-10065420 + S07-16280-TP COSM4991808 c.3756C>A p.G1252G Substitution - coding silent 3:10090364-10090364 + TCGA-06-0879 COSM2152292 c.1642_1643delAG p.S548fs*6 Deletion - Frameshift 3:10052483-10052484 + U373 COSM2915593 c.3106-9T>A p.? Unknown 3:10081337-10081337 + Detroit_562 COSM4152592 c.1179T>C p.T393T Substitution - coding silent 3:10046624-10046624 + sysucc-1640T COSM4152592 c.1179T>C p.T393T Substitution - coding silent 3:10046624-10046624 + sysucc-1240T COSM5766106 c.1413+3A>G p.? Unknown 3:10048054-10048054 + SNU-C4 COSM4653582 c.352G>A p.E118K Substitution - Missense 3:10034773-10034773 + CN-AML-CR-42-Dx COSM4594709 c.1509C>T p.N503N Substitution - coding silent 3:10049469-10049469 + SCC-9 COSM4591323 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + C008 COSM5522653 c.2597G>A p.G866E Substitution - Missense 3:10072973-10072973 + TCGA-D1-A103-01 COSM1035811 c.4052C>T p.T1351M Substitution - Missense 3:10096339-10096339 + UM-SCC-17B COSM4591323 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + UPCI:SCC090 COSM4593247 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + S07-16280-TP COSM4991805 c.1807A>T p.S603C Substitution - Missense 3:10062191-10062191 + p2_VI-2 COSM1738295 c.427G>C p.D143H Substitution - Missense 3:10035222-10035222 + 2011-2370:2012-1299-T COSM4606115 c.916G>C p.D306H Substitution - Missense 3:10043077-10043077 + PD4137a COSM160983 c.3252G>A p.Q1084Q Substitution - coding silent 3:10085839-10085839 + PCSI_0044_Pa_P COSM1130392 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + TCGA-CH-5754-01 COSM1130392 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + TCGA-EE-A29D-06 COSM3584620 c.1924G>A p.E642K Substitution - Missense 3:10063888-10063888 + WSU-HN8 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + BICR_22 COSM4593247 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + TCGA-BR-4184-01 COSM4111833 c.871G>A p.A291T Substitution - Missense 3:10042646-10042646 + TCGA-GC-A3RC-01 COSM3800829 c.2054G>C p.G685A Substitution - Missense 3:10064761-10064761 + YUMEZ COSM5397675 c.1353T>A p.I451I Substitution - coding silent 3:10047991-10047991 + HN_62421 COSM127962 c.4023G>C p.L1341L Substitution - coding silent 3:10095259-10095259 + K118 COSM249507 c.1589G>A p.R530Q Substitution - Missense 3:10052430-10052430 + p2_VI-1 COSM1738297 c.438+5G>C p.? Unknown 3:10035238-10035238 + UM-SCC-4 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + SH-1641 COSM5019433 c.2702G>T p.G901V Substitution - Missense 3:10073349-10073349 + SUDHL7 COSM1580886 c.3494G>A p.R1165Q Substitution - Missense 3:10088476-10088476 + TCGA-EE-A2MJ-06 COSM3584631 c.2016G>A p.P672P Substitution - coding silent 3:10064424-10064424 + TCGA-27-2527-01 COSM3408076 c.2401T>C p.C801R Substitution - Missense 3:10067224-10067224 + BICR_22 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + TCGA-DK-A1AC-01 COSM1308311 c.14G>C p.R5T Substitution - Missense 3:10028671-10028671 + RK306_C01 COSM3766820 c.2613A>C p.K871N Substitution - Missense 3:10073260-10073260 + TCGA-AD-6889-01 COSM1417225 c.906G>A p.R302R Substitution - coding silent 3:10043067-10043067 + sysucc-826T COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + ESCC-F6 COSM5048182 c.1876C>G p.Q626E Substitution - Missense 3:10063840-10063840 + SH-5693 COSM5020236 c.1367T>G p.L456R Substitution - Missense 3:10048005-10048005 + TCGA-DK-A3IV-01 COSM1308322 c.2257G>A p.D753N Substitution - Missense 3:10065482-10065482 + MB_Exm645 COSM215886 c.3962G>A p.R1321Q Substitution - Missense 3:10094362-10094362 + TCGA-D1-A103-01 COSM1593181 c.4052C>T p.T1351M Substitution - Missense 3:10096339-10096339 + TCGA-BS-A0UF-01 COSM1593184 c.3628G>T p.E1210* Substitution - Nonsense 3:10088895-10088895 + 505 COSM5611877 c.788G>A p.R263H Substitution - Missense 3:10042563-10042563 + PD7307a COSM5789086 c.1263C>T p.F421F Substitution - coding silent 3:10046708-10046708 + TCGA-B5-A11E-01 COSM1035749 c.1035C>T p.L345L Substitution - coding silent 3:10043529-10043529 + TCGA-CC-A3MC-01 COSM4919595 c.3351C>T p.Y1117Y Substitution - coding silent 3:10087149-10087149 + Pat_06_A COSM5863108 c.2775_2776delCC p.F925fs*6 Deletion - Frameshift 3:10074589-10074590 + 170T COSM1251993 c.3895C>T p.R1299C Substitution - Missense 3:10094295-10094295 + TCGA-D3-A51T-06 COSM3584577 c.655C>T p.L219L Substitution - coding silent 3:10039805-10039805 + ESCC_74 COSM5634762 c.4234A>G p.S1412G Substitution - Missense 3:10098768-10098768 + TCGA-D1-A1NU-01 COSM1035773 c.2045C>T p.A682V Substitution - Missense 3:10064752-10064752 + UM-SCC-4 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + ORL-48 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-IR-A3LK-01 COSM4817087 c.65-1G>C p.? Unknown 3:10032831-10032831 + TCGA-AA-3715-01 COSM269144 c.2053G>A p.G685R Substitution - Missense 3:10064760-10064760 + S07-16280-TP COSM4991804 c.1807A>T p.S603C Substitution - Missense 3:10062191-10062191 + WSU-HN13 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-B0-4827-01 COSM3364905 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + NOKSI COSM4593247 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + TCGA-AP-A0LM-01 COSM1593205 c.1294T>C p.C432R Substitution - Missense 3:10047932-10047932 + p2_VI-1 COSM1738292 c.463G>A p.E155K Substitution - Missense 3:10036311-10036311 + TCGA-E2-A10C-01 COSM445217 c.2296G>T p.E766* Substitution - Nonsense 3:10065890-10065890 + TCGA-AM-5820-01 COSM3759566 c.4098T>G p.L1366L Substitution - coding silent 3:10096385-10096385 + DLBCL781 COSM1580885 c.3446C>T p.A1149V Substitution - Missense 3:10087244-10087244 + 587376 COSM1206502 c.3817C>T p.R1273* Substitution - Nonsense 3:10092220-10092220 + RK306_C01 COSM3766819 c.2613A>C p.K871N Substitution - Missense 3:10073260-10073260 + UM-SCC-17B COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + 93VU147T COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + DN11190 COSM5789086 c.1263C>T p.F421F Substitution - coding silent 3:10046708-10046708 + TCGA-EE-A2MR-06 COSM3584579 c.1280T>C p.V427A Substitution - Missense 3:10047918-10047918 + TCGA-IM-A3U2-01 COSM3372930 c.2138G>A p.G713D Substitution - Missense 3:10064845-10064845 + PTC-7C COSM4157100 c.1820G>T p.C607F Substitution - Missense 3:10062204-10062204 + TCGA-BP-4971-01 COSM3364905 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + TCGA-B5-A11E-01 COSM1035774 c.2104C>T p.L702L Substitution - coding silent 3:10064811-10064811 + Detroit_562 COSM4152593 c.1179T>C p.T393T Substitution - coding silent 3:10046624-10046624 + LAU63 COSM233948 c.2169-8C>T p.? Unknown 3:10065386-10065386 + C0034T COSM4422612 c.1170C>T p.S390S Substitution - coding silent 3:10046615-10046615 + SUDHL7 COSM1580876 c.2180C>T p.P727L Substitution - Missense 3:10065405-10065405 + sysucc-1240T COSM4157099 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + C135 COSM4618273 c.2886C>G p.P962P Substitution - coding silent 3:10078107-10078107 + UM-SCC-17B COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + PD13756a COSM5800531 c.661G>T p.D221Y Substitution - Missense 3:10039811-10039811 + TCGA-AH-6544-01 COSM1566379 c.813G>T p.S271S Substitution - coding silent 3:10042588-10042588 + Detroit_562 COSM4422612 c.1170C>T p.S390S Substitution - coding silent 3:10046615-10046615 + TCGA-DK-A1A5-01 COSM419483 c.481T>G p.F161V Substitution - Missense 3:10036329-10036329 + 168 COSM146182 c.2168+1G>T p.? Unknown 3:10064876-10064876 + TCGA-DB-A64X-01 COSM3974044 c.3195G>A p.L1065L Substitution - coding silent 3:10081435-10081435 + PTC-7C COSM4157101 c.1820G>T p.C607F Substitution - Missense 3:10062204-10062204 + PDA_055 COSM4593246 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + SH-3133 COSM5019050 c.1440T>C p.H480H Substitution - coding silent 3:10049400-10049400 + ESO-0292 COSM1241156 c.1222C>T p.R408* Substitution - Nonsense 3:10046667-10046667 + 587376 COSM275089 c.3817C>T p.R1273* Substitution - Nonsense 3:10092220-10092220 + TCGA-D8-A1XK-01 COSM3845669 c.2610G>T p.R870S Substitution - Missense 3:10073257-10073257 + sysucc-1838T COSM4769962 c.2022-5C>T p.? Unknown 3:10064724-10064724 + sysucc-1878T COSM4157099 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + 587376 COSM1206500 c.3373A>G p.I1125V Substitution - Missense 3:10087171-10087171 + p2_VI-1 COSM1738299 c.475G>T p.E159* Substitution - Nonsense 3:10036323-10036323 + TCGA-E2-A15T-01 COSM1484372 c.2095C>T p.L699F Substitution - Missense 3:10064802-10064802 + TCGA-BJ-A0ZB-01 COSM3372925 c.1519A>G p.M507V Substitution - Missense 3:10049479-10049479 + TARGET-30-PASWYR COSM1284876 c.958C>A p.Q320K Substitution - Missense 3:10043119-10043119 + TCGA-HU-A4G8-01 COSM4111901 c.4183C>T p.Q1395* Substitution - Nonsense 3:10096470-10096470 + WSU-HN13 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + 9227_T COSM5040202 c.1202G>A p.R401K Substitution - Missense 3:10046647-10046647 + YUKAT COSM5397673 c.435G>A p.L145L Substitution - coding silent 3:10035230-10035230 + TCGA-DA-A1HY-06 COSM3584587 c.1450G>A p.G484R Substitution - Missense 3:10049410-10049410 + U343 COSM1417229 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + sysucc-1317T COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + 2_FL COSM4171188 c.2914C>A p.L972I Substitution - Missense 3:10078135-10078135 + U343 COSM1417230 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + ESCC-F6 COSM5048183 c.1876C>G p.Q626E Substitution - Missense 3:10063840-10063840 + 93VU147T COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-EE-A2MR-06 COSM3584578 c.1280T>C p.V427A Substitution - Missense 3:10047918-10047918 + MBRep_T2 COSM306978 c.1932G>A p.L644L Substitution - coding silent 3:10063896-10063896 + U87 COSM1417229 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + TCGA-EE-A2MJ-06 COSM3584630 c.2016G>A p.P672P Substitution - coding silent 3:10064424-10064424 + Pat_28_B COSM3584582 c.1288G>A p.D430N Substitution - Missense 3:10047926-10047926 + GC1_T COSM3748789 c.3828T>G p.S1276R Substitution - Missense 3:10092231-10092231 + TCGA-FS-A4F5-06 COSM3584656 c.3960C>T p.H1320H Substitution - coding silent 3:10094360-10094360 + TCGA-FS-A1ZM-06 COSM3584665 c.4403C>T p.P1468L Substitution - Missense 3:10098937-10098937 + 2012-705:2012-1310-T COSM4605103 c.3187C>T p.Q1063* Substitution - Nonsense 3:10081427-10081427 + TCGA-AP-A0LG-01 COSM1035748 c.1015G>A p.G339S Substitution - Missense 3:10043509-10043509 + T3064 COSM4683343 c.617A>G p.N206S Substitution - Missense 3:10039767-10039767 + S01733 COSM1417232 c.1278+1delG p.? Unknown 3:10046724-10046724 + TCGA-CC-A3MC-01 COSM4919596 c.3351C>T p.Y1117Y Substitution - coding silent 3:10087149-10087149 + SCC-9 COSM4591322 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + UPCI:SCC090 COSM4591322 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + TCGA-FD-A3SS-01 COSM3800820 c.935T>G p.L312W Substitution - Missense 3:10043096-10043096 + TCGA-AX-A05S-01 COSM1035781 c.2454C>T p.H818H Substitution - coding silent 3:10067277-10067277 + Detroit_562 COSM3759562 c.1122A>G p.V374V Substitution - coding silent 3:10043852-10043852 + TCGA-FS-A1ZW-06 COSM3584583 c.1288G>A p.D430N Substitution - Missense 3:10047926-10047926 + sysucc-1577T COSM1417229 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + CAL27 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + PTC-73C COSM1417230 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + CSCC-37-T COSM4494822 c.4402C>T p.P1468S Substitution - Missense 3:10098936-10098936 + 505 COSM5611876 c.788G>A p.R263H Substitution - Missense 3:10042563-10042563 + CSCC-56-T COSM4473785 c.1873C>T p.P625S Substitution - Missense 3:10063837-10063837 + TCGA-FS-A4F5-06 COSM3584655 c.3960C>T p.H1320H Substitution - coding silent 3:10094360-10094360 + TCGA-FW-A3R5-06 COSM3914410 c.4286C>T p.S1429F Substitution - Missense 3:10098820-10098820 + Detroit_562 COSM4422613 c.1170C>T p.S390S Substitution - coding silent 3:10046615-10046615 + S09-31237-TP COSM4991803 c.1598T>G p.F533C Substitution - Missense 3:10052439-10052439 + 170T COSM180509 c.3895C>T p.R1299C Substitution - Missense 3:10094295-10094295 + TCGA-F1-A448-01 COSM2915481 c.2067C>T p.Y689Y Substitution - coding silent 3:10064774-10064774 + CN-AML-CR-57-Dx COSM4157095 c.1137G>T p.V379V Substitution - coding silent 3:10046582-10046582 + PTC-46C COSM3766820 c.2613A>C p.K871N Substitution - Missense 3:10073260-10073260 + SJRHB003 COSM1130392 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + PTC-88C COSM1417229 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + PT26 COSM3766819 c.2613A>C p.K871N Substitution - Missense 3:10073260-10073260 + sysucc-1397T COSM4152592 c.1179T>C p.T393T Substitution - coding silent 3:10046624-10046624 + TCGA-D1-A17Q-01 COSM1593208 c.688G>T p.E230* Substitution - Nonsense 3:10039838-10039838 + TCGA-BT-A3PJ-01 COSM3800834 c.4080C>G p.L1360L Substitution - coding silent 3:10096367-10096367 + SH-0348 COSM5019050 c.1440T>C p.H480H Substitution - coding silent 3:10049400-10049400 + 587222 COSM1206496 c.3031G>T p.E1011* Substitution - Nonsense 3:10081154-10081154 + TCGA-D8-A1XK-01 COSM3845670 c.2610G>T p.R870S Substitution - Missense 3:10073257-10073257 + LUAD-NYU408 COSM374451 c.4349G>A p.W1450* Substitution - Nonsense 3:10098883-10098883 + TCGA-B5-A0JY-01 COSM1593206 c.1188G>T p.K396N Substitution - Missense 3:10046633-10046633 + UPCI:SCC090 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-DA-A3F8-06 COSM3584585 c.1355C>T p.S452L Substitution - Missense 3:10047993-10047993 + HT COSM1580875 c.1696A>G p.T566A Substitution - Missense 3:10060333-10060333 + TCGA-EE-A3AG-06 COSM3584657 c.3990C>T p.T1330T Substitution - coding silent 3:10095226-10095226 + TCGA-DK-A1A5-01 COSM1133668 c.481T>G p.F161V Substitution - Missense 3:10036329-10036329 + TCGA-J8-A3O0-01 COSM3372927 c.2009T>C p.V670A Substitution - Missense 3:10064417-10064417 + TCGA-EB-A3XB-01 COSM3584651 c.3624C>T p.V1208V Substitution - coding silent 3:10088891-10088891 + UD-SCC-2 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + PTC-7C COSM4157097 c.1348A>G p.I450V Substitution - Missense 3:10047986-10047986 + 93VU147T COSM4591322 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + PCSI_0044_Pa_P COSM3845666 c.2391A>G p.V797V Substitution - coding silent 3:10067214-10067214 + sysucc-1838T COSM4769961 c.2022-5C>T p.? Unknown 3:10064724-10064724 + p2_VI-2 COSM1738296 c.438+5G>C p.? Unknown 3:10035238-10035238 + HCC152T COSM3660057 c.2133T>G p.D711E Substitution - Missense 3:10064840-10064840 + TCGA-CG-4465-01 COSM4111824 c.69C>T p.T23T Substitution - coding silent 3:10032836-10032836 + 8034048 COSM3391930 c.4177G>T p.D1393Y Substitution - Missense 3:10096464-10096464 + 1261_T COSM3944606 c.2866G>C p.E956Q Substitution - Missense 3:10078087-10078087 + C086 COSM5531026 c.3208C>T p.H1070Y Substitution - Missense 3:10081448-10081448 + TCGA-23-1123-01 COSM79183 c.1948G>T p.E650* Substitution - Nonsense 3:10064356-10064356 + UM-SCC-4 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + UM-SCC-11B COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + 8 COSM4166891 c.3706C>T p.R1236C Substitution - Missense 3:10090314-10090314 + T98G COSM1417230 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + Detroit_562 COSM4594708 c.1509C>T p.N503N Substitution - coding silent 3:10049469-10049469 + TCGA-BS-A0UV-01 COSM1035802 c.3987A>G p.E1329E Substitution - coding silent 3:10095223-10095223 + CSCC-45-T COSM4534162 c.2054G>A p.G685E Substitution - Missense 3:10064761-10064761 + BICR_22 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + UD-SCC-2 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + CSCC-16-T COSM4477898 c.2194C>T p.P732S Substitution - Missense 3:10065419-10065419 + sysucc-783T COSM1593198 c.2104C>T p.L702L Substitution - coding silent 3:10064811-10064811 + TCGA-AP-A0LG-01 COSM1154051 c.1015G>A p.G339S Substitution - Missense 3:10043509-10043509 + sysucc-1397T COSM5474527 c.1748G>A p.G583D Substitution - Missense 3:10060385-10060385 + WSU-HN6 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-DV-5574-01 COSM1417230 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + sysucc-1397T COSM4152593 c.1179T>C p.T393T Substitution - coding silent 3:10046624-10046624 + sysucc-1247T COSM5037546 c.1414-9C>T p.? Unknown 3:10049365-10049365 + TCGA-AP-A0LM-01 COSM1593180 c.4118C>A p.A1373D Substitution - Missense 3:10096405-10096405 + sysucc-1397T COSM4422612 c.1170C>T p.S390S Substitution - coding silent 3:10046615-10046615 + TCGA-BR-6452-01 COSM4111891 c.3529A>G p.I1177V Substitution - Missense 3:10088511-10088511 + T3190 COSM4683347 c.2068G>A p.D690N Substitution - Missense 3:10064775-10064775 + SH-5693 COSM5020329 c.2712C>T p.N904N Substitution - coding silent 3:10073359-10073359 + TCGA-JW-A852-01 COSM4823755 c.2195C>T p.P732L Substitution - Missense 3:10065420-10065420 + TCGA-CD-5803-01 COSM4111829 c.649G>A p.E217K Substitution - Missense 3:10039799-10039799 + YUSEL COSM1692355 c.2516C>T p.P839L Substitution - Missense 3:10072892-10072892 + CSCC-15-T COSM4482813 c.2642C>T p.S881F Substitution - Missense 3:10073289-10073289 + HCC90 COSM1616665 c.2938C>G p.L980V Substitution - Missense 3:10078159-10078159 + p2_VI-2 COSM1738298 c.475G>T p.E159* Substitution - Nonsense 3:10036323-10036323 + SUDHL7 COSM1580887 c.3494G>A p.R1165Q Substitution - Missense 3:10088476-10088476 + TCGA-BC-A112-01 COSM3364905 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + ME009T COSM222775 c.3031G>A p.E1011K Substitution - Missense 3:10081154-10081154 + TCGA-GC-A3RC-01 COSM3800830 c.2238C>A p.N746K Substitution - Missense 3:10065463-10065463 + Br02X COSM39696 c.2774_2775insT p.R926fs*6 Insertion - Frameshift 3:10074588-10074589 + TCGA-AX-A05S-01 COSM1154053 c.2454C>T p.H818H Substitution - coding silent 3:10067277-10067277 + PTC-77C COSM4157098 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + DLBCL891 COSM1580873 c.311T>C p.I104T Substitution - Missense 3:10034732-10034732 + TCGA-B6-A0I1-01 COSM3845667 c.2527T>A p.F843I Substitution - Missense 3:10072903-10072903 + TCGA-BR-6452-01 COSM4111890 c.3529A>G p.I1177V Substitution - Missense 3:10088511-10088511 + TCGA-RP-A695-06 COSM4897046 c.913T>C p.L305L Substitution - coding silent 3:10043074-10043074 + Farage COSM1580878 c.2725G>T p.G909W Substitution - Missense 3:10074539-10074539 + T3080 COSM4683351 c.2884delC p.P963fs*18 Deletion - Frameshift 3:10078105-10078105 + PTC-73C COSM1417229 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + WSU-HN13 COSM4593246 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + C0091T COSM4152597 c.1827G>T p.Q609H Substitution - Missense 3:10062211-10062211 + TCGA-DA-A1HY-06 COSM3584629 c.1998G>A p.V666V Substitution - coding silent 3:10064406-10064406 + TCGA-BC-A112-01 COSM3845666 c.2391A>G p.V797V Substitution - coding silent 3:10067214-10067214 + TCGA-D3-A51T-06 COSM3584576 c.655C>T p.L219L Substitution - coding silent 3:10039805-10039805 + LN18 COSM1417229 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + 8047835 COSM3391925 c.1301C>T p.S434F Substitution - Missense 3:10047939-10047939 + ESCC_18 COSM4157099 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + TCGA-FG-A4MY-01 COSM3974039 c.772T>G p.F258V Substitution - Missense 3:10041699-10041699 + CRC-02T COSM5455110 c.2550A>G p.I850M Substitution - Missense 3:10072926-10072926 + TCGA-BT-A0YX-01 COSM1133670 c.1489C>G p.L497V Substitution - Missense 3:10049449-10049449 + 154T COSM5576314 c.3563_3564delTC p.Y1189fs*27 Deletion - Frameshift 3:10088830-10088831 + BZ09 COSM5758093 c.3859A>T p.S1287C Substitution - Missense 3:10093294-10093294 + TCGA-BR-4368-01 COSM4111895 c.3840C>G p.N1280K Substitution - Missense 3:10092243-10092243 + TCGA-CG-4305-01 COSM4111893 c.3584G>A p.S1195N Substitution - Missense 3:10088851-10088851 + PTC_441 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + BICR_22 COSM4593246 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + CSCC-56-T COSM4473784 c.1873C>T p.P625S Substitution - Missense 3:10063837-10063837 + NOKSI COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + SH-1439 COSM5019051 c.1440T>C p.H480H Substitution - coding silent 3:10049400-10049400 + TCGA-CH-5764-01 COSM1130393 c.2391A>G p.V797V Substitution - coding silent 3:10067214-10067214 + TCGA-BC-A10T-01 COSM1130393 c.2391A>G p.V797V Substitution - coding silent 3:10067214-10067214 + BICR_22 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-DA-A1HY-06 COSM3584586 c.1450G>A p.G484R Substitution - Missense 3:10049410-10049410 + HCC051T COSM5820712 c.3369A>T p.Q1123H Substitution - Missense 3:10087167-10087167 + TCGA-C8-A274-01 COSM1484368 c.1318C>T p.Q440* Substitution - Nonsense 3:10047956-10047956 + 47T COSM5575768 c.3092A>G p.H1031R Substitution - Missense 3:10081215-10081215 + PT52 COSM5939099 c.904C>T p.R302W Substitution - Missense 3:10043065-10043065 + CRC-02T COSM5455107 c.2142G>T p.P714P Substitution - coding silent 3:10064849-10064849 + TCGA-B5-A0JY-01 COSM1593186 c.2826G>A p.T942T Substitution - coding silent 3:10074640-10074640 + TCGA-B0-4712-01 COSM1136901 c.473C>A p.P158Q Substitution - Missense 3:10036321-10036321 + 278T COSM4381594 c.4376A>G p.Y1459C Substitution - Missense 3:10098910-10098910 + UM-SCC-17B COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + Detroit_562 COSM4157099 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + HCC002T COSM5819318 c.1099-2A>T p.? Unknown 3:10043827-10043827 + TCGA-D1-A17Q-01 COSM1035746 c.688G>T p.E230* Substitution - Nonsense 3:10039838-10039838 + HCC051T COSM5820711 c.3369A>T p.Q1123H Substitution - Missense 3:10087167-10087167 + UM-SCC-2 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + SH-5693 COSM5020328 c.2712C>T p.N904N Substitution - coding silent 3:10073359-10073359 + sysucc-867T COSM4422612 c.1170C>T p.S390S Substitution - coding silent 3:10046615-10046615 + TCGA-BH-A18V-06 COSM3845676 c.3519G>C p.E1173D Substitution - Missense 3:10088501-10088501 + 93VU147T COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + WSU-HN8 COSM4593247 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + LUAD-S01467 COSM399474 c.2355C>G p.L785L Substitution - coding silent 3:10065949-10065949 + TCGA-B5-A11E-01 COSM1593198 c.2104C>T p.L702L Substitution - coding silent 3:10064811-10064811 + TCGA-BT-A0YX-01 COSM419482 c.1298C>T p.S433L Substitution - Missense 3:10047936-10047936 + 168-02-2TD COSM146182 c.2168+1G>T p.? Unknown 3:10064876-10064876 + TCGA-AC-A2QJ-01 COSM1130392 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + TCGA-DK-A3IV-01 COSM1308321 c.2257G>A p.D753N Substitution - Missense 3:10065482-10065482 + GC1_T COSM3748788 c.3828T>G p.S1276R Substitution - Missense 3:10092231-10092231 + PCSI_0194_Pa_P COSM4157098 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + HCC152 COSM3660057 c.2133T>G p.D711E Substitution - Missense 3:10064840-10064840 + CLL158 COSM1291562 c.1368C>G p.L456L Substitution - coding silent 3:10048006-10048006 + TCGA-06-2561-01 COSM2152757 c.2339C>T p.S780L Substitution - Missense 3:10065933-10065933 + TCGA-AP-A0LM-01 COSM1035751 c.1294T>C p.C432R Substitution - Missense 3:10047932-10047932 + ORL-48 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + WSU-HN6 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + SH-1439 COSM5019050 c.1440T>C p.H480H Substitution - coding silent 3:10049400-10049400 + UM-SCC-11B COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + PCSI_0044_Pa_P COSM1130393 c.2391A>G p.V797V Substitution - coding silent 3:10067214-10067214 + TCGA-DA-A1HY-06 COSM3584628 c.1998G>A p.V666V Substitution - coding silent 3:10064406-10064406 + TCGA-AD-6964-01 COSM1417223 c.583A>G p.K195E Substitution - Missense 3:10039733-10039733 + TCGA-D3-A51T-06 COSM3584605 c.1674G>A p.V558V Substitution - coding silent 3:10060311-10060311 + 8047835 COSM3391926 c.1301C>T p.S434F Substitution - Missense 3:10047939-10047939 + CAL33 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-FD-A3B6-01 COSM1308314 c.1596C>G p.L532L Substitution - coding silent 3:10052437-10052437 + pfg008T COSM1642025 c.879T>C p.D293D Substitution - coding silent 3:10042654-10042654 + TCGA-CH-5764-01 COSM1130392 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + TCGA-BC-A112-01 COSM1130392 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + PD23570a COSM5768149 c.1856C>T p.S619F Substitution - Missense 3:10063820-10063820 + LS411 COSM2915665 c.3715A>G p.M1239V Substitution - Missense 3:10090323-10090323 + CAL33 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + C0034T COSM4152592 c.1179T>C p.T393T Substitution - coding silent 3:10046624-10046624 + sysucc-1397T COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + WSU-HN13 COSM4591323 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + QC2-25-T2 COSM1669961 c.3818G>A p.R1273Q Substitution - Missense 3:10092221-10092221 + TCGA-BC-A10T-01 COSM3845666 c.2391A>G p.V797V Substitution - coding silent 3:10067214-10067214 + TCGA-EE-A29X-06 COSM3584584 c.1355C>T p.S452L Substitution - Missense 3:10047993-10047993 + TCGA-D1-A1NU-01 COSM1154052 c.2045C>T p.A682V Substitution - Missense 3:10064752-10064752 + BHY COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + PT32 COSM4157094 c.1137G>T p.V379V Substitution - coding silent 3:10046582-10046582 + PDA_011 COSM4593246 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + U87 COSM1417230 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + p2_V-1 COSM1738293 c.463G>A p.E155K Substitution - Missense 3:10036311-10036311 + UM-SCC-17B COSM4591322 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + I2L-P31-Tumor-Organoid COSM5355500 c.1890T>A p.L630L Substitution - coding silent 3:10063854-10063854 + NOKSI COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + 1N45-VS-1T45 COSM4975872 c.3707G>T p.R1236L Substitution - Missense 3:10090315-10090315 + CRC-02T COSM5455108 c.2142G>T p.P714P Substitution - coding silent 3:10064849-10064849 + ESCC_168 COSM5648776 c.2381G>T p.R794L Substitution - Missense 3:10065975-10065975 + PT13 COSM5895677 c.3225-6C>T p.? Unknown 3:10085806-10085806 + KPOPBR-35-T COSM5963289 c.3777+5G>C p.? Unknown 3:10090390-10090390 + ACINAR03 COSM1732713 c.2769_2770insT p.R926fs*6 Insertion - Frameshift 3:10074583-10074584 + TCGA-G3-A6UC-01 COSM4929757 c.4028G>A p.G1343E Substitution - Missense 3:10095264-10095264 + CSCC-54-T COSM4540562 c.2860G>A p.A954T Substitution - Missense 3:10078081-10078081 + TCGA-CG-5721-01 COSM4111827 c.424A>T p.I142F Substitution - Missense 3:10035219-10035219 + sysucc-1640T COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + Detroit_562 COSM4157098 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + CSCC-45-T COSM4534163 c.2054G>A p.G685E Substitution - Missense 3:10064761-10064761 + TCGA-G4-6588-01 COSM1417238 c.2665delA p.N890fs*14 Deletion - Frameshift 3:10073312-10073312 + PT35 COSM4157095 c.1137G>T p.V379V Substitution - coding silent 3:10046582-10046582 + TCGA-MI-A75H-01 COSM4918273 c.1742T>C p.M581T Substitution - Missense 3:10060379-10060379 + T2284 COSM2915670 c.3896G>A p.R1299H Substitution - Missense 3:10094296-10094296 + SCC-25 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-DB-A64X-01 COSM3974043 c.3195G>A p.L1065L Substitution - coding silent 3:10081435-10081435 + UM-SCC-17B COSM4593246 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + T263 COSM4683345 c.943C>T p.R315W Substitution - Missense 3:10043104-10043104 + SH-4435 COSM5019434 c.2702G>T p.G901V Substitution - Missense 3:10073349-10073349 + p2_VI-2 COSM1738292 c.463G>A p.E155K Substitution - Missense 3:10036311-10036311 + p2_VI-2 COSM1738297 c.438+5G>C p.? Unknown 3:10035238-10035238 + 2233440 COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + sysucc-966T COSM4157099 c.1401G>A p.T467T Substitution - coding silent 3:10048039-10048039 + MPCC_0032_Pa_C COSM3380316 c.744C>A p.V248V Substitution - coding silent 3:10041671-10041671 + TCGA-A8-A09Z-01 COSM3845678 c.3609T>C p.I1203I Substitution - coding silent 3:10088876-10088876 + DLBCL783 COSM1580882 c.2942C>T p.T981I Substitution - Missense 3:10078163-10078163 + HN_62854 COSM127961 c.1608C>T p.L536L Substitution - coding silent 3:10052449-10052449 + TCGA-D3-A1Q1-06 COSM3584575 c.591G>C p.M197I Substitution - Missense 3:10039741-10039741 + TCGA-CG-5726-01 COSM4111885 c.2606-1G>T p.? Unknown 3:10073252-10073252 + NOKSI COSM4152594 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + UPCI:SCC090 COSM4591323 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + C658 COSM4443452 c.3760G>T p.A1254S Substitution - Missense 3:10090368-10090368 + sysucc-867T COSM4422613 c.1170C>T p.S390S Substitution - coding silent 3:10046615-10046615 + TCGA-MI-A75H-01 COSM4918274 c.1742T>C p.M581T Substitution - Missense 3:10060379-10060379 + PD13756a COSM5800530 c.661G>T p.D221Y Substitution - Missense 3:10039811-10039811 + TCGA-FW-A3R5-06 COSM3914396 c.654C>T p.I218I Substitution - coding silent 3:10039804-10039804 + HCA46 COSM4629480 c.3367C>G p.Q1123E Substitution - Missense 3:10087165-10087165 + TCGA-AC-A5XS-01 COSM4390880 c.4142G>C p.R1381T Substitution - Missense 3:10096429-10096429 + UM-SCC-11B COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + BHY COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + U373 COSM2915592 c.3106-9T>A p.? Unknown 3:10081337-10081337 + SW48 COSM2915698 c.4048G>A p.D1350N Substitution - Missense 3:10096335-10096335 + pfg008T COSM1642024 c.879T>C p.D293D Substitution - coding silent 3:10042654-10042654 + DLBCL895 COSM1580880 c.2801C>G p.S934C Substitution - Missense 3:10074615-10074615 + UD-SCC-2 COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + UM-SCC-4 COSM4591323 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + ESO-837 COSM1251996 c.3223T>C p.W1075R Substitution - Missense 3:10081463-10081463 + YUMEZ COSM5397676 c.1353T>A p.I451I Substitution - coding silent 3:10047991-10047991 + PT32 COSM4157095 c.1137G>T p.V379V Substitution - coding silent 3:10046582-10046582 + TCGA-06-0237-01 COSM1154050 c.813G>A p.S271S Substitution - coding silent 3:10042588-10042588 + S06-38853-TP COSM4991806 c.3434C>G p.S1145* Substitution - Nonsense 3:10087232-10087232 + CAL27 COSM2915288 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + 8031704 COSM1168973 c.2335C>T p.R779C Substitution - Missense 3:10065929-10065929 + PT42 COSM5925045 c.787C>T p.R263C Substitution - Missense 3:10042562-10042562 + MZ7-mel COSM13875 c.3367C>T p.Q1123* Substitution - Nonsense 3:10087165-10087165 + TCGA-AM-5820-01 COSM3759565 c.4098T>G p.L1366L Substitution - coding silent 3:10096385-10096385 + 93VU147T COSM4591323 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + TCGA-IA-A40Y-01 COSM3992608 c.1311G>A p.S437S Substitution - coding silent 3:10047949-10047949 + TCGA-AP-A051-01 COSM1035752 c.1588C>T p.R530* Substitution - Nonsense 3:10052429-10052429 + UM-SCC-17B COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + TCGA-AA-A02F-01 COSM300653 c.436C>T p.Q146* Substitution - Nonsense 3:10035231-10035231 + CSCC-54-T COSM4540563 c.2860G>A p.A954T Substitution - Missense 3:10078081-10078081 + HCC002T COSM5819319 c.1099-2A>T p.? Unknown 3:10043827-10043827 + TCGA-DS-A0VM-01 COSM460967 c.4356G>C p.*1452Y Nonstop extension 3:10101262-10101262 + TCGA-AA-3663-01 COSM1417233 c.1759G>A p.A587T Substitution - Missense 3:10060396-10060396 + SJRHB003 COSM3364905 c.2406G>T p.Q802H Substitution - Missense 3:10067229-10067229 + TCGA-D1-A160-01 COSM1035778 c.2203C>T p.R735W Substitution - Missense 3:10065428-10065428 + U373 COSM1417230 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + PTC-88C COSM1417230 c.1275C>T p.Y425Y Substitution - coding silent 3:10046720-10046720 + QC2-25-T2 COSM1669962 c.3818G>A p.R1273Q Substitution - Missense 3:10092221-10092221 + p2_V-1 COSM1738292 c.463G>A p.E155K Substitution - Missense 3:10036311-10036311 + HCA46 COSM4629479 c.3367C>G p.Q1123E Substitution - Missense 3:10087165-10087165 + H1703 COSM1196591 c.289G>A p.V97I Substitution - Missense 3:10034710-10034710 + sysucc-1038T COSM4152595 c.1214A>G p.N405S Substitution - Missense 3:10046659-10046659 + CN-AML-CR-57-Dx COSM4157094 c.1137G>T p.V379V Substitution - coding silent 3:10046582-10046582 + TCGA-DB-A64O-01 COSM3974041 c.1106A>G p.E369G Substitution - Missense 3:10043836-10043836 + TCGA-06-0879 COSM2152293 c.1642_1643delAG p.S548fs*6 Deletion - Frameshift 3:10052483-10052484 + T2284 COSM2915669 c.3896G>A p.R1299H Substitution - Missense 3:10094296-10094296 + sysucc-1315T COSM4157094 c.1137G>T p.V379V Substitution - coding silent 3:10046582-10046582 + WSU-HN30 COSM4593246 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + TCGA-IR-A3LK-01 COSM4817088 c.65-1G>C p.? Unknown 3:10032831-10032831 + TCGA-EB-A3XB-01 COSM3584652 c.3624C>T p.V1208V Substitution - coding silent 3:10088891-10088891 + T3190 COSM4683348 c.2068G>A p.D690N Substitution - Missense 3:10064775-10064775 + SCC-25 COSM4591322 c.3457G>A p.E1153K Substitution - Missense 3:10087255-10087255 + PCSI_0090_Pa_X COSM3380315 c.173T>C p.I58T Substitution - Missense 3:10032940-10032940 + TCGA-BJ-A0ZB-01 COSM3372926 c.1519A>G p.M507V Substitution - Missense 3:10049479-10049479 + WSU-HN6 COSM2915289 c.1278_1278+3delAGTA p.? Unknown 3:10046723-10046726 + TCGA-BR-8372-01 COSM4111830 c.809T>C p.L270S Substitution - Missense 3:10042584-10042584 + TCGA-FW-A3R5-06 COSM3914399 c.1366C>T p.L456F Substitution - Missense 3:10048004-10048004 + C086 COSM3584584 c.1355C>T p.S452L Substitution - Missense 3:10047993-10047993 + TCGA-06-2561-01 COSM2152756 c.2339C>T p.S780L Substitution - Missense 3:10065933-10065933 + PTC-46C COSM3766819 c.2613A>C p.K871N Substitution - Missense 3:10073260-10073260 + UPCI:SCC090 COSM4593246 c.2141C>T p.P714L Substitution - Missense 3:10064848-10064848 + sysucc-1397T COSM5474528 c.1748G>A p.G583D Substitution - Missense 3:10060385-10060385 + ESCC_74 COSM5634765 c.4235G>A p.S1412N Substitution - Missense 3:10098769-10098769 + 154T COSM5576315 c.3563_3564delTC p.Y1189fs*27 Deletion - Frameshift 3:10088830-10088831 + sysucc-1315T COSM4157095 c.1137G>T p.V379V Substitution - coding silent 3:10046582-10046582 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.208388 3p26 613984

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.E1262D c.3786A>C 3 10133873 BLCA A G Missense p.M507V c.1519A>G 3 10091163 THCA A G Missense p.N637S c.1910A>G 3 10105558 CM A G Missense p.Q1010R c.3029A>G 3 10122836 HNSC A G Missense p.Y1457C c.4370A>G 3 10140588 STAD AGTA - SpliceDonorDeletion . c.1278+3_1278+6delAAGT 3 10088407 HNSC AGTA - SpliceDonorDeletion . c.1278+3_1278+6delAAGT 3 10088407 LUAD A - IntronicDeletion . c.1767-15delA 3 10103812 STAD C A Missense p.Q320K c.958C>A 3 10084803 NB C A Synonymous p.P1126P c.3378C>A 3 10128860 CM CC TT Missense p.R735W c.2202_2203delinsTT 3 10107111 CM C G Missense p.L1134V c.3400C>G 3 10128882 BRCA C G Missense p.L497V c.1489C>G 3 10091133 BLCA C G Missense p.N1280K c.3840C>G 3 10133927 STAD C G Synonymous p.L1360L c.4080C>G 3 10138051 BLCA C G Synonymous p.L456L c.1368C>G 3 10089690 CLL C G Synonymous p.L532L c.1596C>G 3 10094121 BLCA C G Synonymous p.V512V c.1536C>G 3 10091180 MM C T IntronicSNV . c.2022-8C>T 3 10106405 CM C T Missense p.A731V c.2192C>T 3 10107101 BRCA C T Missense p.H1042Y c.3124C>T 3 10123048 BRCA C T Missense p.H618Y c.1852C>T 3 10105500 CM C T Missense p.L1377F c.4129C>T 3 10138100 ESCA C T Missense p.L428F c.1282C>T 3 10089604 CM C T Missense p.L630F c.1888C>T 3 10105536 CM C T Missense p.L699F c.2095C>T 3 10106486 BRCA C T Missense p.P1468L c.4403C>T 3 10140621 CM C T Missense p.R1299C c.3895C>T 3 10135979 ESCA C T Missense p.R735W c.2203C>T 3 10107112 UCEC C T Missense p.S433L c.1298C>T 3 10089620 BLCA C T Missense p.S452L c.1355C>T 3 10089677 CM C T Missense p.S780L c.2339C>T 3 10107617 GBM C T Nonsense p.Q146* c.436C>T 3 10076915 COREAD C T Nonsense p.Q440* c.1318C>T 3 10089640 BRCA C T Nonsense p.Q640* c.1918C>T 3 10105566 CM C T Synonymous p.F386F c.1158C>T 3 10088287 HNSC C T Synonymous p.H818H c.2454C>T 3 10108961 UCEC C T Synonymous p.L219L c.655C>T 3 10081489 CM C T Synonymous p.L536L c.1608C>T 3 10094133 HNSC C T Synonymous p.L699L c.2097C>T 3 10106488 LUAD C T Synonymous p.S319S c.957C>T 3 10084802 HC C T Synonymous p.S668S c.2004C>T 3 10106096 LUAD C T Synonymous p.T1330T c.3990C>T 3 10136910 CM C T Synonymous p.T23T c.69C>T 3 10074520 STAD G A IntronicSNV . c.1135-414G>A 3 10087850 CLL G A Missense p.A682T c.2044G>A 3 10106435 CM G A Missense p.D430N c.1288G>A 3 10089610 CM G A Missense p.D753N c.2257G>A 3 10107166 BLCA G A Missense p.E1011K c.3031G>A 3 10122838 CM G A Missense p.E217K c.649G>A 3 10081483 STAD G A Missense p.E650K c.1948G>A 3 10106040 CM G A Missense p.G484R c.1450G>A 3 10091094 CM G A Missense p.G62R c.184G>A 3 10074635 CM G A Missense p.G713D c.2138G>A 3 10106529 THCA G A Missense p.R1321Q c.3962G>A 3 10136046 MB G A Missense p.R735Q c.2204G>A 3 10107113 CM G A Missense p.S1195N c.3584G>A 3 10130535 STAD G A Synonymous p.P672P c.2016G>A 3 10106108 CM G A Synonymous p.Q1084Q c.3252G>A 3 10127523 BRCA G A Synonymous p.S271S c.813G>A 3 10084272 GBM G A Synonymous p.S271S c.813G>A 3 10084272 UCEC G A Synonymous p.V666V c.1998G>A 3 10106090 CM G C Missense p.M197I c.591G>C 3 10081425 CM G C Synonymous p.L1341L c.4023G>C 3 10136943 HNSC G T IntronicSNV . c.1135-884G>T 3 10087380 HC G T Nonsense p.E650* c.1948G>T 3 10106040 OV G T SpliceAcceptorSNV . c.2606-1G>T 3 10114936 STAD G T Synonymous p.L644L c.1932G>T 3 10105580 LUAD G T Synonymous p.P727P c.2181G>T 3 10107090 LUAD T A IntronicSNV . c.1656+1978T>A 3 10096159 CLL T A Missense p.S250T c.748T>A 3 10083359 HNSC T C 3-UTRSNV . c.4413+78T>C 3 10140709 CM T C IntronicSNV . c.491+1261T>C 3 10079284 HC T C IntronicSNV . c.696-131T>C 3 10083176 CM T C Missense p.C801R c.2401T>C 3 10108908 GBM T C Missense p.F1223L c.3667T>C 3 10130618 CM T C Missense p.V670A c.2009T>C 3 10106101 THCA T C Missense p.W1075R c.3223T>C 3 10123147 ESCA T C Synonymous p.D293D c.879T>C 3 10084338 STAD T C Synonymous p.I298I c.894T>C 3 10084739 LUAD - T Frameshift p.R926Sfs*6 c.2775_2776insT 3 10116273 GBM T G Missense p.F161V c.481T>G 3 10078013 BLCA T G Missense p.S590R c.1770T>G 3 10103838 BRCA T - IntronicDeletion . c.570+74delT 3 10081107 ESCA