Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 11 11913616 11913616 + Silent SNP C C T TCGA-C4-A0F0-01A-12D-A10S-08 TCGA-C4-A0F0-10A-01D-A10S-08 g.chr11:11913616C>T c.519C>T c.(517-519)agC>agT p.S173S BLCA 11 11913630 11913630 + Missense_Mutation SNP C C G TCGA-DK-A3IN-01A-11D-A20D-08 TCGA-DK-A3IN-10A-01D-A20D-08 g.chr11:11913630C>G c.533C>G c.(532-534)tCt>tGt p.S178C BLCA 11 11924404 11924404 + Missense_Mutation SNP G G A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr11:11924404G>A c.796G>A c.(796-798)Gag>Aag p.E266K BLCA 11 11924854 11924854 + Missense_Mutation SNP G G A TCGA-GU-AATP-01A-11D-A391-08 TCGA-GU-AATP-10A-01D-A394-08 g.chr11:11924854G>A c.844G>A c.(844-846)Gat>Aat p.D282N BLCA 11 11941735 11941735 + Missense_Mutation SNP G G C TCGA-4Z-AA87-01A-11D-A391-08 TCGA-4Z-AA87-10A-01D-A394-08 g.chr11:11941735G>C c.1062G>C c.(1060-1062)gaG>gaC p.E354D BLCA 11 11942014 11942014 + Missense_Mutation SNP G G A TCGA-BT-A0YX-01A-11D-A10S-08 TCGA-BT-A0YX-10A-01D-A10S-08 g.chr11:11942014G>A c.1251G>A c.(1249-1251)atG>atA p.M417I BLCA 11 11944391 11944391 + Missense_Mutation SNP G G C TCGA-4Z-AA7R-01A-11D-A391-08 TCGA-4Z-AA7R-10A-01D-A394-08 g.chr11:11944391G>C c.1399G>C c.(1399-1401)Gaa>Caa p.E467Q BLCA 11 11954622 11954622 + Missense_Mutation SNP C C G TCGA-BL-A13I-01A-11D-A13W-08 TCGA-BL-A13I-11A-11D-A13W-08 g.chr11:11954622C>G c.1783C>G c.(1783-1785)Caa>Gaa p.Q595E BLCA 11 11955432 11955432 + Nonsense_Mutation SNP G G T TCGA-4Z-AA7Y-01A-11D-A391-08 TCGA-4Z-AA7Y-10A-01D-A394-08 g.chr11:11955432G>T c.1879G>T c.(1879-1881)Gag>Tag p.E627* BLCA 11 11957849 11957849 + Splice_Site SNP G G A TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr11:11957849G>A c.e18-1 BLCA 11 11957937 11957937 + Missense_Mutation SNP G G A TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr11:11957937G>A c.2017G>A c.(2017-2019)Gaa>Aaa p.E673K BLCA 11 11958017 11958017 + Silent SNP G G A TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr11:11958017G>A c.2097G>A c.(2095-2097)acG>acA p.T699T BLCA 11 11963917 11963917 + Silent SNP G G A TCGA-4Z-AA89-01A-11D-A391-08 TCGA-4Z-AA89-10A-01D-A394-08 g.chr11:11963917G>A c.2409G>A c.(2407-2409)caG>caA p.Q803Q BLCA 11 11964064 11964064 + Silent SNP G G T TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr11:11964064G>T c.2556G>T c.(2554-2556)gtG>gtT p.V852V BLCA 11 11964244 11964244 + Silent SNP C C G TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chr11:11964244C>G c.2736C>G c.(2734-2736)ctC>ctG p.L912L BLCA 11 11964323 11964323 + Missense_Mutation SNP C C A TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chr11:11964323C>A c.2815C>A c.(2815-2817)Cag>Aag p.Q939K BLCA 11 11964413 11964413 + Missense_Mutation SNP G G C TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr11:11964413G>C c.2905G>C c.(2905-2907)Gat>Cat p.D969H BLCA 11 11971470 11971470 + Missense_Mutation SNP A A G TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr11:11971470A>G c.3443A>G c.(3442-3444)aAa>aGa p.K1148R BLCA 11 11972017 11972017 + Nonsense_Mutation SNP G G T TCGA-G2-AA3D-01A-11D-A391-08 TCGA-G2-AA3D-10A-01D-A394-08 g.chr11:11972017G>T c.3631G>T c.(3631-3633)Gaa>Taa p.E1211* BLCA 11 11977561 11977561 + Missense_Mutation SNP G G C TCGA-GD-A3OP-01A-21D-A21Z-08 TCGA-GD-A3OP-10A-01D-A21Z-08 g.chr11:11977561G>C c.3967G>C c.(3967-3969)Gaa>Caa p.E1323Q BRCA 11 11951662 11951662 + Silent SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:11951662C>T c.1650C>T c.(1648-1650)ttC>ttT p.F550F BRCA 11 11962036 11962036 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr11:11962036C>T c.2314C>T c.(2314-2316)Cgt>Tgt p.R772C BRCA 11 11964198 11964198 + Missense_Mutation SNP G G T TCGA-AR-A1AI-01A-11D-A12Q-09 TCGA-AR-A1AI-10A-01D-A12Q-09 g.chr11:11964198G>T c.2690G>T c.(2689-2691)aGc>aTc p.S897I BRCA 11 11964387 11964387 + Missense_Mutation SNP A A G TCGA-D8-A27I-01A-11D-A16D-09 TCGA-D8-A27I-10A-02D-A16D-09 g.chr11:11964387A>G c.2879A>G c.(2878-2880)gAt>gGt p.D960G BRCA 11 11977640 11977640 + Missense_Mutation SNP G G A TCGA-BH-A18F-01A-11D-A12B-09 TCGA-BH-A18F-11A-22D-A12B-09 g.chr11:11977640G>A c.4046G>A c.(4045-4047)cGt>cAt p.R1349H CESC 11 11924287 11924287 + Missense_Mutation SNP G G C TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr11:11924287G>C c.679G>C c.(679-681)Gat>Cat p.D227H CESC 11 11962085 11962085 + Missense_Mutation SNP G G C TCGA-EK-A2PL-01A-11D-A18J-09 TCGA-EK-A2PL-10A-01D-A18J-09 g.chr11:11962085G>C c.2363G>C c.(2362-2364)aGa>aCa p.R788T CESC 11 11964023 11964023 + Missense_Mutation SNP A A G TCGA-RA-A741-01A-11D-A33O-09 TCGA-RA-A741-10B-01D-A33O-09 g.chr11:11964023A>G c.2515A>G c.(2515-2517)Agg>Ggg p.R839G CHOL 11 11969496 11969496 + Missense_Mutation SNP G G C TCGA-W6-AA0S-01A-11D-A417-09 TCGA-W6-AA0S-10A-01D-A41A-09 g.chr11:11969496G>C c.3156G>C c.(3154-3156)ttG>ttC p.L1052F COAD 11 11863744 11863744 + Silent SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr11:11863744C>T c.12C>T c.(10-12)ggC>ggT p.G4G COAD 11 11919204 11919204 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:11919204T>G c.617T>G c.(616-618)cTt>cGt p.L206R COAD 11 11941719 11941719 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr11:11941719C>T c.1046C>T c.(1045-1047)gCa>gTa p.A349V COAD 11 11941793 11941793 + Silent SNP C C A TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr11:11941793C>A c.1120C>A c.(1120-1122)Cgg>Agg p.R374R COAD 11 11941794 11941794 + Missense_Mutation SNP G G A TCGA-CK-6751-01A-11D-1835-10 TCGA-CK-6751-10A-01D-1835-10 g.chr11:11941794G>A c.1121G>A c.(1120-1122)cGg>cAg p.R374Q COAD 11 11944367 11944367 + Missense_Mutation SNP G G T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr11:11944367G>T c.1375G>T c.(1375-1377)Ggt>Tgt p.G459C COAD 11 11957978 11957978 + Silent SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:11957978C>T c.2058C>T c.(2056-2058)ggC>ggT p.G686G COAD 11 11959817 11959817 + Missense_Mutation SNP A A C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr11:11959817A>C c.2151A>C c.(2149-2151)aaA>aaC p.K717N COAD 11 11963957 11963957 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr11:11963957C>T c.2449C>T c.(2449-2451)Cgg>Tgg p.R817W COAD 11 11964113 11964113 + Missense_Mutation SNP G G T TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr11:11964113G>T c.2605G>T c.(2605-2607)Gtg>Ttg p.V869L COAD 11 11964232 11964232 + Silent SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:11964232C>T c.2724C>T c.(2722-2724)atC>atT p.I908I COAD 11 11964320 11964320 + Missense_Mutation SNP T T G TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr11:11964320T>G c.2812T>G c.(2812-2814)Ttt>Gtt p.F938V COAD 11 11970052 11970052 + Frame_Shift_Del DEL A A - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr11:11970052delA c.3355delA c.(3355-3357)aaafs p.K1120fs COAD 11 11974328 11974328 + Silent SNP G G A TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr11:11974328G>A c.3684G>A c.(3682-3684)ttG>ttA p.L1228L COAD 11 11977548 11977548 + Splice_Site SNP G G T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr11:11977548G>T c.3954G>T c.(3952-3954)agG>agT p.R1318S COAD 11 11977678 11977678 + Missense_Mutation SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:11977678A>G c.4084A>G c.(4084-4086)Ata>Gta p.I1362V COADREAD 11 11863744 11863744 + Silent SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr11:11863744C>T c.12C>T c.(10-12)ggC>ggT p.G4G COADREAD 11 11919204 11919204 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:11919204T>G c.617T>G c.(616-618)cTt>cGt p.L206R COADREAD 11 11941719 11941719 + Missense_Mutation SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr11:11941719C>T c.1046C>T c.(1045-1047)gCa>gTa p.A349V COADREAD 11 11941793 11941793 + Silent SNP C C A TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr11:11941793C>A c.1120C>A c.(1120-1122)Cgg>Agg p.R374R COADREAD 11 11941794 11941794 + Missense_Mutation SNP G G A TCGA-CK-6751-01A-11D-1835-10 TCGA-CK-6751-10A-01D-1835-10 g.chr11:11941794G>A c.1121G>A c.(1120-1122)cGg>cAg p.R374Q COADREAD 11 11941794 11941794 + Missense_Mutation SNP G G T TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr11:11941794G>T c.1121G>T c.(1120-1122)cGg>cTg p.R374L COADREAD 11 11941795 11941795 + Silent SNP G G A TCGA-G5-6641-01A-11D-1826-10 TCGA-G5-6641-10A-01D-1826-10 g.chr11:11941795G>A c.1122G>A c.(1120-1122)cgG>cgA p.R374R COADREAD 11 11944367 11944367 + Missense_Mutation SNP G G T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr11:11944367G>T c.1375G>T c.(1375-1377)Ggt>Tgt p.G459C COADREAD 11 11957967 11957967 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:11957967C>A c.2047C>A c.(2047-2049)Cta>Ata p.L683I COADREAD 11 11957978 11957978 + Silent SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr11:11957978C>T c.2058C>T c.(2056-2058)ggC>ggT p.G686G COADREAD 11 11959817 11959817 + Missense_Mutation SNP A A C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr11:11959817A>C c.2151A>C c.(2149-2151)aaA>aaC p.K717N COADREAD 11 11963957 11963957 + Missense_Mutation SNP C C T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr11:11963957C>T c.2449C>T c.(2449-2451)Cgg>Tgg p.R817W COADREAD 11 11964113 11964113 + Missense_Mutation SNP G G T TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr11:11964113G>T c.2605G>T c.(2605-2607)Gtg>Ttg p.V869L COADREAD 11 11964232 11964232 + Silent SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr11:11964232C>T c.2724C>T c.(2722-2724)atC>atT p.I908I COADREAD 11 11964320 11964320 + Missense_Mutation SNP T T G TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr11:11964320T>G c.2812T>G c.(2812-2814)Ttt>Gtt p.F938V COADREAD 11 11969545 11969545 + Missense_Mutation SNP T T G TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr11:11969545T>G c.3205T>G c.(3205-3207)Tta>Gta p.L1069V COADREAD 11 11969590 11969590 + Nonsense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:11969590C>T c.3250C>T c.(3250-3252)Cga>Tga p.R1084* COADREAD 11 11970052 11970052 + Frame_Shift_Del DEL A A - TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr11:11970052delA c.3355delA c.(3355-3357)aaafs p.K1120fs COADREAD 11 11974328 11974328 + Silent SNP G G A TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr11:11974328G>A c.3684G>A c.(3682-3684)ttG>ttA p.L1228L COADREAD 11 11976696 11976696 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:11976696C>T c.3938C>T c.(3937-3939)gCg>gTg p.A1313V COADREAD 11 11977548 11977548 + Splice_Site SNP G G T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr11:11977548G>T c.3954G>T c.(3952-3954)agG>agT p.R1318S COADREAD 11 11977678 11977678 + Missense_Mutation SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:11977678A>G c.4084A>G c.(4084-4086)Ata>Gta p.I1362V ESCA 11 11958055 11958055 + Missense_Mutation SNP G G A TCGA-LN-A49L-01A-11D-A247-09 TCGA-LN-A49L-10A-01D-A247-09 g.chr11:11958055G>A c.2135G>A c.(2134-2136)gGa>gAa p.G712E ESCA 11 11969622 11969622 + Silent SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr11:11969622C>T c.3282C>T c.(3280-3282)agC>agT p.S1094S ESCA 11 11974404 11974404 + Missense_Mutation SNP G G A TCGA-L5-A88W-01A-11D-A351-09 TCGA-L5-A88W-11A-11D-A351-09 g.chr11:11974404G>A c.3760G>A c.(3760-3762)Gaa>Aaa p.E1254K GBM 11 11969542 11969542 + Missense_Mutation SNP C C T TCGA-32-2495-01A-01D-1353-08 TCGA-32-2495-10B-01D-1353-08 g.chr11:11969542C>T c.3202C>T c.(3202-3204)Cat>Tat p.H1068Y GBMLGG 11 11959846 11959846 + Missense_Mutation SNP C C T TCGA-VM-A8C8-01A-11D-A36O-08 TCGA-VM-A8C8-10A-01D-A367-08 g.chr11:11959846C>T c.2180C>T c.(2179-2181)tCt>tTt p.S727F GBMLGG 11 11961975 11961975 + Splice_Site SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:11961975G>T c.e20-1 GBMLGG 11 11969542 11969542 + Missense_Mutation SNP C C T TCGA-32-2495-01A-01D-1353-08 TCGA-32-2495-10B-01D-1353-08 g.chr11:11969542C>T c.3202C>T c.(3202-3204)Cat>Tat p.H1068Y HNSC 11 11913622 11913622 + Silent SNP C C G TCGA-DQ-7588-01A-11D-2078-08 TCGA-DQ-7588-10B-01D-2078-08 g.chr11:11913622C>G c.525C>G c.(523-525)tcC>tcG p.S175S HNSC 11 11924275 11924275 + Missense_Mutation SNP G G A TCGA-CR-6472-01A-11D-1870-08 TCGA-CR-6472-10A-01D-1870-08 g.chr11:11924275G>A c.667G>A c.(667-669)Gaa>Aaa p.E223K HNSC 11 11926970 11926970 + Nonsense_Mutation SNP C C T TCGA-T3-A92N-01A-11D-A391-08 TCGA-T3-A92N-10A-01D-A394-08 g.chr11:11926970C>T c.904C>T c.(904-906)Caa>Taa p.Q302* HNSC 11 11964241 11964241 + Silent SNP T T C TCGA-CQ-5327-01A-01D-1683-08 TCGA-CQ-5327-10A-01D-1683-08 g.chr11:11964241T>C c.2733T>C c.(2731-2733)ccT>ccC p.P911P HNSC 11 11964389 11964389 + Missense_Mutation SNP A A G TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr11:11964389A>G c.2881A>G c.(2881-2883)Att>Gtt p.I961V HNSC 11 11964459 11964459 + Missense_Mutation SNP G G A TCGA-P3-A6T0-01A-12D-A34J-08 TCGA-P3-A6T0-10A-01D-A34M-08 g.chr11:11964459G>A c.2951G>A c.(2950-2952)gGa>gAa p.G984E HNSC 11 11971469 11971469 + Missense_Mutation SNP A A G TCGA-CR-6487-01A-11D-1870-08 TCGA-CR-6487-10A-01D-1870-08 g.chr11:11971469A>G c.3442A>G c.(3442-3444)Aaa>Gaa p.K1148E HNSC 11 11971484 11971484 + Missense_Mutation SNP C C T TCGA-CR-6487-01A-11D-1870-08 TCGA-CR-6487-10A-01D-1870-08 g.chr11:11971484C>T c.3457C>T c.(3457-3459)Cgg>Tgg p.R1153W KIPAN 11 11924349 11924349 + Silent SNP A A G TCGA-GL-A9DC-01A-11D-A36X-10 TCGA-GL-A9DC-10A-01D-A370-10 g.chr11:11924349A>G c.741A>G c.(739-741)aaA>aaG p.K247K KIPAN 11 11964635 11964635 + Missense_Mutation SNP G G A TCGA-B0-5081-01A-01D-1462-08 TCGA-B0-5081-11A-01D-1462-08 g.chr11:11964635G>A c.3127G>A c.(3127-3129)Gaa>Aaa p.E1043K KIPAN 11 11971443 11971443 + Missense_Mutation SNP A A G TCGA-J7-A8I2-01A-12D-A35Z-10 TCGA-J7-A8I2-10A-01D-A35Z-10 g.chr11:11971443A>G c.3416A>G c.(3415-3417)aAg>aGg p.K1139R KIRC 11 11964635 11964635 + Missense_Mutation SNP G G A TCGA-B0-5081-01A-01D-1462-08 TCGA-B0-5081-11A-01D-1462-08 g.chr11:11964635G>A c.3127G>A c.(3127-3129)Gaa>Aaa p.E1043K KIRP 11 11924349 11924349 + Silent SNP A A G TCGA-GL-A9DC-01A-11D-A36X-10 TCGA-GL-A9DC-10A-01D-A370-10 g.chr11:11924349A>G c.741A>G c.(739-741)aaA>aaG p.K247K KIRP 11 11971443 11971443 + Missense_Mutation SNP A A G TCGA-J7-A8I2-01A-12D-A35Z-10 TCGA-J7-A8I2-10A-01D-A35Z-10 g.chr11:11971443A>G c.3416A>G c.(3415-3417)aAg>aGg p.K1139R LGG 11 11959846 11959846 + Missense_Mutation SNP C C T TCGA-VM-A8C8-01A-11D-A36O-08 TCGA-VM-A8C8-10A-01D-A367-08 g.chr11:11959846C>T c.2180C>T c.(2179-2181)tCt>tTt p.S727F LGG 11 11961975 11961975 + Splice_Site SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:11961975G>T c.e20-1 LIHC 11 11927068 11927068 + Silent SNP T T C TCGA-DD-A116-01A-11D-A12Z-10 TCGA-DD-A116-10A-01D-A12Z-10 g.chr11:11927068T>C c.1002T>C c.(1000-1002)taT>taC p.Y334Y LIHC 11 11941963 11941963 + Missense_Mutation SNP G G A TCGA-CC-A3MA-01A-11D-A20W-10 TCGA-CC-A3MA-10A-01D-A20W-10 g.chr11:11941963G>A c.1200G>A c.(1198-1200)atG>atA p.M400I LIHC 11 11944273 11944273 + Silent SNP A A G TCGA-DD-AACI-01A-11D-A40R-10 TCGA-DD-AACI-10A-01D-A40U-10 g.chr11:11944273A>G c.1281A>G c.(1279-1281)aaA>aaG p.K427K LIHC 11 11963990 11963990 + Missense_Mutation SNP C C G TCGA-EP-A3JL-01A-11D-A20W-10 TCGA-EP-A3JL-10A-01D-A20W-10 g.chr11:11963990C>G c.2482C>G c.(2482-2484)Cta>Gta p.L828V LIHC 11 11964527 11964527 + Missense_Mutation SNP G G T TCGA-BC-A10U-01A-11D-A12Z-10 TCGA-BC-A10U-11A-11D-A12Z-10 g.chr11:11964527G>T c.3019G>T c.(3019-3021)Gat>Tat p.D1007Y LIHC 11 11970052 11970052 + Frame_Shift_Del DEL A A - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr11:11970052delA c.3355delA c.(3355-3357)aaafs p.K1120fs LIHC 11 11977603 11977603 + Frame_Shift_Del DEL A A - TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr11:11977603delA c.4009delA c.(4009-4011)aaafs p.K1338fs LUAD 11 11926949 11926949 + Missense_Mutation SNP G G A TCGA-17-Z014-01A-01W-0746-08 TCGA-17-Z014-11A-01W-0746-08 g.chr11:11926949G>A c.883G>A c.(883-885)Gat>Aat p.D295N LUAD 11 11942041 11942041 + Splice_Site SNP G G C TCGA-17-Z055-01A-01W-0747-08 TCGA-17-Z055-11A-01W-0747-08 g.chr11:11942041G>C c.1278G>C c.(1276-1278)gaG>gaC p.E426D LUAD 11 11944424 11944424 + Missense_Mutation SNP T T A TCGA-17-Z000-01A-01W-0746-08 TCGA-17-Z000-11A-01W-0746-08 g.chr11:11944424T>A c.1432T>A c.(1432-1434)Tct>Act p.S478T LUAD 11 11954630 11954630 + Missense_Mutation SNP G G C TCGA-NJ-A4YI-01A-11D-A25L-08 TCGA-NJ-A4YI-10A-01D-A25L-08 g.chr11:11954630G>C c.1791G>C c.(1789-1791)aaG>aaC p.K597N LUAD 11 11957904 11957904 + Missense_Mutation SNP G G T TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr11:11957904G>T c.1984G>T c.(1984-1986)Gat>Tat p.D662Y LUAD 11 11959861 11959861 + Missense_Mutation SNP T T A TCGA-62-8398-01A-11D-2323-08 TCGA-62-8398-10A-01D-2323-08 g.chr11:11959861T>A c.2195T>A c.(2194-2196)aTa>aAa p.I732K LUAD 11 11964407 11964407 + Missense_Mutation SNP A A T TCGA-44-7659-01A-11D-2063-08 TCGA-44-7659-10A-01D-2063-08 g.chr11:11964407A>T c.2899A>T c.(2899-2901)Agc>Tgc p.S967C LUAD 11 11972026 11972026 + Missense_Mutation SNP G G C TCGA-55-6982-01A-11D-1945-08 TCGA-55-6982-11A-01D-1945-08 g.chr11:11972026G>C c.3640G>C c.(3640-3642)Gat>Cat p.D1214H LUAD 11 11976665 11976665 + Missense_Mutation SNP G G T TCGA-91-6828-01A-11D-1855-08 TCGA-91-6828-10A-01D-1855-08 g.chr11:11976665G>T c.3907G>T c.(3907-3909)Gtc>Ttc p.V1303F LUAD 11 11977639 11977639 + Missense_Mutation SNP C C T TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr11:11977639C>T c.4045C>T c.(4045-4047)Cgt>Tgt p.R1349C LUSC 11 11962033 11962033 + Missense_Mutation SNP T T G TCGA-60-2713-01A-01D-1522-08 TCGA-60-2713-11A-01D-1522-08 g.chr11:11962033T>G c.2311T>G c.(2311-2313)Ttg>Gtg p.L771V LUSC 11 11964541 11964541 + Missense_Mutation SNP A A C TCGA-56-6546-01A-11D-1817-08 TCGA-56-6546-10A-01D-1817-08 g.chr11:11964541A>C c.3033A>C c.(3031-3033)gaA>gaC p.E1011D LUSC 11 11969555 11969555 + Missense_Mutation SNP T T G TCGA-18-3417-01A-01D-1441-08 TCGA-18-3417-11A-01D-1441-08 g.chr11:11969555T>G c.3215T>G c.(3214-3216)tTt>tGt p.F1072C LUSC 11 11970068 11970068 + Missense_Mutation SNP G G C TCGA-18-3406-01A-01D-0983-08 TCGA-18-3406-11A-01D-0983-08 g.chr11:11970068G>C c.3371G>C c.(3370-3372)aGa>aCa p.R1124T LUSC 11 11977671 11977671 + Silent SNP A A G TCGA-66-2754-01A-01D-0983-08 TCGA-66-2754-11A-01D-0983-08 g.chr11:11977671A>G c.4077A>G c.(4075-4077)gcA>gcG p.A1359A OV 11 11964115 11964115 + Silent SNP G G A TCGA-04-1338-01A-01W-0484-10 TCGA-04-1338-11A-01W-0485-10 g.chr11:11964115G>A c.2607G>A c.(2605-2607)gtG>gtA p.V869V PRAD 11 11913565 11913565 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr11:11913565G>A c.468G>A c.(466-468)ccG>ccA p.P156P PRAD 11 11957962 11957962 + Missense_Mutation SNP G G A TCGA-ZG-A9ND-01A-11D-A41K-08 TCGA-ZG-A9ND-10A-01D-A41N-08 g.chr11:11957962G>A c.2042G>A c.(2041-2043)gGg>gAg p.G681E PRAD 11 11963959 11963959 + Silent SNP G G A TCGA-XK-AAJA-01A-11D-A41K-08 TCGA-XK-AAJA-10A-01D-A41N-08 g.chr11:11963959G>A c.2451G>A c.(2449-2451)cgG>cgA p.R817R PRAD 11 11969590 11969590 + Silent SNP C C A TCGA-HC-7750-01A-11D-2114-08 TCGA-HC-7750-10A-01D-2115-08 g.chr11:11969590C>A c.3250C>A c.(3250-3252)Cga>Aga p.R1084R READ 11 11941794 11941794 + Missense_Mutation SNP G G T TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr11:11941794G>T c.1121G>T c.(1120-1122)cGg>cTg p.R374L READ 11 11941795 11941795 + Silent SNP G G A TCGA-G5-6641-01A-11D-1826-10 TCGA-G5-6641-10A-01D-1826-10 g.chr11:11941795G>A c.1122G>A c.(1120-1122)cgG>cgA p.R374R READ 11 11957967 11957967 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:11957967C>A c.2047C>A c.(2047-2049)Cta>Ata p.L683I READ 11 11969545 11969545 + Missense_Mutation SNP T T G TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr11:11969545T>G c.3205T>G c.(3205-3207)Tta>Gta p.L1069V READ 11 11969590 11969590 + Nonsense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:11969590C>T c.3250C>T c.(3250-3252)Cga>Tga p.R1084* READ 11 11976696 11976696 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:11976696C>T c.3938C>T c.(3937-3939)gCg>gTg p.A1313V SARC 11 11969622 11969622 + Silent SNP C C T TCGA-DX-AB32-01A-11D-A417-09 TCGA-DX-AB32-10A-01D-A41A-09 g.chr11:11969622C>T c.3282C>T c.(3280-3282)agC>agT p.S1094S SARC 11 11970051 11970052 + Frame_Shift_Ins INS - - A TCGA-DX-A1L1-01A-11D-A24N-09 TCGA-DX-A1L1-10A-01D-A24N-09 g.chr11:11970051_11970052insA c.3354_3355insA c.(3355-3357)aaafs p.K1119fs SARC 11 11976640 11976640 + Missense_Mutation SNP G G T TCGA-X6-A8C4-01A-11D-A36J-09 TCGA-X6-A8C4-10A-01D-A36M-09 g.chr11:11976640G>T c.3882G>T c.(3880-3882)tgG>tgT p.W1294C SKCM 11 11919184 11919184 + Silent SNP G G A TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr11:11919184G>A c.597G>A c.(595-597)ttG>ttA p.L199L SKCM 11 11941997 11941997 + Missense_Mutation SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr11:11941997C>T c.1234C>T c.(1234-1236)Ccc>Tcc p.P412S SKCM 11 11944273 11944273 + Missense_Mutation SNP A A T TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chr11:11944273A>T c.1281A>T c.(1279-1281)aaA>aaT p.K427N SKCM 11 11951662 11951662 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:11951662C>T c.1650C>T c.(1648-1650)ttC>ttT p.F550F SKCM 11 11971966 11971966 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr11:11971966C>T c.3580C>T c.(3580-3582)Cat>Tat p.H1194Y SKCM 11 11976465 11976465 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr11:11976465C>T c.3796C>T c.(3796-3798)Cct>Tct p.P1266S SKCM 11 11976597 11976597 + Missense_Mutation SNP C C T TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr11:11976597C>T c.3839C>T c.(3838-3840)cCc>cTc p.P1280L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 11 11955458 11955458 single base substitution G C 5_prime_UTR_variant BLCA-CN 11 11955458 11955458 single base substitution G C missense_variant K547N 1641G>C BLCA-CN 11 11955458 11955458 single base substitution G C missense_variant K615N 1845G>C BLCA-CN 11 11955458 11955458 single base substitution G C missense_variant K635N 1905G>C BLCA-CN 11 11955458 11955458 single base substitution G C upstream_gene_variant BLCA-CN 11 11957981 11957981 single base substitution C G 5_prime_UTR_variant BLCA-CN 11 11957981 11957981 single base substitution C G synonymous_variant V599V 1797C>G BLCA-CN 11 11957981 11957981 single base substitution C G synonymous_variant V667V 2001C>G BLCA-CN 11 11957981 11957981 single base substitution C G synonymous_variant V687V 2061C>G BLCA-CN 11 11957981 11957981 single base substitution C G upstream_gene_variant BLCA-CN 11 11969541 11969541 single base substitution A G 5_prime_UTR_variant BLCA-CN 11 11969541 11969541 single base substitution A G downstream_gene_variant BLCA-CN 11 11969541 11969541 single base substitution A G exon_variant BLCA-CN 11 11969541 11969541 single base substitution A G synonymous_variant Q1047Q 3141A>G BLCA-CN 11 11969541 11969541 single base substitution A G synonymous_variant Q1067Q 3201A>G BLCA-CN 11 11969541 11969541 single base substitution A G synonymous_variant Q979Q 2937A>G BLCA-CN 11 11969541 11969541 single base substitution A G upstream_gene_variant BLCA-CN 11 11976689 11976689 single base substitution G A downstream_gene_variant BLCA-CN 11 11976689 11976689 single base substitution G A exon_variant BLCA-CN 11 11976689 11976689 single base substitution G A missense_variant D1223N 3667G>A BLCA-CN 11 11976689 11976689 single base substitution G A missense_variant D1291N 3871G>A BLCA-CN 11 11976689 11976689 single base substitution G A missense_variant D1311N 3931G>A BLCA-CN 11 11976689 11976689 single base substitution G A missense_variant D93N 277G>A BLCA-US 11 11913630 11913630 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant BLCA-US 11 11913630 11913630 single base substitution C G missense_variant S158C 473C>G BLCA-US 11 11913630 11913630 single base substitution C G missense_variant S178C 533C>G BLCA-US 11 11913630 11913630 single base substitution C G missense_variant S90C 269C>G BLCA-US 11 11942014 11942014 single base substitution G A 5_prime_UTR_variant BLCA-US 11 11942014 11942014 single base substitution G A missense_variant M329I 987G>A BLCA-US 11 11942014 11942014 single base substitution G A missense_variant M397I 1191G>A BLCA-US 11 11942014 11942014 single base substitution G A missense_variant M417I 1251G>A BLCA-US 11 11954622 11954622 single base substitution C G 5_prime_UTR_variant BLCA-US 11 11954622 11954622 single base substitution C G missense_variant Q507E 1519C>G BLCA-US 11 11954622 11954622 single base substitution C G missense_variant Q575E 1723C>G BLCA-US 11 11954622 11954622 single base substitution C G missense_variant Q595E 1783C>G BLCA-US 11 11971470 11971470 single base substitution A G 5_prime_UTR_variant BLCA-US 11 11971470 11971470 single base substitution A G downstream_gene_variant BLCA-US 11 11971470 11971470 single base substitution A G exon_variant BLCA-US 11 11971470 11971470 single base substitution A G missense_variant K1060R 3179A>G BLCA-US 11 11971470 11971470 single base substitution A G missense_variant K1128R 3383A>G BLCA-US 11 11971470 11971470 single base substitution A G missense_variant K1148R 3443A>G BLCA-US 11 11971470 11971470 single base substitution A G upstream_gene_variant BRCA-EU 11 11858101 11858101 single base substitution G C upstream_gene_variant BRCA-EU 11 11858227 11858227 single base substitution G C upstream_gene_variant BRCA-EU 11 11858748 11858748 single base substitution T G upstream_gene_variant BRCA-EU 11 11861253 11861253 single base substitution T C upstream_gene_variant BRCA-EU 11 11862456 11862456 deletion of <=200bp T - upstream_gene_variant BRCA-EU 11 11866906 11866906 insertion of <=200bp - T intron_variant BRCA-EU 11 11869486 11869486 single base substitution G C intron_variant BRCA-EU 11 11869590 11869590 single base substitution G C intron_variant BRCA-EU 11 11869973 11869973 single base substitution A C intron_variant BRCA-EU 11 11870976 11870976 single base substitution C T intron_variant BRCA-EU 11 11874998 11874998 single base substitution T A intron_variant BRCA-EU 11 11875087 11875087 single base substitution A G intron_variant BRCA-EU 11 11876145 11876147 deletion of <=200bp ACA - intron_variant BRCA-EU 11 11877604 11877604 single base substitution A C intron_variant BRCA-EU 11 11879263 11879263 single base substitution C T intron_variant BRCA-EU 11 11880139 11880139 single base substitution C A intron_variant BRCA-EU 11 11880729 11880729 single base substitution T G intron_variant BRCA-EU 11 11882411 11882411 single base substitution G A intron_variant BRCA-EU 11 11883024 11883024 single base substitution T G intron_variant BRCA-EU 11 11884136 11884136 single base substitution A G intron_variant BRCA-EU 11 11886642 11886642 single base substitution T G intron_variant BRCA-EU 11 11887509 11887509 single base substitution G C intron_variant BRCA-EU 11 11887540 11887540 single base substitution G A intron_variant BRCA-EU 11 11888196 11888196 deletion of <=200bp T - intron_variant BRCA-EU 11 11890373 11890373 single base substitution C T intron_variant BRCA-EU 11 11892539 11892539 single base substitution T C intron_variant BRCA-EU 11 11896391 11896391 single base substitution C T intron_variant BRCA-EU 11 11896884 11896884 single base substitution T G intron_variant BRCA-EU 11 11896884 11896884 single base substitution T G upstream_gene_variant BRCA-EU 11 11898177 11898177 single base substitution G T intron_variant BRCA-EU 11 11898177 11898177 single base substitution G T upstream_gene_variant BRCA-EU 11 11898466 11898466 single base substitution A G intron_variant BRCA-EU 11 11898466 11898466 single base substitution A G upstream_gene_variant BRCA-EU 11 11899611 11899611 single base substitution T C intron_variant BRCA-EU 11 11899611 11899611 single base substitution T C upstream_gene_variant BRCA-EU 11 11900111 11900111 insertion of <=200bp - T intron_variant BRCA-EU 11 11900111 11900111 insertion of <=200bp - T upstream_gene_variant BRCA-EU 11 11900443 11900443 single base substitution T C intron_variant BRCA-EU 11 11900443 11900443 single base substitution T C upstream_gene_variant BRCA-EU 11 11901019 11901019 single base substitution G A intron_variant BRCA-EU 11 11901019 11901019 single base substitution G A upstream_gene_variant BRCA-EU 11 11902591 11902591 single base substitution C T intron_variant BRCA-EU 11 11903522 11903522 single base substitution G C intron_variant BRCA-EU 11 11905054 11905054 single base substitution C G intron_variant BRCA-EU 11 11906040 11906040 single base substitution G C 5_prime_UTR_variant BRCA-EU 11 11906040 11906040 single base substitution G C exon_variant BRCA-EU 11 11906040 11906040 single base substitution G C missense_variant K110N 330G>C BRCA-EU 11 11906040 11906040 single base substitution G C missense_variant K22N 66G>C BRCA-EU 11 11906040 11906040 single base substitution G C missense_variant K90N 270G>C BRCA-EU 11 11907740 11907740 single base substitution C G downstream_gene_variant BRCA-EU 11 11907740 11907740 single base substitution C G intron_variant BRCA-EU 11 11908151 11908151 single base substitution A G downstream_gene_variant BRCA-EU 11 11908151 11908151 single base substitution A G intron_variant BRCA-EU 11 11909085 11909085 single base substitution A G downstream_gene_variant BRCA-EU 11 11909085 11909085 single base substitution A G intron_variant BRCA-EU 11 11910145 11910145 single base substitution T G downstream_gene_variant BRCA-EU 11 11910145 11910145 single base substitution T G intron_variant BRCA-EU 11 11911966 11911966 single base substitution T C intron_variant BRCA-EU 11 11915444 11915444 single base substitution G T intron_variant BRCA-EU 11 11915909 11915909 single base substitution A G intron_variant BRCA-EU 11 11916299 11916299 single base substitution C A intron_variant BRCA-EU 11 11916318 11916318 deletion of <=200bp T - intron_variant BRCA-EU 11 11917346 11917346 single base substitution C T intron_variant BRCA-EU 11 11918462 11918462 single base substitution A G intron_variant BRCA-EU 11 11920138 11920138 single base substitution G C intron_variant BRCA-EU 11 11921288 11921288 single base substitution C T intron_variant BRCA-EU 11 11922836 11922836 single base substitution T A intron_variant BRCA-EU 11 11923129 11923129 single base substitution A G intron_variant BRCA-EU 11 11926273 11926273 single base substitution T C intron_variant BRCA-EU 11 11926291 11926291 single base substitution G C intron_variant BRCA-EU 11 11927619 11927619 single base substitution C T intron_variant BRCA-EU 11 11928889 11928889 single base substitution C T intron_variant BRCA-EU 11 11928928 11928928 single base substitution G C intron_variant BRCA-EU 11 11929411 11929411 single base substitution G C intron_variant BRCA-EU 11 11929695 11929695 single base substitution C G intron_variant BRCA-EU 11 11931521 11931523 deletion of <=200bp GAA - intron_variant BRCA-EU 11 11932720 11932720 single base substitution G C intron_variant BRCA-EU 11 11933489 11933489 single base substitution C G intron_variant BRCA-EU 11 11934188 11934188 deletion of <=200bp A - intron_variant BRCA-EU 11 11934789 11934789 single base substitution T C intron_variant BRCA-EU 11 11937225 11937225 deletion of <=200bp A - intron_variant BRCA-EU 11 11937225 11937225 insertion of <=200bp - A intron_variant BRCA-EU 11 11941515 11941515 deletion of <=200bp T - intron_variant BRCA-EU 11 11942092 11942092 single base substitution C G intron_variant BRCA-EU 11 11942934 11942934 single base substitution A C intron_variant BRCA-EU 11 11943429 11943429 single base substitution T C intron_variant BRCA-EU 11 11944858 11944858 insertion of <=200bp - TT intron_variant BRCA-EU 11 11946077 11946077 single base substitution T A intron_variant BRCA-EU 11 11946210 11946210 single base substitution C G intron_variant BRCA-EU 11 11946448 11946448 single base substitution T A intron_variant BRCA-EU 11 11947055 11947061 deletion of <=200bp TTCTTAA - intron_variant BRCA-EU 11 11947126 11947126 single base substitution T A intron_variant BRCA-EU 11 11947332 11947332 single base substitution G A intron_variant BRCA-EU 11 11950036 11950068 deletion of <=200bp TCTACAATGCTTTTTAGGAAAAGAATAAAGAAG - intron_variant BRCA-EU 11 11950360 11950360 single base substitution C T intron_variant BRCA-EU 11 11950639 11950640 deletion of <=200bp TG - intron_variant BRCA-EU 11 11950946 11950946 single base substitution T A intron_variant BRCA-EU 11 11951632 11951632 single base substitution A G 5_prime_UTR_variant BRCA-EU 11 11951632 11951632 single base substitution A G synonymous_variant S452S 1356A>G BRCA-EU 11 11951632 11951632 single base substitution A G synonymous_variant S520S 1560A>G BRCA-EU 11 11951632 11951632 single base substitution A G synonymous_variant S540S 1620A>G BRCA-EU 11 11952132 11952132 single base substitution T C intron_variant BRCA-EU 11 11953444 11953444 single base substitution T A intron_variant BRCA-EU 11 11955659 11955659 single base substitution T C intron_variant BRCA-EU 11 11955659 11955659 single base substitution T C upstream_gene_variant BRCA-EU 11 11957022 11957022 single base substitution G T intron_variant BRCA-EU 11 11957022 11957022 single base substitution G T upstream_gene_variant BRCA-EU 11 11958122 11958122 single base substitution T A intron_variant BRCA-EU 11 11958122 11958122 single base substitution T A upstream_gene_variant BRCA-EU 11 11958585 11958585 single base substitution C G intron_variant BRCA-EU 11 11958585 11958585 single base substitution C G upstream_gene_variant BRCA-EU 11 11960261 11960261 single base substitution C T intron_variant BRCA-EU 11 11960261 11960261 single base substitution C T upstream_gene_variant BRCA-EU 11 11961261 11961261 single base substitution G C intron_variant BRCA-EU 11 11961261 11961261 single base substitution G C upstream_gene_variant BRCA-EU 11 11961876 11961876 single base substitution C G intron_variant BRCA-EU 11 11961876 11961876 single base substitution C G upstream_gene_variant BRCA-EU 11 11962321 11962321 single base substitution T C intron_variant BRCA-EU 11 11962321 11962321 single base substitution T C upstream_gene_variant BRCA-EU 11 11964871 11964871 deletion of <=200bp A - downstream_gene_variant BRCA-EU 11 11964871 11964871 deletion of <=200bp A - intron_variant BRCA-EU 11 11964871 11964871 deletion of <=200bp A - upstream_gene_variant BRCA-EU 11 11967319 11967319 deletion of <=200bp A - downstream_gene_variant BRCA-EU 11 11967319 11967319 deletion of <=200bp A - intron_variant BRCA-EU 11 11967319 11967319 deletion of <=200bp A - upstream_gene_variant BRCA-EU 11 11967616 11967616 single base substitution G C downstream_gene_variant BRCA-EU 11 11967616 11967616 single base substitution G C intron_variant BRCA-EU 11 11967616 11967616 single base substitution G C upstream_gene_variant BRCA-EU 11 11968471 11968471 single base substitution A G downstream_gene_variant BRCA-EU 11 11968471 11968471 single base substitution A G intron_variant BRCA-EU 11 11968471 11968471 single base substitution A G upstream_gene_variant BRCA-EU 11 11969122 11969122 single base substitution C T downstream_gene_variant BRCA-EU 11 11969122 11969122 single base substitution C T intron_variant BRCA-EU 11 11969122 11969122 single base substitution C T upstream_gene_variant BRCA-EU 11 11970331 11970331 single base substitution C T exon_variant BRCA-EU 11 11970331 11970331 single base substitution C T intron_variant BRCA-EU 11 11970331 11970331 single base substitution C T upstream_gene_variant BRCA-EU 11 11970980 11971002 deletion of <=200bp TCTCTTAATGTGACCCATTACAG - downstream_gene_variant BRCA-EU 11 11970980 11971002 deletion of <=200bp TCTCTTAATGTGACCCATTACAG - intron_variant BRCA-EU 11 11970980 11971002 deletion of <=200bp TCTCTTAATGTGACCCATTACAG - upstream_gene_variant BRCA-EU 11 11972973 11972976 deletion of <=200bp ACAT - downstream_gene_variant BRCA-EU 11 11972973 11972976 deletion of <=200bp ACAT - exon_variant BRCA-EU 11 11972973 11972976 deletion of <=200bp ACAT - intron_variant BRCA-EU 11 11973107 11973107 deletion of <=200bp T - downstream_gene_variant BRCA-EU 11 11973107 11973107 deletion of <=200bp T - exon_variant BRCA-EU 11 11973107 11973107 deletion of <=200bp T - intron_variant BRCA-EU 11 11973427 11973427 single base substitution C G downstream_gene_variant BRCA-EU 11 11973427 11973427 single base substitution C G exon_variant BRCA-EU 11 11973427 11973427 single base substitution C G intron_variant BRCA-EU 11 11975389 11975389 single base substitution G A downstream_gene_variant BRCA-EU 11 11975389 11975389 single base substitution G A intron_variant BRCA-EU 11 11975730 11975730 single base substitution G A downstream_gene_variant BRCA-EU 11 11975730 11975730 single base substitution G A intron_variant BRCA-EU 11 11977064 11977064 single base substitution C G downstream_gene_variant BRCA-EU 11 11977064 11977064 single base substitution C G intron_variant BRCA-EU 11 11978867 11978867 single base substitution A G 3_prime_UTR_variant BRCA-EU 11 11978867 11978867 single base substitution A G downstream_gene_variant BRCA-EU 11 11978867 11978867 single base substitution A G exon_variant BRCA-EU 11 11979032 11979032 single base substitution A G 3_prime_UTR_variant BRCA-EU 11 11979032 11979032 single base substitution A G downstream_gene_variant BRCA-EU 11 11979032 11979032 single base substitution A G exon_variant BRCA-EU 11 11981323 11981323 single base substitution C T downstream_gene_variant BRCA-EU 11 11982655 11982655 single base substitution G T downstream_gene_variant BRCA-EU 11 11982669 11982669 single base substitution C G downstream_gene_variant BRCA-FR 11 11858227 11858227 single base substitution G C upstream_gene_variant BRCA-FR 11 11866797 11866797 single base substitution C A intron_variant BRCA-FR 11 11869973 11869973 single base substitution A C intron_variant BRCA-FR 11 11873206 11873206 single base substitution T C intron_variant BRCA-FR 11 11874998 11874998 single base substitution T A intron_variant BRCA-FR 11 11875087 11875087 single base substitution A G intron_variant BRCA-FR 11 11920289 11920289 single base substitution G A intron_variant BRCA-FR 11 11922049 11922049 single base substitution C G intron_variant BRCA-FR 11 11927619 11927619 single base substitution C T intron_variant BRCA-FR 11 11928928 11928928 single base substitution G C intron_variant BRCA-FR 11 11933489 11933489 single base substitution C G intron_variant BRCA-FR 11 11936923 11936923 single base substitution G C intron_variant BRCA-FR 11 11947332 11947332 single base substitution G A intron_variant BRCA-FR 11 11967616 11967616 single base substitution G C downstream_gene_variant BRCA-FR 11 11967616 11967616 single base substitution G C intron_variant BRCA-FR 11 11967616 11967616 single base substitution G C upstream_gene_variant BRCA-FR 11 11968471 11968471 single base substitution A G downstream_gene_variant BRCA-FR 11 11968471 11968471 single base substitution A G intron_variant BRCA-FR 11 11968471 11968471 single base substitution A G upstream_gene_variant BRCA-FR 11 11973470 11973470 single base substitution T C downstream_gene_variant BRCA-FR 11 11973470 11973470 single base substitution T C exon_variant BRCA-FR 11 11973470 11973470 single base substitution T C intron_variant BRCA-FR 11 11984198 11984198 single base substitution C A downstream_gene_variant BRCA-KR 11 11976447 11976447 single base substitution A G downstream_gene_variant BRCA-KR 11 11976447 11976447 single base substitution A G exon_variant BRCA-KR 11 11976447 11976447 single base substitution A G missense_variant S1172G 3514A>G BRCA-KR 11 11976447 11976447 single base substitution A G missense_variant S1240G 3718A>G BRCA-KR 11 11976447 11976447 single base substitution A G missense_variant S1260G 3778A>G BRCA-KR 11 11976447 11976447 single base substitution A G missense_variant S42G 124A>G BRCA-UK 11 11876145 11876147 deletion of <=200bp ACA - intron_variant BRCA-UK 11 11882411 11882411 single base substitution G A intron_variant BRCA-UK 11 11919210 11919210 single base substitution T A 5_prime_UTR_variant BRCA-UK 11 11919210 11919210 single base substitution T A missense_variant M120K 359T>A BRCA-UK 11 11919210 11919210 single base substitution T A missense_variant M188K 563T>A BRCA-UK 11 11919210 11919210 single base substitution T A missense_variant M208K 623T>A BRCA-UK 11 11919236 11919236 single base substitution T C 5_prime_UTR_variant BRCA-UK 11 11919236 11919236 single base substitution T C missense_variant Y129H 385T>C BRCA-UK 11 11919236 11919236 single base substitution T C missense_variant Y197H 589T>C BRCA-UK 11 11919236 11919236 single base substitution T C missense_variant Y217H 649T>C BRCA-UK 11 11944286 11944286 single base substitution G C 5_prime_UTR_variant BRCA-UK 11 11944286 11944286 single base substitution G C missense_variant E344Q 1030G>C BRCA-UK 11 11944286 11944286 single base substitution G C missense_variant E412Q 1234G>C BRCA-UK 11 11944286 11944286 single base substitution G C missense_variant E432Q 1294G>C BRCA-UK 11 11944409 11944409 single base substitution G A 5_prime_UTR_variant BRCA-UK 11 11944409 11944409 single base substitution G A missense_variant E385K 1153G>A BRCA-UK 11 11944409 11944409 single base substitution G A missense_variant E453K 1357G>A BRCA-UK 11 11944409 11944409 single base substitution G A missense_variant E473K 1417G>A BRCA-UK 11 11950946 11950946 single base substitution T A intron_variant BRCA-UK 11 11978708 11978708 single base substitution A C 3_prime_UTR_variant BRCA-UK 11 11978708 11978708 single base substitution A C downstream_gene_variant BRCA-UK 11 11978708 11978708 single base substitution A C exon_variant BRCA-US 11 11895388 11895388 single base substitution G C intron_variant BRCA-US 11 11895388 11895388 single base substitution G C missense_variant M27I 81G>C BRCA-US 11 11951662 11951662 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-US 11 11951662 11951662 single base substitution C T synonymous_variant F462F 1386C>T BRCA-US 11 11951662 11951662 single base substitution C T synonymous_variant F530F 1590C>T BRCA-US 11 11951662 11951662 single base substitution C T synonymous_variant F550F 1650C>T BRCA-US 11 11962036 11962036 single base substitution C T 5_prime_UTR_variant BRCA-US 11 11962036 11962036 single base substitution C T exon_variant BRCA-US 11 11962036 11962036 single base substitution C T missense_variant R684C 2050C>T BRCA-US 11 11962036 11962036 single base substitution C T missense_variant R752C 2254C>T BRCA-US 11 11962036 11962036 single base substitution C T missense_variant R772C 2314C>T BRCA-US 11 11962036 11962036 single base substitution C T upstream_gene_variant BRCA-US 11 11964198 11964198 single base substitution G T 5_prime_UTR_variant BRCA-US 11 11964198 11964198 single base substitution G T exon_variant BRCA-US 11 11964198 11964198 single base substitution G T missense_variant S809I 2426G>T BRCA-US 11 11964198 11964198 single base substitution G T missense_variant S877I 2630G>T BRCA-US 11 11964198 11964198 single base substitution G T missense_variant S897I 2690G>T BRCA-US 11 11964198 11964198 single base substitution G T upstream_gene_variant BRCA-US 11 11964387 11964387 single base substitution A G 5_prime_UTR_variant BRCA-US 11 11964387 11964387 single base substitution A G exon_variant BRCA-US 11 11964387 11964387 single base substitution A G missense_variant D872G 2615A>G BRCA-US 11 11964387 11964387 single base substitution A G missense_variant D940G 2819A>G BRCA-US 11 11964387 11964387 single base substitution A G missense_variant D960G 2879A>G BRCA-US 11 11964387 11964387 single base substitution A G upstream_gene_variant BRCA-US 11 11977640 11977640 single base substitution G A downstream_gene_variant BRCA-US 11 11977640 11977640 single base substitution G A exon_variant BRCA-US 11 11977640 11977640 single base substitution G A missense_variant R1261H 3782G>A BRCA-US 11 11977640 11977640 single base substitution G A missense_variant R131H 392G>A BRCA-US 11 11977640 11977640 single base substitution G A missense_variant R1329H 3986G>A BRCA-US 11 11977640 11977640 single base substitution G A missense_variant R1349H 4046G>A BRCA-US 11 11979020 11979020 single base substitution C A 3_prime_UTR_variant BRCA-US 11 11979020 11979020 single base substitution C A downstream_gene_variant BRCA-US 11 11979020 11979020 single base substitution C A exon_variant BTCA-JP 11 11913705 11913705 single base substitution T G intron_variant BTCA-JP 11 11941881 11941881 deletion of <=200bp T - splice_region_variant BTCA-JP 11 11957890 11957890 single base substitution G A 5_prime_UTR_variant BTCA-JP 11 11957890 11957890 single base substitution G A missense_variant R569H 1706G>A BTCA-JP 11 11957890 11957890 single base substitution G A missense_variant R637H 1910G>A BTCA-JP 11 11957890 11957890 single base substitution G A missense_variant R657H 1970G>A BTCA-JP 11 11957890 11957890 single base substitution G A upstream_gene_variant BTCA-JP 11 11974519 11974519 single base substitution C T downstream_gene_variant BTCA-JP 11 11974519 11974519 single base substitution C T intron_variant CESC-US 11 11924287 11924287 single base substitution G C 5_prime_UTR_variant CESC-US 11 11924287 11924287 single base substitution G C missense_variant D139H 415G>C CESC-US 11 11924287 11924287 single base substitution G C missense_variant D207H 619G>C CESC-US 11 11924287 11924287 single base substitution G C missense_variant D227H 679G>C CESC-US 11 11962085 11962085 single base substitution G C 5_prime_UTR_variant CESC-US 11 11962085 11962085 single base substitution G C exon_variant CESC-US 11 11962085 11962085 single base substitution G C missense_variant R700T 2099G>C CESC-US 11 11962085 11962085 single base substitution G C missense_variant R768T 2303G>C CESC-US 11 11962085 11962085 single base substitution G C missense_variant R788T 2363G>C CESC-US 11 11962085 11962085 single base substitution G C upstream_gene_variant CESC-US 11 11964023 11964023 single base substitution A G 5_prime_UTR_variant CESC-US 11 11964023 11964023 single base substitution A G exon_variant CESC-US 11 11964023 11964023 single base substitution A G missense_variant R751G 2251A>G CESC-US 11 11964023 11964023 single base substitution A G missense_variant R819G 2455A>G CESC-US 11 11964023 11964023 single base substitution A G missense_variant R839G 2515A>G CESC-US 11 11964023 11964023 single base substitution A G upstream_gene_variant CLLE-ES 11 11868123 11868123 single base substitution A G intron_variant CLLE-ES 11 11880604 11880604 single base substitution A G intron_variant CLLE-ES 11 11896618 11896618 single base substitution G T intron_variant CLLE-ES 11 11897465 11897465 single base substitution A G intron_variant CLLE-ES 11 11897465 11897465 single base substitution A G upstream_gene_variant CLLE-ES 11 11914459 11914459 single base substitution T G intron_variant CLLE-ES 11 11942002 11942002 single base substitution G A 5_prime_UTR_variant CLLE-ES 11 11942002 11942002 single base substitution G A synonymous_variant E325E 975G>A CLLE-ES 11 11942002 11942002 single base substitution G A synonymous_variant E393E 1179G>A CLLE-ES 11 11942002 11942002 single base substitution G A synonymous_variant E413E 1239G>A CLLE-ES 11 11944573 11944573 single base substitution T C intron_variant CLLE-ES 11 11950062 11950062 single base substitution A G intron_variant CLLE-ES 11 11952312 11952312 single base substitution C A intron_variant CLLE-ES 11 11967451 11967451 single base substitution C T downstream_gene_variant CLLE-ES 11 11967451 11967451 single base substitution C T intron_variant CLLE-ES 11 11967451 11967451 single base substitution C T upstream_gene_variant CLLE-ES 11 11977165 11977166 deletion of <=200bp TC - downstream_gene_variant CLLE-ES 11 11977165 11977166 deletion of <=200bp TC - intron_variant COAD-US 11 11863744 11863744 single base substitution C T 5_prime_UTR_variant COAD-US 11 11863744 11863744 single base substitution C T exon_variant COAD-US 11 11863744 11863744 single base substitution C T synonymous_variant G4G 12C>T COAD-US 11 11913585 11913585 single base substitution G T 5_prime_UTR_variant COAD-US 11 11913585 11913585 single base substitution G T missense_variant G143V 428G>T COAD-US 11 11913585 11913585 single base substitution G T missense_variant G163V 488G>T COAD-US 11 11913585 11913585 single base substitution G T missense_variant G75V 224G>T COAD-US 11 11919204 11919204 single base substitution T G 5_prime_UTR_variant COAD-US 11 11919204 11919204 single base substitution T G missense_variant L118R 353T>G COAD-US 11 11919204 11919204 single base substitution T G missense_variant L186R 557T>G COAD-US 11 11919204 11919204 single base substitution T G missense_variant L206R 617T>G COAD-US 11 11941719 11941719 single base substitution C T 5_prime_UTR_variant COAD-US 11 11941719 11941719 single base substitution C T missense_variant A261V 782C>T COAD-US 11 11941719 11941719 single base substitution C T missense_variant A329V 986C>T COAD-US 11 11941719 11941719 single base substitution C T missense_variant A349V 1046C>T COAD-US 11 11957978 11957978 single base substitution C T 5_prime_UTR_variant COAD-US 11 11957978 11957978 single base substitution C T synonymous_variant G598G 1794C>T COAD-US 11 11957978 11957978 single base substitution C T synonymous_variant G666G 1998C>T COAD-US 11 11957978 11957978 single base substitution C T synonymous_variant G686G 2058C>T COAD-US 11 11957978 11957978 single base substitution C T upstream_gene_variant COAD-US 11 11964320 11964320 single base substitution T G 5_prime_UTR_premature_start_codon_gain_variant COAD-US 11 11964320 11964320 single base substitution T G exon_variant COAD-US 11 11964320 11964320 single base substitution T G missense_variant F850V 2548T>G COAD-US 11 11964320 11964320 single base substitution T G missense_variant F918V 2752T>G COAD-US 11 11964320 11964320 single base substitution T G missense_variant F938V 2812T>G COAD-US 11 11964320 11964320 single base substitution T G upstream_gene_variant COAD-US 11 11970052 11970052 deletion of <=200bp A - 5_prime_UTR_variant COAD-US 11 11970052 11970052 deletion of <=200bp A - exon_variant COAD-US 11 11970052 11970052 deletion of <=200bp A - frameshift_variant K1031 COAD-US 11 11970052 11970052 deletion of <=200bp A - frameshift_variant K1099 COAD-US 11 11970052 11970052 deletion of <=200bp A - frameshift_variant K1119 COAD-US 11 11970052 11970052 deletion of <=200bp A - upstream_gene_variant COAD-US 11 11974328 11974328 single base substitution G A downstream_gene_variant COAD-US 11 11974328 11974328 single base substitution G A exon_variant COAD-US 11 11974328 11974328 single base substitution G A synonymous_variant L10L 30G>A COAD-US 11 11974328 11974328 single base substitution G A synonymous_variant L1140L 3420G>A COAD-US 11 11974328 11974328 single base substitution G A synonymous_variant L1208L 3624G>A COAD-US 11 11974328 11974328 single base substitution G A synonymous_variant L1228L 3684G>A COAD-US 11 11977548 11977548 single base substitution G T downstream_gene_variant COAD-US 11 11977548 11977548 single base substitution G T missense_variant R100S 300G>T COAD-US 11 11977548 11977548 single base substitution G T missense_variant R1230S 3690G>T COAD-US 11 11977548 11977548 single base substitution G T missense_variant R1298S 3894G>T COAD-US 11 11977548 11977548 single base substitution G T missense_variant R1318S 3954G>T COAD-US 11 11977548 11977548 single base substitution G T splice_region_variant COAD-US 11 11977678 11977678 single base substitution A G downstream_gene_variant COAD-US 11 11977678 11977678 single base substitution A G exon_variant COAD-US 11 11977678 11977678 single base substitution A G missense_variant I1274V 3820A>G COAD-US 11 11977678 11977678 single base substitution A G missense_variant I1342V 4024A>G COAD-US 11 11977678 11977678 single base substitution A G missense_variant I1362V 4084A>G COAD-US 11 11977678 11977678 single base substitution A G missense_variant I144V 430A>G COCA-CN 11 11863701 11863701 single base substitution G A 5_prime_UTR_variant COCA-CN 11 11863701 11863701 single base substitution G A exon_variant COCA-CN 11 11896586 11896586 single base substitution G A intron_variant COCA-CN 11 11896624 11896624 single base substitution G T intron_variant COCA-CN 11 11906052 11906052 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 11 11906052 11906052 single base substitution C T downstream_gene_variant COCA-CN 11 11906052 11906052 single base substitution C T exon_variant COCA-CN 11 11906052 11906052 single base substitution C T synonymous_variant D114D 342C>T COCA-CN 11 11906052 11906052 single base substitution C T synonymous_variant D26D 78C>T COCA-CN 11 11906052 11906052 single base substitution C T synonymous_variant D94D 282C>T COCA-CN 11 11947889 11947889 single base substitution G T intron_variant COCA-CN 11 11959869 11959869 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 11 11959869 11959869 single base substitution C T missense_variant R647C 1939C>T COCA-CN 11 11959869 11959869 single base substitution C T missense_variant R715C 2143C>T COCA-CN 11 11959869 11959869 single base substitution C T missense_variant R735C 2203C>T COCA-CN 11 11959869 11959869 single base substitution C T upstream_gene_variant COCA-CN 11 11964238 11964238 single base substitution A G 5_prime_UTR_variant COCA-CN 11 11964238 11964238 single base substitution A G exon_variant COCA-CN 11 11964238 11964238 single base substitution A G synonymous_variant S822S 2466A>G COCA-CN 11 11964238 11964238 single base substitution A G synonymous_variant S890S 2670A>G COCA-CN 11 11964238 11964238 single base substitution A G synonymous_variant S910S 2730A>G COCA-CN 11 11964238 11964238 single base substitution A G upstream_gene_variant COCA-CN 11 11964496 11964496 single base substitution G A 5_prime_UTR_variant COCA-CN 11 11964496 11964496 single base substitution G A exon_variant COCA-CN 11 11964496 11964496 single base substitution G A synonymous_variant T908T 2724G>A COCA-CN 11 11964496 11964496 single base substitution G A synonymous_variant T976T 2928G>A COCA-CN 11 11964496 11964496 single base substitution G A synonymous_variant T996T 2988G>A COCA-CN 11 11964496 11964496 single base substitution G A upstream_gene_variant COCA-CN 11 11969484 11969484 single base substitution G T downstream_gene_variant COCA-CN 11 11969484 11969484 single base substitution G T splice_region_variant COCA-CN 11 11969484 11969484 single base substitution G T upstream_gene_variant COCA-CN 11 11969971 11969971 single base substitution G A intron_variant COCA-CN 11 11969971 11969971 single base substitution G A upstream_gene_variant COCA-CN 11 11976487 11976487 single base substitution C T downstream_gene_variant COCA-CN 11 11976487 11976487 single base substitution C T exon_variant COCA-CN 11 11976487 11976487 single base substitution C T missense_variant A1185V 3554C>T COCA-CN 11 11976487 11976487 single base substitution C T missense_variant A1253V 3758C>T COCA-CN 11 11976487 11976487 single base substitution C T missense_variant A1273V 3818C>T COCA-CN 11 11976487 11976487 single base substitution C T missense_variant A55V 164C>T COCA-CN 11 11983434 11983434 single base substitution C A downstream_gene_variant EOPC-DE 11 11864245 11864245 single base substitution C T intron_variant EOPC-DE 11 11882672 11882672 single base substitution C T intron_variant EOPC-DE 11 11913784 11913784 single base substitution C G intron_variant EOPC-DE 11 11937184 11937184 single base substitution C T intron_variant ESAD-UK 11 11859644 11859644 single base substitution A T upstream_gene_variant ESAD-UK 11 11860114 11860114 single base substitution G C upstream_gene_variant ESAD-UK 11 11861702 11861702 deletion of <=200bp G - upstream_gene_variant ESAD-UK 11 11863121 11863121 single base substitution G C 5_prime_UTR_variant ESAD-UK 11 11863121 11863121 single base substitution G C upstream_gene_variant ESAD-UK 11 11864143 11864143 single base substitution T C intron_variant ESAD-UK 11 11865449 11865452 deletion of <=200bp CTTT - intron_variant ESAD-UK 11 11868837 11868837 single base substitution T G intron_variant ESAD-UK 11 11869923 11869923 single base substitution C T intron_variant ESAD-UK 11 11870608 11870608 single base substitution C T intron_variant ESAD-UK 11 11877577 11877577 single base substitution A G intron_variant ESAD-UK 11 11877797 11877797 single base substitution A T intron_variant ESAD-UK 11 11877850 11877850 single base substitution C G intron_variant ESAD-UK 11 11880105 11880105 single base substitution C G intron_variant ESAD-UK 11 11882297 11882297 single base substitution G C intron_variant ESAD-UK 11 11885891 11885891 insertion of <=200bp - A intron_variant ESAD-UK 11 11886315 11886315 single base substitution T G intron_variant ESAD-UK 11 11888102 11888102 single base substitution G T intron_variant ESAD-UK 11 11890095 11890095 single base substitution G A intron_variant ESAD-UK 11 11891857 11891857 single base substitution A C intron_variant ESAD-UK 11 11894025 11894025 single base substitution G C intron_variant ESAD-UK 11 11895632 11895632 single base substitution A G intron_variant ESAD-UK 11 11896862 11896862 single base substitution G A intron_variant ESAD-UK 11 11896862 11896862 single base substitution G A upstream_gene_variant ESAD-UK 11 11899933 11899933 single base substitution C T intron_variant ESAD-UK 11 11899933 11899933 single base substitution C T upstream_gene_variant ESAD-UK 11 11900702 11900702 single base substitution T G intron_variant ESAD-UK 11 11900702 11900702 single base substitution T G upstream_gene_variant ESAD-UK 11 11901298 11901298 single base substitution A T intron_variant ESAD-UK 11 11901298 11901298 single base substitution A T upstream_gene_variant ESAD-UK 11 11907984 11907984 single base substitution T C downstream_gene_variant ESAD-UK 11 11907984 11907984 single base substitution T C intron_variant ESAD-UK 11 11912919 11912919 single base substitution C A intron_variant ESAD-UK 11 11915235 11915235 single base substitution G T intron_variant ESAD-UK 11 11915949 11915949 single base substitution G A intron_variant ESAD-UK 11 11919085 11919085 single base substitution G A intron_variant ESAD-UK 11 11922809 11922809 single base substitution A G intron_variant ESAD-UK 11 11923399 11923399 single base substitution G A intron_variant ESAD-UK 11 11923618 11923618 single base substitution C T intron_variant ESAD-UK 11 11924671 11924671 single base substitution G A intron_variant ESAD-UK 11 11930797 11930797 single base substitution T A intron_variant ESAD-UK 11 11932277 11932277 single base substitution C T intron_variant ESAD-UK 11 11936396 11936396 single base substitution T C intron_variant ESAD-UK 11 11936950 11936950 single base substitution G A intron_variant ESAD-UK 11 11937530 11937530 insertion of <=200bp - A intron_variant ESAD-UK 11 11941108 11941108 single base substitution C G intron_variant ESAD-UK 11 11944421 11944421 single base substitution A G 5_prime_UTR_variant ESAD-UK 11 11944421 11944421 single base substitution A G missense_variant K389E 1165A>G ESAD-UK 11 11944421 11944421 single base substitution A G missense_variant K457E 1369A>G ESAD-UK 11 11944421 11944421 single base substitution A G missense_variant K477E 1429A>G ESAD-UK 11 11955331 11955331 single base substitution T G intron_variant ESAD-UK 11 11955331 11955331 single base substitution T G upstream_gene_variant ESAD-UK 11 11956727 11956727 single base substitution T A intron_variant ESAD-UK 11 11956727 11956727 single base substitution T A upstream_gene_variant ESAD-UK 11 11963368 11963368 single base substitution A C intron_variant ESAD-UK 11 11963368 11963368 single base substitution A C upstream_gene_variant ESAD-UK 11 11963972 11963972 single base substitution A G 5_prime_UTR_variant ESAD-UK 11 11963972 11963972 single base substitution A G exon_variant ESAD-UK 11 11963972 11963972 single base substitution A G missense_variant I734V 2200A>G ESAD-UK 11 11963972 11963972 single base substitution A G missense_variant I802V 2404A>G ESAD-UK 11 11963972 11963972 single base substitution A G missense_variant I822V 2464A>G ESAD-UK 11 11963972 11963972 single base substitution A G upstream_gene_variant ESAD-UK 11 11965125 11965125 single base substitution C T downstream_gene_variant ESAD-UK 11 11965125 11965125 single base substitution C T exon_variant ESAD-UK 11 11965125 11965125 single base substitution C T intron_variant ESAD-UK 11 11965125 11965125 single base substitution C T upstream_gene_variant ESAD-UK 11 11966294 11966296 deletion of <=200bp TAG - downstream_gene_variant ESAD-UK 11 11966294 11966296 deletion of <=200bp TAG - intron_variant ESAD-UK 11 11966294 11966296 deletion of <=200bp TAG - upstream_gene_variant ESAD-UK 11 11968599 11968599 single base substitution C T downstream_gene_variant ESAD-UK 11 11968599 11968599 single base substitution C T intron_variant ESAD-UK 11 11968599 11968599 single base substitution C T upstream_gene_variant ESAD-UK 11 11973487 11973487 single base substitution G A downstream_gene_variant ESAD-UK 11 11973487 11973487 single base substitution G A exon_variant ESAD-UK 11 11973487 11973487 single base substitution G A intron_variant ESAD-UK 11 11975557 11975557 single base substitution G T downstream_gene_variant ESAD-UK 11 11975557 11975557 single base substitution G T intron_variant ESAD-UK 11 11975634 11975634 single base substitution T G downstream_gene_variant ESAD-UK 11 11975634 11975634 single base substitution T G intron_variant ESAD-UK 11 11977282 11977282 single base substitution C T downstream_gene_variant ESAD-UK 11 11977282 11977282 single base substitution C T intron_variant ESAD-UK 11 11977898 11977898 single base substitution C T 3_prime_UTR_variant ESAD-UK 11 11977898 11977898 single base substitution C T downstream_gene_variant ESAD-UK 11 11977898 11977898 single base substitution C T exon_variant ESAD-UK 11 11981571 11981571 single base substitution C A downstream_gene_variant ESAD-UK 11 11981858 11981858 single base substitution C G downstream_gene_variant ESAD-UK 11 11982639 11982639 single base substitution G A downstream_gene_variant ESAD-UK 11 11984598 11984598 single base substitution G A downstream_gene_variant ESCA-CN 11 11955416 11955416 single base substitution G C 5_prime_UTR_variant ESCA-CN 11 11955416 11955416 single base substitution G C missense_variant M533I 1599G>C ESCA-CN 11 11955416 11955416 single base substitution G C missense_variant M601I 1803G>C ESCA-CN 11 11955416 11955416 single base substitution G C missense_variant M621I 1863G>C ESCA-CN 11 11955416 11955416 single base substitution G C upstream_gene_variant GBM-US 11 11969542 11969542 single base substitution C T 5_prime_UTR_variant GBM-US 11 11969542 11969542 single base substitution C T downstream_gene_variant GBM-US 11 11969542 11969542 single base substitution C T exon_variant GBM-US 11 11969542 11969542 single base substitution C T missense_variant H1048Y 3142C>T GBM-US 11 11969542 11969542 single base substitution C T missense_variant H1068Y 3202C>T GBM-US 11 11969542 11969542 single base substitution C T missense_variant H980Y 2938C>T GBM-US 11 11969542 11969542 single base substitution C T upstream_gene_variant KIRC-US 11 11964635 11964635 single base substitution G A 5_prime_UTR_variant KIRC-US 11 11964635 11964635 single base substitution G A exon_variant KIRC-US 11 11964635 11964635 single base substitution G A missense_variant E1023K 3067G>A KIRC-US 11 11964635 11964635 single base substitution G A missense_variant E1043K 3127G>A KIRC-US 11 11964635 11964635 single base substitution G A missense_variant E955K 2863G>A KIRC-US 11 11964635 11964635 single base substitution G A upstream_gene_variant KIRP-US 11 11941997 11941997 single base substitution C T 5_prime_UTR_variant KIRP-US 11 11941997 11941997 single base substitution C T missense_variant P324S 970C>T KIRP-US 11 11941997 11941997 single base substitution C T missense_variant P392S 1174C>T KIRP-US 11 11941997 11941997 single base substitution C T missense_variant P412S 1234C>T KIRP-US 11 11942036 11942036 single base substitution G T 5_prime_UTR_variant KIRP-US 11 11942036 11942036 single base substitution G T missense_variant D337Y 1009G>T KIRP-US 11 11942036 11942036 single base substitution G T missense_variant D405Y 1213G>T KIRP-US 11 11942036 11942036 single base substitution G T missense_variant D425Y 1273G>T LAML-KR 11 11976628 11976628 single base substitution G A downstream_gene_variant LAML-KR 11 11976628 11976628 single base substitution G A exon_variant LAML-KR 11 11976628 11976628 single base substitution G A synonymous_variant Q1202Q 3606G>A LAML-KR 11 11976628 11976628 single base substitution G A synonymous_variant Q1270Q 3810G>A LAML-KR 11 11976628 11976628 single base substitution G A synonymous_variant Q1290Q 3870G>A LAML-KR 11 11976628 11976628 single base substitution G A synonymous_variant Q72Q 216G>A LICA-CN 11 11970067 11970067 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant LICA-CN 11 11970067 11970067 single base substitution A T exon_variant LICA-CN 11 11970067 11970067 single base substitution A T stop_gained R1036* 3106A>T LICA-CN 11 11970067 11970067 single base substitution A T stop_gained R1104* 3310A>T LICA-CN 11 11970067 11970067 single base substitution A T stop_gained R1124* 3370A>T LICA-CN 11 11970067 11970067 single base substitution A T upstream_gene_variant LICA-FR 11 11859422 11859422 single base substitution T C upstream_gene_variant LICA-FR 11 11888431 11888431 single base substitution T G intron_variant LICA-FR 11 11899762 11899762 single base substitution T G intron_variant LICA-FR 11 11899762 11899762 single base substitution T G upstream_gene_variant LICA-FR 11 11971500 11971500 single base substitution A T 5_prime_UTR_variant LICA-FR 11 11971500 11971500 single base substitution A T downstream_gene_variant LICA-FR 11 11971500 11971500 single base substitution A T exon_variant LICA-FR 11 11971500 11971500 single base substitution A T missense_variant E1070V 3209A>T LICA-FR 11 11971500 11971500 single base substitution A T missense_variant E1138V 3413A>T LICA-FR 11 11971500 11971500 single base substitution A T missense_variant E1158V 3473A>T LICA-FR 11 11971500 11971500 single base substitution A T upstream_gene_variant LIHC-US 11 11927068 11927068 single base substitution T C 5_prime_UTR_variant LIHC-US 11 11927068 11927068 single base substitution T C synonymous_variant Y246Y 738T>C LIHC-US 11 11927068 11927068 single base substitution T C synonymous_variant Y314Y 942T>C LIHC-US 11 11927068 11927068 single base substitution T C synonymous_variant Y334Y 1002T>C LIHC-US 11 11941963 11941963 single base substitution G A 5_prime_UTR_variant LIHC-US 11 11941963 11941963 single base substitution G A missense_variant M312I 936G>A LIHC-US 11 11941963 11941963 single base substitution G A missense_variant M380I 1140G>A LIHC-US 11 11941963 11941963 single base substitution G A missense_variant M400I 1200G>A LIHC-US 11 11963990 11963990 single base substitution C G 5_prime_UTR_variant LIHC-US 11 11963990 11963990 single base substitution C G exon_variant LIHC-US 11 11963990 11963990 single base substitution C G missense_variant L740V 2218C>G LIHC-US 11 11963990 11963990 single base substitution C G missense_variant L808V 2422C>G LIHC-US 11 11963990 11963990 single base substitution C G missense_variant L828V 2482C>G LIHC-US 11 11963990 11963990 single base substitution C G upstream_gene_variant LIHC-US 11 11964527 11964527 single base substitution G T 5_prime_UTR_variant LIHC-US 11 11964527 11964527 single base substitution G T exon_variant LIHC-US 11 11964527 11964527 single base substitution G T missense_variant D1007Y 3019G>T LIHC-US 11 11964527 11964527 single base substitution G T missense_variant D919Y 2755G>T LIHC-US 11 11964527 11964527 single base substitution G T missense_variant D987Y 2959G>T LIHC-US 11 11964527 11964527 single base substitution G T upstream_gene_variant LINC-JP 11 11876156 11876156 single base substitution A T intron_variant LINC-JP 11 11877716 11877716 single base substitution A G intron_variant LINC-JP 11 11895475 11895475 single base substitution A G intron_variant LINC-JP 11 11895901 11895901 single base substitution A G intron_variant LINC-JP 11 11896843 11896843 single base substitution C A intron_variant LINC-JP 11 11896843 11896843 single base substitution C A upstream_gene_variant LINC-JP 11 11918167 11918167 single base substitution G T intron_variant LINC-JP 11 11933456 11933456 single base substitution A G intron_variant LINC-JP 11 11934047 11934047 single base substitution A G intron_variant LINC-JP 11 11938164 11938164 single base substitution A G intron_variant LINC-JP 11 11942009 11942009 single base substitution G C 5_prime_UTR_variant LINC-JP 11 11942009 11942009 single base substitution G C missense_variant D328H 982G>C LINC-JP 11 11942009 11942009 single base substitution G C missense_variant D396H 1186G>C LINC-JP 11 11942009 11942009 single base substitution G C missense_variant D416H 1246G>C LINC-JP 11 11951727 11951727 deletion of <=200bp T - intron_variant LINC-JP 11 11952058 11952058 single base substitution A C intron_variant LINC-JP 11 11952269 11952269 single base substitution A G 5_prime_UTR_premature_start_codon_gain_variant LINC-JP 11 11952269 11952269 single base substitution A G missense_variant Y473C 1418A>G LINC-JP 11 11952269 11952269 single base substitution A G missense_variant Y541C 1622A>G LINC-JP 11 11952269 11952269 single base substitution A G missense_variant Y561C 1682A>G LINC-JP 11 11957930 11957930 single base substitution G T 5_prime_UTR_variant LINC-JP 11 11957930 11957930 single base substitution G T synonymous_variant R582R 1746G>T LINC-JP 11 11957930 11957930 single base substitution G T synonymous_variant R650R 1950G>T LINC-JP 11 11957930 11957930 single base substitution G T synonymous_variant R670R 2010G>T LINC-JP 11 11957930 11957930 single base substitution G T upstream_gene_variant LINC-JP 11 11967488 11967488 single base substitution A C downstream_gene_variant LINC-JP 11 11967488 11967488 single base substitution A C intron_variant LINC-JP 11 11967488 11967488 single base substitution A C upstream_gene_variant LINC-JP 11 11968902 11968902 single base substitution A G downstream_gene_variant LINC-JP 11 11968902 11968902 single base substitution A G intron_variant LINC-JP 11 11968902 11968902 single base substitution A G upstream_gene_variant LINC-JP 11 11970175 11970175 single base substitution T C exon_variant LINC-JP 11 11970175 11970175 single base substitution T C intron_variant LINC-JP 11 11970175 11970175 single base substitution T C upstream_gene_variant LINC-JP 11 11971171 11971171 single base substitution T C downstream_gene_variant LINC-JP 11 11971171 11971171 single base substitution T C intron_variant LINC-JP 11 11971171 11971171 single base substitution T C upstream_gene_variant LINC-JP 11 11971176 11971176 single base substitution T C downstream_gene_variant LINC-JP 11 11971176 11971176 single base substitution T C intron_variant LINC-JP 11 11971176 11971176 single base substitution T C upstream_gene_variant LINC-JP 11 11976340 11976340 single base substitution A G downstream_gene_variant LINC-JP 11 11976340 11976340 single base substitution A G intron_variant LINC-JP 11 11985522 11985522 single base substitution A G downstream_gene_variant LIRI-JP 11 11859276 11859276 single base substitution A G upstream_gene_variant LIRI-JP 11 11862781 11862781 single base substitution C G upstream_gene_variant LIRI-JP 11 11864922 11864922 insertion of <=200bp - A intron_variant LIRI-JP 11 11865139 11865139 single base substitution A G intron_variant LIRI-JP 11 11866302 11866302 single base substitution A G intron_variant LIRI-JP 11 11866554 11866554 single base substitution C T intron_variant LIRI-JP 11 11867219 11867219 single base substitution G A intron_variant LIRI-JP 11 11867916 11867916 single base substitution T C intron_variant LIRI-JP 11 11868052 11868052 single base substitution A G intron_variant LIRI-JP 11 11868389 11868389 single base substitution G A intron_variant LIRI-JP 11 11869777 11869777 single base substitution A G intron_variant LIRI-JP 11 11872980 11872980 single base substitution A C intron_variant LIRI-JP 11 11873887 11873887 single base substitution T C intron_variant LIRI-JP 11 11873892 11873892 single base substitution A G intron_variant LIRI-JP 11 11878765 11878766 deletion of <=200bp TA - intron_variant LIRI-JP 11 11883824 11883824 single base substitution A G intron_variant LIRI-JP 11 11884928 11884928 single base substitution A G intron_variant LIRI-JP 11 11886092 11886092 single base substitution C G intron_variant LIRI-JP 11 11886917 11886917 single base substitution C T intron_variant LIRI-JP 11 11887945 11887945 single base substitution A G intron_variant LIRI-JP 11 11892455 11892455 single base substitution A G intron_variant LIRI-JP 11 11895688 11895688 single base substitution A G intron_variant LIRI-JP 11 11896097 11896097 single base substitution A G intron_variant LIRI-JP 11 11896231 11896231 single base substitution G A intron_variant LIRI-JP 11 11900133 11900133 single base substitution T C intron_variant LIRI-JP 11 11900133 11900133 single base substitution T C upstream_gene_variant LIRI-JP 11 11900442 11900442 single base substitution A G intron_variant LIRI-JP 11 11900442 11900442 single base substitution A G upstream_gene_variant LIRI-JP 11 11900698 11900698 single base substitution A G intron_variant LIRI-JP 11 11900698 11900698 single base substitution A G upstream_gene_variant LIRI-JP 11 11901085 11901085 single base substitution A G intron_variant LIRI-JP 11 11901085 11901085 single base substitution A G upstream_gene_variant LIRI-JP 11 11904870 11904870 single base substitution A G intron_variant LIRI-JP 11 11906408 11906408 single base substitution G T downstream_gene_variant LIRI-JP 11 11906408 11906408 single base substitution G T intron_variant LIRI-JP 11 11907955 11907955 single base substitution T A downstream_gene_variant LIRI-JP 11 11907955 11907955 single base substitution T A intron_variant LIRI-JP 11 11908615 11908615 single base substitution A T downstream_gene_variant LIRI-JP 11 11908615 11908615 single base substitution A T intron_variant LIRI-JP 11 11909484 11909484 single base substitution A G downstream_gene_variant LIRI-JP 11 11909484 11909484 single base substitution A G intron_variant LIRI-JP 11 11912221 11912221 single base substitution G T intron_variant LIRI-JP 11 11912255 11912255 single base substitution C G intron_variant LIRI-JP 11 11912366 11912366 single base substitution A G intron_variant LIRI-JP 11 11914487 11914487 single base substitution C T intron_variant LIRI-JP 11 11916406 11916406 single base substitution A G intron_variant LIRI-JP 11 11917455 11917455 single base substitution C T intron_variant LIRI-JP 11 11920846 11920846 single base substitution A G intron_variant LIRI-JP 11 11921254 11921254 single base substitution A G intron_variant LIRI-JP 11 11922538 11922538 single base substitution A G intron_variant LIRI-JP 11 11923543 11923543 single base substitution A G intron_variant LIRI-JP 11 11926322 11926322 single base substitution A G intron_variant LIRI-JP 11 11926685 11926685 single base substitution A G intron_variant LIRI-JP 11 11927179 11927179 single base substitution A G intron_variant LIRI-JP 11 11929029 11929029 single base substitution A G intron_variant LIRI-JP 11 11929540 11929540 single base substitution C T intron_variant LIRI-JP 11 11929732 11929732 single base substitution A G intron_variant LIRI-JP 11 11930480 11930480 single base substitution A G intron_variant LIRI-JP 11 11930905 11930905 single base substitution A G intron_variant LIRI-JP 11 11931141 11931141 single base substitution A G intron_variant LIRI-JP 11 11931480 11931480 single base substitution C T intron_variant LIRI-JP 11 11931993 11931993 single base substitution C G intron_variant LIRI-JP 11 11933563 11933563 single base substitution A G intron_variant LIRI-JP 11 11935594 11935594 single base substitution A G intron_variant LIRI-JP 11 11936056 11936056 single base substitution C T intron_variant LIRI-JP 11 11937267 11937282 deletion of <=200bp TCCTAGTTAAAAAGTA - intron_variant LIRI-JP 11 11945061 11945061 single base substitution T A intron_variant LIRI-JP 11 11946091 11946091 single base substitution A C intron_variant LIRI-JP 11 11946382 11946382 single base substitution A G intron_variant LIRI-JP 11 11946754 11946754 single base substitution A G intron_variant LIRI-JP 11 11948879 11948879 single base substitution A G intron_variant LIRI-JP 11 11948939 11948939 single base substitution A G intron_variant LIRI-JP 11 11950062 11950062 single base substitution A G intron_variant LIRI-JP 11 11951553 11951553 single base substitution A G intron_variant LIRI-JP 11 11952650 11952650 single base substitution G A intron_variant LIRI-JP 11 11955271 11955271 single base substitution G A intron_variant LIRI-JP 11 11955271 11955271 single base substitution G A upstream_gene_variant LIRI-JP 11 11955298 11955298 single base substitution A G intron_variant LIRI-JP 11 11955298 11955298 single base substitution A G upstream_gene_variant LIRI-JP 11 11957010 11957010 single base substitution C T intron_variant LIRI-JP 11 11957010 11957010 single base substitution C T upstream_gene_variant LIRI-JP 11 11957215 11957215 single base substitution A G intron_variant LIRI-JP 11 11957215 11957215 single base substitution A G upstream_gene_variant LIRI-JP 11 11957864 11957864 single base substitution A G 5_prime_UTR_variant LIRI-JP 11 11957864 11957864 single base substitution A G synonymous_variant E560E 1680A>G LIRI-JP 11 11957864 11957864 single base substitution A G synonymous_variant E628E 1884A>G LIRI-JP 11 11957864 11957864 single base substitution A G synonymous_variant E648E 1944A>G LIRI-JP 11 11957864 11957864 single base substitution A G upstream_gene_variant LIRI-JP 11 11959237 11959237 single base substitution A G intron_variant LIRI-JP 11 11959237 11959237 single base substitution A G upstream_gene_variant LIRI-JP 11 11961623 11961623 single base substitution C G intron_variant LIRI-JP 11 11961623 11961623 single base substitution C G upstream_gene_variant LIRI-JP 11 11963198 11963198 single base substitution T A intron_variant LIRI-JP 11 11963198 11963198 single base substitution T A upstream_gene_variant LIRI-JP 11 11963223 11963223 single base substitution G T intron_variant LIRI-JP 11 11963223 11963223 single base substitution G T upstream_gene_variant LIRI-JP 11 11965872 11965872 single base substitution A G downstream_gene_variant LIRI-JP 11 11965872 11965872 single base substitution A G intron_variant LIRI-JP 11 11965872 11965872 single base substitution A G upstream_gene_variant LIRI-JP 11 11966237 11966237 single base substitution G C downstream_gene_variant LIRI-JP 11 11966237 11966237 single base substitution G C intron_variant LIRI-JP 11 11966237 11966237 single base substitution G C upstream_gene_variant LIRI-JP 11 11968375 11968375 single base substitution C A downstream_gene_variant LIRI-JP 11 11968375 11968375 single base substitution C A intron_variant LIRI-JP 11 11968375 11968375 single base substitution C A upstream_gene_variant LIRI-JP 11 11969102 11969102 single base substitution G A downstream_gene_variant LIRI-JP 11 11969102 11969102 single base substitution G A intron_variant LIRI-JP 11 11969102 11969102 single base substitution G A upstream_gene_variant LIRI-JP 11 11971115 11971139 deletion of <=200bp TGGTTCTTTTTGCTTTCAAAATTAT - downstream_gene_variant LIRI-JP 11 11971115 11971139 deletion of <=200bp TGGTTCTTTTTGCTTTCAAAATTAT - intron_variant LIRI-JP 11 11971115 11971139 deletion of <=200bp TGGTTCTTTTTGCTTTCAAAATTAT - upstream_gene_variant LIRI-JP 11 11971269 11971269 single base substitution C G downstream_gene_variant LIRI-JP 11 11971269 11971269 single base substitution C G intron_variant LIRI-JP 11 11971269 11971269 single base substitution C G upstream_gene_variant LIRI-JP 11 11974924 11974924 single base substitution A G downstream_gene_variant LIRI-JP 11 11974924 11974924 single base substitution A G intron_variant LIRI-JP 11 11974952 11974952 single base substitution A G downstream_gene_variant LIRI-JP 11 11974952 11974952 single base substitution A G intron_variant LIRI-JP 11 11975099 11975099 single base substitution A G downstream_gene_variant LIRI-JP 11 11975099 11975099 single base substitution A G intron_variant LIRI-JP 11 11978224 11978224 single base substitution A T 3_prime_UTR_variant LIRI-JP 11 11978224 11978224 single base substitution A T downstream_gene_variant LIRI-JP 11 11978224 11978224 single base substitution A T exon_variant LIRI-JP 11 11978695 11978695 single base substitution G A 3_prime_UTR_variant LIRI-JP 11 11978695 11978695 single base substitution G A downstream_gene_variant LIRI-JP 11 11978695 11978695 single base substitution G A exon_variant LIRI-JP 11 11979126 11979126 single base substitution C T 3_prime_UTR_variant LIRI-JP 11 11979126 11979126 single base substitution C T downstream_gene_variant LIRI-JP 11 11979126 11979126 single base substitution C T exon_variant LIRI-JP 11 11983916 11983916 single base substitution A G downstream_gene_variant LIRI-JP 11 11984277 11984277 single base substitution C A downstream_gene_variant LIRI-JP 11 11985526 11985526 single base substitution G T downstream_gene_variant LUSC-KR 11 11863080 11863080 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant LUSC-KR 11 11863080 11863080 single base substitution G A upstream_gene_variant LUSC-KR 11 11866130 11866130 single base substitution A G intron_variant LUSC-KR 11 11879550 11879550 single base substitution A G intron_variant LUSC-KR 11 11887919 11887919 single base substitution C T intron_variant LUSC-KR 11 11899946 11899946 single base substitution A G intron_variant LUSC-KR 11 11899946 11899946 single base substitution A G upstream_gene_variant LUSC-KR 11 11902891 11902891 single base substitution G A intron_variant LUSC-KR 11 11915217 11915217 single base substitution G A intron_variant LUSC-KR 11 11915389 11915389 single base substitution T C intron_variant LUSC-KR 11 11916318 11916318 single base substitution T C intron_variant LUSC-KR 11 11920805 11920805 single base substitution A T intron_variant LUSC-KR 11 11922367 11922367 single base substitution A T intron_variant LUSC-KR 11 11925393 11925393 single base substitution G T intron_variant LUSC-KR 11 11926221 11926221 single base substitution A G intron_variant LUSC-KR 11 11926629 11926629 single base substitution C G intron_variant LUSC-KR 11 11929928 11929928 single base substitution C G intron_variant LUSC-KR 11 11936956 11936956 single base substitution G T intron_variant LUSC-KR 11 11942039 11942039 single base substitution G A missense_variant E338K 1012G>A LUSC-KR 11 11942039 11942039 single base substitution G A missense_variant E406K 1216G>A LUSC-KR 11 11942039 11942039 single base substitution G A missense_variant E426K 1276G>A LUSC-KR 11 11942039 11942039 single base substitution G A splice_region_variant LUSC-KR 11 11944347 11944347 single base substitution A G 5_prime_UTR_variant LUSC-KR 11 11944347 11944347 single base substitution A G missense_variant N364S 1091A>G LUSC-KR 11 11944347 11944347 single base substitution A G missense_variant N432S 1295A>G LUSC-KR 11 11944347 11944347 single base substitution A G missense_variant N452S 1355A>G LUSC-KR 11 11944505 11944505 single base substitution A G intron_variant LUSC-KR 11 11945705 11945705 single base substitution A G intron_variant LUSC-KR 11 11951492 11951492 single base substitution G A intron_variant LUSC-KR 11 11952434 11952434 single base substitution G A intron_variant LUSC-KR 11 11979592 11979592 single base substitution G A 3_prime_UTR_variant LUSC-KR 11 11979592 11979592 single base substitution G A downstream_gene_variant LUSC-KR 11 11979592 11979592 single base substitution G A exon_variant LUSC-KR 11 11979674 11979674 single base substitution A G 3_prime_UTR_variant LUSC-KR 11 11979674 11979674 single base substitution A G downstream_gene_variant LUSC-KR 11 11979674 11979674 single base substitution A G exon_variant LUSC-KR 11 11980449 11980449 single base substitution A G 3_prime_UTR_variant LUSC-KR 11 11980449 11980449 single base substitution A G downstream_gene_variant LUSC-KR 11 11980449 11980449 single base substitution A G exon_variant LUSC-KR 11 11984614 11984614 single base substitution C G downstream_gene_variant LUSC-KR 11 11985233 11985233 single base substitution T G downstream_gene_variant LUSC-US 11 11962033 11962033 single base substitution T G 5_prime_UTR_premature_start_codon_gain_variant LUSC-US 11 11962033 11962033 single base substitution T G exon_variant LUSC-US 11 11962033 11962033 single base substitution T G missense_variant L683V 2047T>G LUSC-US 11 11962033 11962033 single base substitution T G missense_variant L751V 2251T>G LUSC-US 11 11962033 11962033 single base substitution T G missense_variant L771V 2311T>G LUSC-US 11 11962033 11962033 single base substitution T G upstream_gene_variant LUSC-US 11 11964541 11964541 single base substitution A C 5_prime_UTR_variant LUSC-US 11 11964541 11964541 single base substitution A C exon_variant LUSC-US 11 11964541 11964541 single base substitution A C missense_variant E1011D 3033A>C LUSC-US 11 11964541 11964541 single base substitution A C missense_variant E923D 2769A>C LUSC-US 11 11964541 11964541 single base substitution A C missense_variant E991D 2973A>C LUSC-US 11 11964541 11964541 single base substitution A C upstream_gene_variant LUSC-US 11 11969555 11969555 single base substitution T G 5_prime_UTR_premature_start_codon_gain_variant LUSC-US 11 11969555 11969555 single base substitution T G downstream_gene_variant LUSC-US 11 11969555 11969555 single base substitution T G exon_variant LUSC-US 11 11969555 11969555 single base substitution T G missense_variant F1052C 3155T>G LUSC-US 11 11969555 11969555 single base substitution T G missense_variant F1072C 3215T>G LUSC-US 11 11969555 11969555 single base substitution T G missense_variant F984C 2951T>G LUSC-US 11 11969555 11969555 single base substitution T G upstream_gene_variant LUSC-US 11 11970068 11970068 single base substitution G C 5_prime_UTR_variant LUSC-US 11 11970068 11970068 single base substitution G C exon_variant LUSC-US 11 11970068 11970068 single base substitution G C missense_variant R1036T 3107G>C LUSC-US 11 11970068 11970068 single base substitution G C missense_variant R1104T 3311G>C LUSC-US 11 11970068 11970068 single base substitution G C missense_variant R1124T 3371G>C LUSC-US 11 11970068 11970068 single base substitution G C upstream_gene_variant LUSC-US 11 11977671 11977671 single base substitution A G downstream_gene_variant LUSC-US 11 11977671 11977671 single base substitution A G exon_variant LUSC-US 11 11977671 11977671 single base substitution A G synonymous_variant A1271A 3813A>G LUSC-US 11 11977671 11977671 single base substitution A G synonymous_variant A1339A 4017A>G LUSC-US 11 11977671 11977671 single base substitution A G synonymous_variant A1359A 4077A>G LUSC-US 11 11977671 11977671 single base substitution A G synonymous_variant A141A 423A>G MALY-DE 11 11858362 11858362 single base substitution C A upstream_gene_variant MALY-DE 11 11860209 11860209 single base substitution G T upstream_gene_variant MALY-DE 11 11867169 11867169 single base substitution T G intron_variant MALY-DE 11 11869112 11869112 single base substitution C T intron_variant MALY-DE 11 11872259 11872259 single base substitution A C intron_variant MALY-DE 11 11874355 11874355 single base substitution T G intron_variant MALY-DE 11 11875006 11875006 single base substitution G A intron_variant MALY-DE 11 11877011 11877011 single base substitution A C intron_variant MALY-DE 11 11883300 11883300 single base substitution C G intron_variant MALY-DE 11 11885709 11885709 single base substitution A G intron_variant MALY-DE 11 11899956 11899956 single base substitution G A intron_variant MALY-DE 11 11899956 11899956 single base substitution G A upstream_gene_variant MALY-DE 11 11901588 11901588 single base substitution C T intron_variant MALY-DE 11 11901588 11901588 single base substitution C T upstream_gene_variant MALY-DE 11 11903586 11903586 single base substitution T C intron_variant MALY-DE 11 11904026 11904026 single base substitution A G intron_variant MALY-DE 11 11909151 11909151 single base substitution T A downstream_gene_variant MALY-DE 11 11909151 11909151 single base substitution T A intron_variant MALY-DE 11 11909867 11909867 single base substitution T G downstream_gene_variant MALY-DE 11 11909867 11909867 single base substitution T G intron_variant MALY-DE 11 11919716 11919716 single base substitution C T intron_variant MALY-DE 11 11923841 11923841 single base substitution G T intron_variant MALY-DE 11 11930925 11930925 single base substitution G T intron_variant MALY-DE 11 11936541 11936541 single base substitution A G intron_variant MALY-DE 11 11936661 11936661 single base substitution G T intron_variant MALY-DE 11 11936820 11936820 single base substitution T C intron_variant MALY-DE 11 11950875 11950875 single base substitution A G intron_variant MALY-DE 11 11956810 11956810 single base substitution G C intron_variant MALY-DE 11 11956810 11956810 single base substitution G C upstream_gene_variant MALY-DE 11 11957933 11957933 single base substitution A G 5_prime_UTR_variant MALY-DE 11 11957933 11957933 single base substitution A G synonymous_variant S583S 1749A>G MALY-DE 11 11957933 11957933 single base substitution A G synonymous_variant S651S 1953A>G MALY-DE 11 11957933 11957933 single base substitution A G synonymous_variant S671S 2013A>G MALY-DE 11 11957933 11957933 single base substitution A G upstream_gene_variant MALY-DE 11 11962549 11962549 single base substitution T G intron_variant MALY-DE 11 11962549 11962549 single base substitution T G upstream_gene_variant MALY-DE 11 11975456 11975456 single base substitution G A downstream_gene_variant MALY-DE 11 11975456 11975456 single base substitution G A intron_variant MALY-DE 11 11985647 11985647 single base substitution A C downstream_gene_variant MELA-AU 11 11858074 11858074 single base substitution G A upstream_gene_variant MELA-AU 11 11858154 11858154 single base substitution G A upstream_gene_variant MELA-AU 11 11858227 11858227 single base substitution G A upstream_gene_variant MELA-AU 11 11858257 11858257 single base substitution G A upstream_gene_variant MELA-AU 11 11858388 11858388 single base substitution G A upstream_gene_variant MELA-AU 11 11858767 11858767 single base substitution G A upstream_gene_variant MELA-AU 11 11859368 11859368 single base substitution C T upstream_gene_variant MELA-AU 11 11859373 11859373 single base substitution G T upstream_gene_variant MELA-AU 11 11859598 11859598 single base substitution C T upstream_gene_variant MELA-AU 11 11859600 11859600 single base substitution C T upstream_gene_variant MELA-AU 11 11859719 11859719 single base substitution C T upstream_gene_variant MELA-AU 11 11860009 11860009 single base substitution C T upstream_gene_variant MELA-AU 11 11860250 11860250 single base substitution G A upstream_gene_variant MELA-AU 11 11860595 11860595 single base substitution G A upstream_gene_variant MELA-AU 11 11860973 11860973 single base substitution G A upstream_gene_variant MELA-AU 11 11861147 11861147 single base substitution G A upstream_gene_variant MELA-AU 11 11863106 11863106 single base substitution G A 5_prime_UTR_variant MELA-AU 11 11863106 11863106 single base substitution G A upstream_gene_variant MELA-AU 11 11863247 11863248 multiple base substitution (>=2bp and <=200bp) GG AA 5_prime_UTR_variant MELA-AU 11 11863247 11863248 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 11863269 11863269 single base substitution T C 5_prime_UTR_variant MELA-AU 11 11863269 11863269 single base substitution T C upstream_gene_variant MELA-AU 11 11863469 11863470 multiple base substitution (>=2bp and <=200bp) GG AA 5_prime_UTR_variant MELA-AU 11 11863469 11863470 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 11 11864295 11864295 single base substitution G A intron_variant MELA-AU 11 11864581 11864581 single base substitution T C intron_variant MELA-AU 11 11864873 11864873 single base substitution G A intron_variant MELA-AU 11 11864894 11864894 single base substitution G A intron_variant MELA-AU 11 11866231 11866231 single base substitution C T intron_variant MELA-AU 11 11867142 11867142 single base substitution T G intron_variant MELA-AU 11 11867471 11867471 single base substitution G A intron_variant MELA-AU 11 11868276 11868276 deletion of <=200bp A - intron_variant MELA-AU 11 11868974 11868974 single base substitution C T intron_variant MELA-AU 11 11870025 11870025 single base substitution C G intron_variant MELA-AU 11 11870854 11870854 single base substitution C T intron_variant MELA-AU 11 11871529 11871529 single base substitution C T intron_variant MELA-AU 11 11871709 11871709 single base substitution A T intron_variant MELA-AU 11 11872920 11872920 single base substitution T C intron_variant MELA-AU 11 11872955 11872955 single base substitution C T intron_variant MELA-AU 11 11875475 11875475 single base substitution C T intron_variant MELA-AU 11 11875775 11875775 single base substitution C T intron_variant MELA-AU 11 11875894 11875894 single base substitution C T intron_variant MELA-AU 11 11876006 11876011 deletion of <=200bp TGAGTT - intron_variant MELA-AU 11 11877768 11877768 single base substitution C T intron_variant MELA-AU 11 11878102 11878102 single base substitution G A intron_variant MELA-AU 11 11878862 11878862 single base substitution T A intron_variant MELA-AU 11 11879129 11879129 single base substitution T G intron_variant MELA-AU 11 11879629 11879629 single base substitution C T intron_variant MELA-AU 11 11879720 11879720 single base substitution C T intron_variant MELA-AU 11 11881535 11881535 single base substitution C T intron_variant MELA-AU 11 11881726 11881726 single base substitution C T intron_variant MELA-AU 11 11884066 11884066 single base substitution C T intron_variant MELA-AU 11 11884611 11884611 single base substitution G A intron_variant MELA-AU 11 11884948 11884948 single base substitution C T intron_variant MELA-AU 11 11885104 11885104 single base substitution G A intron_variant MELA-AU 11 11885971 11885971 single base substitution G A intron_variant MELA-AU 11 11886247 11886247 single base substitution C T intron_variant MELA-AU 11 11886927 11886927 single base substitution T C intron_variant MELA-AU 11 11887143 11887143 single base substitution G A intron_variant MELA-AU 11 11887899 11887899 single base substitution A G intron_variant MELA-AU 11 11888353 11888353 single base substitution T G intron_variant MELA-AU 11 11888634 11888634 single base substitution G A intron_variant MELA-AU 11 11889843 11889843 single base substitution C T intron_variant MELA-AU 11 11889995 11889995 single base substitution C T intron_variant MELA-AU 11 11890113 11890113 single base substitution T A intron_variant MELA-AU 11 11890156 11890156 single base substitution G A intron_variant MELA-AU 11 11890268 11890268 single base substitution C T intron_variant MELA-AU 11 11890689 11890689 single base substitution C T intron_variant MELA-AU 11 11890846 11890846 single base substitution G A intron_variant MELA-AU 11 11891174 11891174 single base substitution C T intron_variant MELA-AU 11 11891365 11891365 single base substitution C T intron_variant MELA-AU 11 11892135 11892135 single base substitution C T intron_variant MELA-AU 11 11892285 11892285 single base substitution C T intron_variant MELA-AU 11 11892579 11892579 single base substitution C T intron_variant MELA-AU 11 11893036 11893036 single base substitution G A intron_variant MELA-AU 11 11893224 11893224 single base substitution C T intron_variant MELA-AU 11 11893698 11893698 single base substitution C T intron_variant MELA-AU 11 11893827 11893827 single base substitution A C intron_variant MELA-AU 11 11893970 11893970 single base substitution C T intron_variant MELA-AU 11 11895324 11895324 single base substitution C T intron_variant MELA-AU 11 11897046 11897046 single base substitution C T intron_variant MELA-AU 11 11897046 11897046 single base substitution C T upstream_gene_variant MELA-AU 11 11897326 11897326 single base substitution T C intron_variant MELA-AU 11 11897326 11897326 single base substitution T C upstream_gene_variant MELA-AU 11 11897394 11897394 single base substitution C T intron_variant MELA-AU 11 11897394 11897394 single base substitution C T upstream_gene_variant MELA-AU 11 11899079 11899079 single base substitution G A intron_variant MELA-AU 11 11899079 11899079 single base substitution G A upstream_gene_variant MELA-AU 11 11899164 11899164 single base substitution C T intron_variant MELA-AU 11 11899164 11899164 single base substitution C T upstream_gene_variant MELA-AU 11 11899356 11899356 single base substitution G C intron_variant MELA-AU 11 11899356 11899356 single base substitution G C upstream_gene_variant MELA-AU 11 11899668 11899668 single base substitution G T intron_variant MELA-AU 11 11899668 11899668 single base substitution G T upstream_gene_variant MELA-AU 11 11900420 11900420 single base substitution C T intron_variant MELA-AU 11 11900420 11900420 single base substitution C T upstream_gene_variant MELA-AU 11 11900625 11900625 single base substitution G A intron_variant MELA-AU 11 11900625 11900625 single base substitution G A upstream_gene_variant MELA-AU 11 11900666 11900666 single base substitution G A intron_variant MELA-AU 11 11900666 11900666 single base substitution G A upstream_gene_variant MELA-AU 11 11901047 11901047 single base substitution A G intron_variant MELA-AU 11 11901047 11901047 single base substitution A G upstream_gene_variant MELA-AU 11 11901106 11901106 single base substitution C T intron_variant MELA-AU 11 11901106 11901106 single base substitution C T upstream_gene_variant MELA-AU 11 11901330 11901330 single base substitution A T intron_variant MELA-AU 11 11901330 11901330 single base substitution A T upstream_gene_variant MELA-AU 11 11902585 11902585 single base substitution C T intron_variant MELA-AU 11 11902609 11902609 single base substitution T A intron_variant MELA-AU 11 11902656 11902656 single base substitution C T intron_variant MELA-AU 11 11902961 11902961 single base substitution G C intron_variant MELA-AU 11 11903106 11903106 single base substitution C T intron_variant MELA-AU 11 11903356 11903356 single base substitution C T intron_variant MELA-AU 11 11903374 11903375 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 11903601 11903601 single base substitution C T intron_variant MELA-AU 11 11903774 11903774 single base substitution G A intron_variant MELA-AU 11 11903794 11903794 single base substitution A T intron_variant MELA-AU 11 11903828 11903828 single base substitution A G intron_variant MELA-AU 11 11904146 11904146 single base substitution G A intron_variant MELA-AU 11 11905191 11905191 single base substitution G A intron_variant MELA-AU 11 11905402 11905402 single base substitution C T intron_variant MELA-AU 11 11905579 11905579 single base substitution C T intron_variant MELA-AU 11 11905674 11905674 single base substitution C T intron_variant MELA-AU 11 11905677 11905677 single base substitution A T intron_variant MELA-AU 11 11905877 11905877 single base substitution T A intron_variant MELA-AU 11 11906643 11906643 single base substitution C T downstream_gene_variant MELA-AU 11 11906643 11906643 single base substitution C T intron_variant MELA-AU 11 11906886 11906886 single base substitution C T downstream_gene_variant MELA-AU 11 11906886 11906886 single base substitution C T intron_variant MELA-AU 11 11907088 11907088 single base substitution C T downstream_gene_variant MELA-AU 11 11907088 11907088 single base substitution C T intron_variant MELA-AU 11 11907348 11907348 single base substitution C T downstream_gene_variant MELA-AU 11 11907348 11907348 single base substitution C T intron_variant MELA-AU 11 11907630 11907630 single base substitution C T downstream_gene_variant MELA-AU 11 11907630 11907630 single base substitution C T intron_variant MELA-AU 11 11908026 11908026 single base substitution G C downstream_gene_variant MELA-AU 11 11908026 11908026 single base substitution G C intron_variant MELA-AU 11 11908060 11908060 single base substitution C T downstream_gene_variant MELA-AU 11 11908060 11908060 single base substitution C T intron_variant MELA-AU 11 11908513 11908513 single base substitution C T downstream_gene_variant MELA-AU 11 11908513 11908513 single base substitution C T intron_variant MELA-AU 11 11908947 11908947 single base substitution G A downstream_gene_variant MELA-AU 11 11908947 11908947 single base substitution G A intron_variant MELA-AU 11 11909045 11909045 single base substitution A T downstream_gene_variant MELA-AU 11 11909045 11909045 single base substitution A T intron_variant MELA-AU 11 11910015 11910015 single base substitution C T downstream_gene_variant MELA-AU 11 11910015 11910015 single base substitution C T intron_variant MELA-AU 11 11910466 11910466 single base substitution T A downstream_gene_variant MELA-AU 11 11910466 11910466 single base substitution T A intron_variant MELA-AU 11 11910468 11910468 single base substitution C T downstream_gene_variant MELA-AU 11 11910468 11910468 single base substitution C T intron_variant MELA-AU 11 11911700 11911700 single base substitution C T intron_variant MELA-AU 11 11914635 11914635 single base substitution G A intron_variant MELA-AU 11 11914716 11914716 single base substitution C T intron_variant MELA-AU 11 11915567 11915567 single base substitution A G intron_variant MELA-AU 11 11915809 11915809 single base substitution C T intron_variant MELA-AU 11 11915824 11915824 single base substitution G A intron_variant MELA-AU 11 11916602 11916602 single base substitution T G intron_variant MELA-AU 11 11917120 11917120 single base substitution G A intron_variant MELA-AU 11 11918682 11918682 single base substitution G T intron_variant MELA-AU 11 11918747 11918747 single base substitution T G intron_variant MELA-AU 11 11919557 11919557 single base substitution C T intron_variant MELA-AU 11 11919916 11919916 single base substitution C T intron_variant MELA-AU 11 11921037 11921037 single base substitution C T intron_variant MELA-AU 11 11921274 11921274 single base substitution C T intron_variant MELA-AU 11 11921511 11921511 single base substitution C G intron_variant MELA-AU 11 11921628 11921629 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 11921817 11921817 single base substitution C T intron_variant MELA-AU 11 11921920 11921920 single base substitution G A intron_variant MELA-AU 11 11922526 11922526 single base substitution A G intron_variant MELA-AU 11 11922568 11922568 single base substitution G A intron_variant MELA-AU 11 11922851 11922851 single base substitution C T intron_variant MELA-AU 11 11923169 11923169 single base substitution C T intron_variant MELA-AU 11 11923801 11923801 single base substitution A T intron_variant MELA-AU 11 11923827 11923827 single base substitution C T intron_variant MELA-AU 11 11924910 11924910 single base substitution C T intron_variant MELA-AU 11 11926641 11926641 single base substitution C T intron_variant MELA-AU 11 11926871 11926871 deletion of <=200bp A - intron_variant MELA-AU 11 11927184 11927184 single base substitution C T intron_variant MELA-AU 11 11927695 11927695 single base substitution C T intron_variant MELA-AU 11 11928050 11928050 single base substitution C T intron_variant MELA-AU 11 11929530 11929530 single base substitution G A intron_variant MELA-AU 11 11929814 11929814 single base substitution T C intron_variant MELA-AU 11 11930198 11930198 single base substitution C T intron_variant MELA-AU 11 11931348 11931348 single base substitution A G intron_variant MELA-AU 11 11932206 11932207 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 11933166 11933166 single base substitution G C intron_variant MELA-AU 11 11933415 11933415 single base substitution C A intron_variant MELA-AU 11 11933683 11933683 single base substitution C T intron_variant MELA-AU 11 11934476 11934476 single base substitution G A intron_variant MELA-AU 11 11935325 11935325 single base substitution C T intron_variant MELA-AU 11 11935365 11935365 single base substitution C T intron_variant MELA-AU 11 11936124 11936124 single base substitution C T intron_variant MELA-AU 11 11936714 11936714 single base substitution T C intron_variant MELA-AU 11 11936755 11936755 single base substitution C T intron_variant MELA-AU 11 11936756 11936756 single base substitution C T intron_variant MELA-AU 11 11937810 11937810 single base substitution C T intron_variant MELA-AU 11 11938750 11938750 single base substitution C T intron_variant MELA-AU 11 11938792 11938792 single base substitution C T intron_variant MELA-AU 11 11940840 11940840 single base substitution G A intron_variant MELA-AU 11 11941024 11941025 multiple base substitution (>=2bp and <=200bp) CT TC intron_variant MELA-AU 11 11943894 11943894 single base substitution T C intron_variant MELA-AU 11 11944544 11944544 single base substitution T C intron_variant MELA-AU 11 11944546 11944546 single base substitution A T intron_variant MELA-AU 11 11945104 11945104 single base substitution A T intron_variant MELA-AU 11 11945173 11945173 single base substitution C T intron_variant MELA-AU 11 11946496 11946496 single base substitution C T intron_variant MELA-AU 11 11946693 11946693 single base substitution C T intron_variant MELA-AU 11 11946994 11946994 single base substitution C A intron_variant MELA-AU 11 11947388 11947388 single base substitution C T intron_variant MELA-AU 11 11948590 11948590 single base substitution C T intron_variant MELA-AU 11 11952193 11952193 single base substitution C T intron_variant MELA-AU 11 11952859 11952859 single base substitution A T intron_variant MELA-AU 11 11954247 11954247 single base substitution G C intron_variant MELA-AU 11 11956045 11956045 single base substitution C T intron_variant MELA-AU 11 11956045 11956045 single base substitution C T upstream_gene_variant MELA-AU 11 11956332 11956332 single base substitution C T intron_variant MELA-AU 11 11956332 11956332 single base substitution C T upstream_gene_variant MELA-AU 11 11957351 11957351 single base substitution G A intron_variant MELA-AU 11 11957351 11957351 single base substitution G A upstream_gene_variant MELA-AU 11 11958267 11958267 single base substitution A G intron_variant MELA-AU 11 11958267 11958267 single base substitution A G upstream_gene_variant MELA-AU 11 11958697 11958697 single base substitution C T intron_variant MELA-AU 11 11958697 11958697 single base substitution C T upstream_gene_variant MELA-AU 11 11959541 11959541 single base substitution G A intron_variant MELA-AU 11 11959541 11959541 single base substitution G A upstream_gene_variant MELA-AU 11 11959857 11959857 single base substitution C T 5_prime_UTR_variant MELA-AU 11 11959857 11959857 single base substitution C T missense_variant P643S 1927C>T MELA-AU 11 11959857 11959857 single base substitution C T missense_variant P711S 2131C>T MELA-AU 11 11959857 11959857 single base substitution C T missense_variant P731S 2191C>T MELA-AU 11 11959857 11959857 single base substitution C T upstream_gene_variant MELA-AU 11 11960735 11960735 single base substitution G A intron_variant MELA-AU 11 11960735 11960735 single base substitution G A upstream_gene_variant MELA-AU 11 11961351 11961351 single base substitution G A intron_variant MELA-AU 11 11961351 11961351 single base substitution G A upstream_gene_variant MELA-AU 11 11961677 11961677 single base substitution C T intron_variant MELA-AU 11 11961677 11961677 single base substitution C T upstream_gene_variant MELA-AU 11 11961977 11961978 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant A664V 1991CC>TT MELA-AU 11 11961977 11961978 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant A732V 2195CC>TT MELA-AU 11 11961977 11961978 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant A752V 2255CC>TT MELA-AU 11 11961977 11961978 multiple base substitution (>=2bp and <=200bp) CC TT splice_region_variant MELA-AU 11 11961977 11961978 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 11962264 11962264 single base substitution C T intron_variant MELA-AU 11 11962264 11962264 single base substitution C T upstream_gene_variant MELA-AU 11 11962395 11962395 single base substitution C T intron_variant MELA-AU 11 11962395 11962395 single base substitution C T upstream_gene_variant MELA-AU 11 11962440 11962440 single base substitution C T intron_variant MELA-AU 11 11962440 11962440 single base substitution C T upstream_gene_variant MELA-AU 11 11963144 11963144 single base substitution C T intron_variant MELA-AU 11 11963144 11963144 single base substitution C T upstream_gene_variant MELA-AU 11 11963712 11963712 single base substitution T A intron_variant MELA-AU 11 11963712 11963712 single base substitution T A upstream_gene_variant MELA-AU 11 11963866 11963866 single base substitution C T intron_variant MELA-AU 11 11963866 11963866 single base substitution C T upstream_gene_variant MELA-AU 11 11964452 11964452 single base substitution G A 5_prime_UTR_variant MELA-AU 11 11964452 11964452 single base substitution G A exon_variant MELA-AU 11 11964452 11964452 single base substitution G A missense_variant A894T 2680G>A MELA-AU 11 11964452 11964452 single base substitution G A missense_variant A962T 2884G>A MELA-AU 11 11964452 11964452 single base substitution G A missense_variant A982T 2944G>A MELA-AU 11 11964452 11964452 single base substitution G A upstream_gene_variant MELA-AU 11 11964988 11964988 single base substitution T A downstream_gene_variant MELA-AU 11 11964988 11964988 single base substitution T A exon_variant MELA-AU 11 11964988 11964988 single base substitution T A intron_variant MELA-AU 11 11964988 11964988 single base substitution T A upstream_gene_variant MELA-AU 11 11965041 11965041 single base substitution C T downstream_gene_variant MELA-AU 11 11965041 11965041 single base substitution C T exon_variant MELA-AU 11 11965041 11965041 single base substitution C T intron_variant MELA-AU 11 11965041 11965041 single base substitution C T upstream_gene_variant MELA-AU 11 11965716 11965716 single base substitution C T downstream_gene_variant MELA-AU 11 11965716 11965716 single base substitution C T intron_variant MELA-AU 11 11965716 11965716 single base substitution C T upstream_gene_variant MELA-AU 11 11967196 11967196 single base substitution C T downstream_gene_variant MELA-AU 11 11967196 11967196 single base substitution C T intron_variant MELA-AU 11 11967196 11967196 single base substitution C T upstream_gene_variant MELA-AU 11 11967248 11967248 single base substitution C T downstream_gene_variant MELA-AU 11 11967248 11967248 single base substitution C T intron_variant MELA-AU 11 11967248 11967248 single base substitution C T upstream_gene_variant MELA-AU 11 11967274 11967274 single base substitution G A downstream_gene_variant MELA-AU 11 11967274 11967274 single base substitution G A intron_variant MELA-AU 11 11967274 11967274 single base substitution G A upstream_gene_variant MELA-AU 11 11967326 11967326 single base substitution A T downstream_gene_variant MELA-AU 11 11967326 11967326 single base substitution A T intron_variant MELA-AU 11 11967326 11967326 single base substitution A T upstream_gene_variant MELA-AU 11 11967327 11967327 deletion of <=200bp T - downstream_gene_variant MELA-AU 11 11967327 11967327 deletion of <=200bp T - intron_variant MELA-AU 11 11967327 11967327 deletion of <=200bp T - upstream_gene_variant MELA-AU 11 11967482 11967482 single base substitution C T downstream_gene_variant MELA-AU 11 11967482 11967482 single base substitution C T intron_variant MELA-AU 11 11967482 11967482 single base substitution C T upstream_gene_variant MELA-AU 11 11968195 11968195 single base substitution G A downstream_gene_variant MELA-AU 11 11968195 11968195 single base substitution G A intron_variant MELA-AU 11 11968195 11968195 single base substitution G A upstream_gene_variant MELA-AU 11 11968367 11968367 single base substitution C T downstream_gene_variant MELA-AU 11 11968367 11968367 single base substitution C T intron_variant MELA-AU 11 11968367 11968367 single base substitution C T upstream_gene_variant MELA-AU 11 11968925 11968925 single base substitution C T downstream_gene_variant MELA-AU 11 11968925 11968925 single base substitution C T intron_variant MELA-AU 11 11968925 11968925 single base substitution C T upstream_gene_variant MELA-AU 11 11969282 11969282 single base substitution C T downstream_gene_variant MELA-AU 11 11969282 11969282 single base substitution C T intron_variant MELA-AU 11 11969282 11969282 single base substitution C T upstream_gene_variant MELA-AU 11 11969686 11969686 single base substitution C T downstream_gene_variant MELA-AU 11 11969686 11969686 single base substitution C T exon_variant MELA-AU 11 11969686 11969686 single base substitution C T intron_variant MELA-AU 11 11969686 11969686 single base substitution C T upstream_gene_variant MELA-AU 11 11970309 11970309 single base substitution A G exon_variant MELA-AU 11 11970309 11970309 single base substitution A G intron_variant MELA-AU 11 11970309 11970309 single base substitution A G upstream_gene_variant MELA-AU 11 11971724 11971743 deletion of <=200bp ATTTCCTATACAGAATTCTA - downstream_gene_variant MELA-AU 11 11971724 11971743 deletion of <=200bp ATTTCCTATACAGAATTCTA - intron_variant MELA-AU 11 11971724 11971743 deletion of <=200bp ATTTCCTATACAGAATTCTA - upstream_gene_variant MELA-AU 11 11972211 11972212 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 11972211 11972212 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 11972211 11972212 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 11972364 11972364 single base substitution C T downstream_gene_variant MELA-AU 11 11972364 11972364 single base substitution C T intron_variant MELA-AU 11 11972364 11972364 single base substitution C T upstream_gene_variant MELA-AU 11 11972430 11972430 single base substitution C T downstream_gene_variant MELA-AU 11 11972430 11972430 single base substitution C T exon_variant MELA-AU 11 11972430 11972430 single base substitution C T intron_variant MELA-AU 11 11972434 11972444 deletion of <=200bp GCCACGTTTGT - downstream_gene_variant MELA-AU 11 11972434 11972444 deletion of <=200bp GCCACGTTTGT - exon_variant MELA-AU 11 11972434 11972444 deletion of <=200bp GCCACGTTTGT - intron_variant MELA-AU 11 11972435 11972435 single base substitution C T downstream_gene_variant MELA-AU 11 11972435 11972435 single base substitution C T exon_variant MELA-AU 11 11972435 11972435 single base substitution C T intron_variant MELA-AU 11 11972599 11972599 single base substitution C T downstream_gene_variant MELA-AU 11 11972599 11972599 single base substitution C T exon_variant MELA-AU 11 11972599 11972599 single base substitution C T intron_variant MELA-AU 11 11972847 11972847 single base substitution C T downstream_gene_variant MELA-AU 11 11972847 11972847 single base substitution C T exon_variant MELA-AU 11 11972847 11972847 single base substitution C T intron_variant MELA-AU 11 11972877 11972877 single base substitution C G downstream_gene_variant MELA-AU 11 11972877 11972877 single base substitution C G exon_variant MELA-AU 11 11972877 11972877 single base substitution C G intron_variant MELA-AU 11 11973141 11973141 single base substitution C T downstream_gene_variant MELA-AU 11 11973141 11973141 single base substitution C T exon_variant MELA-AU 11 11973141 11973141 single base substitution C T intron_variant MELA-AU 11 11975594 11975594 single base substitution C T downstream_gene_variant MELA-AU 11 11975594 11975594 single base substitution C T intron_variant MELA-AU 11 11976904 11976904 single base substitution G A downstream_gene_variant MELA-AU 11 11976904 11976904 single base substitution G A intron_variant MELA-AU 11 11978134 11978134 single base substitution C T 3_prime_UTR_variant MELA-AU 11 11978134 11978134 single base substitution C T downstream_gene_variant MELA-AU 11 11978134 11978134 single base substitution C T exon_variant MELA-AU 11 11979279 11979279 single base substitution C T 3_prime_UTR_variant MELA-AU 11 11979279 11979279 single base substitution C T downstream_gene_variant MELA-AU 11 11979279 11979279 single base substitution C T exon_variant MELA-AU 11 11981032 11981032 single base substitution A G downstream_gene_variant MELA-AU 11 11981099 11981099 single base substitution C T downstream_gene_variant MELA-AU 11 11981566 11981566 single base substitution C T downstream_gene_variant MELA-AU 11 11982053 11982053 single base substitution C G downstream_gene_variant MELA-AU 11 11983371 11983371 single base substitution G A downstream_gene_variant MELA-AU 11 11984902 11984902 single base substitution G A downstream_gene_variant MELA-AU 11 11984963 11984963 single base substitution C T downstream_gene_variant MELA-AU 11 11985178 11985178 single base substitution G A downstream_gene_variant MELA-AU 11 11985582 11985582 single base substitution C T downstream_gene_variant MELA-AU 11 11985666 11985666 single base substitution C T downstream_gene_variant ORCA-IN 11 11871679 11871679 single base substitution C T intron_variant ORCA-IN 11 11886302 11886302 single base substitution C G intron_variant ORCA-IN 11 11908432 11908432 single base substitution C T downstream_gene_variant ORCA-IN 11 11908432 11908432 single base substitution C T intron_variant ORCA-IN 11 11941834 11941834 single base substitution G A intron_variant ORCA-IN 11 11942030 11942030 single base substitution G T 5_prime_UTR_variant ORCA-IN 11 11942030 11942030 single base substitution G T missense_variant V335F 1003G>T ORCA-IN 11 11942030 11942030 single base substitution G T missense_variant V403F 1207G>T ORCA-IN 11 11942030 11942030 single base substitution G T missense_variant V423F 1267G>T ORCA-IN 11 11975406 11975406 single base substitution A T downstream_gene_variant ORCA-IN 11 11975406 11975406 single base substitution A T intron_variant ORCA-IN 11 11976304 11976304 single base substitution C T downstream_gene_variant ORCA-IN 11 11976304 11976304 single base substitution C T intron_variant OV-AU 11 11858532 11858532 single base substitution G T upstream_gene_variant OV-AU 11 11895494 11895494 single base substitution C G intron_variant OV-AU 11 11896779 11896779 single base substitution C A intron_variant OV-AU 11 11896779 11896779 single base substitution C A upstream_gene_variant OV-AU 11 11918153 11918153 single base substitution G T intron_variant OV-AU 11 11918576 11918576 single base substitution G A intron_variant OV-AU 11 11923373 11923373 single base substitution G A intron_variant OV-AU 11 11930924 11930924 single base substitution T C intron_variant OV-AU 11 11933770 11933770 single base substitution C T intron_variant OV-AU 11 11935392 11935392 single base substitution A C intron_variant OV-AU 11 11941002 11941002 single base substitution A G intron_variant OV-AU 11 11945115 11945115 single base substitution T A intron_variant OV-AU 11 11946330 11946330 single base substitution T G intron_variant OV-AU 11 11967595 11967595 single base substitution A G downstream_gene_variant OV-AU 11 11967595 11967595 single base substitution A G intron_variant OV-AU 11 11967595 11967595 single base substitution A G upstream_gene_variant OV-AU 11 11970463 11970463 single base substitution A T exon_variant OV-AU 11 11970463 11970463 single base substitution A T intron_variant OV-AU 11 11970463 11970463 single base substitution A T upstream_gene_variant OV-AU 11 11970667 11970667 single base substitution T C downstream_gene_variant OV-AU 11 11970667 11970667 single base substitution T C intron_variant OV-AU 11 11970667 11970667 single base substitution T C upstream_gene_variant OV-AU 11 11973126 11973126 single base substitution G T downstream_gene_variant OV-AU 11 11973126 11973126 single base substitution G T exon_variant OV-AU 11 11973126 11973126 single base substitution G T intron_variant OV-AU 11 11974350 11974350 single base substitution G T downstream_gene_variant OV-AU 11 11974350 11974350 single base substitution G T exon_variant OV-AU 11 11974350 11974350 single base substitution G T stop_gained E1148* 3442G>T OV-AU 11 11974350 11974350 single base substitution G T stop_gained E1216* 3646G>T OV-AU 11 11974350 11974350 single base substitution G T stop_gained E1236* 3706G>T OV-AU 11 11974350 11974350 single base substitution G T stop_gained E18* 52G>T PACA-AU 11 11858153 11858153 single base substitution A T upstream_gene_variant PACA-AU 11 11858476 11858476 single base substitution C A upstream_gene_variant PACA-AU 11 11866782 11866782 single base substitution C G intron_variant PACA-AU 11 11871958 11871958 single base substitution T G intron_variant PACA-AU 11 11877568 11877568 single base substitution T G intron_variant PACA-AU 11 11882902 11882902 single base substitution G T intron_variant PACA-AU 11 11885652 11885652 single base substitution A G intron_variant PACA-AU 11 11887242 11887242 single base substitution C T intron_variant PACA-AU 11 11887754 11887754 single base substitution T C intron_variant PACA-AU 11 11888127 11888127 single base substitution C T intron_variant PACA-AU 11 11893532 11893532 single base substitution A T intron_variant PACA-AU 11 11896163 11896163 single base substitution A G intron_variant PACA-AU 11 11897698 11897698 single base substitution T C intron_variant PACA-AU 11 11897698 11897698 single base substitution T C upstream_gene_variant PACA-AU 11 11898969 11898969 deletion of <=200bp T - intron_variant PACA-AU 11 11898969 11898969 deletion of <=200bp T - upstream_gene_variant PACA-AU 11 11900100 11900100 single base substitution A G intron_variant PACA-AU 11 11900100 11900100 single base substitution A G upstream_gene_variant PACA-AU 11 11905342 11905342 single base substitution G A intron_variant PACA-AU 11 11907619 11907619 deletion of <=200bp C - downstream_gene_variant PACA-AU 11 11907619 11907619 deletion of <=200bp C - intron_variant PACA-AU 11 11910146 11910146 single base substitution T A downstream_gene_variant PACA-AU 11 11910146 11910146 single base substitution T A intron_variant PACA-AU 11 11910896 11910896 single base substitution C T downstream_gene_variant PACA-AU 11 11910896 11910896 single base substitution C T intron_variant PACA-AU 11 11914371 11914382 deletion of <=200bp AAAAAAAAAAAG - intron_variant PACA-AU 11 11914716 11914716 single base substitution C T intron_variant PACA-AU 11 11925794 11925794 single base substitution G A intron_variant PACA-AU 11 11930574 11930574 single base substitution G T intron_variant PACA-AU 11 11931771 11931771 single base substitution G A intron_variant PACA-AU 11 11941881 11941881 deletion of <=200bp T - splice_region_variant PACA-AU 11 11943030 11943030 single base substitution A G intron_variant PACA-AU 11 11945081 11945081 deletion of <=200bp T - intron_variant PACA-AU 11 11946323 11946323 single base substitution T C intron_variant PACA-AU 11 11952670 11952670 insertion of <=200bp - G intron_variant PACA-AU 11 11954550 11954550 single base substitution G C splice_acceptor_variant PACA-AU 11 11960693 11960693 deletion of <=200bp G - intron_variant PACA-AU 11 11960693 11960693 deletion of <=200bp G - upstream_gene_variant PACA-AU 11 11963203 11963203 single base substitution A T intron_variant PACA-AU 11 11963203 11963203 single base substitution A T upstream_gene_variant PACA-AU 11 11972182 11972185 deletion of <=200bp GATT - downstream_gene_variant PACA-AU 11 11972182 11972185 deletion of <=200bp GATT - intron_variant PACA-AU 11 11972182 11972185 deletion of <=200bp GATT - upstream_gene_variant PACA-AU 11 11974873 11974873 single base substitution A G downstream_gene_variant PACA-AU 11 11974873 11974873 single base substitution A G intron_variant PACA-AU 11 11983098 11983098 insertion of <=200bp - A downstream_gene_variant PACA-AU 11 11984961 11984961 single base substitution G A downstream_gene_variant PACA-CA 11 11860227 11860227 single base substitution C G upstream_gene_variant PACA-CA 11 11861976 11861976 single base substitution T C upstream_gene_variant PACA-CA 11 11864510 11864510 single base substitution G C intron_variant PACA-CA 11 11864853 11864853 single base substitution T C intron_variant PACA-CA 11 11868045 11868045 single base substitution A C intron_variant PACA-CA 11 11869214 11869214 single base substitution C A intron_variant PACA-CA 11 11869388 11869388 single base substitution A G intron_variant PACA-CA 11 11870349 11870349 single base substitution G A intron_variant PACA-CA 11 11876117 11876117 single base substitution T C intron_variant PACA-CA 11 11885721 11885721 single base substitution A T intron_variant PACA-CA 11 11887039 11887040 deletion of <=200bp TC - intron_variant PACA-CA 11 11899336 11899336 single base substitution T C intron_variant PACA-CA 11 11899336 11899336 single base substitution T C upstream_gene_variant PACA-CA 11 11901534 11901534 single base substitution C T intron_variant PACA-CA 11 11901534 11901534 single base substitution C T upstream_gene_variant PACA-CA 11 11903991 11903991 single base substitution T A intron_variant PACA-CA 11 11904548 11904548 single base substitution A G intron_variant PACA-CA 11 11909149 11909149 single base substitution C T downstream_gene_variant PACA-CA 11 11909149 11909149 single base substitution C T intron_variant PACA-CA 11 11916753 11916753 insertion of <=200bp - A intron_variant PACA-CA 11 11918703 11918703 single base substitution A G intron_variant PACA-CA 11 11922120 11922120 single base substitution C T intron_variant PACA-CA 11 11926239 11926239 insertion of <=200bp - TAG intron_variant PACA-CA 11 11929305 11929305 single base substitution A G intron_variant PACA-CA 11 11929391 11929391 single base substitution C T intron_variant PACA-CA 11 11934084 11934099 deletion of <=200bp TTAAAACCTCTTGAAA - intron_variant PACA-CA 11 11936318 11936318 single base substitution C A intron_variant PACA-CA 11 11937457 11937457 single base substitution T A intron_variant PACA-CA 11 11938213 11938213 single base substitution T A intron_variant PACA-CA 11 11938866 11938866 single base substitution G C intron_variant PACA-CA 11 11941711 11941711 single base substitution A G 5_prime_UTR_variant PACA-CA 11 11941711 11941711 single base substitution A G synonymous_variant A258A 774A>G PACA-CA 11 11941711 11941711 single base substitution A G synonymous_variant A326A 978A>G PACA-CA 11 11941711 11941711 single base substitution A G synonymous_variant A346A 1038A>G PACA-CA 11 11943696 11943696 single base substitution A G intron_variant PACA-CA 11 11943882 11943882 single base substitution G T intron_variant PACA-CA 11 11953686 11953686 single base substitution G A intron_variant PACA-CA 11 11953687 11953687 single base substitution C T intron_variant PACA-CA 11 11961868 11961888 deletion of <=200bp CTCTGCTGCTTTTAAGAAGAA - intron_variant PACA-CA 11 11961868 11961888 deletion of <=200bp CTCTGCTGCTTTTAAGAAGAA - upstream_gene_variant PACA-CA 11 11964756 11964756 single base substitution G T downstream_gene_variant PACA-CA 11 11964756 11964756 single base substitution G T intron_variant PACA-CA 11 11964756 11964756 single base substitution G T upstream_gene_variant PACA-CA 11 11972090 11972090 single base substitution C G downstream_gene_variant PACA-CA 11 11972090 11972090 single base substitution C G intron_variant PACA-CA 11 11972090 11972090 single base substitution C G upstream_gene_variant PACA-CA 11 11976445 11976445 single base substitution T G downstream_gene_variant PACA-CA 11 11976445 11976445 single base substitution T G missense_variant L1171R 3512T>G PACA-CA 11 11976445 11976445 single base substitution T G missense_variant L1239R 3716T>G PACA-CA 11 11976445 11976445 single base substitution T G missense_variant L1259R 3776T>G PACA-CA 11 11976445 11976445 single base substitution T G missense_variant L41R 122T>G PACA-CA 11 11976445 11976445 single base substitution T G splice_region_variant PAEN-AU 11 11865773 11865773 single base substitution T A intron_variant PAEN-AU 11 11881826 11881826 single base substitution G A intron_variant PAEN-AU 11 11887639 11887639 single base substitution G A intron_variant PAEN-AU 11 11896976 11896976 single base substitution A G intron_variant PAEN-AU 11 11896976 11896976 single base substitution A G upstream_gene_variant PAEN-IT 11 11877636 11877636 single base substitution A C intron_variant PAEN-IT 11 11931303 11931303 single base substitution C T intron_variant PBCA-DE 11 11861193 11861193 single base substitution C T upstream_gene_variant PBCA-DE 11 11876901 11876901 single base substitution G T intron_variant PBCA-DE 11 11899520 11899520 insertion of <=200bp - A intron_variant PBCA-DE 11 11899520 11899520 insertion of <=200bp - A upstream_gene_variant PBCA-DE 11 11902629 11902629 single base substitution C A intron_variant PBCA-DE 11 11907010 11907010 single base substitution C A downstream_gene_variant PBCA-DE 11 11907010 11907010 single base substitution C A intron_variant PBCA-DE 11 11921230 11921230 single base substitution G A intron_variant PBCA-DE 11 11930853 11930856 deletion of <=200bp TAGA - intron_variant PBCA-DE 11 11942785 11942785 single base substitution T G intron_variant PBCA-DE 11 11945262 11945262 single base substitution T A intron_variant PBCA-DE 11 11956536 11956536 single base substitution C T intron_variant PBCA-DE 11 11956536 11956536 single base substitution C T upstream_gene_variant PBCA-DE 11 11960887 11960887 single base substitution T C intron_variant PBCA-DE 11 11960887 11960887 single base substitution T C upstream_gene_variant PBCA-DE 11 11974639 11974639 single base substitution T G downstream_gene_variant PBCA-DE 11 11974639 11974639 single base substitution T G intron_variant PRAD-CA 11 11877633 11877633 single base substitution G A intron_variant PRAD-CA 11 11896586 11896586 single base substitution G A intron_variant PRAD-CA 11 11899336 11899336 single base substitution T C intron_variant PRAD-CA 11 11899336 11899336 single base substitution T C upstream_gene_variant PRAD-CA 11 11922843 11922843 single base substitution T G intron_variant PRAD-CA 11 11979264 11979264 single base substitution G T 3_prime_UTR_variant PRAD-CA 11 11979264 11979264 single base substitution G T downstream_gene_variant PRAD-CA 11 11979264 11979264 single base substitution G T exon_variant PRAD-UK 11 11882522 11882522 single base substitution G C intron_variant PRAD-UK 11 11886112 11886112 single base substitution A G intron_variant PRAD-UK 11 11909081 11909081 single base substitution A G downstream_gene_variant PRAD-UK 11 11909081 11909081 single base substitution A G intron_variant PRAD-UK 11 11914439 11914439 single base substitution C G intron_variant PRAD-UK 11 11928898 11928898 single base substitution G C intron_variant PRAD-UK 11 11934440 11934440 single base substitution G A intron_variant PRAD-UK 11 11941152 11941152 insertion of <=200bp - CA intron_variant PRAD-UK 11 11941794 11941794 single base substitution G A 5_prime_UTR_variant PRAD-UK 11 11941794 11941794 single base substitution G A missense_variant R286Q 857G>A PRAD-UK 11 11941794 11941794 single base substitution G A missense_variant R354Q 1061G>A PRAD-UK 11 11941794 11941794 single base substitution G A missense_variant R374Q 1121G>A PRAD-UK 11 11944321 11944321 single base substitution T A 5_prime_UTR_variant PRAD-UK 11 11944321 11944321 single base substitution T A synonymous_variant G355G 1065T>A PRAD-UK 11 11944321 11944321 single base substitution T A synonymous_variant G423G 1269T>A PRAD-UK 11 11944321 11944321 single base substitution T A synonymous_variant G443G 1329T>A PRAD-UK 11 11958400 11958400 single base substitution C T intron_variant PRAD-UK 11 11958400 11958400 single base substitution C T upstream_gene_variant PRAD-UK 11 11976547 11976547 single base substitution G C downstream_gene_variant PRAD-UK 11 11976547 11976547 single base substitution G C intron_variant PRAD-UK 11 11980756 11980756 single base substitution T G 3_prime_UTR_variant PRAD-UK 11 11980756 11980756 single base substitution T G downstream_gene_variant PRAD-US 11 11969590 11969590 single base substitution C A 5_prime_UTR_variant PRAD-US 11 11969590 11969590 single base substitution C A downstream_gene_variant PRAD-US 11 11969590 11969590 single base substitution C A exon_variant PRAD-US 11 11969590 11969590 single base substitution C A synonymous_variant R1064R 3190C>A PRAD-US 11 11969590 11969590 single base substitution C A synonymous_variant R1084R 3250C>A PRAD-US 11 11969590 11969590 single base substitution C A synonymous_variant R996R 2986C>A PRAD-US 11 11969590 11969590 single base substitution C A upstream_gene_variant READ-US 11 11913582 11913582 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant READ-US 11 11913582 11913582 single base substitution C A missense_variant S142Y 425C>A READ-US 11 11913582 11913582 single base substitution C A missense_variant S162Y 485C>A READ-US 11 11913582 11913582 single base substitution C A missense_variant S74Y 221C>A READ-US 11 11941739 11941739 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant READ-US 11 11941739 11941739 single base substitution C A missense_variant L268M 802C>A READ-US 11 11941739 11941739 single base substitution C A missense_variant L336M 1006C>A READ-US 11 11941739 11941739 single base substitution C A missense_variant L356M 1066C>A RECA-EU 11 11865013 11865013 single base substitution T C intron_variant RECA-EU 11 11865421 11865421 single base substitution T C intron_variant RECA-EU 11 11866916 11866916 single base substitution A G intron_variant RECA-EU 11 11868037 11868037 single base substitution A T intron_variant RECA-EU 11 11876007 11876007 single base substitution G T intron_variant RECA-EU 11 11885459 11885459 single base substitution A T intron_variant RECA-EU 11 11890501 11890501 single base substitution C G intron_variant RECA-EU 11 11896319 11896319 single base substitution T C intron_variant RECA-EU 11 11899815 11899815 single base substitution A C intron_variant RECA-EU 11 11899815 11899815 single base substitution A C upstream_gene_variant RECA-EU 11 11904149 11904149 single base substitution A G intron_variant RECA-EU 11 11904150 11904150 single base substitution G A intron_variant RECA-EU 11 11916924 11916924 single base substitution G A intron_variant RECA-EU 11 11919298 11919298 single base substitution T A intron_variant RECA-EU 11 11944323 11944323 single base substitution G C 5_prime_UTR_variant RECA-EU 11 11944323 11944323 single base substitution G C missense_variant S356T 1067G>C RECA-EU 11 11944323 11944323 single base substitution G C missense_variant S424T 1271G>C RECA-EU 11 11944323 11944323 single base substitution G C missense_variant S444T 1331G>C RECA-EU 11 11946524 11946524 single base substitution T A intron_variant RECA-EU 11 11954887 11954887 single base substitution G A intron_variant RECA-EU 11 11954887 11954887 single base substitution G A upstream_gene_variant RECA-EU 11 11967788 11967788 single base substitution G C downstream_gene_variant RECA-EU 11 11967788 11967788 single base substitution G C intron_variant RECA-EU 11 11967788 11967788 single base substitution G C upstream_gene_variant RECA-EU 11 11971033 11971033 single base substitution T C downstream_gene_variant RECA-EU 11 11971033 11971033 single base substitution T C intron_variant RECA-EU 11 11971033 11971033 single base substitution T C upstream_gene_variant RECA-EU 11 11979787 11979787 single base substitution A G 3_prime_UTR_variant RECA-EU 11 11979787 11979787 single base substitution A G downstream_gene_variant RECA-EU 11 11979787 11979787 single base substitution A G exon_variant RECA-EU 11 11984407 11984407 single base substitution A T downstream_gene_variant SKCA-BR 11 11858446 11858447 deletion of <=200bp GT - upstream_gene_variant SKCA-BR 11 11858471 11858471 single base substitution A G upstream_gene_variant SKCA-BR 11 11858925 11858925 single base substitution G A upstream_gene_variant SKCA-BR 11 11859846 11859846 single base substitution C T upstream_gene_variant SKCA-BR 11 11860380 11860380 single base substitution T G upstream_gene_variant SKCA-BR 11 11870991 11870991 single base substitution A G intron_variant SKCA-BR 11 11871421 11871421 single base substitution T C intron_variant SKCA-BR 11 11877757 11877757 single base substitution A G intron_variant SKCA-BR 11 11884485 11884485 single base substitution A C intron_variant SKCA-BR 11 11884873 11884873 insertion of <=200bp - GA intron_variant SKCA-BR 11 11887757 11887757 single base substitution C T intron_variant SKCA-BR 11 11896584 11896584 single base substitution G A intron_variant SKCA-BR 11 11896828 11896828 single base substitution C T intron_variant SKCA-BR 11 11896828 11896828 single base substitution C T upstream_gene_variant SKCA-BR 11 11897830 11897830 single base substitution C T intron_variant SKCA-BR 11 11897830 11897830 single base substitution C T upstream_gene_variant SKCA-BR 11 11899352 11899362 deletion of <=200bp CTGTGTGTGTG - intron_variant SKCA-BR 11 11899352 11899362 deletion of <=200bp CTGTGTGTGTG - upstream_gene_variant SKCA-BR 11 11899358 11899358 single base substitution G C intron_variant SKCA-BR 11 11899358 11899358 single base substitution G C upstream_gene_variant SKCA-BR 11 11899389 11899407 deletion of <=200bp TGTGTGTGTGTGTGTGTGC - intron_variant SKCA-BR 11 11899389 11899407 deletion of <=200bp TGTGTGTGTGTGTGTGTGC - upstream_gene_variant SKCA-BR 11 11899391 11899407 deletion of <=200bp TGTGTGTGTGTGTGTGC - intron_variant SKCA-BR 11 11899391 11899407 deletion of <=200bp TGTGTGTGTGTGTGTGC - upstream_gene_variant SKCA-BR 11 11899393 11899407 deletion of <=200bp TGTGTGTGTGTGTGC - intron_variant SKCA-BR 11 11899393 11899407 deletion of <=200bp TGTGTGTGTGTGTGC - upstream_gene_variant SKCA-BR 11 11899395 11899407 deletion of <=200bp TGTGTGTGTGTGC - intron_variant SKCA-BR 11 11899395 11899407 deletion of <=200bp TGTGTGTGTGTGC - upstream_gene_variant SKCA-BR 11 11899397 11899407 deletion of <=200bp TGTGTGTGTGC - intron_variant SKCA-BR 11 11899397 11899407 deletion of <=200bp TGTGTGTGTGC - upstream_gene_variant SKCA-BR 11 11899407 11899407 single base substitution C T intron_variant SKCA-BR 11 11899407 11899407 single base substitution C T upstream_gene_variant SKCA-BR 11 11902685 11902685 single base substitution T C intron_variant SKCA-BR 11 11906771 11906771 single base substitution G A downstream_gene_variant SKCA-BR 11 11906771 11906771 single base substitution G A intron_variant SKCA-BR 11 11914381 11914382 deletion of <=200bp AG - intron_variant SKCA-BR 11 11914382 11914382 single base substitution G A intron_variant SKCA-BR 11 11918196 11918196 single base substitution G A intron_variant SKCA-BR 11 11918991 11918991 single base substitution C T intron_variant SKCA-BR 11 11921701 11921701 insertion of <=200bp - CT intron_variant SKCA-BR 11 11927472 11927472 single base substitution C T intron_variant SKCA-BR 11 11928392 11928392 single base substitution C T intron_variant SKCA-BR 11 11930250 11930250 single base substitution C A intron_variant SKCA-BR 11 11935182 11935182 single base substitution A G intron_variant SKCA-BR 11 11936941 11936941 single base substitution C T intron_variant SKCA-BR 11 11937873 11937873 single base substitution A T intron_variant SKCA-BR 11 11943117 11943117 single base substitution C T intron_variant SKCA-BR 11 11944588 11944590 deletion of <=200bp CAT - intron_variant SKCA-BR 11 11944595 11944595 single base substitution A G intron_variant SKCA-BR 11 11944609 11944609 single base substitution A G intron_variant SKCA-BR 11 11947492 11947492 single base substitution C T intron_variant SKCA-BR 11 11948773 11948773 insertion of <=200bp - AT intron_variant SKCA-BR 11 11949488 11949488 single base substitution C T intron_variant SKCA-BR 11 11950776 11950776 single base substitution T A intron_variant SKCA-BR 11 11954362 11954362 single base substitution C T intron_variant SKCA-BR 11 11959544 11959547 deletion of <=200bp ATAT - intron_variant SKCA-BR 11 11959544 11959547 deletion of <=200bp ATAT - upstream_gene_variant SKCA-BR 11 11965468 11965468 single base substitution C T downstream_gene_variant SKCA-BR 11 11965468 11965468 single base substitution C T intron_variant SKCA-BR 11 11965468 11965468 single base substitution C T upstream_gene_variant SKCA-BR 11 11967081 11967081 single base substitution T G downstream_gene_variant SKCA-BR 11 11967081 11967081 single base substitution T G intron_variant SKCA-BR 11 11967081 11967081 single base substitution T G upstream_gene_variant SKCA-BR 11 11977656 11977656 single base substitution T G downstream_gene_variant SKCA-BR 11 11977656 11977656 single base substitution T G exon_variant SKCA-BR 11 11977656 11977656 single base substitution T G synonymous_variant P1266P 3798T>G SKCA-BR 11 11977656 11977656 single base substitution T G synonymous_variant P1334P 4002T>G SKCA-BR 11 11977656 11977656 single base substitution T G synonymous_variant P1354P 4062T>G SKCA-BR 11 11977656 11977656 single base substitution T G synonymous_variant P136P 408T>G SKCA-BR 11 11980089 11980089 single base substitution C T 3_prime_UTR_variant SKCA-BR 11 11980089 11980089 single base substitution C T downstream_gene_variant SKCA-BR 11 11980089 11980089 single base substitution C T exon_variant SKCA-BR 11 11982253 11982253 single base substitution T A downstream_gene_variant SKCM-US 11 11919184 11919184 single base substitution G A 5_prime_UTR_variant SKCM-US 11 11919184 11919184 single base substitution G A synonymous_variant L111L 333G>A SKCM-US 11 11919184 11919184 single base substitution G A synonymous_variant L179L 537G>A SKCM-US 11 11919184 11919184 single base substitution G A synonymous_variant L199L 597G>A SKCM-US 11 11941997 11941997 single base substitution C T 5_prime_UTR_variant SKCM-US 11 11941997 11941997 single base substitution C T missense_variant P324S 970C>T SKCM-US 11 11941997 11941997 single base substitution C T missense_variant P392S 1174C>T SKCM-US 11 11941997 11941997 single base substitution C T missense_variant P412S 1234C>T SKCM-US 11 11944273 11944273 single base substitution A T missense_variant K339N 1017A>T SKCM-US 11 11944273 11944273 single base substitution A T missense_variant K407N 1221A>T SKCM-US 11 11944273 11944273 single base substitution A T missense_variant K427N 1281A>T SKCM-US 11 11944273 11944273 single base substitution A T splice_region_variant SKCM-US 11 11964207 11964207 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 11 11964207 11964207 single base substitution C T exon_variant SKCM-US 11 11964207 11964207 single base substitution C T missense_variant T812I 2435C>T SKCM-US 11 11964207 11964207 single base substitution C T missense_variant T880I 2639C>T SKCM-US 11 11964207 11964207 single base substitution C T missense_variant T900I 2699C>T SKCM-US 11 11964207 11964207 single base substitution C T upstream_gene_variant SKCM-US 11 11971966 11971966 single base substitution C T 5_prime_UTR_variant SKCM-US 11 11971966 11971966 single base substitution C T downstream_gene_variant SKCM-US 11 11971966 11971966 single base substitution C T exon_variant SKCM-US 11 11971966 11971966 single base substitution C T missense_variant H1106Y 3316C>T SKCM-US 11 11971966 11971966 single base substitution C T missense_variant H1174Y 3520C>T SKCM-US 11 11971966 11971966 single base substitution C T missense_variant H1194Y 3580C>T SKCM-US 11 11971966 11971966 single base substitution C T upstream_gene_variant SKCM-US 11 11976465 11976465 single base substitution C T downstream_gene_variant SKCM-US 11 11976465 11976465 single base substitution C T exon_variant SKCM-US 11 11976465 11976465 single base substitution C T missense_variant P1178S 3532C>T SKCM-US 11 11976465 11976465 single base substitution C T missense_variant P1246S 3736C>T SKCM-US 11 11976465 11976465 single base substitution C T missense_variant P1266S 3796C>T SKCM-US 11 11976465 11976465 single base substitution C T missense_variant P48S 142C>T SKCM-US 11 11976597 11976597 single base substitution C T downstream_gene_variant SKCM-US 11 11976597 11976597 single base substitution C T exon_variant SKCM-US 11 11976597 11976597 single base substitution C T missense_variant P1192L 3575C>T SKCM-US 11 11976597 11976597 single base substitution C T missense_variant P1260L 3779C>T SKCM-US 11 11976597 11976597 single base substitution C T missense_variant P1280L 3839C>T SKCM-US 11 11976597 11976597 single base substitution C T missense_variant P62L 185C>T SKCM-US 11 11977655 11977655 single base substitution C T downstream_gene_variant SKCM-US 11 11977655 11977655 single base substitution C T exon_variant SKCM-US 11 11977655 11977655 single base substitution C T missense_variant P1266L 3797C>T SKCM-US 11 11977655 11977655 single base substitution C T missense_variant P1334L 4001C>T SKCM-US 11 11977655 11977655 single base substitution C T missense_variant P1354L 4061C>T SKCM-US 11 11977655 11977655 single base substitution C T missense_variant P136L 407C>T STAD-US 11 11926990 11926990 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant STAD-US 11 11926990 11926990 single base substitution C T synonymous_variant Y220Y 660C>T STAD-US 11 11926990 11926990 single base substitution C T synonymous_variant Y288Y 864C>T STAD-US 11 11926990 11926990 single base substitution C T synonymous_variant Y308Y 924C>T STAD-US 11 11927031 11927031 single base substitution A G 5_prime_UTR_variant STAD-US 11 11927031 11927031 single base substitution A G missense_variant D234G 701A>G STAD-US 11 11927031 11927031 single base substitution A G missense_variant D302G 905A>G STAD-US 11 11927031 11927031 single base substitution A G missense_variant D322G 965A>G STAD-US 11 11944340 11944340 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant STAD-US 11 11944340 11944340 single base substitution A T missense_variant M362L 1084A>T STAD-US 11 11944340 11944340 single base substitution A T missense_variant M430L 1288A>T STAD-US 11 11944340 11944340 single base substitution A T missense_variant M450L 1348A>T STAD-US 11 11954637 11954637 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant STAD-US 11 11954637 11954637 single base substitution C T stop_gained R512* 1534C>T STAD-US 11 11954637 11954637 single base substitution C T stop_gained R580* 1738C>T STAD-US 11 11954637 11954637 single base substitution C T stop_gained R600* 1798C>T STAD-US 11 11957978 11957978 single base substitution C T 5_prime_UTR_variant STAD-US 11 11957978 11957978 single base substitution C T synonymous_variant G598G 1794C>T STAD-US 11 11957978 11957978 single base substitution C T synonymous_variant G666G 1998C>T STAD-US 11 11957978 11957978 single base substitution C T synonymous_variant G686G 2058C>T STAD-US 11 11957978 11957978 single base substitution C T upstream_gene_variant STAD-US 11 11969622 11969622 single base substitution C T 5_prime_UTR_variant STAD-US 11 11969622 11969622 single base substitution C T downstream_gene_variant STAD-US 11 11969622 11969622 single base substitution C T exon_variant STAD-US 11 11969622 11969622 single base substitution C T synonymous_variant S1006S 3018C>T STAD-US 11 11969622 11969622 single base substitution C T synonymous_variant S1074S 3222C>T STAD-US 11 11969622 11969622 single base substitution C T synonymous_variant S1094S 3282C>T STAD-US 11 11969622 11969622 single base substitution C T upstream_gene_variant STAD-US 11 11971915 11971915 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant STAD-US 11 11971915 11971915 single base substitution C T downstream_gene_variant STAD-US 11 11971915 11971915 single base substitution C T exon_variant STAD-US 11 11971915 11971915 single base substitution C T missense_variant R1089C 3265C>T STAD-US 11 11971915 11971915 single base substitution C T missense_variant R1157C 3469C>T STAD-US 11 11971915 11971915 single base substitution C T missense_variant R1177C 3529C>T STAD-US 11 11971915 11971915 single base substitution C T upstream_gene_variant STAD-US 11 11971986 11971986 single base substitution T G 5_prime_UTR_premature_start_codon_gain_variant STAD-US 11 11971986 11971986 single base substitution T G downstream_gene_variant STAD-US 11 11971986 11971986 single base substitution T G exon_variant STAD-US 11 11971986 11971986 single base substitution T G missense_variant I1112M 3336T>G STAD-US 11 11971986 11971986 single base substitution T G missense_variant I1180M 3540T>G STAD-US 11 11971986 11971986 single base substitution T G missense_variant I1200M 3600T>G STAD-US 11 11971986 11971986 single base substitution T G upstream_gene_variant STAD-US 11 11974317 11974317 single base substitution C T downstream_gene_variant STAD-US 11 11974317 11974317 single base substitution C T exon_variant STAD-US 11 11974317 11974317 single base substitution C T missense_variant L1137F 3409C>T STAD-US 11 11974317 11974317 single base substitution C T missense_variant L1205F 3613C>T STAD-US 11 11974317 11974317 single base substitution C T missense_variant L1225F 3673C>T STAD-US 11 11974317 11974317 single base substitution C T missense_variant L7F 19C>T STAD-US 11 11974417 11974417 single base substitution A C downstream_gene_variant STAD-US 11 11974417 11974417 single base substitution A C missense_variant K1170T 3509A>C STAD-US 11 11974417 11974417 single base substitution A C missense_variant K1238T 3713A>C STAD-US 11 11974417 11974417 single base substitution A C missense_variant K1258T 3773A>C STAD-US 11 11974417 11974417 single base substitution A C missense_variant K40T 119A>C STAD-US 11 11974417 11974417 single base substitution A C splice_region_variant STAD-US 11 11977643 11977643 single base substitution T C downstream_gene_variant STAD-US 11 11977643 11977643 single base substitution T C exon_variant STAD-US 11 11977643 11977643 single base substitution T C missense_variant V1262A 3785T>C STAD-US 11 11977643 11977643 single base substitution T C missense_variant V132A 395T>C STAD-US 11 11977643 11977643 single base substitution T C missense_variant V1330A 3989T>C STAD-US 11 11977643 11977643 single base substitution T C missense_variant V1350A 4049T>C THCA-SA 11 11941765 11941765 single base substitution T C 5_prime_UTR_variant THCA-SA 11 11941765 11941765 single base substitution T C synonymous_variant C276C 828T>C THCA-SA 11 11941765 11941765 single base substitution T C synonymous_variant C344C 1032T>C THCA-SA 11 11941765 11941765 single base substitution T C synonymous_variant C364C 1092T>C THCA-SA 11 11979592 11979592 single base substitution G A 3_prime_UTR_variant THCA-SA 11 11979592 11979592 single base substitution G A downstream_gene_variant THCA-SA 11 11979592 11979592 single base substitution G A exon_variant THCA-SA 11 11979674 11979674 single base substitution A G 3_prime_UTR_variant THCA-SA 11 11979674 11979674 single base substitution A G downstream_gene_variant THCA-SA 11 11979674 11979674 single base substitution A G exon_variant THCA-SA 11 11980449 11980449 single base substitution A G 3_prime_UTR_variant THCA-SA 11 11980449 11980449 single base substitution A G downstream_gene_variant THCA-SA 11 11980449 11980449 single base substitution A G exon_variant UCEC-US 11 11906129 11906129 single base substitution T C downstream_gene_variant UCEC-US 11 11906129 11906129 single base substitution T C exon_variant UCEC-US 11 11906129 11906129 single base substitution T C splice_donor_variant UCEC-US 11 11919204 11919204 single base substitution T G 5_prime_UTR_variant UCEC-US 11 11919204 11919204 single base substitution T G missense_variant L118R 353T>G UCEC-US 11 11919204 11919204 single base substitution T G missense_variant L186R 557T>G UCEC-US 11 11919204 11919204 single base substitution T G missense_variant L206R 617T>G UCEC-US 11 11926958 11926958 single base substitution A C 5_prime_UTR_variant UCEC-US 11 11926958 11926958 single base substitution A C missense_variant N210H 628A>C UCEC-US 11 11926958 11926958 single base substitution A C missense_variant N278H 832A>C UCEC-US 11 11926958 11926958 single base substitution A C missense_variant N298H 892A>C UCEC-US 11 11941934 11941934 single base substitution A G 5_prime_UTR_variant UCEC-US 11 11941934 11941934 single base substitution A G missense_variant K303E 907A>G UCEC-US 11 11941934 11941934 single base substitution A G missense_variant K371E 1111A>G UCEC-US 11 11941934 11941934 single base substitution A G missense_variant K391E 1171A>G UCEC-US 11 11941938 11941938 single base substitution G T 5_prime_UTR_variant UCEC-US 11 11941938 11941938 single base substitution G T missense_variant R304I 911G>T UCEC-US 11 11941938 11941938 single base substitution G T missense_variant R372I 1115G>T UCEC-US 11 11941938 11941938 single base substitution G T missense_variant R392I 1175G>T UCEC-US 11 11941986 11941986 single base substitution G A 5_prime_UTR_variant UCEC-US 11 11941986 11941986 single base substitution G A missense_variant R320Q 959G>A UCEC-US 11 11941986 11941986 single base substitution G A missense_variant R388Q 1163G>A UCEC-US 11 11941986 11941986 single base substitution G A missense_variant R408Q 1223G>A UCEC-US 11 11944322 11944322 single base substitution A G 5_prime_UTR_variant UCEC-US 11 11944322 11944322 single base substitution A G missense_variant S356G 1066A>G UCEC-US 11 11944322 11944322 single base substitution A G missense_variant S424G 1270A>G UCEC-US 11 11944322 11944322 single base substitution A G missense_variant S444G 1330A>G UCEC-US 11 11944349 11944349 single base substitution G A 5_prime_UTR_variant UCEC-US 11 11944349 11944349 single base substitution G A missense_variant D365N 1093G>A UCEC-US 11 11944349 11944349 single base substitution G A missense_variant D433N 1297G>A UCEC-US 11 11944349 11944349 single base substitution G A missense_variant D453N 1357G>A UCEC-US 11 11944361 11944361 single base substitution G A 5_prime_UTR_variant UCEC-US 11 11944361 11944361 single base substitution G A missense_variant D369N 1105G>A UCEC-US 11 11944361 11944361 single base substitution G A missense_variant D437N 1309G>A UCEC-US 11 11944361 11944361 single base substitution G A missense_variant D457N 1369G>A UCEC-US 11 11951042 11951044 deletion of <=200bp ATT - 5_prime_UTR_variant UCEC-US 11 11951042 11951044 deletion of <=200bp ATT - inframe_deletion HY415H UCEC-US 11 11951042 11951044 deletion of <=200bp ATT - inframe_deletion HY483H UCEC-US 11 11951042 11951044 deletion of <=200bp ATT - inframe_deletion HY503H UCEC-US 11 11951046 11951046 single base substitution T G 5_prime_UTR_variant UCEC-US 11 11951046 11951046 single base substitution T G stop_gained Y416* 1248T>G UCEC-US 11 11951046 11951046 single base substitution T G stop_gained Y484* 1452T>G UCEC-US 11 11951046 11951046 single base substitution T G stop_gained Y504* 1512T>G UCEC-US 11 11955420 11955420 single base substitution G T 5_prime_UTR_variant UCEC-US 11 11955420 11955420 single base substitution G T stop_gained E535* 1603G>T UCEC-US 11 11955420 11955420 single base substitution G T stop_gained E603* 1807G>T UCEC-US 11 11955420 11955420 single base substitution G T stop_gained E623* 1867G>T UCEC-US 11 11955420 11955420 single base substitution G T upstream_gene_variant UCEC-US 11 11959901 11959901 single base substitution C A 5_prime_UTR_variant UCEC-US 11 11959901 11959901 single base substitution C A exon_variant UCEC-US 11 11959901 11959901 single base substitution C A missense_variant F657L 1971C>A UCEC-US 11 11959901 11959901 single base substitution C A missense_variant F725L 2175C>A UCEC-US 11 11959901 11959901 single base substitution C A missense_variant F745L 2235C>A UCEC-US 11 11959901 11959901 single base substitution C A upstream_gene_variant UCEC-US 11 11964050 11964050 single base substitution G A 5_prime_UTR_variant UCEC-US 11 11964050 11964050 single base substitution G A exon_variant UCEC-US 11 11964050 11964050 single base substitution G A missense_variant D760N 2278G>A UCEC-US 11 11964050 11964050 single base substitution G A missense_variant D828N 2482G>A UCEC-US 11 11964050 11964050 single base substitution G A missense_variant D848N 2542G>A UCEC-US 11 11964050 11964050 single base substitution G A upstream_gene_variant UCEC-US 11 11964232 11964232 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant UCEC-US 11 11964232 11964232 single base substitution C T exon_variant UCEC-US 11 11964232 11964232 single base substitution C T synonymous_variant I820I 2460C>T UCEC-US 11 11964232 11964232 single base substitution C T synonymous_variant I888I 2664C>T UCEC-US 11 11964232 11964232 single base substitution C T synonymous_variant I908I 2724C>T UCEC-US 11 11964232 11964232 single base substitution C T upstream_gene_variant UCEC-US 11 11964360 11964360 single base substitution A G 5_prime_UTR_variant UCEC-US 11 11964360 11964360 single base substitution A G exon_variant UCEC-US 11 11964360 11964360 single base substitution A G missense_variant D863G 2588A>G UCEC-US 11 11964360 11964360 single base substitution A G missense_variant D931G 2792A>G UCEC-US 11 11964360 11964360 single base substitution A G missense_variant D951G 2852A>G UCEC-US 11 11964360 11964360 single base substitution A G upstream_gene_variant UCEC-US 11 11964496 11964496 single base substitution G T 5_prime_UTR_variant UCEC-US 11 11964496 11964496 single base substitution G T exon_variant UCEC-US 11 11964496 11964496 single base substitution G T synonymous_variant T908T 2724G>T UCEC-US 11 11964496 11964496 single base substitution G T synonymous_variant T976T 2928G>T UCEC-US 11 11964496 11964496 single base substitution G T synonymous_variant T996T 2988G>T UCEC-US 11 11964496 11964496 single base substitution G T upstream_gene_variant UCEC-US 11 11969594 11969594 single base substitution T C 5_prime_UTR_variant UCEC-US 11 11969594 11969594 single base substitution T C downstream_gene_variant UCEC-US 11 11969594 11969594 single base substitution T C exon_variant UCEC-US 11 11969594 11969594 single base substitution T C missense_variant V1065A 3194T>C UCEC-US 11 11969594 11969594 single base substitution T C missense_variant V1085A 3254T>C UCEC-US 11 11969594 11969594 single base substitution T C missense_variant V997A 2990T>C UCEC-US 11 11969594 11969594 single base substitution T C upstream_gene_variant UCEC-US 11 11969599 11969599 single base substitution G A 5_prime_UTR_variant UCEC-US 11 11969599 11969599 single base substitution G A downstream_gene_variant UCEC-US 11 11969599 11969599 single base substitution G A exon_variant UCEC-US 11 11969599 11969599 single base substitution G A missense_variant A1067T 3199G>A UCEC-US 11 11969599 11969599 single base substitution G A missense_variant A1087T 3259G>A UCEC-US 11 11969599 11969599 single base substitution G A missense_variant A999T 2995G>A UCEC-US 11 11969599 11969599 single base substitution G A upstream_gene_variant UCEC-US 11 11969622 11969622 deletion of <=200bp C - 5_prime_UTR_variant UCEC-US 11 11969622 11969622 deletion of <=200bp C - downstream_gene_variant UCEC-US 11 11969622 11969622 deletion of <=200bp C - exon_variant UCEC-US 11 11969622 11969622 deletion of <=200bp C - frameshift_variant S1006 UCEC-US 11 11969622 11969622 deletion of <=200bp C - frameshift_variant S1074 UCEC-US 11 11969622 11969622 deletion of <=200bp C - frameshift_variant S1094 UCEC-US 11 11969622 11969622 deletion of <=200bp C - upstream_gene_variant UCEC-US 11 11969623 11969623 single base substitution G A 5_prime_UTR_variant UCEC-US 11 11969623 11969623 single base substitution G A downstream_gene_variant UCEC-US 11 11969623 11969623 single base substitution G A exon_variant UCEC-US 11 11969623 11969623 single base substitution G A missense_variant V1007I 3019G>A UCEC-US 11 11969623 11969623 single base substitution G A missense_variant V1075I 3223G>A UCEC-US 11 11969623 11969623 single base substitution G A missense_variant V1095I 3283G>A UCEC-US 11 11969623 11969623 single base substitution G A upstream_gene_variant UCEC-US 11 11974391 11974391 single base substitution C T downstream_gene_variant UCEC-US 11 11974391 11974391 single base substitution C T exon_variant UCEC-US 11 11974391 11974391 single base substitution C T synonymous_variant S1161S 3483C>T UCEC-US 11 11974391 11974391 single base substitution C T synonymous_variant S1229S 3687C>T UCEC-US 11 11974391 11974391 single base substitution C T synonymous_variant S1249S 3747C>T UCEC-US 11 11974391 11974391 single base substitution C T synonymous_variant S31S 93C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand T3118 COSM4739873 c.40-1G>T p.? Unknown 11:11884466-11884466 + S01023 COSM5666362 c.2506T>C p.Y836H Substitution - Missense 11:11942467-11942467 + pfg089T COSM4765044 c.3302_3303insTTTCA p.S1102fs*43 Insertion - Frameshift 11:11948095-11948096 + C086 COSM5541498 c.2231C>T p.S744F Substitution - Missense 11:11942456-11942456 + SNUH_G10_S1 COSM3998260 c.3870G>A p.Q1290Q Substitution - coding silent 11:11955081-11955081 + TCGA-BH-A18F-01 COSM5218143 c.4046G>A p.R1349H Substitution - Missense 11:11956093-11956093 + SNUH_G16_S1 COSM3998263 c.3715T>G p.L1239V Substitution - Missense 11:11956026-11956026 + TCGA-AP-A0LT-01 COSM923872 c.1244_1246delATT p.Y417delY Deletion - In frame 11:11929495-11929497 + S02237 COSM5676410 c.3447G>T p.M1149I Substitution - Missense 11:11952808-11952808 + HCC154T COSM3666131 c.1746G>T p.R582R Substitution - coding silent 11:11936383-11936383 + 313 COSM1741962 c.3376G>A p.D1126N Substitution - Missense 11:11950479-11950479 + 9227_T COSM5039678 c.2128G>A p.E710K Substitution - Missense 11:11942353-11942353 + CT-TC COSM4989691 c.1387G>A p.A463T Substitution - Missense 11:11930116-11930116 + TCGA-AN-A046-01 COSM3808569 c.1386C>T p.F462F Substitution - coding silent 11:11930115-11930115 + TCGA-EK-A2PL-01 COSM4838412 c.2363G>C p.R788T Substitution - Missense 11:11940538-11940538 + SC_9055 COSM5547817 c.2574_2579delAGTCAA p.V859_K860delVK Deletion - In frame 11:11942535-11942540 + TCGA-D1-A160-01 COSM923807 c.153+2T>C p.? Unknown 11:11884582-11884582 + CN-AML-08-T COSM3998260 c.3870G>A p.Q1290Q Substitution - coding silent 11:11955081-11955081 + HCC136 COSM1604204 c.1418A>G p.Y473C Substitution - Missense 11:11930722-11930722 + HCC066T COSM5821497 c.3370A>T p.R1124* Substitution - Nonsense 11:11948520-11948520 + 3N55-VS-3T55 COSM4983697 c.3989A>C p.E1330A Substitution - Missense 11:11956036-11956036 + 16461 COSM5613302 c.3859G>T p.D1287Y Substitution - Missense 11:11956170-11956170 + TCGA-A4-7996-01 COSM3985992 c.1009G>T p.D337Y Substitution - Missense 11:11920489-11920489 + TCGA-BR-4362-01 COSM4018587 c.3785T>C p.V1262A Substitution - Missense 11:11956096-11956096 + B37-Tumor COSM1746090 c.1641G>C p.K547N Substitution - Missense 11:11933911-11933911 + 4537_T COSM3979186 c.4098A>T p.G1366G Substitution - coding silent 11:11956145-11956145 + S00539 COSM5658701 c.1029+1G>C p.? Unknown 11:11905549-11905549 + sysucc-1370T COSM5469514 c.2988G>A p.T996T Substitution - coding silent 11:11942949-11942949 + LUAD-YINHD COSM348357 c.3205G>C p.E1069Q Substitution - Missense 11:11949949-11949949 + 3N55-VS-3T55 COSM4983698 c.3725A>C p.E1242A Substitution - Missense 11:11956036-11956036 + SJDOSTEOS005 COSM5759851 c.1314+2T>C p.? Unknown 11:11929567-11929567 + TCGA-B1-A47O-01 COSM4404911 c.1234C>T p.P412S Substitution - Missense 11:11920450-11920450 + YUFERY COSM5371820 c.2663A>C p.N888T Substitution - Missense 11:11942888-11942888 + TCGA-D5-6928-01 COSM1351887 c.782C>T p.A261V Substitution - Missense 11:11920172-11920172 + TCGA-AR-A1AI-01 COSM428547 c.2426G>T p.S809I Substitution - Missense 11:11942651-11942651 + BD135T COSM5516917 c.1126-8delT p.? Unknown 11:11920334-11920334 + RK308_C01 COSM3738893 c.1944A>G p.E648E Substitution - coding silent 11:11936317-11936317 + 24 COSM4777982 c.609G>T p.L203F Substitution - Missense 11:11897649-11897649 + TCGA-BH-A0B6-01 COSM3808531 c.81G>C p.M27I Substitution - Missense 11:11873841-11873841 + YUKAT COSM5371806 c.305T>C p.L102P Substitution - Missense 11:11897609-11897609 + sysucc-1370T COSM5469515 c.2724G>A p.T908T Substitution - coding silent 11:11942949-11942949 + TCGA-AX-A0J0-01 COSM923834 c.353T>G p.L118R Substitution - Missense 11:11897657-11897657 + PD4128a COSM165452 c.359T>A p.M120K Substitution - Missense 11:11897663-11897663 + TCGA-CA-6718-01 COSM5144290 c.2812T>G p.F938V Substitution - Missense 11:11942773-11942773 + T3090 COSM4333872 c.3355delA p.G1121fs*22 Deletion - Frameshift 11:11948505-11948505 + TCGA-EP-A3JL-01 COSM4913932 c.2218C>G p.L740V Substitution - Missense 11:11942443-11942443 + sysucc-880T COSM5461925 c.2466A>G p.S822S Substitution - coding silent 11:11942691-11942691 + ME048T COSM229775 c.1516G>A p.E506K Substitution - Missense 11:11933072-11933072 + YUPAER COSM5371821 c.3184C>T p.L1062L Substitution - coding silent 11:11947977-11947977 + TCGA-EE-A2MI-06 COSM3444174 c.333G>A p.L111L Substitution - coding silent 11:11897637-11897637 + HCC119 COSM3666128 c.1246G>C p.D416H Substitution - Missense 11:11920462-11920462 + TCGA-AN-A046-01 COSM3808575 c.2314C>T p.R772C Substitution - Missense 11:11940489-11940489 + T3446 COSM4739882 c.3191C>A p.A1064D Substitution - Missense 11:11947984-11947984 + PD4953a COSM5771538 c.330G>C p.K110N Substitution - Missense 11:11884493-11884493 + TCGA-EE-A3JB-06 COSM4898492 c.1281A>T p.K427N Substitution - Missense 11:11922726-11922726 + TCGA-EP-A3JL-01 COSM4913931 c.2482C>G p.L828V Substitution - Missense 11:11942443-11942443 + TCGA-FW-A3R5-06 COSM3868576 c.3316C>T p.H1106Y Substitution - Missense 11:11950419-11950419 + MZ7-mel COSM24323 c.857G>A p.R286Q Substitution - Missense 11:11920247-11920247 + HCC154T COSM3666130 c.2010G>T p.R670R Substitution - coding silent 11:11936383-11936383 + TCGA-HU-A4GU-01 COSM1351905 c.1794C>T p.G598G Substitution - coding silent 11:11936431-11936431 + Mel18 COSM3726963 c.3308T>C p.L1103S Substitution - Missense 11:11950411-11950411 + HCA7 COSM4018556 c.660C>T p.Y220Y Substitution - coding silent 11:11905443-11905443 + LS180 COSM4185330 c.2204G>A p.R735H Substitution - Missense 11:11938323-11938323 + TCGA-CA-6717-01 COSM5826913 c.617T>G p.L206R Substitution - Missense 11:11897657-11897657 + TCGA-DA-A3F8-06 COSM3444224 c.3839C>T p.P1280L Substitution - Missense 11:11955050-11955050 + RK308_C01 COSM3738894 c.1680A>G p.E560E Substitution - coding silent 11:11936317-11936317 + TCGA-BS-A0UL-01 COSM923906 c.3019G>A p.V1007I Substitution - Missense 11:11948076-11948076 + ESCC_157 COSM5646191 c.1634A>G p.Y545C Substitution - Missense 11:11930099-11930099 + TCGA-BT-A0YX-01 COSM415308 c.987G>A p.M329I Substitution - Missense 11:11920467-11920467 + CSCC-10-T COSM4565018 c.1641_1642GG>AA p.E548K Substitution - Missense 11:11933911-11933912 + PD4953a COSM5771539 c.66G>C p.K22N Substitution - Missense 11:11884493-11884493 + TCGA-BR-8680-01 COSM4018580 c.3600T>G p.I1200M Substitution - Missense 11:11950439-11950439 + TCGA-AN-A046-01 COSM3808576 c.2050C>T p.R684C Substitution - Missense 11:11940489-11940489 + S02237 COSM5676409 c.3711G>T p.M1237I Substitution - Missense 11:11952808-11952808 + TCGA-CA-6717-01 COSM923834 c.353T>G p.L118R Substitution - Missense 11:11897657-11897657 + OV207 COSM252912 c.1940G>A p.R647H Substitution - Missense 11:11938323-11938323 + QC2-32-T2 COSM3998261 c.3606G>A p.Q1202Q Substitution - coding silent 11:11955081-11955081 + TCGA-EE-A29D-06 COSM3444222 c.3796C>T p.P1266S Substitution - Missense 11:11954918-11954918 + TCGA-B5-A0JY-01 COSM180941 c.2460C>T p.I820I Substitution - coding silent 11:11942685-11942685 + sysucc-880T COSM5461924 c.2730A>G p.S910S Substitution - coding silent 11:11942691-11942691 + TCGA-BR-4362-01 COSM4018555 c.924C>T p.Y308Y Substitution - coding silent 11:11905443-11905443 + Pat_41_B COSM5837994 c.2148G>A p.M716I Substitution - Missense 11:11942373-11942373 + TCGA-A4-7996-01 COSM3985991 c.1273G>T p.D425Y Substitution - Missense 11:11920489-11920489 + B104-0-Tumor COSM3931237 c.2061C>G p.V687V Substitution - coding silent 11:11936434-11936434 + T298 COSM4739874 c.1133G>A p.R378Q Substitution - Missense 11:11920349-11920349 + CSCC-60-T COSM4018579 c.3265C>T p.R1089C Substitution - Missense 11:11950368-11950368 + SH-1537 COSM5017593 c.832A>C p.R278R Substitution - coding silent 11:11903295-11903295 + TCGA-D9-A6EC-06 COSM4404912 c.970C>T p.P324S Substitution - Missense 11:11920450-11920450 + A3 COSM5349625 c.1781A>G p.E594G Substitution - Missense 11:11933073-11933073 + 134413 COSM326843 c.839A>G p.K280R Substitution - Missense 11:11920229-11920229 + SNUH_G76_S1 COSM3998261 c.3606G>A p.Q1202Q Substitution - coding silent 11:11955081-11955081 + SNUH_G10_S1 COSM3998261 c.3606G>A p.Q1202Q Substitution - coding silent 11:11955081-11955081 + 16461 COSM5613301 c.4123G>T p.D1375Y Substitution - Missense 11:11956170-11956170 + TCGA-DD-A116-01 COSM4912233 c.738T>C p.Y246Y Substitution - coding silent 11:11905521-11905521 + TCGA-HU-A4GU-01 COSM4018575 c.2058C>T p.G686G Substitution - coding silent 11:11936431-11936431 + TCGA-AP-A0LM-01 COSM923900 c.2588A>G p.D863G Substitution - Missense 11:11942813-11942813 + HDC101 COSM4635853 c.1394C>G p.S465C Substitution - Missense 11:11930698-11930698 + TCGA-GD-A3OP-01 COSM1297729 c.3703G>C p.E1235Q Substitution - Missense 11:11956014-11956014 + LIM1215 COSM4185264 c.646T>A p.L216I Substitution - Missense 11:11897686-11897686 + TCGA-A6-5661-01 COSM4018575 c.2058C>T p.G686G Substitution - coding silent 11:11936431-11936431 + TCGA-DI-A0WH-01 COSM923875 c.1281G>A p.Q427Q Substitution - coding silent 11:11929532-11929532 + sysucc-1972T COSM5480319 c.342C>T p.D114D Substitution - coding silent 11:11884505-11884505 + B37-Tumor COSM3931236 c.1905G>C p.K635N Substitution - Missense 11:11933911-11933911 + TCGA-32-2495-01 COSM3397474 c.3202C>T p.H1068Y Substitution - Missense 11:11947995-11947995 + BD121T COSM5515410 c.1706G>A p.R569H Substitution - Missense 11:11936343-11936343 + LS174T COSM252912 c.1940G>A p.R647H Substitution - Missense 11:11938323-11938323 + T3021 COSM4739876 c.1953A>G p.I651M Substitution - Missense 11:11936326-11936326 + pfg089T COSM4765045 c.3038_3039insTTTCA p.S1014fs*43 Insertion - Frameshift 11:11948095-11948096 + TCGA-HU-8602-01 COSM4018565 c.1534C>T p.R512* Substitution - Nonsense 11:11933090-11933090 + HN_01000 COSM128451 c.3022C>A p.R1008R Substitution - coding silent 11:11948079-11948079 + LUAD-F00018 COSM338948 c.1615G>C p.E539Q Substitution - Missense 11:11933885-11933885 + T298 COSM4739875 c.869G>A p.R290Q Substitution - Missense 11:11920349-11920349 + TCGA-CJ-5677-01 COSM466461 c.3615C>T p.D1205D Substitution - coding silent 11:11955090-11955090 + OSCC-GB_00450111 COSM3710111 c.1267G>T p.V423F Substitution - Missense 11:11920483-11920483 + CSCC-31-T COSM4470958 c.1691C>T p.P564L Substitution - Missense 11:11936328-11936328 + TCGA-AP-A0LM-01 COSM923870 c.1093G>A p.D365N Substitution - Missense 11:11922802-11922802 + 2492729 COSM5725991 c.1347G>A p.Q449Q Substitution - coding silent 11:11922792-11922792 + CN-AML-NR-08-Dx COSM3998261 c.3606G>A p.Q1202Q Substitution - coding silent 11:11955081-11955081 + TCGA-AX-A0J1-01 COSM923871 c.1105G>A p.D369N Substitution - Missense 11:11922814-11922814 + TCGA-F5-6814-01 COSM3415595 c.221C>A p.S74Y Substitution - Missense 11:11892035-11892035 + B104-0 COSM1746091 c.1797C>G p.V599V Substitution - coding silent 11:11936434-11936434 + TCGA-AY-5543-01 COSM5136149 c.3684G>A p.L1228L Substitution - coding silent 11:11952781-11952781 + HCC154 COSM3666130 c.2010G>T p.R670R Substitution - coding silent 11:11936383-11936383 + pfg053T COSM4746685 c.2694_2705del12 p.T900_S903delTETS Deletion - In frame 11:11942655-11942666 + TCGA-BS-A0UA-01 COSM923907 c.3483C>T p.S1161S Substitution - coding silent 11:11952844-11952844 + C086 COSM5541497 c.2495C>T p.S832F Substitution - Missense 11:11942456-11942456 + TCGA-CM-4743-01 COSM4333872 c.3355delA p.G1121fs*22 Deletion - Frameshift 11:11948505-11948505 + TCGA-Q1-A73O-01 COSM4834544 c.415G>C p.D139H Substitution - Missense 11:11902740-11902740 + S00539 COSM316418 c.765+1G>C p.? Unknown 11:11905549-11905549 + S01023 COSM5666363 c.2242T>C p.Y748H Substitution - Missense 11:11942467-11942467 + S00539 COSM316418 c.765+1G>C p.? Unknown 11:11905549-11905549 + SH-1537 COSM5017594 c.568A>C p.R190R Substitution - coding silent 11:11903295-11903295 + CSCC-10-T COSM4565017 c.1905_1906GG>AA p.E636K Substitution - Missense 11:11933911-11933912 + ESCC_BICR_038T COSM5434497 c.1863G>C p.M621I Substitution - Missense 11:11933869-11933869 + CHC121T COSM216943 c.3209A>T p.E1070V Substitution - Missense 11:11949953-11949953 + Pat_41_B COSM5837993 c.2412G>A p.M804I Substitution - Missense 11:11942373-11942373 + TCGA-EB-A551-01 COSM3444226 c.4061C>T p.P1354L Substitution - Missense 11:11956108-11956108 + TCGA-EB-A5SE-01 COSM3444221 c.2435C>T p.T812I Substitution - Missense 11:11942660-11942660 + 587376 COSM1232085 c.2549T>G p.F850C Substitution - Missense 11:11942774-11942774 + 24 COSM4777983 c.345G>T p.L115F Substitution - Missense 11:11897649-11897649 + TCGA-HU-A4GU-01 COSM4018576 c.3282C>T p.S1094S Substitution - coding silent 11:11948075-11948075 + TCGA-BT-A2LB-01 COSM3791262 c.3443A>G p.K1148R Substitution - Missense 11:11949923-11949923 + ccRCC-30 COSM1664924 c.2692G>T p.D898Y Substitution - Missense 11:11942917-11942917 + TCGA-DK-A3IN-01 COSM3791244 c.533C>G p.S178C Substitution - Missense 11:11892083-11892083 + CT-TC COSM4989690 c.1651G>A p.A551T Substitution - Missense 11:11930116-11930116 + PCSI_0170_Pa_P_526 COSM4964954 c.3776T>G p.L1259R Substitution - Missense 11:11954898-11954898 + TCGA-F5-6814-01 COSM3415594 c.485C>A p.S162Y Substitution - Missense 11:11892035-11892035 + TCGA-BS-A0UL-01 COSM923869 c.1066A>G p.S356G Substitution - Missense 11:11922775-11922775 + TCGA-B0-5081-01 COSM466460 c.2863G>A p.E955K Substitution - Missense 11:11943088-11943088 + B47-Tumor COSM3931238 c.3201A>G p.Q1067Q Substitution - coding silent 11:11947994-11947994 + TCGA-BS-A0UF-01 COSM923897 c.1603G>T p.E535* Substitution - Nonsense 11:11933873-11933873 + TCGA-F5-6814-01 COSM3415603 c.802C>A p.L268M Substitution - Missense 11:11920192-11920192 + TCGA-CG-5721-01 COSM4018558 c.701A>G p.D234G Substitution - Missense 11:11905484-11905484 + sysucc-863T COSM5765259 c.3152-8G>T p.? Unknown 11:11947937-11947937 + PCSI_0170_Pa_P_526 COSM4964955 c.3512T>G p.L1171R Substitution - Missense 11:11954898-11954898 + PCSI_0090_Pa_X COSM5419913 c.774A>G p.A258A Substitution - coding silent 11:11920164-11920164 + TCGA-AP-A0LM-01 COSM923899 c.2278G>A p.D760N Substitution - Missense 11:11942503-11942503 + TCGA-F5-6814-01 COSM3415602 c.1066C>A p.L356M Substitution - Missense 11:11920192-11920192 + LIM2551 COSM4643510 c.3464A>G p.Q1155R Substitution - Missense 11:11952825-11952825 + TCGA-B5-A0K3-01 COSM923806 c.61G>C p.D21H Substitution - Missense 11:11884488-11884488 + TCGA-Q1-A73O-01 COSM4834543 c.679G>C p.D227H Substitution - Missense 11:11902740-11902740 + TCGA-EE-A3JB-06 COSM4898493 c.1017A>T p.K339N Substitution - Missense 11:11922726-11922726 + KM12 COSM2107002 c.1270A>G p.S424G Substitution - Missense 11:11929521-11929521 + TCGA-CC-A3MA-01 COSM4942735 c.1200G>A p.M400I Substitution - Missense 11:11920416-11920416 + TCGA-BR-8361-01 COSM4018584 c.3773A>C p.K1258T Substitution - Missense 11:11952870-11952870 + TCGA-DK-A3IN-01 COSM3791245 c.269C>G p.S90C Substitution - Missense 11:11892083-11892083 + TCGA-AG-A002-01 COSM264620 c.3674C>T p.A1225V Substitution - Missense 11:11955149-11955149 + TCGA-BR-8680-01 COSM4018578 c.3529C>T p.R1177C Substitution - Missense 11:11950368-11950368 + TCGA-AR-A1AI-01 COSM5831676 c.2690G>T p.S897I Substitution - Missense 11:11942651-11942651 + TCGA-56-6546-01 COSM686871 c.2769A>C p.E923D Substitution - Missense 11:11942994-11942994 + LIM1215 COSM4185265 c.382T>A p.L128I Substitution - Missense 11:11897686-11897686 + TCGA-BC-A10U-01 COSM4942382 c.3019G>T p.D1007Y Substitution - Missense 11:11942980-11942980 + 449 COSM4435329 c.1651G>C p.E551Q Substitution - Missense 11:11933921-11933921 + 205T COSM1726774 c.1462G>A p.D488N Substitution - Missense 11:11933018-11933018 + TCGA-RA-A741-01 COSM4818887 c.2251A>G p.R751G Substitution - Missense 11:11942476-11942476 + TCGA-D1-A101-01 COSM923904 c.2995G>A p.A999T Substitution - Missense 11:11948052-11948052 + HCC066T COSM5821498 c.3106A>T p.R1036* Substitution - Nonsense 11:11948520-11948520 + T1154 COSM4739880 c.2760A>G p.S920S Substitution - coding silent 11:11942721-11942721 + PT41 COSM5924552 c.1510T>C p.Y504H Substitution - Missense 11:11929497-11929497 + 0057_CRUK_PC_0057_T1_DNA COSM4185297 c.1121G>A p.R374Q Substitution - Missense 11:11920247-11920247 + TCGA-BR-8680-01 COSM4018581 c.3336T>G p.I1112M Substitution - Missense 11:11950439-11950439 + SJDOSTEOS005 COSM5759850 c.1578+2T>C p.? Unknown 11:11929567-11929567 + LP6005334-DNA_E03 COSM5032773 c.2200A>G p.I734V Substitution - Missense 11:11942425-11942425 + SJDES001-R COSM4574116 c.2569G>T p.D857Y Substitution - Missense 11:11942794-11942794 + 9227_T COSM5039670 c.1417G>A p.E473K Substitution - Missense 11:11922862-11922862 + TCGA-D5-6928-01 COSM5165525 c.1046C>T p.A349V Substitution - Missense 11:11920172-11920172 + HCA7 COSM4018555 c.924C>T p.Y308Y Substitution - coding silent 11:11905443-11905443 + LP6005334-DNA_E03 COSM5032772 c.2464A>G p.I822V Substitution - Missense 11:11942425-11942425 + T3090 COSM1351908 c.3091delA p.G1033fs*22 Deletion - Frameshift 11:11948505-11948505 + 9227_T COSM5039677 c.2392G>A p.E798K Substitution - Missense 11:11942353-11942353 + TCGA-AY-5543-01 COSM1351909 c.3420G>A p.L1140L Substitution - coding silent 11:11952781-11952781 + 49M COSM5593903 c.1364C>T p.S455F Substitution - Missense 11:11922809-11922809 + TCGA-D8-A27I-01 COSM1475117 c.2615A>G p.D872G Substitution - Missense 11:11942840-11942840 + 8058333 COSM3383254 c.1712-1G>C p.? Unknown 11:11933003-11933003 + CSCC-17-T COSM4448981 c.418-2A>T p.? Unknown 11:11891966-11891966 + 0057_CRUK_PC_0057_T1_DNA COSM24323 c.857G>A p.R286Q Substitution - Missense 11:11920247-11920247 + TCGA-AN-A046-01 COSM3808568 c.1650C>T p.F550F Substitution - coding silent 11:11930115-11930115 + 49M COSM5593906 c.2592G>A p.R864R Substitution - coding silent 11:11942817-11942817 + B37 COSM1746090 c.1641G>C p.K547N Substitution - Missense 11:11933911-11933911 + TCGA-CM-4743-01 COSM1351908 c.3091delA p.G1033fs*22 Deletion - Frameshift 11:11948505-11948505 + 49M COSM5593904 c.1100C>T p.S367F Substitution - Missense 11:11922809-11922809 + LS180 COSM252912 c.1940G>A p.R647H Substitution - Missense 11:11938323-11938323 + BD121T COSM5515409 c.1970G>A p.R657H Substitution - Missense 11:11936343-11936343 + TCGA-A6-5661-01 COSM1351905 c.1794C>T p.G598G Substitution - coding silent 11:11936431-11936431 + HN_62338 COSM130127 c.3583A>G p.I1195V Substitution - Missense 11:11955058-11955058 + TCGA-AA-3715-01 COSM270531 c.1887A>C p.K629N Substitution - Missense 11:11938270-11938270 + B109-Tumor COSM1746093 c.3667G>A p.D1223N Substitution - Missense 11:11955142-11955142 + J13_T COSM3979183 c.1355A>G p.N452S Substitution - Missense 11:11922800-11922800 + HDC101 COSM4635852 c.1658C>G p.S553C Substitution - Missense 11:11930698-11930698 + B47 COSM1746092 c.2937A>G p.Q979Q Substitution - coding silent 11:11947994-11947994 + TCGA-AG-3892-01 COSM258340 c.2941T>G p.L981V Substitution - Missense 11:11947998-11947998 + Gp2D COSM4626756 c.1187C>T p.S396F Substitution - Missense 11:11929438-11929438 + 1N52-VS-1T52 COSM4976742 c.853G>A p.E285K Substitution - Missense 11:11903316-11903316 + 1339-01-03TD COSM5417922 c.1239G>A p.E413E Substitution - coding silent 11:11920455-11920455 + CSCC-7-T COSM4490668 c.3938C>G p.A1313G Substitution - Missense 11:11955149-11955149 + CSCC-7-T COSM4490669 c.3674C>G p.A1225G Substitution - Missense 11:11955149-11955149 + B109-Tumor COSM3931239 c.3931G>A p.D1311N Substitution - Missense 11:11955142-11955142 + Mel18 COSM3726962 c.3572T>C p.L1191S Substitution - Missense 11:11950411-11950411 + TCGA-A5-A0GA-01 COSM923902 c.2849C>A p.P950H Substitution - Missense 11:11943074-11943074 + HCC154 COSM3666131 c.1746G>T p.R582R Substitution - coding silent 11:11936383-11936383 + TCGA-B1-A47O-01 COSM4404912 c.970C>T p.P324S Substitution - Missense 11:11920450-11920450 + TCGA-CA-6717-01 COSM1351911 c.3820A>G p.I1274V Substitution - Missense 11:11956131-11956131 + B104-0-Tumor COSM1746091 c.1797C>G p.V599V Substitution - coding silent 11:11936434-11936434 + TCGA-CC-A3MA-01 COSM4942736 c.936G>A p.M312I Substitution - Missense 11:11920416-11920416 + TCGA-EB-A551-01 COSM3444227 c.3797C>T p.P1266L Substitution - Missense 11:11956108-11956108 + TCGA-RA-A741-01 COSM4818886 c.2515A>G p.R839G Substitution - Missense 11:11942476-11942476 + ESCC_113 COSM5649825 c.624G>T p.M208I Substitution - Missense 11:11897664-11897664 + TCGA-D1-A16Y-01 COSM923868 c.959G>A p.R320Q Substitution - Missense 11:11920439-11920439 + TCGA-D1-A160-01 COSM923905 c.3018delC p.S1006fs*4 Deletion - Frameshift 11:11948075-11948075 + SJHYPO021 COSM4775517 c.3545_3546insA p.E1183fs*1 Insertion - Frameshift 11:11954931-11954932 + B109 COSM1746093 c.3667G>A p.D1223N Substitution - Missense 11:11955142-11955142 + TCGA-BL-A13I-01 COSM415307 c.1519C>G p.Q507E Substitution - Missense 11:11933075-11933075 + TCGA-AM-5820-01 COSM3752174 c.224G>T p.G75V Substitution - Missense 11:11892038-11892038 + sysucc-863T COSM5765260 c.2888-8G>T p.? Unknown 11:11947937-11947937 + ESCC_BICR_038T COSM5434498 c.1599G>C p.M533I Substitution - Missense 11:11933869-11933869 + ESCC_113 COSM5649826 c.360G>T p.M120I Substitution - Missense 11:11897664-11897664 + YUKAT COSM5371817 c.1548G>A p.W516* Substitution - Nonsense 11:11929535-11929535 + CN-AML-NR-08-Dx COSM3998260 c.3870G>A p.Q1290Q Substitution - coding silent 11:11955081-11955081 + TCGA-18-3417-01 COSM686870 c.2951T>G p.F984C Substitution - Missense 11:11948008-11948008 + LIM2551 COSM4643509 c.3728A>G p.Q1243R Substitution - Missense 11:11952825-11952825 + S02350 COSM5694573 c.1788A>G p.L596L Substitution - coding silent 11:11936425-11936425 + TCGA-HU-8602-01 COSM4018582 c.3673C>T p.L1225F Substitution - Missense 11:11952770-11952770 + HCT116 COSM4333872 c.3355delA p.G1121fs*22 Deletion - Frameshift 11:11948505-11948505 + TCGA-HU-8602-01 COSM4018583 c.3409C>T p.L1137F Substitution - Missense 11:11952770-11952770 + 9227_T COSM165450 c.1153G>A p.E385K Substitution - Missense 11:11922862-11922862 + HCC136T COSM1604204 c.1418A>G p.Y473C Substitution - Missense 11:11930722-11930722 + 1339-01-03TD COSM5417923 c.975G>A p.E325E Substitution - coding silent 11:11920455-11920455 + SCC-15 COSM4185283 c.667G>A p.E223K Substitution - Missense 11:11902728-11902728 + TCGA-D8-A27I-01 COSM5226742 c.2879A>G p.D960G Substitution - Missense 11:11942840-11942840 + HCC119T COSM1604203 c.982G>C p.D328H Substitution - Missense 11:11920462-11920462 + 8058333 COSM3383255 c.1448-1G>C p.? Unknown 11:11933003-11933003 + TCGA-AM-5820-01 COSM3752173 c.488G>T p.G163V Substitution - Missense 11:11892038-11892038 + TCGA-HC-7750-01 COSM3670689 c.2986C>A p.R996R Substitution - coding silent 11:11948043-11948043 + 6115121 COSM2107089 c.2032C>T p.R678C Substitution - Missense 11:11940471-11940471 + TCGA-61-2611-02 COSM1321860 c.534G>T p.E178D Substitution - Missense 11:11902859-11902859 + KPOPBR-03-T COSM5964846 c.3778A>G p.S1260G Substitution - Missense 11:11954900-11954900 + TCGA-CG-5721-01 COSM4018557 c.965A>G p.D322G Substitution - Missense 11:11905484-11905484 + CSCC-60-T COSM4018578 c.3529C>T p.R1177C Substitution - Missense 11:11950368-11950368 + 4537_T COSM3979187 c.3834A>T p.G1278G Substitution - coding silent 11:11956145-11956145 + TCGA-AA-3715-01 COSM270530 c.1111G>T p.G371C Substitution - Missense 11:11922820-11922820 + YUWIA COSM5371823 c.3410C>T p.P1137L Substitution - Missense 11:11949890-11949890 + TCGA-DD-A116-01 COSM4912232 c.1002T>C p.Y334Y Substitution - coding silent 11:11905521-11905521 + CHC121T COSM5348911 c.3473A>T p.E1158V Substitution - Missense 11:11949953-11949953 + SNUH_G16_S1 COSM3998261 c.3606G>A p.Q1202Q Substitution - coding silent 11:11955081-11955081 + SNUH_G16_S1 COSM3998260 c.3870G>A p.Q1290Q Substitution - coding silent 11:11955081-11955081 + C0051T COSM4165668 c.1331G>C p.S444T Substitution - Missense 11:11922776-11922776 + PD4120a COSM165451 c.1030G>C p.E344Q Substitution - Missense 11:11922739-11922739 + HCT116 COSM1351908 c.3091delA p.G1033fs*22 Deletion - Frameshift 11:11948505-11948505 + CSCC-17-T COSM4448982 c.154-2A>T p.? Unknown 11:11891966-11891966 + TCGA-B5-A11N-01 COSM923873 c.1248T>G p.Y416* Substitution - Nonsense 11:11929499-11929499 + B47-Tumor COSM1746092 c.2937A>G p.Q979Q Substitution - coding silent 11:11947994-11947994 + KPOPBR-03-T COSM5964847 c.3514A>G p.S1172G Substitution - Missense 11:11954900-11954900 + 6115121 COSM4185332 c.2296C>T p.R766C Substitution - Missense 11:11940471-11940471 + BD135T COSM5516918 c.862-8delT p.? Unknown 11:11920334-11920334 + LUAD-B00523 COSM331696 c.3771G>T p.K1257N Substitution - Missense 11:11956082-11956082 + TCGA-EK-A2PL-01 COSM4838413 c.2099G>C p.R700T Substitution - Missense 11:11940538-11940538 + T3446 COSM4739883 c.2927C>A p.A976D Substitution - Missense 11:11947984-11947984 + AOCS-145-1-6 COSM3981341 c.3442G>T p.E1148* Substitution - Nonsense 11:11952803-11952803 + sysucc-1397T COSM5473083 c.3818C>T p.A1273V Substitution - Missense 11:11954940-11954940 + T3118 COSM4739872 c.304-1G>T p.? Unknown 11:11884466-11884466 + 45T COSM3710112 c.1003G>T p.V335F Substitution - Missense 11:11920483-11920483 + TCGA-FW-A3R5-06 COSM3868575 c.3580C>T p.H1194Y Substitution - Missense 11:11950419-11950419 + YUKAT COSM5371805 c.569T>C p.L190P Substitution - Missense 11:11897609-11897609 + TCGA-60-2713-01 COSM686872 c.2047T>G p.L683V Substitution - Missense 11:11940486-11940486 + TCGA-AX-A0J0-01 COSM923867 c.911G>T p.R304I Substitution - Missense 11:11920391-11920391 + TCGA-BH-A18F-01 COSM428548 c.3782G>A p.R1261H Substitution - Missense 11:11956093-11956093 + TCGA-HC-7750-01 COSM3670688 c.3250C>A p.R1084R Substitution - coding silent 11:11948043-11948043 + TCGA-BR-4362-01 COSM4018586 c.4049T>C p.V1350A Substitution - Missense 11:11956096-11956096 + SC_9055 COSM5547818 c.2310_2315delAGTCAA p.V771_K772delVK Deletion - In frame 11:11942535-11942540 + TCGA-AD-6889-01 COSM1351910 c.3690G>T p.R1230S Substitution - Missense 11:11956001-11956001 + YUPAER COSM5371822 c.2920C>T p.L974L Substitution - coding silent 11:11947977-11947977 + TCGA-BC-A10U-01 COSM4942383 c.2755G>T p.D919Y Substitution - Missense 11:11942980-11942980 + TCGA-D1-A16N-01 COSM923878 c.1465G>A p.E489K Substitution - Missense 11:11933021-11933021 + TCGA-D9-A6EC-06 COSM4404911 c.1234C>T p.P412S Substitution - Missense 11:11920450-11920450 + TCGA-BR-6452-01 COSM4018562 c.1348A>T p.M450L Substitution - Missense 11:11922793-11922793 + KM12 COSM4185306 c.1534A>G p.S512G Substitution - Missense 11:11929521-11929521 + TCGA-BR-6452-01 COSM4018563 c.1084A>T p.M362L Substitution - Missense 11:11922793-11922793 + CSCC-31-T COSM4470957 c.1955C>T p.P652L Substitution - Missense 11:11936328-11936328 + TCGA-BT-A2LB-01 COSM3791263 c.3179A>G p.K1060R Substitution - Missense 11:11949923-11949923 + 2521259 COSM5890666 c.2632C>T p.H878Y Substitution - Missense 11:11942857-11942857 + LS174T COSM4185330 c.2204G>A p.R735H Substitution - Missense 11:11938323-11938323 + ESCC_157 COSM5646192 c.1370A>G p.Y457C Substitution - Missense 11:11930099-11930099 + TCGA-EB-A5SE-01 COSM3444220 c.2699C>T p.T900I Substitution - Missense 11:11942660-11942660 + QC2-32-T2 COSM3998260 c.3870G>A p.Q1290Q Substitution - coding silent 11:11955081-11955081 + Gp2D COSM4626755 c.1451C>T p.S484F Substitution - Missense 11:11929438-11929438 + S02350 COSM5694572 c.2052A>G p.L684L Substitution - coding silent 11:11936425-11936425 + PR-00-1165 COSM248254 c.2986C>T p.R996* Substitution - Nonsense 11:11948043-11948043 + J13_T COSM3979184 c.1091A>G p.N364S Substitution - Missense 11:11922800-11922800 + 1N52-VS-1T52 COSM4976743 c.589G>A p.E197K Substitution - Missense 11:11903316-11903316 + TCGA-32-2495-01 COSM3397475 c.2938C>T p.H980Y Substitution - Missense 11:11947995-11947995 + TCGA-HU-A4GU-01 COSM4018577 c.3018C>T p.S1006S Substitution - coding silent 11:11948075-11948075 + PT41 COSM5924553 c.1246T>C p.Y416H Substitution - Missense 11:11929497-11929497 + TCGA-BR-8361-01 COSM4018585 c.3509A>C p.K1170T Substitution - Missense 11:11952870-11952870 + TCGA-AA-3492-01 COSM5097039 c.12C>T p.G4G Substitution - coding silent 11:11842197-11842197 + TCGA-BR-4362-01 COSM4018556 c.660C>T p.Y220Y Substitution - coding silent 11:11905443-11905443 + TCGA-04-1338-01 COSM82441 c.2343G>A p.V781V Substitution - coding silent 11:11942568-11942568 + SJHYPO021 COSM4775516 c.3809_3810insA p.E1271fs*1 Insertion - Frameshift 11:11954931-11954932 + TCGA-BR-8680-01 COSM4018579 c.3265C>T p.R1089C Substitution - Missense 11:11950368-11950368 + AOCS-145-1-6 COSM3981340 c.3706G>T p.E1236* Substitution - Nonsense 11:11952803-11952803 + TCGA-AA-3492-01 COSM1351712 c.12C>T p.G4G Substitution - coding silent 11:11842197-11842197 + T578 COSM4739878 c.2541C>T p.G847G Substitution - coding silent 11:11942502-11942502 + TCGA-CA-6717-01 COSM5826915 c.4084A>G p.I1362V Substitution - Missense 11:11956131-11956131 + PCSI_0090_Pa_X COSM5419912 c.1038A>G p.A346A Substitution - coding silent 11:11920164-11920164 + C0051T COSM4165669 c.1067G>C p.S356T Substitution - Missense 11:11922776-11922776 + TCGA-D1-A17Q-01 COSM923864 c.628A>C p.N210H Substitution - Missense 11:11905411-11905411 + sysucc-1397T COSM5473084 c.3554C>T p.A1185V Substitution - Missense 11:11954940-11954940 + TCGA-EE-A29D-06 COSM3444223 c.3532C>T p.P1178S Substitution - Missense 11:11954918-11954918 + TCGA-AD-6889-01 COSM5826914 c.3954G>T p.R1318S Substitution - Missense 11:11956001-11956001 + TCGA-AX-A060-01 COSM923903 c.2990T>C p.V997A Substitution - Missense 11:11948047-11948047 + TCGA-18-3406-01 COSM686869 c.3107G>C p.R1036T Substitution - Missense 11:11948521-11948521 + 2521259 COSM5890665 c.2896C>T p.H966Y Substitution - Missense 11:11942857-11942857 + T578 COSM4739879 c.2277C>T p.G759G Substitution - coding silent 11:11942502-11942502 + CN-AML-08-T COSM3998261 c.3606G>A p.Q1202Q Substitution - coding silent 11:11955081-11955081 + CSCC-31-T COSM4543301 c.3357G>A p.E1119E Substitution - coding silent 11:11950460-11950460 + CSCC-31-T COSM4543300 c.3621G>A p.E1207E Substitution - coding silent 11:11950460-11950460 + CHC121T COSM216943 c.3209A>T p.E1070V Substitution - Missense 11:11949953-11949953 + 49M COSM5593905 c.2856G>A p.R952R Substitution - coding silent 11:11942817-11942817 + TCGA-EE-A2MI-06 COSM3444173 c.597G>A p.L199L Substitution - coding silent 11:11897637-11897637 + SNUH_G16_S1 COSM3998262 c.3979T>G p.L1327V Substitution - Missense 11:11956026-11956026 + TCGA-DA-A3F8-06 COSM3444225 c.3575C>T p.P1192L Substitution - Missense 11:11955050-11955050 + pfg053T COSM4746686 c.2430_2441del12 p.T812_S815delTETS Deletion - In frame 11:11942655-11942666 + OSCC-GB_00450111 COSM3710112 c.1003G>T p.V335F Substitution - Missense 11:11920483-11920483 + YUFERY COSM5371819 c.2927A>C p.N976T Substitution - Missense 11:11942888-11942888 + PTC-14C COSM4145400 c.1657G>T p.A553S Substitution - Missense 11:11933927-11933927 + TCGA-HU-8602-01 COSM4018564 c.1798C>T p.R600* Substitution - Nonsense 11:11933090-11933090 + TCGA-A5-A0GP-01 COSM923898 c.1971C>A p.F657L Substitution - Missense 11:11938354-11938354 + TCGA-D1-A16F-01 COSM923901 c.2724G>T p.T908T Substitution - coding silent 11:11942949-11942949 + HCC119 COSM1604203 c.982G>C p.D328H Substitution - Missense 11:11920462-11920462 + T1154 COSM4739881 c.2496A>G p.S832S Substitution - coding silent 11:11942721-11942721 + TCGA-AG-A002-01 COSM248254 c.2986C>T p.R996* Substitution - Nonsense 11:11948043-11948043 + YUKAT COSM5371818 c.1284G>A p.W428* Substitution - Nonsense 11:11929535-11929535 + PD4128a COSM165453 c.385T>C p.Y129H Substitution - Missense 11:11897689-11897689 + SCC-15 COSM2106952 c.403G>A p.E135K Substitution - Missense 11:11902728-11902728 + sysucc-1972T COSM5480320 c.78C>T p.D26D Substitution - coding silent 11:11884505-11884505 + HCC136 COSM3666129 c.1682A>G p.Y561C Substitution - Missense 11:11930722-11930722 + YUWIA COSM5371824 c.3146C>T p.P1049L Substitution - Missense 11:11949890-11949890 + TCGA-66-2754-01 COSM686868 c.3813A>G p.A1271A Substitution - coding silent 11:11956124-11956124 + PTC-14C COSM4145399 c.1921G>T p.A641S Substitution - Missense 11:11933927-11933927 + SJDES001-R COSM4574115 c.2833G>T p.D945Y Substitution - Missense 11:11942794-11942794 + T3021 COSM4739877 c.1689A>G p.I563M Substitution - Missense 11:11936326-11936326 + CHC121T COSM216943 c.3209A>T p.E1070V Substitution - Missense 11:11949953-11949953 + TCGA-B5-A11N-01 COSM923866 c.907A>G p.K303E Substitution - Missense 11:11920387-11920387 + 45T COSM3710111 c.1267G>T p.V423F Substitution - Missense 11:11920483-11920483 + SNUH_G76_S1 COSM3998260 c.3870G>A p.Q1290Q Substitution - coding silent 11:11955081-11955081 + PD4120a COSM165450 c.1153G>A p.E385K Substitution - Missense 11:11922862-11922862 + TCGA-CA-6718-01 COSM1351907 c.2548T>G p.F850V Substitution - Missense 11:11942773-11942773 + A3 COSM5349626 c.1517A>G p.E506G Substitution - Missense 11:11933073-11933073 + 449 COSM4435328 c.1915G>C p.E639Q Substitution - Missense 11:11933921-11933921 + 2492729 COSM5725992 c.1083G>A p.Q361Q Substitution - coding silent 11:11922792-11922792 + TCGA-AG-A002-01 COSM264619 c.1783C>A p.L595I Substitution - Missense 11:11936420-11936420 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.577253;Hs.577254;Hs.577256 11p15.3 614460

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.E923D c.2769A>C 11 11964541 LUSC A - Frameshift p.G1033Efs*22 c.3096delA 11 11970052 STAD A G IntronicSNV . c.1183-919A>G 11 11950062 CLL A G Missense p.D872G c.2615A>G 11 11964387 BRCA A G Missense p.I1195V c.3583A>G 11 11976605 HNSC A G Missense p.K1060E c.3178A>G 11 11971469 HNSC A G Missense p.K1060R c.3179A>G 11 11971470 BLCA A G Missense p.K280R c.839A>G 11 11941776 SCLC A G Missense p.S356G c.1066A>G 11 11944322 UCEC A G Synonymous p.A1271A c.3813A>G 11 11977671 LUSC ATCT - IntronicDeletion . c.3690-384_3690-381delATCT 11 11977164 CLL A T Missense p.E1070V c.3209A>T 11 11971500 HC A T Missense p.K339N c.1017A>T 11 11944273 CM A T Missense p.R751W c.2251A>T 11 11964023 LUAD ATT - InFrameDeletion p.Y417delY c.1249_1251delTAT 11 11951042 UCEC C A Missense p.F657L c.1971C>A 11 11959901 UCEC C A Missense p.P1098T c.3292C>A 11 11971942 MM C A Synonymous p.R1008R c.3022C>A 11 11969626 HNSC C A Synonymous p.R996R c.2986C>A 11 11969590 PRAD C - Frameshift p.S1006Rfs*4 c.3018delC 11 11969622 UCEC C G Missense p.Q507E c.1519C>G 11 11954622 BLCA C G Missense p.R320G c.958C>G 11 11941985 LGG C G Missense p.S90C c.269C>G 11 11913630 BLCA C G Synonymous p.S87S c.261C>G 11 11913622 HNSC C T IntronicSNV . c.39+15492C>T 11 11879263 PIA C T Missense p.H980Y c.2938C>T 11 11969542 GBM C T Missense p.P1192L c.3575C>T 11 11976597 CM C T Missense p.R1065W c.3193C>T 11 11971484 HNSC C T Missense p.S709F c.2126C>T 11 11963898 CM C T Missense p.T165I c.494C>T 11 11924366 CM C T Synonymous p.F305F c.915C>T 11 11941942 LUAD C T Synonymous p.G598G c.1794C>T 11 11957978 BRCA C T Synonymous p.S1161S c.3483C>T 11 11974391 UCEC G A Missense p.A999T c.2995G>A 11 11969599 UCEC G A Missense p.D207N c.619G>A 11 11926949 LUAD G A Missense p.E135K c.403G>A 11 11924275 HNSC G A Missense p.E385K c.1153G>A 11 11944409 BRCA G A Missense p.E506K c.1516G>A 11 11954619 CM G A Missense p.E955K c.2863G>A 11 11964635 RCCC G A Missense p.M329I c.987G>A 11 11942014 BLCA G A Missense p.R1261H c.3782G>A 11 11977640 BRCA G A Missense p.R320Q c.959G>A 11 11941986 UCEC G A Missense p.V1007I c.3019G>A 11 11969623 UCEC G A Missense p.V1037I c.3109G>A 11 11970070 MM G A Synonymous p.L111L c.333G>A 11 11919184 CM G A Synonymous p.V781V c.2343G>A 11 11964115 OV G C Missense p.E1235Q c.3703G>C 11 11977561 BLCA G C Missense p.E338D c.1014G>C 11 11942041 LUAD G C Missense p.E344Q c.1030G>C 11 11944286 BRCA G C Missense p.G57A c.170G>C 11 11913531 CM G C Missense p.R1036T c.3107G>C 11 11970068 LUSC G C SpliceDonorSNV . c.765+1G>C 11 11927096 SCLC G T Missense p.D1287Y c.3859G>T 11 11977717 NSCLC G T Missense p.D574Y c.1720G>T 11 11957904 LUAD G T Missense p.S809I c.2426G>T 11 11964198 BRCA G T Missense p.V1215F c.3643G>T 11 11976665 LUAD G T Synonymous p.T908T c.2724G>T 11 11964496 UCEC T A Missense p.M120K c.359T>A 11 11919210 BRCA T A Missense p.S390T c.1168T>A 11 11944424 LUAD T C Missense p.V997A c.2990T>C 11 11969594 UCEC T C Missense p.Y129H c.385T>C 11 11919236 BRCA T C SpliceDonorSNV . c.153+2T>C 11 11906129 UCEC T C Synonymous p.P823P c.2469T>C 11 11964241 HNSC T G Missense p.F984C c.2951T>G 11 11969555 LUSC T G Missense p.L683V c.2047T>G 11 11962033 LUSC