Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 10 8006163 8006163 + Silent SNP A A G TCGA-OR-A5LO-01A-11D-A29I-10 TCGA-OR-A5LO-10A-01D-A29L-10 g.chr10:8006163A>G c.690A>G c.(688-690)ccA>ccG p.P230P ACC 10 8007680 8007682 + In_Frame_Del DEL AGA AGA - TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chr10:8007680_8007682delAGA c.2207_2209delAGA c.(2206-2211)gagaag>gag p.K737del ACC 10 8051255 8051255 + Missense_Mutation SNP G G A TCGA-OR-A5LB-01A-11D-A29I-10 TCGA-OR-A5LB-10A-01D-A29L-10 g.chr10:8051255G>A c.2530G>A c.(2530-2532)Gtg>Atg p.V844M BLCA 10 7860702 7860702 + Missense_Mutation SNP G G C TCGA-ZF-AA54-01A-11D-A391-08 TCGA-ZF-AA54-10A-01D-A394-08 g.chr10:7860702G>C c.30G>C c.(28-30)ttG>ttC p.L10F BLCA 10 7866376 7866376 + Missense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr10:7866376G>C c.262G>C c.(262-264)Gag>Cag p.E88Q BLCA 10 8006054 8006054 + Missense_Mutation SNP G G A TCGA-S5-AA26-01A-11D-A38G-08 TCGA-S5-AA26-10A-01D-A38J-08 g.chr10:8006054G>A c.581G>A c.(580-582)cGg>cAg p.R194Q BLCA 10 8006521 8006521 + Missense_Mutation SNP G G A TCGA-XF-A9SY-01A-21D-A42E-08 TCGA-XF-A9SY-10A-01D-A42H-08 g.chr10:8006521G>A c.1048G>A c.(1048-1050)Gaa>Aaa p.E350K BLCA 10 8006708 8006708 + Missense_Mutation SNP G G C TCGA-UY-A78M-01A-21D-A34U-08 TCGA-UY-A78M-10A-01D-A34X-08 g.chr10:8006708G>C c.1235G>C c.(1234-1236)gGa>gCa p.G412A BLCA 10 8006853 8006853 + Silent SNP C C T TCGA-GD-A6C6-01A-21D-A31L-08 TCGA-GD-A6C6-10A-01D-A31J-08 g.chr10:8006853C>T c.1380C>T c.(1378-1380)tcC>tcT p.S460S BLCA 10 8007337 8007337 + Missense_Mutation SNP G G C TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr10:8007337G>C c.1864G>C c.(1864-1866)Gat>Cat p.D622H BLCA 10 8007409 8007409 + Missense_Mutation SNP A A G TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr10:8007409A>G c.1936A>G c.(1936-1938)Aag>Gag p.K646E BLCA 10 8007618 8007618 + Missense_Mutation SNP G G C TCGA-XF-A9T0-01A-11D-A391-08 TCGA-XF-A9T0-10A-01D-A394-08 g.chr10:8007618G>C c.2145G>C c.(2143-2145)gaG>gaC p.E715D BLCA 10 8051117 8051128 + In_Frame_Del DEL GCCCCCGCGCCC GCCCCCGCGCCC - TCGA-DK-A3IS-01A-21D-A21A-08 TCGA-DK-A3IS-10A-01D-A21A-08 g.chr10:8051117_8051128delGCCCCCGCGCCC c.2392_2403delGCCCCCGCGCCC c.(2392-2403)gcccccgcgcccdel p.APAP798del BLCA 10 8055748 8055748 + Missense_Mutation SNP G G C TCGA-4Z-AA87-01A-11D-A391-08 TCGA-4Z-AA87-10A-01D-A394-08 g.chr10:8055748G>C c.2623G>C c.(2623-2625)Gac>Cac p.D875H BLCA 10 8055784 8055784 + Missense_Mutation SNP G G A TCGA-4Z-AA87-01A-11D-A391-08 TCGA-4Z-AA87-10A-01D-A394-08 g.chr10:8055784G>A c.2659G>A c.(2659-2661)Gat>Aat p.D887N BLCA 10 8056618 8056618 + Missense_Mutation SNP G G T TCGA-GV-A3QK-01B-11D-A23M-08 TCGA-GV-A3QK-10A-01D-A23K-08 g.chr10:8056618G>T c.2694G>T c.(2692-2694)atG>atT p.M898I BRCA 10 7860723 7860723 + Silent SNP C C A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr10:7860723C>A c.51C>A c.(49-51)atC>atA p.I17I BRCA 10 7866501 7866501 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr10:7866501A>C c.387A>C c.(385-387)ccA>ccC p.P129P BRCA 10 8005972 8005972 + Nonsense_Mutation SNP G G T TCGA-A8-A06X-01A-21W-A019-09 TCGA-A8-A06X-10A-01W-A021-09 g.chr10:8005972G>T c.499G>T c.(499-501)Gaa>Taa p.E167* BRCA 10 8006100 8006103 + Frame_Shift_Del DEL ATTG ATTG - TCGA-AN-A0XS-01A-22D-A10G-09 TCGA-AN-A0XS-10A-01D-A10G-09 g.chr10:8006100_8006103delATTG c.627_630delATTG c.(625-630)ttattgfs p.LL209fs BRCA 10 8006644 8006644 + Missense_Mutation SNP A A G TCGA-BH-A1FD-01A-11W-A14Q-09 TCGA-BH-A1FD-11B-21D-A13O-09 g.chr10:8006644A>G c.1171A>G c.(1171-1173)Atc>Gtc p.I391V BRCA 10 8006835 8006835 + Silent SNP C C G TCGA-E2-A15G-01A-11D-A12B-09 TCGA-E2-A15G-10A-01D-A12B-09 g.chr10:8006835C>G c.1362C>G c.(1360-1362)tcC>tcG p.S454S BRCA 10 8055756 8055756 + Silent SNP G G A TCGA-AN-A0AR-01A-11W-A019-09 TCGA-AN-A0AR-10A-01W-A021-09 g.chr10:8055756G>A c.2631G>A c.(2629-2631)ggG>ggA p.G877G CESC 10 7860774 7860774 + Silent SNP C C G TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr10:7860774C>G c.102C>G c.(100-102)ctC>ctG p.L34L CESC 10 8006327 8006327 + Nonsense_Mutation SNP C C G TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr10:8006327C>G c.854C>G c.(853-855)tCa>tGa p.S285* CESC 10 8006430 8006430 + Silent SNP G G A TCGA-EK-A2H0-01A-11D-A17W-09 TCGA-EK-A2H0-10A-01D-A17W-09 g.chr10:8006430G>A c.957G>A c.(955-957)aaG>aaA p.K319K CHOL 10 8019213 8019213 + Nonsense_Mutation SNP G G T TCGA-W5-AA31-01A-11D-A417-09 TCGA-W5-AA31-10A-01D-A41A-09 g.chr10:8019213G>T c.2242G>T c.(2242-2244)Gaa>Taa p.E748* COAD 10 7866478 7866478 + Nonsense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:7866478G>T c.364G>T c.(364-366)Gaa>Taa p.E122* COAD 10 8005916 8005916 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:8005916G>A c.443G>A c.(442-444)gGc>gAc p.G148D COAD 10 8006195 8006195 + Missense_Mutation SNP C C A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr10:8006195C>A c.722C>A c.(721-723)cCt>cAt p.P241H COAD 10 8006413 8006413 + Missense_Mutation SNP C C T TCGA-AZ-6605-01A-11D-1835-10 TCGA-AZ-6605-11A-01D-1835-10 g.chr10:8006413C>T c.940C>T c.(940-942)Cgt>Tgt p.R314C COAD 10 8006454 8006454 + Silent SNP G G A TCGA-CK-5914-01A-11D-1650-10 TCGA-CK-5914-10A-01D-1650-10 g.chr10:8006454G>A c.981G>A c.(979-981)acG>acA p.T327T COAD 10 8006489 8006489 + Missense_Mutation SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr10:8006489C>T c.1016C>T c.(1015-1017)aCg>aTg p.T339M COAD 10 8006552 8006552 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:8006552A>C c.1079A>C c.(1078-1080)aAa>aCa p.K360T COAD 10 8006647 8006647 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:8006647G>A c.1174G>A c.(1174-1176)Gat>Aat p.D392N COAD 10 8007368 8007369 + Frame_Shift_Del DEL AG AG - TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr10:8007368_8007369delAG c.1895_1896delAG c.(1894-1896)aagfs p.K632fs COAD 10 8007451 8007451 + Nonsense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:8007451G>T c.1978G>T c.(1978-1980)Gag>Tag p.E660* COAD 10 8056609 8056610 + Frame_Shift_Ins INS - - C TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr10:8056609_8056610insC c.2685_2686insC c.(2686-2688)ggafs p.G896fs COAD 10 8056667 8056669 + In_Frame_Del DEL AAG AAG - TCGA-AD-6890-01A-11D-1924-10 TCGA-AD-6890-10A-01D-1924-10 g.chr10:8056667_8056669delAAG c.2743_2745delAAG c.(2743-2745)aagdel p.K917del COADREAD 10 7866478 7866478 + Nonsense_Mutation SNP G G T TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:7866478G>T c.364G>T c.(364-366)Gaa>Taa p.E122* COADREAD 10 8005916 8005916 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:8005916G>A c.443G>A c.(442-444)gGc>gAc p.G148D COADREAD 10 8006195 8006195 + Missense_Mutation SNP C C A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr10:8006195C>A c.722C>A c.(721-723)cCt>cAt p.P241H COADREAD 10 8006413 8006413 + Missense_Mutation SNP C C T TCGA-AZ-6605-01A-11D-1835-10 TCGA-AZ-6605-11A-01D-1835-10 g.chr10:8006413C>T c.940C>T c.(940-942)Cgt>Tgt p.R314C COADREAD 10 8006454 8006454 + Silent SNP G G A TCGA-CK-5914-01A-11D-1650-10 TCGA-CK-5914-10A-01D-1650-10 g.chr10:8006454G>A c.981G>A c.(979-981)acG>acA p.T327T COADREAD 10 8006489 8006489 + Missense_Mutation SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr10:8006489C>T c.1016C>T c.(1015-1017)aCg>aTg p.T339M COADREAD 10 8006552 8006552 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:8006552A>C c.1079A>C c.(1078-1080)aAa>aCa p.K360T COADREAD 10 8006604 8006604 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:8006604G>A c.1131G>A c.(1129-1131)ccG>ccA p.P377P COADREAD 10 8006647 8006647 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:8006647G>A c.1174G>A c.(1174-1176)Gat>Aat p.D392N COADREAD 10 8006792 8006792 + Missense_Mutation SNP C C T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr10:8006792C>T c.1319C>T c.(1318-1320)gCg>gTg p.A440V COADREAD 10 8007368 8007369 + Frame_Shift_Del DEL AG AG - TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr10:8007368_8007369delAG c.1895_1896delAG c.(1894-1896)aagfs p.K632fs COADREAD 10 8007451 8007451 + Nonsense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:8007451G>T c.1978G>T c.(1978-1980)Gag>Tag p.E660* COADREAD 10 8056609 8056610 + Frame_Shift_Ins INS - - C TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr10:8056609_8056610insC c.2685_2686insC c.(2686-2688)ggafs p.G896fs COADREAD 10 8056667 8056669 + In_Frame_Del DEL AAG AAG - TCGA-AD-6890-01A-11D-1924-10 TCGA-AD-6890-10A-01D-1924-10 g.chr10:8056667_8056669delAAG c.2743_2745delAAG c.(2743-2745)aagdel p.K917del DLBC 10 8007260 8007260 + Missense_Mutation SNP A A C TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr10:8007260A>C c.1787A>C c.(1786-1788)gAa>gCa p.E596A ESCA 10 8005880 8005881 + Intron INS - - AGA TCGA-IC-A6RE-01A-11D-A33E-09 TCGA-IC-A6RE-10A-01D-A33H-09 g.chr10:8005880_8005881insAGA ESCA 10 8005922 8005922 + Missense_Mutation SNP C C T TCGA-R6-A6L6-01B-11D-A33E-09 TCGA-R6-A6L6-10A-01D-A33H-09 g.chr10:8005922C>T c.449C>T c.(448-450)tCa>tTa p.S150L ESCA 10 8006229 8006229 + Silent SNP T T A TCGA-LN-A49S-01A-11D-A247-09 TCGA-LN-A49S-10A-01D-A247-09 g.chr10:8006229T>A c.756T>A c.(754-756)gtT>gtA p.V252V ESCA 10 8006695 8006695 + Nonsense_Mutation SNP G G T TCGA-KH-A6WC-01A-11D-A33E-09 TCGA-KH-A6WC-10B-01D-A33H-09 g.chr10:8006695G>T c.1222G>T c.(1222-1224)Gaa>Taa p.E408* ESCA 10 8006704 8006704 + Missense_Mutation SNP T T C TCGA-ZR-A9CJ-01B-11D-A387-09 TCGA-ZR-A9CJ-10A-01D-A38A-09 g.chr10:8006704T>C c.1231T>C c.(1231-1233)Tct>Cct p.S411P ESCA 10 8019276 8019276 + Missense_Mutation SNP C C A TCGA-XP-A8T8-01A-11D-A36J-09 TCGA-XP-A8T8-10A-01D-A36M-09 g.chr10:8019276C>A c.2305C>A c.(2305-2307)Caa>Aaa p.Q769K GBM 10 8006394 8006394 + Silent SNP A A G TCGA-32-2615-01A-01D-1495-08 TCGA-32-2615-10A-01D-1495-08 g.chr10:8006394A>G c.921A>G c.(919-921)aaA>aaG p.K307K GBM 10 8007617 8007625 + In_Frame_Del DEL AGAAGGAGA AGAAGGAGA - TCGA-28-5204-01A-01D-1486-08 TCGA-28-5204-10A-01D-1486-08 g.chr10:8007617_8007625delAGAAGGAGA c.2144_2152delAGAAGGAGA c.(2143-2154)gagaaggagaag>gag p.KEK719del GBMLGG 10 8005992 8005992 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:8005992G>T c.519G>T c.(517-519)gaG>gaT p.E173D GBMLGG 10 8006394 8006394 + Silent SNP A A G TCGA-32-2615-01A-01D-1495-08 TCGA-32-2615-10A-01D-1495-08 g.chr10:8006394A>G c.921A>G c.(919-921)aaA>aaG p.K307K GBMLGG 10 8007427 8007427 + Frame_Shift_Del DEL C C - TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr10:8007427delC c.1954delC c.(1954-1956)cccfs p.P653fs GBMLGG 10 8007617 8007625 + In_Frame_Del DEL AGAAGGAGA AGAAGGAGA - TCGA-28-5204-01A-01D-1486-08 TCGA-28-5204-10A-01D-1486-08 g.chr10:8007617_8007625delAGAAGGAGA c.2144_2152delAGAAGGAGA c.(2143-2154)gagaaggagaag>gag p.KEK719del HNSC 10 8006040 8006040 + Silent SNP G G T TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chr10:8006040G>T c.567G>T c.(565-567)ctG>ctT p.L189L HNSC 10 8006089 8006089 + Missense_Mutation SNP G G A TCGA-CR-7370-01A-11D-2129-08 TCGA-CR-7370-10A-01D-2129-08 g.chr10:8006089G>A c.616G>A c.(616-618)Gat>Aat p.D206N HNSC 10 8006137 8006137 + Nonsense_Mutation SNP C C T TCGA-CN-6021-01A-11D-1683-08 TCGA-CN-6021-10A-01D-1683-08 g.chr10:8006137C>T c.664C>T c.(664-666)Caa>Taa p.Q222* HNSC 10 8006971 8006971 + Missense_Mutation SNP C C T TCGA-P3-A5QF-01A-11D-A28R-08 TCGA-P3-A5QF-10A-01D-A28U-08 g.chr10:8006971C>T c.1498C>T c.(1498-1500)Ccc>Tcc p.P500S HNSC 10 8007660 8007660 + Silent SNP G G A TCGA-CR-7390-01A-11D-2012-08 TCGA-CR-7390-10A-01D-2013-08 g.chr10:8007660G>A c.2187G>A c.(2185-2187)gaG>gaA p.E729E KIPAN 10 8006138 8006138 + Frame_Shift_Del DEL A A - TCGA-MH-A854-01A-11D-A34Z-10 TCGA-MH-A854-10A-01D-A34Z-10 g.chr10:8006138delA c.665delA c.(664-666)caafs p.Q222fs KIPAN 10 8007636 8007636 + Missense_Mutation SNP G G C TCGA-MH-A560-01A-11D-A26P-10 TCGA-MH-A560-10A-01D-A26P-10 g.chr10:8007636G>C c.2163G>C c.(2161-2163)aaG>aaC p.K721N KIPAN 10 8051125 8051125 + Silent SNP G G T TCGA-B0-5096-01A-01D-1421-08 TCGA-B0-5096-11A-01D-1421-08 g.chr10:8051125G>T c.2400G>T c.(2398-2400)gcG>gcT p.A800A KIPAN 10 8055709 8055709 + Missense_Mutation SNP G G A TCGA-B0-4694-01A-01D-1361-10 TCGA-B0-4694-11A-01D-1361-10 g.chr10:8055709G>A c.2584G>A c.(2584-2586)Ggc>Agc p.G862S KIRC 10 8051125 8051125 + Silent SNP G G T TCGA-B0-5096-01A-01D-1421-08 TCGA-B0-5096-11A-01D-1421-08 g.chr10:8051125G>T c.2400G>T c.(2398-2400)gcG>gcT p.A800A KIRC 10 8055709 8055709 + Missense_Mutation SNP G G A TCGA-B0-4694-01A-01D-1361-10 TCGA-B0-4694-11A-01D-1361-10 g.chr10:8055709G>A c.2584G>A c.(2584-2586)Ggc>Agc p.G862S KIRP 10 8006138 8006138 + Frame_Shift_Del DEL A A - TCGA-MH-A854-01A-11D-A34Z-10 TCGA-MH-A854-10A-01D-A34Z-10 g.chr10:8006138delA c.665delA c.(664-666)caafs p.Q222fs KIRP 10 8007636 8007636 + Missense_Mutation SNP G G C TCGA-MH-A560-01A-11D-A26P-10 TCGA-MH-A560-10A-01D-A26P-10 g.chr10:8007636G>C c.2163G>C c.(2161-2163)aaG>aaC p.K721N LGG 10 8005992 8005992 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:8005992G>T c.519G>T c.(517-519)gaG>gaT p.E173D LGG 10 8007427 8007427 + Frame_Shift_Del DEL C C - TCGA-HT-8564-01A-11D-2395-08 TCGA-HT-8564-10A-01D-2396-08 g.chr10:8007427delC c.1954delC c.(1954-1956)cccfs p.P653fs LIHC 10 8006085 8006085 + Silent SNP G G T TCGA-BW-A5NO-01A-11D-A27I-10 TCGA-BW-A5NO-10A-01D-A27I-10 g.chr10:8006085G>T c.612G>T c.(610-612)acG>acT p.T204T LIHC 10 8006438 8006438 + Missense_Mutation SNP A A G TCGA-DD-A3A7-01A-11D-A22F-10 TCGA-DD-A3A7-11A-11D-A22F-10 g.chr10:8006438A>G c.965A>G c.(964-966)aAg>aGg p.K322R LIHC 10 8006861 8006861 + Missense_Mutation SNP C C T TCGA-DD-A3A2-01A-11D-A20W-10 TCGA-DD-A3A2-11A-11D-A20W-10 g.chr10:8006861C>T c.1388C>T c.(1387-1389)tCa>tTa p.S463L LIHC 10 8007022 8007022 + Missense_Mutation SNP T T C TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr10:8007022T>C c.1549T>C c.(1549-1551)Tcc>Ccc p.S517P LIHC 10 8007368 8007368 + Missense_Mutation SNP A A G TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr10:8007368A>G c.1895A>G c.(1894-1896)aAg>aGg p.K632R LIHC 10 8051233 8051233 + Silent SNP C C T TCGA-DD-AACX-01A-11D-A40R-10 TCGA-DD-AACX-10A-01D-A40U-10 g.chr10:8051233C>T c.2508C>T c.(2506-2508)tcC>tcT p.S836S LIHC 10 8051256 8051256 + Missense_Mutation SNP T T A TCGA-CC-A7IE-01A-21D-A382-10 TCGA-CC-A7IE-10A-01D-A385-10 g.chr10:8051256T>A c.2531T>A c.(2530-2532)gTg>gAg p.V844E LUAD 10 7860740 7860740 + Missense_Mutation SNP G G T TCGA-05-5715-01A-01D-1625-08 TCGA-05-5715-10A-01D-1625-08 g.chr10:7860740G>T c.68G>T c.(67-69)tGg>tTg p.W23L LUAD 10 7866286 7866286 + Nonsense_Mutation SNP C C T TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr10:7866286C>T c.172C>T c.(172-174)Cga>Tga p.R58* LUAD 10 7866336 7866336 + Silent SNP G G T TCGA-05-4390-01A-02D-1753-08 TCGA-05-4390-10A-01D-1753-08 g.chr10:7866336G>T c.222G>T c.(220-222)ggG>ggT p.G74G LUAD 10 7866380 7866380 + Missense_Mutation SNP C C T TCGA-55-8507-01A-11D-2393-08 TCGA-55-8507-10A-01D-2393-08 g.chr10:7866380C>T c.266C>T c.(265-267)cCt>cTt p.P89L LUAD 10 7866463 7866463 + Missense_Mutation SNP G G T TCGA-86-6851-01A-11D-1945-08 TCGA-86-6851-10A-01D-1946-08 g.chr10:7866463G>T c.349G>T c.(349-351)Gca>Tca p.A117S LUAD 10 8006002 8006002 + Missense_Mutation SNP G G T TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chr10:8006002G>T c.529G>T c.(529-531)Ggc>Tgc p.G177C LUAD 10 8006476 8006476 + Missense_Mutation SNP G G C TCGA-91-8499-01A-11D-2393-08 TCGA-91-8499-10A-01D-2393-08 g.chr10:8006476G>C c.1003G>C c.(1003-1005)Gtg>Ctg p.V335L LUAD 10 8006708 8006708 + Missense_Mutation SNP G G T TCGA-86-8672-01A-21D-2393-08 TCGA-86-8672-10A-01D-2393-08 g.chr10:8006708G>T c.1235G>T c.(1234-1236)gGa>gTa p.G412V LUAD 10 8006719 8006719 + Nonsense_Mutation SNP G G T TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr10:8006719G>T c.1246G>T c.(1246-1248)Gaa>Taa p.E416* LUAD 10 8006747 8006747 + Missense_Mutation SNP G G T TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr10:8006747G>T c.1274G>T c.(1273-1275)aGa>aTa p.R425I LUAD 10 8006790 8006790 + Silent SNP C C T TCGA-78-7154-01A-11D-2036-08 TCGA-78-7154-10A-01D-2036-08 g.chr10:8006790C>T c.1317C>T c.(1315-1317)tcC>tcT p.S439S LUAD 10 8006869 8006869 + Missense_Mutation SNP A A G TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr10:8006869A>G c.1396A>G c.(1396-1398)Atg>Gtg p.M466V LUAD 10 8007006 8007006 + Silent SNP G G A TCGA-64-1677-01A-01W-0928-08 TCGA-64-1677-10A-01W-0928-08 g.chr10:8007006G>A c.1533G>A c.(1531-1533)gaG>gaA p.E511E LUAD 10 8007078 8007078 + Missense_Mutation SNP G G C TCGA-44-7660-01A-11D-2063-08 TCGA-44-7660-10A-01D-2063-08 g.chr10:8007078G>C c.1605G>C c.(1603-1605)aaG>aaC p.K535N LUAD 10 8007139 8007139 + Missense_Mutation SNP A A G TCGA-78-7148-01A-11D-2036-08 TCGA-78-7148-10A-01D-2036-08 g.chr10:8007139A>G c.1666A>G c.(1666-1668)Aag>Gag p.K556E LUAD 10 8007166 8007166 + Frame_Shift_Del DEL G G - TCGA-69-8255-01A-11D-2284-08 TCGA-69-8255-10A-01D-2284-08 g.chr10:8007166delG c.1693delG c.(1693-1695)gacfs p.D565fs LUAD 10 8007183 8007183 + Missense_Mutation SNP G G T TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr10:8007183G>T c.1710G>T c.(1708-1710)agG>agT p.R570S LUAD 10 8007192 8007192 + Missense_Mutation SNP G G T TCGA-69-7760-01A-11D-2167-08 TCGA-69-7760-10A-01D-2167-08 g.chr10:8007192G>T c.1719G>T c.(1717-1719)aaG>aaT p.K573N LUAD 10 8007307 8007307 + Missense_Mutation SNP G G C TCGA-J2-A4AD-01A-11D-A24D-08 TCGA-J2-A4AD-10A-01D-A24F-08 g.chr10:8007307G>C c.1834G>C c.(1834-1836)Gag>Cag p.E612Q LUAD 10 8007492 8007492 + Missense_Mutation SNP G G T TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chr10:8007492G>T c.2019G>T c.(2017-2019)agG>agT p.R673S LUAD 10 8007624 8007624 + Silent SNP G G A TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr10:8007624G>A c.2151G>A c.(2149-2151)gaG>gaA p.E717E LUAD 10 8007650 8007650 + Missense_Mutation SNP A A G TCGA-44-7662-01A-11D-2063-08 TCGA-44-7662-10A-01D-2063-08 g.chr10:8007650A>G c.2177A>G c.(2176-2178)gAg>gGg p.E726G LUAD 10 8007705 8007705 + Splice_Site SNP A A T TCGA-44-A4SS-01A-11D-A24P-08 TCGA-44-A4SS-10A-01D-A24P-08 g.chr10:8007705A>T c.2232A>T c.(2230-2232)aaA>aaT p.K744N LUAD 10 8019213 8019213 + Nonsense_Mutation SNP G G T TCGA-44-6777-01A-11D-1855-08 TCGA-44-6777-10A-01D-1855-08 g.chr10:8019213G>T c.2242G>T c.(2242-2244)Gaa>Taa p.E748* LUAD 10 8055777 8055777 + Silent SNP C C T TCGA-MP-A4TA-01A-21D-A24P-08 TCGA-MP-A4TA-10A-01D-A24P-08 g.chr10:8055777C>T c.2652C>T c.(2650-2652)gaC>gaT p.D884D LUAD 10 8056639 8056639 + Missense_Mutation SNP G G C TCGA-55-1592-01A-01D-0969-08 TCGA-55-1592-11A-01D-0969-08 g.chr10:8056639G>C c.2715G>C c.(2713-2715)atG>atC p.M905I LUSC 10 7860717 7860717 + Silent SNP G G T TCGA-37-4141-01A-02D-1352-08 TCGA-37-4141-10A-01D-1352-08 g.chr10:7860717G>T c.45G>T c.(43-45)gcG>gcT p.A15A LUSC 10 7860771 7860771 + Silent SNP C C T TCGA-34-5239-01A-21D-1817-08 TCGA-34-5239-10A-01D-1817-08 g.chr10:7860771C>T c.99C>T c.(97-99)ctC>ctT p.L33L LUSC 10 7866291 7866291 + Silent SNP A A T TCGA-66-2782-01A-01D-1522-08 TCGA-66-2782-11A-01D-1522-08 g.chr10:7866291A>T c.177A>T c.(175-177)acA>acT p.T59T LUSC 10 8007024 8007024 + Silent SNP C C A TCGA-37-3789-01A-01D-0983-08 TCGA-37-3789-10A-01D-0983-08 g.chr10:8007024C>A c.1551C>A c.(1549-1551)tcC>tcA p.S517S LUSC 10 8007226 8007226 + Missense_Mutation SNP G G T TCGA-22-5492-01A-01D-1632-08 TCGA-22-5492-11A-01D-1632-08 g.chr10:8007226G>T c.1753G>T c.(1753-1755)Gca>Tca p.A585S LUSC 10 8051097 8051097 + Missense_Mutation SNP G G A TCGA-66-2789-01A-01D-0983-08 TCGA-66-2789-11A-01D-0983-08 g.chr10:8051097G>A c.2372G>A c.(2371-2373)aGg>aAg p.R791K LUSC 10 8055717 8055717 + Missense_Mutation SNP G G T TCGA-66-2787-01A-01D-0983-08 TCGA-66-2787-11A-01D-0983-08 g.chr10:8055717G>T c.2592G>T c.(2590-2592)caG>caT p.Q864H LUSC 10 8055795 8055795 + Nonsense_Mutation SNP C C G TCGA-85-6560-01A-11D-1817-08 TCGA-85-6560-10A-01D-1817-08 g.chr10:8055795C>G c.2670C>G c.(2668-2670)taC>taG p.Y890* OV 10 8007590 8007590 + Missense_Mutation SNP A A G TCGA-24-1474-01A-01W-0551-08 TCGA-24-1474-10A-01W-0551-08 g.chr10:8007590A>G c.2117A>G c.(2116-2118)aAg>aGg p.K706R PAAD 10 8006790 8006790 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:8006790C>T c.1317C>T c.(1315-1317)tcC>tcT p.S439S PAAD 10 8006929 8006929 + Missense_Mutation SNP C C T TCGA-2J-AABO-01A-21D-A40W-08 TCGA-2J-AABO-10A-01D-A40W-08 g.chr10:8006929C>T c.1456C>T c.(1456-1458)Ccc>Tcc p.P486S PAAD 10 8051129 8051129 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:8051129G>A c.2404G>A c.(2404-2406)Gcc>Acc p.A802T PRAD 10 8006411 8006411 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:8006411G>A c.938G>A c.(937-939)gGa>gAa p.G313E PRAD 10 8006929 8006929 + Missense_Mutation SNP C C T TCGA-EJ-A6RC-01A-11D-A32B-08 TCGA-EJ-A6RC-10A-01D-A329-08 g.chr10:8006929C>T c.1456C>T c.(1456-1458)Ccc>Tcc p.P486S PRAD 10 8051082 8051082 + Missense_Mutation SNP C C T TCGA-V1-A9OH-01A-11D-A41K-08 TCGA-V1-A9OH-10A-01D-A41N-08 g.chr10:8051082C>T c.2357C>T c.(2356-2358)gCg>gTg p.A786V READ 10 8006604 8006604 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:8006604G>A c.1131G>A c.(1129-1131)ccG>ccA p.P377P READ 10 8006792 8006792 + Missense_Mutation SNP C C T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr10:8006792C>T c.1319C>T c.(1318-1320)gCg>gTg p.A440V SKCM 10 7860672 7860672 + De_novo_Start_InFrame SNP G G A TCGA-EE-A2M5-06A-12D-A197-08 TCGA-EE-A2M5-10A-01D-A199-08 g.chr10:7860672G>A SKCM 10 7866325 7866325 + Nonsense_Mutation SNP C C T TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr10:7866325C>T c.211C>T c.(211-213)Cag>Tag p.Q71* SKCM 10 7866502 7866502 + Missense_Mutation SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr10:7866502C>T c.388C>T c.(388-390)Ccc>Tcc p.P130S SKCM 10 8006232 8006232 + Silent SNP A A G TCGA-EB-A5UN-06A-11D-A30X-08 TCGA-EB-A5UN-10A-01D-A30X-08 g.chr10:8006232A>G c.759A>G c.(757-759)gcA>gcG p.A253A SKCM 10 8006646 8006646 + Silent SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr10:8006646C>T c.1173C>T c.(1171-1173)atC>atT p.I391I SKCM 10 8006790 8006790 + Silent SNP C C T TCGA-D3-A5GL-06A-11D-A27K-08 TCGA-D3-A5GL-10A-01D-A27N-08 g.chr10:8006790C>T c.1317C>T c.(1315-1317)tcC>tcT p.S439S SKCM 10 8006910 8006910 + Silent SNP G G T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr10:8006910G>T c.1437G>T c.(1435-1437)ctG>ctT p.L479L SKCM 10 8006979 8006979 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:8006979C>T c.1506C>T c.(1504-1506)ccC>ccT p.P502P SKCM 10 8007004 8007004 + Missense_Mutation SNP G G C TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr10:8007004G>C c.1531G>C c.(1531-1533)Gag>Cag p.E511Q SKCM 10 8007196 8007196 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr10:8007196C>T c.1723C>T c.(1723-1725)Ccc>Tcc p.P575S SKCM 10 8007232 8007232 + Missense_Mutation SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr10:8007232C>T c.1759C>T c.(1759-1761)Ccc>Tcc p.P587S SKCM 10 8007463 8007463 + Missense_Mutation SNP C C T TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr10:8007463C>T c.1990C>T c.(1990-1992)Ccc>Tcc p.P664S SKCM 10 8007517 8007517 + Frame_Shift_Del DEL T T - TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr10:8007517delT c.2044delT c.(2044-2046)ttgfs p.L682fs SKCM 10 8051084 8051084 + Missense_Mutation SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr10:8051084C>T c.2359C>T c.(2359-2361)Ccc>Tcc p.P787S SKCM 10 8051106 8051106 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr10:8051106C>T c.2381C>T c.(2380-2382)aCc>aTc p.T794I SKCM 10 8051146 8051146 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:8051146C>T c.2421C>T c.(2419-2421)ctC>ctT p.L807L SKCM 10 8051254 8051254 + Silent SNP C C T TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr10:8051254C>T c.2529C>T c.(2527-2529)ccC>ccT p.P843P

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US 10 8006059 8006059 single base substitution C T missense_variant R196W 586C>T ALL-US 10 8006782 8006782 single base substitution T C missense_variant S437P 1309T>C ALL-US 10 8006791 8006791 single base substitution G A missense_variant A440T 1318G>A BLCA-US 10 8051117 8051128 deletion of <=200bp GCCCCCGCGCCC - inframe_deletion APAP798 BLCA-US 10 8056618 8056618 single base substitution G T missense_variant M898I 2694G>T BOCA-FR 10 7955330 7955330 single base substitution G A intron_variant BRCA-EU 10 7858466 7858466 single base substitution C T upstream_gene_variant BRCA-EU 10 7858569 7858569 single base substitution G A upstream_gene_variant BRCA-EU 10 7859555 7859555 single base substitution G A upstream_gene_variant BRCA-EU 10 7859643 7859643 single base substitution A G upstream_gene_variant BRCA-EU 10 7859902 7859902 single base substitution G T upstream_gene_variant BRCA-EU 10 7860555 7860555 single base substitution G A 5_prime_UTR_variant BRCA-EU 10 7861145 7861145 single base substitution T C intron_variant BRCA-EU 10 7861224 7861224 single base substitution A G intron_variant BRCA-EU 10 7862412 7862412 single base substitution T C intron_variant BRCA-EU 10 7862533 7862533 single base substitution C G intron_variant BRCA-EU 10 7864312 7864312 deletion of <=200bp T - intron_variant BRCA-EU 10 7864566 7864566 single base substitution G A intron_variant BRCA-EU 10 7864970 7864970 single base substitution G C intron_variant BRCA-EU 10 7866517 7866517 single base substitution C G missense_variant Q135E 403C>G BRCA-EU 10 7866556 7866556 single base substitution A G intron_variant BRCA-EU 10 7867517 7867517 single base substitution A G intron_variant BRCA-EU 10 7867755 7867755 single base substitution C T intron_variant BRCA-EU 10 7867772 7867772 single base substitution T G intron_variant BRCA-EU 10 7867806 7867806 deletion of <=200bp T - intron_variant BRCA-EU 10 7868961 7868961 single base substitution C T intron_variant BRCA-EU 10 7871679 7871679 single base substitution G C intron_variant BRCA-EU 10 7871997 7871997 single base substitution C T intron_variant BRCA-EU 10 7874970 7874970 single base substitution C T intron_variant BRCA-EU 10 7875655 7875655 single base substitution G T intron_variant BRCA-EU 10 7876003 7876003 deletion of <=200bp T - intron_variant BRCA-EU 10 7876433 7876433 single base substitution C G intron_variant BRCA-EU 10 7876773 7876773 deletion of <=200bp A - intron_variant BRCA-EU 10 7876781 7876781 insertion of <=200bp - T intron_variant BRCA-EU 10 7877878 7877878 single base substitution C T intron_variant BRCA-EU 10 7878387 7878387 single base substitution G C intron_variant BRCA-EU 10 7878938 7878938 single base substitution C A intron_variant BRCA-EU 10 7878988 7878988 single base substitution G C intron_variant BRCA-EU 10 7879199 7879199 single base substitution G A intron_variant BRCA-EU 10 7880327 7880327 single base substitution T G intron_variant BRCA-EU 10 7880926 7880926 single base substitution C G intron_variant BRCA-EU 10 7881203 7881203 single base substitution G A intron_variant BRCA-EU 10 7883074 7883074 single base substitution A T intron_variant BRCA-EU 10 7883479 7883479 single base substitution G A intron_variant BRCA-EU 10 7883764 7883764 single base substitution G C intron_variant BRCA-EU 10 7884540 7884541 deletion of <=200bp TA - intron_variant BRCA-EU 10 7885568 7885569 deletion of <=200bp TC - intron_variant BRCA-EU 10 7886759 7886759 deletion of <=200bp T - intron_variant BRCA-EU 10 7887062 7887062 single base substitution G A intron_variant BRCA-EU 10 7887631 7887631 single base substitution G C intron_variant BRCA-EU 10 7888602 7888602 single base substitution T A intron_variant BRCA-EU 10 7889447 7889447 single base substitution G A intron_variant BRCA-EU 10 7890779 7890779 single base substitution C G intron_variant BRCA-EU 10 7890800 7890802 deletion of <=200bp TCT - intron_variant BRCA-EU 10 7894118 7894118 single base substitution G T intron_variant BRCA-EU 10 7894193 7894193 single base substitution G A intron_variant BRCA-EU 10 7895185 7895185 single base substitution C T intron_variant BRCA-EU 10 7900659 7900659 single base substitution G T intron_variant BRCA-EU 10 7900759 7900759 single base substitution A T intron_variant BRCA-EU 10 7901122 7901122 single base substitution G T intron_variant BRCA-EU 10 7903509 7903509 single base substitution C G intron_variant BRCA-EU 10 7903647 7903647 deletion of <=200bp C - intron_variant BRCA-EU 10 7904599 7904599 single base substitution C A intron_variant BRCA-EU 10 7904872 7904872 single base substitution A G intron_variant BRCA-EU 10 7908744 7908744 single base substitution C G intron_variant BRCA-EU 10 7908847 7908847 single base substitution G C intron_variant BRCA-EU 10 7910621 7910621 single base substitution A G intron_variant BRCA-EU 10 7912751 7912751 single base substitution G A intron_variant BRCA-EU 10 7913102 7913102 single base substitution T C intron_variant BRCA-EU 10 7913267 7913267 single base substitution T C intron_variant BRCA-EU 10 7913509 7913509 single base substitution T C intron_variant BRCA-EU 10 7913825 7913825 single base substitution A C intron_variant BRCA-EU 10 7914975 7914975 single base substitution A C intron_variant BRCA-EU 10 7915093 7915093 single base substitution G T intron_variant BRCA-EU 10 7915763 7915787 deletion of <=200bp AACTTAATGCTGTTTATAGATAGAA - intron_variant BRCA-EU 10 7916742 7916742 single base substitution C T intron_variant BRCA-EU 10 7917186 7917189 deletion of <=200bp TTGT - intron_variant BRCA-EU 10 7918327 7918327 single base substitution C G intron_variant BRCA-EU 10 7918565 7918565 single base substitution C T intron_variant BRCA-EU 10 7918779 7918779 single base substitution C T intron_variant BRCA-EU 10 7919765 7919765 single base substitution C G intron_variant BRCA-EU 10 7919891 7919891 single base substitution C T intron_variant BRCA-EU 10 7919986 7919986 insertion of <=200bp - T intron_variant BRCA-EU 10 7921432 7921432 single base substitution A G intron_variant BRCA-EU 10 7921900 7921900 single base substitution G A intron_variant BRCA-EU 10 7922554 7922554 single base substitution G A intron_variant BRCA-EU 10 7923946 7923946 single base substitution A T intron_variant BRCA-EU 10 7924159 7924159 single base substitution G T intron_variant BRCA-EU 10 7924325 7924325 single base substitution G A intron_variant BRCA-EU 10 7924577 7924577 single base substitution A G intron_variant BRCA-EU 10 7924609 7924609 single base substitution C G intron_variant BRCA-EU 10 7925473 7925473 single base substitution G T intron_variant BRCA-EU 10 7925700 7925700 single base substitution G A intron_variant BRCA-EU 10 7926044 7926044 single base substitution G A intron_variant BRCA-EU 10 7927701 7927701 single base substitution A G intron_variant BRCA-EU 10 7928151 7928151 single base substitution C G intron_variant BRCA-EU 10 7928425 7928425 single base substitution A G intron_variant BRCA-EU 10 7929130 7929130 single base substitution G A intron_variant BRCA-EU 10 7929605 7929605 single base substitution A G intron_variant BRCA-EU 10 7930056 7930056 single base substitution C G intron_variant BRCA-EU 10 7930293 7930293 single base substitution T C intron_variant BRCA-EU 10 7930354 7930354 deletion of <=200bp A - intron_variant BRCA-EU 10 7930812 7930812 single base substitution C T intron_variant BRCA-EU 10 7932133 7932133 single base substitution G T intron_variant BRCA-EU 10 7932135 7932135 single base substitution T C intron_variant BRCA-EU 10 7934200 7934200 single base substitution G A intron_variant BRCA-EU 10 7936280 7936280 single base substitution G A intron_variant BRCA-EU 10 7936557 7936557 single base substitution G A intron_variant BRCA-EU 10 7938831 7938831 single base substitution G C intron_variant BRCA-EU 10 7940604 7940604 single base substitution G C intron_variant BRCA-EU 10 7940688 7940688 single base substitution T C intron_variant BRCA-EU 10 7940782 7940782 single base substitution T C intron_variant BRCA-EU 10 7941860 7941860 single base substitution C G intron_variant BRCA-EU 10 7942292 7942292 single base substitution G A intron_variant BRCA-EU 10 7942663 7942663 deletion of <=200bp T - intron_variant BRCA-EU 10 7942687 7942687 deletion of <=200bp G - intron_variant BRCA-EU 10 7943380 7943380 single base substitution T A intron_variant BRCA-EU 10 7944159 7944159 single base substitution G C intron_variant BRCA-EU 10 7944457 7944457 single base substitution G C intron_variant BRCA-EU 10 7944685 7944685 single base substitution G T intron_variant BRCA-EU 10 7944847 7944847 deletion of <=200bp T - intron_variant BRCA-EU 10 7945102 7945102 single base substitution G A intron_variant BRCA-EU 10 7946577 7946577 single base substitution A T intron_variant BRCA-EU 10 7946762 7946762 insertion of <=200bp - A intron_variant BRCA-EU 10 7946785 7946785 single base substitution C A intron_variant BRCA-EU 10 7948669 7948669 single base substitution C T intron_variant BRCA-EU 10 7950072 7950072 single base substitution C G intron_variant BRCA-EU 10 7952235 7952235 single base substitution A G intron_variant BRCA-EU 10 7954879 7954879 single base substitution C T intron_variant BRCA-EU 10 7954973 7954973 insertion of <=200bp - GGTTT intron_variant BRCA-EU 10 7955399 7955399 single base substitution C T intron_variant BRCA-EU 10 7955967 7955967 single base substitution C G intron_variant BRCA-EU 10 7956056 7956056 deletion of <=200bp T - intron_variant BRCA-EU 10 7956373 7956373 single base substitution A G intron_variant BRCA-EU 10 7958544 7958544 single base substitution A T intron_variant BRCA-EU 10 7959624 7959624 single base substitution G A intron_variant BRCA-EU 10 7961075 7961075 deletion of <=200bp A - intron_variant BRCA-EU 10 7965681 7965681 deletion of <=200bp A - intron_variant BRCA-EU 10 7965681 7965682 deletion of <=200bp AA - intron_variant BRCA-EU 10 7967407 7967407 single base substitution T C intron_variant BRCA-EU 10 7968930 7968930 single base substitution G C intron_variant BRCA-EU 10 7969107 7969107 insertion of <=200bp - T intron_variant BRCA-EU 10 7969517 7969517 single base substitution C T intron_variant BRCA-EU 10 7969905 7969905 single base substitution A G intron_variant BRCA-EU 10 7970681 7970681 single base substitution A C intron_variant BRCA-EU 10 7971280 7971280 single base substitution G C intron_variant BRCA-EU 10 7971795 7971795 single base substitution T A intron_variant BRCA-EU 10 7972740 7972740 insertion of <=200bp - T intron_variant BRCA-EU 10 7973214 7973214 single base substitution G A intron_variant BRCA-EU 10 7974988 7974988 single base substitution A G intron_variant BRCA-EU 10 7979417 7979417 single base substitution C G intron_variant BRCA-EU 10 7979952 7979952 single base substitution G A intron_variant BRCA-EU 10 7980156 7980156 single base substitution G A intron_variant BRCA-EU 10 7980521 7980521 insertion of <=200bp - A intron_variant BRCA-EU 10 7983423 7983423 single base substitution G C intron_variant BRCA-EU 10 7983628 7983628 single base substitution G C intron_variant BRCA-EU 10 7984766 7984766 single base substitution T A intron_variant BRCA-EU 10 7985099 7985099 single base substitution C T intron_variant BRCA-EU 10 7985987 7985987 single base substitution G T intron_variant BRCA-EU 10 7986000 7986000 single base substitution T G intron_variant BRCA-EU 10 7986040 7986040 single base substitution T G intron_variant BRCA-EU 10 7986909 7986909 single base substitution G C intron_variant BRCA-EU 10 7987703 7987703 single base substitution C T intron_variant BRCA-EU 10 7988172 7988172 single base substitution G T intron_variant BRCA-EU 10 7988387 7988387 single base substitution C G intron_variant BRCA-EU 10 7988450 7988450 single base substitution G A intron_variant BRCA-EU 10 7989298 7989298 single base substitution T G intron_variant BRCA-EU 10 7991010 7991010 single base substitution C G intron_variant BRCA-EU 10 7992676 7992676 single base substitution C T intron_variant BRCA-EU 10 7995651 7995651 single base substitution G C intron_variant BRCA-EU 10 7996024 7996024 single base substitution G T intron_variant BRCA-EU 10 7996135 7996135 single base substitution A C intron_variant BRCA-EU 10 7996683 7996683 single base substitution A G intron_variant BRCA-EU 10 7998450 7998450 insertion of <=200bp - A intron_variant BRCA-EU 10 7998553 7998553 single base substitution A G intron_variant BRCA-EU 10 7998900 7998900 deletion of <=200bp T - intron_variant BRCA-EU 10 7999124 7999124 single base substitution G C intron_variant BRCA-EU 10 7999217 7999217 single base substitution T C intron_variant BRCA-EU 10 7999843 7999843 single base substitution G C intron_variant BRCA-EU 10 7999849 7999849 single base substitution G T intron_variant BRCA-EU 10 7999864 7999864 insertion of <=200bp - A intron_variant BRCA-EU 10 8000713 8000713 insertion of <=200bp - C intron_variant BRCA-EU 10 8000949 8000949 single base substitution C A intron_variant BRCA-EU 10 8001470 8001470 single base substitution A G intron_variant BRCA-EU 10 8002533 8002533 single base substitution G A intron_variant BRCA-EU 10 8003534 8003534 single base substitution C G intron_variant BRCA-EU 10 8003733 8003733 single base substitution C T intron_variant BRCA-EU 10 8003959 8003959 single base substitution C T intron_variant BRCA-EU 10 8004176 8004176 single base substitution C T intron_variant BRCA-EU 10 8005036 8005036 single base substitution C T intron_variant BRCA-EU 10 8005362 8005362 single base substitution G C intron_variant BRCA-EU 10 8005603 8005603 single base substitution C A intron_variant BRCA-EU 10 8006121 8006121 single base substitution C G synonymous_variant L216L 648C>G BRCA-EU 10 8008621 8008621 single base substitution G C intron_variant BRCA-EU 10 8011276 8011294 deletion of <=200bp AAGAGCACTTATATTATCC - intron_variant BRCA-EU 10 8011387 8011387 deletion of <=200bp G - intron_variant BRCA-EU 10 8012126 8012126 single base substitution G A intron_variant BRCA-EU 10 8013329 8013329 deletion of <=200bp T - intron_variant BRCA-EU 10 8015408 8015408 single base substitution G A intron_variant BRCA-EU 10 8015898 8015898 single base substitution C G intron_variant BRCA-EU 10 8017616 8017616 single base substitution G A intron_variant BRCA-EU 10 8017692 8017692 single base substitution C A intron_variant BRCA-EU 10 8018526 8018526 single base substitution C T intron_variant BRCA-EU 10 8018635 8018635 single base substitution G A intron_variant BRCA-EU 10 8019796 8019796 insertion of <=200bp - T intron_variant BRCA-EU 10 8020388 8020388 single base substitution G C intron_variant BRCA-EU 10 8021496 8021496 single base substitution G C intron_variant BRCA-EU 10 8022308 8022327 deletion of <=200bp GATCCAGAAAAGTACTTTGA - intron_variant BRCA-EU 10 8023707 8023707 single base substitution G A intron_variant BRCA-EU 10 8024671 8024671 deletion of <=200bp T - intron_variant BRCA-EU 10 8026226 8026228 deletion of <=200bp CAC - intron_variant BRCA-EU 10 8027274 8027274 single base substitution C G intron_variant BRCA-EU 10 8028105 8028105 single base substitution C T intron_variant BRCA-EU 10 8028541 8028541 single base substitution G A intron_variant BRCA-EU 10 8028821 8028821 single base substitution C G intron_variant BRCA-EU 10 8030092 8030092 single base substitution T C intron_variant BRCA-EU 10 8030470 8030470 single base substitution G A intron_variant BRCA-EU 10 8032929 8032929 single base substitution G A intron_variant BRCA-EU 10 8033249 8033249 deletion of <=200bp T - intron_variant BRCA-EU 10 8034053 8034053 single base substitution C G intron_variant BRCA-EU 10 8034402 8034402 single base substitution G A intron_variant BRCA-EU 10 8035170 8035170 single base substitution C T intron_variant BRCA-EU 10 8035410 8035410 single base substitution G A intron_variant BRCA-EU 10 8036173 8036173 single base substitution C T intron_variant BRCA-EU 10 8037490 8037490 single base substitution T C intron_variant BRCA-EU 10 8038609 8038609 deletion of <=200bp T - intron_variant BRCA-EU 10 8039361 8039361 single base substitution G A intron_variant BRCA-EU 10 8039744 8039744 single base substitution G A intron_variant BRCA-EU 10 8042633 8042633 single base substitution T C intron_variant BRCA-EU 10 8042750 8042750 single base substitution A C intron_variant BRCA-EU 10 8044074 8044074 single base substitution T C intron_variant BRCA-EU 10 8044210 8044210 single base substitution G T intron_variant BRCA-EU 10 8044746 8044746 single base substitution G A intron_variant BRCA-EU 10 8045915 8045915 deletion of <=200bp A - intron_variant BRCA-EU 10 8046024 8046024 insertion of <=200bp - T intron_variant BRCA-EU 10 8046280 8046280 single base substitution G T intron_variant BRCA-EU 10 8046356 8046356 insertion of <=200bp - T intron_variant BRCA-EU 10 8047844 8047844 single base substitution G C intron_variant BRCA-EU 10 8047864 8047864 single base substitution G C intron_variant BRCA-EU 10 8050208 8050208 single base substitution C T intron_variant BRCA-EU 10 8050236 8050236 deletion of <=200bp T - intron_variant BRCA-EU 10 8050366 8050366 single base substitution C T intron_variant BRCA-EU 10 8050447 8050447 single base substitution G C intron_variant BRCA-EU 10 8051112 8051112 single base substitution C T missense_variant P796L 2387C>T BRCA-EU 10 8051658 8051658 single base substitution C G intron_variant BRCA-EU 10 8052218 8052218 single base substitution G A intron_variant BRCA-EU 10 8053293 8053293 single base substitution T C intron_variant BRCA-EU 10 8053706 8053706 single base substitution C G intron_variant BRCA-EU 10 8054881 8054881 deletion of <=200bp C - intron_variant BRCA-EU 10 8058065 8058065 insertion of <=200bp - A 3_prime_UTR_variant BRCA-EU 10 8058414 8058414 single base substitution C G 3_prime_UTR_variant BRCA-EU 10 8058557 8058557 deletion of <=200bp G - 3_prime_UTR_variant BRCA-EU 10 8058723 8058723 deletion of <=200bp C - downstream_gene_variant BRCA-EU 10 8058781 8058781 single base substitution C T downstream_gene_variant BRCA-EU 10 8059494 8059494 single base substitution C T downstream_gene_variant BRCA-EU 10 8059634 8059634 single base substitution G A downstream_gene_variant BRCA-EU 10 8061399 8061399 single base substitution G A downstream_gene_variant BRCA-EU 10 8061794 8061794 single base substitution G A downstream_gene_variant BRCA-EU 10 8063323 8063323 single base substitution A T downstream_gene_variant BRCA-FR 10 7860555 7860555 single base substitution G A 5_prime_UTR_variant BRCA-FR 10 7860689 7860689 single base substitution C G missense_variant S6C 17C>G BRCA-FR 10 7861145 7861145 single base substitution T C intron_variant BRCA-FR 10 7864566 7864566 single base substitution G A intron_variant BRCA-FR 10 7864970 7864970 single base substitution G C intron_variant BRCA-FR 10 7873425 7873425 single base substitution C T intron_variant BRCA-FR 10 7874970 7874970 single base substitution C T intron_variant BRCA-FR 10 7876433 7876433 single base substitution C G intron_variant BRCA-FR 10 7880327 7880327 single base substitution T G intron_variant BRCA-FR 10 7887062 7887062 single base substitution G A intron_variant BRCA-FR 10 7888602 7888602 single base substitution T A intron_variant BRCA-FR 10 7890779 7890779 single base substitution C G intron_variant BRCA-FR 10 7895932 7895932 single base substitution C A intron_variant BRCA-FR 10 7913265 7913265 single base substitution C T intron_variant BRCA-FR 10 7915093 7915093 single base substitution G T intron_variant BRCA-FR 10 7916742 7916742 single base substitution C T intron_variant BRCA-FR 10 7917539 7917539 single base substitution G T intron_variant BRCA-FR 10 7918327 7918327 single base substitution C G intron_variant BRCA-FR 10 7918779 7918779 single base substitution C T intron_variant BRCA-FR 10 7922554 7922554 single base substitution G A intron_variant BRCA-FR 10 7942292 7942292 single base substitution G A intron_variant BRCA-FR 10 7950072 7950072 single base substitution C G intron_variant BRCA-FR 10 7979055 7979055 single base substitution G A intron_variant BRCA-FR 10 7984983 7984983 single base substitution C G intron_variant BRCA-FR 10 7985987 7985987 single base substitution G T intron_variant BRCA-FR 10 7986040 7986040 single base substitution T G intron_variant BRCA-FR 10 8002654 8002654 single base substitution G C intron_variant BRCA-FR 10 8003534 8003534 single base substitution C G intron_variant BRCA-FR 10 8003733 8003733 single base substitution C T intron_variant BRCA-FR 10 8004176 8004176 single base substitution C T intron_variant BRCA-FR 10 8005036 8005036 single base substitution C T intron_variant BRCA-FR 10 8005362 8005362 single base substitution G C intron_variant BRCA-FR 10 8005603 8005603 single base substitution C A intron_variant BRCA-FR 10 8006121 8006121 single base substitution C G synonymous_variant L216L 648C>G BRCA-FR 10 8015874 8015874 single base substitution C G intron_variant BRCA-FR 10 8025446 8025446 single base substitution C T intron_variant BRCA-FR 10 8030470 8030470 single base substitution G A intron_variant BRCA-FR 10 8042633 8042633 single base substitution T C intron_variant BRCA-FR 10 8047844 8047844 single base substitution G C intron_variant BRCA-FR 10 8047864 8047864 single base substitution G C intron_variant BRCA-FR 10 8051658 8051658 single base substitution C G intron_variant BRCA-FR 10 8059494 8059494 single base substitution C T downstream_gene_variant BRCA-KR 10 8051228 8051228 single base substitution G A missense_variant A835T 2503G>A BRCA-UK 10 7863651 7863651 single base substitution G A intron_variant BRCA-UK 10 7869670 7869670 single base substitution G A intron_variant BRCA-UK 10 7897625 7897625 single base substitution G C intron_variant BRCA-UK 10 7974988 7974988 single base substitution A G intron_variant BRCA-UK 10 7996364 7996364 single base substitution A G intron_variant BRCA-UK 10 7996371 7996371 single base substitution T C intron_variant BRCA-UK 10 8006753 8006753 single base substitution C G stop_gained S427* 1280C>G BRCA-UK 10 8015408 8015408 single base substitution G A intron_variant BRCA-UK 10 8042750 8042750 single base substitution A C intron_variant BRCA-UK 10 8055791 8055791 single base substitution G C missense_variant W889S 2666G>C BRCA-US 10 7860723 7860723 single base substitution C A synonymous_variant I17I 51C>A BRCA-US 10 7866501 7866501 single base substitution A C synonymous_variant P129P 387A>C BRCA-US 10 8005972 8005972 single base substitution G T stop_gained E167* 499G>T BRCA-US 10 8006100 8006103 deletion of <=200bp ATTG - frameshift_variant LL209 BRCA-US 10 8006644 8006644 single base substitution A G missense_variant I391V 1171A>G BRCA-US 10 8006835 8006835 single base substitution C G synonymous_variant S454S 1362C>G BRCA-US 10 8055756 8055756 single base substitution G A synonymous_variant G877G 2631G>A BTCA-JP 10 8006085 8006085 single base substitution G A synonymous_variant T204T 612G>A BTCA-JP 10 8006342 8006342 single base substitution A G missense_variant Q290R 869A>G BTCA-JP 10 8006656 8006656 single base substitution A T missense_variant I395F 1183A>T BTCA-JP 10 8006790 8006790 single base substitution C T synonymous_variant S439S 1317C>T BTCA-JP 10 8007495 8007495 single base substitution C T synonymous_variant V674V 2022C>T BTCA-JP 10 8050974 8050974 single base substitution T A intron_variant BTCA-JP 10 8051300 8051300 single base substitution A T splice_region_variant BTCA-JP 10 8055637 8055640 deletion of <=200bp TTTT - intron_variant CESC-US 10 7860774 7860774 single base substitution C G synonymous_variant L34L 102C>G CESC-US 10 8006327 8006327 single base substitution C G stop_gained S285* 854C>G CESC-US 10 8006430 8006430 single base substitution G A synonymous_variant K319K 957G>A CLLE-ES 10 7883293 7883293 single base substitution G C intron_variant CLLE-ES 10 7884128 7884128 single base substitution T G intron_variant CLLE-ES 10 7889476 7889476 single base substitution T C intron_variant CLLE-ES 10 7898320 7898320 single base substitution G A intron_variant CLLE-ES 10 7901243 7901243 single base substitution A C intron_variant CLLE-ES 10 7904000 7904000 single base substitution T A intron_variant CLLE-ES 10 7914469 7914469 single base substitution A G intron_variant CLLE-ES 10 7927427 7927427 single base substitution G A intron_variant CLLE-ES 10 7961381 7961381 single base substitution G A intron_variant CLLE-ES 10 7975067 7975067 single base substitution A T intron_variant CLLE-ES 10 7976765 7976765 single base substitution A G intron_variant CLLE-ES 10 7977120 7977120 single base substitution A G intron_variant CLLE-ES 10 7996185 7996185 deletion of <=200bp C - intron_variant CLLE-ES 10 8040813 8040813 single base substitution G A intron_variant CLLE-ES 10 8042257 8042257 single base substitution T G intron_variant COAD-US 10 8005916 8005916 single base substitution G A missense_variant G148D 443G>A COAD-US 10 8006413 8006413 single base substitution C T missense_variant R314C 940C>T COAD-US 10 8006454 8006454 single base substitution G A synonymous_variant T327T 981G>A COAD-US 10 8006552 8006552 single base substitution A C missense_variant K360T 1079A>C COAD-US 10 8007368 8007369 deletion of <=200bp AG - frameshift_variant K632 COAD-US 10 8007451 8007451 single base substitution G T stop_gained E660* 1978G>T COAD-US 10 8056667 8056669 deletion of <=200bp AAG - inframe_deletion K915 COCA-CN 10 7859695 7859695 single base substitution C T upstream_gene_variant COCA-CN 10 7864257 7864257 single base substitution T C intron_variant COCA-CN 10 7866475 7866475 single base substitution A C missense_variant K121Q 361A>C COCA-CN 10 7868412 7868412 single base substitution G T intron_variant COCA-CN 10 7876659 7876659 single base substitution A G intron_variant COCA-CN 10 7877131 7877131 single base substitution T C intron_variant COCA-CN 10 7884128 7884128 single base substitution T G intron_variant COCA-CN 10 7884576 7884576 single base substitution T A intron_variant COCA-CN 10 7885494 7885494 single base substitution G T intron_variant COCA-CN 10 7887927 7887927 single base substitution T G intron_variant COCA-CN 10 7887928 7887928 single base substitution T G intron_variant COCA-CN 10 7893900 7893900 single base substitution G A intron_variant COCA-CN 10 7894539 7894539 single base substitution G A intron_variant COCA-CN 10 7896049 7896049 single base substitution C G intron_variant COCA-CN 10 7900811 7900811 single base substitution G C intron_variant COCA-CN 10 7900813 7900813 single base substitution A C intron_variant COCA-CN 10 7906796 7906796 single base substitution T C intron_variant COCA-CN 10 7907196 7907196 single base substitution C T intron_variant COCA-CN 10 7911208 7911208 single base substitution C G intron_variant COCA-CN 10 7911209 7911209 single base substitution C T intron_variant COCA-CN 10 7915583 7915583 single base substitution C T intron_variant COCA-CN 10 7916660 7916660 single base substitution G T intron_variant COCA-CN 10 7916662 7916662 single base substitution T A intron_variant COCA-CN 10 7923508 7923508 single base substitution A G intron_variant COCA-CN 10 7957463 7957463 single base substitution G A intron_variant COCA-CN 10 7957771 7957771 single base substitution G A intron_variant COCA-CN 10 7957947 7957947 single base substitution G A intron_variant COCA-CN 10 7963749 7963749 single base substitution T A intron_variant COCA-CN 10 7966062 7966062 single base substitution G A intron_variant COCA-CN 10 7995887 7995887 single base substitution C T intron_variant COCA-CN 10 7996364 7996364 single base substitution A G intron_variant COCA-CN 10 8006085 8006085 single base substitution G A synonymous_variant T204T 612G>A COCA-CN 10 8007138 8007138 single base substitution G T missense_variant E555D 1665G>T COCA-CN 10 8007809 8007809 single base substitution A C intron_variant COCA-CN 10 8011423 8011423 single base substitution A C intron_variant COCA-CN 10 8016134 8016134 single base substitution C A intron_variant COCA-CN 10 8017070 8017070 single base substitution T A intron_variant COCA-CN 10 8017144 8017144 single base substitution G A intron_variant COCA-CN 10 8021530 8021530 single base substitution C G intron_variant COCA-CN 10 8027655 8027655 single base substitution G T intron_variant COCA-CN 10 8036146 8036146 single base substitution C T intron_variant COCA-CN 10 8041532 8041532 single base substitution G A intron_variant COCA-CN 10 8045664 8045664 single base substitution C A intron_variant COCA-CN 10 8048142 8048142 single base substitution T C intron_variant COCA-CN 10 8048146 8048146 single base substitution C T intron_variant COCA-CN 10 8056495 8056495 single base substitution C T intron_variant COCA-CN 10 8056663 8056663 single base substitution G A synonymous_variant A913A 2739G>A COCA-CN 10 8056715 8056715 single base substitution C T 3_prime_UTR_variant EOPC-DE 10 7880332 7880332 single base substitution G T intron_variant EOPC-DE 10 7932226 7932226 single base substitution C G intron_variant EOPC-DE 10 7953013 7953013 single base substitution T C intron_variant EOPC-DE 10 8048601 8048601 single base substitution A G intron_variant ESAD-UK 10 7855920 7855920 single base substitution C T upstream_gene_variant ESAD-UK 10 7857014 7857014 single base substitution G A upstream_gene_variant ESAD-UK 10 7857836 7857836 single base substitution A T upstream_gene_variant ESAD-UK 10 7860434 7860434 single base substitution T G upstream_gene_variant ESAD-UK 10 7864344 7864344 single base substitution A G intron_variant ESAD-UK 10 7867905 7867905 single base substitution G T intron_variant ESAD-UK 10 7868228 7868228 single base substitution C A intron_variant ESAD-UK 10 7870229 7870229 single base substitution G T intron_variant ESAD-UK 10 7870399 7870399 single base substitution A C intron_variant ESAD-UK 10 7874003 7874003 single base substitution A T intron_variant ESAD-UK 10 7874744 7874744 single base substitution C T intron_variant ESAD-UK 10 7874847 7874847 single base substitution C T intron_variant ESAD-UK 10 7875800 7875800 single base substitution C A intron_variant ESAD-UK 10 7876889 7876889 insertion of <=200bp - T intron_variant ESAD-UK 10 7877535 7877535 single base substitution A G intron_variant ESAD-UK 10 7877884 7877884 single base substitution A G intron_variant ESAD-UK 10 7878595 7878595 single base substitution C T intron_variant ESAD-UK 10 7878667 7878667 single base substitution C T intron_variant ESAD-UK 10 7879892 7879892 single base substitution G A intron_variant ESAD-UK 10 7880363 7880363 single base substitution G A intron_variant ESAD-UK 10 7882507 7882507 single base substitution G T intron_variant ESAD-UK 10 7883737 7883737 single base substitution G A intron_variant ESAD-UK 10 7883822 7883822 single base substitution C G intron_variant ESAD-UK 10 7886712 7886712 single base substitution A G intron_variant ESAD-UK 10 7889418 7889418 deletion of <=200bp T - intron_variant ESAD-UK 10 7889532 7889532 single base substitution G A intron_variant ESAD-UK 10 7890671 7890671 single base substitution G A intron_variant ESAD-UK 10 7891255 7891255 single base substitution T A intron_variant ESAD-UK 10 7892693 7892693 single base substitution A T intron_variant ESAD-UK 10 7898089 7898089 single base substitution A T intron_variant ESAD-UK 10 7899200 7899200 single base substitution T A intron_variant ESAD-UK 10 7899406 7899406 single base substitution C T intron_variant ESAD-UK 10 7900536 7900536 single base substitution C T intron_variant ESAD-UK 10 7901817 7901817 single base substitution C T intron_variant ESAD-UK 10 7902280 7902280 single base substitution T C intron_variant ESAD-UK 10 7903358 7903358 single base substitution C T intron_variant ESAD-UK 10 7904624 7904624 single base substitution C T intron_variant ESAD-UK 10 7904911 7904911 single base substitution C T intron_variant ESAD-UK 10 7905714 7905714 insertion of <=200bp - AT intron_variant ESAD-UK 10 7906026 7906026 single base substitution G T intron_variant ESAD-UK 10 7907278 7907278 deletion of <=200bp A - intron_variant ESAD-UK 10 7909163 7909163 single base substitution A T intron_variant ESAD-UK 10 7909933 7909933 single base substitution A G intron_variant ESAD-UK 10 7910659 7910659 single base substitution G T intron_variant ESAD-UK 10 7911280 7911280 single base substitution C A intron_variant ESAD-UK 10 7911943 7911943 single base substitution A C intron_variant ESAD-UK 10 7914127 7914127 single base substitution A C intron_variant ESAD-UK 10 7917203 7917203 single base substitution C G intron_variant ESAD-UK 10 7917883 7917883 single base substitution G A intron_variant ESAD-UK 10 7919986 7919986 insertion of <=200bp - T intron_variant ESAD-UK 10 7925912 7925912 single base substitution A T intron_variant ESAD-UK 10 7927237 7927237 insertion of <=200bp - A intron_variant ESAD-UK 10 7927238 7927238 insertion of <=200bp - A intron_variant ESAD-UK 10 7929390 7929390 single base substitution A G intron_variant ESAD-UK 10 7930062 7930062 single base substitution G C intron_variant ESAD-UK 10 7930850 7930850 single base substitution T G intron_variant ESAD-UK 10 7932216 7932216 single base substitution T C intron_variant ESAD-UK 10 7933036 7933036 single base substitution C T intron_variant ESAD-UK 10 7933489 7933489 single base substitution G C intron_variant ESAD-UK 10 7935021 7935021 single base substitution G A intron_variant ESAD-UK 10 7936277 7936277 single base substitution C T intron_variant ESAD-UK 10 7937327 7937327 single base substitution A T intron_variant ESAD-UK 10 7938069 7938069 single base substitution G T intron_variant ESAD-UK 10 7938196 7938196 single base substitution T G intron_variant ESAD-UK 10 7940705 7940705 single base substitution T G intron_variant ESAD-UK 10 7944122 7944122 single base substitution G A intron_variant ESAD-UK 10 7949716 7949716 single base substitution G A intron_variant ESAD-UK 10 7951212 7951212 single base substitution G T intron_variant ESAD-UK 10 7952095 7952095 single base substitution A C intron_variant ESAD-UK 10 7953557 7953557 single base substitution A G intron_variant ESAD-UK 10 7954552 7954552 single base substitution C T intron_variant ESAD-UK 10 7955142 7955142 single base substitution A G intron_variant ESAD-UK 10 7957716 7957716 single base substitution C T intron_variant ESAD-UK 10 7958973 7958973 single base substitution A G intron_variant ESAD-UK 10 7960067 7960067 single base substitution G A intron_variant ESAD-UK 10 7961693 7961693 single base substitution C G intron_variant ESAD-UK 10 7963417 7963417 single base substitution G C intron_variant ESAD-UK 10 7965546 7965546 insertion of <=200bp - A intron_variant ESAD-UK 10 7965563 7965563 single base substitution C A intron_variant ESAD-UK 10 7965569 7965569 deletion of <=200bp A - intron_variant ESAD-UK 10 7965682 7965682 single base substitution A C intron_variant ESAD-UK 10 7968448 7968448 single base substitution G C intron_variant ESAD-UK 10 7969893 7969893 single base substitution G T intron_variant ESAD-UK 10 7971785 7971785 single base substitution A G intron_variant ESAD-UK 10 7975063 7975063 single base substitution A T intron_variant ESAD-UK 10 7977393 7977393 single base substitution A C intron_variant ESAD-UK 10 7977671 7977671 single base substitution C T intron_variant ESAD-UK 10 7978232 7978232 single base substitution C T intron_variant ESAD-UK 10 7978873 7978873 single base substitution C T intron_variant ESAD-UK 10 7979343 7979343 single base substitution A G intron_variant ESAD-UK 10 7982241 7982241 single base substitution C T intron_variant ESAD-UK 10 7982542 7982542 single base substitution G A intron_variant ESAD-UK 10 7984765 7984765 single base substitution A T intron_variant ESAD-UK 10 7984766 7984766 single base substitution T A intron_variant ESAD-UK 10 7984768 7984768 single base substitution T G intron_variant ESAD-UK 10 7985593 7985593 single base substitution A G intron_variant ESAD-UK 10 7987509 7987509 single base substitution C G intron_variant ESAD-UK 10 7987679 7987679 single base substitution T G intron_variant ESAD-UK 10 7988881 7988881 single base substitution T A intron_variant ESAD-UK 10 7989053 7989053 single base substitution A G intron_variant ESAD-UK 10 7989683 7989683 single base substitution C G intron_variant ESAD-UK 10 7995577 7995577 single base substitution C G intron_variant ESAD-UK 10 7998181 7998181 single base substitution G A intron_variant ESAD-UK 10 7998865 7998865 single base substitution C T intron_variant ESAD-UK 10 7998963 7998963 single base substitution G A intron_variant ESAD-UK 10 8000710 8000710 single base substitution G A intron_variant ESAD-UK 10 8003012 8003012 single base substitution C T intron_variant ESAD-UK 10 8004965 8004965 single base substitution C T intron_variant ESAD-UK 10 8007606 8007606 single base substitution G C missense_variant K711N 2133G>C ESAD-UK 10 8007986 8007986 deletion of <=200bp A - intron_variant ESAD-UK 10 8009823 8009823 single base substitution T G intron_variant ESAD-UK 10 8010036 8010036 single base substitution G A intron_variant ESAD-UK 10 8010428 8010428 single base substitution A T intron_variant ESAD-UK 10 8011961 8011961 single base substitution G C intron_variant ESAD-UK 10 8012193 8012193 single base substitution G A intron_variant ESAD-UK 10 8012910 8012910 deletion of <=200bp T - intron_variant ESAD-UK 10 8013042 8013042 single base substitution C T intron_variant ESAD-UK 10 8020552 8020552 single base substitution T C intron_variant ESAD-UK 10 8020673 8020673 single base substitution C T intron_variant ESAD-UK 10 8023908 8023908 single base substitution T G intron_variant ESAD-UK 10 8025484 8025484 single base substitution G A intron_variant ESAD-UK 10 8028097 8028097 deletion of <=200bp T - intron_variant ESAD-UK 10 8028222 8028222 single base substitution A C intron_variant ESAD-UK 10 8028224 8028224 single base substitution A T intron_variant ESAD-UK 10 8028475 8028475 single base substitution A T intron_variant ESAD-UK 10 8029854 8029854 single base substitution G A intron_variant ESAD-UK 10 8029907 8029907 single base substitution C T intron_variant ESAD-UK 10 8030962 8030962 single base substitution A C intron_variant ESAD-UK 10 8031716 8031716 single base substitution G A intron_variant ESAD-UK 10 8031981 8031981 single base substitution A G intron_variant ESAD-UK 10 8032004 8032004 single base substitution T C intron_variant ESAD-UK 10 8032257 8032257 single base substitution G T intron_variant ESAD-UK 10 8033749 8033749 single base substitution C A intron_variant ESAD-UK 10 8034855 8034855 single base substitution C T intron_variant ESAD-UK 10 8035892 8035892 single base substitution G C intron_variant ESAD-UK 10 8038609 8038609 deletion of <=200bp T - intron_variant ESAD-UK 10 8039652 8039652 single base substitution G A intron_variant ESAD-UK 10 8041145 8041145 single base substitution G A intron_variant ESAD-UK 10 8041365 8041365 single base substitution C G intron_variant ESAD-UK 10 8041898 8041898 single base substitution G C intron_variant ESAD-UK 10 8044640 8044640 deletion of <=200bp T - intron_variant ESAD-UK 10 8046024 8046024 insertion of <=200bp - T intron_variant ESAD-UK 10 8047257 8047257 single base substitution C G intron_variant ESAD-UK 10 8047427 8047427 single base substitution G A intron_variant ESAD-UK 10 8048644 8048644 single base substitution C T intron_variant ESAD-UK 10 8048692 8048692 single base substitution T C intron_variant ESAD-UK 10 8050130 8050130 single base substitution G A intron_variant ESAD-UK 10 8050286 8050286 single base substitution T C intron_variant ESAD-UK 10 8050690 8050690 single base substitution A T intron_variant ESAD-UK 10 8050860 8050860 single base substitution C T intron_variant ESAD-UK 10 8052990 8052990 single base substitution G A intron_variant ESAD-UK 10 8053938 8053938 single base substitution G C intron_variant ESAD-UK 10 8055010 8055010 single base substitution T G intron_variant ESAD-UK 10 8057836 8057836 deletion of <=200bp A - 3_prime_UTR_variant ESAD-UK 10 8057894 8057894 single base substitution G A 3_prime_UTR_variant ESAD-UK 10 8058081 8058081 single base substitution T C 3_prime_UTR_variant ESAD-UK 10 8058366 8058366 single base substitution G A 3_prime_UTR_variant ESAD-UK 10 8059559 8059559 insertion of <=200bp - G downstream_gene_variant ESAD-UK 10 8060445 8060445 single base substitution T G downstream_gene_variant ESAD-UK 10 8062632 8062632 single base substitution A C downstream_gene_variant ESCA-CN 10 8006085 8006085 single base substitution G A synonymous_variant T204T 612G>A ESCA-CN 10 8007136 8007136 single base substitution G C missense_variant E555Q 1663G>C ESCA-CN 10 8007217 8007217 single base substitution G A missense_variant E582K 1744G>A GBM-US 10 8006394 8006394 single base substitution A G synonymous_variant K307K 921A>G GBM-US 10 8007617 8007625 deletion of <=200bp AGAAGGAGA - inframe_deletion EKEK715E KIRC-US 10 8051125 8051125 single base substitution G T synonymous_variant A800A 2400G>T KIRC-US 10 8055709 8055709 single base substitution G A missense_variant G862S 2584G>A KIRP-US 10 8007636 8007636 single base substitution G C missense_variant K721N 2163G>C LAML-KR 10 7995943 7995943 single base substitution C T intron_variant LAML-KR 10 7996101 7996101 single base substitution C T intron_variant LGG-US 10 8007427 8007427 deletion of <=200bp C - frameshift_variant P652 LICA-CN 10 8055792 8055792 single base substitution G A stop_gained W889* 2667G>A LICA-FR 10 7860786 7860786 single base substitution G T synonymous_variant L38L 114G>T LICA-FR 10 7880723 7880723 single base substitution C A intron_variant LICA-FR 10 7881756 7881756 single base substitution A T intron_variant LICA-FR 10 7887923 7887923 deletion of <=200bp T - intron_variant LICA-FR 10 7940413 7940413 single base substitution G A intron_variant LICA-FR 10 8006086 8006086 single base substitution C A missense_variant L205I 613C>A LICA-FR 10 8007490 8007490 single base substitution A G missense_variant R673G 2017A>G LICA-FR 10 8040821 8040821 single base substitution A G intron_variant LICA-FR 10 8041402 8041406 deletion of <=200bp GAAAG - intron_variant LICA-FR 10 8046105 8046105 single base substitution C A intron_variant LIHC-US 10 8006085 8006085 single base substitution G T synonymous_variant T204T 612G>T LIHC-US 10 8006438 8006438 single base substitution A G missense_variant K322R 965A>G LIHC-US 10 8006861 8006861 single base substitution C T missense_variant S463L 1388C>T LINC-JP 10 7859623 7859623 single base substitution C T upstream_gene_variant LINC-JP 10 7865585 7865585 single base substitution A G intron_variant LINC-JP 10 7865991 7865991 single base substitution C G intron_variant LINC-JP 10 7868466 7868466 single base substitution A G intron_variant LINC-JP 10 7872097 7872097 single base substitution C G intron_variant LINC-JP 10 7880871 7880871 single base substitution G T intron_variant LINC-JP 10 7890856 7890856 single base substitution G A intron_variant LINC-JP 10 7892671 7892671 single base substitution C T intron_variant LINC-JP 10 7912998 7912998 single base substitution G T intron_variant LINC-JP 10 7918992 7918992 insertion of <=200bp - T intron_variant LINC-JP 10 7932748 7932748 single base substitution C A intron_variant LINC-JP 10 7960399 7960399 single base substitution G C intron_variant LINC-JP 10 7974465 7974465 single base substitution A G intron_variant LINC-JP 10 7980371 7980371 single base substitution A G intron_variant LINC-JP 10 8006264 8006264 single base substitution A G missense_variant E264G 791A>G LINC-JP 10 8028097 8028097 deletion of <=200bp T - intron_variant LINC-JP 10 8034968 8034968 single base substitution A C intron_variant LINC-JP 10 8052967 8052967 single base substitution A G intron_variant LINC-JP 10 8063405 8063405 single base substitution G A downstream_gene_variant LIRI-JP 10 7858801 7858801 single base substitution T C upstream_gene_variant LIRI-JP 10 7862500 7862500 single base substitution G A intron_variant LIRI-JP 10 7862984 7862984 single base substitution A G intron_variant LIRI-JP 10 7863355 7863355 single base substitution A T intron_variant LIRI-JP 10 7866499 7866499 single base substitution C T missense_variant P129S 385C>T LIRI-JP 10 7869352 7869352 single base substitution G A intron_variant LIRI-JP 10 7870510 7870510 single base substitution G T intron_variant LIRI-JP 10 7875284 7875284 single base substitution G A intron_variant LIRI-JP 10 7876684 7876684 single base substitution G T intron_variant LIRI-JP 10 7876950 7876950 single base substitution A G intron_variant LIRI-JP 10 7878240 7878240 single base substitution G C intron_variant LIRI-JP 10 7880551 7880551 single base substitution G A intron_variant LIRI-JP 10 7882688 7882688 single base substitution G A intron_variant LIRI-JP 10 7883644 7883647 deletion of <=200bp TGGA - intron_variant LIRI-JP 10 7883700 7883700 single base substitution C G intron_variant LIRI-JP 10 7883779 7883779 single base substitution G T intron_variant LIRI-JP 10 7885264 7885264 single base substitution C T intron_variant LIRI-JP 10 7887576 7887576 single base substitution G A intron_variant LIRI-JP 10 7892194 7892194 single base substitution T C intron_variant LIRI-JP 10 7892236 7892236 single base substitution C A intron_variant LIRI-JP 10 7892924 7892924 single base substitution C G intron_variant LIRI-JP 10 7894765 7894765 single base substitution A T intron_variant LIRI-JP 10 7896164 7896164 single base substitution A T intron_variant LIRI-JP 10 7896358 7896358 single base substitution C G intron_variant LIRI-JP 10 7896694 7896694 single base substitution G T intron_variant LIRI-JP 10 7897099 7897099 single base substitution A G intron_variant LIRI-JP 10 7897613 7897613 single base substitution T G intron_variant LIRI-JP 10 7903616 7903616 single base substitution T A intron_variant LIRI-JP 10 7903643 7903643 single base substitution T A intron_variant LIRI-JP 10 7904372 7904372 single base substitution C T intron_variant LIRI-JP 10 7905014 7905014 single base substitution A G intron_variant LIRI-JP 10 7905399 7905399 single base substitution C T intron_variant LIRI-JP 10 7907516 7907516 single base substitution G A intron_variant LIRI-JP 10 7912244 7912244 single base substitution A T intron_variant LIRI-JP 10 7913015 7913015 single base substitution T C intron_variant LIRI-JP 10 7913714 7913714 single base substitution G T intron_variant LIRI-JP 10 7917520 7917520 single base substitution G A intron_variant LIRI-JP 10 7920171 7920171 single base substitution C T intron_variant LIRI-JP 10 7923871 7923871 single base substitution A G intron_variant LIRI-JP 10 7924223 7924223 single base substitution A T intron_variant LIRI-JP 10 7924265 7924265 single base substitution T C intron_variant LIRI-JP 10 7925003 7925003 single base substitution G A intron_variant LIRI-JP 10 7928404 7928404 single base substitution A C intron_variant LIRI-JP 10 7932643 7932643 single base substitution T G intron_variant LIRI-JP 10 7934159 7934159 single base substitution A G intron_variant LIRI-JP 10 7935735 7935735 single base substitution C A intron_variant LIRI-JP 10 7936231 7936231 single base substitution G A intron_variant LIRI-JP 10 7936835 7936835 single base substitution T G intron_variant LIRI-JP 10 7938327 7938327 single base substitution A G intron_variant LIRI-JP 10 7945672 7945672 single base substitution T C intron_variant LIRI-JP 10 7949354 7949354 single base substitution A G intron_variant LIRI-JP 10 7951412 7951412 single base substitution C T intron_variant LIRI-JP 10 7952471 7952471 single base substitution G A intron_variant LIRI-JP 10 7954393 7954393 single base substitution A G intron_variant LIRI-JP 10 7956356 7956356 single base substitution C A intron_variant LIRI-JP 10 7959528 7959528 single base substitution A G intron_variant LIRI-JP 10 7959848 7959848 single base substitution T G intron_variant LIRI-JP 10 7960630 7960630 single base substitution A T intron_variant LIRI-JP 10 7961134 7961134 single base substitution C T intron_variant LIRI-JP 10 7961492 7961492 single base substitution A C intron_variant LIRI-JP 10 7961895 7961895 single base substitution G T intron_variant LIRI-JP 10 7962171 7962171 single base substitution C T intron_variant LIRI-JP 10 7963167 7963167 single base substitution A G intron_variant LIRI-JP 10 7963487 7963487 single base substitution A G intron_variant LIRI-JP 10 7964097 7964097 single base substitution A G intron_variant LIRI-JP 10 7964463 7964463 single base substitution A T intron_variant LIRI-JP 10 7965951 7965951 single base substitution A T intron_variant LIRI-JP 10 7966018 7966018 single base substitution A G intron_variant LIRI-JP 10 7966706 7966709 deletion of <=200bp CTAT - intron_variant LIRI-JP 10 7966864 7966864 single base substitution G T intron_variant LIRI-JP 10 7967389 7967389 single base substitution A G intron_variant LIRI-JP 10 7969082 7969082 single base substitution G A intron_variant LIRI-JP 10 7970822 7970822 single base substitution A G intron_variant LIRI-JP 10 7974492 7974492 single base substitution G A intron_variant LIRI-JP 10 7977401 7977401 single base substitution G T intron_variant LIRI-JP 10 7982623 7982623 single base substitution G A intron_variant LIRI-JP 10 7984507 7984507 single base substitution A G intron_variant LIRI-JP 10 7985946 7985963 deletion of <=200bp TTCTTGTTCTTTCTGCAA - intron_variant LIRI-JP 10 7987294 7987294 single base substitution G T intron_variant LIRI-JP 10 7988354 7988354 single base substitution T C intron_variant LIRI-JP 10 7991131 7991131 single base substitution C G intron_variant LIRI-JP 10 7991317 7991317 single base substitution G A intron_variant LIRI-JP 10 7992004 7992004 single base substitution A G intron_variant LIRI-JP 10 7992523 7992523 single base substitution A G intron_variant LIRI-JP 10 7992575 7992575 single base substitution T C intron_variant LIRI-JP 10 7994618 7994618 single base substitution A T intron_variant LIRI-JP 10 7994852 7994852 single base substitution G A intron_variant LIRI-JP 10 7995666 7995666 single base substitution A G intron_variant LIRI-JP 10 7998128 7998128 single base substitution T C intron_variant LIRI-JP 10 7999848 7999848 single base substitution G T intron_variant LIRI-JP 10 8003048 8003048 single base substitution G A intron_variant LIRI-JP 10 8005839 8005839 single base substitution T G intron_variant LIRI-JP 10 8005912 8005912 single base substitution G A missense_variant G147R 439G>A LIRI-JP 10 8006724 8006724 single base substitution A G synonymous_variant G417G 1251A>G LIRI-JP 10 8009275 8009275 deletion of <=200bp C - intron_variant LIRI-JP 10 8009548 8009548 single base substitution T G intron_variant LIRI-JP 10 8021171 8021171 single base substitution G T intron_variant LIRI-JP 10 8021258 8021258 single base substitution G T intron_variant LIRI-JP 10 8022521 8022521 single base substitution G T intron_variant LIRI-JP 10 8023081 8023081 deletion of <=200bp A - intron_variant LIRI-JP 10 8024859 8024859 single base substitution C G intron_variant LIRI-JP 10 8028787 8028787 single base substitution A G intron_variant LIRI-JP 10 8029423 8029423 single base substitution C T intron_variant LIRI-JP 10 8029547 8029547 single base substitution A T intron_variant LIRI-JP 10 8029952 8029952 single base substitution T C intron_variant LIRI-JP 10 8030699 8030699 single base substitution G A intron_variant LIRI-JP 10 8031362 8031362 single base substitution G T intron_variant LIRI-JP 10 8031940 8031940 single base substitution A G intron_variant LIRI-JP 10 8032891 8032891 single base substitution G A intron_variant LIRI-JP 10 8036571 8036571 single base substitution C A intron_variant LIRI-JP 10 8038086 8038086 single base substitution A G intron_variant LIRI-JP 10 8041039 8041039 single base substitution G A intron_variant LIRI-JP 10 8042377 8042377 single base substitution G A intron_variant LIRI-JP 10 8043872 8043872 single base substitution A G intron_variant LIRI-JP 10 8043927 8043927 single base substitution A G intron_variant LIRI-JP 10 8044256 8044256 single base substitution G A intron_variant LIRI-JP 10 8044924 8044924 single base substitution C A intron_variant LIRI-JP 10 8044944 8044944 single base substitution G T intron_variant LIRI-JP 10 8045950 8045950 single base substitution C A intron_variant LIRI-JP 10 8047186 8047186 single base substitution C A intron_variant LIRI-JP 10 8048532 8048532 single base substitution T G intron_variant LIRI-JP 10 8049177 8049177 single base substitution A G intron_variant LIRI-JP 10 8049937 8049937 single base substitution G T intron_variant LIRI-JP 10 8052030 8052030 single base substitution G T intron_variant LIRI-JP 10 8052369 8052369 single base substitution A G intron_variant LIRI-JP 10 8053243 8053243 single base substitution G C intron_variant LIRI-JP 10 8053361 8053361 single base substitution C T intron_variant LIRI-JP 10 8054050 8054050 single base substitution A G intron_variant LIRI-JP 10 8054213 8054213 single base substitution A G intron_variant LIRI-JP 10 8054970 8054970 single base substitution A G intron_variant LIRI-JP 10 8058047 8058047 single base substitution T C 3_prime_UTR_variant LIRI-JP 10 8060170 8060170 insertion of <=200bp - T downstream_gene_variant LIRI-JP 10 8060292 8060292 single base substitution T G downstream_gene_variant LIRI-JP 10 8061509 8061509 single base substitution G A downstream_gene_variant LIRI-JP 10 8063208 8063208 single base substitution T C downstream_gene_variant LUSC-KR 10 7856347 7856347 single base substitution C T upstream_gene_variant LUSC-KR 10 7859550 7859550 single base substitution C A upstream_gene_variant LUSC-KR 10 7860455 7860455 single base substitution C T upstream_gene_variant LUSC-KR 10 7860514 7860514 single base substitution G T 5_prime_UTR_variant LUSC-KR 10 7866771 7866771 single base substitution G T intron_variant LUSC-KR 10 7878385 7878385 single base substitution G T intron_variant LUSC-KR 10 7879257 7879257 single base substitution T G intron_variant LUSC-KR 10 7882404 7882404 single base substitution C G intron_variant LUSC-KR 10 7882508 7882508 single base substitution T G intron_variant LUSC-KR 10 7889707 7889707 single base substitution A T intron_variant LUSC-KR 10 7891495 7891495 single base substitution G A intron_variant LUSC-KR 10 7892423 7892423 single base substitution G A intron_variant LUSC-KR 10 7897022 7897022 single base substitution G T intron_variant LUSC-KR 10 7898443 7898443 single base substitution C T intron_variant LUSC-KR 10 7901601 7901601 single base substitution A C intron_variant LUSC-KR 10 7908758 7908758 single base substitution G C intron_variant LUSC-KR 10 7910696 7910696 single base substitution G T intron_variant LUSC-KR 10 7911314 7911314 single base substitution G C intron_variant LUSC-KR 10 7912093 7912093 single base substitution C G intron_variant LUSC-KR 10 7912269 7912269 single base substitution C G intron_variant LUSC-KR 10 7912520 7912520 single base substitution G T intron_variant LUSC-KR 10 7914883 7914883 single base substitution G T intron_variant LUSC-KR 10 7916957 7916957 single base substitution A C intron_variant LUSC-KR 10 7917322 7917322 single base substitution G C intron_variant LUSC-KR 10 7927812 7927812 single base substitution G C intron_variant LUSC-KR 10 7927862 7927862 single base substitution A T intron_variant LUSC-KR 10 7928257 7928257 single base substitution G T intron_variant LUSC-KR 10 7941545 7941545 single base substitution G C intron_variant LUSC-KR 10 7942288 7942288 single base substitution G T intron_variant LUSC-KR 10 7942289 7942289 single base substitution G T intron_variant LUSC-KR 10 7943277 7943277 single base substitution G C intron_variant LUSC-KR 10 7946832 7946832 single base substitution C A intron_variant LUSC-KR 10 7947132 7947132 single base substitution G T intron_variant LUSC-KR 10 7955054 7955054 single base substitution C T intron_variant LUSC-KR 10 7955296 7955296 single base substitution G T intron_variant LUSC-KR 10 7955695 7955695 single base substitution G A intron_variant LUSC-KR 10 7957713 7957713 single base substitution G T intron_variant LUSC-KR 10 7966325 7966325 single base substitution T A intron_variant LUSC-KR 10 7968432 7968432 single base substitution G T intron_variant LUSC-KR 10 7969598 7969598 single base substitution C A intron_variant LUSC-KR 10 7974863 7974863 single base substitution G T intron_variant LUSC-KR 10 7979851 7979851 single base substitution C T intron_variant LUSC-KR 10 7980839 7980839 single base substitution G T intron_variant LUSC-KR 10 7983068 7983068 single base substitution G C intron_variant LUSC-KR 10 7989149 7989149 single base substitution G A intron_variant LUSC-KR 10 7996187 7996187 single base substitution T C intron_variant LUSC-KR 10 7998005 7998005 single base substitution A C intron_variant LUSC-KR 10 7998890 7998890 single base substitution A T intron_variant LUSC-KR 10 7998891 7998891 single base substitution T C intron_variant LUSC-KR 10 7999611 7999611 single base substitution G T intron_variant LUSC-KR 10 8002253 8002253 single base substitution C G intron_variant LUSC-KR 10 8002710 8002710 single base substitution C T intron_variant LUSC-KR 10 8002711 8002711 single base substitution C T intron_variant LUSC-KR 10 8005117 8005117 single base substitution T G intron_variant LUSC-KR 10 8009807 8009807 single base substitution C G intron_variant LUSC-KR 10 8011845 8011845 single base substitution G A intron_variant LUSC-KR 10 8017203 8017203 single base substitution C G intron_variant LUSC-KR 10 8020394 8020394 single base substitution A G intron_variant LUSC-KR 10 8021204 8021204 single base substitution G T intron_variant LUSC-KR 10 8021666 8021666 single base substitution G T intron_variant LUSC-KR 10 8022132 8022132 single base substitution G C intron_variant LUSC-KR 10 8022483 8022483 single base substitution C G intron_variant LUSC-KR 10 8022549 8022549 single base substitution C T intron_variant LUSC-KR 10 8030254 8030254 single base substitution A G intron_variant LUSC-KR 10 8032795 8032795 single base substitution A G intron_variant LUSC-KR 10 8038822 8038822 single base substitution G T intron_variant LUSC-KR 10 8039814 8039814 single base substitution A G intron_variant LUSC-KR 10 8040831 8040831 single base substitution T A intron_variant LUSC-KR 10 8044174 8044174 single base substitution C T intron_variant LUSC-KR 10 8050844 8050844 single base substitution T C intron_variant LUSC-KR 10 8053670 8053670 single base substitution G C intron_variant LUSC-KR 10 8059127 8059127 single base substitution A T downstream_gene_variant LUSC-KR 10 8059557 8059557 single base substitution G A downstream_gene_variant LUSC-KR 10 8061241 8061241 single base substitution G A downstream_gene_variant LUSC-US 10 7860717 7860717 single base substitution G T synonymous_variant A15A 45G>T LUSC-US 10 7860771 7860771 single base substitution C T synonymous_variant L33L 99C>T LUSC-US 10 7866291 7866291 single base substitution A T synonymous_variant T59T 177A>T LUSC-US 10 8007024 8007024 single base substitution C A synonymous_variant S517S 1551C>A LUSC-US 10 8007226 8007226 single base substitution G T missense_variant A585S 1753G>T LUSC-US 10 8051097 8051097 single base substitution G A missense_variant R791K 2372G>A LUSC-US 10 8055717 8055717 single base substitution G T missense_variant Q864H 2592G>T LUSC-US 10 8055795 8055795 single base substitution C G stop_gained Y890* 2670C>G MALY-DE 10 7857159 7857159 single base substitution G A upstream_gene_variant MALY-DE 10 7867435 7867435 single base substitution C T intron_variant MALY-DE 10 7894921 7894921 single base substitution A C intron_variant MALY-DE 10 7898886 7898886 single base substitution T A intron_variant MALY-DE 10 7905667 7905667 single base substitution T C intron_variant MALY-DE 10 7905686 7905686 insertion of <=200bp - ACACAT intron_variant MALY-DE 10 7922928 7922928 single base substitution G A intron_variant MALY-DE 10 7926488 7926488 single base substitution T C intron_variant MALY-DE 10 7926490 7926490 single base substitution T C intron_variant MALY-DE 10 7928164 7928164 single base substitution T G intron_variant MALY-DE 10 7931445 7931445 single base substitution C A intron_variant MALY-DE 10 7939141 7939141 single base substitution A T intron_variant MALY-DE 10 7945465 7945465 single base substitution A G intron_variant MALY-DE 10 7945524 7945524 single base substitution T G intron_variant MALY-DE 10 7949178 7949178 single base substitution C T intron_variant MALY-DE 10 7952849 7952849 single base substitution C T intron_variant MALY-DE 10 7953946 7953946 single base substitution G A intron_variant MALY-DE 10 7954527 7954527 single base substitution A G intron_variant MALY-DE 10 7961075 7961075 insertion of <=200bp - A intron_variant MALY-DE 10 7965681 7965681 deletion of <=200bp A - intron_variant MALY-DE 10 7965682 7965682 single base substitution A C intron_variant MALY-DE 10 7974545 7974545 single base substitution T C intron_variant MALY-DE 10 7986177 7986177 single base substitution C G intron_variant MALY-DE 10 7986551 7986551 single base substitution G A intron_variant MALY-DE 10 7997334 7997334 single base substitution A C intron_variant MALY-DE 10 7998195 7998195 single base substitution G A intron_variant MALY-DE 10 8000179 8000179 single base substitution A G intron_variant MALY-DE 10 8000186 8000186 single base substitution A T intron_variant MALY-DE 10 8000898 8000898 single base substitution C G intron_variant MALY-DE 10 8008505 8008505 single base substitution G T intron_variant MALY-DE 10 8008730 8008730 single base substitution C G intron_variant MALY-DE 10 8017086 8017086 single base substitution A C intron_variant MALY-DE 10 8018948 8018948 single base substitution A C intron_variant MALY-DE 10 8044037 8044037 single base substitution C T intron_variant MALY-DE 10 8046188 8046194 deletion of <=200bp ATTTTTA - intron_variant MALY-DE 10 8054639 8054639 single base substitution C G intron_variant MALY-DE 10 8061004 8061004 single base substitution A T downstream_gene_variant MELA-AU 10 7855789 7855789 single base substitution A G upstream_gene_variant MELA-AU 10 7855908 7855908 single base substitution G A upstream_gene_variant MELA-AU 10 7856429 7856429 single base substitution G A upstream_gene_variant MELA-AU 10 7856465 7856465 single base substitution G A upstream_gene_variant MELA-AU 10 7856489 7856489 single base substitution G A upstream_gene_variant MELA-AU 10 7856514 7856514 single base substitution G A upstream_gene_variant MELA-AU 10 7857133 7857133 single base substitution C T upstream_gene_variant MELA-AU 10 7857159 7857159 single base substitution G A upstream_gene_variant MELA-AU 10 7857179 7857179 single base substitution G A upstream_gene_variant MELA-AU 10 7857440 7857440 single base substitution C T upstream_gene_variant MELA-AU 10 7858070 7858070 single base substitution C T upstream_gene_variant MELA-AU 10 7858881 7858881 single base substitution A G upstream_gene_variant MELA-AU 10 7859226 7859226 single base substitution G A upstream_gene_variant MELA-AU 10 7859252 7859252 single base substitution G A upstream_gene_variant MELA-AU 10 7859300 7859300 single base substitution C T upstream_gene_variant MELA-AU 10 7859364 7859364 single base substitution T G upstream_gene_variant MELA-AU 10 7859405 7859405 single base substitution G A upstream_gene_variant MELA-AU 10 7859624 7859624 single base substitution G A upstream_gene_variant MELA-AU 10 7859821 7859821 single base substitution A T upstream_gene_variant MELA-AU 10 7859928 7859928 single base substitution T G upstream_gene_variant MELA-AU 10 7860397 7860397 single base substitution C T upstream_gene_variant MELA-AU 10 7860596 7860596 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 10 7860672 7860672 single base substitution G A 5_prime_UTR_variant MELA-AU 10 7860832 7860832 single base substitution G A missense_variant E54K 160G>A MELA-AU 10 7861713 7861713 single base substitution T G intron_variant MELA-AU 10 7862275 7862275 single base substitution G A intron_variant MELA-AU 10 7862471 7862471 single base substitution C T intron_variant MELA-AU 10 7862572 7862572 single base substitution C T intron_variant MELA-AU 10 7862950 7862950 single base substitution C T intron_variant MELA-AU 10 7863319 7863319 single base substitution C T intron_variant MELA-AU 10 7863772 7863772 single base substitution C T intron_variant MELA-AU 10 7864308 7864308 single base substitution T A intron_variant MELA-AU 10 7864941 7864941 single base substitution G A intron_variant MELA-AU 10 7865081 7865081 single base substitution A C intron_variant MELA-AU 10 7865313 7865313 single base substitution G T intron_variant MELA-AU 10 7865708 7865708 single base substitution C T intron_variant MELA-AU 10 7867553 7867558 deletion of <=200bp TTTGTC - intron_variant MELA-AU 10 7867633 7867633 single base substitution C T intron_variant MELA-AU 10 7869297 7869297 deletion of <=200bp T - intron_variant MELA-AU 10 7869484 7869484 single base substitution C T intron_variant MELA-AU 10 7869730 7869730 single base substitution G A intron_variant MELA-AU 10 7869774 7869774 single base substitution T C intron_variant MELA-AU 10 7871839 7871839 single base substitution G A intron_variant MELA-AU 10 7871992 7871992 single base substitution C T intron_variant MELA-AU 10 7872290 7872290 single base substitution C T intron_variant MELA-AU 10 7872378 7872378 single base substitution C T intron_variant MELA-AU 10 7873418 7873418 single base substitution C T intron_variant MELA-AU 10 7873602 7873602 single base substitution C T intron_variant MELA-AU 10 7873842 7873842 single base substitution C T intron_variant MELA-AU 10 7874151 7874151 single base substitution C T intron_variant MELA-AU 10 7874336 7874336 single base substitution C T intron_variant MELA-AU 10 7874495 7874495 single base substitution A T intron_variant MELA-AU 10 7874620 7874620 single base substitution C T intron_variant MELA-AU 10 7874870 7874870 single base substitution T A intron_variant MELA-AU 10 7875356 7875356 single base substitution A G intron_variant MELA-AU 10 7875596 7875596 single base substitution C T intron_variant MELA-AU 10 7876261 7876261 single base substitution C T intron_variant MELA-AU 10 7876575 7876575 single base substitution C T intron_variant MELA-AU 10 7877347 7877347 single base substitution C T intron_variant MELA-AU 10 7877748 7877748 single base substitution C G intron_variant MELA-AU 10 7877994 7877994 single base substitution C T intron_variant MELA-AU 10 7878243 7878243 single base substitution T A intron_variant MELA-AU 10 7878283 7878283 single base substitution C T intron_variant MELA-AU 10 7878969 7878969 single base substitution C T intron_variant MELA-AU 10 7880137 7880137 single base substitution C T intron_variant MELA-AU 10 7880226 7880226 single base substitution C T intron_variant MELA-AU 10 7880390 7880390 single base substitution G T intron_variant MELA-AU 10 7881374 7881374 single base substitution T C intron_variant MELA-AU 10 7881626 7881626 single base substitution C G intron_variant MELA-AU 10 7881721 7881721 single base substitution C T intron_variant MELA-AU 10 7881842 7881842 single base substitution T C intron_variant MELA-AU 10 7881957 7881957 single base substitution C T intron_variant MELA-AU 10 7882581 7882581 single base substitution C T intron_variant MELA-AU 10 7883053 7883053 single base substitution A C intron_variant MELA-AU 10 7883313 7883313 single base substitution T C intron_variant MELA-AU 10 7883351 7883351 single base substitution G A intron_variant MELA-AU 10 7883838 7883838 single base substitution T A intron_variant MELA-AU 10 7883901 7883902 multiple base substitution (>=2bp and <=200bp) CA TG intron_variant MELA-AU 10 7885740 7885740 single base substitution G A intron_variant MELA-AU 10 7886237 7886237 single base substitution T A intron_variant MELA-AU 10 7886956 7886956 single base substitution C T intron_variant MELA-AU 10 7886996 7886996 single base substitution T C intron_variant MELA-AU 10 7887149 7887149 deletion of <=200bp T - intron_variant MELA-AU 10 7887736 7887736 single base substitution A T intron_variant MELA-AU 10 7887920 7887920 single base substitution T C intron_variant MELA-AU 10 7887988 7887988 single base substitution C T intron_variant MELA-AU 10 7887990 7887990 single base substitution C T intron_variant MELA-AU 10 7888263 7888263 single base substitution C T intron_variant MELA-AU 10 7888617 7888617 single base substitution A T intron_variant MELA-AU 10 7888962 7888962 single base substitution C T intron_variant MELA-AU 10 7889003 7889003 single base substitution T C intron_variant MELA-AU 10 7889415 7889415 single base substitution T A intron_variant MELA-AU 10 7889517 7889517 single base substitution C T intron_variant MELA-AU 10 7890263 7890263 single base substitution T C intron_variant MELA-AU 10 7890362 7890362 single base substitution C T intron_variant MELA-AU 10 7891135 7891135 single base substitution T C intron_variant MELA-AU 10 7891310 7891310 single base substitution C T intron_variant MELA-AU 10 7892048 7892048 single base substitution C T intron_variant MELA-AU 10 7892236 7892236 single base substitution C T intron_variant MELA-AU 10 7892387 7892387 single base substitution C T intron_variant MELA-AU 10 7893648 7893648 single base substitution T C intron_variant MELA-AU 10 7893745 7893745 single base substitution T C intron_variant MELA-AU 10 7893839 7893839 single base substitution C T intron_variant MELA-AU 10 7893858 7893858 single base substitution C T intron_variant MELA-AU 10 7893950 7893950 single base substitution T C intron_variant MELA-AU 10 7894051 7894051 single base substitution C T intron_variant MELA-AU 10 7894228 7894228 single base substitution C T intron_variant MELA-AU 10 7894695 7894695 single base substitution T C intron_variant MELA-AU 10 7894872 7894872 single base substitution C T intron_variant MELA-AU 10 7895192 7895193 multiple base substitution (>=2bp and <=200bp) AC TT intron_variant MELA-AU 10 7895292 7895292 single base substitution G A intron_variant MELA-AU 10 7895580 7895580 single base substitution C T intron_variant MELA-AU 10 7897051 7897051 single base substitution A C intron_variant MELA-AU 10 7897237 7897237 single base substitution C T intron_variant MELA-AU 10 7897371 7897371 single base substitution G A intron_variant MELA-AU 10 7897594 7897594 single base substitution C G intron_variant MELA-AU 10 7897595 7897595 single base substitution T C intron_variant MELA-AU 10 7897937 7897937 single base substitution G A intron_variant MELA-AU 10 7898267 7898267 single base substitution C T intron_variant MELA-AU 10 7898335 7898335 single base substitution C T intron_variant MELA-AU 10 7898423 7898423 single base substitution G A intron_variant MELA-AU 10 7898987 7898987 single base substitution C T intron_variant MELA-AU 10 7900045 7900045 single base substitution G C intron_variant MELA-AU 10 7900080 7900080 single base substitution C T intron_variant MELA-AU 10 7900203 7900203 single base substitution C T intron_variant MELA-AU 10 7900562 7900573 deletion of <=200bp AACTAAGTTCAG - intron_variant MELA-AU 10 7900565 7900565 single base substitution T G intron_variant MELA-AU 10 7901713 7901713 single base substitution C T intron_variant MELA-AU 10 7902974 7902974 single base substitution G A intron_variant MELA-AU 10 7903048 7903048 single base substitution C T intron_variant MELA-AU 10 7903786 7903786 single base substitution T C intron_variant MELA-AU 10 7903868 7903868 single base substitution C T intron_variant MELA-AU 10 7904136 7904136 single base substitution C T intron_variant MELA-AU 10 7904384 7904384 single base substitution C T intron_variant MELA-AU 10 7904737 7904737 single base substitution C T intron_variant MELA-AU 10 7905225 7905225 single base substitution A T intron_variant MELA-AU 10 7905226 7905226 single base substitution C T intron_variant MELA-AU 10 7905826 7905826 single base substitution C T intron_variant MELA-AU 10 7905988 7905988 single base substitution C T intron_variant MELA-AU 10 7906250 7906250 single base substitution C T intron_variant MELA-AU 10 7906574 7906574 single base substitution G T intron_variant MELA-AU 10 7906796 7906796 single base substitution T C intron_variant MELA-AU 10 7906797 7906797 single base substitution C T intron_variant MELA-AU 10 7906976 7906976 single base substitution C T intron_variant MELA-AU 10 7907297 7907297 single base substitution C T intron_variant MELA-AU 10 7907330 7907331 deletion of <=200bp TA - intron_variant MELA-AU 10 7907690 7907690 single base substitution A G intron_variant MELA-AU 10 7907861 7907861 single base substitution A G intron_variant MELA-AU 10 7907984 7907984 single base substitution C T intron_variant MELA-AU 10 7908066 7908066 single base substitution C T intron_variant MELA-AU 10 7908155 7908155 single base substitution C T intron_variant MELA-AU 10 7909789 7909789 single base substitution C T intron_variant MELA-AU 10 7909865 7909865 single base substitution C T intron_variant MELA-AU 10 7910850 7910850 single base substitution C T intron_variant MELA-AU 10 7911887 7911887 single base substitution C T intron_variant MELA-AU 10 7912262 7912262 single base substitution A C intron_variant MELA-AU 10 7912474 7912474 single base substitution T A intron_variant MELA-AU 10 7912796 7912796 single base substitution C T intron_variant MELA-AU 10 7913338 7913338 single base substitution A C intron_variant MELA-AU 10 7913840 7913840 single base substitution C T intron_variant MELA-AU 10 7915322 7915322 single base substitution C T intron_variant MELA-AU 10 7915617 7915618 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 7915640 7915640 single base substitution C T intron_variant MELA-AU 10 7915912 7915912 single base substitution C T intron_variant MELA-AU 10 7916264 7916264 single base substitution T A intron_variant MELA-AU 10 7916467 7916467 single base substitution T C intron_variant MELA-AU 10 7916526 7916526 single base substitution C T intron_variant MELA-AU 10 7916611 7916611 single base substitution T A intron_variant MELA-AU 10 7916760 7916760 single base substitution G T intron_variant MELA-AU 10 7916973 7916973 single base substitution C T intron_variant MELA-AU 10 7917736 7917736 single base substitution C T intron_variant MELA-AU 10 7918373 7918373 single base substitution G A intron_variant MELA-AU 10 7919241 7919241 single base substitution C T intron_variant MELA-AU 10 7919543 7919544 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 10 7921194 7921194 single base substitution C T intron_variant MELA-AU 10 7921847 7921847 single base substitution C T intron_variant MELA-AU 10 7921848 7921848 single base substitution C T intron_variant MELA-AU 10 7922125 7922125 single base substitution C T intron_variant MELA-AU 10 7922431 7922431 single base substitution T G intron_variant MELA-AU 10 7922598 7922598 single base substitution C T intron_variant MELA-AU 10 7922658 7922658 single base substitution C T intron_variant MELA-AU 10 7922910 7922910 single base substitution T G intron_variant MELA-AU 10 7924754 7924754 single base substitution C T intron_variant MELA-AU 10 7924755 7924755 single base substitution C T intron_variant MELA-AU 10 7926000 7926000 single base substitution C T intron_variant MELA-AU 10 7926136 7926136 single base substitution C T intron_variant MELA-AU 10 7926830 7926830 single base substitution C T intron_variant MELA-AU 10 7927239 7927239 single base substitution C A intron_variant MELA-AU 10 7927687 7927687 single base substitution C T intron_variant MELA-AU 10 7927862 7927862 single base substitution A G intron_variant MELA-AU 10 7928100 7928100 single base substitution T C intron_variant MELA-AU 10 7928325 7928325 single base substitution C T intron_variant MELA-AU 10 7929291 7929291 single base substitution T G intron_variant MELA-AU 10 7929410 7929410 single base substitution C T intron_variant MELA-AU 10 7930227 7930227 single base substitution C T intron_variant MELA-AU 10 7931214 7931214 single base substitution C T intron_variant MELA-AU 10 7931444 7931444 single base substitution C T intron_variant MELA-AU 10 7932037 7932037 single base substitution C T intron_variant MELA-AU 10 7932206 7932206 single base substitution C T intron_variant MELA-AU 10 7932806 7932806 single base substitution C T intron_variant MELA-AU 10 7933386 7933386 single base substitution G A intron_variant MELA-AU 10 7933507 7933507 single base substitution G A intron_variant MELA-AU 10 7934057 7934057 single base substitution T G intron_variant MELA-AU 10 7934122 7934122 single base substitution C T intron_variant MELA-AU 10 7934731 7934732 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 7934794 7934794 single base substitution T A intron_variant MELA-AU 10 7934906 7934906 single base substitution C T intron_variant MELA-AU 10 7934987 7934987 single base substitution T G intron_variant MELA-AU 10 7935017 7935017 single base substitution C T intron_variant MELA-AU 10 7935916 7935916 single base substitution C T intron_variant MELA-AU 10 7936021 7936021 single base substitution T A intron_variant MELA-AU 10 7936330 7936330 single base substitution C T intron_variant MELA-AU 10 7936342 7936342 single base substitution C T intron_variant MELA-AU 10 7936410 7936410 single base substitution C T intron_variant MELA-AU 10 7936547 7936547 single base substitution C T intron_variant MELA-AU 10 7936589 7936589 single base substitution T C intron_variant MELA-AU 10 7937268 7937268 single base substitution C T intron_variant MELA-AU 10 7937335 7937335 single base substitution C T intron_variant MELA-AU 10 7937724 7937724 single base substitution T C intron_variant MELA-AU 10 7938197 7938197 single base substitution C T intron_variant MELA-AU 10 7938404 7938404 single base substitution A G intron_variant MELA-AU 10 7938496 7938496 single base substitution C T intron_variant MELA-AU 10 7938604 7938604 single base substitution C T intron_variant MELA-AU 10 7938621 7938621 single base substitution T A intron_variant MELA-AU 10 7938848 7938848 single base substitution C T intron_variant MELA-AU 10 7938903 7938903 single base substitution C T intron_variant MELA-AU 10 7938957 7938957 single base substitution C G intron_variant MELA-AU 10 7939494 7939494 single base substitution C T intron_variant MELA-AU 10 7939540 7939540 single base substitution C T intron_variant MELA-AU 10 7939874 7939874 single base substitution C T intron_variant MELA-AU 10 7940062 7940062 single base substitution C T intron_variant MELA-AU 10 7940362 7940362 single base substitution A T intron_variant MELA-AU 10 7940678 7940678 single base substitution C T intron_variant MELA-AU 10 7940790 7940790 single base substitution C A intron_variant MELA-AU 10 7940879 7940879 single base substitution C T intron_variant MELA-AU 10 7942016 7942016 single base substitution T G intron_variant MELA-AU 10 7942165 7942165 single base substitution C T intron_variant MELA-AU 10 7942250 7942250 single base substitution G A intron_variant MELA-AU 10 7942419 7942419 single base substitution C T intron_variant MELA-AU 10 7944011 7944011 single base substitution C T intron_variant MELA-AU 10 7944705 7944705 single base substitution C T intron_variant MELA-AU 10 7946169 7946169 single base substitution G C intron_variant MELA-AU 10 7946861 7946861 single base substitution C T intron_variant MELA-AU 10 7946924 7946924 single base substitution C T intron_variant MELA-AU 10 7947042 7947042 single base substitution G A intron_variant MELA-AU 10 7947285 7947285 single base substitution G A intron_variant MELA-AU 10 7948152 7948152 single base substitution T C intron_variant MELA-AU 10 7948153 7948153 single base substitution C T intron_variant MELA-AU 10 7948298 7948298 single base substitution T C intron_variant MELA-AU 10 7948307 7948307 single base substitution C A intron_variant MELA-AU 10 7948693 7948693 single base substitution T G intron_variant MELA-AU 10 7948787 7948787 single base substitution C T intron_variant MELA-AU 10 7948889 7948889 single base substitution C T intron_variant MELA-AU 10 7949132 7949132 single base substitution G A intron_variant MELA-AU 10 7950041 7950041 single base substitution C T intron_variant MELA-AU 10 7950879 7950879 single base substitution C T intron_variant MELA-AU 10 7951048 7951048 single base substitution C T intron_variant MELA-AU 10 7952058 7952058 single base substitution C T intron_variant MELA-AU 10 7953112 7953112 single base substitution T C intron_variant MELA-AU 10 7954258 7954258 single base substitution C T intron_variant MELA-AU 10 7954434 7954434 single base substitution T G intron_variant MELA-AU 10 7954799 7954799 single base substitution C T intron_variant MELA-AU 10 7954999 7954999 single base substitution C T intron_variant MELA-AU 10 7955044 7955044 single base substitution C T intron_variant MELA-AU 10 7955563 7955564 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 7956330 7956330 single base substitution C T intron_variant MELA-AU 10 7957124 7957124 single base substitution C T intron_variant MELA-AU 10 7957218 7957218 single base substitution C T intron_variant MELA-AU 10 7957524 7957524 single base substitution T G intron_variant MELA-AU 10 7958174 7958174 single base substitution G A intron_variant MELA-AU 10 7958206 7958206 single base substitution C T intron_variant MELA-AU 10 7958359 7958359 single base substitution A T intron_variant MELA-AU 10 7958633 7958634 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 7958884 7958884 single base substitution C G intron_variant MELA-AU 10 7959589 7959589 single base substitution C T intron_variant MELA-AU 10 7959792 7959792 single base substitution C T intron_variant MELA-AU 10 7960867 7960867 single base substitution T C intron_variant MELA-AU 10 7961453 7961453 single base substitution C T intron_variant MELA-AU 10 7961823 7961823 single base substitution C T intron_variant MELA-AU 10 7962342 7962342 single base substitution C T intron_variant MELA-AU 10 7962968 7962968 single base substitution C T intron_variant MELA-AU 10 7963187 7963187 single base substitution G A intron_variant MELA-AU 10 7964242 7964242 single base substitution A G intron_variant MELA-AU 10 7964358 7964358 single base substitution C T intron_variant MELA-AU 10 7964385 7964385 single base substitution T A intron_variant MELA-AU 10 7966025 7966025 single base substitution C T intron_variant MELA-AU 10 7966233 7966233 single base substitution C T intron_variant MELA-AU 10 7966590 7966590 single base substitution C T intron_variant MELA-AU 10 7966670 7966670 single base substitution G A intron_variant MELA-AU 10 7967574 7967574 single base substitution C T intron_variant MELA-AU 10 7968534 7968534 single base substitution C T intron_variant MELA-AU 10 7970643 7970643 single base substitution C T intron_variant MELA-AU 10 7970781 7970781 single base substitution T C intron_variant MELA-AU 10 7970803 7970803 single base substitution G A intron_variant MELA-AU 10 7970818 7970818 single base substitution G T intron_variant MELA-AU 10 7971182 7971182 single base substitution C T intron_variant MELA-AU 10 7971250 7971250 single base substitution A G intron_variant MELA-AU 10 7972152 7972152 single base substitution C T intron_variant MELA-AU 10 7972654 7972654 single base substitution C T intron_variant MELA-AU 10 7973293 7973293 single base substitution C T intron_variant MELA-AU 10 7973308 7973308 single base substitution C T intron_variant MELA-AU 10 7973396 7973396 single base substitution C T intron_variant MELA-AU 10 7974629 7974629 single base substitution T C intron_variant MELA-AU 10 7976006 7976006 single base substitution T G intron_variant MELA-AU 10 7976228 7976228 single base substitution C G intron_variant MELA-AU 10 7976326 7976326 single base substitution G A intron_variant MELA-AU 10 7976334 7976334 single base substitution G A intron_variant MELA-AU 10 7976597 7976597 single base substitution G A intron_variant MELA-AU 10 7977448 7977448 single base substitution G T intron_variant MELA-AU 10 7977501 7977501 single base substitution C T intron_variant MELA-AU 10 7977603 7977603 single base substitution C T intron_variant MELA-AU 10 7978802 7978802 single base substitution C T intron_variant MELA-AU 10 7979146 7979146 single base substitution C T intron_variant MELA-AU 10 7979325 7979325 single base substitution C T intron_variant MELA-AU 10 7979378 7979378 single base substitution C T intron_variant MELA-AU 10 7979385 7979385 single base substitution C T intron_variant MELA-AU 10 7979681 7979681 single base substitution A C intron_variant MELA-AU 10 7979883 7979883 single base substitution C T intron_variant MELA-AU 10 7980415 7980415 single base substitution G A intron_variant MELA-AU 10 7980815 7980815 single base substitution G A intron_variant MELA-AU 10 7981889 7981889 single base substitution A C intron_variant MELA-AU 10 7982216 7982216 single base substitution C T intron_variant MELA-AU 10 7982690 7982690 single base substitution G A intron_variant MELA-AU 10 7983102 7983102 single base substitution G A intron_variant MELA-AU 10 7984294 7984294 single base substitution C T intron_variant MELA-AU 10 7984340 7984340 single base substitution C T intron_variant MELA-AU 10 7984512 7984512 single base substitution C T intron_variant MELA-AU 10 7984524 7984524 single base substitution C T intron_variant MELA-AU 10 7987142 7987142 single base substitution G A intron_variant MELA-AU 10 7987521 7987521 single base substitution G A intron_variant MELA-AU 10 7988134 7988134 single base substitution T A intron_variant MELA-AU 10 7988464 7988464 single base substitution A C intron_variant MELA-AU 10 7989081 7989081 single base substitution C T intron_variant MELA-AU 10 7989094 7989094 single base substitution C T intron_variant MELA-AU 10 7989196 7989203 deletion of <=200bp GTGCAATC - intron_variant MELA-AU 10 7989351 7989351 single base substitution C T intron_variant MELA-AU 10 7989574 7989574 single base substitution G A intron_variant MELA-AU 10 7990063 7990063 single base substitution T C intron_variant MELA-AU 10 7990141 7990141 single base substitution C T intron_variant MELA-AU 10 7990896 7990896 single base substitution G A intron_variant MELA-AU 10 7991835 7991835 single base substitution C T intron_variant MELA-AU 10 7992123 7992123 single base substitution A G intron_variant MELA-AU 10 7992540 7992540 single base substitution G A intron_variant MELA-AU 10 7992718 7992718 single base substitution C T intron_variant MELA-AU 10 7993411 7993411 single base substitution C T intron_variant MELA-AU 10 7993563 7993563 single base substitution C T intron_variant MELA-AU 10 7993964 7993964 single base substitution C T intron_variant MELA-AU 10 7994194 7994194 single base substitution T A intron_variant MELA-AU 10 7994263 7994263 single base substitution C T intron_variant MELA-AU 10 7994345 7994345 single base substitution T C intron_variant MELA-AU 10 7994364 7994364 single base substitution C T intron_variant MELA-AU 10 7995152 7995152 single base substitution C T intron_variant MELA-AU 10 7995168 7995168 single base substitution C T intron_variant MELA-AU 10 7995966 7995966 single base substitution T G intron_variant MELA-AU 10 7996212 7996212 single base substitution C T intron_variant MELA-AU 10 7996415 7996415 single base substitution C T intron_variant MELA-AU 10 7996686 7996686 single base substitution C T intron_variant MELA-AU 10 7996994 7996994 single base substitution G A intron_variant MELA-AU 10 7997169 7997169 single base substitution C T intron_variant MELA-AU 10 7997567 7997567 single base substitution C T intron_variant MELA-AU 10 7997745 7997745 single base substitution A G intron_variant MELA-AU 10 7997875 7997875 single base substitution T A intron_variant MELA-AU 10 7998054 7998054 single base substitution T G intron_variant MELA-AU 10 7998193 7998193 single base substitution C T intron_variant MELA-AU 10 7998219 7998219 single base substitution G A intron_variant MELA-AU 10 7998650 7998650 single base substitution C T intron_variant MELA-AU 10 8000060 8000060 single base substitution C T intron_variant MELA-AU 10 8000339 8000339 single base substitution T C intron_variant MELA-AU 10 8000687 8000687 single base substitution T A intron_variant MELA-AU 10 8000761 8000761 single base substitution A G intron_variant MELA-AU 10 8002701 8002701 single base substitution T G intron_variant MELA-AU 10 8003005 8003005 single base substitution C T intron_variant MELA-AU 10 8003033 8003033 single base substitution G A intron_variant MELA-AU 10 8003449 8003449 single base substitution C G intron_variant MELA-AU 10 8003506 8003506 single base substitution C T intron_variant MELA-AU 10 8003582 8003582 single base substitution C T intron_variant MELA-AU 10 8003733 8003733 single base substitution C T intron_variant MELA-AU 10 8003849 8003849 single base substitution G A intron_variant MELA-AU 10 8004039 8004039 single base substitution C T intron_variant MELA-AU 10 8004061 8004061 single base substitution C T intron_variant MELA-AU 10 8004175 8004175 single base substitution T A intron_variant MELA-AU 10 8004196 8004196 single base substitution C T intron_variant MELA-AU 10 8004219 8004219 single base substitution T A intron_variant MELA-AU 10 8004375 8004375 single base substitution C T intron_variant MELA-AU 10 8004938 8004938 single base substitution C T intron_variant MELA-AU 10 8004984 8004985 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 8005459 8005459 single base substitution A C intron_variant MELA-AU 10 8005464 8005465 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 8005505 8005505 single base substitution C T intron_variant MELA-AU 10 8005674 8005674 single base substitution T G intron_variant MELA-AU 10 8006465 8006465 single base substitution C T missense_variant P331L 992C>T MELA-AU 10 8006989 8006989 single base substitution C T missense_variant H506Y 1516C>T MELA-AU 10 8007116 8007116 single base substitution A T missense_variant K548M 1643A>T MELA-AU 10 8007196 8007197 multiple base substitution (>=2bp and <=200bp) CC GT missense_variant P575V 1723CC>GT MELA-AU 10 8007406 8007406 single base substitution G A missense_variant D645N 1933G>A MELA-AU 10 8007513 8007513 single base substitution T A synonymous_variant S680S 2040T>A MELA-AU 10 8007849 8007849 single base substitution T A intron_variant MELA-AU 10 8007969 8007977 deletion of <=200bp GTGATCTCT - intron_variant MELA-AU 10 8009000 8009000 single base substitution C T intron_variant MELA-AU 10 8009964 8009964 single base substitution C T intron_variant MELA-AU 10 8009975 8009975 single base substitution A G intron_variant MELA-AU 10 8010060 8010060 single base substitution C T intron_variant MELA-AU 10 8012588 8012588 single base substitution C T intron_variant MELA-AU 10 8013014 8013014 single base substitution T A intron_variant MELA-AU 10 8013524 8013524 single base substitution C G intron_variant MELA-AU 10 8013627 8013627 single base substitution C T intron_variant MELA-AU 10 8014023 8014023 single base substitution C T intron_variant MELA-AU 10 8015206 8015207 multiple base substitution (>=2bp and <=200bp) CC TG intron_variant MELA-AU 10 8015426 8015426 single base substitution C T intron_variant MELA-AU 10 8015601 8015601 single base substitution C T intron_variant MELA-AU 10 8016803 8016803 single base substitution T A intron_variant MELA-AU 10 8017664 8017664 single base substitution G C intron_variant MELA-AU 10 8017949 8017949 single base substitution C T intron_variant MELA-AU 10 8018468 8018468 single base substitution C T intron_variant MELA-AU 10 8018677 8018677 single base substitution C T intron_variant MELA-AU 10 8018695 8018695 single base substitution T C intron_variant MELA-AU 10 8019221 8019221 single base substitution C T synonymous_variant V750V 2250C>T MELA-AU 10 8019422 8019422 single base substitution C T intron_variant MELA-AU 10 8019537 8019537 single base substitution T C intron_variant MELA-AU 10 8020229 8020229 single base substitution G A intron_variant MELA-AU 10 8020314 8020314 single base substitution C T intron_variant MELA-AU 10 8020467 8020467 single base substitution C T intron_variant MELA-AU 10 8020521 8020521 single base substitution C T intron_variant MELA-AU 10 8020559 8020559 single base substitution T C intron_variant MELA-AU 10 8020575 8020575 single base substitution C G intron_variant MELA-AU 10 8020847 8020847 single base substitution G A intron_variant MELA-AU 10 8021261 8021261 single base substitution C T intron_variant MELA-AU 10 8021552 8021552 single base substitution C T intron_variant MELA-AU 10 8021967 8021967 single base substitution C T intron_variant MELA-AU 10 8022362 8022362 single base substitution C T intron_variant MELA-AU 10 8023245 8023245 single base substitution C T intron_variant MELA-AU 10 8023447 8023447 single base substitution C T intron_variant MELA-AU 10 8024130 8024130 single base substitution C T intron_variant MELA-AU 10 8024174 8024174 single base substitution C T intron_variant MELA-AU 10 8024260 8024261 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 8024370 8024370 single base substitution T C intron_variant MELA-AU 10 8024388 8024388 single base substitution C T intron_variant MELA-AU 10 8024597 8024597 single base substitution C T intron_variant MELA-AU 10 8024694 8024694 single base substitution C T intron_variant MELA-AU 10 8024800 8024800 single base substitution C T intron_variant MELA-AU 10 8024850 8024850 single base substitution A G intron_variant MELA-AU 10 8025583 8025583 single base substitution C T intron_variant MELA-AU 10 8025809 8025809 single base substitution A G intron_variant MELA-AU 10 8026681 8026681 single base substitution G T intron_variant MELA-AU 10 8027320 8027320 single base substitution C T intron_variant MELA-AU 10 8027429 8027429 single base substitution C T intron_variant MELA-AU 10 8027795 8027795 single base substitution G A intron_variant MELA-AU 10 8028308 8028308 single base substitution T A intron_variant MELA-AU 10 8028360 8028360 single base substitution C T intron_variant MELA-AU 10 8028645 8028645 single base substitution C T intron_variant MELA-AU 10 8028648 8028648 single base substitution C T intron_variant MELA-AU 10 8028928 8028928 single base substitution C T intron_variant MELA-AU 10 8028930 8028930 single base substitution C T intron_variant MELA-AU 10 8029091 8029091 single base substitution C T intron_variant MELA-AU 10 8029369 8029369 single base substitution C T intron_variant MELA-AU 10 8029438 8029438 single base substitution C T intron_variant MELA-AU 10 8029611 8029611 single base substitution C T intron_variant MELA-AU 10 8029739 8029739 single base substitution C T intron_variant MELA-AU 10 8030637 8030637 single base substitution C T intron_variant MELA-AU 10 8030798 8030798 single base substitution C T intron_variant MELA-AU 10 8031955 8031955 single base substitution C T intron_variant MELA-AU 10 8033180 8033180 single base substitution C T intron_variant MELA-AU 10 8033386 8033386 insertion of <=200bp - C intron_variant MELA-AU 10 8033798 8033798 single base substitution C T intron_variant MELA-AU 10 8034613 8034613 single base substitution C T intron_variant MELA-AU 10 8034886 8034886 single base substitution C T intron_variant MELA-AU 10 8035229 8035229 single base substitution A G intron_variant MELA-AU 10 8035400 8035401 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 8035622 8035622 single base substitution T C intron_variant MELA-AU 10 8035773 8035773 single base substitution C T intron_variant MELA-AU 10 8035776 8035776 single base substitution C T intron_variant MELA-AU 10 8035799 8035799 single base substitution C T intron_variant MELA-AU 10 8035979 8035979 single base substitution C T intron_variant MELA-AU 10 8037414 8037414 single base substitution C T intron_variant MELA-AU 10 8037581 8037581 single base substitution A T intron_variant MELA-AU 10 8037595 8037595 single base substitution C T intron_variant MELA-AU 10 8037706 8037706 single base substitution C T intron_variant MELA-AU 10 8037762 8037762 single base substitution A G intron_variant MELA-AU 10 8037764 8037764 single base substitution C T intron_variant MELA-AU 10 8037907 8037907 single base substitution C T intron_variant MELA-AU 10 8037980 8037980 single base substitution C T intron_variant MELA-AU 10 8038022 8038022 single base substitution G A intron_variant MELA-AU 10 8038044 8038044 single base substitution C T intron_variant MELA-AU 10 8038402 8038402 single base substitution C T intron_variant MELA-AU 10 8038882 8038882 single base substitution C T intron_variant MELA-AU 10 8039426 8039426 single base substitution G A intron_variant MELA-AU 10 8039549 8039549 single base substitution C T intron_variant MELA-AU 10 8039618 8039619 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 8039854 8039854 single base substitution T A intron_variant MELA-AU 10 8040306 8040306 single base substitution C T intron_variant MELA-AU 10 8040692 8040692 single base substitution C T intron_variant MELA-AU 10 8040770 8040770 single base substitution C T intron_variant MELA-AU 10 8041325 8041325 single base substitution C T intron_variant MELA-AU 10 8041580 8041580 single base substitution C T intron_variant MELA-AU 10 8042032 8042032 single base substitution T C intron_variant MELA-AU 10 8042033 8042033 single base substitution C T intron_variant MELA-AU 10 8042083 8042083 single base substitution C T intron_variant MELA-AU 10 8042385 8042385 single base substitution C T intron_variant MELA-AU 10 8043187 8043187 single base substitution C T intron_variant MELA-AU 10 8043770 8043770 single base substitution A G intron_variant MELA-AU 10 8044219 8044219 single base substitution C T intron_variant MELA-AU 10 8044719 8044719 single base substitution C T intron_variant MELA-AU 10 8045227 8045227 single base substitution C T intron_variant MELA-AU 10 8045262 8045262 single base substitution T C intron_variant MELA-AU 10 8045341 8045341 single base substitution C T intron_variant MELA-AU 10 8046165 8046165 single base substitution C T intron_variant MELA-AU 10 8046649 8046649 single base substitution C T intron_variant MELA-AU 10 8047007 8047007 single base substitution C T intron_variant MELA-AU 10 8047087 8047087 single base substitution C T intron_variant MELA-AU 10 8047088 8047088 single base substitution C T intron_variant MELA-AU 10 8048530 8048530 single base substitution C T intron_variant MELA-AU 10 8048937 8048937 single base substitution G A intron_variant MELA-AU 10 8048978 8048978 single base substitution C T intron_variant MELA-AU 10 8048979 8048979 single base substitution C T intron_variant MELA-AU 10 8049021 8049021 single base substitution C T intron_variant MELA-AU 10 8049043 8049043 single base substitution A G intron_variant MELA-AU 10 8049661 8049661 single base substitution C T intron_variant MELA-AU 10 8050402 8050403 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 8050565 8050565 single base substitution C T intron_variant MELA-AU 10 8050860 8050860 single base substitution C T intron_variant MELA-AU 10 8050939 8050939 single base substitution C T intron_variant MELA-AU 10 8051211 8051211 single base substitution C T missense_variant P829L 2486C>T MELA-AU 10 8051782 8051782 single base substitution C T intron_variant MELA-AU 10 8052233 8052233 single base substitution C T intron_variant MELA-AU 10 8052393 8052393 single base substitution C T intron_variant MELA-AU 10 8052768 8052768 single base substitution G T intron_variant MELA-AU 10 8052894 8052894 single base substitution C T intron_variant MELA-AU 10 8052898 8052898 single base substitution C T intron_variant MELA-AU 10 8053259 8053259 single base substitution C T intron_variant MELA-AU 10 8053560 8053560 single base substitution G A intron_variant MELA-AU 10 8053602 8053602 single base substitution T A intron_variant MELA-AU 10 8053697 8053697 single base substitution C T intron_variant MELA-AU 10 8054315 8054315 single base substitution C T intron_variant MELA-AU 10 8054324 8054324 single base substitution C T intron_variant MELA-AU 10 8054711 8054711 single base substitution C T intron_variant MELA-AU 10 8055138 8055138 single base substitution G A intron_variant MELA-AU 10 8055319 8055319 single base substitution C T intron_variant MELA-AU 10 8055569 8055569 single base substitution A G intron_variant MELA-AU 10 8055651 8055651 single base substitution C T intron_variant MELA-AU 10 8056104 8056104 single base substitution C T intron_variant MELA-AU 10 8056176 8056176 single base substitution C T intron_variant MELA-AU 10 8056735 8056735 single base substitution C T 3_prime_UTR_variant MELA-AU 10 8056779 8056779 single base substitution G A 3_prime_UTR_variant MELA-AU 10 8056883 8056883 single base substitution C T 3_prime_UTR_variant MELA-AU 10 8056905 8056905 single base substitution C T 3_prime_UTR_variant MELA-AU 10 8057619 8057619 single base substitution C T 3_prime_UTR_variant MELA-AU 10 8057691 8057691 single base substitution T C 3_prime_UTR_variant MELA-AU 10 8057966 8057966 single base substitution C T 3_prime_UTR_variant MELA-AU 10 8058009 8058013 deletion of <=200bp TTTAT - 3_prime_UTR_variant MELA-AU 10 8058325 8058325 single base substitution A G 3_prime_UTR_variant MELA-AU 10 8059448 8059448 single base substitution C T downstream_gene_variant MELA-AU 10 8059697 8059697 single base substitution T C downstream_gene_variant MELA-AU 10 8060068 8060068 single base substitution C T downstream_gene_variant MELA-AU 10 8060357 8060357 single base substitution C T downstream_gene_variant MELA-AU 10 8060420 8060420 single base substitution C T downstream_gene_variant MELA-AU 10 8060863 8060863 single base substitution C T downstream_gene_variant MELA-AU 10 8061097 8061097 single base substitution T C downstream_gene_variant MELA-AU 10 8061675 8061675 single base substitution G A downstream_gene_variant MELA-AU 10 8061784 8061784 single base substitution G A downstream_gene_variant MELA-AU 10 8061864 8061864 single base substitution C T downstream_gene_variant MELA-AU 10 8061967 8061967 single base substitution T C downstream_gene_variant MELA-AU 10 8063271 8063271 single base substitution C T downstream_gene_variant MELA-AU 10 8063519 8063519 single base substitution G A downstream_gene_variant MELA-AU 10 8063538 8063538 single base substitution C T downstream_gene_variant ORCA-IN 10 7902998 7902998 single base substitution C T intron_variant ORCA-IN 10 7920692 7920692 single base substitution G A intron_variant ORCA-IN 10 7931152 7931152 single base substitution G T intron_variant ORCA-IN 10 7941020 7941020 single base substitution G T intron_variant ORCA-IN 10 7964527 7964527 single base substitution G C intron_variant ORCA-IN 10 7966693 7966693 single base substitution C A intron_variant ORCA-IN 10 7986098 7986098 single base substitution G T intron_variant ORCA-IN 10 8016104 8016104 single base substitution C T intron_variant ORCA-IN 10 8037013 8037013 single base substitution A T intron_variant OV-AU 10 7855664 7855664 single base substitution T G upstream_gene_variant OV-AU 10 7864129 7864129 single base substitution A T intron_variant OV-AU 10 7866555 7866555 single base substitution G T intron_variant OV-AU 10 7867117 7867117 single base substitution T C intron_variant OV-AU 10 7867697 7867697 single base substitution A T intron_variant OV-AU 10 7869914 7869914 single base substitution C G intron_variant OV-AU 10 7881565 7881565 single base substitution T A intron_variant OV-AU 10 7881934 7881934 single base substitution C A intron_variant OV-AU 10 7883952 7883952 single base substitution A G intron_variant OV-AU 10 7886739 7886739 single base substitution C G intron_variant OV-AU 10 7887256 7887256 single base substitution G A intron_variant OV-AU 10 7887982 7887982 single base substitution C A intron_variant OV-AU 10 7891761 7891761 single base substitution G T intron_variant OV-AU 10 7899377 7899377 single base substitution C G intron_variant OV-AU 10 7900682 7900682 single base substitution A T intron_variant OV-AU 10 7904360 7904360 single base substitution C G intron_variant OV-AU 10 7905106 7905106 single base substitution C G intron_variant OV-AU 10 7906588 7906588 single base substitution G A intron_variant OV-AU 10 7920763 7920763 single base substitution C T intron_variant OV-AU 10 7922263 7922263 single base substitution G C intron_variant OV-AU 10 7927239 7927239 single base substitution C A intron_variant OV-AU 10 7936077 7936077 single base substitution G T intron_variant OV-AU 10 7953837 7953837 single base substitution T G intron_variant OV-AU 10 7956321 7956321 single base substitution A C intron_variant OV-AU 10 7956419 7956419 single base substitution T G intron_variant OV-AU 10 7968434 7968434 single base substitution A G intron_variant OV-AU 10 7974422 7974422 single base substitution G A intron_variant OV-AU 10 7979997 7979997 single base substitution C G intron_variant OV-AU 10 7982181 7982181 single base substitution G T intron_variant OV-AU 10 7985304 7985304 single base substitution T C intron_variant OV-AU 10 7988477 7988477 single base substitution A C intron_variant OV-AU 10 7999345 7999345 single base substitution A C intron_variant OV-AU 10 8000663 8000663 single base substitution G A intron_variant OV-AU 10 8000831 8000831 single base substitution C G intron_variant OV-AU 10 8011096 8011096 single base substitution C T intron_variant OV-AU 10 8011208 8011208 single base substitution G A intron_variant OV-AU 10 8013615 8013615 single base substitution A T intron_variant OV-AU 10 8016889 8016889 single base substitution T C intron_variant OV-AU 10 8017366 8017366 single base substitution A T intron_variant OV-AU 10 8025810 8025810 single base substitution T C intron_variant OV-AU 10 8027944 8027944 single base substitution G C intron_variant OV-AU 10 8028416 8028416 single base substitution G C intron_variant OV-AU 10 8041819 8041819 single base substitution C A intron_variant OV-AU 10 8042722 8042722 single base substitution G A intron_variant OV-AU 10 8045571 8045571 single base substitution C G intron_variant OV-AU 10 8047503 8047503 single base substitution C T intron_variant OV-AU 10 8051488 8051488 single base substitution C G intron_variant OV-AU 10 8054938 8054938 single base substitution C T intron_variant OV-AU 10 8057928 8057928 single base substitution G A 3_prime_UTR_variant OV-AU 10 8061007 8061007 single base substitution A T downstream_gene_variant OV-AU 10 8061965 8061965 single base substitution T C downstream_gene_variant OV-AU 10 8062715 8062715 single base substitution C T downstream_gene_variant PACA-AU 10 7856187 7856187 single base substitution G A upstream_gene_variant PACA-AU 10 7859200 7859200 single base substitution C G upstream_gene_variant PACA-AU 10 7875651 7875651 single base substitution G C intron_variant PACA-AU 10 7875826 7875826 single base substitution G C intron_variant PACA-AU 10 7876781 7876781 single base substitution T A intron_variant PACA-AU 10 7877164 7877164 single base substitution C T intron_variant PACA-AU 10 7877386 7877386 single base substitution A C intron_variant PACA-AU 10 7877655 7877655 single base substitution C T intron_variant PACA-AU 10 7882217 7882217 single base substitution G A intron_variant PACA-AU 10 7886251 7886253 deletion of <=200bp ATT - intron_variant PACA-AU 10 7891377 7891377 single base substitution C T intron_variant PACA-AU 10 7892920 7892920 single base substitution G A intron_variant PACA-AU 10 7897334 7897334 single base substitution C T intron_variant PACA-AU 10 7899695 7899695 single base substitution C T intron_variant PACA-AU 10 7899721 7899721 single base substitution C T intron_variant PACA-AU 10 7900008 7900008 single base substitution C T intron_variant PACA-AU 10 7901086 7901086 single base substitution G A intron_variant PACA-AU 10 7903753 7903753 single base substitution T C intron_variant PACA-AU 10 7903851 7903851 deletion of <=200bp T - intron_variant PACA-AU 10 7911648 7911648 single base substitution T C intron_variant PACA-AU 10 7913250 7913250 single base substitution G A intron_variant PACA-AU 10 7913683 7913683 single base substitution A G intron_variant PACA-AU 10 7929804 7929804 single base substitution A G intron_variant PACA-AU 10 7932542 7932545 deletion of <=200bp TCTT - intron_variant PACA-AU 10 7942873 7942873 single base substitution G A intron_variant PACA-AU 10 7945677 7945677 single base substitution C G intron_variant PACA-AU 10 7950367 7950367 single base substitution C T intron_variant PACA-AU 10 7953571 7953571 single base substitution C T intron_variant PACA-AU 10 7957463 7957463 single base substitution G A intron_variant PACA-AU 10 7964526 7964526 single base substitution T G intron_variant PACA-AU 10 7968332 7968332 single base substitution A G intron_variant PACA-AU 10 7974065 7974065 single base substitution C A intron_variant PACA-AU 10 7981906 7981906 single base substitution A C intron_variant PACA-AU 10 7984766 7984766 single base substitution T A intron_variant PACA-AU 10 7985144 7985144 single base substitution G A intron_variant PACA-AU 10 7987322 7987322 deletion of <=200bp T - intron_variant PACA-AU 10 7989676 7989676 single base substitution G T intron_variant PACA-AU 10 7989964 7989964 single base substitution T G intron_variant PACA-AU 10 7997260 7997260 single base substitution A G intron_variant PACA-AU 10 7999046 7999046 single base substitution T C intron_variant PACA-AU 10 8000514 8000514 single base substitution C G intron_variant PACA-AU 10 8001293 8001293 single base substitution A G intron_variant PACA-AU 10 8004500 8004500 single base substitution C G intron_variant PACA-AU 10 8005675 8005675 single base substitution G A intron_variant PACA-AU 10 8006662 8006662 single base substitution C T stop_gained R397* 1189C>T PACA-AU 10 8008745 8008745 single base substitution G T intron_variant PACA-AU 10 8010787 8010787 deletion of <=200bp A - intron_variant PACA-AU 10 8013737 8013737 single base substitution A G intron_variant PACA-AU 10 8015305 8015305 single base substitution G A intron_variant PACA-AU 10 8016128 8016128 single base substitution C A intron_variant PACA-AU 10 8016130 8016130 single base substitution C A intron_variant PACA-AU 10 8018102 8018102 single base substitution C T intron_variant PACA-AU 10 8027540 8027540 single base substitution G A intron_variant PACA-AU 10 8034641 8034641 single base substitution T A intron_variant PACA-AU 10 8037506 8037506 single base substitution G C intron_variant PACA-AU 10 8038608 8038608 single base substitution G T intron_variant PACA-AU 10 8039343 8039343 single base substitution A G intron_variant PACA-AU 10 8042936 8042936 single base substitution C G intron_variant PACA-AU 10 8042957 8042957 single base substitution G C intron_variant PACA-AU 10 8043069 8043069 single base substitution G C intron_variant PACA-AU 10 8043279 8043279 single base substitution G C intron_variant PACA-AU 10 8043404 8043404 single base substitution G C intron_variant PACA-AU 10 8043732 8043732 single base substitution G C intron_variant PACA-AU 10 8043833 8043833 single base substitution G A intron_variant PACA-AU 10 8044081 8044081 single base substitution A T intron_variant PACA-AU 10 8045171 8045171 single base substitution C T intron_variant PACA-AU 10 8045915 8045915 single base substitution A T intron_variant PACA-AU 10 8049613 8049613 single base substitution G C intron_variant PACA-AU 10 8050205 8050205 single base substitution G A intron_variant PACA-AU 10 8051341 8051341 single base substitution G A intron_variant PACA-AU 10 8052481 8052481 single base substitution T G intron_variant PACA-AU 10 8053237 8053237 single base substitution G C intron_variant PACA-AU 10 8053414 8053414 single base substitution G T intron_variant PACA-CA 10 7856114 7856114 single base substitution C T upstream_gene_variant PACA-CA 10 7871272 7871272 single base substitution C A intron_variant PACA-CA 10 7872316 7872316 single base substitution C A intron_variant PACA-CA 10 7873857 7873857 insertion of <=200bp - T intron_variant PACA-CA 10 7874703 7874703 single base substitution C T intron_variant PACA-CA 10 7874762 7874762 single base substitution C A intron_variant PACA-CA 10 7875334 7875334 single base substitution T C intron_variant PACA-CA 10 7882273 7882273 single base substitution G A intron_variant PACA-CA 10 7888994 7888994 single base substitution A T intron_variant PACA-CA 10 7889418 7889418 deletion of <=200bp T - intron_variant PACA-CA 10 7889486 7889486 single base substitution A G intron_variant PACA-CA 10 7889525 7889525 single base substitution G A intron_variant PACA-CA 10 7891877 7891877 single base substitution C T intron_variant PACA-CA 10 7891964 7891964 deletion of <=200bp A - intron_variant PACA-CA 10 7896986 7896986 single base substitution G T intron_variant PACA-CA 10 7898599 7898599 single base substitution G C intron_variant PACA-CA 10 7898624 7898624 single base substitution A C intron_variant PACA-CA 10 7905114 7905114 single base substitution C T intron_variant PACA-CA 10 7914832 7914832 single base substitution G A intron_variant PACA-CA 10 7918626 7918626 single base substitution A G intron_variant PACA-CA 10 7920037 7920037 single base substitution G T intron_variant PACA-CA 10 7921718 7921718 single base substitution T C intron_variant PACA-CA 10 7923006 7923006 single base substitution C A intron_variant PACA-CA 10 7933643 7933643 single base substitution T C intron_variant PACA-CA 10 7933733 7933733 insertion of <=200bp - T intron_variant PACA-CA 10 7936946 7936946 single base substitution C T intron_variant PACA-CA 10 7942976 7942976 insertion of <=200bp - A intron_variant PACA-CA 10 7947292 7947292 single base substitution A C intron_variant PACA-CA 10 7951722 7951722 single base substitution T C intron_variant PACA-CA 10 7957661 7957661 single base substitution C G intron_variant PACA-CA 10 7959577 7959577 single base substitution G A intron_variant PACA-CA 10 7960912 7960912 single base substitution G A intron_variant PACA-CA 10 7962293 7962293 single base substitution G A intron_variant PACA-CA 10 7963494 7963494 single base substitution T A intron_variant PACA-CA 10 7963983 7963983 single base substitution G C intron_variant PACA-CA 10 7972024 7972024 single base substitution G A intron_variant PACA-CA 10 7975797 7975797 single base substitution A G intron_variant PACA-CA 10 7976489 7976489 single base substitution C T intron_variant PACA-CA 10 7977342 7977342 single base substitution C T intron_variant PACA-CA 10 7979793 7979793 deletion of <=200bp T - intron_variant PACA-CA 10 7979941 7979941 single base substitution C A intron_variant PACA-CA 10 7980521 7980521 deletion of <=200bp A - intron_variant PACA-CA 10 7981891 7981891 single base substitution T A intron_variant PACA-CA 10 7988107 7988107 single base substitution C G intron_variant PACA-CA 10 7988653 7988653 single base substitution T C intron_variant PACA-CA 10 7993432 7993432 single base substitution T A intron_variant PACA-CA 10 7997459 7997459 single base substitution T C intron_variant PACA-CA 10 7997470 7997470 single base substitution T C intron_variant PACA-CA 10 7998817 7998817 single base substitution A G intron_variant PACA-CA 10 7999231 7999251 deletion of <=200bp CGATGGGGAGATTAGGGCAGA - intron_variant PACA-CA 10 8001103 8001103 single base substitution A T intron_variant PACA-CA 10 8001943 8001943 single base substitution C T intron_variant PACA-CA 10 8004963 8004963 single base substitution C T intron_variant PACA-CA 10 8007028 8007028 single base substitution G A missense_variant V519M 1555G>A PACA-CA 10 8007626 8007626 insertion of <=200bp - GCC disruptive_inframe_insertion K718SQ PACA-CA 10 8007986 8007986 deletion of <=200bp A - intron_variant PACA-CA 10 8009679 8009679 single base substitution G A intron_variant PACA-CA 10 8011258 8011258 single base substitution A T intron_variant PACA-CA 10 8014670 8014670 deletion of <=200bp T - intron_variant PACA-CA 10 8014682 8014682 single base substitution A G intron_variant PACA-CA 10 8017961 8017961 single base substitution C T intron_variant PACA-CA 10 8020435 8020435 single base substitution T G intron_variant PACA-CA 10 8022833 8022833 single base substitution C T intron_variant PACA-CA 10 8024809 8024809 deletion of <=200bp T - intron_variant PACA-CA 10 8025547 8025547 insertion of <=200bp - A intron_variant PACA-CA 10 8026201 8026201 single base substitution C T intron_variant PACA-CA 10 8028096 8028096 insertion of <=200bp - T intron_variant PACA-CA 10 8030855 8030855 single base substitution T C intron_variant PACA-CA 10 8031116 8031116 single base substitution G A intron_variant PACA-CA 10 8031423 8031423 single base substitution T A intron_variant PACA-CA 10 8038609 8038609 deletion of <=200bp T - intron_variant PACA-CA 10 8039754 8039754 single base substitution A G intron_variant PACA-CA 10 8042385 8042385 insertion of <=200bp - T intron_variant PACA-CA 10 8042386 8042386 deletion of <=200bp T - intron_variant PACA-CA 10 8046024 8046024 deletion of <=200bp T - intron_variant PACA-CA 10 8047881 8047881 single base substitution C G intron_variant PACA-CA 10 8048200 8048200 single base substitution G A intron_variant PACA-CA 10 8052504 8052504 single base substitution G T intron_variant PACA-CA 10 8052739 8052739 single base substitution G C intron_variant PACA-CA 10 8055642 8055642 insertion of <=200bp - T intron_variant PACA-CA 10 8056820 8056820 single base substitution T C 3_prime_UTR_variant PACA-CA 10 8058455 8058455 insertion of <=200bp - T 3_prime_UTR_variant PACA-CA 10 8059558 8059558 insertion of <=200bp - G downstream_gene_variant PACA-CA 10 8059745 8059745 single base substitution G C downstream_gene_variant PACA-CA 10 8060165 8060165 single base substitution A G downstream_gene_variant PACA-CA 10 8060175 8060175 single base substitution G T downstream_gene_variant PACA-CA 10 8060504 8060504 single base substitution T A downstream_gene_variant PACA-CA 10 8060771 8060771 single base substitution G A downstream_gene_variant PACA-CA 10 8060786 8060786 single base substitution G C downstream_gene_variant PAEN-AU 10 7941499 7941499 single base substitution T A intron_variant PAEN-AU 10 7986201 7986201 single base substitution T C intron_variant PAEN-AU 10 8000455 8000455 single base substitution T A intron_variant PAEN-AU 10 8045621 8045621 single base substitution G T intron_variant PAEN-IT 10 7943055 7943055 single base substitution A G intron_variant PAEN-IT 10 7954257 7954257 single base substitution C G intron_variant PAEN-IT 10 7962259 7962259 single base substitution A G intron_variant PAEN-IT 10 8002489 8002489 single base substitution G A intron_variant PBCA-DE 10 7858157 7858157 single base substitution G A upstream_gene_variant PBCA-DE 10 7859025 7859025 single base substitution T C upstream_gene_variant PBCA-DE 10 7859817 7859817 single base substitution T A upstream_gene_variant PBCA-DE 10 7865759 7865759 single base substitution G A intron_variant PBCA-DE 10 7877885 7877885 single base substitution C T intron_variant PBCA-DE 10 7884540 7884541 deletion of <=200bp TA - intron_variant PBCA-DE 10 7898563 7898563 single base substitution C T intron_variant PBCA-DE 10 7899406 7899406 single base substitution C T intron_variant PBCA-DE 10 7900770 7900771 deletion of <=200bp TG - intron_variant PBCA-DE 10 7908252 7908252 single base substitution G A intron_variant PBCA-DE 10 7918781 7918781 single base substitution C G intron_variant PBCA-DE 10 7925669 7925669 single base substitution C T intron_variant PBCA-DE 10 7927213 7927214 deletion of <=200bp AC - intron_variant PBCA-DE 10 7929955 7929955 single base substitution C A intron_variant PBCA-DE 10 7935174 7935174 single base substitution C G intron_variant PBCA-DE 10 7940707 7940707 single base substitution T C intron_variant PBCA-DE 10 7948903 7948903 single base substitution G A intron_variant PBCA-DE 10 7949327 7949329 deletion of <=200bp ATA - intron_variant PBCA-DE 10 7951650 7951650 single base substitution G A intron_variant PBCA-DE 10 7979016 7979016 single base substitution G A intron_variant PBCA-DE 10 7984171 7984171 single base substitution C T intron_variant PBCA-DE 10 7999856 7999856 single base substitution A C intron_variant PBCA-DE 10 8002422 8002422 single base substitution C T intron_variant PBCA-DE 10 8008434 8008434 single base substitution C A intron_variant PBCA-DE 10 8015299 8015299 single base substitution G C intron_variant PBCA-DE 10 8015370 8015370 single base substitution C A intron_variant PBCA-DE 10 8019990 8019990 insertion of <=200bp - T intron_variant PBCA-DE 10 8025461 8025461 single base substitution C T intron_variant PBCA-DE 10 8028691 8028691 single base substitution A G intron_variant PBCA-DE 10 8029599 8029599 single base substitution T A intron_variant PBCA-DE 10 8032213 8032213 single base substitution T C intron_variant PBCA-DE 10 8038321 8038321 single base substitution G C intron_variant PBCA-DE 10 8038607 8038607 single base substitution G T intron_variant PBCA-DE 10 8040802 8040802 insertion of <=200bp - A intron_variant PBCA-DE 10 8041398 8041398 single base substitution A G intron_variant PBCA-DE 10 8046443 8046443 single base substitution A T intron_variant PBCA-DE 10 8048522 8048522 single base substitution C A intron_variant PRAD-CA 10 7860115 7860115 single base substitution G A upstream_gene_variant PRAD-CA 10 7887255 7887255 single base substitution C T intron_variant PRAD-CA 10 7891652 7891652 single base substitution C T intron_variant PRAD-CA 10 7915193 7915193 single base substitution A G intron_variant PRAD-CA 10 7919406 7919406 single base substitution A G intron_variant PRAD-CA 10 7955752 7955752 single base substitution T G intron_variant PRAD-CA 10 7958385 7958385 single base substitution G A intron_variant PRAD-CA 10 7959985 7959985 single base substitution G C intron_variant PRAD-CA 10 7962295 7962295 single base substitution A G intron_variant PRAD-CA 10 7967975 7967975 single base substitution G A intron_variant PRAD-CA 10 8029161 8029161 single base substitution T G intron_variant PRAD-CA 10 8056538 8056538 single base substitution G A intron_variant PRAD-UK 10 7866145 7866145 single base substitution A G intron_variant PRAD-UK 10 7877026 7877026 single base substitution T G intron_variant PRAD-UK 10 7888867 7888867 deletion of <=200bp T - intron_variant PRAD-UK 10 7907403 7907403 single base substitution C T intron_variant PRAD-UK 10 7917784 7917784 single base substitution T C intron_variant PRAD-UK 10 7918626 7918626 single base substitution A G intron_variant PRAD-UK 10 7929055 7929055 single base substitution G A intron_variant PRAD-UK 10 7930977 7930977 single base substitution T G intron_variant PRAD-UK 10 7961799 7961799 single base substitution G A intron_variant PRAD-UK 10 7991032 7991032 single base substitution G A intron_variant PRAD-UK 10 8000886 8000886 single base substitution A C intron_variant PRAD-UK 10 8000887 8000887 single base substitution G A intron_variant PRAD-UK 10 8007638 8007638 single base substitution A G missense_variant E722G 2165A>G PRAD-UK 10 8036742 8036742 single base substitution A C intron_variant PRAD-UK 10 8063441 8063441 single base substitution G A downstream_gene_variant READ-US 10 8006695 8006695 single base substitution G A missense_variant E408K 1222G>A RECA-EU 10 7856891 7856891 single base substitution C A upstream_gene_variant RECA-EU 10 7869836 7869836 single base substitution G C intron_variant RECA-EU 10 7881639 7881639 single base substitution T G intron_variant RECA-EU 10 7886926 7886926 single base substitution T G intron_variant RECA-EU 10 7894566 7894566 single base substitution G T intron_variant RECA-EU 10 7903535 7903535 single base substitution A G intron_variant RECA-EU 10 7908593 7908593 single base substitution C A intron_variant RECA-EU 10 7911414 7911414 single base substitution C G intron_variant RECA-EU 10 7918437 7918437 single base substitution G C intron_variant RECA-EU 10 7920521 7920521 single base substitution G C intron_variant RECA-EU 10 7922600 7922600 single base substitution A T intron_variant RECA-EU 10 7925075 7925075 single base substitution A T intron_variant RECA-EU 10 7929365 7929365 single base substitution C G intron_variant RECA-EU 10 7937854 7937854 single base substitution C G intron_variant RECA-EU 10 7941427 7941427 single base substitution A C intron_variant RECA-EU 10 7946534 7946534 single base substitution A T intron_variant RECA-EU 10 7960742 7960742 single base substitution A T intron_variant RECA-EU 10 7966102 7966102 single base substitution T G intron_variant RECA-EU 10 7973789 7973789 single base substitution A T intron_variant RECA-EU 10 7974492 7974492 single base substitution G C intron_variant RECA-EU 10 7975713 7975713 single base substitution A T intron_variant RECA-EU 10 7988189 7988189 single base substitution T G intron_variant RECA-EU 10 7993100 7993100 single base substitution G A intron_variant RECA-EU 10 7994791 7994791 single base substitution A G intron_variant RECA-EU 10 7997361 7997361 single base substitution A C intron_variant RECA-EU 10 8001684 8001684 single base substitution T G intron_variant RECA-EU 10 8009679 8009679 single base substitution G A intron_variant RECA-EU 10 8010396 8010396 single base substitution G A intron_variant RECA-EU 10 8019969 8019969 single base substitution A T intron_variant RECA-EU 10 8028296 8028296 single base substitution C T intron_variant RECA-EU 10 8051408 8051408 single base substitution A T intron_variant RECA-EU 10 8053732 8053732 single base substitution T C intron_variant RECA-EU 10 8056594 8056594 single base substitution G A intron_variant SKCA-BR 10 7857802 7857802 single base substitution A T upstream_gene_variant SKCA-BR 10 7858479 7858479 single base substitution C T upstream_gene_variant SKCA-BR 10 7858480 7858480 single base substitution C T upstream_gene_variant SKCA-BR 10 7858550 7858550 single base substitution G C upstream_gene_variant SKCA-BR 10 7859006 7859006 single base substitution G A upstream_gene_variant SKCA-BR 10 7860407 7860407 single base substitution G A upstream_gene_variant SKCA-BR 10 7860554 7860554 single base substitution C G 5_prime_UTR_variant SKCA-BR 10 7865908 7865910 deletion of <=200bp TAA - intron_variant SKCA-BR 10 7866263 7866264 deletion of <=200bp CT - intron_variant SKCA-BR 10 7866267 7866268 deletion of <=200bp TC - intron_variant SKCA-BR 10 7866442 7866442 single base substitution C T missense_variant P110S 328C>T SKCA-BR 10 7874833 7874833 single base substitution T G intron_variant SKCA-BR 10 7875340 7875340 single base substitution C G intron_variant SKCA-BR 10 7877464 7877464 single base substitution C T intron_variant SKCA-BR 10 7878969 7878969 single base substitution C T intron_variant SKCA-BR 10 7880329 7880329 insertion of <=200bp - TTTG intron_variant SKCA-BR 10 7882120 7882120 insertion of <=200bp - GT intron_variant SKCA-BR 10 7884121 7884139 deletion of <=200bp TTTTTTGTTTTTTTTTTTG - intron_variant SKCA-BR 10 7884125 7884127 deletion of <=200bp TTG - intron_variant SKCA-BR 10 7884138 7884139 deletion of <=200bp TG - intron_variant SKCA-BR 10 7884920 7884920 single base substitution C T intron_variant SKCA-BR 10 7885528 7885528 single base substitution C T intron_variant SKCA-BR 10 7887922 7887924 deletion of <=200bp GTT - intron_variant SKCA-BR 10 7889761 7889761 single base substitution C T intron_variant SKCA-BR 10 7896619 7896619 single base substitution T G intron_variant SKCA-BR 10 7897149 7897149 single base substitution C T intron_variant SKCA-BR 10 7897150 7897150 single base substitution C G intron_variant SKCA-BR 10 7902767 7902767 single base substitution C T intron_variant SKCA-BR 10 7905516 7905516 single base substitution C T intron_variant SKCA-BR 10 7905534 7905534 single base substitution C G intron_variant SKCA-BR 10 7905637 7905637 single base substitution T C intron_variant SKCA-BR 10 7906107 7906107 single base substitution G T intron_variant SKCA-BR 10 7906133 7906133 single base substitution A C intron_variant SKCA-BR 10 7907903 7907903 single base substitution C T intron_variant SKCA-BR 10 7908155 7908155 single base substitution C T intron_variant SKCA-BR 10 7913257 7913257 single base substitution G C intron_variant SKCA-BR 10 7913702 7913702 single base substitution A C intron_variant SKCA-BR 10 7917237 7917237 single base substitution C T intron_variant SKCA-BR 10 7925979 7925979 single base substitution C T intron_variant SKCA-BR 10 7926035 7926035 single base substitution A C intron_variant SKCA-BR 10 7927212 7927212 insertion of <=200bp - GAC intron_variant SKCA-BR 10 7932509 7932509 single base substitution T G intron_variant SKCA-BR 10 7934723 7934723 single base substitution C T intron_variant SKCA-BR 10 7936495 7936495 single base substitution T G intron_variant SKCA-BR 10 7937738 7937738 single base substitution G A intron_variant SKCA-BR 10 7939296 7939296 single base substitution C T intron_variant SKCA-BR 10 7941013 7941013 single base substitution C T intron_variant SKCA-BR 10 7941158 7941158 single base substitution C T intron_variant SKCA-BR 10 7943840 7943840 single base substitution C T intron_variant SKCA-BR 10 7945970 7945970 single base substitution C T intron_variant SKCA-BR 10 7946265 7946265 single base substitution C T intron_variant SKCA-BR 10 7947164 7947164 single base substitution T C intron_variant SKCA-BR 10 7950184 7950184 single base substitution C A intron_variant SKCA-BR 10 7953457 7953457 single base substitution T G intron_variant SKCA-BR 10 7954086 7954086 single base substitution C T intron_variant SKCA-BR 10 7955401 7955401 single base substitution C T intron_variant SKCA-BR 10 7958418 7958418 single base substitution C T intron_variant SKCA-BR 10 7960570 7960570 single base substitution G A intron_variant SKCA-BR 10 7967524 7967524 single base substitution C T intron_variant SKCA-BR 10 7975001 7975001 single base substitution C T intron_variant SKCA-BR 10 7976611 7976611 single base substitution T G intron_variant SKCA-BR 10 7977589 7977591 deletion of <=200bp AGG - intron_variant SKCA-BR 10 7977716 7977716 single base substitution C T intron_variant SKCA-BR 10 7978615 7978615 single base substitution T G intron_variant SKCA-BR 10 7980608 7980608 single base substitution C T intron_variant SKCA-BR 10 7981522 7981522 single base substitution T C intron_variant SKCA-BR 10 7982139 7982139 single base substitution A G intron_variant SKCA-BR 10 7984669 7984669 single base substitution C T intron_variant SKCA-BR 10 7987826 7987826 single base substitution G T intron_variant SKCA-BR 10 7988690 7988690 insertion of <=200bp - CAAAAAAAAAA intron_variant SKCA-BR 10 7988751 7988751 single base substitution C T intron_variant SKCA-BR 10 7988874 7988874 single base substitution C T intron_variant SKCA-BR 10 7990635 7990635 single base substitution G T intron_variant SKCA-BR 10 7996664 7996664 single base substitution C A intron_variant SKCA-BR 10 7996898 7996898 single base substitution G A intron_variant SKCA-BR 10 7997981 7997981 single base substitution G A intron_variant SKCA-BR 10 7999645 7999645 single base substitution C T intron_variant SKCA-BR 10 7999755 7999755 insertion of <=200bp - GCTCT intron_variant SKCA-BR 10 8001571 8001571 single base substitution A G intron_variant SKCA-BR 10 8002841 8002841 single base substitution G C intron_variant SKCA-BR 10 8004049 8004049 single base substitution G A intron_variant SKCA-BR 10 8006145 8006145 single base substitution C T synonymous_variant I224I 672C>T SKCA-BR 10 8007467 8007467 single base substitution T G missense_variant L665W 1994T>G SKCA-BR 10 8012896 8012896 single base substitution C T intron_variant SKCA-BR 10 8014337 8014337 single base substitution C T intron_variant SKCA-BR 10 8018180 8018180 single base substitution G A intron_variant SKCA-BR 10 8020023 8020023 single base substitution C T intron_variant SKCA-BR 10 8021325 8021326 deletion of <=200bp GA - intron_variant SKCA-BR 10 8021903 8021903 single base substitution A G intron_variant SKCA-BR 10 8022634 8022634 single base substitution A T intron_variant SKCA-BR 10 8022636 8022636 single base substitution C T intron_variant SKCA-BR 10 8024699 8024699 single base substitution T A intron_variant SKCA-BR 10 8029409 8029409 single base substitution C T intron_variant SKCA-BR 10 8030535 8030551 deletion of <=200bp CAAAAAAAAAAAAAAAA - intron_variant SKCA-BR 10 8032792 8032792 single base substitution C T intron_variant SKCA-BR 10 8033426 8033426 single base substitution C T intron_variant SKCA-BR 10 8035250 8035250 single base substitution T C intron_variant SKCA-BR 10 8036020 8036020 single base substitution C T intron_variant SKCA-BR 10 8038805 8038805 insertion of <=200bp - AT intron_variant SKCA-BR 10 8043353 8043353 single base substitution T G intron_variant SKCA-BR 10 8043366 8043366 single base substitution A T intron_variant SKCA-BR 10 8043376 8043376 single base substitution C T intron_variant SKCA-BR 10 8044669 8044669 single base substitution C T intron_variant SKCA-BR 10 8046829 8046829 single base substitution C T intron_variant SKCA-BR 10 8047534 8047534 single base substitution C T intron_variant SKCA-BR 10 8049525 8049529 deletion of <=200bp TTATA - intron_variant SKCA-BR 10 8051827 8051827 single base substitution A C intron_variant SKCA-BR 10 8061734 8061734 single base substitution G A downstream_gene_variant SKCM-US 10 7866325 7866325 single base substitution C T stop_gained Q71* 211C>T SKCM-US 10 7866502 7866502 single base substitution C T missense_variant P130S 388C>T SKCM-US 10 8006232 8006232 single base substitution A G synonymous_variant A253A 759A>G SKCM-US 10 8006646 8006646 single base substitution C T synonymous_variant I391I 1173C>T SKCM-US 10 8006663 8006663 single base substitution G A missense_variant R397Q 1190G>A SKCM-US 10 8006910 8006910 single base substitution G T synonymous_variant L479L 1437G>T SKCM-US 10 8006979 8006979 single base substitution C T synonymous_variant P502P 1506C>T SKCM-US 10 8007004 8007004 single base substitution G C missense_variant E511Q 1531G>C SKCM-US 10 8007196 8007196 single base substitution C T missense_variant P575S 1723C>T SKCM-US 10 8007232 8007232 single base substitution C T missense_variant P587S 1759C>T SKCM-US 10 8007463 8007463 single base substitution C T missense_variant P664S 1990C>T SKCM-US 10 8007517 8007517 deletion of <=200bp T - frameshift_variant L682 SKCM-US 10 8051084 8051084 single base substitution C T missense_variant P787S 2359C>T SKCM-US 10 8051106 8051106 single base substitution C T missense_variant T794I 2381C>T SKCM-US 10 8051146 8051146 single base substitution C T synonymous_variant L807L 2421C>T SKCM-US 10 8051254 8051254 single base substitution C T synonymous_variant P843P 2529C>T STAD-US 10 7866365 7866365 single base substitution T C missense_variant I84T 251T>C STAD-US 10 7866405 7866405 single base substitution G A synonymous_variant P97P 291G>A STAD-US 10 7866512 7866512 single base substitution C T missense_variant S133F 398C>T STAD-US 10 8005989 8005989 single base substitution T C synonymous_variant D172D 516T>C STAD-US 10 8006080 8006080 single base substitution G A missense_variant D203N 607G>A STAD-US 10 8006284 8006284 deletion of <=200bp A - frameshift_variant K271 STAD-US 10 8006390 8006390 single base substitution C T missense_variant S306F 917C>T STAD-US 10 8006409 8006409 single base substitution T C synonymous_variant P312P 936T>C STAD-US 10 8006770 8006770 single base substitution A G missense_variant T433A 1297A>G STAD-US 10 8007107 8007107 deletion of <=200bp A - frameshift_variant E545 STAD-US 10 8007187 8007187 single base substitution A G missense_variant T572A 1714A>G STAD-US 10 8007477 8007477 single base substitution T C synonymous_variant P668P 2004T>C STAD-US 10 8007484 8007484 single base substitution G A missense_variant A671T 2011G>A STAD-US 10 8055793 8055793 single base substitution T C missense_variant Y890H 2668T>C STAD-US 10 8056685 8056685 single base substitution C T missense_variant H921Y 2761C>T STAD-US 10 8056703 8056703 single base substitution C T stop_gained R927* 2779C>T UCEC-US 10 7866349 7866349 single base substitution G T stop_gained E79* 235G>T UCEC-US 10 7866478 7866478 single base substitution G T stop_gained E122* 364G>T UCEC-US 10 8006053 8006053 single base substitution C T missense_variant R194W 580C>T UCEC-US 10 8006111 8006111 single base substitution G A missense_variant R213Q 638G>A UCEC-US 10 8006372 8006372 single base substitution G A missense_variant R300Q 899G>A UCEC-US 10 8006478 8006478 single base substitution G A synonymous_variant V335V 1005G>A UCEC-US 10 8006695 8006695 single base substitution G A missense_variant E408K 1222G>A UCEC-US 10 8006793 8006793 single base substitution G A synonymous_variant A440A 1320G>A UCEC-US 10 8007069 8007069 single base substitution A C missense_variant K532N 1596A>C UCEC-US 10 8007250 8007250 single base substitution A T stop_gained K593* 1777A>T UCEC-US 10 8007652 8007652 insertion of <=200bp - AG frameshift_variant K727R? UCEC-US 10 8051225 8051225 single base substitution G A missense_variant A834T 2500G>A UCEC-US 10 8055697 8055697 single base substitution C T stop_gained R858* 2572C>T UCEC-US 10 8056704 8056704 single base substitution G A missense_variant R927Q 2780G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand T1743 COSM4731996 c.222G>A p.G74G Substitution - coding silent 10:7824373-7824373 + ESCC_BICR_064T COSM5437043 c.612G>A p.T204T Substitution - coding silent 10:7964122-7964122 + Gp5D COSM1966275 c.2095A>G p.K699E Substitution - Missense 10:7965605-7965605 + BD49T COSM5437043 c.612G>A p.T204T Substitution - coding silent 10:7964122-7964122 + 49M COSM5593372 c.328C>T p.P110S Substitution - Missense 10:7824479-7824479 + TCGA-BR-8368-01 COSM4016194 c.516T>C p.D172D Substitution - coding silent 10:7964026-7964026 + TCGA-AX-A0J1-01 COSM920697 c.580C>T p.R194W Substitution - Missense 10:7964090-7964090 + Gp5D COSM1966235 c.426G>A p.Q142Q Substitution - coding silent 10:7963936-7963936 + TCGA-66-2789-01 COSM685256 c.2372G>A p.R791K Substitution - Missense 10:8009134-8009134 + CHC1756T COSM4804487 c.114G>T p.L38L Substitution - coding silent 10:7818823-7818823 + NCI-H23 COSM1196468 c.221G>T p.G74V Substitution - Missense 10:7824372-7824372 + T407 COSM4732003 c.2553G>A p.T851T Substitution - coding silent 10:8009315-8009315 + ESCC_54 COSM5631412 c.2147A>G p.K716R Substitution - Missense 10:7965657-7965657 + 2492722 COSM5721460 c.2601C>T p.I867I Substitution - coding silent 10:8013763-8013763 + TCGA-AD-6889-01 COSM1349253 c.1895_1896delAG p.K635fs*6 Deletion - Frameshift 10:7965405-7965406 + TCGA-AX-A062-01 COSM920707 c.2500G>A p.A834T Substitution - Missense 10:8009262-8009262 + TCGA-BP-4987-01 COSM1492364 c.2021T>C p.V674A Substitution - Missense 10:7965531-7965531 + TCGA-DA-A1IC-06 COSM3440910 c.1531G>C p.E511Q Substitution - Missense 10:7965041-7965041 + TCGA-AZ-4315-01 COSM1349254 c.1978G>T p.E660* Substitution - Nonsense 10:7965488-7965488 + CRC-2 COSM304263 c.1238C>T p.S413L Substitution - Missense 10:7964748-7964748 + TCGA-BW-A5NO-01 COSM381791 c.612G>T p.T204T Substitution - coding silent 10:7964122-7964122 + Au4 COSM4732002 c.2040T>A p.S680S Substitution - coding silent 10:7965550-7965550 + T2269 COSM920701 c.1222G>A p.E408K Substitution - Missense 10:7964732-7964732 + CSCC-27-T COSM4457072 c.1031C>T p.P344L Substitution - Missense 10:7964541-7964541 + C086 COSM5540098 c.1550C>T p.S517F Substitution - Missense 10:7965060-7965060 + TCGA-HU-A4GU-01 COSM4016036 c.291G>A p.P97P Substitution - coding silent 10:7824442-7824442 + RK106_C01 COSM1627640 c.385C>T p.P129S Substitution - Missense 10:7824536-7824536 + ESCC_84 COSM5636359 c.1875A>G p.K625K Substitution - coding silent 10:7965385-7965385 + PT23_2 COSM5903769 c.1493C>T p.S498F Substitution - Missense 10:7965003-7965003 + CSCC-62-T COSM1966261 c.1484C>T p.P495L Substitution - Missense 10:7964994-7964994 + TCGA-FW-A3R5-06 COSM3867909 c.2421C>T p.L807L Substitution - coding silent 10:8009183-8009183 + TCGA-34-5239-01 COSM685282 c.99C>T p.L33L Substitution - coding silent 10:7818808-7818808 + 19M COSM5579692 c.366A>T p.E122D Substitution - Missense 10:7824517-7824517 + LUAD-RT-S01777 COSM381791 c.612G>T p.T204T Substitution - coding silent 10:7964122-7964122 + TCGA-B5-A11E-01 COSM920709 c.2780G>A p.R927Q Substitution - Missense 10:8014741-8014741 + TCGA-AG-A002-01 COSM263956 c.1131G>A p.P377P Substitution - coding silent 10:7964641-7964641 + TCGA-AP-A0LF-01 COSM920705 c.1777A>T p.K593* Substitution - Nonsense 10:7965287-7965287 + CSB16 COSM5027184 c.2735G>A p.C912Y Substitution - Missense 10:8014696-8014696 + TCGA-AZ-4315-01 COSM1349249 c.443G>A p.G148D Substitution - Missense 10:7963953-7963953 + SJHGG069_A COSM4969838 c.1437G>C p.L479L Substitution - coding silent 10:7964947-7964947 + TCGA-DD-A3A7-01 COSM4916251 c.965A>G p.K322R Substitution - Missense 10:7964475-7964475 + EGC15 COSM5050356 c.1485G>A p.P495P Substitution - coding silent 10:7964995-7964995 + TCGA-B0-4694-01 COSM3358880 c.2584G>A p.G862S Substitution - Missense 10:8013746-8013746 + TCGA-BR-A4QL-01 COSM4016195 c.607G>A p.D203N Substitution - Missense 10:7964117-7964117 + TCGA-CA-6717-01 COSM1349252 c.1079A>C p.K360T Substitution - Missense 10:7964589-7964589 + HCT8 COSM4633209 c.2223G>A p.K741K Substitution - coding silent 10:7965733-7965733 + TCGA-AD-6890-01 COSM1349265 c.2743_2745delAAG p.K917delK Deletion - In frame 10:8014704-8014706 + 2492723 COSM5721460 c.2601C>T p.I867I Substitution - coding silent 10:8013763-8013763 + SNU-175 COSM1966295 c.2764_2766delAAG p.K923delK Deletion - In frame 10:8014725-8014727 + TCGA-AX-A0J0-01 COSM920701 c.1222G>A p.E408K Substitution - Missense 10:7964732-7964732 + CHEWS001 COSM4573845 c.1635A>G p.E545E Substitution - coding silent 10:7965145-7965145 + 1N31-VS-1T31 COSM4974228 c.2019G>A p.R673R Substitution - coding silent 10:7965529-7965529 + T3509 COSM4732001 c.1554C>T p.S518S Substitution - coding silent 10:7965064-7965064 + Pat_60_B COSM5837363 c.962C>T p.P321L Substitution - Missense 10:7964472-7964472 + CHEWS008 COSM4573844 c.1584A>C p.E528D Substitution - Missense 10:7965094-7965094 + 2492721 COSM5721460 c.2601C>T p.I867I Substitution - coding silent 10:8013763-8013763 + LUAD-CHTN-MAD06-00668 COSM358393 c.562G>T p.E188* Substitution - Nonsense 10:7964072-7964072 + 3030_T COSM3978814 c.2147A>C p.K716T Substitution - Missense 10:7965657-7965657 + BD124T COSM5492629 c.869A>G p.Q290R Substitution - Missense 10:7964379-7964379 + TCGA-BR-8680-01 COSM4016035 c.251T>C p.I84T Substitution - Missense 10:7824402-7824402 + T2926 COSM4732002 c.2040T>A p.S680S Substitution - coding silent 10:7965550-7965550 + ESCC_BICR_070T COSM5444798 c.1744G>A p.E582K Substitution - Missense 10:7965254-7965254 + cSCCP4 COSM138746 c.2335C>T p.P779S Substitution - Missense 10:8009097-8009097 + 587376 COSM1228436 c.1782A>C p.E594D Substitution - Missense 10:7965292-7965292 + TCGA-24-1474-01 COSM72902 c.2117A>G p.K706R Substitution - Missense 10:7965627-7965627 + T3080 COSM4732000 c.1503T>C p.T501T Substitution - coding silent 10:7965013-7965013 + C135 COSM1966248 c.980C>T p.T327M Substitution - Missense 10:7964490-7964490 + TCGA-BR-4362-01 COSM4016202 c.2668T>C p.Y890H Substitution - Missense 10:8013830-8013830 + CHC326T COSM4951287 c.613C>A p.L205I Substitution - Missense 10:7964123-7964123 + T38 COSM5341310 c.744G>A p.M248I Substitution - Missense 10:7964254-7964254 + BK0042 COSM4187309 c.2534G>T p.R845L Substitution - Missense 10:8009296-8009296 + T3099 COSM1966276 c.2098G>T p.E700* Substitution - Nonsense 10:7965608-7965608 + CHC326T COSM4951287 c.613C>A p.L205I Substitution - Missense 10:7964123-7964123 + I2L-P19Tb-Tumor-Biopsy COSM1349251 c.981G>A p.T327T Substitution - coding silent 10:7964491-7964491 + 13 COSM3383049 c.1189C>T p.R397* Substitution - Nonsense 10:7964699-7964699 + TCGA-AZ-6605-01 COSM1349250 c.940C>T p.R314C Substitution - Missense 10:7964450-7964450 + COLO-205 COSM1675049 c.29T>C p.L10S Substitution - Missense 10:7818738-7818738 + WA26 COSM238274 c.384G>A p.L128L Substitution - coding silent 10:7824535-7824535 + S0078 COSM5881959 c.1780G>C p.E594Q Substitution - Missense 10:7965290-7965290 + TCGA-CK-5914-01 COSM1349251 c.981G>A p.T327T Substitution - coding silent 10:7964491-7964491 + LUAD-CHTN-3090415 COSM357178 c.1604A>G p.K535R Substitution - Missense 10:7965114-7965114 + TCGA-CG-5721-01 COSM4016037 c.398C>T p.S133F Substitution - Missense 10:7824549-7824549 + HCC57T COSM1603777 c.791A>G p.E264G Substitution - Missense 10:7964301-7964301 + Gp2D COSM1966235 c.426G>A p.Q142Q Substitution - coding silent 10:7963936-7963936 + TCGA-EE-A2GC-06 COSM228521 c.211C>T p.Q71* Substitution - Nonsense 10:7824362-7824362 + TCGA-37-4141-01 COSM685283 c.45G>T p.A15A Substitution - coding silent 10:7818754-7818754 + HCC2998 COSM1966277 c.2103G>T p.K701N Substitution - Missense 10:7965613-7965613 + S01563 COSM5669894 c.1652A>G p.D551G Substitution - Missense 10:7965162-7965162 + sysucc-1370T COSM5437043 c.612G>A p.T204T Substitution - coding silent 10:7964122-7964122 + CHC2358T COSM4953184 c.2017A>G p.R673G Substitution - Missense 10:7965527-7965527 + WA48 COSM241835 c.283C>A p.Q95K Substitution - Missense 10:7824434-7824434 + TCGA-E2-A15G-01 COSM427971 c.1362C>G p.S454S Substitution - coding silent 10:7964872-7964872 + TCGA-AC-A23H-01 COSM3807762 c.51C>A p.I17I Substitution - coding silent 10:7818760-7818760 + Pat_24_A COSM5837365 c.2716C>G p.Q906E Substitution - Missense 10:8014677-8014677 + TCGA-AA-A010-01 COSM285562 c.1174G>A p.D392N Substitution - Missense 10:7964684-7964684 + TCGA-EB-A551-01 COSM3440908 c.1190G>A p.R397Q Substitution - Missense 10:7964700-7964700 + TCGA-GF-A6C9-06 COSM4903704 c.388C>T p.P130S Substitution - Missense 10:7824539-7824539 + PTC-7C COSM4144891 c.2737G>A p.A913T Substitution - Missense 10:8014698-8014698 + CHC1756T COSM4804487 c.114G>T p.L38L Substitution - coding silent 10:7818823-7818823 + BD104T COSM5490758 c.2022C>T p.V674V Substitution - coding silent 10:7965532-7965532 + ESCC_46 COSM466004 c.2400G>T p.A800A Substitution - coding silent 10:8009162-8009162 + ME043T COSM228521 c.211C>T p.Q71* Substitution - Nonsense 10:7824362-7824362 + HCC118T COSM5813588 c.2667G>A p.W889* Substitution - Nonsense 10:8013829-8013829 + TCGA-CG-4442-01 COSM4016200 c.2004T>C p.P668P Substitution - coding silent 10:7965514-7965514 + Pat_60_A COSM5837363 c.962C>T p.P321L Substitution - Missense 10:7964472-7964472 + LC_S3 COSM1187891 c.173G>T p.R58L Substitution - Missense 10:7824324-7824324 + PTC-10C COSM4144890 c.2517T>G p.S839R Substitution - Missense 10:8009279-8009279 + C135 COSM4617049 c.2782G>A p.A928T Substitution - Missense 10:8014743-8014743 + PT48 COSM138746 c.2335C>T p.P779S Substitution - Missense 10:8009097-8009097 + ESCC_109 COSM5649818 c.739C>G p.P247A Substitution - Missense 10:7964249-7964249 + TCGA-IR-A3LK-01 COSM4816745 c.102C>G p.L34L Substitution - coding silent 10:7818811-7818811 + TCGA-CG-5723-01 COSM4016196 c.917C>T p.S306F Substitution - Missense 10:7964427-7964427 + CSCC-31-T COSM920701 c.1222G>A p.E408K Substitution - Missense 10:7964732-7964732 + TCGA-BH-A1FD-01 COSM1474801 c.1171A>G p.I391V Substitution - Missense 10:7964681-7964681 + TCGA-EE-A2GR-06 COSM3440914 c.2529C>T p.P843P Substitution - coding silent 10:8009291-8009291 + DN14067 COSM5963021 c.17C>G p.S6C Substitution - Missense 10:7818726-7818726 + TCGA-BS-A0UV-01 COSM920698 c.638G>A p.R213Q Substitution - Missense 10:7964148-7964148 + LUAD-RT-S01818 COSM383779 c.1895A>C p.K632T Substitution - Missense 10:7965405-7965405 + TCGA-AX-A05Z-01 COSM920617 c.235G>T p.E79* Substitution - Nonsense 10:7824386-7824386 + I2L-P19Tb-Tumor-Organoid COSM1349251 c.981G>A p.T327T Substitution - coding silent 10:7964491-7964491 + 587376 COSM1228435 c.1274G>T p.R425I Substitution - Missense 10:7964784-7964784 + PASFXA COSM5005821 c.1309T>C p.S437P Substitution - Missense 10:7964819-7964819 + 8031556 COSM3383049 c.1189C>T p.R397* Substitution - Nonsense 10:7964699-7964699 + TCGA-EE-A181-06 COSM3440911 c.1723C>T p.P575S Substitution - Missense 10:7965233-7965233 + T578 COSM4731997 c.637C>T p.R213* Substitution - Nonsense 10:7964147-7964147 + TCGA-BS-A0UV-01 COSM920699 c.899G>A p.R300Q Substitution - Missense 10:7964409-7964409 + TCGA-EE-A2MJ-06 COSM3867908 c.1759C>T p.P587S Substitution - Missense 10:7965269-7965269 + WA16 COSM241836 c.1097_1098insC p.D367fs*1 Insertion - Frameshift 10:7964607-7964608 + CSCC-32-T COSM4525985 c.1367G>A p.G456E Substitution - Missense 10:7964877-7964877 + TCGA-BR-4257-01 COSM4016197 c.936T>C p.P312P Substitution - coding silent 10:7964446-7964446 + BD114T COSM5503581 c.2568+7A>T p.? Unknown 10:8009337-8009337 + RMS110_ COSM4987253 c.1046G>C p.S349T Substitution - Missense 10:7964556-7964556 + TCGA-AN-A0XS-01 COSM427969 c.627_630delATTG p.L210fs*9 Deletion - Frameshift 10:7964137-7964140 + T2999 COSM4731999 c.1081C>T p.Q361* Substitution - Nonsense 10:7964591-7964591 + S00836 COSM315773 c.175A>G p.T59A Substitution - Missense 10:7824326-7824326 + TCGA-AP-A0LM-01 COSM920708 c.2572C>T p.R858* Substitution - Nonsense 10:8013734-8013734 + HCC57 COSM1603777 c.791A>G p.E264G Substitution - Missense 10:7964301-7964301 + TCGA-EE-A3J5-06 COSM3440909 c.1437G>T p.L479L Substitution - coding silent 10:7964947-7964947 + TCGA-CG-5721-01 COSM4016198 c.1297A>G p.T433A Substitution - Missense 10:7964807-7964807 + TCGA-DD-A3A2-01 COSM4928951 c.1388C>T p.S463L Substitution - Missense 10:7964898-7964898 + HCC2998 COSM1966258 c.1433A>C p.K478T Substitution - Missense 10:7964943-7964943 + S00539 COSM5658694 c.1868G>T p.R623I Substitution - Missense 10:7965378-7965378 + WA16 COSM241837 c.1461_1462insC p.N488fs*23 Insertion - Frameshift 10:7964971-7964972 + CSCC-35-T COSM4532299 c.1872G>A p.E624E Substitution - coding silent 10:7965382-7965382 + TCGA-A8-A06X-01 COSM427968 c.499G>T p.E167* Substitution - Nonsense 10:7964009-7964009 + LUAD-F00121 COSM365607 c.691G>T p.V231F Substitution - Missense 10:7964201-7964201 + TCGA-B0-5096-01 COSM466004 c.2400G>T p.A800A Substitution - coding silent 10:8009162-8009162 + T3147 COSM4732004 c.2706A>T p.P902P Substitution - coding silent 10:8014667-8014667 + Pat_24_A COSM5837364 c.1738C>T p.L580F Substitution - Missense 10:7965248-7965248 + HT115 COSM1966267 c.1780G>T p.E594* Substitution - Nonsense 10:7965290-7965290 + T3152 COSM4731998 c.661A>G p.T221A Substitution - Missense 10:7964171-7964171 + LUAD-E01278 COSM394059 c.2676G>T p.W892C Substitution - Missense 10:8014637-8014637 + HCC2998 COSM1966276 c.2098G>T p.E700* Substitution - Nonsense 10:7965608-7965608 + pfg092T COSM4749546 c.1372T>G p.S458A Substitution - Missense 10:7964882-7964882 + TCGA-D1-A17Q-01 COSM920704 c.1596A>C p.K532N Substitution - Missense 10:7965106-7965106 + TCGA-DS-A1OD-01 COSM1293297 c.1866T>A p.D622E Substitution - Missense 10:7965376-7965376 + ESCC_BICR_007T COSM5434021 c.1663G>C p.E555Q Substitution - Missense 10:7965173-7965173 + QC2-32-T2 COSM5654150 c.2087T>C p.V696A Substitution - Missense 10:7965597-7965597 + TCGA-A5-A0R6-01 COSM920703 c.1381G>A p.D461N Substitution - Missense 10:7964891-7964891 + DLD1 COSM1966238 c.465G>T p.Q155H Substitution - Missense 10:7963975-7963975 + LUAD-RT-S01477 COSM377392 c.2640G>C p.M880I Substitution - Missense 10:8013802-8013802 + ORL-48 COSM4596833 c.1928G>T p.R643I Substitution - Missense 10:7965438-7965438 + TCGA-AP-A05N-01 COSM920706 c.2179_2180insAG p.R730fs*17 Insertion - Frameshift 10:7965689-7965690 + TCGA-EY-A1GS-01 COSM920700 c.1005G>A p.V335V Substitution - coding silent 10:7964515-7964515 + TCGA-AX-A05Z-01 COSM920702 c.1320G>A p.A440A Substitution - coding silent 10:7964830-7964830 + TCGA-66-2782-01 COSM685281 c.177A>T p.T59T Substitution - coding silent 10:7824328-7824328 + TCGA-25-2042-01 COSM118916 c.1695C>T p.D565D Substitution - coding silent 10:7965205-7965205 + A9 COSM5349589 c.1307C>T p.A436V Substitution - Missense 10:7964817-7964817 + TCGA-BR-8361-01 COSM4016204 c.2779C>T p.R927* Substitution - Nonsense 10:8014740-8014740 + ME049T COSM230183 c.1973C>T p.P658L Substitution - Missense 10:7965483-7965483 + ME049T COSM230182 c.1969C>G p.P657A Substitution - Missense 10:7965479-7965479 + HCT116 COSM4631961 c.1762T>A p.Y588N Substitution - Missense 10:7965272-7965272 + TCGA-37-3789-01 COSM685258 c.1551C>A p.S517S Substitution - coding silent 10:7965061-7965061 + TCGA-66-2787-01 COSM685255 c.2592G>T p.Q864H Substitution - Missense 10:8013754-8013754 + PTC-7C COSM4144893 c.2745G>A p.K915K Substitution - coding silent 10:8014706-8014706 + PTC-7C COSM4144892 c.2739G>A p.A913A Substitution - coding silent 10:8014700-8014700 + Gp2D COSM4626693 c.1816G>A p.D606N Substitution - Missense 10:7965326-7965326 + TCGA-CG-5723-01 COSM4016203 c.2761C>T p.H921Y Substitution - Missense 10:8014722-8014722 + C0081T COSM4165551 c.2676-6G>A p.? Unknown 10:8014631-8014631 + RMS111_ COSM4987501 c.452C>T p.A151V Substitution - Missense 10:7963962-7963962 + TCGA-EE-A2GJ-06 COSM3440912 c.1990C>T p.P664S Substitution - Missense 10:7965500-7965500 + 1517_CLM COSM5753545 c.2564A>G p.Y855C Substitution - Missense 10:8009326-8009326 + TCGA-AN-A0AR-01 COSM427972 c.2631G>A p.G877G Substitution - coding silent 10:8013793-8013793 + TCGA-BS-A0UF-01 COSM179972 c.364G>T p.E122* Substitution - Nonsense 10:7824515-7824515 + TCGA-EI-6917-01 COSM920701 c.1222G>A p.E408K Substitution - Missense 10:7964732-7964732 + TCGA-EE-A29E-06 COSM3440907 c.1173C>T p.I391I Substitution - coding silent 10:7964683-7964683 + PD11341a COSM5782731 c.403C>G p.Q135E Substitution - Missense 10:7824554-7824554 + COLO201 COSM1675049 c.29T>C p.L10S Substitution - Missense 10:7818738-7818738 + 587376 COSM179972 c.364G>T p.E122* Substitution - Nonsense 10:7824515-7824515 + 0120_CRUK_PC_0120_T1_DNA COSM5422753 c.2165A>G p.E722G Substitution - Missense 10:7965675-7965675 + S0029 COSM5881958 c.1376G>A p.S459N Substitution - Missense 10:7964886-7964886 + PD13755a COSM5777096 c.2387C>T p.P796L Substitution - Missense 10:8009149-8009149 + PASFXA COSM252858 c.1318G>A p.A440T Substitution - Missense 10:7964828-7964828 + PD4125a COSM164781 c.2666G>C p.W889S Substitution - Missense 10:8013828-8013828 + RK065_C01 COSM1627645 c.439G>A p.G147R Substitution - Missense 10:7963949-7963949 + SC_9008 COSM5562027 c.810T>C p.P270P Substitution - coding silent 10:7964320-7964320 + CSCC-30-T COSM4471530 c.1724C>T p.P575L Substitution - Missense 10:7965234-7965234 + TCGA-MH-A560-01 COSM3985775 c.2163G>C p.K721N Substitution - Missense 10:7965673-7965673 + TCGA-BR-4201-01 COSM4016201 c.2011G>A p.A671T Substitution - Missense 10:7965521-7965521 + TCGA-GV-A3QK-01 COSM3790980 c.2694G>T p.M898I Substitution - Missense 10:8014655-8014655 + TCGA-22-5492-01 COSM685257 c.1753G>T p.A585S Substitution - Missense 10:7965263-7965263 + TCGA-IR-A3LK-01 COSM4818089 c.854C>G p.S285* Substitution - Nonsense 10:7964364-7964364 + OV207 COSM252858 c.1318G>A p.A440T Substitution - Missense 10:7964828-7964828 + SNU-C4 COSM4651826 c.1499C>A p.P500H Substitution - Missense 10:7965009-7965009 + TCGA-32-2615-01 COSM3397262 c.921A>G p.K307K Substitution - coding silent 10:7964431-7964431 + H23 COSM1196468 c.221G>T p.G74V Substitution - Missense 10:7824372-7824372 + GB07 COSM1744513 c.2213A>G p.E738G Substitution - Missense 10:7965723-7965723 + LUAD-CHTN-Z4716A COSM361471 c.1105G>T p.G369W Substitution - Missense 10:7964615-7964615 + TCGA-EK-A2H0-01 COSM4818952 c.957G>A p.K319K Substitution - coding silent 10:7964467-7964467 + TCGA-EE-A3JD-06 COSM4394565 c.2359C>T p.P787S Substitution - Missense 10:8009121-8009121 + 2492720 COSM5721460 c.2601C>T p.I867I Substitution - coding silent 10:8013763-8013763 + TCGA-EE-A29D-06 COSM3440913 c.2381C>T p.T794I Substitution - Missense 10:8009143-8009143 + TCGA-FW-A3R5-06 COSM3867907 c.1506C>T p.P502P Substitution - coding silent 10:7965016-7965016 + KPOPBR-34-T COSM5963338 c.2503G>A p.A835T Substitution - Missense 10:8009265-8009265 + TCGA-85-6560-01 COSM685254 c.2670C>G p.Y890* Substitution - Nonsense 10:8013832-8013832 + HCC2998 COSM920701 c.1222G>A p.E408K Substitution - Missense 10:7964732-7964732 + PT35 COSM5913122 c.1301C>T p.P434L Substitution - Missense 10:7964811-7964811 + RK186_C01 COSM3738744 c.1251A>G p.G417G Substitution - coding silent 10:7964761-7964761 + HCC2998 COSM920701 c.1222G>A p.E408K Substitution - Missense 10:7964732-7964732 + TCGA-A8-A0A6-01 COSM3807775 c.387A>C p.P129P Substitution - coding silent 10:7824538-7824538 + TCGA-CG-5721-01 COSM4016199 c.1714A>G p.T572A Substitution - Missense 10:7965224-7965224 + PD4125a COSM164782 c.1280C>G p.S427* Substitution - Nonsense 10:7964790-7964790 + Gp2D COSM1966275 c.2095A>G p.K699E Substitution - Missense 10:7965605-7965605 + COLO205 COSM1675049 c.29T>C p.L10S Substitution - Missense 10:7818738-7818738 + S02296 COSM5689351 c.1118G>T p.S373I Substitution - Missense 10:7964628-7964628 + PCSI_0044_Pa_P COSM5420292 c.2153_2154insGCC p.K718_K719insP Insertion - In frame 10:7965663-7965664 + Pat_24_B COSM5837365 c.2716C>G p.Q906E Substitution - Missense 10:8014677-8014677 + CHC2358T COSM4953184 c.2017A>G p.R673G Substitution - Missense 10:7965527-7965527 + TCGA-EB-A5UN-06 COSM3440906 c.759A>G p.A253A Substitution - coding silent 10:7964269-7964269 + 3N49-VS-3T49 COSM4982838 c.2167A>G p.R723G Substitution - Missense 10:7965677-7965677 + WSU-HN30 COSM4600861 c.581G>A p.R194Q Substitution - Missense 10:7964091-7964091 + PASLZM COSM5006490 c.586C>T p.R196W Substitution - Missense 10:7964096-7964096 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.527669;Hs.527671;Hs.527684;Hs.527688 10p15.1 606576 Hs.709984;Hs.709987;Hs.709990;Hs.709992;Hs.709993;Hs.709995 10p15.1 606576

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - Frameshift p.D547Tfs*13 c.1638delA 10 8007107 STAD AGAAGGAGA - InFrameDeletion p.K719_K721delKEK c.2155_2163delAAGGAGAAG 10 8007617 GBM - AG Frameshift p.R728Gfs*19 c.2180_2181insAG 10 8007653 UCEC A G IntronicSNV . c.410-28763A>G 10 7977120 CLL A G Missense p.I391V c.1171A>G 10 8006644 BRCA A G Missense p.K271E c.811A>G 10 8006284 LUAD A G Missense p.K706R c.2117A>G 10 8007590 OV A G Missense p.T59A c.175A>G 10 7866289 SCLC A G Synonymous p.K307K c.921A>G 10 8006394 GBM A T Missense p.Q108L c.323A>T 10 7866437 LUAD A T Nonsense p.K527* c.1579A>T 10 8007052 CM A T Nonsense p.K593* c.1777A>T 10 8007250 UCEC A T Synonymous p.T59T c.177A>T 10 7866291 LUSC ATTG - Frameshift p.L210Kfs*9 c.627_630delATTG 10 8006100 BRCA C A Synonymous p.S517S c.1551C>A 10 8007024 LUSC C G Missense p.P657A c.1969C>G 10 8007442 CM C G Nonsense p.S427* c.1280C>G 10 8006753 BRCA C G Nonsense p.Y890* c.2670C>G 10 8055795 LUSC C G Synonymous p.S454S c.1362C>G 10 8006835 BRCA C T Missense p.P129S c.385C>T 10 7866499 HC C T Missense p.P241L c.722C>T 10 8006195 CM C T Missense p.P490S c.1468C>T 10 8006941 CM C T Missense p.P575S c.1723C>T 10 8007196 CM C T Missense p.P587S c.1759C>T 10 8007232 CM C T Missense p.P658L c.1973C>T 10 8007446 CM C T Missense p.P664S c.1990C>T 10 8007463 CM C T Missense p.P787S c.2359C>T 10 8051084 CM C T Missense p.S518F c.1553C>T 10 8007026 CM C T Nonsense p.Q222* c.664C>T 10 8006137 HNSC C T Nonsense p.Q71* c.211C>T 10 7866325 CM C T Synonymous p.D565D c.1695C>T 10 8007168 OV C T Synonymous p.I592I c.1776C>T 10 8007249 CM C T Synonymous p.L33L c.99C>T 10 7860771 LUSC C T Synonymous p.P843P c.2529C>T 10 8051254 CM G A Missense p.A671T c.2011G>A 10 8007484 STAD G A Missense p.C912Y c.2735G>A 10 8056659 BRCA G A Missense p.D206N c.616G>A 10 8006089 HNSC G A Missense p.G862D c.2585G>A 10 8055710 STAD G A Missense p.G862S c.2584G>A 10 8055709 RCCC G A Missense p.R791K c.2372G>A 10 8051097 LUSC G A Synonymous p.E511E c.1533G>A 10 8007006 LUAD G A Synonymous p.E729E c.2187G>A 10 8007660 HNSC G A Synonymous p.G877G c.2631G>A 10 8055756 BRCA G A Synonymous p.V335V c.1005G>A 10 8006478 UCEC GCCCCCGCGCCC - InFrameDeletion p.A800_P803delAPAP c.2399_2410delCGCCCGCCCCCG 10 8051117 BLCA G C Missense p.E511Q c.1531G>C 10 8007004 CM G C Missense p.M905I c.2715G>C 10 8056639 LUAD G C Missense p.W889S c.2666G>C 10 8055791 BRCA G - IntronicDeletion . c.409+9325delG 10 7875847 CM G T Missense p.A585S c.1753G>T 10 8007226 LUSC G T Missense p.Q864H c.2592G>T 10 8055717 LUSC G T Missense p.V207F c.619G>T 10 8006092 RCCC G T Missense p.W23L c.68G>T 10 7860740 LUAD G T Nonsense p.E167* c.499G>T 10 8005972 BRCA G T Nonsense p.E748* c.2242G>T 10 8019213 LUAD G T Synonymous p.A15A c.45G>T 10 7860717 LUSC G T Synonymous p.A800A c.2400G>T 10 8051125 RCCC G T Synonymous p.G74G c.222G>T 10 7866336 LUAD G T Synonymous p.L479L c.1437G>T 10 8006910 CM T C Synonymous p.P312P c.936T>C 10 8006409 STAD T - Frameshift p.L682Cfs*15 c.2045delT 10 8007517 CM