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 50691492 50691492 + Missense_Mutation SNP A A C TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chr10:50691492A>C c.1892T>G c.(1891-1893)aTg>aGg p.M631R ACC 10 50714007 50714007 + Missense_Mutation SNP C C A TCGA-OR-A5K9-01A-11D-A29I-10 TCGA-OR-A5K9-11A-11D-A29L-10 g.chr10:50714007C>A c.1449G>T c.(1447-1449)gaG>gaT p.E483D BLCA 10 50666943 50666943 + Missense_Mutation SNP C C T TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr10:50666943C>T c.4400G>A c.(4399-4401)cGa>cAa p.R1467Q BLCA 10 50667018 50667018 + Missense_Mutation SNP T T A TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr10:50667018T>A c.4325A>T c.(4324-4326)gAt>gTt p.D1442V BLCA 10 50669504 50669504 + Missense_Mutation SNP C C T TCGA-DK-A3IM-01A-11D-A20D-08 TCGA-DK-A3IM-10A-01D-A20D-08 g.chr10:50669504C>T c.3877G>A c.(3877-3879)Gcc>Acc p.A1293T BLCA 10 50678385 50678385 + Missense_Mutation SNP C C G TCGA-KQ-A41S-01A-12D-A339-08 TCGA-KQ-A41S-10C-01D-A339-08 g.chr10:50678385C>G c.3621G>C c.(3619-3621)aaG>aaC p.K1207N BLCA 10 50678733 50678733 + Missense_Mutation SNP C C G TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr10:50678733C>G c.3273G>C c.(3271-3273)ttG>ttC p.L1091F BLCA 10 50678885 50678885 + Nonsense_Mutation SNP G G A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr10:50678885G>A c.3121C>T c.(3121-3123)Caa>Taa p.Q1041* BLCA 10 50682233 50682233 + Missense_Mutation SNP G G A TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr10:50682233G>A c.2438C>T c.(2437-2439)tCt>tTt p.S813F BLCA 10 50690842 50690842 + Missense_Mutation SNP G G C TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr10:50690842G>C c.2060C>G c.(2059-2061)tCg>tGg p.S687W BLCA 10 50691406 50691406 + Missense_Mutation SNP G G T TCGA-DK-A3IM-01A-11D-A20D-08 TCGA-DK-A3IM-10A-01D-A20D-08 g.chr10:50691406G>T c.1978C>A c.(1978-1980)Ctt>Att p.L660I BLCA 10 50708622 50708622 + Silent SNP C C G TCGA-GC-A3OO-01A-11D-A22Z-08 TCGA-GC-A3OO-10C-01D-A22Z-08 g.chr10:50708622C>G c.1647G>C c.(1645-1647)ctG>ctC p.L549L BLCA 10 50732248 50732248 + Missense_Mutation SNP C C T TCGA-BT-A20O-01A-21D-A14W-08 TCGA-BT-A20O-11A-11D-A14W-08 g.chr10:50732248C>T c.1228G>A c.(1228-1230)Ggc>Agc p.G410S BLCA 10 50732714 50732714 + Silent SNP C C T TCGA-XF-AAN3-01A-11D-A42E-08 TCGA-XF-AAN3-10A-01D-A42H-08 g.chr10:50732714C>T c.762G>A c.(760-762)caG>caA p.Q254Q BLCA 10 50740776 50740776 + Nonsense_Mutation SNP G G A TCGA-GC-A3BM-01A-11D-A22Z-08 TCGA-GC-A3BM-10A-01D-A22Z-08 g.chr10:50740776G>A c.235C>T c.(235-237)Cag>Tag p.Q79* BLCA 10 50740821 50740821 + Missense_Mutation SNP C C T TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr10:50740821C>T c.190G>A c.(190-192)Gca>Aca p.A64T BLCA 10 50740961 50740961 + Missense_Mutation SNP C C T TCGA-2F-A9KP-01A-11D-A38G-08 TCGA-2F-A9KP-10A-01D-A38J-08 g.chr10:50740961C>T c.50G>A c.(49-51)tGt>tAt p.C17Y BRCA 10 50667150 50667150 + Missense_Mutation SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr10:50667150T>G c.4193A>C c.(4192-4194)cAc>cCc p.H1398P BRCA 10 50667204 50667204 + Missense_Mutation SNP G G A TCGA-BH-A0AW-01A-11W-A071-09 TCGA-BH-A0AW-10A-01W-A071-09 g.chr10:50667204G>A c.4139C>T c.(4138-4140)tCa>tTa p.S1380L BRCA 10 50668419 50668419 + Splice_Site SNP C C A TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr10:50668419C>A c.4062G>T c.(4060-4062)caG>caT p.Q1354H BRCA 10 50668447 50668447 + Missense_Mutation SNP G G A TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr10:50668447G>A c.4034C>T c.(4033-4035)tCa>tTa p.S1345L BRCA 10 50678264 50678264 + Missense_Mutation SNP C C A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr10:50678264C>A c.3742G>T c.(3742-3744)Gac>Tac p.D1248Y BRCA 10 50678496 50678496 + Silent SNP C C T TCGA-E2-A10C-01A-21D-A10M-09 TCGA-E2-A10C-10A-01D-A10M-09 g.chr10:50678496C>T c.3510G>A c.(3508-3510)gaG>gaA p.E1170E BRCA 10 50678569 50678569 + Missense_Mutation SNP C C G TCGA-EW-A1J5-01A-11D-A13L-09 TCGA-EW-A1J5-10A-01D-A13O-09 g.chr10:50678569C>G c.3437G>C c.(3436-3438)aGc>aCc p.S1146T BRCA 10 50679156 50679156 + Missense_Mutation SNP T T C TCGA-A8-A08F-01A-11W-A019-09 TCGA-A8-A08F-10A-01W-A021-09 g.chr10:50679156T>C c.2935A>G c.(2935-2937)Aag>Gag p.K979E BRCA 10 50681546 50681546 + Missense_Mutation SNP G G A TCGA-BH-A0BZ-01A-31D-A12Q-09 TCGA-BH-A0BZ-11A-61D-A12Q-09 g.chr10:50681546G>A c.2686C>T c.(2686-2688)Cca>Tca p.P896S BRCA 10 50681587 50681587 + Missense_Mutation SNP T T G TCGA-E9-A22G-01A-11D-A159-09 TCGA-E9-A22G-10A-01D-A159-09 g.chr10:50681587T>G c.2645A>C c.(2644-2646)tAt>tCt p.Y882S BRCA 10 50682204 50682204 + Missense_Mutation SNP G G T TCGA-AR-A2LE-01A-11D-A17W-09 TCGA-AR-A2LE-10A-01D-A17W-09 g.chr10:50682204G>T c.2467C>A c.(2467-2469)Cct>Act p.P823T BRCA 10 50684343 50684343 + Missense_Mutation SNP C C T TCGA-AO-A03O-01A-11W-A019-09 TCGA-AO-A03O-10A-01W-A021-09 g.chr10:50684343C>T c.2300G>A c.(2299-2301)cGt>cAt p.R767H BRCA 10 50690757 50690758 + Frame_Shift_Ins INS - - C TCGA-E9-A1NI-01A-11W-A16H-09 TCGA-E9-A1NI-10A-01D-A17G-09 g.chr10:50690757_50690758insC c.2144_2145insG c.(2143-2145)ggafs p.G715fs BRCA 10 50690883 50690883 + Silent SNP C C A TCGA-A2-A04P-01A-31D-A128-09 TCGA-A2-A04P-10A-01W-A055-09 g.chr10:50690883C>A c.2019G>T c.(2017-2019)ctG>ctT p.L673L BRCA 10 50708659 50708659 + Missense_Mutation SNP C C T TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chr10:50708659C>T c.1610G>A c.(1609-1611)gGc>gAc p.G537D BRCA 10 50732269 50732269 + Missense_Mutation SNP C C T TCGA-AO-A03M-01B-11D-A10M-09 TCGA-AO-A03M-10A-01D-A10M-09 g.chr10:50732269C>T c.1207G>A c.(1207-1209)Gag>Aag p.E403K BRCA 10 50732504 50732504 + Silent SNP T T C TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr10:50732504T>C c.972A>G c.(970-972)aaA>aaG p.K324K BRCA 10 50732557 50732557 + Missense_Mutation SNP G G C TCGA-A7-A2KD-01A-31D-A21Q-09 TCGA-A7-A2KD-10A-01D-A21Q-09 g.chr10:50732557G>C c.919C>G c.(919-921)Cca>Gca p.P307A BRCA 10 50732662 50732662 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr10:50732662C>T c.814G>A c.(814-816)Gaa>Aaa p.E272K BRCA 10 50732756 50732756 + Silent SNP G G A TCGA-A7-A2KD-01A-31D-A21Q-09 TCGA-A7-A2KD-10A-01D-A21Q-09 g.chr10:50732756G>A c.720C>T c.(718-720)atC>atT p.I240I BRCA 10 50736490 50736490 + Missense_Mutation SNP C C G TCGA-E2-A10C-01A-21D-A10M-09 TCGA-E2-A10C-10A-01D-A10M-09 g.chr10:50736490C>G c.625G>C c.(625-627)Gat>Cat p.D209H CESC 10 50678926 50678926 + Nonsense_Mutation SNP G G C TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr10:50678926G>C c.3080C>G c.(3079-3081)tCa>tGa p.S1027* CESC 10 50732496 50732496 + Missense_Mutation SNP C C T TCGA-EK-A2PG-01A-11D-A18J-09 TCGA-EK-A2PG-10A-01D-A18J-09 g.chr10:50732496C>T c.980G>A c.(979-981)cGt>cAt p.R327H CESC 10 50732662 50732662 + Missense_Mutation SNP C C T TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr10:50732662C>T c.814G>A c.(814-816)Gaa>Aaa p.E272K CESC 10 50732789 50732789 + Missense_Mutation SNP C C T TCGA-C5-A1M8-01A-21D-A13W-08 TCGA-C5-A1M8-10A-01D-A13W-08 g.chr10:50732789C>T c.687G>A c.(685-687)atG>atA p.M229I CESC 10 50740702 50740702 + Silent SNP G G A TCGA-EA-A556-01A-11D-A26G-09 TCGA-EA-A556-10A-01D-A26G-09 g.chr10:50740702G>A c.309C>T c.(307-309)gaC>gaT p.D103D COAD 10 50666893 50666893 + Missense_Mutation SNP C C T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr10:50666893C>T c.4450G>A c.(4450-4452)Gga>Aga p.G1484R COAD 10 50667015 50667015 + Missense_Mutation SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr10:50667015C>T c.4328G>A c.(4327-4329)gGc>gAc p.G1443D COAD 10 50667140 50667140 + Silent SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr10:50667140C>T c.4203G>A c.(4201-4203)ctG>ctA p.L1401L COAD 10 50669513 50669513 + Missense_Mutation SNP C C A TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr10:50669513C>A c.3868G>T c.(3868-3870)Gcc>Tcc p.A1290S COAD 10 50669533 50669533 + Missense_Mutation SNP T T C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr10:50669533T>C c.3848A>G c.(3847-3849)gAg>gGg p.E1283G COAD 10 50678483 50678483 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:50678483C>T c.3523G>A c.(3523-3525)Gaa>Aaa p.E1175K COAD 10 50678650 50678650 + Missense_Mutation SNP T T C TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr10:50678650T>C c.3356A>G c.(3355-3357)gAg>gGg p.E1119G COAD 10 50678650 50678650 + Missense_Mutation SNP T T C TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr10:50678650T>C c.3356A>G c.(3355-3357)gAg>gGg p.E1119G COAD 10 50678651 50678651 + Nonsense_Mutation SNP C C A TCGA-A6-6652-01A-11D-1771-10 TCGA-A6-6652-10A-01D-1771-10 g.chr10:50678651C>A c.3355G>T c.(3355-3357)Gag>Tag p.E1119* COAD 10 50678848 50678848 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr10:50678848C>T c.3158G>A c.(3157-3159)cGc>cAc p.R1053H COAD 10 50678893 50678893 + Missense_Mutation SNP C C T TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr10:50678893C>T c.3113G>A c.(3112-3114)aGa>aAa p.R1038K COAD 10 50679049 50679049 + Missense_Mutation SNP C C A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr10:50679049C>A c.3042G>T c.(3040-3042)caG>caT p.Q1014H COAD 10 50679126 50679126 + Missense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:50679126C>A c.2965G>T c.(2965-2967)Gac>Tac p.D989Y COAD 10 50679166 50679166 + Splice_Site SNP T T C TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr10:50679166T>C c.2925A>G c.(2923-2925)cgA>cgG p.R975R COAD 10 50679168 50679168 + Splice_Site SNP T T C TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr10:50679168T>C c.e17-2 COAD 10 50681008 50681008 + Frame_Shift_Del DEL C C - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr10:50681008delC c.2776delG c.(2776-2778)gcafs p.A926fs COAD 10 50681527 50681527 + Missense_Mutation SNP T T A TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr10:50681527T>A c.2705A>T c.(2704-2706)aAt>aTt p.N902I COAD 10 50681626 50681626 + Missense_Mutation SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:50681626T>C c.2606A>G c.(2605-2607)gAc>gGc p.D869G COAD 10 50682211 50682211 + Missense_Mutation SNP T T G TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chr10:50682211T>G c.2460A>C c.(2458-2460)aaA>aaC p.K820N COAD 10 50684289 50684289 + Missense_Mutation SNP A A T TCGA-AA-3666-01A-02W-0900-09 TCGA-AA-3666-10A-01W-0900-09 g.chr10:50684289A>T c.2354T>A c.(2353-2355)gTt>gAt p.V785D COAD 10 50684305 50684305 + Missense_Mutation SNP C C T TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr10:50684305C>T c.2338G>A c.(2338-2340)Gtt>Att p.V780I COAD 10 50684305 50684305 + Missense_Mutation SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr10:50684305C>T c.2338G>A c.(2338-2340)Gtt>Att p.V780I COAD 10 50690778 50690778 + Silent SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr10:50690778G>A c.2124C>T c.(2122-2124)tcC>tcT p.S708S COAD 10 50690872 50690872 + Missense_Mutation SNP G G A TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr10:50690872G>A c.2030C>T c.(2029-2031)cCg>cTg p.P677L COAD 10 50691429 50691429 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr10:50691429C>T c.1955G>A c.(1954-1956)cGa>cAa p.R652Q COAD 10 50691429 50691429 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:50691429C>T c.1955G>A c.(1954-1956)cGa>cAa p.R652Q COAD 10 50701211 50701211 + Silent SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr10:50701211C>T c.1773G>A c.(1771-1773)ccG>ccA p.P591P COAD 10 50701212 50701212 + Missense_Mutation SNP G G T TCGA-AA-3496-01A-21D-1835-10 TCGA-AA-3496-11A-01D-1835-10 g.chr10:50701212G>T c.1772C>A c.(1771-1773)cCg>cAg p.P591Q COAD 10 50708699 50708699 + Nonsense_Mutation SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr10:50708699G>A c.1570C>T c.(1570-1572)Cag>Tag p.Q524* COAD 10 50713973 50713973 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:50713973C>T c.1483G>A c.(1483-1485)Gaa>Aaa p.E495K COAD 10 50732131 50732131 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:50732131C>T c.1345G>A c.(1345-1347)Gtg>Atg p.V449M COAD 10 50732496 50732496 + Missense_Mutation SNP C C T TCGA-DM-A1D4-01A-21D-A152-10 TCGA-DM-A1D4-10A-01D-A152-10 g.chr10:50732496C>T c.980G>A c.(979-981)cGt>cAt p.R327H COAD 10 50732705 50732705 + Missense_Mutation SNP C C A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr10:50732705C>A c.771G>T c.(769-771)gaG>gaT p.E257D COADREAD 10 50666882 50666882 + Silent SNP T T C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:50666882T>C c.4461A>G c.(4459-4461)aaA>aaG p.K1487K COADREAD 10 50666893 50666893 + Missense_Mutation SNP C C T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr10:50666893C>T c.4450G>A c.(4450-4452)Gga>Aga p.G1484R COADREAD 10 50667015 50667015 + Missense_Mutation SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr10:50667015C>T c.4328G>A c.(4327-4329)gGc>gAc p.G1443D COADREAD 10 50667133 50667133 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:50667133G>A c.4210C>T c.(4210-4212)Cgt>Tgt p.R1404C COADREAD 10 50667140 50667140 + Silent SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr10:50667140C>T c.4203G>A c.(4201-4203)ctG>ctA p.L1401L COADREAD 10 50669513 50669513 + Missense_Mutation SNP C C A TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr10:50669513C>A c.3868G>T c.(3868-3870)Gcc>Tcc p.A1290S COADREAD 10 50669533 50669533 + Missense_Mutation SNP T T C TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr10:50669533T>C c.3848A>G c.(3847-3849)gAg>gGg p.E1283G COADREAD 10 50678483 50678483 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:50678483C>T c.3523G>A c.(3523-3525)Gaa>Aaa p.E1175K COADREAD 10 50678590 50678590 + Missense_Mutation SNP G G A TCGA-AG-A02G-01A-01W-A00E-09 TCGA-AG-A02G-10A-01W-A00E-09 g.chr10:50678590G>A c.3416C>T c.(3415-3417)tCt>tTt p.S1139F COADREAD 10 50678650 50678650 + Missense_Mutation SNP T T C TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr10:50678650T>C c.3356A>G c.(3355-3357)gAg>gGg p.E1119G COADREAD 10 50678650 50678650 + Missense_Mutation SNP T T C TCGA-EI-6506-01A-11D-1733-10 TCGA-EI-6506-10A-01D-1733-10 g.chr10:50678650T>C c.3356A>G c.(3355-3357)gAg>gGg p.E1119G COADREAD 10 50678650 50678650 + Missense_Mutation SNP T T C TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr10:50678650T>C c.3356A>G c.(3355-3357)gAg>gGg p.E1119G COADREAD 10 50678651 50678651 + Nonsense_Mutation SNP C C A TCGA-A6-6652-01A-11D-1771-10 TCGA-A6-6652-10A-01D-1771-10 g.chr10:50678651C>A c.3355G>T c.(3355-3357)Gag>Tag p.E1119* COADREAD 10 50678848 50678848 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr10:50678848C>T c.3158G>A c.(3157-3159)cGc>cAc p.R1053H COADREAD 10 50678893 50678893 + Missense_Mutation SNP C C T TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr10:50678893C>T c.3113G>A c.(3112-3114)aGa>aAa p.R1038K COADREAD 10 50678894 50678894 + Missense_Mutation SNP T T C TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr10:50678894T>C c.3112A>G c.(3112-3114)Aga>Gga p.R1038G COADREAD 10 50678894 50678894 + Missense_Mutation SNP T T C TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr10:50678894T>C c.3112A>G c.(3112-3114)Aga>Gga p.R1038G COADREAD 10 50679049 50679049 + Missense_Mutation SNP C C A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr10:50679049C>A c.3042G>T c.(3040-3042)caG>caT p.Q1014H COADREAD 10 50679126 50679126 + Missense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr10:50679126C>A c.2965G>T c.(2965-2967)Gac>Tac p.D989Y COADREAD 10 50679166 50679166 + Splice_Site SNP T T C TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr10:50679166T>C c.2925A>G c.(2923-2925)cgA>cgG p.R975R COADREAD 10 50679168 50679168 + Splice_Site SNP T T C TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr10:50679168T>C c.e17-2 COADREAD 10 50681008 50681008 + Frame_Shift_Del DEL C C - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr10:50681008delC c.2776delG c.(2776-2778)gcafs p.A926fs COADREAD 10 50681527 50681527 + Missense_Mutation SNP T T A TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr10:50681527T>A c.2705A>T c.(2704-2706)aAt>aTt p.N902I COADREAD 10 50681626 50681626 + Missense_Mutation SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:50681626T>C c.2606A>G c.(2605-2607)gAc>gGc p.D869G COADREAD 10 50682211 50682211 + Missense_Mutation SNP T T G TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chr10:50682211T>G c.2460A>C c.(2458-2460)aaA>aaC p.K820N COADREAD 10 50684289 50684289 + Missense_Mutation SNP A A T TCGA-AA-3666-01A-02W-0900-09 TCGA-AA-3666-10A-01W-0900-09 g.chr10:50684289A>T c.2354T>A c.(2353-2355)gTt>gAt p.V785D COADREAD 10 50684305 50684305 + Missense_Mutation SNP C C T TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr10:50684305C>T c.2338G>A c.(2338-2340)Gtt>Att p.V780I COADREAD 10 50684305 50684305 + Missense_Mutation SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr10:50684305C>T c.2338G>A c.(2338-2340)Gtt>Att p.V780I COADREAD 10 50690778 50690778 + Silent SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr10:50690778G>A c.2124C>T c.(2122-2124)tcC>tcT p.S708S COADREAD 10 50690872 50690872 + Missense_Mutation SNP G G A TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr10:50690872G>A c.2030C>T c.(2029-2031)cCg>cTg p.P677L COADREAD 10 50691429 50691429 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr10:50691429C>T c.1955G>A c.(1954-1956)cGa>cAa p.R652Q COADREAD 10 50691429 50691429 + Missense_Mutation SNP C C T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr10:50691429C>T c.1955G>A c.(1954-1956)cGa>cAa p.R652Q COADREAD 10 50701211 50701211 + Silent SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr10:50701211C>T c.1773G>A c.(1771-1773)ccG>ccA p.P591P COADREAD 10 50701212 50701212 + Missense_Mutation SNP G G T TCGA-AA-3496-01A-21D-1835-10 TCGA-AA-3496-11A-01D-1835-10 g.chr10:50701212G>T c.1772C>A c.(1771-1773)cCg>cAg p.P591Q COADREAD 10 50708699 50708699 + Nonsense_Mutation SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr10:50708699G>A c.1570C>T c.(1570-1572)Cag>Tag p.Q524* COADREAD 10 50713973 50713973 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:50713973C>T c.1483G>A c.(1483-1485)Gaa>Aaa p.E495K COADREAD 10 50732131 50732131 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr10:50732131C>T c.1345G>A c.(1345-1347)Gtg>Atg p.V449M COADREAD 10 50732496 50732496 + Missense_Mutation SNP C C T TCGA-DM-A1D4-01A-21D-A152-10 TCGA-DM-A1D4-10A-01D-A152-10 g.chr10:50732496C>T c.980G>A c.(979-981)cGt>cAt p.R327H COADREAD 10 50732705 50732705 + Missense_Mutation SNP C C A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr10:50732705C>A c.771G>T c.(769-771)gaG>gaT p.E257D COADREAD 10 50736558 50736558 + Missense_Mutation SNP T T C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:50736558T>C c.557A>G c.(556-558)aAa>aGa p.K186R DLBC 10 50678544 50678544 + Silent SNP A A C TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr10:50678544A>C c.3462T>G c.(3460-3462)tcT>tcG p.S1154S ESCA 10 50678883 50678883 + Silent SNP T T C TCGA-LN-A8HZ-01A-11D-A36J-09 TCGA-LN-A8HZ-10A-01D-A36M-09 g.chr10:50678883T>C c.3123A>G c.(3121-3123)caA>caG p.Q1041Q ESCA 10 50681583 50681583 + Silent SNP G G T TCGA-2H-A9GI-01A-11D-A37C-09 TCGA-2H-A9GI-11A-11D-A37F-09 g.chr10:50681583G>T c.2649C>A c.(2647-2649)ctC>ctA p.L883L ESCA 10 50684358 50684358 + Splice_Site SNP T T C TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr10:50684358T>C c.e12-2 ESCA 10 50691461 50691461 + Missense_Mutation SNP G G T TCGA-L5-A88Z-01A-11D-A36J-09 TCGA-L5-A88Z-11A-11D-A36M-09 g.chr10:50691461G>T c.1923C>A c.(1921-1923)caC>caA p.H641Q ESCA 10 50714021 50714021 + Missense_Mutation SNP G G A TCGA-L5-A43I-01A-11D-A247-09 TCGA-L5-A43I-11A-11D-A247-09 g.chr10:50714021G>A c.1435C>T c.(1435-1437)Cgt>Tgt p.R479C ESCA 10 50740752 50740752 + Missense_Mutation SNP C C T TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr10:50740752C>T c.259G>A c.(259-261)Gcc>Acc p.A87T GBM 10 50667268 50667268 + Missense_Mutation SNP T T C TCGA-06-0649-01B-01W-0348-08 TCGA-06-0649-10A-01W-0348-08 g.chr10:50667268T>C c.4075A>G c.(4075-4077)Aaa>Gaa p.K1359E GBM 10 50690763 50690763 + Missense_Mutation SNP C C T TCGA-32-4208-01A-01D-1353-08 TCGA-32-4208-10A-01D-1353-08 g.chr10:50690763C>T c.2139G>A c.(2137-2139)atG>atA p.M713I GBM 10 50690803 50690803 + Missense_Mutation SNP A A G TCGA-26-5134-01A-01D-1486-08 TCGA-26-5134-10A-01D-1486-08 g.chr10:50690803A>G c.2099T>C c.(2098-2100)tTg>tCg p.L700S GBMLGG 10 50667030 50667030 + Missense_Mutation SNP T T C TCGA-HT-7687-01A-11D-2253-08 TCGA-HT-7687-10A-01D-2253-08 g.chr10:50667030T>C c.4313A>G c.(4312-4314)cAg>cGg p.Q1438R GBMLGG 10 50667171 50667171 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:50667171G>A c.4172C>T c.(4171-4173)gCt>gTt p.A1391V GBMLGG 10 50667268 50667268 + Missense_Mutation SNP T T C TCGA-06-0649-01B-01W-0348-08 TCGA-06-0649-10A-01W-0348-08 g.chr10:50667268T>C c.4075A>G c.(4075-4077)Aaa>Gaa p.K1359E GBMLGG 10 50669556 50669556 + Silent SNP G G A TCGA-E1-A7YL-01A-11D-A34A-08 TCGA-E1-A7YL-10A-01D-A34A-08 g.chr10:50669556G>A c.3825C>T c.(3823-3825)gcC>gcT p.A1275A GBMLGG 10 50690763 50690763 + Missense_Mutation SNP C C T TCGA-32-4208-01A-01D-1353-08 TCGA-32-4208-10A-01D-1353-08 g.chr10:50690763C>T c.2139G>A c.(2137-2139)atG>atA p.M713I GBMLGG 10 50690803 50690803 + Missense_Mutation SNP A A G TCGA-26-5134-01A-01D-1486-08 TCGA-26-5134-10A-01D-1486-08 g.chr10:50690803A>G c.2099T>C c.(2098-2100)tTg>tCg p.L700S HNSC 10 50667067 50667067 + Missense_Mutation SNP C C G TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr10:50667067C>G c.4276G>C c.(4276-4278)Gac>Cac p.D1426H HNSC 10 50669597 50669597 + Missense_Mutation SNP C C T TCGA-BB-7870-01A-11D-2229-08 TCGA-BB-7870-10A-01D-2229-08 g.chr10:50669597C>T c.3784G>A c.(3784-3786)Gtg>Atg p.V1262M HNSC 10 50678260 50678260 + Missense_Mutation SNP T T A TCGA-CV-6940-01A-11D-1912-08 TCGA-CV-6940-10A-01D-1912-08 g.chr10:50678260T>A c.3746A>T c.(3745-3747)gAt>gTt p.D1249V HNSC 10 50678456 50678456 + Missense_Mutation SNP T T C TCGA-CV-7253-01A-11D-2012-08 TCGA-CV-7253-10A-01D-2013-08 g.chr10:50678456T>C c.3550A>G c.(3550-3552)Aaa>Gaa p.K1184E HNSC 10 50686430 50686430 + Missense_Mutation SNP C C G TCGA-F7-A50J-01A-21D-A28R-08 TCGA-F7-A50J-10A-01D-A28U-08 g.chr10:50686430C>G c.2256G>C c.(2254-2256)atG>atC p.M752I HNSC 10 50690871 50690871 + Silent SNP C C G TCGA-CN-A63U-01A-11D-A30E-08 TCGA-CN-A63U-10A-01D-A30H-08 g.chr10:50690871C>G c.2031G>C c.(2029-2031)ccG>ccC p.P677P HNSC 10 50691445 50691445 + Missense_Mutation SNP C C T TCGA-CV-A6K1-01A-11D-A31L-08 TCGA-CV-A6K1-10A-01D-A31J-08 g.chr10:50691445C>T c.1939G>A c.(1939-1941)Gaa>Aaa p.E647K HNSC 10 50732560 50732560 + Missense_Mutation SNP C C A TCGA-CN-6012-01A-11D-1683-08 TCGA-CN-6012-10A-01D-1683-08 g.chr10:50732560C>A c.916G>T c.(916-918)Gcc>Tcc p.A306S HNSC 10 50732641 50732641 + Missense_Mutation SNP C C T TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr10:50732641C>T c.835G>A c.(835-837)Gca>Aca p.A279T KIPAN 10 50668440 50668440 + Silent SNP T T C TCGA-O9-A75Z-01A-11D-A33Q-10 TCGA-O9-A75Z-10A-01D-A33Q-10 g.chr10:50668440T>C c.4041A>G c.(4039-4041)acA>acG p.T1347T KIPAN 10 50678573 50678573 + Missense_Mutation SNP C C T TCGA-A3-3357-01A-02D-1421-08 TCGA-A3-3357-11A-01D-1421-08 g.chr10:50678573C>T c.3433G>A c.(3433-3435)Gaa>Aaa p.E1145K KIPAN 10 50679145 50679146 + Frame_Shift_Ins INS - - A TCGA-UZ-A9PS-01A-11D-A42J-10 TCGA-UZ-A9PS-10A-01D-A42M-10 g.chr10:50679145_50679146insA c.2945_2946insT c.(2944-2946)ttgfs p.L982fs KIPAN 10 50681040 50681040 + Missense_Mutation SNP C C T TCGA-P4-A5E6-01A-11D-A28G-10 TCGA-P4-A5E6-11A-22D-A28G-10 g.chr10:50681040C>T c.2744G>A c.(2743-2745)cGg>cAg p.R915Q KIPAN 10 50690813 50690813 + Silent SNP A A G TCGA-B0-5099-01A-01D-1421-08 TCGA-B0-5099-11A-01D-1421-08 g.chr10:50690813A>G c.2089T>C c.(2089-2091)Tta>Cta p.L697L KIPAN 10 50708590 50708590 + Missense_Mutation SNP T T C TCGA-WN-A9G9-01A-12D-A36X-10 TCGA-WN-A9G9-10A-01D-A370-10 g.chr10:50708590T>C c.1679A>G c.(1678-1680)aAt>aGt p.N560S KIPAN 10 50732231 50732231 + Silent SNP C C T TCGA-B0-5104-01A-01D-1421-08 TCGA-B0-5104-11A-01D-1421-08 g.chr10:50732231C>T c.1245G>A c.(1243-1245)aaG>aaA p.K415K KIPAN 10 50732744 50732744 + Missense_Mutation SNP C C A TCGA-CJ-5679-01A-11D-1534-10 TCGA-CJ-5679-11A-01D-1535-10 g.chr10:50732744C>A c.732G>T c.(730-732)caG>caT p.Q244H KIPAN 10 50738880 50738880 + Missense_Mutation SNP A A C TCGA-BP-4981-01A-01D-1462-08 TCGA-BP-4981-11A-01D-1462-08 g.chr10:50738880A>C c.429T>G c.(427-429)tgT>tgG p.C143W KIRC 10 50678573 50678573 + Missense_Mutation SNP C C T TCGA-A3-3357-01A-02D-1421-08 TCGA-A3-3357-11A-01D-1421-08 g.chr10:50678573C>T c.3433G>A c.(3433-3435)Gaa>Aaa p.E1145K KIRC 10 50690813 50690813 + Silent SNP A A G TCGA-B0-5099-01A-01D-1421-08 TCGA-B0-5099-11A-01D-1421-08 g.chr10:50690813A>G c.2089T>C c.(2089-2091)Tta>Cta p.L697L KIRC 10 50732231 50732231 + Silent SNP C C T TCGA-B0-5104-01A-01D-1421-08 TCGA-B0-5104-11A-01D-1421-08 g.chr10:50732231C>T c.1245G>A c.(1243-1245)aaG>aaA p.K415K KIRC 10 50732744 50732744 + Missense_Mutation SNP C C A TCGA-CJ-5679-01A-11D-1534-10 TCGA-CJ-5679-11A-01D-1535-10 g.chr10:50732744C>A c.732G>T c.(730-732)caG>caT p.Q244H KIRC 10 50738880 50738880 + Missense_Mutation SNP A A C TCGA-BP-4981-01A-01D-1462-08 TCGA-BP-4981-11A-01D-1462-08 g.chr10:50738880A>C c.429T>G c.(427-429)tgT>tgG p.C143W KIRP 10 50668440 50668440 + Silent SNP T T C TCGA-O9-A75Z-01A-11D-A33Q-10 TCGA-O9-A75Z-10A-01D-A33Q-10 g.chr10:50668440T>C c.4041A>G c.(4039-4041)acA>acG p.T1347T KIRP 10 50679145 50679146 + Frame_Shift_Ins INS - - A TCGA-UZ-A9PS-01A-11D-A42J-10 TCGA-UZ-A9PS-10A-01D-A42M-10 g.chr10:50679145_50679146insA c.2945_2946insT c.(2944-2946)ttgfs p.L982fs KIRP 10 50681040 50681040 + Missense_Mutation SNP C C T TCGA-P4-A5E6-01A-11D-A28G-10 TCGA-P4-A5E6-11A-22D-A28G-10 g.chr10:50681040C>T c.2744G>A c.(2743-2745)cGg>cAg p.R915Q KIRP 10 50708590 50708590 + Missense_Mutation SNP T T C TCGA-WN-A9G9-01A-12D-A36X-10 TCGA-WN-A9G9-10A-01D-A370-10 g.chr10:50708590T>C c.1679A>G c.(1678-1680)aAt>aGt p.N560S LGG 10 50667030 50667030 + Missense_Mutation SNP T T C TCGA-HT-7687-01A-11D-2253-08 TCGA-HT-7687-10A-01D-2253-08 g.chr10:50667030T>C c.4313A>G c.(4312-4314)cAg>cGg p.Q1438R LGG 10 50667171 50667171 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:50667171G>A c.4172C>T c.(4171-4173)gCt>gTt p.A1391V LGG 10 50669556 50669556 + Silent SNP G G A TCGA-E1-A7YL-01A-11D-A34A-08 TCGA-E1-A7YL-10A-01D-A34A-08 g.chr10:50669556G>A c.3825C>T c.(3823-3825)gcC>gcT p.A1275A LIHC 10 50681069 50681069 + Silent SNP T T C TCGA-G3-AAV6-01A-21D-A36X-10 TCGA-G3-AAV6-10A-01D-A370-10 g.chr10:50681069T>C c.2715A>G c.(2713-2715)acA>acG p.T905T LIHC 10 50690818 50690818 + Missense_Mutation SNP C C A TCGA-DD-A39X-01A-11D-A20W-10 TCGA-DD-A39X-11A-11D-A20W-10 g.chr10:50690818C>A c.2084G>T c.(2083-2085)gGa>gTa p.G695V LIHC 10 50701191 50701191 + Missense_Mutation SNP T T C TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr10:50701191T>C c.1793A>G c.(1792-1794)cAt>cGt p.H598R LIHC 10 50701217 50701217 + Nonsense_Mutation SNP C C T TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr10:50701217C>T c.1767G>A c.(1765-1767)tgG>tgA p.W589* LIHC 10 50732464 50732464 + Missense_Mutation SNP T T A TCGA-CC-5263-01A-01D-A12Z-10 TCGA-CC-5263-10B-01D-A12Z-10 g.chr10:50732464T>A c.1012A>T c.(1012-1014)Agg>Tgg p.R338W LUAD 10 50666958 50666958 + Missense_Mutation SNP T T A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr10:50666958T>A c.4385A>T c.(4384-4386)cAg>cTg p.Q1462L LUAD 10 50667128 50667128 + Silent SNP T T C TCGA-55-A48Z-01A-12D-A24P-08 TCGA-55-A48Z-10A-01D-A24P-08 g.chr10:50667128T>C c.4215A>G c.(4213-4215)ttA>ttG p.L1405L LUAD 10 50667157 50667157 + Missense_Mutation SNP T T C TCGA-55-7573-01A-11D-2036-08 TCGA-55-7573-11A-01D-2036-08 g.chr10:50667157T>C c.4186A>G c.(4186-4188)Aga>Gga p.R1396G LUAD 10 50667200 50667200 + Silent SNP G G A TCGA-05-4244-01A-01D-1105-08 TCGA-05-4244-10A-01D-1105-08 g.chr10:50667200G>A c.4143C>T c.(4141-4143)tcC>tcT p.S1381S LUAD 10 50668435 50668435 + Missense_Mutation SNP G G T TCGA-17-Z025-01A-01W-0746-08 TCGA-17-Z025-11A-01W-0746-08 g.chr10:50668435G>T c.4046C>A c.(4045-4047)cCa>cAa p.P1349Q LUAD 10 50668476 50668476 + Missense_Mutation SNP C C A TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr10:50668476C>A c.4005G>T c.(4003-4005)agG>agT p.R1335S LUAD 10 50678401 50678401 + Missense_Mutation SNP G G A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr10:50678401G>A c.3605C>T c.(3604-3606)cCa>cTa p.P1202L LUAD 10 50678798 50678798 + Missense_Mutation SNP C C T TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr10:50678798C>T c.3208G>A c.(3208-3210)Gaa>Aaa p.E1070K LUAD 10 50679084 50679084 + Missense_Mutation SNP C C G TCGA-67-3771-01A-01D-1040-01 TCGA-67-3771-10A-01D-1040-01 g.chr10:50679084C>G c.3007G>C c.(3007-3009)Gag>Cag p.E1003Q LUAD 10 50679103 50679103 + Missense_Mutation SNP G G C TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr10:50679103G>C c.2988C>G c.(2986-2988)ttC>ttG p.F996L LUAD 10 50680512 50680512 + Missense_Mutation SNP C C A TCGA-73-4658-01A-01D-1753-08 TCGA-73-4658-11A-01D-1753-08 g.chr10:50680512C>A c.2834G>T c.(2833-2835)cGg>cTg p.R945L LUAD 10 50681630 50681630 + Silent SNP G G A TCGA-86-8056-01A-11D-2238-08 TCGA-86-8056-10A-01D-2238-08 g.chr10:50681630G>A c.2602C>T c.(2602-2604)Ctg>Ttg p.L868L LUAD 10 50686483 50686483 + Nonsense_Mutation SNP G G A TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr10:50686483G>A c.2203C>T c.(2203-2205)Cga>Tga p.R735* LUAD 10 50690785 50690785 + Missense_Mutation SNP T T A TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr10:50690785T>A c.2117A>T c.(2116-2118)cAg>cTg p.Q706L LUAD 10 50691563 50691563 + Splice_Site SNP C C A TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr10:50691563C>A c.e9-1 LUAD 10 50708677 50708677 + Missense_Mutation SNP C C G TCGA-75-7031-01A-11D-1945-08 TCGA-75-7031-10A-01D-1946-08 g.chr10:50708677C>G c.1592G>C c.(1591-1593)gGa>gCa p.G531A LUAD 10 50732182 50732182 + Frame_Shift_Del DEL C C - TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr10:50732182delC c.1294delG c.(1294-1296)gaafs p.E433fs LUAD 10 50732274 50732274 + Missense_Mutation SNP T T C TCGA-91-6848-01A-11D-1945-08 TCGA-91-6848-11A-01D-1945-08 g.chr10:50732274T>C c.1202A>G c.(1201-1203)gAc>gGc p.D401G LUAD 10 50732305 50732305 + Frame_Shift_Del DEL C C - TCGA-17-Z051-01A-01W-0747-08 TCGA-17-Z051-11A-01W-0747-08 g.chr10:50732305delC c.1171delG c.(1171-1173)gcafs p.A391fs LUAD 10 50732561 50732561 + Silent SNP T T A TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-10A-01D-2036-08 g.chr10:50732561T>A c.915A>T c.(913-915)ccA>ccT p.P305P LUAD 10 50732718 50732718 + Missense_Mutation SNP G G C TCGA-91-6836-01A-21D-1855-08 TCGA-91-6836-11A-01D-1855-08 g.chr10:50732718G>C c.758C>G c.(757-759)cCt>cGt p.P253R LUAD 10 50732741 50732741 + Missense_Mutation SNP C C T TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr10:50732741C>T c.735G>A c.(733-735)atG>atA p.M245I LUAD 10 50732792 50732792 + Silent SNP G G A TCGA-97-A4M0-01A-11D-A24P-08 TCGA-97-A4M0-10A-01D-A24P-08 g.chr10:50732792G>A c.684C>T c.(682-684)ctC>ctT p.L228L LUAD 10 50736571 50736571 + Splice_Site SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr10:50736571C>A c.544G>T c.(544-546)Gaa>Taa p.E182* LUAD 10 50740724 50740724 + Frame_Shift_Del DEL C C - TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr10:50740724delC c.287delG c.(286-288)ggtfs p.G96fs LUAD 10 50740740 50740740 + Missense_Mutation SNP C C G TCGA-99-8025-01A-11D-2238-08 TCGA-99-8025-10A-01D-2238-08 g.chr10:50740740C>G c.271G>C c.(271-273)Gag>Cag p.E91Q LUAD 10 50740774 50740774 + Missense_Mutation SNP C C G TCGA-17-Z062-01A-01W-0747-08 TCGA-17-Z062-11A-01W-0747-08 g.chr10:50740774C>G c.237G>C c.(235-237)caG>caC p.Q79H LUSC 10 50678601 50678601 + Silent SNP T T C TCGA-39-5037-01A-01D-1441-08 TCGA-39-5037-11A-01D-1441-08 g.chr10:50678601T>C c.3405A>G c.(3403-3405)acA>acG p.T1135T LUSC 10 50690811 50690811 + Missense_Mutation SNP T T A TCGA-60-2707-01A-01D-1522-08 TCGA-60-2707-11A-01D-1522-08 g.chr10:50690811T>A c.2091A>T c.(2089-2091)ttA>ttT p.L697F LUSC 10 50691393 50691393 + Splice_Site SNP T T A TCGA-66-2792-01A-01D-0983-08 TCGA-66-2792-11A-01D-0983-08 g.chr10:50691393T>A c.1991A>T c.(1990-1992)cAg>cTg p.Q664L LUSC 10 50732520 50732520 + Missense_Mutation SNP C C G TCGA-63-5131-01A-01D-1441-08 TCGA-63-5131-10A-01D-1441-08 g.chr10:50732520C>G c.956G>C c.(955-957)aGa>aCa p.R319T OV 10 50701242 50701242 + Nonsense_Mutation SNP C C T TCGA-29-1698-01A-01W-0633-09 TCGA-29-1698-10A-01W-0633-09 g.chr10:50701242C>T c.1742G>A c.(1741-1743)tGg>tAg p.W581* OV 10 50708600 50708600 + Missense_Mutation SNP G G C TCGA-04-1332-01A-01W-0488-09 TCGA-04-1332-10A-01W-0489-09 g.chr10:50708600G>C c.1669C>G c.(1669-1671)Cgt>Ggt p.R557G OV 10 50708699 50708699 + Nonsense_Mutation SNP G G A TCGA-24-1104-01A-01W-0488-09 TCGA-24-1104-10A-01W-0488-09 g.chr10:50708699G>A c.1570C>T c.(1570-1572)Cag>Tag p.Q524* OV 10 50738887 50738887 + Splice_Site SNP C C A TCGA-61-2008-01A-02W-0722-08 TCGA-61-2008-11A-01W-0722-08 g.chr10:50738887C>A c.e3-1 PAAD 10 50678238 50678238 + Missense_Mutation SNP G G T TCGA-YB-A89D-01A-12D-A36O-08 TCGA-YB-A89D-10A-01D-A367-08 g.chr10:50678238G>T c.3768C>A c.(3766-3768)ttC>ttA p.F1256L PAAD 10 50678363 50678363 + Missense_Mutation SNP C C T TCGA-RL-AAAS-01A-32D-A397-08 TCGA-RL-AAAS-10A-01D-A39A-08 g.chr10:50678363C>T c.3643G>A c.(3643-3645)Gcc>Acc p.A1215T PAAD 10 50678629 50678629 + Missense_Mutation SNP T T C TCGA-OE-A75W-01A-12D-A32N-08 TCGA-OE-A75W-10A-01D-A32N-08 g.chr10:50678629T>C c.3377A>G c.(3376-3378)aAt>aGt p.N1126S PAAD 10 50678905 50678905 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:50678905C>T c.3101G>A c.(3100-3102)tGc>tAc p.C1034Y PRAD 10 50666944 50666944 + Nonsense_Mutation SNP G G A TCGA-EJ-5542-01A-01D-1576-08 TCGA-EJ-5542-10A-01D-1577-08 g.chr10:50666944G>A c.4399C>T c.(4399-4401)Cga>Tga p.R1467* PRAD 10 50669577 50669577 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:50669577G>A c.3804C>T c.(3802-3804)caC>caT p.H1268H PRAD 10 50680468 50680469 + Frame_Shift_Del DEL AC AC - TCGA-CH-5769-01A-11D-1576-08 TCGA-CH-5769-11A-01D-1576-08 g.chr10:50680468_50680469delAC c.2877_2878delGT c.(2875-2880)gtgtacfs p.Y960fs PRAD 10 50736488 50736492 + Frame_Shift_Del DEL ATCTA ATCTA - TCGA-G9-6494-01A-11D-1786-08 TCGA-G9-6494-10A-01D-1786-08 g.chr10:50736488_50736492delATCTA c.623_627delTAGAT c.(622-627)ctagatfs p.LD208fs PRAD 10 50740946 50740946 + Missense_Mutation SNP G G C TCGA-KK-A7AW-01A-11D-A32B-08 TCGA-KK-A7AW-11A-11D-A329-08 g.chr10:50740946G>C c.65C>G c.(64-66)cCt>cGt p.P22R PRAD 10 50740993 50740993 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:50740993G>A c.18C>T c.(16-18)atC>atT p.I6I READ 10 50666882 50666882 + Silent SNP T T C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:50666882T>C c.4461A>G c.(4459-4461)aaA>aaG p.K1487K READ 10 50667133 50667133 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:50667133G>A c.4210C>T c.(4210-4212)Cgt>Tgt p.R1404C READ 10 50678590 50678590 + Missense_Mutation SNP G G A TCGA-AG-A02G-01A-01W-A00E-09 TCGA-AG-A02G-10A-01W-A00E-09 g.chr10:50678590G>A c.3416C>T c.(3415-3417)tCt>tTt p.S1139F READ 10 50678650 50678650 + Missense_Mutation SNP T T C TCGA-EI-6506-01A-11D-1733-10 TCGA-EI-6506-10A-01D-1733-10 g.chr10:50678650T>C c.3356A>G c.(3355-3357)gAg>gGg p.E1119G READ 10 50678894 50678894 + Missense_Mutation SNP T T C TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr10:50678894T>C c.3112A>G c.(3112-3114)Aga>Gga p.R1038G READ 10 50678894 50678894 + Missense_Mutation SNP T T C TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr10:50678894T>C c.3112A>G c.(3112-3114)Aga>Gga p.R1038G READ 10 50736558 50736558 + Missense_Mutation SNP T T C TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:50736558T>C c.557A>G c.(556-558)aAa>aGa p.K186R SKCM 10 50666971 50666971 + Silent SNP A A G TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr10:50666971A>G c.4372T>C c.(4372-4374)Tta>Cta p.L1458L SKCM 10 50667245 50667245 + Silent SNP G G A TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr10:50667245G>A c.4098C>T c.(4096-4098)gtC>gtT p.V1366V SKCM 10 50678350 50678350 + Missense_Mutation SNP C C T TCGA-GN-A4U4-06A-11D-A32N-08 TCGA-GN-A4U4-10B-01D-A32N-08 g.chr10:50678350C>T c.3656G>A c.(3655-3657)gGa>gAa p.G1219E SKCM 10 50678838 50678838 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr10:50678838G>A c.3168C>T c.(3166-3168)ttC>ttT p.F1056F SKCM 10 50679123 50679123 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:50679123G>A c.2968C>T c.(2968-2970)Cca>Tca p.P990S SKCM 10 50682166 50682166 + Nonsense_Mutation SNP C C T TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr10:50682166C>T c.2505G>A c.(2503-2505)tgG>tgA p.W835* SKCM 10 50682237 50682237 + Missense_Mutation SNP A A T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr10:50682237A>T c.2434T>A c.(2434-2436)Ttt>Att p.F812I SKCM 10 50682238 50682238 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr10:50682238G>A c.2433C>T c.(2431-2433)ctC>ctT p.L811L SKCM 10 50684298 50684298 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:50684298G>A c.2345C>T c.(2344-2346)tCc>tTc p.S782F SKCM 10 50684306 50684306 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr10:50684306G>A c.2337C>T c.(2335-2337)ttC>ttT p.F779F SKCM 10 50686467 50686467 + Missense_Mutation SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr10:50686467G>A c.2219C>T c.(2218-2220)cCa>cTa p.P740L SKCM 10 50690779 50690779 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr10:50690779G>A c.2123C>T c.(2122-2124)tCc>tTc p.S708F SKCM 10 50690901 50690901 + Silent SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr10:50690901G>A c.2001C>T c.(1999-2001)acC>acT p.T667T SKCM 10 50691522 50691522 + Missense_Mutation SNP A A G TCGA-GN-A265-06A-21D-A197-08 TCGA-GN-A265-10A-01D-A199-08 g.chr10:50691522A>G c.1862T>C c.(1861-1863)tTg>tCg p.L621S SKCM 10 50691550 50691550 + Nonsense_Mutation SNP G G A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr10:50691550G>A c.1834C>T c.(1834-1836)Cga>Tga p.R612* SKCM 10 50691556 50691556 + Silent SNP G G A TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr10:50691556G>A c.1828C>T c.(1828-1830)Cta>Tta p.L610L SKCM 10 50701195 50701195 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:50701195G>A c.1789C>T c.(1789-1791)Cta>Tta p.L597L SKCM 10 50701288 50701288 + Silent SNP A A G TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr10:50701288A>G c.1696T>C c.(1696-1698)Ttg>Ctg p.L566L SKCM 10 50736487 50736487 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:50736487G>A c.628C>T c.(628-630)Cac>Tac p.H210Y SKCM 10 50740647 50740647 + Missense_Mutation SNP G G A TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr10:50740647G>A c.364C>T c.(364-366)Cgt>Tgt p.R122C SKCM 10 50740648 50740648 + Missense_Mutation SNP G G T TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr10:50740648G>T c.363C>A c.(361-363)agC>agA p.S121R SKCM 10 50740841 50740841 + Missense_Mutation SNP G G A TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr10:50740841G>A c.170C>T c.(169-171)tCt>tTt p.S57F SKCM 10 50740971 50740971 + Missense_Mutation SNP C C T TCGA-EE-A29C-06A-21D-A197-08 TCGA-EE-A29C-10A-01D-A199-08 g.chr10:50740971C>T c.40G>A c.(40-42)Gag>Aag p.E14K SKCM 10 50740990 50740990 + Silent SNP G G A TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr10:50740990G>A c.21C>T c.(19-21)ccC>ccT p.P7P

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 10 50669504 50669504 single base substitution C T exon_variant BLCA-US 10 50669504 50669504 single base substitution C T missense_variant A1293T 3877G>A BLCA-US 10 50669504 50669504 single base substitution C T missense_variant A663T 1987G>A BLCA-US 10 50678885 50678885 single base substitution G A stop_gained Q1041* 3121C>T BLCA-US 10 50678885 50678885 single base substitution G A stop_gained Q411* 1231C>T BLCA-US 10 50678885 50678885 single base substitution G A upstream_gene_variant BLCA-US 10 50682233 50682233 single base substitution G A missense_variant S183F 548C>T BLCA-US 10 50682233 50682233 single base substitution G A missense_variant S813F 2438C>T BLCA-US 10 50682233 50682233 single base substitution G A upstream_gene_variant BLCA-US 10 50690842 50690842 single base substitution G C downstream_gene_variant BLCA-US 10 50690842 50690842 single base substitution G C missense_variant S57W 170C>G BLCA-US 10 50690842 50690842 single base substitution G C missense_variant S687W 2060C>G BLCA-US 10 50708622 50708622 single base substitution C G 5_prime_UTR_variant BLCA-US 10 50708622 50708622 single base substitution C G exon_variant BLCA-US 10 50708622 50708622 single base substitution C G synonymous_variant L549L 1647G>C BLCA-US 10 50732248 50732248 single base substitution C T downstream_gene_variant BLCA-US 10 50732248 50732248 single base substitution C T missense_variant G410S 1228G>A BLCA-US 10 50740776 50740776 single base substitution G A stop_gained Q79* 235C>T BLCA-US 10 50740776 50740776 single base substitution G A upstream_gene_variant BLCA-US 10 50740821 50740821 single base substitution C T missense_variant A64T 190G>A BLCA-US 10 50740821 50740821 single base substitution C T upstream_gene_variant BOCA-UK 10 50724488 50724488 single base substitution T C intron_variant BRCA-EU 10 50658599 50658599 single base substitution G C downstream_gene_variant BRCA-EU 10 50659833 50659833 single base substitution C A downstream_gene_variant BRCA-EU 10 50660900 50660900 single base substitution C G downstream_gene_variant BRCA-EU 10 50661609 50661609 single base substitution G A downstream_gene_variant BRCA-EU 10 50663212 50663212 single base substitution C T downstream_gene_variant BRCA-EU 10 50663788 50663788 single base substitution C T 3_prime_UTR_variant BRCA-EU 10 50663788 50663788 single base substitution C T downstream_gene_variant BRCA-EU 10 50665740 50665740 single base substitution T C 3_prime_UTR_variant BRCA-EU 10 50665740 50665740 single base substitution T C downstream_gene_variant BRCA-EU 10 50665880 50665880 single base substitution A C 3_prime_UTR_variant BRCA-EU 10 50665880 50665880 single base substitution A C downstream_gene_variant BRCA-EU 10 50665921 50665921 single base substitution G A 3_prime_UTR_variant BRCA-EU 10 50665921 50665921 single base substitution G A downstream_gene_variant BRCA-EU 10 50666497 50666497 deletion of <=200bp A - 3_prime_UTR_variant BRCA-EU 10 50666497 50666497 deletion of <=200bp A - downstream_gene_variant BRCA-EU 10 50668117 50668117 single base substitution C T exon_variant BRCA-EU 10 50668117 50668117 single base substitution C T intron_variant BRCA-EU 10 50668371 50668371 single base substitution C T exon_variant BRCA-EU 10 50668371 50668371 single base substitution C T intron_variant BRCA-EU 10 50676013 50676013 single base substitution C G intron_variant BRCA-EU 10 50676355 50676355 single base substitution G C intron_variant BRCA-EU 10 50677535 50677535 deletion of <=200bp T - intron_variant BRCA-EU 10 50677755 50677755 single base substitution C A intron_variant BRCA-EU 10 50678366 50678366 single base substitution C T missense_variant D1214N 3640G>A BRCA-EU 10 50678366 50678366 single base substitution C T missense_variant D584N 1750G>A BRCA-EU 10 50678366 50678366 single base substitution C T upstream_gene_variant BRCA-EU 10 50682005 50682005 single base substitution C A intron_variant BRCA-EU 10 50682005 50682005 single base substitution C A upstream_gene_variant BRCA-EU 10 50683171 50683171 single base substitution T A intron_variant BRCA-EU 10 50683171 50683171 single base substitution T A upstream_gene_variant BRCA-EU 10 50683895 50683895 single base substitution C T intron_variant BRCA-EU 10 50686006 50686006 single base substitution C T intron_variant BRCA-EU 10 50686087 50686087 single base substitution C G intron_variant BRCA-EU 10 50686171 50686171 single base substitution G A intron_variant BRCA-EU 10 50686389 50686389 single base substitution G A intron_variant BRCA-EU 10 50686418 50686418 single base substitution C G downstream_gene_variant BRCA-EU 10 50686418 50686418 single base substitution C G missense_variant L126F 378G>C BRCA-EU 10 50686418 50686418 single base substitution C G missense_variant L756F 2268G>C BRCA-EU 10 50686443 50686443 single base substitution G A downstream_gene_variant BRCA-EU 10 50686443 50686443 single base substitution G A missense_variant S118L 353C>T BRCA-EU 10 50686443 50686443 single base substitution G A missense_variant S748L 2243C>T BRCA-EU 10 50687067 50687067 single base substitution C A downstream_gene_variant BRCA-EU 10 50687067 50687067 single base substitution C A intron_variant BRCA-EU 10 50687241 50687241 insertion of <=200bp - A downstream_gene_variant BRCA-EU 10 50687241 50687241 insertion of <=200bp - A intron_variant BRCA-EU 10 50688070 50688070 single base substitution C T downstream_gene_variant BRCA-EU 10 50688070 50688070 single base substitution C T intron_variant BRCA-EU 10 50689282 50689282 single base substitution C T downstream_gene_variant BRCA-EU 10 50689282 50689282 single base substitution C T intron_variant BRCA-EU 10 50689645 50689645 single base substitution G A downstream_gene_variant BRCA-EU 10 50689645 50689645 single base substitution G A intron_variant BRCA-EU 10 50690352 50690352 single base substitution C A downstream_gene_variant BRCA-EU 10 50690352 50690352 single base substitution C A intron_variant BRCA-EU 10 50690883 50690883 single base substitution C T downstream_gene_variant BRCA-EU 10 50690883 50690883 single base substitution C T synonymous_variant L43L 129G>A BRCA-EU 10 50690883 50690883 single base substitution C T synonymous_variant L673L 2019G>A BRCA-EU 10 50692160 50692160 deletion of <=200bp A - intron_variant BRCA-EU 10 50692172 50692172 single base substitution T A intron_variant BRCA-EU 10 50693023 50693023 single base substitution A C intron_variant BRCA-EU 10 50694284 50694284 single base substitution G C intron_variant BRCA-EU 10 50694758 50694758 single base substitution A T intron_variant BRCA-EU 10 50696492 50696492 deletion of <=200bp A - intron_variant BRCA-EU 10 50696898 50696898 single base substitution C T intron_variant BRCA-EU 10 50697491 50697491 single base substitution C T intron_variant BRCA-EU 10 50699197 50699197 single base substitution T C intron_variant BRCA-EU 10 50703953 50703953 single base substitution C T intron_variant BRCA-EU 10 50707956 50707956 single base substitution A G intron_variant BRCA-EU 10 50708808 50708808 single base substitution G A intron_variant BRCA-EU 10 50709372 50709372 single base substitution G T intron_variant BRCA-EU 10 50709993 50709993 single base substitution G A intron_variant BRCA-EU 10 50710042 50710042 deletion of <=200bp T - intron_variant BRCA-EU 10 50712289 50712289 single base substitution A G intron_variant BRCA-EU 10 50712289 50712289 single base substitution A G upstream_gene_variant BRCA-EU 10 50712476 50712476 single base substitution T C intron_variant BRCA-EU 10 50712476 50712476 single base substitution T C upstream_gene_variant BRCA-EU 10 50715540 50715540 single base substitution C A intron_variant BRCA-EU 10 50715540 50715540 single base substitution C A upstream_gene_variant BRCA-EU 10 50715542 50715542 single base substitution C A intron_variant BRCA-EU 10 50715542 50715542 single base substitution C A upstream_gene_variant BRCA-EU 10 50715932 50715932 single base substitution G C intron_variant BRCA-EU 10 50715932 50715932 single base substitution G C upstream_gene_variant BRCA-EU 10 50715962 50715962 single base substitution G A intron_variant BRCA-EU 10 50715962 50715962 single base substitution G A upstream_gene_variant BRCA-EU 10 50716751 50716751 single base substitution C G intron_variant BRCA-EU 10 50716751 50716751 single base substitution C G upstream_gene_variant BRCA-EU 10 50718158 50718158 single base substitution C T intron_variant BRCA-EU 10 50718158 50718158 single base substitution C T upstream_gene_variant BRCA-EU 10 50718299 50718299 single base substitution C T intron_variant BRCA-EU 10 50718299 50718299 single base substitution C T upstream_gene_variant BRCA-EU 10 50719265 50719265 single base substitution C A intron_variant BRCA-EU 10 50719896 50719896 single base substitution G C intron_variant BRCA-EU 10 50720102 50720102 single base substitution T C intron_variant BRCA-EU 10 50720637 50720637 single base substitution G T intron_variant BRCA-EU 10 50720773 50720773 single base substitution T C intron_variant BRCA-EU 10 50720823 50720823 single base substitution A G intron_variant BRCA-EU 10 50721717 50721717 single base substitution T G intron_variant BRCA-EU 10 50723033 50723033 single base substitution A G intron_variant BRCA-EU 10 50723391 50723391 single base substitution A C intron_variant BRCA-EU 10 50723473 50723473 single base substitution C T intron_variant BRCA-EU 10 50724515 50724515 single base substitution C A intron_variant BRCA-EU 10 50725059 50725059 single base substitution T A intron_variant BRCA-EU 10 50725539 50725539 single base substitution G C intron_variant BRCA-EU 10 50726036 50726036 deletion of <=200bp A - intron_variant BRCA-EU 10 50728839 50728839 single base substitution T C downstream_gene_variant BRCA-EU 10 50728839 50728839 single base substitution T C intron_variant BRCA-EU 10 50729824 50729824 single base substitution G A downstream_gene_variant BRCA-EU 10 50729824 50729824 single base substitution G A intron_variant BRCA-EU 10 50731711 50731711 single base substitution C T downstream_gene_variant BRCA-EU 10 50731711 50731711 single base substitution C T intron_variant BRCA-EU 10 50731975 50731975 single base substitution G A downstream_gene_variant BRCA-EU 10 50731975 50731975 single base substitution G A intron_variant BRCA-EU 10 50735397 50735397 single base substitution A G downstream_gene_variant BRCA-EU 10 50735397 50735397 single base substitution A G intron_variant BRCA-EU 10 50735586 50735586 single base substitution G A downstream_gene_variant BRCA-EU 10 50735586 50735586 single base substitution G A intron_variant BRCA-EU 10 50735614 50735614 single base substitution G C downstream_gene_variant BRCA-EU 10 50735614 50735614 single base substitution G C intron_variant BRCA-EU 10 50736107 50736107 single base substitution C G downstream_gene_variant BRCA-EU 10 50736107 50736107 single base substitution C G intron_variant BRCA-EU 10 50736367 50736367 single base substitution C G downstream_gene_variant BRCA-EU 10 50736367 50736367 single base substitution C G intron_variant BRCA-EU 10 50736881 50736881 single base substitution A T downstream_gene_variant BRCA-EU 10 50736881 50736881 single base substitution A T intron_variant BRCA-EU 10 50738334 50738334 single base substitution C T downstream_gene_variant BRCA-EU 10 50738334 50738334 single base substitution C T intron_variant BRCA-EU 10 50739664 50739664 single base substitution C T intron_variant BRCA-EU 10 50739664 50739664 single base substitution C T upstream_gene_variant BRCA-EU 10 50741730 50741730 single base substitution T C intron_variant BRCA-EU 10 50741730 50741730 single base substitution T C upstream_gene_variant BRCA-EU 10 50743054 50743054 single base substitution C G intron_variant BRCA-EU 10 50743054 50743054 single base substitution C G upstream_gene_variant BRCA-EU 10 50747658 50747658 single base substitution C G upstream_gene_variant BRCA-EU 10 50747871 50747871 single base substitution G A upstream_gene_variant BRCA-EU 10 50750405 50750405 single base substitution C G upstream_gene_variant BRCA-EU 10 50751351 50751351 single base substitution A G upstream_gene_variant BRCA-EU 10 50752453 50752453 deletion of <=200bp G - upstream_gene_variant BRCA-FR 10 50668117 50668117 single base substitution C T exon_variant BRCA-FR 10 50668117 50668117 single base substitution C T intron_variant BRCA-FR 10 50678556 50678556 single base substitution C A missense_variant K1150N 3450G>T BRCA-FR 10 50678556 50678556 single base substitution C A missense_variant K520N 1560G>T BRCA-FR 10 50678556 50678556 single base substitution C A upstream_gene_variant BRCA-FR 10 50686087 50686087 single base substitution C G intron_variant BRCA-FR 10 50694758 50694758 single base substitution A T intron_variant BRCA-FR 10 50698894 50698894 single base substitution G T intron_variant BRCA-FR 10 50709993 50709993 single base substitution G A intron_variant BRCA-FR 10 50712476 50712476 single base substitution T C intron_variant BRCA-FR 10 50712476 50712476 single base substitution T C upstream_gene_variant BRCA-FR 10 50719896 50719896 single base substitution G C intron_variant BRCA-FR 10 50736367 50736367 single base substitution C G downstream_gene_variant BRCA-FR 10 50736367 50736367 single base substitution C G intron_variant BRCA-KR 10 50669464 50669464 single base substitution C T exon_variant BRCA-KR 10 50669464 50669464 single base substitution C T missense_variant G1306E 3917G>A BRCA-KR 10 50669464 50669464 single base substitution C T missense_variant G676E 2027G>A BRCA-UK 10 50676355 50676355 single base substitution G C intron_variant BRCA-UK 10 50677755 50677755 single base substitution C A intron_variant BRCA-UK 10 50697338 50697338 single base substitution G A intron_variant BRCA-UK 10 50712289 50712289 single base substitution A G intron_variant BRCA-UK 10 50712289 50712289 single base substitution A G upstream_gene_variant BRCA-UK 10 50715540 50715540 single base substitution C A intron_variant BRCA-UK 10 50715540 50715540 single base substitution C A upstream_gene_variant BRCA-UK 10 50723493 50723493 single base substitution G C intron_variant BRCA-UK 10 50727981 50727981 single base substitution C G intron_variant BRCA-US 10 50667150 50667150 single base substitution T G downstream_gene_variant BRCA-US 10 50667150 50667150 single base substitution T G missense_variant H1398P 4193A>C BRCA-US 10 50667150 50667150 single base substitution T G missense_variant H768P 2303A>C BRCA-US 10 50667204 50667204 single base substitution G A downstream_gene_variant BRCA-US 10 50667204 50667204 single base substitution G A missense_variant S1380L 4139C>T BRCA-US 10 50667204 50667204 single base substitution G A missense_variant S750L 2249C>T BRCA-US 10 50668419 50668419 single base substitution C A exon_variant BRCA-US 10 50668419 50668419 single base substitution C A missense_variant Q1354H 4062G>T BRCA-US 10 50668419 50668419 single base substitution C A missense_variant Q724H 2172G>T BRCA-US 10 50668447 50668447 single base substitution G A exon_variant BRCA-US 10 50668447 50668447 single base substitution G A missense_variant S1345L 4034C>T BRCA-US 10 50668447 50668447 single base substitution G A missense_variant S715L 2144C>T BRCA-US 10 50678264 50678264 single base substitution C A exon_variant BRCA-US 10 50678264 50678264 single base substitution C A missense_variant D1248Y 3742G>T BRCA-US 10 50678264 50678264 single base substitution C A missense_variant D618Y 1852G>T BRCA-US 10 50678496 50678496 single base substitution C T synonymous_variant E1170E 3510G>A BRCA-US 10 50678496 50678496 single base substitution C T synonymous_variant E540E 1620G>A BRCA-US 10 50678496 50678496 single base substitution C T upstream_gene_variant BRCA-US 10 50678569 50678569 single base substitution C G missense_variant S1146T 3437G>C BRCA-US 10 50678569 50678569 single base substitution C G missense_variant S516T 1547G>C BRCA-US 10 50678569 50678569 single base substitution C G upstream_gene_variant BRCA-US 10 50679156 50679156 single base substitution T C missense_variant K349E 1045A>G BRCA-US 10 50679156 50679156 single base substitution T C missense_variant K979E 2935A>G BRCA-US 10 50679156 50679156 single base substitution T C upstream_gene_variant BRCA-US 10 50681546 50681546 single base substitution G A missense_variant P266S 796C>T BRCA-US 10 50681546 50681546 single base substitution G A missense_variant P896S 2686C>T BRCA-US 10 50681546 50681546 single base substitution G A upstream_gene_variant BRCA-US 10 50681587 50681587 single base substitution T G missense_variant Y252S 755A>C BRCA-US 10 50681587 50681587 single base substitution T G missense_variant Y882S 2645A>C BRCA-US 10 50681587 50681587 single base substitution T G upstream_gene_variant BRCA-US 10 50682204 50682204 single base substitution G T missense_variant P193T 577C>A BRCA-US 10 50682204 50682204 single base substitution G T missense_variant P823T 2467C>A BRCA-US 10 50682204 50682204 single base substitution G T upstream_gene_variant BRCA-US 10 50684343 50684343 single base substitution C T missense_variant R137H 410G>A BRCA-US 10 50684343 50684343 single base substitution C T missense_variant R767H 2300G>A BRCA-US 10 50690757 50690757 insertion of <=200bp - C downstream_gene_variant BRCA-US 10 50690757 50690757 insertion of <=200bp - C frameshift_variant G715G? BRCA-US 10 50690757 50690757 insertion of <=200bp - C frameshift_variant G85G? BRCA-US 10 50690883 50690883 single base substitution C A downstream_gene_variant BRCA-US 10 50690883 50690883 single base substitution C A synonymous_variant L43L 129G>T BRCA-US 10 50690883 50690883 single base substitution C A synonymous_variant L673L 2019G>T BRCA-US 10 50708659 50708659 single base substitution C T 5_prime_UTR_variant BRCA-US 10 50708659 50708659 single base substitution C T exon_variant BRCA-US 10 50708659 50708659 single base substitution C T missense_variant G537D 1610G>A BRCA-US 10 50723441 50723441 single base substitution G A intron_variant BRCA-US 10 50724809 50724809 single base substitution C T intron_variant BRCA-US 10 50725153 50725153 single base substitution C T intron_variant BRCA-US 10 50732269 50732269 single base substitution C T downstream_gene_variant BRCA-US 10 50732269 50732269 single base substitution C T missense_variant E403K 1207G>A BRCA-US 10 50732504 50732504 single base substitution T C downstream_gene_variant BRCA-US 10 50732504 50732504 single base substitution T C synonymous_variant K324K 972A>G BRCA-US 10 50732557 50732557 single base substitution G C downstream_gene_variant BRCA-US 10 50732557 50732557 single base substitution G C missense_variant P307A 919C>G BRCA-US 10 50732662 50732662 single base substitution C T downstream_gene_variant BRCA-US 10 50732662 50732662 single base substitution C T missense_variant E272K 814G>A BRCA-US 10 50732756 50732756 single base substitution G A downstream_gene_variant BRCA-US 10 50732756 50732756 single base substitution G A synonymous_variant I240I 720C>T BRCA-US 10 50736490 50736490 single base substitution C G downstream_gene_variant BRCA-US 10 50736490 50736490 single base substitution C G exon_variant BRCA-US 10 50736490 50736490 single base substitution C G missense_variant D209H 625G>C BTCA-JP 10 50686601 50686601 deletion of <=200bp A - downstream_gene_variant BTCA-JP 10 50686601 50686601 deletion of <=200bp A - intron_variant BTCA-JP 10 50723839 50723839 single base substitution A G intron_variant BTCA-JP 10 50736546 50736546 single base substitution G A downstream_gene_variant BTCA-JP 10 50736546 50736546 single base substitution G A exon_variant BTCA-JP 10 50736546 50736546 single base substitution G A missense_variant A190V 569C>T BTCA-JP 10 50740974 50740974 single base substitution G C missense_variant Q13E 37C>G BTCA-JP 10 50740974 50740974 single base substitution G C upstream_gene_variant BTCA-JP 10 50741033 50741033 insertion of <=200bp - A intron_variant BTCA-JP 10 50741033 50741033 insertion of <=200bp - A upstream_gene_variant CESC-US 10 50678926 50678926 single base substitution G C stop_gained S1027* 3080C>G CESC-US 10 50678926 50678926 single base substitution G C stop_gained S397* 1190C>G CESC-US 10 50678926 50678926 single base substitution G C upstream_gene_variant CESC-US 10 50732496 50732496 single base substitution C T downstream_gene_variant CESC-US 10 50732496 50732496 single base substitution C T missense_variant R327H 980G>A CESC-US 10 50732662 50732662 single base substitution C T downstream_gene_variant CESC-US 10 50732662 50732662 single base substitution C T missense_variant E272K 814G>A CESC-US 10 50732789 50732789 single base substitution C T downstream_gene_variant CESC-US 10 50732789 50732789 single base substitution C T missense_variant M229I 687G>A CESC-US 10 50740702 50740702 single base substitution G A synonymous_variant D103D 309C>T CESC-US 10 50740702 50740702 single base substitution G A upstream_gene_variant CLLE-ES 10 50661109 50661109 single base substitution T C downstream_gene_variant CLLE-ES 10 50712192 50712192 single base substitution T C intron_variant CLLE-ES 10 50712192 50712192 single base substitution T C upstream_gene_variant CLLE-ES 10 50735963 50735963 single base substitution C T downstream_gene_variant CLLE-ES 10 50735963 50735963 single base substitution C T intron_variant COAD-US 10 50667015 50667015 single base substitution C T downstream_gene_variant COAD-US 10 50667015 50667015 single base substitution C T missense_variant G1443D 4328G>A COAD-US 10 50667015 50667015 single base substitution C T missense_variant G813D 2438G>A COAD-US 10 50667140 50667140 single base substitution C T downstream_gene_variant COAD-US 10 50667140 50667140 single base substitution C T synonymous_variant L1401L 4203G>A COAD-US 10 50667140 50667140 single base substitution C T synonymous_variant L771L 2313G>A COAD-US 10 50669513 50669513 single base substitution C A exon_variant COAD-US 10 50669513 50669513 single base substitution C A missense_variant A1290S 3868G>T COAD-US 10 50669513 50669513 single base substitution C A missense_variant A660S 1978G>T COAD-US 10 50669533 50669533 single base substitution T C exon_variant COAD-US 10 50669533 50669533 single base substitution T C missense_variant E1283G 3848A>G COAD-US 10 50669533 50669533 single base substitution T C missense_variant E653G 1958A>G COAD-US 10 50678317 50678317 single base substitution C G exon_variant COAD-US 10 50678317 50678317 single base substitution C G missense_variant R1230P 3689G>C COAD-US 10 50678317 50678317 single base substitution C G missense_variant R600P 1799G>C COAD-US 10 50678369 50678369 single base substitution T C missense_variant R1213G 3637A>G COAD-US 10 50678369 50678369 single base substitution T C missense_variant R583G 1747A>G COAD-US 10 50678369 50678369 single base substitution T C upstream_gene_variant COAD-US 10 50678483 50678483 single base substitution C T missense_variant E1175K 3523G>A COAD-US 10 50678483 50678483 single base substitution C T missense_variant E545K 1633G>A COAD-US 10 50678483 50678483 single base substitution C T upstream_gene_variant COAD-US 10 50678717 50678717 single base substitution T C missense_variant M1097V 3289A>G COAD-US 10 50678717 50678717 single base substitution T C missense_variant M467V 1399A>G COAD-US 10 50678717 50678717 single base substitution T C upstream_gene_variant COAD-US 10 50679049 50679049 single base substitution C A missense_variant Q1014H 3042G>T COAD-US 10 50679049 50679049 single base substitution C A missense_variant Q384H 1152G>T COAD-US 10 50679049 50679049 single base substitution C A upstream_gene_variant COAD-US 10 50679169 50679169 deletion of <=200bp A - splice_region_variant COAD-US 10 50679169 50679169 deletion of <=200bp A - upstream_gene_variant COAD-US 10 50681008 50681008 deletion of <=200bp C - frameshift_variant A296 COAD-US 10 50681008 50681008 deletion of <=200bp C - frameshift_variant A926 COAD-US 10 50681008 50681008 deletion of <=200bp C - upstream_gene_variant COAD-US 10 50681033 50681033 single base substitution G A synonymous_variant G287G 861C>T COAD-US 10 50681033 50681033 single base substitution G A synonymous_variant G917G 2751C>T COAD-US 10 50681033 50681033 single base substitution G A upstream_gene_variant COAD-US 10 50690778 50690778 single base substitution G A downstream_gene_variant COAD-US 10 50690778 50690778 single base substitution G A synonymous_variant S708S 2124C>T COAD-US 10 50690778 50690778 single base substitution G A synonymous_variant S78S 234C>T COAD-US 10 50690872 50690872 single base substitution G A downstream_gene_variant COAD-US 10 50690872 50690872 single base substitution G A missense_variant P47L 140C>T COAD-US 10 50690872 50690872 single base substitution G A missense_variant P677L 2030C>T COAD-US 10 50691429 50691429 single base substitution C T exon_variant COAD-US 10 50691429 50691429 single base substitution C T missense_variant R22Q 65G>A COAD-US 10 50691429 50691429 single base substitution C T missense_variant R652Q 1955G>A COAD-US 10 50713973 50713973 single base substitution C T exon_variant COAD-US 10 50713973 50713973 single base substitution C T missense_variant E495K 1483G>A COAD-US 10 50713973 50713973 single base substitution C T upstream_gene_variant COAD-US 10 50723399 50723399 single base substitution C T intron_variant COAD-US 10 50723415 50723415 single base substitution T C intron_variant COAD-US 10 50723735 50723735 single base substitution A G intron_variant COAD-US 10 50724637 50724637 single base substitution A G intron_variant COAD-US 10 50725028 50725028 single base substitution C A intron_variant COAD-US 10 50732496 50732496 single base substitution C T downstream_gene_variant COAD-US 10 50732496 50732496 single base substitution C T missense_variant R327H 980G>A COAD-US 10 50738781 50738781 single base substitution T C exon_variant COAD-US 10 50738781 50738781 single base substitution T C synonymous_variant R176R 528A>G COCA-CN 10 50666943 50666943 single base substitution C T downstream_gene_variant COCA-CN 10 50666943 50666943 single base substitution C T missense_variant R1467Q 4400G>A COCA-CN 10 50666943 50666943 single base substitution C T missense_variant R837Q 2510G>A COCA-CN 10 50666994 50666994 single base substitution A G downstream_gene_variant COCA-CN 10 50666994 50666994 single base substitution A G missense_variant I1450T 4349T>C COCA-CN 10 50666994 50666994 single base substitution A G missense_variant I820T 2459T>C COCA-CN 10 50667132 50667132 single base substitution C T downstream_gene_variant COCA-CN 10 50667132 50667132 single base substitution C T missense_variant R1404H 4211G>A COCA-CN 10 50667132 50667132 single base substitution C T missense_variant R774H 2321G>A COCA-CN 10 50678251 50678251 single base substitution A C exon_variant COCA-CN 10 50678251 50678251 single base substitution A C missense_variant L1252W 3755T>G COCA-CN 10 50678251 50678251 single base substitution A C missense_variant L622W 1865T>G COCA-CN 10 50678476 50678476 single base substitution T G missense_variant N1177T 3530A>C COCA-CN 10 50678476 50678476 single base substitution T G missense_variant N547T 1640A>C COCA-CN 10 50678476 50678476 single base substitution T G upstream_gene_variant COCA-CN 10 50680895 50680895 single base substitution G A intron_variant COCA-CN 10 50680895 50680895 single base substitution G A upstream_gene_variant COCA-CN 10 50680933 50680933 single base substitution T A intron_variant COCA-CN 10 50680933 50680933 single base substitution T A upstream_gene_variant COCA-CN 10 50686409 50686409 single base substitution T G missense_variant K129N 387A>C COCA-CN 10 50686409 50686409 single base substitution T G missense_variant K759N 2277A>C COCA-CN 10 50690686 50690686 single base substitution A G downstream_gene_variant COCA-CN 10 50690686 50690686 single base substitution A G intron_variant COCA-CN 10 50691009 50691009 single base substitution C T downstream_gene_variant COCA-CN 10 50691009 50691009 single base substitution C T intron_variant COCA-CN 10 50692337 50692337 single base substitution A G intron_variant COCA-CN 10 50696705 50696705 single base substitution A T intron_variant COCA-CN 10 50705709 50705709 single base substitution C T intron_variant COCA-CN 10 50708681 50708681 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant COCA-CN 10 50708681 50708681 single base substitution G A exon_variant COCA-CN 10 50708681 50708681 single base substitution G A synonymous_variant L530L 1588C>T COCA-CN 10 50723687 50723687 single base substitution C T intron_variant COCA-CN 10 50723778 50723778 single base substitution T C intron_variant COCA-CN 10 50725153 50725153 single base substitution C T intron_variant COCA-CN 10 50732662 50732662 single base substitution C T downstream_gene_variant COCA-CN 10 50732662 50732662 single base substitution C T missense_variant E272K 814G>A COCA-CN 10 50745554 50745554 single base substitution T C intron_variant EOPC-DE 10 50723399 50723399 single base substitution C T intron_variant ESAD-UK 10 50658687 50658687 insertion of <=200bp - T downstream_gene_variant ESAD-UK 10 50658751 50658751 single base substitution A C downstream_gene_variant ESAD-UK 10 50658753 50658753 single base substitution T G downstream_gene_variant ESAD-UK 10 50660654 50660654 single base substitution G A downstream_gene_variant ESAD-UK 10 50661623 50661623 single base substitution T A downstream_gene_variant ESAD-UK 10 50661944 50661944 single base substitution T A downstream_gene_variant ESAD-UK 10 50663010 50663010 single base substitution C G downstream_gene_variant ESAD-UK 10 50663914 50663914 single base substitution C T 3_prime_UTR_variant ESAD-UK 10 50663914 50663914 single base substitution C T downstream_gene_variant ESAD-UK 10 50664271 50664271 single base substitution T G 3_prime_UTR_variant ESAD-UK 10 50664271 50664271 single base substitution T G downstream_gene_variant ESAD-UK 10 50665546 50665546 single base substitution C T 3_prime_UTR_variant ESAD-UK 10 50665546 50665546 single base substitution C T downstream_gene_variant ESAD-UK 10 50668628 50668628 single base substitution C T intron_variant ESAD-UK 10 50669816 50669816 single base substitution C G intron_variant ESAD-UK 10 50670545 50670545 single base substitution A T intron_variant ESAD-UK 10 50671041 50671041 single base substitution G A intron_variant ESAD-UK 10 50672019 50672019 single base substitution G T intron_variant ESAD-UK 10 50672243 50672243 single base substitution T C intron_variant ESAD-UK 10 50672294 50672294 single base substitution C T intron_variant ESAD-UK 10 50672543 50672543 single base substitution C T intron_variant ESAD-UK 10 50673113 50673113 single base substitution G A intron_variant ESAD-UK 10 50673518 50673518 single base substitution T C intron_variant ESAD-UK 10 50673838 50673838 single base substitution T C intron_variant ESAD-UK 10 50676307 50676307 single base substitution C T intron_variant ESAD-UK 10 50678442 50678442 single base substitution A G synonymous_variant H1188H 3564T>C ESAD-UK 10 50678442 50678442 single base substitution A G synonymous_variant H558H 1674T>C ESAD-UK 10 50678442 50678442 single base substitution A G upstream_gene_variant ESAD-UK 10 50679384 50679384 single base substitution A T intron_variant ESAD-UK 10 50679384 50679384 single base substitution A T upstream_gene_variant ESAD-UK 10 50680524 50680524 insertion of <=200bp - AG splice_region_variant ESAD-UK 10 50680524 50680524 insertion of <=200bp - AG upstream_gene_variant ESAD-UK 10 50680933 50680933 single base substitution T A intron_variant ESAD-UK 10 50680933 50680933 single base substitution T A upstream_gene_variant ESAD-UK 10 50680934 50680934 single base substitution A T intron_variant ESAD-UK 10 50680934 50680934 single base substitution A T upstream_gene_variant ESAD-UK 10 50681042 50681042 single base substitution C T synonymous_variant T284T 852G>A ESAD-UK 10 50681042 50681042 single base substitution C T synonymous_variant T914T 2742G>A ESAD-UK 10 50681042 50681042 single base substitution C T upstream_gene_variant ESAD-UK 10 50681347 50681347 single base substitution C T intron_variant ESAD-UK 10 50681347 50681347 single base substitution C T upstream_gene_variant ESAD-UK 10 50682677 50682677 single base substitution T C intron_variant ESAD-UK 10 50682677 50682677 single base substitution T C upstream_gene_variant ESAD-UK 10 50683237 50683237 single base substitution T C intron_variant ESAD-UK 10 50683237 50683237 single base substitution T C upstream_gene_variant ESAD-UK 10 50684914 50684914 single base substitution C G intron_variant ESAD-UK 10 50685125 50685125 single base substitution G A intron_variant ESAD-UK 10 50685750 50685750 single base substitution C T intron_variant ESAD-UK 10 50688141 50688141 single base substitution C A downstream_gene_variant ESAD-UK 10 50688141 50688141 single base substitution C A intron_variant ESAD-UK 10 50688403 50688403 single base substitution T C downstream_gene_variant ESAD-UK 10 50688403 50688403 single base substitution T C intron_variant ESAD-UK 10 50689388 50689388 single base substitution A T downstream_gene_variant ESAD-UK 10 50689388 50689388 single base substitution A T intron_variant ESAD-UK 10 50691604 50691604 single base substitution A C intron_variant ESAD-UK 10 50692947 50692947 single base substitution C T intron_variant ESAD-UK 10 50693056 50693056 single base substitution T G intron_variant ESAD-UK 10 50694711 50694711 single base substitution A C intron_variant ESAD-UK 10 50698495 50698495 single base substitution G T intron_variant ESAD-UK 10 50698646 50698646 single base substitution G A intron_variant ESAD-UK 10 50701052 50701052 deletion of <=200bp A - intron_variant ESAD-UK 10 50704884 50704884 single base substitution A T intron_variant ESAD-UK 10 50705354 50705354 single base substitution T C intron_variant ESAD-UK 10 50707652 50707652 single base substitution C A intron_variant ESAD-UK 10 50709352 50709352 deletion of <=200bp A - intron_variant ESAD-UK 10 50709482 50709482 single base substitution G A intron_variant ESAD-UK 10 50709828 50709828 single base substitution C T intron_variant ESAD-UK 10 50711228 50711228 single base substitution A C intron_variant ESAD-UK 10 50711228 50711228 single base substitution A C upstream_gene_variant ESAD-UK 10 50713678 50713678 single base substitution A T intron_variant ESAD-UK 10 50713678 50713678 single base substitution A T upstream_gene_variant ESAD-UK 10 50716938 50716938 single base substitution G A intron_variant ESAD-UK 10 50716938 50716938 single base substitution G A upstream_gene_variant ESAD-UK 10 50717184 50717184 single base substitution A C intron_variant ESAD-UK 10 50717184 50717184 single base substitution A C upstream_gene_variant ESAD-UK 10 50718227 50718227 single base substitution C T intron_variant ESAD-UK 10 50718227 50718227 single base substitution C T upstream_gene_variant ESAD-UK 10 50718992 50718992 deletion of <=200bp A - intron_variant ESAD-UK 10 50718992 50718992 deletion of <=200bp A - upstream_gene_variant ESAD-UK 10 50721274 50721274 single base substitution C T intron_variant ESAD-UK 10 50723036 50723036 single base substitution G A intron_variant ESAD-UK 10 50723413 50723413 single base substitution T G intron_variant ESAD-UK 10 50723614 50723614 single base substitution C T intron_variant ESAD-UK 10 50724457 50724457 single base substitution G A intron_variant ESAD-UK 10 50725423 50725423 single base substitution T C intron_variant ESAD-UK 10 50726087 50726087 single base substitution G A intron_variant ESAD-UK 10 50726177 50726177 single base substitution C T intron_variant ESAD-UK 10 50728773 50728773 single base substitution C T downstream_gene_variant ESAD-UK 10 50728773 50728773 single base substitution C T intron_variant ESAD-UK 10 50729249 50729249 single base substitution G A downstream_gene_variant ESAD-UK 10 50729249 50729249 single base substitution G A intron_variant ESAD-UK 10 50731136 50731136 single base substitution C G downstream_gene_variant ESAD-UK 10 50731136 50731136 single base substitution C G intron_variant ESAD-UK 10 50731971 50731971 deletion of <=200bp G - downstream_gene_variant ESAD-UK 10 50731971 50731971 deletion of <=200bp G - intron_variant ESAD-UK 10 50732194 50732194 single base substitution G A downstream_gene_variant ESAD-UK 10 50732194 50732194 single base substitution G A missense_variant P428S 1282C>T ESAD-UK 10 50733045 50733045 single base substitution T G exon_variant ESAD-UK 10 50733045 50733045 single base substitution T G intron_variant ESAD-UK 10 50738002 50738002 single base substitution A C downstream_gene_variant ESAD-UK 10 50738002 50738002 single base substitution A C intron_variant ESAD-UK 10 50738101 50738101 single base substitution G A downstream_gene_variant ESAD-UK 10 50738101 50738101 single base substitution G A intron_variant ESAD-UK 10 50738554 50738554 single base substitution A G downstream_gene_variant ESAD-UK 10 50738554 50738554 single base substitution A G intron_variant ESAD-UK 10 50742268 50742268 single base substitution C A intron_variant ESAD-UK 10 50742268 50742268 single base substitution C A upstream_gene_variant ESAD-UK 10 50742777 50742777 single base substitution G T intron_variant ESAD-UK 10 50742777 50742777 single base substitution G T upstream_gene_variant ESAD-UK 10 50743724 50743724 single base substitution T C intron_variant ESAD-UK 10 50743724 50743724 single base substitution T C upstream_gene_variant ESAD-UK 10 50743813 50743813 single base substitution G A intron_variant ESAD-UK 10 50744190 50744190 single base substitution G A intron_variant ESAD-UK 10 50746212 50746212 single base substitution C T intron_variant ESAD-UK 10 50746244 50746244 single base substitution G A intron_variant ESAD-UK 10 50747004 50747004 single base substitution T A intron_variant ESAD-UK 10 50747909 50747909 single base substitution C T upstream_gene_variant ESAD-UK 10 50750566 50750566 single base substitution T C upstream_gene_variant ESAD-UK 10 50750687 50750687 single base substitution T G upstream_gene_variant ESAD-UK 10 50750847 50750847 single base substitution G A upstream_gene_variant ESAD-UK 10 50752453 50752453 deletion of <=200bp G - upstream_gene_variant ESCA-CN 10 50668440 50668440 single base substitution T A exon_variant ESCA-CN 10 50668440 50668440 single base substitution T A synonymous_variant T1347T 4041A>T ESCA-CN 10 50668440 50668440 single base substitution T A synonymous_variant T717T 2151A>T ESCA-CN 10 50684305 50684305 single base substitution C T missense_variant V150I 448G>A ESCA-CN 10 50684305 50684305 single base substitution C T missense_variant V780I 2338G>A GBM-US 10 50667268 50667268 single base substitution T C downstream_gene_variant GBM-US 10 50667268 50667268 single base substitution T C missense_variant K1359E 4075A>G GBM-US 10 50667268 50667268 single base substitution T C missense_variant K729E 2185A>G GBM-US 10 50690763 50690763 single base substitution C T downstream_gene_variant GBM-US 10 50690763 50690763 single base substitution C T missense_variant M713I 2139G>A GBM-US 10 50690763 50690763 single base substitution C T missense_variant M83I 249G>A GBM-US 10 50690803 50690803 single base substitution A G downstream_gene_variant GBM-US 10 50690803 50690803 single base substitution A G missense_variant L700S 2099T>C GBM-US 10 50690803 50690803 single base substitution A G missense_variant L70S 209T>C KIRC-US 10 50678573 50678573 single base substitution C T missense_variant E1145K 3433G>A KIRC-US 10 50678573 50678573 single base substitution C T missense_variant E515K 1543G>A KIRC-US 10 50678573 50678573 single base substitution C T upstream_gene_variant KIRC-US 10 50690813 50690813 single base substitution A G downstream_gene_variant KIRC-US 10 50690813 50690813 single base substitution A G synonymous_variant L67L 199T>C KIRC-US 10 50690813 50690813 single base substitution A G synonymous_variant L697L 2089T>C KIRC-US 10 50725062 50725062 single base substitution A T intron_variant KIRC-US 10 50732227 50732227 deletion of <=200bp C - downstream_gene_variant KIRC-US 10 50732227 50732227 deletion of <=200bp C - frameshift_variant V417 KIRC-US 10 50732231 50732231 single base substitution C T downstream_gene_variant KIRC-US 10 50732231 50732231 single base substitution C T synonymous_variant K415K 1245G>A KIRC-US 10 50732744 50732744 single base substitution C A downstream_gene_variant KIRC-US 10 50732744 50732744 single base substitution C A missense_variant Q244H 732G>T KIRC-US 10 50738880 50738880 single base substitution A C missense_variant C143W 429T>G KIRC-US 10 50738880 50738880 single base substitution A C upstream_gene_variant KIRP-US 10 50681040 50681040 single base substitution C T missense_variant R285Q 854G>A KIRP-US 10 50681040 50681040 single base substitution C T missense_variant R915Q 2744G>A KIRP-US 10 50681040 50681040 single base substitution C T upstream_gene_variant LAML-KR 10 50691009 50691009 single base substitution C T downstream_gene_variant LAML-KR 10 50691009 50691009 single base substitution C T intron_variant LAML-KR 10 50732280 50732280 single base substitution C T downstream_gene_variant LAML-KR 10 50732280 50732280 single base substitution C T missense_variant G399D 1196G>A LAML-KR 10 50740600 50740600 single base substitution C T synonymous_variant L137L 411G>A LAML-KR 10 50740600 50740600 single base substitution C T upstream_gene_variant LAML-KR 10 50745554 50745554 single base substitution T C intron_variant LGG-US 10 50667030 50667030 single base substitution T C downstream_gene_variant LGG-US 10 50667030 50667030 single base substitution T C missense_variant Q1438R 4313A>G LGG-US 10 50667030 50667030 single base substitution T C missense_variant Q808R 2423A>G LICA-CN 10 50686407 50686407 single base substitution T G missense_variant N130T 389A>C LICA-CN 10 50686407 50686407 single base substitution T G missense_variant N760T 2279A>C LICA-CN 10 50732268 50732268 single base substitution T A downstream_gene_variant LICA-CN 10 50732268 50732268 single base substitution T A missense_variant E403V 1208A>T LICA-CN 10 50732825 50732825 single base substitution T A downstream_gene_variant LICA-CN 10 50732825 50732825 single base substitution T A splice_acceptor_variant LICA-FR 10 50666942 50666942 single base substitution T C downstream_gene_variant LICA-FR 10 50666942 50666942 single base substitution T C synonymous_variant R1467R 4401A>G LICA-FR 10 50666942 50666942 single base substitution T C synonymous_variant R837R 2511A>G LICA-FR 10 50679320 50679320 single base substitution G A intron_variant LICA-FR 10 50679320 50679320 single base substitution G A upstream_gene_variant LICA-FR 10 50690779 50690779 single base substitution G A downstream_gene_variant LICA-FR 10 50690779 50690779 single base substitution G A missense_variant S708F 2123C>T LICA-FR 10 50690779 50690779 single base substitution G A missense_variant S78F 233C>T LICA-FR 10 50724089 50724089 single base substitution T C intron_variant LIHC-US 10 50669432 50669432 single base substitution G A exon_variant LIHC-US 10 50669432 50669432 single base substitution G A missense_variant H1317Y 3949C>T LIHC-US 10 50669432 50669432 single base substitution G A missense_variant H687Y 2059C>T LIHC-US 10 50690818 50690818 single base substitution C A downstream_gene_variant LIHC-US 10 50690818 50690818 single base substitution C A missense_variant G65V 194G>T LIHC-US 10 50690818 50690818 single base substitution C A missense_variant G695V 2084G>T LIHC-US 10 50724703 50724703 single base substitution T A intron_variant LIHC-US 10 50732464 50732464 single base substitution T A downstream_gene_variant LIHC-US 10 50732464 50732464 single base substitution T A missense_variant R338W 1012A>T LINC-JP 10 50661976 50661976 single base substitution T C downstream_gene_variant LINC-JP 10 50670272 50670272 single base substitution G A intron_variant LINC-JP 10 50670827 50670827 single base substitution T C intron_variant LINC-JP 10 50671981 50671981 single base substitution G A intron_variant LINC-JP 10 50684316 50684316 single base substitution T G missense_variant Y146S 437A>C LINC-JP 10 50684316 50684316 single base substitution T G missense_variant Y776S 2327A>C LINC-JP 10 50684902 50684902 single base substitution G A intron_variant LINC-JP 10 50686600 50686600 single base substitution T C downstream_gene_variant LINC-JP 10 50686600 50686600 single base substitution T C intron_variant LINC-JP 10 50690669 50690669 single base substitution T C downstream_gene_variant LINC-JP 10 50690669 50690669 single base substitution T C intron_variant LINC-JP 10 50692339 50692339 single base substitution A G intron_variant LINC-JP 10 50696280 50696280 single base substitution C T intron_variant LINC-JP 10 50708894 50708894 single base substitution T C intron_variant LINC-JP 10 50714857 50714857 deletion of <=200bp A - intron_variant LINC-JP 10 50714857 50714857 deletion of <=200bp A - upstream_gene_variant LINC-JP 10 50724899 50724899 single base substitution C T intron_variant LINC-JP 10 50727636 50727636 single base substitution T C intron_variant LINC-JP 10 50729299 50729304 deletion of <=200bp TGATCT - downstream_gene_variant LINC-JP 10 50729299 50729304 deletion of <=200bp TGATCT - intron_variant LINC-JP 10 50731295 50731295 single base substitution G A downstream_gene_variant LINC-JP 10 50731295 50731295 single base substitution G A intron_variant LINC-JP 10 50732689 50732689 single base substitution T C downstream_gene_variant LINC-JP 10 50732689 50732689 single base substitution T C missense_variant I263V 787A>G LINC-JP 10 50733483 50733483 single base substitution T C intron_variant LINC-JP 10 50738926 50738926 single base substitution A G intron_variant LINC-JP 10 50738926 50738926 single base substitution A G upstream_gene_variant LINC-JP 10 50741066 50741066 single base substitution T G intron_variant LINC-JP 10 50741066 50741066 single base substitution T G upstream_gene_variant LIRI-JP 10 50659095 50659095 single base substitution G T downstream_gene_variant LIRI-JP 10 50662907 50662907 single base substitution G A downstream_gene_variant LIRI-JP 10 50663400 50663400 single base substitution A G downstream_gene_variant LIRI-JP 10 50663598 50663598 single base substitution T A 3_prime_UTR_variant LIRI-JP 10 50663598 50663598 single base substitution T A downstream_gene_variant LIRI-JP 10 50665165 50665165 single base substitution C T 3_prime_UTR_variant LIRI-JP 10 50665165 50665165 single base substitution C T downstream_gene_variant LIRI-JP 10 50665890 50665890 single base substitution G C 3_prime_UTR_variant LIRI-JP 10 50665890 50665890 single base substitution G C downstream_gene_variant LIRI-JP 10 50666453 50666453 single base substitution T C 3_prime_UTR_variant LIRI-JP 10 50666453 50666453 single base substitution T C downstream_gene_variant LIRI-JP 10 50672999 50672999 single base substitution C T intron_variant LIRI-JP 10 50673559 50673559 single base substitution T C intron_variant LIRI-JP 10 50674235 50674235 single base substitution T C intron_variant LIRI-JP 10 50676432 50676432 single base substitution C T intron_variant LIRI-JP 10 50677181 50677181 single base substitution T C intron_variant LIRI-JP 10 50679398 50679398 single base substitution A G intron_variant LIRI-JP 10 50679398 50679398 single base substitution A G upstream_gene_variant LIRI-JP 10 50680367 50680367 deletion of <=200bp C - intron_variant LIRI-JP 10 50680367 50680367 deletion of <=200bp C - upstream_gene_variant LIRI-JP 10 50680589 50680589 single base substitution C T intron_variant LIRI-JP 10 50680589 50680589 single base substitution C T upstream_gene_variant LIRI-JP 10 50682053 50682053 single base substitution T C intron_variant LIRI-JP 10 50682053 50682053 single base substitution T C upstream_gene_variant LIRI-JP 10 50682698 50682698 single base substitution T A intron_variant LIRI-JP 10 50682698 50682698 single base substitution T A upstream_gene_variant LIRI-JP 10 50684465 50684465 single base substitution T C intron_variant LIRI-JP 10 50685203 50685203 single base substitution T A intron_variant LIRI-JP 10 50685471 50685471 single base substitution G T intron_variant LIRI-JP 10 50686378 50686378 single base substitution G A intron_variant LIRI-JP 10 50688377 50688377 single base substitution C T downstream_gene_variant LIRI-JP 10 50688377 50688377 single base substitution C T intron_variant LIRI-JP 10 50689051 50689051 single base substitution G A downstream_gene_variant LIRI-JP 10 50689051 50689051 single base substitution G A intron_variant LIRI-JP 10 50690518 50690518 single base substitution C G downstream_gene_variant LIRI-JP 10 50690518 50690518 single base substitution C G intron_variant LIRI-JP 10 50690894 50690894 single base substitution G C downstream_gene_variant LIRI-JP 10 50690894 50690894 single base substitution G C missense_variant R40G 118C>G LIRI-JP 10 50690894 50690894 single base substitution G C missense_variant R670G 2008C>G LIRI-JP 10 50693661 50693661 single base substitution T C intron_variant LIRI-JP 10 50693698 50693698 single base substitution T G intron_variant LIRI-JP 10 50702656 50702656 single base substitution G A intron_variant LIRI-JP 10 50702716 50702716 single base substitution T G intron_variant LIRI-JP 10 50704392 50704392 single base substitution C A intron_variant LIRI-JP 10 50704415 50704415 single base substitution G A intron_variant LIRI-JP 10 50704969 50704969 single base substitution T C intron_variant LIRI-JP 10 50705047 50705047 single base substitution A T intron_variant LIRI-JP 10 50705676 50705676 single base substitution C A intron_variant LIRI-JP 10 50706439 50706439 single base substitution T C intron_variant LIRI-JP 10 50707882 50707882 single base substitution T C intron_variant LIRI-JP 10 50708164 50708164 single base substitution T A intron_variant LIRI-JP 10 50708311 50708311 single base substitution C T intron_variant LIRI-JP 10 50708736 50708736 single base substitution C T 5_prime_UTR_variant LIRI-JP 10 50708736 50708736 single base substitution C T exon_variant LIRI-JP 10 50708736 50708736 single base substitution C T synonymous_variant Q511Q 1533G>A LIRI-JP 10 50714773 50714773 single base substitution A C intron_variant LIRI-JP 10 50714773 50714773 single base substitution A C upstream_gene_variant LIRI-JP 10 50715839 50715839 single base substitution C T intron_variant LIRI-JP 10 50715839 50715839 single base substitution C T upstream_gene_variant LIRI-JP 10 50716143 50716143 single base substitution A C intron_variant LIRI-JP 10 50716143 50716143 single base substitution A C upstream_gene_variant LIRI-JP 10 50718299 50718299 single base substitution C T intron_variant LIRI-JP 10 50718299 50718299 single base substitution C T upstream_gene_variant LIRI-JP 10 50723479 50723479 single base substitution T C intron_variant LIRI-JP 10 50724090 50724090 single base substitution A G intron_variant LIRI-JP 10 50724421 50724421 single base substitution C A intron_variant LIRI-JP 10 50725399 50725399 single base substitution T C intron_variant LIRI-JP 10 50730874 50730874 single base substitution C T downstream_gene_variant LIRI-JP 10 50730874 50730874 single base substitution C T intron_variant LIRI-JP 10 50732449 50732449 single base substitution G A downstream_gene_variant LIRI-JP 10 50732449 50732449 single base substitution G A stop_gained Q343* 1027C>T LIRI-JP 10 50737011 50737011 single base substitution T C downstream_gene_variant LIRI-JP 10 50737011 50737011 single base substitution T C intron_variant LIRI-JP 10 50737698 50737698 single base substitution A T downstream_gene_variant LIRI-JP 10 50737698 50737698 single base substitution A T intron_variant LIRI-JP 10 50740276 50740276 single base substitution T C intron_variant LIRI-JP 10 50740276 50740276 single base substitution T C upstream_gene_variant LIRI-JP 10 50741631 50741631 single base substitution C T intron_variant LIRI-JP 10 50741631 50741631 single base substitution C T upstream_gene_variant LIRI-JP 10 50749346 50749346 single base substitution A G upstream_gene_variant LIRI-JP 10 50750361 50750361 single base substitution G T upstream_gene_variant LIRI-JP 10 50750902 50750902 single base substitution T C upstream_gene_variant LIRI-JP 10 50751684 50751684 single base substitution T C upstream_gene_variant LIRI-JP 10 50751920 50751920 single base substitution T A upstream_gene_variant LIRI-JP 10 50752119 50752119 single base substitution G C upstream_gene_variant LIRI-JP 10 50752419 50752419 single base substitution A T upstream_gene_variant LUSC-KR 10 50659200 50659200 single base substitution G A downstream_gene_variant LUSC-KR 10 50667105 50667105 single base substitution T C downstream_gene_variant LUSC-KR 10 50667105 50667105 single base substitution T C missense_variant Q1413R 4238A>G LUSC-KR 10 50667105 50667105 single base substitution T C missense_variant Q783R 2348A>G LUSC-KR 10 50667220 50667220 single base substitution C G downstream_gene_variant LUSC-KR 10 50667220 50667220 single base substitution C G missense_variant E1375Q 4123G>C LUSC-KR 10 50667220 50667220 single base substitution C G missense_variant E745Q 2233G>C LUSC-KR 10 50667571 50667571 single base substitution C G downstream_gene_variant LUSC-KR 10 50667571 50667571 single base substitution C G intron_variant LUSC-KR 10 50670766 50670766 single base substitution A T intron_variant LUSC-KR 10 50675314 50675314 single base substitution A G intron_variant LUSC-KR 10 50678212 50678212 single base substitution G A intron_variant LUSC-KR 10 50678369 50678369 single base substitution T C missense_variant R1213G 3637A>G LUSC-KR 10 50678369 50678369 single base substitution T C missense_variant R583G 1747A>G LUSC-KR 10 50678369 50678369 single base substitution T C upstream_gene_variant LUSC-KR 10 50678717 50678717 single base substitution T C missense_variant M1097V 3289A>G LUSC-KR 10 50678717 50678717 single base substitution T C missense_variant M467V 1399A>G LUSC-KR 10 50678717 50678717 single base substitution T C upstream_gene_variant LUSC-KR 10 50680066 50680066 single base substitution A T intron_variant LUSC-KR 10 50680066 50680066 single base substitution A T upstream_gene_variant LUSC-KR 10 50681033 50681033 single base substitution G A synonymous_variant G287G 861C>T LUSC-KR 10 50681033 50681033 single base substitution G A synonymous_variant G917G 2751C>T LUSC-KR 10 50681033 50681033 single base substitution G A upstream_gene_variant LUSC-KR 10 50681169 50681169 single base substitution G T intron_variant LUSC-KR 10 50681169 50681169 single base substitution G T upstream_gene_variant LUSC-KR 10 50682097 50682097 single base substitution T C synonymous_variant V228V 684A>G LUSC-KR 10 50682097 50682097 single base substitution T C synonymous_variant V858V 2574A>G LUSC-KR 10 50682097 50682097 single base substitution T C upstream_gene_variant LUSC-KR 10 50683646 50683646 single base substitution G A intron_variant LUSC-KR 10 50684306 50684306 single base substitution G A synonymous_variant F149F 447C>T LUSC-KR 10 50684306 50684306 single base substitution G A synonymous_variant F779F 2337C>T LUSC-KR 10 50687182 50687182 single base substitution A G downstream_gene_variant LUSC-KR 10 50687182 50687182 single base substitution A G intron_variant LUSC-KR 10 50689171 50689171 single base substitution T A downstream_gene_variant LUSC-KR 10 50689171 50689171 single base substitution T A intron_variant LUSC-KR 10 50690301 50690301 single base substitution C A downstream_gene_variant LUSC-KR 10 50690301 50690301 single base substitution C A intron_variant LUSC-KR 10 50690302 50690302 single base substitution C A downstream_gene_variant LUSC-KR 10 50690302 50690302 single base substitution C A intron_variant LUSC-KR 10 50690701 50690701 single base substitution A T downstream_gene_variant LUSC-KR 10 50690701 50690701 single base substitution A T intron_variant LUSC-KR 10 50696004 50696004 single base substitution T C intron_variant LUSC-KR 10 50707261 50707261 single base substitution C T intron_variant LUSC-KR 10 50709659 50709659 single base substitution G A intron_variant LUSC-KR 10 50710394 50710394 single base substitution C G intron_variant LUSC-KR 10 50710394 50710394 single base substitution C G upstream_gene_variant LUSC-KR 10 50717921 50717921 single base substitution A T intron_variant LUSC-KR 10 50717921 50717921 single base substitution A T upstream_gene_variant LUSC-KR 10 50718580 50718580 single base substitution C T intron_variant LUSC-KR 10 50718580 50718580 single base substitution C T upstream_gene_variant LUSC-KR 10 50719770 50719770 single base substitution C A intron_variant LUSC-KR 10 50720127 50720127 single base substitution T A intron_variant LUSC-KR 10 50722400 50722400 single base substitution G T intron_variant LUSC-KR 10 50727858 50727858 single base substitution C A intron_variant LUSC-KR 10 50730138 50730138 single base substitution T C downstream_gene_variant LUSC-KR 10 50730138 50730138 single base substitution T C intron_variant LUSC-KR 10 50730661 50730661 single base substitution T C downstream_gene_variant LUSC-KR 10 50730661 50730661 single base substitution T C intron_variant LUSC-KR 10 50739841 50739841 single base substitution C A intron_variant LUSC-KR 10 50739841 50739841 single base substitution C A upstream_gene_variant LUSC-KR 10 50745196 50745196 single base substitution C A intron_variant LUSC-KR 10 50746943 50746943 single base substitution G A intron_variant LUSC-KR 10 50749647 50749647 single base substitution C G upstream_gene_variant LUSC-KR 10 50750355 50750355 single base substitution G A upstream_gene_variant LUSC-KR 10 50751187 50751187 single base substitution C A upstream_gene_variant LUSC-US 10 50678601 50678601 single base substitution T C synonymous_variant T1135T 3405A>G LUSC-US 10 50678601 50678601 single base substitution T C synonymous_variant T505T 1515A>G LUSC-US 10 50678601 50678601 single base substitution T C upstream_gene_variant LUSC-US 10 50690811 50690811 single base substitution T A downstream_gene_variant LUSC-US 10 50690811 50690811 single base substitution T A missense_variant L67F 201A>T LUSC-US 10 50690811 50690811 single base substitution T A missense_variant L697F 2091A>T LUSC-US 10 50691393 50691393 single base substitution T A downstream_gene_variant LUSC-US 10 50691393 50691393 single base substitution T A missense_variant Q34L 101A>T LUSC-US 10 50691393 50691393 single base substitution T A missense_variant Q664L 1991A>T LUSC-US 10 50723759 50723759 single base substitution C T intron_variant LUSC-US 10 50723771 50723771 single base substitution C G intron_variant LUSC-US 10 50723876 50723876 single base substitution G T intron_variant LUSC-US 10 50723928 50723928 single base substitution G T intron_variant LUSC-US 10 50723929 50723929 single base substitution C T intron_variant LUSC-US 10 50724411 50724411 single base substitution T A intron_variant LUSC-US 10 50724810 50724810 single base substitution G A intron_variant LUSC-US 10 50725112 50725112 single base substitution C A intron_variant LUSC-US 10 50732520 50732520 single base substitution C G downstream_gene_variant LUSC-US 10 50732520 50732520 single base substitution C G missense_variant R319T 956G>C MALY-DE 10 50664518 50664518 single base substitution G A 3_prime_UTR_variant MALY-DE 10 50664518 50664518 single base substitution G A downstream_gene_variant MALY-DE 10 50673225 50673225 single base substitution C A intron_variant MALY-DE 10 50673814 50673814 single base substitution T C intron_variant MALY-DE 10 50675594 50675594 single base substitution A G intron_variant MALY-DE 10 50683169 50683169 single base substitution A C intron_variant MALY-DE 10 50683169 50683169 single base substitution A C upstream_gene_variant MALY-DE 10 50700831 50700831 single base substitution C T intron_variant MALY-DE 10 50714885 50714885 single base substitution C G intron_variant MALY-DE 10 50714885 50714885 single base substitution C G upstream_gene_variant MALY-DE 10 50715812 50715812 single base substitution G A intron_variant MALY-DE 10 50715812 50715812 single base substitution G A upstream_gene_variant MALY-DE 10 50723649 50723649 single base substitution T C intron_variant MALY-DE 10 50743106 50743106 single base substitution A G intron_variant MALY-DE 10 50743106 50743106 single base substitution A G upstream_gene_variant MALY-DE 10 50744031 50744031 single base substitution G A intron_variant MALY-DE 10 50746004 50746004 single base substitution G A intron_variant MALY-DE 10 50752404 50752404 single base substitution C T upstream_gene_variant MELA-AU 10 50658880 50658880 single base substitution T C downstream_gene_variant MELA-AU 10 50659202 50659202 single base substitution A G downstream_gene_variant MELA-AU 10 50659848 50659848 single base substitution G A downstream_gene_variant MELA-AU 10 50660203 50660203 single base substitution G A downstream_gene_variant MELA-AU 10 50660608 50660608 single base substitution G A downstream_gene_variant MELA-AU 10 50661760 50661760 single base substitution A T downstream_gene_variant MELA-AU 10 50662134 50662134 single base substitution G A downstream_gene_variant MELA-AU 10 50662459 50662459 single base substitution G A downstream_gene_variant MELA-AU 10 50662890 50662890 single base substitution G A downstream_gene_variant MELA-AU 10 50663360 50663360 single base substitution T C downstream_gene_variant MELA-AU 10 50663519 50663519 single base substitution G A 3_prime_UTR_variant MELA-AU 10 50663519 50663519 single base substitution G A downstream_gene_variant MELA-AU 10 50663603 50663603 single base substitution C T 3_prime_UTR_variant MELA-AU 10 50663603 50663603 single base substitution C T downstream_gene_variant MELA-AU 10 50663736 50663736 single base substitution G A 3_prime_UTR_variant MELA-AU 10 50663736 50663736 single base substitution G A downstream_gene_variant MELA-AU 10 50663791 50663791 single base substitution T A 3_prime_UTR_variant MELA-AU 10 50663791 50663791 single base substitution T A downstream_gene_variant MELA-AU 10 50663848 50663848 single base substitution G A 3_prime_UTR_variant MELA-AU 10 50663848 50663848 single base substitution G A downstream_gene_variant MELA-AU 10 50663994 50663994 single base substitution T C 3_prime_UTR_variant MELA-AU 10 50663994 50663994 single base substitution T C downstream_gene_variant MELA-AU 10 50665644 50665644 single base substitution G A 3_prime_UTR_variant MELA-AU 10 50665644 50665644 single base substitution G A downstream_gene_variant MELA-AU 10 50665915 50665915 single base substitution C A 3_prime_UTR_variant MELA-AU 10 50665915 50665915 single base substitution C A downstream_gene_variant MELA-AU 10 50666318 50666318 single base substitution G A 3_prime_UTR_variant MELA-AU 10 50666318 50666318 single base substitution G A downstream_gene_variant MELA-AU 10 50667415 50667415 single base substitution T A downstream_gene_variant MELA-AU 10 50667415 50667415 single base substitution T A intron_variant MELA-AU 10 50668765 50668765 single base substitution G A intron_variant MELA-AU 10 50669034 50669034 single base substitution G A intron_variant MELA-AU 10 50669286 50669286 single base substitution G A intron_variant MELA-AU 10 50670463 50670463 single base substitution A T intron_variant MELA-AU 10 50670704 50670704 single base substitution G A intron_variant MELA-AU 10 50670842 50670842 single base substitution G A intron_variant MELA-AU 10 50671405 50671405 single base substitution G A intron_variant MELA-AU 10 50671437 50671437 single base substitution G C intron_variant MELA-AU 10 50671479 50671479 single base substitution G A intron_variant MELA-AU 10 50671723 50671723 single base substitution G A intron_variant MELA-AU 10 50671925 50671925 single base substitution G A intron_variant MELA-AU 10 50671963 50671963 single base substitution G A intron_variant MELA-AU 10 50672055 50672055 single base substitution G A intron_variant MELA-AU 10 50672228 50672228 single base substitution G A intron_variant MELA-AU 10 50672252 50672252 single base substitution G A intron_variant MELA-AU 10 50672486 50672486 single base substitution G A intron_variant MELA-AU 10 50672641 50672641 single base substitution G A intron_variant MELA-AU 10 50672975 50672975 single base substitution G A intron_variant MELA-AU 10 50673251 50673251 single base substitution G A intron_variant MELA-AU 10 50673447 50673447 single base substitution G A intron_variant MELA-AU 10 50673453 50673453 single base substitution G A intron_variant MELA-AU 10 50673466 50673466 single base substitution G A intron_variant MELA-AU 10 50673588 50673588 single base substitution G A intron_variant MELA-AU 10 50674111 50674111 single base substitution G A intron_variant MELA-AU 10 50674179 50674179 single base substitution G A intron_variant MELA-AU 10 50674202 50674202 single base substitution A T intron_variant MELA-AU 10 50674281 50674281 single base substitution T A intron_variant MELA-AU 10 50674476 50674476 single base substitution G A intron_variant MELA-AU 10 50674722 50674722 single base substitution G A intron_variant MELA-AU 10 50675134 50675134 single base substitution T A intron_variant MELA-AU 10 50675415 50675415 single base substitution T C intron_variant MELA-AU 10 50675464 50675464 single base substitution G T intron_variant MELA-AU 10 50675605 50675605 single base substitution T C intron_variant MELA-AU 10 50676142 50676142 single base substitution G C intron_variant MELA-AU 10 50676407 50676407 single base substitution C T intron_variant MELA-AU 10 50676516 50676516 single base substitution A T intron_variant MELA-AU 10 50677015 50677015 single base substitution G A intron_variant MELA-AU 10 50677282 50677282 single base substitution A C intron_variant MELA-AU 10 50677500 50677500 single base substitution G A intron_variant MELA-AU 10 50677533 50677533 single base substitution G A intron_variant MELA-AU 10 50677875 50677875 single base substitution G A intron_variant MELA-AU 10 50678073 50678073 deletion of <=200bp A - intron_variant MELA-AU 10 50678206 50678206 single base substitution G A intron_variant MELA-AU 10 50678415 50678415 single base substitution C T synonymous_variant E1197E 3591G>A MELA-AU 10 50678415 50678415 single base substitution C T synonymous_variant E567E 1701G>A MELA-AU 10 50678415 50678415 single base substitution C T upstream_gene_variant MELA-AU 10 50678617 50678617 single base substitution G A missense_variant S1130L 3389C>T MELA-AU 10 50678617 50678617 single base substitution G A missense_variant S500L 1499C>T MELA-AU 10 50678617 50678617 single base substitution G A upstream_gene_variant MELA-AU 10 50678838 50678838 single base substitution G A synonymous_variant F1056F 3168C>T MELA-AU 10 50678838 50678838 single base substitution G A synonymous_variant F426F 1278C>T MELA-AU 10 50678838 50678838 single base substitution G A upstream_gene_variant MELA-AU 10 50678974 50678974 single base substitution C T intron_variant MELA-AU 10 50678974 50678974 single base substitution C T upstream_gene_variant MELA-AU 10 50679649 50679649 single base substitution G A intron_variant MELA-AU 10 50679649 50679649 single base substitution G A upstream_gene_variant MELA-AU 10 50679864 50679864 single base substitution G A intron_variant MELA-AU 10 50679864 50679864 single base substitution G A upstream_gene_variant MELA-AU 10 50679956 50679956 single base substitution G A intron_variant MELA-AU 10 50679956 50679956 single base substitution G A upstream_gene_variant MELA-AU 10 50679970 50679970 single base substitution G A intron_variant MELA-AU 10 50679970 50679970 single base substitution G A upstream_gene_variant MELA-AU 10 50680701 50680701 single base substitution G A intron_variant MELA-AU 10 50680701 50680701 single base substitution G A upstream_gene_variant MELA-AU 10 50680831 50680831 single base substitution G A intron_variant MELA-AU 10 50680831 50680831 single base substitution G A upstream_gene_variant MELA-AU 10 50681050 50681050 single base substitution G A synonymous_variant L282L 844C>T MELA-AU 10 50681050 50681050 single base substitution G A synonymous_variant L912L 2734C>T MELA-AU 10 50681050 50681050 single base substitution G A upstream_gene_variant MELA-AU 10 50681713 50681713 single base substitution A G intron_variant MELA-AU 10 50681713 50681713 single base substitution A G upstream_gene_variant MELA-AU 10 50681912 50681912 single base substitution C T intron_variant MELA-AU 10 50681912 50681912 single base substitution C T upstream_gene_variant MELA-AU 10 50682007 50682007 single base substitution C T intron_variant MELA-AU 10 50682007 50682007 single base substitution C T upstream_gene_variant MELA-AU 10 50682343 50682343 single base substitution C T intron_variant MELA-AU 10 50682343 50682343 single base substitution C T upstream_gene_variant MELA-AU 10 50682361 50682361 single base substitution T G intron_variant MELA-AU 10 50682361 50682361 single base substitution T G upstream_gene_variant MELA-AU 10 50682530 50682531 multiple base substitution (>=2bp and <=200bp) GG CA intron_variant MELA-AU 10 50682530 50682531 multiple base substitution (>=2bp and <=200bp) GG CA upstream_gene_variant MELA-AU 10 50682617 50682617 single base substitution G A intron_variant MELA-AU 10 50682617 50682617 single base substitution G A upstream_gene_variant MELA-AU 10 50682866 50682866 single base substitution G A intron_variant MELA-AU 10 50682866 50682866 single base substitution G A upstream_gene_variant MELA-AU 10 50683329 50683329 single base substitution A G intron_variant MELA-AU 10 50683457 50683457 single base substitution G A intron_variant MELA-AU 10 50684100 50684100 single base substitution A G intron_variant MELA-AU 10 50684297 50684297 single base substitution G A synonymous_variant S152S 456C>T MELA-AU 10 50684297 50684297 single base substitution G A synonymous_variant S782S 2346C>T MELA-AU 10 50684298 50684298 single base substitution G A missense_variant S152F 455C>T MELA-AU 10 50684298 50684298 single base substitution G A missense_variant S782F 2345C>T MELA-AU 10 50684306 50684306 single base substitution G A synonymous_variant F149F 447C>T MELA-AU 10 50684306 50684306 single base substitution G A synonymous_variant F779F 2337C>T MELA-AU 10 50684460 50684460 single base substitution G A intron_variant MELA-AU 10 50685142 50685142 single base substitution A G intron_variant MELA-AU 10 50685283 50685283 single base substitution G A intron_variant MELA-AU 10 50685337 50685337 single base substitution C T intron_variant MELA-AU 10 50685633 50685633 single base substitution A C intron_variant MELA-AU 10 50685671 50685671 single base substitution C T intron_variant MELA-AU 10 50686877 50686877 single base substitution G A downstream_gene_variant MELA-AU 10 50686877 50686877 single base substitution G A intron_variant MELA-AU 10 50687055 50687055 single base substitution G A downstream_gene_variant MELA-AU 10 50687055 50687055 single base substitution G A intron_variant MELA-AU 10 50687069 50687069 single base substitution C T downstream_gene_variant MELA-AU 10 50687069 50687069 single base substitution C T intron_variant MELA-AU 10 50687076 50687076 single base substitution G A downstream_gene_variant MELA-AU 10 50687076 50687076 single base substitution G A intron_variant MELA-AU 10 50688631 50688631 single base substitution G A downstream_gene_variant MELA-AU 10 50688631 50688631 single base substitution G A intron_variant MELA-AU 10 50688733 50688733 single base substitution T C downstream_gene_variant MELA-AU 10 50688733 50688733 single base substitution T C intron_variant MELA-AU 10 50688793 50688793 single base substitution T C downstream_gene_variant MELA-AU 10 50688793 50688793 single base substitution T C intron_variant MELA-AU 10 50689046 50689046 single base substitution T A downstream_gene_variant MELA-AU 10 50689046 50689046 single base substitution T A intron_variant MELA-AU 10 50689134 50689134 single base substitution G A downstream_gene_variant MELA-AU 10 50689134 50689134 single base substitution G A intron_variant MELA-AU 10 50689159 50689159 single base substitution C G downstream_gene_variant MELA-AU 10 50689159 50689159 single base substitution C G intron_variant MELA-AU 10 50689198 50689198 single base substitution G A downstream_gene_variant MELA-AU 10 50689198 50689198 single base substitution G A intron_variant MELA-AU 10 50690083 50690083 single base substitution C T downstream_gene_variant MELA-AU 10 50690083 50690083 single base substitution C T intron_variant MELA-AU 10 50690901 50690901 single base substitution G A downstream_gene_variant MELA-AU 10 50690901 50690901 single base substitution G A synonymous_variant T37T 111C>T MELA-AU 10 50690901 50690901 single base substitution G A synonymous_variant T667T 2001C>T MELA-AU 10 50691430 50691430 single base substitution G A exon_variant MELA-AU 10 50691430 50691430 single base substitution G A stop_gained R22* 64C>T MELA-AU 10 50691430 50691430 single base substitution G A stop_gained R652* 1954C>T MELA-AU 10 50694455 50694455 single base substitution A T intron_variant MELA-AU 10 50695226 50695226 single base substitution G A intron_variant MELA-AU 10 50695650 50695650 single base substitution T C intron_variant MELA-AU 10 50696176 50696176 single base substitution G A intron_variant MELA-AU 10 50696282 50696282 single base substitution C T intron_variant MELA-AU 10 50696964 50696964 single base substitution G A intron_variant MELA-AU 10 50697097 50697097 single base substitution G A intron_variant MELA-AU 10 50697563 50697563 single base substitution G A intron_variant MELA-AU 10 50697657 50697657 single base substitution G A intron_variant MELA-AU 10 50698149 50698149 single base substitution C T intron_variant MELA-AU 10 50698299 50698299 single base substitution G A intron_variant MELA-AU 10 50698377 50698377 single base substitution G A intron_variant MELA-AU 10 50699265 50699265 single base substitution G A intron_variant MELA-AU 10 50699336 50699336 single base substitution C T intron_variant MELA-AU 10 50699364 50699364 single base substitution G A intron_variant MELA-AU 10 50699550 50699550 single base substitution G A intron_variant MELA-AU 10 50699888 50699888 single base substitution A T intron_variant MELA-AU 10 50699911 50699911 single base substitution G A intron_variant MELA-AU 10 50700342 50700342 single base substitution G A intron_variant MELA-AU 10 50700709 50700709 single base substitution A G intron_variant MELA-AU 10 50701288 50701288 single base substitution A G intron_variant MELA-AU 10 50701288 50701288 single base substitution A G synonymous_variant L566L 1696T>C MELA-AU 10 50701923 50701923 single base substitution G A intron_variant MELA-AU 10 50702264 50702264 single base substitution G A intron_variant MELA-AU 10 50702292 50702292 single base substitution G A intron_variant MELA-AU 10 50702448 50702448 single base substitution A T intron_variant MELA-AU 10 50703098 50703098 single base substitution C T intron_variant MELA-AU 10 50704017 50704017 single base substitution G A intron_variant MELA-AU 10 50704037 50704037 single base substitution G A intron_variant MELA-AU 10 50705174 50705174 single base substitution G A intron_variant MELA-AU 10 50705480 50705480 single base substitution A G intron_variant MELA-AU 10 50705857 50705857 single base substitution G A intron_variant MELA-AU 10 50706466 50706466 single base substitution G A intron_variant MELA-AU 10 50707531 50707531 single base substitution G A intron_variant MELA-AU 10 50708153 50708153 single base substitution T A intron_variant MELA-AU 10 50708461 50708461 single base substitution G A intron_variant MELA-AU 10 50709079 50709079 single base substitution G A intron_variant MELA-AU 10 50709526 50709526 single base substitution A G intron_variant MELA-AU 10 50709600 50709600 single base substitution G A intron_variant MELA-AU 10 50709768 50709768 single base substitution G A intron_variant MELA-AU 10 50709796 50709796 single base substitution G A intron_variant MELA-AU 10 50709912 50709912 single base substitution G A intron_variant MELA-AU 10 50710303 50710303 single base substitution G A intron_variant MELA-AU 10 50710303 50710303 single base substitution G A upstream_gene_variant MELA-AU 10 50711805 50711805 single base substitution G A intron_variant MELA-AU 10 50711805 50711805 single base substitution G A upstream_gene_variant MELA-AU 10 50711838 50711838 single base substitution G A intron_variant MELA-AU 10 50711838 50711838 single base substitution G A upstream_gene_variant MELA-AU 10 50711847 50711847 single base substitution G A intron_variant MELA-AU 10 50711847 50711847 single base substitution G A upstream_gene_variant MELA-AU 10 50712105 50712105 single base substitution C T intron_variant MELA-AU 10 50712105 50712105 single base substitution C T upstream_gene_variant MELA-AU 10 50712715 50712715 single base substitution C T intron_variant MELA-AU 10 50712715 50712715 single base substitution C T upstream_gene_variant MELA-AU 10 50713567 50713567 single base substitution T C intron_variant MELA-AU 10 50713567 50713567 single base substitution T C upstream_gene_variant MELA-AU 10 50714344 50714344 single base substitution G A intron_variant MELA-AU 10 50714344 50714344 single base substitution G A upstream_gene_variant MELA-AU 10 50715669 50715669 single base substitution G A intron_variant MELA-AU 10 50715669 50715669 single base substitution G A upstream_gene_variant MELA-AU 10 50718053 50718053 single base substitution G A intron_variant MELA-AU 10 50718053 50718053 single base substitution G A upstream_gene_variant MELA-AU 10 50718686 50718686 single base substitution G A intron_variant MELA-AU 10 50718686 50718686 single base substitution G A upstream_gene_variant MELA-AU 10 50718794 50718794 single base substitution G A intron_variant MELA-AU 10 50718794 50718794 single base substitution G A upstream_gene_variant MELA-AU 10 50718828 50718828 single base substitution G A intron_variant MELA-AU 10 50718828 50718828 single base substitution G A upstream_gene_variant MELA-AU 10 50719084 50719084 single base substitution A G intron_variant MELA-AU 10 50719148 50719148 single base substitution G A intron_variant MELA-AU 10 50719365 50719365 single base substitution G A intron_variant MELA-AU 10 50719862 50719862 single base substitution A G intron_variant MELA-AU 10 50720732 50720732 single base substitution G A intron_variant MELA-AU 10 50720842 50720842 single base substitution G A intron_variant MELA-AU 10 50721330 50721330 single base substitution G A intron_variant MELA-AU 10 50721348 50721348 single base substitution G A intron_variant MELA-AU 10 50721737 50721737 single base substitution G A intron_variant MELA-AU 10 50722211 50722211 single base substitution G A intron_variant MELA-AU 10 50722493 50722493 single base substitution C T intron_variant MELA-AU 10 50722649 50722649 single base substitution G A intron_variant MELA-AU 10 50723015 50723015 single base substitution G A intron_variant MELA-AU 10 50723087 50723087 single base substitution G A intron_variant MELA-AU 10 50723570 50723570 single base substitution G A intron_variant MELA-AU 10 50723948 50723948 single base substitution C T intron_variant MELA-AU 10 50723970 50723970 single base substitution G T intron_variant MELA-AU 10 50724230 50724230 single base substitution G A intron_variant MELA-AU 10 50724856 50724856 single base substitution G A intron_variant MELA-AU 10 50726804 50726804 single base substitution G A intron_variant MELA-AU 10 50726982 50726982 single base substitution A T intron_variant MELA-AU 10 50728274 50728275 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 10 50728274 50728275 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 50728697 50728697 single base substitution G A downstream_gene_variant MELA-AU 10 50728697 50728697 single base substitution G A intron_variant MELA-AU 10 50728715 50728715 single base substitution A G downstream_gene_variant MELA-AU 10 50728715 50728715 single base substitution A G intron_variant MELA-AU 10 50728762 50728762 single base substitution G A downstream_gene_variant MELA-AU 10 50728762 50728762 single base substitution G A intron_variant MELA-AU 10 50729022 50729022 single base substitution G A downstream_gene_variant MELA-AU 10 50729022 50729022 single base substitution G A intron_variant MELA-AU 10 50729416 50729416 single base substitution G A downstream_gene_variant MELA-AU 10 50729416 50729416 single base substitution G A intron_variant MELA-AU 10 50729492 50729492 single base substitution A T downstream_gene_variant MELA-AU 10 50729492 50729492 single base substitution A T intron_variant MELA-AU 10 50729689 50729689 single base substitution G C downstream_gene_variant MELA-AU 10 50729689 50729689 single base substitution G C intron_variant MELA-AU 10 50730597 50730597 single base substitution G A downstream_gene_variant MELA-AU 10 50730597 50730597 single base substitution G A intron_variant MELA-AU 10 50730875 50730875 single base substitution G A downstream_gene_variant MELA-AU 10 50730875 50730875 single base substitution G A intron_variant MELA-AU 10 50731181 50731181 single base substitution G A downstream_gene_variant MELA-AU 10 50731181 50731181 single base substitution G A intron_variant MELA-AU 10 50731721 50731721 single base substitution T A downstream_gene_variant MELA-AU 10 50731721 50731721 single base substitution T A intron_variant MELA-AU 10 50731856 50731856 single base substitution C A downstream_gene_variant MELA-AU 10 50731856 50731856 single base substitution C A intron_variant MELA-AU 10 50731961 50731961 single base substitution C T downstream_gene_variant MELA-AU 10 50731961 50731961 single base substitution C T intron_variant MELA-AU 10 50732515 50732515 single base substitution G A downstream_gene_variant MELA-AU 10 50732515 50732515 single base substitution G A synonymous_variant L321L 961C>T MELA-AU 10 50733290 50733290 single base substitution A G intron_variant MELA-AU 10 50733687 50733687 single base substitution G A intron_variant MELA-AU 10 50734409 50734409 single base substitution G A downstream_gene_variant MELA-AU 10 50734409 50734409 single base substitution G A intron_variant MELA-AU 10 50734441 50734441 single base substitution G A downstream_gene_variant MELA-AU 10 50734441 50734441 single base substitution G A intron_variant MELA-AU 10 50734633 50734633 single base substitution A T downstream_gene_variant MELA-AU 10 50734633 50734633 single base substitution A T intron_variant MELA-AU 10 50734780 50734780 single base substitution G A downstream_gene_variant MELA-AU 10 50734780 50734780 single base substitution G A intron_variant MELA-AU 10 50734863 50734863 single base substitution G A downstream_gene_variant MELA-AU 10 50734863 50734863 single base substitution G A intron_variant MELA-AU 10 50735376 50735376 single base substitution A G downstream_gene_variant MELA-AU 10 50735376 50735376 single base substitution A G intron_variant MELA-AU 10 50735518 50735518 single base substitution C T downstream_gene_variant MELA-AU 10 50735518 50735518 single base substitution C T intron_variant MELA-AU 10 50735540 50735540 single base substitution G A downstream_gene_variant MELA-AU 10 50735540 50735540 single base substitution G A intron_variant MELA-AU 10 50737266 50737266 single base substitution T C downstream_gene_variant MELA-AU 10 50737266 50737266 single base substitution T C intron_variant MELA-AU 10 50737282 50737282 single base substitution G A downstream_gene_variant MELA-AU 10 50737282 50737282 single base substitution G A intron_variant MELA-AU 10 50737291 50737291 single base substitution G A downstream_gene_variant MELA-AU 10 50737291 50737291 single base substitution G A intron_variant MELA-AU 10 50737546 50737546 single base substitution C T downstream_gene_variant MELA-AU 10 50737546 50737546 single base substitution C T intron_variant MELA-AU 10 50737684 50737684 single base substitution G A downstream_gene_variant MELA-AU 10 50737684 50737684 single base substitution G A intron_variant MELA-AU 10 50739003 50739003 single base substitution G A intron_variant MELA-AU 10 50739003 50739003 single base substitution G A upstream_gene_variant MELA-AU 10 50739262 50739262 single base substitution G A intron_variant MELA-AU 10 50739262 50739262 single base substitution G A upstream_gene_variant MELA-AU 10 50740591 50740591 single base substitution G A splice_region_variant MELA-AU 10 50740591 50740591 single base substitution G A upstream_gene_variant MELA-AU 10 50740971 50740971 single base substitution C T missense_variant E14K 40G>A MELA-AU 10 50740971 50740971 single base substitution C T upstream_gene_variant MELA-AU 10 50741012 50741012 single base substitution C T 5_prime_UTR_variant MELA-AU 10 50741012 50741012 single base substitution C T upstream_gene_variant MELA-AU 10 50741032 50741032 single base substitution G A splice_region_variant MELA-AU 10 50741032 50741032 single base substitution G A upstream_gene_variant MELA-AU 10 50741279 50741279 single base substitution G A intron_variant MELA-AU 10 50741279 50741279 single base substitution G A upstream_gene_variant MELA-AU 10 50741302 50741302 single base substitution G A intron_variant MELA-AU 10 50741302 50741302 single base substitution G A upstream_gene_variant MELA-AU 10 50741659 50741659 single base substitution G A intron_variant MELA-AU 10 50741659 50741659 single base substitution G A upstream_gene_variant MELA-AU 10 50742431 50742431 single base substitution A G intron_variant MELA-AU 10 50742431 50742431 single base substitution A G upstream_gene_variant MELA-AU 10 50742635 50742635 single base substitution G A intron_variant MELA-AU 10 50742635 50742635 single base substitution G A upstream_gene_variant MELA-AU 10 50743563 50743563 single base substitution G A intron_variant MELA-AU 10 50743563 50743563 single base substitution G A upstream_gene_variant MELA-AU 10 50744581 50744581 single base substitution C T intron_variant MELA-AU 10 50745534 50745534 insertion of <=200bp - TA intron_variant MELA-AU 10 50745749 50745749 single base substitution G A intron_variant MELA-AU 10 50747155 50747155 single base substitution G A intron_variant MELA-AU 10 50747155 50747155 single base substitution G A upstream_gene_variant MELA-AU 10 50749483 50749483 single base substitution G A upstream_gene_variant MELA-AU 10 50749606 50749606 single base substitution C T upstream_gene_variant MELA-AU 10 50749956 50749956 single base substitution G A upstream_gene_variant MELA-AU 10 50750044 50750044 single base substitution C T upstream_gene_variant MELA-AU 10 50750226 50750226 single base substitution G A upstream_gene_variant MELA-AU 10 50750609 50750609 single base substitution A C upstream_gene_variant MELA-AU 10 50750778 50750778 single base substitution G A upstream_gene_variant MELA-AU 10 50750927 50750927 single base substitution C T upstream_gene_variant MELA-AU 10 50751687 50751687 single base substitution C T upstream_gene_variant MELA-AU 10 50751903 50751903 single base substitution T A upstream_gene_variant MELA-AU 10 50752025 50752025 single base substitution G A upstream_gene_variant MELA-AU 10 50752356 50752356 single base substitution T C upstream_gene_variant MELA-AU 10 50752450 50752450 single base substitution G A upstream_gene_variant MELA-AU 10 50752530 50752530 single base substitution C T upstream_gene_variant ORCA-IN 10 50666893 50666893 single base substitution C G downstream_gene_variant ORCA-IN 10 50666893 50666893 single base substitution C G missense_variant G1484R 4450G>C ORCA-IN 10 50666893 50666893 single base substitution C G missense_variant G854R 2560G>C ORCA-IN 10 50672968 50672968 single base substitution G A intron_variant ORCA-IN 10 50678426 50678426 single base substitution C G missense_variant E1194Q 3580G>C ORCA-IN 10 50678426 50678426 single base substitution C G missense_variant E564Q 1690G>C ORCA-IN 10 50678426 50678426 single base substitution C G upstream_gene_variant ORCA-IN 10 50678746 50678746 single base substitution C T missense_variant R1087Q 3260G>A ORCA-IN 10 50678746 50678746 single base substitution C T missense_variant R457Q 1370G>A ORCA-IN 10 50678746 50678746 single base substitution C T upstream_gene_variant ORCA-IN 10 50679731 50679731 single base substitution C G intron_variant ORCA-IN 10 50679731 50679731 single base substitution C G upstream_gene_variant ORCA-IN 10 50687419 50687419 single base substitution C T downstream_gene_variant ORCA-IN 10 50687419 50687419 single base substitution C T intron_variant ORCA-IN 10 50690596 50690596 insertion of <=200bp - A downstream_gene_variant ORCA-IN 10 50690596 50690596 insertion of <=200bp - A intron_variant ORCA-IN 10 50715790 50715790 single base substitution T C intron_variant ORCA-IN 10 50715790 50715790 single base substitution T C upstream_gene_variant ORCA-IN 10 50737876 50737876 single base substitution C T downstream_gene_variant ORCA-IN 10 50737876 50737876 single base substitution C T intron_variant OV-AU 10 50662491 50662491 single base substitution G A downstream_gene_variant OV-AU 10 50668007 50668007 single base substitution G A downstream_gene_variant OV-AU 10 50668007 50668007 single base substitution G A intron_variant OV-AU 10 50668009 50668009 single base substitution G A downstream_gene_variant OV-AU 10 50668009 50668009 single base substitution G A intron_variant OV-AU 10 50676481 50676481 single base substitution C A intron_variant OV-AU 10 50680305 50680305 single base substitution A C intron_variant OV-AU 10 50680305 50680305 single base substitution A C upstream_gene_variant OV-AU 10 50686819 50686819 single base substitution C G downstream_gene_variant OV-AU 10 50686819 50686819 single base substitution C G intron_variant OV-AU 10 50692552 50692552 single base substitution G A intron_variant OV-AU 10 50696018 50696018 single base substitution C T intron_variant OV-AU 10 50697256 50697256 single base substitution G T intron_variant OV-AU 10 50726182 50726182 single base substitution C G intron_variant OV-AU 10 50735616 50735616 single base substitution G C downstream_gene_variant OV-AU 10 50735616 50735616 single base substitution G C intron_variant OV-AU 10 50741159 50741159 single base substitution A C intron_variant OV-AU 10 50741159 50741159 single base substitution A C upstream_gene_variant OV-AU 10 50745200 50745200 single base substitution A G intron_variant OV-AU 10 50746377 50746377 single base substitution G C intron_variant OV-AU 10 50752295 50752295 single base substitution G C upstream_gene_variant OV-US 10 50708600 50708600 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant OV-US 10 50708600 50708600 single base substitution G C exon_variant OV-US 10 50708600 50708600 single base substitution G C missense_variant R557G 1669C>G OV-US 10 50708699 50708699 single base substitution G A 5_prime_UTR_variant OV-US 10 50708699 50708699 single base substitution G A exon_variant OV-US 10 50708699 50708699 single base substitution G A stop_gained Q524* 1570C>T PACA-AU 10 50670579 50670579 single base substitution A T intron_variant PACA-AU 10 50681033 50681033 single base substitution G A synonymous_variant G287G 861C>T PACA-AU 10 50681033 50681033 single base substitution G A synonymous_variant G917G 2751C>T PACA-AU 10 50681033 50681033 single base substitution G A upstream_gene_variant PACA-AU 10 50681478 50681478 single base substitution C T intron_variant PACA-AU 10 50681478 50681478 single base substitution C T upstream_gene_variant PACA-AU 10 50681711 50681711 single base substitution T C intron_variant PACA-AU 10 50681711 50681711 single base substitution T C upstream_gene_variant PACA-AU 10 50686482 50686482 single base substitution C T downstream_gene_variant PACA-AU 10 50686482 50686482 single base substitution C T missense_variant R105Q 314G>A PACA-AU 10 50686482 50686482 single base substitution C T missense_variant R735Q 2204G>A PACA-AU 10 50687801 50687801 single base substitution G C downstream_gene_variant PACA-AU 10 50687801 50687801 single base substitution G C intron_variant PACA-AU 10 50689388 50689388 single base substitution A T downstream_gene_variant PACA-AU 10 50689388 50689388 single base substitution A T intron_variant PACA-AU 10 50692337 50692337 single base substitution A G intron_variant PACA-AU 10 50702153 50702153 single base substitution G T intron_variant PACA-AU 10 50708673 50708673 single base substitution A G 5_prime_UTR_variant PACA-AU 10 50708673 50708673 single base substitution A G exon_variant PACA-AU 10 50708673 50708673 single base substitution A G synonymous_variant D532D 1596T>C PACA-AU 10 50710456 50710456 single base substitution C T intron_variant PACA-AU 10 50710456 50710456 single base substitution C T upstream_gene_variant PACA-AU 10 50710541 50710541 single base substitution A T intron_variant PACA-AU 10 50710541 50710541 single base substitution A T upstream_gene_variant PACA-AU 10 50711561 50711561 single base substitution C T intron_variant PACA-AU 10 50711561 50711561 single base substitution C T upstream_gene_variant PACA-AU 10 50714735 50714735 deletion of <=200bp A - intron_variant PACA-AU 10 50714735 50714735 deletion of <=200bp A - upstream_gene_variant PACA-AU 10 50716428 50716428 single base substitution G A intron_variant PACA-AU 10 50716428 50716428 single base substitution G A upstream_gene_variant PACA-AU 10 50725814 50725814 single base substitution T A intron_variant PACA-AU 10 50726903 50726903 single base substitution A T intron_variant PACA-AU 10 50729240 50729240 single base substitution A G downstream_gene_variant PACA-AU 10 50729240 50729240 single base substitution A G intron_variant PACA-AU 10 50738246 50738246 single base substitution G A downstream_gene_variant PACA-AU 10 50738246 50738246 single base substitution G A intron_variant PACA-AU 10 50738565 50738565 deletion of <=200bp T - downstream_gene_variant PACA-AU 10 50738565 50738565 deletion of <=200bp T - intron_variant PACA-AU 10 50746614 50746615 deletion of <=200bp TT - intron_variant PACA-AU 10 50750929 50750929 single base substitution T A upstream_gene_variant PACA-AU 10 50751730 50751730 single base substitution C T upstream_gene_variant PACA-AU 10 50752453 50752453 deletion of <=200bp G - upstream_gene_variant PACA-CA 10 50659365 50659365 single base substitution T C downstream_gene_variant PACA-CA 10 50659562 50659562 single base substitution C A downstream_gene_variant PACA-CA 10 50660947 50660947 single base substitution T A downstream_gene_variant PACA-CA 10 50664695 50664695 insertion of <=200bp - T 3_prime_UTR_variant PACA-CA 10 50664695 50664695 insertion of <=200bp - T downstream_gene_variant PACA-CA 10 50675231 50675231 single base substitution C T intron_variant PACA-CA 10 50677368 50677368 single base substitution T G intron_variant PACA-CA 10 50681596 50681596 single base substitution T G missense_variant K249T 746A>C PACA-CA 10 50681596 50681596 single base substitution T G missense_variant K879T 2636A>C PACA-CA 10 50681596 50681596 single base substitution T G upstream_gene_variant PACA-CA 10 50684402 50684402 single base substitution T A intron_variant PACA-CA 10 50688396 50688396 single base substitution A G downstream_gene_variant PACA-CA 10 50688396 50688396 single base substitution A G intron_variant PACA-CA 10 50688503 50688503 single base substitution G T downstream_gene_variant PACA-CA 10 50688503 50688503 single base substitution G T intron_variant PACA-CA 10 50689388 50689388 single base substitution A T downstream_gene_variant PACA-CA 10 50689388 50689388 single base substitution A T intron_variant PACA-CA 10 50690959 50690959 single base substitution C T downstream_gene_variant PACA-CA 10 50690959 50690959 single base substitution C T intron_variant PACA-CA 10 50693318 50693318 single base substitution G A intron_variant PACA-CA 10 50695892 50695892 single base substitution G A intron_variant PACA-CA 10 50696291 50696291 single base substitution C A intron_variant PACA-CA 10 50700875 50700875 single base substitution C A intron_variant PACA-CA 10 50705673 50705673 single base substitution C T intron_variant PACA-CA 10 50709616 50709616 single base substitution T A intron_variant PACA-CA 10 50710189 50710189 single base substitution G A intron_variant PACA-CA 10 50710189 50710189 single base substitution G A upstream_gene_variant PACA-CA 10 50711885 50711885 single base substitution G C intron_variant PACA-CA 10 50711885 50711885 single base substitution G C upstream_gene_variant PACA-CA 10 50713172 50713172 single base substitution T C intron_variant PACA-CA 10 50713172 50713172 single base substitution T C upstream_gene_variant PACA-CA 10 50713442 50713442 single base substitution G A intron_variant PACA-CA 10 50713442 50713442 single base substitution G A upstream_gene_variant PACA-CA 10 50715495 50715495 insertion of <=200bp - A intron_variant PACA-CA 10 50715495 50715495 insertion of <=200bp - A upstream_gene_variant PACA-CA 10 50719533 50719533 single base substitution C T intron_variant PACA-CA 10 50724097 50724098 deletion of <=200bp AA - intron_variant PACA-CA 10 50724321 50724321 single base substitution G A intron_variant PACA-CA 10 50727215 50727215 single base substitution G A intron_variant PACA-CA 10 50734335 50734335 single base substitution T C downstream_gene_variant PACA-CA 10 50734335 50734335 single base substitution T C intron_variant PACA-CA 10 50740239 50740239 single base substitution G A intron_variant PACA-CA 10 50740239 50740239 single base substitution G A upstream_gene_variant PACA-CA 10 50743419 50743419 single base substitution T C intron_variant PACA-CA 10 50743419 50743419 single base substitution T C upstream_gene_variant PACA-CA 10 50746252 50746252 single base substitution G A intron_variant PACA-CA 10 50746588 50746588 single base substitution G A intron_variant PACA-CA 10 50749005 50749005 single base substitution A G upstream_gene_variant PACA-CA 10 50751339 50751339 single base substitution C T upstream_gene_variant PACA-CA 10 50751548 50751548 single base substitution T G upstream_gene_variant PACA-CA 10 50751931 50751931 single base substitution C T upstream_gene_variant PACA-CA 10 50752450 50752450 insertion of <=200bp - A upstream_gene_variant PACA-CA 10 50752522 50752522 single base substitution T A upstream_gene_variant PAEN-AU 10 50678065 50678065 single base substitution C T intron_variant PAEN-AU 10 50739300 50739300 single base substitution C T intron_variant PAEN-AU 10 50739300 50739300 single base substitution C T upstream_gene_variant PBCA-DE 10 50663881 50663881 single base substitution C T 3_prime_UTR_variant PBCA-DE 10 50663881 50663881 single base substitution C T downstream_gene_variant PBCA-DE 10 50667132 50667132 single base substitution C T downstream_gene_variant PBCA-DE 10 50667132 50667132 single base substitution C T missense_variant R1404H 4211G>A PBCA-DE 10 50667132 50667132 single base substitution C T missense_variant R774H 2321G>A PBCA-DE 10 50670545 50670545 insertion of <=200bp - A intron_variant PBCA-DE 10 50678066 50678066 single base substitution G A intron_variant PBCA-DE 10 50703709 50703709 single base substitution G T intron_variant PBCA-DE 10 50705461 50705461 single base substitution G T intron_variant PBCA-DE 10 50719080 50719080 single base substitution A T intron_variant PBCA-DE 10 50725246 50725246 deletion of <=200bp T - intron_variant PBCA-DE 10 50742651 50742651 single base substitution G A intron_variant PBCA-DE 10 50742651 50742651 single base substitution G A upstream_gene_variant PRAD-CA 10 50667133 50667133 single base substitution G A downstream_gene_variant PRAD-CA 10 50667133 50667133 single base substitution G A missense_variant R1404C 4210C>T PRAD-CA 10 50667133 50667133 single base substitution G A missense_variant R774C 2320C>T PRAD-CA 10 50680093 50680093 single base substitution T A intron_variant PRAD-CA 10 50680093 50680093 single base substitution T A upstream_gene_variant PRAD-CA 10 50681205 50681205 single base substitution G C intron_variant PRAD-CA 10 50681205 50681205 single base substitution G C upstream_gene_variant PRAD-CA 10 50690168 50690168 single base substitution C A downstream_gene_variant PRAD-CA 10 50690168 50690168 single base substitution C A intron_variant PRAD-CA 10 50692338 50692338 single base substitution G A intron_variant PRAD-CA 10 50695786 50695786 single base substitution A C intron_variant PRAD-CA 10 50712397 50712397 single base substitution A G intron_variant PRAD-CA 10 50712397 50712397 single base substitution A G upstream_gene_variant PRAD-CA 10 50718221 50718221 single base substitution C T intron_variant PRAD-CA 10 50718221 50718221 single base substitution C T upstream_gene_variant PRAD-UK 10 50662443 50662443 single base substitution G T downstream_gene_variant PRAD-UK 10 50669364 50669364 single base substitution C T intron_variant PRAD-UK 10 50676480 50676480 single base substitution C G intron_variant PRAD-UK 10 50683169 50683169 deletion of <=200bp A - intron_variant PRAD-UK 10 50683169 50683169 deletion of <=200bp A - upstream_gene_variant PRAD-UK 10 50697786 50697786 insertion of <=200bp - A intron_variant PRAD-UK 10 50703171 50703171 single base substitution C T intron_variant PRAD-UK 10 50737922 50737922 single base substitution T A downstream_gene_variant PRAD-UK 10 50737922 50737922 single base substitution T A intron_variant PRAD-UK 10 50742941 50742941 single base substitution C T intron_variant PRAD-UK 10 50742941 50742941 single base substitution C T upstream_gene_variant PRAD-UK 10 50746636 50746636 single base substitution G A intron_variant PRAD-UK 10 50751581 50751581 single base substitution G A upstream_gene_variant PRAD-US 10 50666944 50666944 single base substitution G A downstream_gene_variant PRAD-US 10 50666944 50666944 single base substitution G A stop_gained R1467* 4399C>T PRAD-US 10 50666944 50666944 single base substitution G A stop_gained R837* 2509C>T PRAD-US 10 50680468 50680469 deletion of <=200bp AC - frameshift_variant VY329 PRAD-US 10 50680468 50680469 deletion of <=200bp AC - frameshift_variant VY959 PRAD-US 10 50680468 50680469 deletion of <=200bp AC - upstream_gene_variant PRAD-US 10 50732139 50732141 deletion of <=200bp CCT - disruptive_inframe_deletion GG445G PRAD-US 10 50732139 50732141 deletion of <=200bp CCT - downstream_gene_variant PRAD-US 10 50736488 50736492 deletion of <=200bp ATCTA - downstream_gene_variant PRAD-US 10 50736488 50736492 deletion of <=200bp ATCTA - exon_variant PRAD-US 10 50736488 50736492 deletion of <=200bp ATCTA - frameshift_variant LD208 READ-US 10 50678729 50678729 single base substitution C A missense_variant D1093Y 3277G>T READ-US 10 50678729 50678729 single base substitution C A missense_variant D463Y 1387G>T READ-US 10 50678729 50678729 single base substitution C A upstream_gene_variant READ-US 10 50679088 50679088 single base substitution G A synonymous_variant L1001L 3003C>T READ-US 10 50679088 50679088 single base substitution G A synonymous_variant L371L 1113C>T READ-US 10 50679088 50679088 single base substitution G A upstream_gene_variant READ-US 10 50691430 50691430 single base substitution G A exon_variant READ-US 10 50691430 50691430 single base substitution G A stop_gained R22* 64C>T READ-US 10 50691430 50691430 single base substitution G A stop_gained R652* 1954C>T READ-US 10 50723441 50723441 single base substitution G A intron_variant RECA-EU 10 50681367 50681367 single base substitution T A intron_variant RECA-EU 10 50681367 50681367 single base substitution T A upstream_gene_variant RECA-EU 10 50689157 50689157 single base substitution A T downstream_gene_variant RECA-EU 10 50689157 50689157 single base substitution A T intron_variant RECA-EU 10 50695289 50695289 single base substitution A C intron_variant RECA-EU 10 50707298 50707298 single base substitution C A intron_variant RECA-EU 10 50720212 50720212 single base substitution C T intron_variant RECA-EU 10 50726350 50726350 single base substitution A C intron_variant RECA-EU 10 50729808 50729808 single base substitution C A downstream_gene_variant RECA-EU 10 50729808 50729808 single base substitution C A intron_variant RECA-EU 10 50730666 50730666 single base substitution C T downstream_gene_variant RECA-EU 10 50730666 50730666 single base substitution C T intron_variant RECA-EU 10 50732580 50732580 single base substitution G A downstream_gene_variant RECA-EU 10 50732580 50732580 single base substitution G A missense_variant P299L 896C>T RECA-EU 10 50747925 50747925 single base substitution C T upstream_gene_variant SKCA-BR 10 50659494 50659494 single base substitution G C downstream_gene_variant SKCA-BR 10 50672653 50672653 single base substitution G A intron_variant SKCA-BR 10 50674614 50674614 single base substitution A G intron_variant SKCA-BR 10 50679600 50679600 single base substitution C T intron_variant SKCA-BR 10 50679600 50679600 single base substitution C T upstream_gene_variant SKCA-BR 10 50679951 50679951 single base substitution T A intron_variant SKCA-BR 10 50679951 50679951 single base substitution T A upstream_gene_variant SKCA-BR 10 50679970 50679970 single base substitution G A intron_variant SKCA-BR 10 50679970 50679970 single base substitution G A upstream_gene_variant SKCA-BR 10 50686072 50686072 single base substitution T C intron_variant SKCA-BR 10 50689038 50689038 single base substitution G A downstream_gene_variant SKCA-BR 10 50689038 50689038 single base substitution G A intron_variant SKCA-BR 10 50689817 50689817 single base substitution G A downstream_gene_variant SKCA-BR 10 50689817 50689817 single base substitution G A intron_variant SKCA-BR 10 50690585 50690585 insertion of <=200bp - ATTT downstream_gene_variant SKCA-BR 10 50690585 50690585 insertion of <=200bp - ATTT intron_variant SKCA-BR 10 50692346 50692346 single base substitution A G intron_variant SKCA-BR 10 50692467 50692467 single base substitution C T intron_variant SKCA-BR 10 50692939 50692941 deletion of <=200bp AAT - intron_variant SKCA-BR 10 50692942 50692942 single base substitution C T intron_variant SKCA-BR 10 50693350 50693350 single base substitution C T intron_variant SKCA-BR 10 50693632 50693632 single base substitution A T intron_variant SKCA-BR 10 50696315 50696315 single base substitution A C intron_variant SKCA-BR 10 50698403 50698403 insertion of <=200bp - CT intron_variant SKCA-BR 10 50703230 50703230 single base substitution G A intron_variant SKCA-BR 10 50706549 50706549 single base substitution G A intron_variant SKCA-BR 10 50710620 50710620 single base substitution G A intron_variant SKCA-BR 10 50710620 50710620 single base substitution G A upstream_gene_variant SKCA-BR 10 50714214 50714214 single base substitution G A intron_variant SKCA-BR 10 50714214 50714214 single base substitution G A upstream_gene_variant SKCA-BR 10 50716026 50716026 single base substitution G A intron_variant SKCA-BR 10 50716026 50716026 single base substitution G A upstream_gene_variant SKCA-BR 10 50721516 50721516 single base substitution C T intron_variant SKCA-BR 10 50721579 50721579 single base substitution G A intron_variant SKCA-BR 10 50722210 50722210 single base substitution G A intron_variant SKCA-BR 10 50725253 50725253 single base substitution C T intron_variant SKCA-BR 10 50730262 50730262 single base substitution A C downstream_gene_variant SKCA-BR 10 50730262 50730262 single base substitution A C intron_variant SKCA-BR 10 50731029 50731029 single base substitution C T downstream_gene_variant SKCA-BR 10 50731029 50731029 single base substitution C T intron_variant SKCA-BR 10 50731693 50731693 single base substitution G A downstream_gene_variant SKCA-BR 10 50731693 50731693 single base substitution G A intron_variant SKCA-BR 10 50734139 50734163 deletion of <=200bp ATATATTTATATATTTATATATTTT - downstream_gene_variant SKCA-BR 10 50734139 50734163 deletion of <=200bp ATATATTTATATATTTATATATTTT - intron_variant SKCA-BR 10 50734153 50734179 deletion of <=200bp TTATATATTTTTATATATATATATATA - downstream_gene_variant SKCA-BR 10 50734153 50734179 deletion of <=200bp TTATATATTTTTATATATATATATATA - intron_variant SKCA-BR 10 50734169 50734169 single base substitution A T downstream_gene_variant SKCA-BR 10 50734169 50734169 single base substitution A T intron_variant SKCA-BR 10 50734177 50734177 single base substitution A T downstream_gene_variant SKCA-BR 10 50734177 50734177 single base substitution A T intron_variant SKCA-BR 10 50734185 50734185 single base substitution A T downstream_gene_variant SKCA-BR 10 50734185 50734185 single base substitution A T intron_variant SKCA-BR 10 50736979 50736979 single base substitution A G downstream_gene_variant SKCA-BR 10 50736979 50736979 single base substitution A G intron_variant SKCA-BR 10 50738275 50738275 single base substitution G A downstream_gene_variant SKCA-BR 10 50738275 50738275 single base substitution G A intron_variant SKCA-BR 10 50738855 50738855 single base substitution T C missense_variant K152E 454A>G SKCA-BR 10 50738855 50738855 single base substitution T C upstream_gene_variant SKCA-BR 10 50740894 50740894 single base substitution C T synonymous_variant G39G 117G>A SKCA-BR 10 50740894 50740894 single base substitution C T upstream_gene_variant SKCA-BR 10 50741429 50741429 single base substitution T C intron_variant SKCA-BR 10 50741429 50741429 single base substitution T C upstream_gene_variant SKCA-BR 10 50742047 50742047 single base substitution G A intron_variant SKCA-BR 10 50742047 50742047 single base substitution G A upstream_gene_variant SKCA-BR 10 50742488 50742488 single base substitution T C intron_variant SKCA-BR 10 50742488 50742488 single base substitution T C upstream_gene_variant SKCA-BR 10 50745554 50745554 insertion of <=200bp - TACACAC intron_variant SKCM-US 10 50666971 50666971 single base substitution A G downstream_gene_variant SKCM-US 10 50666971 50666971 single base substitution A G synonymous_variant L1458L 4372T>C SKCM-US 10 50666971 50666971 single base substitution A G synonymous_variant L828L 2482T>C SKCM-US 10 50667245 50667245 single base substitution G A downstream_gene_variant SKCM-US 10 50667245 50667245 single base substitution G A synonymous_variant V1366V 4098C>T SKCM-US 10 50667245 50667245 single base substitution G A synonymous_variant V736V 2208C>T SKCM-US 10 50678838 50678838 single base substitution G A synonymous_variant F1056F 3168C>T SKCM-US 10 50678838 50678838 single base substitution G A synonymous_variant F426F 1278C>T SKCM-US 10 50678838 50678838 single base substitution G A upstream_gene_variant SKCM-US 10 50679123 50679123 single base substitution G A missense_variant P360S 1078C>T SKCM-US 10 50679123 50679123 single base substitution G A missense_variant P990S 2968C>T SKCM-US 10 50679123 50679123 single base substitution G A upstream_gene_variant SKCM-US 10 50681610 50681610 single base substitution G A synonymous_variant F244F 732C>T SKCM-US 10 50681610 50681610 single base substitution G A synonymous_variant F874F 2622C>T SKCM-US 10 50681610 50681610 single base substitution G A upstream_gene_variant SKCM-US 10 50682166 50682166 single base substitution C T stop_gained W205* 615G>A SKCM-US 10 50682166 50682166 single base substitution C T stop_gained W835* 2505G>A SKCM-US 10 50682166 50682166 single base substitution C T upstream_gene_variant SKCM-US 10 50684298 50684298 single base substitution G A missense_variant S152F 455C>T SKCM-US 10 50684298 50684298 single base substitution G A missense_variant S782F 2345C>T SKCM-US 10 50686456 50686456 single base substitution G A downstream_gene_variant SKCM-US 10 50686456 50686456 single base substitution G A missense_variant R114W 340C>T SKCM-US 10 50686456 50686456 single base substitution G A missense_variant R744W 2230C>T SKCM-US 10 50686467 50686467 single base substitution G A downstream_gene_variant SKCM-US 10 50686467 50686467 single base substitution G A missense_variant P110L 329C>T SKCM-US 10 50686467 50686467 single base substitution G A missense_variant P740L 2219C>T SKCM-US 10 50686468 50686468 single base substitution G A downstream_gene_variant SKCM-US 10 50686468 50686468 single base substitution G A missense_variant P110S 328C>T SKCM-US 10 50686468 50686468 single base substitution G A missense_variant P740S 2218C>T SKCM-US 10 50690779 50690779 single base substitution G A downstream_gene_variant SKCM-US 10 50690779 50690779 single base substitution G A missense_variant S708F 2123C>T SKCM-US 10 50690779 50690779 single base substitution G A missense_variant S78F 233C>T SKCM-US 10 50690901 50690901 single base substitution G A downstream_gene_variant SKCM-US 10 50690901 50690901 single base substitution G A synonymous_variant T37T 111C>T SKCM-US 10 50690901 50690901 single base substitution G A synonymous_variant T667T 2001C>T SKCM-US 10 50690906 50690906 single base substitution G A downstream_gene_variant SKCM-US 10 50690906 50690906 single base substitution G A missense_variant R36C 106C>T SKCM-US 10 50690906 50690906 single base substitution G A missense_variant R666C 1996C>T SKCM-US 10 50691522 50691522 single base substitution A G 5_prime_UTR_variant SKCM-US 10 50691522 50691522 single base substitution A G exon_variant SKCM-US 10 50691522 50691522 single base substitution A G missense_variant L621S 1862T>C SKCM-US 10 50691550 50691550 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 10 50691550 50691550 single base substitution G A exon_variant SKCM-US 10 50691550 50691550 single base substitution G A stop_gained R612* 1834C>T SKCM-US 10 50691556 50691556 single base substitution G A 5_prime_UTR_variant SKCM-US 10 50691556 50691556 single base substitution G A exon_variant SKCM-US 10 50691556 50691556 single base substitution G A synonymous_variant L610L 1828C>T SKCM-US 10 50701195 50701195 single base substitution G A intron_variant SKCM-US 10 50701195 50701195 single base substitution G A synonymous_variant L597L 1789C>T SKCM-US 10 50701288 50701288 single base substitution A G intron_variant SKCM-US 10 50701288 50701288 single base substitution A G synonymous_variant L566L 1696T>C SKCM-US 10 50708721 50708721 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant SKCM-US 10 50708721 50708721 single base substitution C A exon_variant SKCM-US 10 50708721 50708721 single base substitution C A missense_variant R516S 1548G>T SKCM-US 10 50732569 50732569 single base substitution T C downstream_gene_variant SKCM-US 10 50732569 50732569 single base substitution T C missense_variant T303A 907A>G SKCM-US 10 50732687 50732687 single base substitution G A downstream_gene_variant SKCM-US 10 50732687 50732687 single base substitution G A synonymous_variant I263I 789C>T SKCM-US 10 50736487 50736487 single base substitution G A downstream_gene_variant SKCM-US 10 50736487 50736487 single base substitution G A exon_variant SKCM-US 10 50736487 50736487 single base substitution G A missense_variant H210Y 628C>T SKCM-US 10 50740841 50740841 single base substitution G A missense_variant S57F 170C>T SKCM-US 10 50740841 50740841 single base substitution G A upstream_gene_variant SKCM-US 10 50740971 50740971 single base substitution C T missense_variant E14K 40G>A SKCM-US 10 50740971 50740971 single base substitution C T upstream_gene_variant SKCM-US 10 50740990 50740990 single base substitution G A synonymous_variant P7P 21C>T SKCM-US 10 50740990 50740990 single base substitution G A upstream_gene_variant STAD-US 10 50667115 50667115 single base substitution C T downstream_gene_variant STAD-US 10 50667115 50667115 single base substitution C T missense_variant G1410R 4228G>A STAD-US 10 50667115 50667115 single base substitution C T missense_variant G780R 2338G>A STAD-US 10 50669423 50669423 insertion of <=200bp - C exon_variant STAD-US 10 50669423 50669423 insertion of <=200bp - C frameshift_variant I1320S? STAD-US 10 50669423 50669423 insertion of <=200bp - C frameshift_variant I690S? STAD-US 10 50669424 50669424 insertion of <=200bp - C exon_variant STAD-US 10 50669424 50669424 insertion of <=200bp - C frameshift_variant G1319G? STAD-US 10 50669424 50669424 insertion of <=200bp - C frameshift_variant G689G? STAD-US 10 50678232 50678232 single base substitution T G exon_variant STAD-US 10 50678232 50678232 single base substitution T G missense_variant K1258N 3774A>C STAD-US 10 50678232 50678232 single base substitution T G missense_variant K628N 1884A>C STAD-US 10 50678283 50678286 deletion of <=200bp CTCA - exon_variant STAD-US 10 50678283 50678286 deletion of <=200bp CTCA - frameshift_variant SE1240 STAD-US 10 50678283 50678286 deletion of <=200bp CTCA - frameshift_variant SE610 STAD-US 10 50678377 50678377 single base substitution T G missense_variant K1210T 3629A>C STAD-US 10 50678377 50678377 single base substitution T G missense_variant K580T 1739A>C STAD-US 10 50678377 50678377 single base substitution T G upstream_gene_variant STAD-US 10 50678501 50678501 deletion of <=200bp A - frameshift_variant W1169 STAD-US 10 50678501 50678501 deletion of <=200bp A - frameshift_variant W539 STAD-US 10 50678501 50678501 deletion of <=200bp A - upstream_gene_variant STAD-US 10 50678712 50678712 single base substitution A G synonymous_variant S1098S 3294T>C STAD-US 10 50678712 50678712 single base substitution A G synonymous_variant S468S 1404T>C STAD-US 10 50678712 50678712 single base substitution A G upstream_gene_variant STAD-US 10 50678849 50678849 single base substitution G A missense_variant R1053C 3157C>T STAD-US 10 50678849 50678849 single base substitution G A missense_variant R423C 1267C>T STAD-US 10 50678849 50678849 single base substitution G A upstream_gene_variant STAD-US 10 50679169 50679169 deletion of <=200bp A - splice_region_variant STAD-US 10 50679169 50679169 deletion of <=200bp A - upstream_gene_variant STAD-US 10 50680490 50680490 single base substitution G A synonymous_variant G322G 966C>T STAD-US 10 50680490 50680490 single base substitution G A synonymous_variant G952G 2856C>T STAD-US 10 50680490 50680490 single base substitution G A upstream_gene_variant STAD-US 10 50680508 50680508 single base substitution C A missense_variant E316D 948G>T STAD-US 10 50680508 50680508 single base substitution C A missense_variant E946D 2838G>T STAD-US 10 50680508 50680508 single base substitution C A upstream_gene_variant STAD-US 10 50681583 50681583 single base substitution G C synonymous_variant L253L 759C>G STAD-US 10 50681583 50681583 single base substitution G C synonymous_variant L883L 2649C>G STAD-US 10 50681583 50681583 single base substitution G C upstream_gene_variant STAD-US 10 50682250 50682250 single base substitution G A synonymous_variant N177N 531C>T STAD-US 10 50682250 50682250 single base substitution G A synonymous_variant N807N 2421C>T STAD-US 10 50682250 50682250 single base substitution G A upstream_gene_variant STAD-US 10 50686478 50686478 single base substitution A G downstream_gene_variant STAD-US 10 50686478 50686478 single base substitution A G synonymous_variant D106D 318T>C STAD-US 10 50686478 50686478 single base substitution A G synonymous_variant D736D 2208T>C STAD-US 10 50686483 50686483 single base substitution G A downstream_gene_variant STAD-US 10 50686483 50686483 single base substitution G A stop_gained R105* 313C>T STAD-US 10 50686483 50686483 single base substitution G A stop_gained R735* 2203C>T STAD-US 10 50690777 50690777 single base substitution C T downstream_gene_variant STAD-US 10 50690777 50690777 single base substitution C T missense_variant V709I 2125G>A STAD-US 10 50690777 50690777 single base substitution C T missense_variant V79I 235G>A STAD-US 10 50691467 50691467 single base substitution G A exon_variant STAD-US 10 50691467 50691467 single base substitution G A synonymous_variant D639D 1917C>T STAD-US 10 50691467 50691467 single base substitution G A synonymous_variant D9D 27C>T STAD-US 10 50701183 50701183 single base substitution C T intron_variant STAD-US 10 50701183 50701183 single base substitution C T missense_variant G601S 1801G>A STAD-US 10 50701224 50701224 single base substitution G A intron_variant STAD-US 10 50701224 50701224 single base substitution G A missense_variant T587M 1760C>T STAD-US 10 50723435 50723435 single base substitution C T intron_variant STAD-US 10 50723502 50723502 single base substitution A G intron_variant STAD-US 10 50724274 50724274 single base substitution T G intron_variant STAD-US 10 50724334 50724334 single base substitution T C intron_variant STAD-US 10 50732109 50732109 single base substitution C T downstream_gene_variant STAD-US 10 50732109 50732109 single base substitution C T missense_variant G456E 1367G>A STAD-US 10 50732318 50732318 single base substitution G A downstream_gene_variant STAD-US 10 50732318 50732318 single base substitution G A synonymous_variant D386D 1158C>T STAD-US 10 50732687 50732687 single base substitution G A downstream_gene_variant STAD-US 10 50732687 50732687 single base substitution G A synonymous_variant I263I 789C>T STAD-US 10 50736484 50736484 single base substitution C T downstream_gene_variant STAD-US 10 50736484 50736484 single base substitution C T exon_variant STAD-US 10 50736484 50736484 single base substitution C T missense_variant A211T 631G>A STAD-US 10 50736485 50736485 single base substitution G A downstream_gene_variant STAD-US 10 50736485 50736485 single base substitution G A exon_variant STAD-US 10 50736485 50736485 single base substitution G A synonymous_variant H210H 630C>T STAD-US 10 50740632 50740632 single base substitution C T missense_variant V127I 379G>A STAD-US 10 50740632 50740632 single base substitution C T upstream_gene_variant STAD-US 10 50740814 50740814 single base substitution G A missense_variant P66L 197C>T STAD-US 10 50740814 50740814 single base substitution G A upstream_gene_variant THCA-SA 10 50678317 50678317 single base substitution C G exon_variant THCA-SA 10 50678317 50678317 single base substitution C G missense_variant R1230P 3689G>C THCA-SA 10 50678317 50678317 single base substitution C G missense_variant R600P 1799G>C THCA-US 10 50723850 50723850 single base substitution G A intron_variant THCA-US 10 50732508 50732508 single base substitution T C downstream_gene_variant THCA-US 10 50732508 50732508 single base substitution T C missense_variant K323R 968A>G UCEC-US 10 50667076 50667076 single base substitution C A downstream_gene_variant UCEC-US 10 50667076 50667076 single base substitution C A stop_gained E1423* 4267G>T UCEC-US 10 50667076 50667076 single base substitution C A stop_gained E793* 2377G>T UCEC-US 10 50667132 50667132 single base substitution C T downstream_gene_variant UCEC-US 10 50667132 50667132 single base substitution C T missense_variant R1404H 4211G>A UCEC-US 10 50667132 50667132 single base substitution C T missense_variant R774H 2321G>A UCEC-US 10 50669518 50669518 single base substitution C T exon_variant UCEC-US 10 50669518 50669518 single base substitution C T missense_variant R1288Q 3863G>A UCEC-US 10 50669518 50669518 single base substitution C T missense_variant R658Q 1973G>A UCEC-US 10 50678344 50678344 single base substitution C T missense_variant R1221Q 3662G>A UCEC-US 10 50678344 50678344 single base substitution C T missense_variant R591Q 1772G>A UCEC-US 10 50678344 50678344 single base substitution C T upstream_gene_variant UCEC-US 10 50678569 50678569 single base substitution C A missense_variant S1146I 3437G>T UCEC-US 10 50678569 50678569 single base substitution C A missense_variant S516I 1547G>T UCEC-US 10 50678569 50678569 single base substitution C A upstream_gene_variant UCEC-US 10 50678746 50678746 single base substitution C T missense_variant R1087Q 3260G>A UCEC-US 10 50678746 50678746 single base substitution C T missense_variant R457Q 1370G>A UCEC-US 10 50678746 50678746 single base substitution C T upstream_gene_variant UCEC-US 10 50680487 50680487 single base substitution C G missense_variant Q323H 969G>C UCEC-US 10 50680487 50680487 single base substitution C G missense_variant Q953H 2859G>C UCEC-US 10 50680487 50680487 single base substitution C G upstream_gene_variant UCEC-US 10 50681042 50681042 single base substitution C T synonymous_variant T284T 852G>A UCEC-US 10 50681042 50681042 single base substitution C T synonymous_variant T914T 2742G>A UCEC-US 10 50681042 50681042 single base substitution C T upstream_gene_variant UCEC-US 10 50681554 50681554 single base substitution G T stop_gained S263* 788C>A UCEC-US 10 50681554 50681554 single base substitution G T stop_gained S893* 2678C>A UCEC-US 10 50681554 50681554 single base substitution G T upstream_gene_variant UCEC-US 10 50682119 50682119 single base substitution C A missense_variant W221L 662G>T UCEC-US 10 50682119 50682119 single base substitution C A missense_variant W851L 2552G>T UCEC-US 10 50682119 50682119 single base substitution C A upstream_gene_variant UCEC-US 10 50682124 50682124 single base substitution T G missense_variant K219N 657A>C UCEC-US 10 50682124 50682124 single base substitution T G missense_variant K849N 2547A>C UCEC-US 10 50682124 50682124 single base substitution T G upstream_gene_variant UCEC-US 10 50682263 50682263 single base substitution C A missense_variant R173I 518G>T UCEC-US 10 50682263 50682263 single base substitution C A missense_variant R803I 2408G>T UCEC-US 10 50682263 50682263 single base substitution C A upstream_gene_variant UCEC-US 10 50684283 50684283 single base substitution C T missense_variant R157K 470G>A UCEC-US 10 50684283 50684283 single base substitution C T missense_variant R787K 2360G>A UCEC-US 10 50686488 50686488 single base substitution A G downstream_gene_variant UCEC-US 10 50686488 50686488 single base substitution A G missense_variant V103A 308T>C UCEC-US 10 50686488 50686488 single base substitution A G missense_variant V733A 2198T>C UCEC-US 10 50690857 50690857 single base substitution A C downstream_gene_variant UCEC-US 10 50690857 50690857 single base substitution A C missense_variant L52R 155T>G UCEC-US 10 50690857 50690857 single base substitution A C missense_variant L682R 2045T>G UCEC-US 10 50723611 50723611 single base substitution C T intron_variant UCEC-US 10 50723687 50723687 single base substitution C T intron_variant UCEC-US 10 50723721 50723721 single base substitution C A intron_variant UCEC-US 10 50723827 50723827 single base substitution A T intron_variant UCEC-US 10 50723956 50723956 single base substitution C T intron_variant UCEC-US 10 50724040 50724040 single base substitution G A intron_variant UCEC-US 10 50724704 50724704 single base substitution C T intron_variant UCEC-US 10 50725153 50725153 single base substitution C T intron_variant UCEC-US 10 50732357 50732357 single base substitution C A downstream_gene_variant UCEC-US 10 50732357 50732357 single base substitution C A missense_variant E373D 1119G>T UCEC-US 10 50732498 50732498 single base substitution C A downstream_gene_variant UCEC-US 10 50732498 50732498 single base substitution C A missense_variant E326D 978G>T UCEC-US 10 50732596 50732596 single base substitution C T downstream_gene_variant UCEC-US 10 50732596 50732596 single base substitution C T missense_variant A294T 880G>A UCEC-US 10 50732662 50732662 single base substitution C T downstream_gene_variant UCEC-US 10 50732662 50732662 single base substitution C T missense_variant E272K 814G>A UCEC-US 10 50738878 50738878 single base substitution G A missense_variant T144M 431C>T UCEC-US 10 50738878 50738878 single base substitution G A upstream_gene_variant UCEC-US 10 50740606 50740606 single base substitution C T synonymous_variant S135S 405G>A UCEC-US 10 50740606 50740606 single base substitution C T upstream_gene_variant UCEC-US 10 50740827 50740827 single base substitution C T missense_variant A62T 184G>A UCEC-US 10 50740827 50740827 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 2521262 COSM5892072 c.307G>A p.D103N Substitution - Missense 10:49532658-49532658 - TCGA-D8-A1XK-01 COSM3807284 c.972A>G p.K324K Substitution - coding silent 10:49524458-49524458 - CRC-04T COSM5468419 c.3755T>G p.L1252W Substitution - Missense 10:49470205-49470205 - PD23560a COSM5768132 c.2243C>T p.S748L Substitution - Missense 10:49478397-49478397 - TCGA-B0-5104-01 COSM3358771 c.1245G>A p.K415K Substitution - coding silent 10:49524185-49524185 - HCC2218 COSM13871 c.3113G>C p.R1038T Substitution - Missense 10:49470847-49470847 - LUAD-NYU330 COSM373758 c.1226A>T p.K409M Substitution - Missense 10:49524204-49524204 - SH-3133 COSM5019758 c.2048G>A p.R683Q Substitution - Missense 10:49482808-49482808 - 8066067 COSM2145472 c.1596T>C p.D532D Substitution - coding silent 10:49500627-49500627 - QC2-22-T2 COSM4014448 c.2203C>T p.R735* Substitution - Nonsense 10:49478437-49478437 - CHEWS028 COSM4573643 c.1670G>A p.R557H Substitution - Missense 10:49500553-49500553 - Mx3 COSM33281 c.1955G>T p.R652L Substitution - Missense 10:49483383-49483383 - CHC1751T COSM3438383 c.2123C>T p.S708F Substitution - Missense 10:49482733-49482733 - LUAD-S01331 COSM396358 c.871A>T p.N291Y Substitution - Missense 10:49524559-49524559 - CT-TC COSM3751837 c.3289A>G p.M1097V Substitution - Missense 10:49470671-49470671 - TCGA-AX-A0J1-01 COSM918664 c.2360G>A p.R787K Substitution - Missense 10:49476237-49476237 - TCGA-A8-A0A6-01 COSM3807277 c.4193A>C p.H1398P Substitution - Missense 10:49459104-49459104 - DU-145 COSM1675222 c.2382G>T p.Q794H Substitution - Missense 10:49476215-49476215 - LOVO COSM1348079 c.1773G>A p.P591P Substitution - coding silent 10:49493165-49493165 - PR-04-3113 COSM244303 c.341A>G p.D114G Substitution - Missense 10:49532624-49532624 - TCGA-AX-A05Z-01 COSM918663 c.2408G>T p.R803I Substitution - Missense 10:49474217-49474217 - GC8_T COSM146933 c.3689G>C p.R1230P Substitution - Missense 10:49470271-49470271 - PD24207a COSM5768259 c.2019G>A p.L673L Substitution - coding silent 10:49482837-49482837 - TCGA-EE-A3JA-06 COSM3438378 c.4098C>T p.V1366V Substitution - coding silent 10:49459199-49459199 - RMS80_ COSM427630 c.4238A>G p.Q1413R Substitution - Missense 10:49459059-49459059 - S02246 COSM5678761 c.3882G>A p.L1294L Substitution - coding silent 10:49461453-49461453 - CHC703T COSM4957478 c.4401A>G p.R1467R Substitution - coding silent 10:49458896-49458896 - TCGA-AP-A0LM-01 COSM918659 c.2742G>A p.T914T Substitution - coding silent 10:49472996-49472996 - S12-11594-TP COSM4989965 c.3995G>A p.G1332D Substitution - Missense 10:49460440-49460440 - CSCC-40-T COSM4484641 c.2834G>A p.R945Q Substitution - Missense 10:49472466-49472466 - SMS-CTR COSM3751836 c.3637A>G p.R1213G Substitution - Missense 10:49470323-49470323 - RK089_C01 COSM1627521 c.1027C>T p.Q343* Substitution - Nonsense 10:49524403-49524403 - Au5 COSM5605705 c.420C>T p.L140L Substitution - coding silent 10:49532545-49532545 - TCGA-60-2707-01 COSM684145 c.2091A>T p.L697F Substitution - Missense 10:49482765-49482765 - TCGA-EB-A3XC-01 COSM3438392 c.789C>T p.I263I Substitution - coding silent 10:49524641-49524641 - ESCC-185T COSM3935075 c.4041A>T p.T1347T Substitution - coding silent 10:49460394-49460394 - TCGA-AD-6964-01 COSM1348065 c.4203G>A p.L1401L Substitution - coding silent 10:49459094-49459094 - TCGA-A8-A08F-01 COSM427633 c.2935A>G p.K979E Substitution - Missense 10:49471110-49471110 - CN-AML-08-T COSM5019040 c.1196G>A p.G399D Substitution - Missense 10:49524234-49524234 - ESCC_52 COSM5631123 c.769G>T p.E257* Substitution - Nonsense 10:49524661-49524661 - TCGA-BS-A0UV-01 COSM918662 c.2547A>C p.K849N Substitution - Missense 10:49474078-49474078 - 1N36-VS-1T36 COSM4974883 c.2135C>G p.T712S Substitution - Missense 10:49482721-49482721 - TCGA-BT-A20O-01 COSM415010 c.1228G>A p.G410S Substitution - Missense 10:49524202-49524202 - RH18C COSM3751837 c.3289A>G p.M1097V Substitution - Missense 10:49470671-49470671 - 587332 COSM1205621 c.1987A>G p.K663E Substitution - Missense 10:49483351-49483351 - TCGA-BR-A4PE-01 COSM4014449 c.2125G>A p.V709I Substitution - Missense 10:49482731-49482731 - STC248 COSM5050208 c.3700C>A p.Q1234K Substitution - Missense 10:49470260-49470260 - SH-6055 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - TCGA-04-1332-01 COSM74540 c.1669C>G p.R557G Substitution - Missense 10:49500554-49500554 - 12M COSM5577432 c.1558G>A p.E520K Substitution - Missense 10:49500665-49500665 - TCGA-AX-A05Z-01 COSM918665 c.2198T>C p.V733A Substitution - Missense 10:49478442-49478442 - PT48 COSM5932605 c.1403G>A p.W468* Substitution - Nonsense 10:49506007-49506007 - HCC2218 COSM13871 c.3113G>C p.R1038T Substitution - Missense 10:49470847-49470847 - RH18C COSM427630 c.4238A>G p.Q1413R Substitution - Missense 10:49459059-49459059 - CHC1751T COSM3438383 c.2123C>T p.S708F Substitution - Missense 10:49482733-49482733 - 2334202 COSM320163 c.4121C>T p.A1374V Substitution - Missense 10:49459176-49459176 - ESO-682 COSM1251473 c.3862C>T p.R1288* Substitution - Nonsense 10:49461473-49461473 - SNUH_G76_S1 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - 61 COSM5738894 c.2626A>G p.R876G Substitution - Missense 10:49473560-49473560 - TCGA-F4-6856-01 COSM1348074 c.2776delG p.A926fs*26 Deletion - Frameshift 10:49472962-49472962 - TCGA-CD-5800-01 COSM4014458 c.1158C>T p.D386D Substitution - coding silent 10:49524272-49524272 - TCGA-EJ-5542-01 COSM1128042 c.4399C>T p.R1467* Substitution - Nonsense 10:49458898-49458898 - TCGA-AP-A059-01 COSM918676 c.1119G>T p.E373D Substitution - Missense 10:49524311-49524311 - PT52 COSM5940023 c.1621C>T p.Q541* Substitution - Nonsense 10:49500602-49500602 - TCGA-CG-5730-01 COSM4014457 c.1367G>A p.G456E Substitution - Missense 10:49524063-49524063 - TCGA-AM-5821-01 COSM3751838 c.528A>G p.R176R Substitution - coding silent 10:49530735-49530735 - STC252 COSM5050209 c.1726A>G p.T576A Substitution - Missense 10:49493212-49493212 - 545 COSM5612596 c.422+1G>A p.? Unknown 10:49532542-49532542 - TCGA-EY-A1GS-01 COSM918658 c.2859G>C p.Q953H Substitution - Missense 10:49472441-49472441 - PT36 COSM5915933 c.1805C>T p.S602F Substitution - Missense 10:49493133-49493133 - HCC156T COSM3665756 c.2327A>C p.Y776S Substitution - Missense 10:49476270-49476270 - TCGA-D1-A16O-01 COSM918660 c.2678C>A p.S893* Substitution - Nonsense 10:49473508-49473508 - 234 COSM3731072 c.364C>T p.R122C Substitution - Missense 10:49532601-49532601 - 112644 COSM94246 c.1248A>C p.K416N Substitution - Missense 10:49524182-49524182 - DLD1 COSM1675221 c.2569C>T p.R857* Substitution - Nonsense 10:49474056-49474056 - CSCC-10-T COSM4565139 c.1771_1772CC>TT p.P591L Substitution - Missense 10:49493166-49493167 - 394 COSM4428476 c.1340G>A p.R447Q Substitution - Missense 10:49524090-49524090 - TCGA-FU-A3HZ-01 COSM918679 c.814G>A p.E272K Substitution - Missense 10:49524616-49524616 - TCGA-EA-A556-01 COSM2145539 c.309C>T p.D103D Substitution - coding silent 10:49532656-49532656 - TCGA-E2-A10C-01 COSM427637 c.625G>C p.D209H Substitution - Missense 10:49528444-49528444 - Pat_06_A COSM4681604 c.401G>A p.R134Q Substitution - Missense 10:49532564-49532564 - PD8609a COSM5782059 c.3640G>A p.D1214N Substitution - Missense 10:49470320-49470320 - TCGA-AA-3666-01 COSM265800 c.2354T>A p.V785D Substitution - Missense 10:49476243-49476243 - TCGA-63-5131-01 COSM684133 c.956G>C p.R319T Substitution - Missense 10:49524474-49524474 - SH-1641 COSM5019449 c.411G>A p.L137L Substitution - coding silent 10:49532554-49532554 - TCGA-26-5134-01 COSM3397154 c.2099T>C p.L700S Substitution - Missense 10:49482757-49482757 - RMS105_ COSM3751836 c.3637A>G p.R1213G Substitution - Missense 10:49470323-49470323 - TCGA-HU-A4G8-01 COSM4014452 c.1760C>T p.T587M Substitution - Missense 10:49493178-49493178 - CCK81 COSM2145532 c.560delA p.K187fs*18 Deletion - Frameshift 10:49528509-49528509 - TCGA-A7-A2KD-01 COSM3807286 c.720C>T p.I240I Substitution - coding silent 10:49524710-49524710 - 98748381 COSM1582063 c.1408A>G p.K470E Substitution - Missense 10:49506002-49506002 - TCGA-EW-A1J5-01 COSM1474644 c.3437G>C p.S1146T Substitution - Missense 10:49470523-49470523 - TCGA-B0-5099-01 COSM465702 c.2089T>C p.L697L Substitution - coding silent 10:49482767-49482767 - TCGA-EE-A2GI-06 COSM3438382 c.2219C>T p.P740L Substitution - Missense 10:49478421-49478421 - TCGA-AX-A0J1-01 COSM918678 c.880G>A p.A294T Substitution - Missense 10:49524550-49524550 - TCGA-D1-A17Q-01 COSM918652 c.3863G>A p.R1288Q Substitution - Missense 10:49461472-49461472 - TCGA-GN-A266-06 COSM3438389 c.1696T>C p.L566L Substitution - coding silent 10:49493242-49493242 - TCGA-39-5037-01 COSM684147 c.3405A>G p.T1135T Substitution - coding silent 10:49470555-49470555 - CSCC-35-T COSM4462503 c.124G>T p.E42* Substitution - Nonsense 10:49532841-49532841 - ID25 COSM1166714 c.3461C>T p.S1154F Substitution - Missense 10:49470499-49470499 - SH-102782 COSM5019449 c.411G>A p.L137L Substitution - coding silent 10:49532554-49532554 - TCGA-06-0649-01 COSM2151469 c.4075A>G p.K1359E Substitution - Missense 10:49459222-49459222 - ESCC-112T COSM190811 c.2338G>A p.V780I Substitution - Missense 10:49476259-49476259 - TCGA-DK-A3WW-01 COSM3790814 c.3121C>T p.Q1041* Substitution - Nonsense 10:49470839-49470839 - PTC-14C COSM4144743 c.2551T>G p.W851G Substitution - Missense 10:49474074-49474074 - 179T COSM1726216 c.2833C>T p.R945W Substitution - Missense 10:49472467-49472467 - I2L-P10-Tumor-Organoid COSM3438385 c.1996C>T p.R666C Substitution - Missense 10:49482860-49482860 - TCGA-AA-3697-01 COSM1348066 c.3868G>T p.A1290S Substitution - Missense 10:49461467-49461467 - HCT15 COSM1675221 c.2569C>T p.R857* Substitution - Nonsense 10:49474056-49474056 - pfg122T COSM4755027 c.3805G>A p.D1269N Substitution - Missense 10:49461530-49461530 - TCGA-EK-A2PG-01 COSM1348088 c.980G>A p.R327H Substitution - Missense 10:49524450-49524450 - ESO-2143 COSM1251472 c.3053C>A p.T1018K Substitution - Missense 10:49470992-49470992 - TCGA-HU-A4GU-01 COSM4014443 c.2856C>T p.G952G Substitution - coding silent 10:49472444-49472444 - TCGA-BH-A0BZ-01 COSM427634 c.2686C>T p.P896S Substitution - Missense 10:49473500-49473500 - SH-1362 COSM5019253 c.1337G>A p.G446D Substitution - Missense 10:49524093-49524093 - YUPAT COSM1702348 c.3493_3494AC>TT p.T1165L Substitution - Missense 10:49470466-49470467 - TCGA-AA-A00N-01 COSM275005 c.3158G>A p.R1053H Substitution - Missense 10:49470802-49470802 - S06-38853-TP COSM4989968 c.2046C>T p.L682L Substitution - coding silent 10:49482810-49482810 - S01022 COSM5665615 c.4150delC p.L1384fs*10 Deletion - Frameshift 10:49459147-49459147 - CRC-23T COSM5482499 c.4349T>C p.I1450T Substitution - Missense 10:49458948-49458948 - 112182 COSM94245 c.3082G>A p.D1028N Substitution - Missense 10:49470878-49470878 - 587332 COSM1205622 c.437C>T p.S146F Substitution - Missense 10:49530826-49530826 - TCGA-F1-6874-01 COSM2145537 c.379G>A p.V127I Substitution - Missense 10:49532586-49532586 - TCGA-AM-5821-01 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - TCGA-A3-3357-01 COSM465701 c.3433G>A p.E1145K Substitution - Missense 10:49470527-49470527 - TCGA-06-0649 COSM2151469 c.4075A>G p.K1359E Substitution - Missense 10:49459222-49459222 - 67 COSM5014911 c.2135C>A p.T712N Substitution - Missense 10:49482721-49482721 - RMS105_ COSM427630 c.4238A>G p.Q1413R Substitution - Missense 10:49459059-49459059 - SWE-4B COSM1179543 c.1449G>T p.E483D Substitution - Missense 10:49505961-49505961 - TCGA-AO-A03O-01 COSM427635 c.2300G>A p.R767H Substitution - Missense 10:49476297-49476297 - TCGA-P4-A5E6-01 COSM3985631 c.2744G>A p.R915Q Substitution - Missense 10:49472994-49472994 - TCGA-32-4208-01 COSM3397153 c.2139G>A p.M713I Substitution - Missense 10:49482717-49482717 - TCGA-61-2008-01 COSM1321326 c.423-1G>T p.? Unknown 10:49530841-49530841 - YUKLAB COSM218274 c.2204G>A p.R735Q Substitution - Missense 10:49478436-49478436 - CN-AML-08-T COSM5019449 c.411G>A p.L137L Substitution - coding silent 10:49532554-49532554 - TCGA-D8-A1JA-01 COSM2145418 c.4034C>T p.S1345L Substitution - Missense 10:49460401-49460401 - TCGA-EB-A41B-01 COSM3438391 c.907A>G p.T303A Substitution - Missense 10:49524523-49524523 - T3174 COSM4681597 c.2461G>T p.G821C Substitution - Missense 10:49474164-49474164 - TCGA-EE-A29V-06 COSM3438388 c.1828C>T p.L610L Substitution - coding silent 10:49483510-49483510 - 18 COSM2145532 c.560delA p.K187fs*18 Deletion - Frameshift 10:49528509-49528509 - TCGA-DM-A1D4-01 COSM1348088 c.980G>A p.R327H Substitution - Missense 10:49524450-49524450 - RK131_C01 COSM3699909 c.2008C>G p.R670G Substitution - Missense 10:49482848-49482848 - CN-AML-NR-08-Dx COSM5019449 c.411G>A p.L137L Substitution - coding silent 10:49532554-49532554 - TCGA-BR-8487-01 COSM4014444 c.2838G>T p.E946D Substitution - Missense 10:49472462-49472462 - TCGA-GC-A3BM-01 COSM3790816 c.235C>T p.Q79* Substitution - Nonsense 10:49532730-49532730 - SNUH_G76_S1 COSM4418778 c.3637A>C p.R1213R Substitution - coding silent 10:49470323-49470323 - S10-24679-TP COSM4989967 c.2073C>T p.F691F Substitution - coding silent 10:49482783-49482783 - pfg057T COSM4755029 c.3164A>C p.K1055T Substitution - Missense 10:49470796-49470796 - PTC-7C COSM427630 c.4238A>G p.Q1413R Substitution - Missense 10:49459059-49459059 - SH-0348 COSM5019040 c.1196G>A p.G399D Substitution - Missense 10:49524234-49524234 - SH-1641 COSM5019040 c.1196G>A p.G399D Substitution - Missense 10:49524234-49524234 - ATL089 COSM5703626 c.1676C>A p.S559* Substitution - Nonsense 10:49500547-49500547 - RMS105_ COSM3751837 c.3289A>G p.M1097V Substitution - Missense 10:49470671-49470671 - TCGA-66-2792-01 COSM684144 c.1991A>T p.Q664L Substitution - Missense 10:49483347-49483347 - TCGA-D5-6540-01 COSM1348064 c.4328G>A p.G1443D Substitution - Missense 10:49458969-49458969 - pfg008T COSM1638575 c.2145_2146insG p.Y716fs*44 Insertion - Frameshift 10:49482710-49482711 - CT-TC COSM3751836 c.3637A>G p.R1213G Substitution - Missense 10:49470323-49470323 - TCGA-CG-5728-01 COSM4014446 c.2421C>T p.N807N Substitution - coding silent 10:49474204-49474204 - CT-TC COSM427630 c.4238A>G p.Q1413R Substitution - Missense 10:49459059-49459059 - CSCC-35-T COSM4528253 c.1521T>A p.L507L Substitution - coding silent 10:49505889-49505889 - 513 COSM3721667 c.3915G>A p.L1305L Substitution - coding silent 10:49461420-49461420 - SH-1439 COSM5019040 c.1196G>A p.G399D Substitution - Missense 10:49524234-49524234 - LC_S6 COSM1187941 c.3842T>C p.L1281P Substitution - Missense 10:49461493-49461493 - TCGA-Q1-A73O-01 COSM4834678 c.3080C>G p.S1027* Substitution - Nonsense 10:49470880-49470880 - TCGA-AA-A010-01 COSM280852 c.1345G>A p.V449M Substitution - Missense 10:49524085-49524085 - DU-145 COSM1675219 c.4309T>A p.F1437I Substitution - Missense 10:49458988-49458988 - TCGA-A2-A04P-01 COSM427636 c.2019G>T p.L673L Substitution - coding silent 10:49482837-49482837 - OSCC-GB_00740111 COSM4890930 c.3580G>C p.E1194Q Substitution - Missense 10:49470380-49470380 - SH-3327 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - SMS-CTR COSM427630 c.4238A>G p.Q1413R Substitution - Missense 10:49459059-49459059 - TCGA-EE-A29L-06 COSM3438384 c.2001C>T p.T667T Substitution - coding silent 10:49482855-49482855 - RMS109_ COSM3751836 c.3637A>G p.R1213G Substitution - Missense 10:49470323-49470323 - TCGA-D9-A4Z5-01 COSM2145457 c.2230C>T p.R744W Substitution - Missense 10:49478410-49478410 - TCGA-AO-A03M-01 COSM3807283 c.1207G>A p.E403K Substitution - Missense 10:49524223-49524223 - PD8610a COSM5789126 c.2268G>C p.L756F Substitution - Missense 10:49478372-49478372 - TCGA-DD-A39X-01 COSM4940739 c.2084G>T p.G695V Substitution - Missense 10:49482772-49482772 - MO_1339 COSM5548466 c.3573A>G p.A1191A Substitution - coding silent 10:49470387-49470387 - SH-1641 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - SH-1439 COSM146933 c.3689G>C p.R1230P Substitution - Missense 10:49470271-49470271 - TCGA-CC-5263-01 COSM4919409 c.1012A>T p.R338W Substitution - Missense 10:49524418-49524418 - HN_62897 COSM122894 c.2783G>C p.R928T Substitution - Missense 10:49472955-49472955 - ICGC_0067 COSM218274 c.2204G>A p.R735Q Substitution - Missense 10:49478436-49478436 - TCGA-EE-A2GR-06 COSM3438381 c.2505G>A p.W835* Substitution - Nonsense 10:49474120-49474120 - TCGA-FW-A3R5-06 COSM3867355 c.628C>T p.H210Y Substitution - Missense 10:49528441-49528441 - OSCC-GB_01080111 COSM918656 c.3260G>A p.R1087Q Substitution - Missense 10:49470700-49470700 - SH-0348 COSM146933 c.3689G>C p.R1230P Substitution - Missense 10:49470271-49470271 - TCGA-AD-6964-01 COSM1348076 c.2124C>T p.S708S Substitution - coding silent 10:49482732-49482732 - SH-102782 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - CSCC-49-T COSM4524601 c.1281C>T p.F427F Substitution - coding silent 10:49524149-49524149 - SNUH_G26_S1 COSM3675777 c.2751C>G p.G917G Substitution - coding silent 10:49472987-49472987 - TCGA-BR-4280-01 COSM4014448 c.2203C>T p.R735* Substitution - Nonsense 10:49478437-49478437 - SH-3133 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - TCGA-A5-A0GB-01 COSM918680 c.431C>T p.T144M Substitution - Missense 10:49530832-49530832 - TCGA-E9-A1NI-01 COSM1474645 c.2144_2145insG p.Y716fs*44 Insertion - Frameshift 10:49482711-49482712 - TCGA-B5-A11E-01 COSM918661 c.2552G>T p.W851L Substitution - Missense 10:49474073-49474073 - TCGA-BF-A1Q0-01 COSM3438380 c.2622C>T p.F874F Substitution - coding silent 10:49473564-49473564 - RMS80_ COSM3751837 c.3289A>G p.M1097V Substitution - Missense 10:49470671-49470671 - TCGA-AP-A056-01 COSM918654 c.3437G>T p.S1146I Substitution - Missense 10:49470523-49470523 - TCGA-D1-A16Y-01 COSM918653 c.3662G>A p.R1221Q Substitution - Missense 10:49470298-49470298 - TCGA-DA-A1HV-06 COSM3438393 c.170C>T p.S57F Substitution - Missense 10:49532795-49532795 - sysucc-968T COSM216221 c.4211G>A p.R1404H Substitution - Missense 10:49459086-49459086 - SNUH_G76_S1 COSM3751837 c.3289A>G p.M1097V Substitution - Missense 10:49470671-49470671 - 19M COSM5578493 c.4113T>A p.S1371R Substitution - Missense 10:49459184-49459184 - TCGA-BH-A0AW-01 COSM427631 c.4139C>T p.S1380L Substitution - Missense 10:49459158-49459158 - S10-44607-TP COSM4989966 c.2298C>T p.C766C Substitution - coding silent 10:49476299-49476299 - TCGA-AY-6197-01 COSM1348067 c.3848A>G p.E1283G Substitution - Missense 10:49461487-49461487 - TCGA-AM-5820-01 COSM3751837 c.3289A>G p.M1097V Substitution - Missense 10:49470671-49470671 - TCGA-EE-A3JA-06 COSM3438385 c.1996C>T p.R666C Substitution - Missense 10:49482860-49482860 - 587234 COSM1205623 c.2008C>T p.R670W Substitution - Missense 10:49482848-49482848 - TCGA-29-1698-01 COSM1321328 c.1742G>A p.W581* Substitution - Nonsense 10:49493196-49493196 - TCGA-BK-A0C9-01 COSM918681 c.405G>A p.S135S Substitution - coding silent 10:49532560-49532560 - TCGA-BR-4362-01 COSM4014441 c.3294T>C p.S1098S Substitution - coding silent 10:49470666-49470666 - TCGA-CG-4442-01 COSM3438392 c.789C>T p.I263I Substitution - coding silent 10:49524641-49524641 - TCGA-AG-A02G-01 COSM265378 c.3416C>T p.S1139F Substitution - Missense 10:49470544-49470544 - TCGA-AR-A2LE-01 COSM3807281 c.2467C>A p.P823T Substitution - Missense 10:49474158-49474158 - TCGA-EE-A182-06 COSM3438395 c.21C>T p.P7P Substitution - coding silent 10:49532944-49532944 - CPCG0369-F1 COSM172076 c.4210C>T p.R1404C Substitution - Missense 10:49459087-49459087 - HCT-15 COSM1675221 c.2569C>T p.R857* Substitution - Nonsense 10:49474056-49474056 - TCGA-DK-A2I4-01 COSM3790817 c.190G>A p.A64T Substitution - Missense 10:49532775-49532775 - LFS_MB2 COSM216221 c.4211G>A p.R1404H Substitution - Missense 10:49459086-49459086 - TCGA-24-1104-01 COSM79178 c.1570C>T p.Q524* Substitution - Nonsense 10:49500653-49500653 - TCGA-CD-5801-01 COSM4014440 c.3629A>C p.K1210T Substitution - Missense 10:49470331-49470331 - TCGA-A6-5665-01 COSM1348072 c.3042G>T p.Q1014H Substitution - Missense 10:49471003-49471003 - 2492729 COSM5726742 c.1169G>A p.G390E Substitution - Missense 10:49524261-49524261 - RMS111_ COSM427630 c.4238A>G p.Q1413R Substitution - Missense 10:49459059-49459059 - RMS111_ COSM3751836 c.3637A>G p.R1213G Substitution - Missense 10:49470323-49470323 - HCC156 COSM3665756 c.2327A>C p.Y776S Substitution - Missense 10:49476270-49476270 - I2L-P7-Tumor-Organoid COSM5360226 c.1188T>C p.S396S Substitution - coding silent 10:49524242-49524242 - SH-7282 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - T3202 COSM4681598 c.1861T>C p.L621L Substitution - coding silent 10:49483477-49483477 - SH-9771 COSM5019449 c.411G>A p.L137L Substitution - coding silent 10:49532554-49532554 - TCGA-CG-5728-01 COSM4014447 c.2208T>C p.D736D Substitution - coding silent 10:49478432-49478432 - CHEWS027 COSM4573644 c.1347G>A p.V449V Substitution - coding silent 10:49524083-49524083 - Mx38 COSM32310 c.1771C>G p.P591A Substitution - Missense 10:49493167-49493167 - 86569 COSM95871 c.378C>T p.L126L Substitution - coding silent 10:49532587-49532587 - SH-9161 COSM5019040 c.1196G>A p.G399D Substitution - Missense 10:49524234-49524234 - LUAD-NYU847 COSM376544 c.295G>T p.V99F Substitution - Missense 10:49532670-49532670 - TCGA-GN-A265-06 COSM3438386 c.1862T>C p.L621S Substitution - Missense 10:49483476-49483476 - 13394 COSM684145 c.2091A>T p.L697F Substitution - Missense 10:49482765-49482765 - CN-AML-NR-08-Dx COSM5019040 c.1196G>A p.G399D Substitution - Missense 10:49524234-49524234 - SH-9161 COSM146933 c.3689G>C p.R1230P Substitution - Missense 10:49470271-49470271 - BD177T COSM5517407 c.569C>T p.A190V Substitution - Missense 10:49528500-49528500 - J90_T COSM3978580 c.2574A>G p.V858V Substitution - coding silent 10:49474051-49474051 - RH18C COSM3751836 c.3637A>G p.R1213G Substitution - Missense 10:49470323-49470323 - Pat_15_B COSM5836943 c.1335_1337delAGG p.G446delG Deletion - In frame 10:49524093-49524095 - PDA_046 COSM5000494 c.3494C>T p.T1165I Substitution - Missense 10:49470466-49470466 - CSCC-40-T COSM4455828 c.916G>A p.A306T Substitution - Missense 10:49524514-49524514 - T3021 COSM4681596 c.2890A>G p.T964A Substitution - Missense 10:49472410-49472410 - 587256 COSM190811 c.2338G>A p.V780I Substitution - Missense 10:49476259-49476259 - PTC-14C COSM4144744 c.2546A>G p.K849R Substitution - Missense 10:49474079-49474079 - TCGA-HU-A4GN-01 COSM4014460 c.197C>T p.P66L Substitution - Missense 10:49532768-49532768 - WSU-HN30 COSM4600488 c.3481A>C p.S1161R Substitution - Missense 10:49470479-49470479 - HCC058T COSM5804929 c.1208A>T p.E403V Substitution - Missense 10:49524222-49524222 - 1604875 COSM141289 c.2138T>C p.M713T Substitution - Missense 10:49482718-49482718 - pfg008T COSM1638575 c.2145_2146insG p.Y716fs*44 Insertion - Frameshift 10:49482710-49482711 - LUAD-NYU1219 COSM369778 c.745G>A p.G249S Substitution - Missense 10:49524685-49524685 - PD18280a COSM3770313 c.4332G>T p.Q1444H Substitution - Missense 10:49458965-49458965 - KPOPBR-36-T COSM5963467 c.3917G>A p.G1306E Substitution - Missense 10:49461418-49461418 - TCGA-EE-A3J5-06 COSM3438387 c.1834C>T p.R612* Substitution - Nonsense 10:49483504-49483504 - TCGA-BG-A0M4-01 COSM918655 c.3400G>A p.G1134R Substitution - Missense 10:49470560-49470560 - SNU-175 COSM2145533 c.527G>A p.R176Q Substitution - Missense 10:49530736-49530736 - TCGA-AZ-6598-01 COSM5826725 c.2925-3delT p.? Unknown 10:49471123-49471123 - TCGA-G2-A2EO-01 COSM1297294 c.2060C>G p.S687W Substitution - Missense 10:49482796-49482796 - TCGA-CG-5728-01 COSM4014438 c.4228G>A p.G1410R Substitution - Missense 10:49459069-49459069 - J88_T COSM3978581 c.2337C>T p.F779F Substitution - coding silent 10:49476260-49476260 - TCGA-GC-A3OO-01 COSM3790815 c.1647G>C p.L549L Substitution - coding silent 10:49500576-49500576 - 86576 COSM94244 c.3954G>T p.R1318S Substitution - Missense 10:49461381-49461381 - RMS2074 COSM1251473 c.3862C>T p.R1288* Substitution - Nonsense 10:49461473-49461473 - T3535 COSM4681604 c.401G>A p.R134Q Substitution - Missense 10:49532564-49532564 - 587222 COSM1205620 c.1360G>T p.D454Y Substitution - Missense 10:49524070-49524070 - Pat_06_A COSM918653 c.3662G>A p.R1221Q Substitution - Missense 10:49470298-49470298 - TCGA-EB-A553-01 COSM3438390 c.1548G>T p.R516S Substitution - Missense 10:49500675-49500675 - TCGA-FW-A3R5-06 COSM3867353 c.2345C>T p.S782F Substitution - Missense 10:49476252-49476252 - SH-4435 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - NB2186 COSM5703045 c.4417C>A p.L1473M Substitution - Missense 10:49458880-49458880 - HCC2218 COSM32243 c.3356A>T p.E1119V Substitution - Missense 10:49470604-49470604 - TCGA-AX-A0J0-01 COSM918656 c.3260G>A p.R1087Q Substitution - Missense 10:49470700-49470700 - TCGA-AM-5820-01 COSM146933 c.3689G>C p.R1230P Substitution - Missense 10:49470271-49470271 - CSCC-55-T COSM4524601 c.1281C>T p.F427F Substitution - coding silent 10:49524149-49524149 - TCGA-CD-A4MG-01 COSM4014442 c.3157C>T p.R1053C Substitution - Missense 10:49470803-49470803 - SH-7329 COSM5019040 c.1196G>A p.G399D Substitution - Missense 10:49524234-49524234 - 3101B7_032_T COSM5041340 c.1568G>C p.C523S Substitution - Missense 10:49500655-49500655 - TCGA-BP-4981-01 COSM465705 c.429T>G p.C143W Substitution - Missense 10:49530834-49530834 - TCGA-E9-A22G-01 COSM3807280 c.2645A>C p.Y882S Substitution - Missense 10:49473541-49473541 - C086 COSM5530604 c.813C>T p.F271F Substitution - coding silent 10:49524617-49524617 - HCC119T COSM5811228 c.2279A>C p.N760T Substitution - Missense 10:49478361-49478361 - TCGA-CJ-5679-01 COSM465704 c.732G>T p.Q244H Substitution - Missense 10:49524698-49524698 - TCGA-D7-A4Z0-01 COSM4014445 c.2649C>G p.L883L Substitution - coding silent 10:49473537-49473537 - TCGA-A7-A2KD-01 COSM3807285 c.919C>G p.P307A Substitution - Missense 10:49524511-49524511 - TCGA-D8-A1XQ-01 COSM3807282 c.1610G>A p.G537D Substitution - Missense 10:49500613-49500613 - TCGA-BR-6452-01 COSM2145530 c.631G>A p.A211T Substitution - Missense 10:49528438-49528438 - TCGA-AZ-4315-01 COSM1348078 c.1955G>A p.R652Q Substitution - Missense 10:49483383-49483383 - TCGA-HT-7687-01 COSM3967087 c.4313A>G p.Q1438R Substitution - Missense 10:49458984-49458984 - TCGA-FW-A3R5-06 COSM3867354 c.1789C>T p.L597L Substitution - coding silent 10:49493149-49493149 - TCGA-E2-A10C-01 COSM427632 c.3510G>A p.E1170E Substitution - coding silent 10:49470450-49470450 - MOLT-4 COSM1675220 c.3844G>A p.V1282M Substitution - Missense 10:49461491-49461491 - TCGA-CA-6717-01 COSM1348068 c.3523G>A p.E1175K Substitution - Missense 10:49470437-49470437 - CHC703T COSM4957478 c.4401A>G p.R1467R Substitution - coding silent 10:49458896-49458896 - pfg006T COSM1638574 c.2316G>T p.Q772H Substitution - Missense 10:49476281-49476281 - PCSI_0083_Pa_P COSM3375479 c.2636A>C p.K879T Substitution - Missense 10:49473550-49473550 - SH-3133 COSM5019783 c.3650T>G p.F1217C Substitution - Missense 10:49470310-49470310 - 24T COSM110127 c.756C>T p.I252I Substitution - coding silent 10:49524674-49524674 - TCGA-CA-6717-01 COSM1348081 c.1483G>A p.E495K Substitution - Missense 10:49505927-49505927 - TGH COSM1582062 c.3023C>T p.T1008I Substitution - Missense 10:49471022-49471022 - DN15001 COSM5962181 c.3450G>T p.K1150N Substitution - Missense 10:49470510-49470510 - SH-7329 COSM146933 c.3689G>C p.R1230P Substitution - Missense 10:49470271-49470271 - TCGA-AA-A010-01 COSM280851 c.2606A>G p.D869G Substitution - Missense 10:49473580-49473580 - LB647-SCLC COSM13944 c.2925A>G p.R975R Substitution - coding silent 10:49471120-49471120 - SN12C COSM1675218 c.4333G>T p.A1445S Substitution - Missense 10:49458964-49458964 - T2269 COSM3358771 c.1245G>A p.K415K Substitution - coding silent 10:49524185-49524185 - TCGA-AN-A046-01 COSM3807279 c.3742G>T p.D1248Y Substitution - Missense 10:49470218-49470218 - TCGA-D8-A1XK-01 COSM3807278 c.4062G>T p.Q1354H Substitution - Missense 10:49460373-49460373 - QC2-32-T2 COSM427630 c.4238A>G p.Q1413R Substitution - Missense 10:49459059-49459059 - TCGA-AP-A056-01 COSM918679 c.814G>A p.E272K Substitution - Missense 10:49524616-49524616 - RK007_C01 COSM1627519 c.1533G>A p.Q511Q Substitution - coding silent 10:49500690-49500690 - LS411 COSM2145468 c.1783G>T p.A595S Substitution - Missense 10:49493155-49493155 - TCGA-EE-A2MR-06 COSM3438379 c.3168C>T p.F1056F Substitution - coding silent 10:49470792-49470792 - 86570 COSM95870 c.4467G>A p.K1489K Substitution - coding silent 10:49458830-49458830 - SH-1679 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - TCGA-FW-A3R5-06 COSM3867352 c.2968C>T p.P990S Substitution - Missense 10:49471077-49471077 - SMS-CTR COSM3751837 c.3289A>G p.M1097V Substitution - Missense 10:49470671-49470671 - TCGA-AM-5820-01 COSM3751836 c.3637A>G p.R1213G Substitution - Missense 10:49470323-49470323 - TCGA-D9-A4Z3-01 COSM2145458 c.2218C>T p.P740S Substitution - Missense 10:49478422-49478422 - TCGA-DD-A4NV-01 COSM4916431 c.3949C>T p.H1317Y Substitution - Missense 10:49461386-49461386 - C0027T COSM4165494 c.896C>T p.P299L Substitution - Missense 10:49524534-49524534 - HN_62897 COSM127906 c.4122A>G p.A1374A Substitution - coding silent 10:49459175-49459175 - LC_C6 COSM1187942 c.1970C>T p.A657V Substitution - Missense 10:49483368-49483368 - U87 COSM2145451 c.2538T>C p.S846S Substitution - coding silent 10:49474087-49474087 - RMS109_ COSM3751837 c.3289A>G p.M1097V Substitution - Missense 10:49470671-49470671 - SH-9771 COSM5019040 c.1196G>A p.G399D Substitution - Missense 10:49524234-49524234 - TCGA-BT-A3PH-01 COSM1297293 c.2438C>T p.S813F Substitution - Missense 10:49474187-49474187 - DLD1 COSM4621852 c.3615G>T p.K1205N Substitution - Missense 10:49470345-49470345 - TCGA-BS-A0UV-01 COSM918682 c.184G>A p.A62T Substitution - Missense 10:49532781-49532781 - TCGA-EE-A2MI-06 COSM3438377 c.4372T>C p.L1458L Substitution - coding silent 10:49458925-49458925 - LB647-SCLC COSM13944 c.2925A>G p.R975R Substitution - coding silent 10:49471120-49471120 - SH-102782 COSM5019040 c.1196G>A p.G399D Substitution - Missense 10:49524234-49524234 - PCSI_0083_Pa_X COSM3375479 c.2636A>C p.K879T Substitution - Missense 10:49473550-49473550 - TCGA-B5-A11Y-01 COSM216221 c.4211G>A p.R1404H Substitution - Missense 10:49459086-49459086 - TCGA-EE-A2GC-06 COSM3438383 c.2123C>T p.S708F Substitution - Missense 10:49482733-49482733 - CSCC-37-T COSM4450995 c.1011G>A p.K337K Substitution - coding silent 10:49524419-49524419 - HX17T COSM1603494 c.787A>G p.I263V Substitution - Missense 10:49524643-49524643 - HT55 COSM2145543 c.99A>T p.Q33H Substitution - Missense 10:49532866-49532866 - T3064 COSM4681603 c.856A>T p.K286* Substitution - Nonsense 10:49524574-49524574 - SH-1439 COSM5021135 c.1772C>T p.P591L Substitution - Missense 10:49493166-49493166 - WSU-HN30 COSM4600928 c.3482G>C p.S1161T Substitution - Missense 10:49470478-49470478 - SH-7166 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - RMS109_ COSM427630 c.4238A>G p.Q1413R Substitution - Missense 10:49459059-49459059 - RMS80_ COSM3751836 c.3637A>G p.R1213G Substitution - Missense 10:49470323-49470323 - 8048567 COSM218274 c.2204G>A p.R735Q Substitution - Missense 10:49478436-49478436 - HCC058T COSM5805334 c.653-2A>T p.? Unknown 10:49524779-49524779 - pfg009T COSM1638573 c.4431T>C p.H1477H Substitution - coding silent 10:49458866-49458866 - PT45 COSM5927582 c.2710-7C>T p.? Unknown 10:49473035-49473035 - OSCC-GB_00740111 COSM4890855 c.4450G>C p.G1484R Substitution - Missense 10:49458847-49458847 - SNUH_G76_S1 COSM427630 c.4238A>G p.Q1413R Substitution - Missense 10:49459059-49459059 - HCC2218 COSM32242 c.3355G>C p.E1119Q Substitution - Missense 10:49470605-49470605 - TCGA-EE-A29C-06 COSM3438394 c.40G>A p.E14K Substitution - Missense 10:49532925-49532925 - ESO-913 COSM1251474 c.2932T>A p.F978I Substitution - Missense 10:49471113-49471113 - TCGA-DM-A28H-01 COSM1348077 c.2030C>T p.P677L Substitution - Missense 10:49482826-49482826 - SH-1439 COSM5019449 c.411G>A p.L137L Substitution - coding silent 10:49532554-49532554 - SH-3776 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - TCGA-AN-A046-01 COSM918679 c.814G>A p.E272K Substitution - Missense 10:49524616-49524616 - TCGA-BG-A0LX-01 COSM918677 c.978G>T p.E326D Substitution - Missense 10:49524452-49524452 - TCGA-DJ-A2PP-01 COSM3368054 c.968A>G p.K323R Substitution - Missense 10:49524462-49524462 - PT52 COSM3415080 c.1954C>T p.R652* Substitution - Nonsense 10:49483384-49483384 - RKO COSM4647189 c.4384C>T p.Q1462* Substitution - Nonsense 10:49458913-49458913 - LUAD-RT-S01774 COSM381292 c.727G>T p.G243C Substitution - Missense 10:49524703-49524703 - TCGA-DK-A3IM-01 COSM1297292 c.3877G>A p.A1293T Substitution - Missense 10:49461458-49461458 - HCC2218 COSM13869 c.3355_3356GA>CT p.E1119L Substitution - Missense 10:49470604-49470605 - 1517_PT COSM2145467 c.1820delA p.K607fs*4 Deletion - Frameshift 10:49493118-49493118 - TCGA-AX-A0IW-01 COSM918657 c.2944T>G p.L982V Substitution - Missense 10:49471101-49471101 - T9 COSM4014442 c.3157C>T p.R1053C Substitution - Missense 10:49470803-49470803 - RMS111_ COSM3751837 c.3289A>G p.M1097V Substitution - Missense 10:49470671-49470671 - SC_9107 COSM5568788 c.2160C>G p.S720S Substitution - coding silent 10:49482696-49482696 - TCGA-HU-A4GQ-01 COSM4014450 c.1917C>T p.D639D Substitution - coding silent 10:49483421-49483421 - TCGA-B5-A11G-01 COSM918666 c.2045T>G p.L682R Substitution - Missense 10:49482811-49482811 - TCGA-F5-6814-01 COSM3415078 c.3277G>T p.D1093Y Substitution - Missense 10:49470683-49470683 - TCGA-BR-8589-01 COSM4014439 c.3774A>C p.K1258N Substitution - Missense 10:49470186-49470186 - TCGA-C5-A1M8-01 COSM4837296 c.687G>A p.M229I Substitution - Missense 10:49524743-49524743 - TCGA-BR-4184-01 COSM4014451 c.1801G>A p.G601S Substitution - Missense 10:49493137-49493137 - GC8_T COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - MCF7 COSM1675224 c.247G>A p.V83I Substitution - Missense 10:49532718-49532718 - LUAD-B00416 COSM330755 c.2388C>T p.F796F Substitution - coding silent 10:49474237-49474237 - T30 COSM5019449 c.411G>A p.L137L Substitution - coding silent 10:49532554-49532554 - HCC2218 COSM13871 c.3113G>C p.R1038T Substitution - Missense 10:49470847-49470847 - SH-9248 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - T27 COSM5341257 c.4330C>T p.Q1444* Substitution - Nonsense 10:49458967-49458967 - S09-31237-TP COSM4989969 c.2013C>T p.I671I Substitution - coding silent 10:49482843-49482843 - HCC2218 COSM13869 c.3355_3356GA>CT p.E1119L Substitution - Missense 10:49470604-49470605 - TCGA-BR-4370-01 COSM4014459 c.630C>T p.H210H Substitution - coding silent 10:49528439-49528439 - SH-1362 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - HCC2998 COSM2145420 c.4010C>A p.S1337Y Substitution - Missense 10:49460425-49460425 - 8016470 COSM146934 c.2751C>T p.G917G Substitution - coding silent 10:49472987-49472987 - TCGA-D1-A17Q-01 COSM918651 c.4267G>T p.E1423* Substitution - Nonsense 10:49459030-49459030 - TCGA-F5-6814-01 COSM3415079 c.3003C>T p.L1001L Substitution - coding silent 10:49471042-49471042 - CSCC-31-T COSM4451555 c.1282C>T p.P428S Substitution - Missense 10:49524148-49524148 - TCGA-EI-6917-01 COSM3415080 c.1954C>T p.R652* Substitution - Nonsense 10:49483384-49483384 - 8033610 COSM218274 c.2204G>A p.R735Q Substitution - Missense 10:49478436-49478436 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.654449 10q11.23 609413

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.C143W c.429T>G 10 50738880 RCCC A C Missense p.L682R c.2045T>G 10 50690857 UCEC A G Missense p.L621S c.1862T>C 10 50691522 CM A G Missense p.L700S c.2099T>C 10 50690803 GBM A G Synonymous p.D736D c.2208T>C 10 50686478 STAD A G Synonymous p.H1477H c.4431T>C 10 50666912 STAD A G Synonymous p.L1458L c.4372T>C 10 50666971 CM A G Synonymous p.L697L c.2089T>C 10 50690813 RCCC AG TA Missense p.F812I c.2433_2434delinsTA 10 50682237 CM A - IntronicDeletion . c.2829+21delT 10 50680934 STAD ATCTA - Frameshift p.L208Pfs*57 c.623_627delTAGAT 10 50736488 PRAD A T Missense p.E1119V c.3356A>T 10 50678650 BRCA A T Missense p.F978I c.2932T>A 10 50679159 ESCA A T Missense p.N310K c.930T>A 10 50732546 BRCA A T Missense p.V785D c.2354T>A 10 50684289 COREAD C A Missense p.A306S c.916G>T 10 50732560 HNSC C A Missense p.E326D c.978G>T 10 50732498 UCEC C A Missense p.Q244H c.732G>T 10 50732744 RCCC C A Missense p.Q772H c.2316G>T 10 50684327 STAD C A Missense p.R945L c.2834G>T 10 50680512 LUAD C A Nonsense p.E182* c.544G>T 10 50736571 LUAD C A SpliceAcceptorSNV . c.423-1G>T 10 50738887 OV C A Synonymous p.L673L c.2019G>T 10 50690883 BRCA C A Synonymous p.T699T c.2097G>T 10 50690805 HNSC CCT - InFrameDeletion p.G446delG c.1335_1337delAGG 10 50732139 PRAD C - Frameshift p.A391Qfs*14 c.1171delG 10 50732305 LUAD C - Frameshift p.V417Cfs*23 c.1249delG 10 50732227 RCCC - C Frameshift p.Y716Ifs*44 c.2144dupG 10 50690758 BRCA - C Frameshift p.Y716Ifs*44 c.2144dupG 10 50690759 STAD C G Missense p.E1003Q c.3007G>C 10 50679084 LUAD C G Missense p.P591A c.1771C>G 10 50701213 COREAD C G Missense p.Q79H c.237G>C 10 50740774 LUAD C G Missense p.Q953H c.2859G>C 10 50680487 UCEC C G Missense p.R319T c.956G>C 10 50732520 LUSC C G Missense p.R928T c.2783G>C 10 50681001 HNSC C T Missense p.A1293T c.3877G>A 10 50669504 BLCA C T Missense p.A64T c.190G>A 10 50740821 BLCA C T Missense p.D1248N c.3742G>A 10 50678264 STAD C T Missense p.E1145K c.3433G>A 10 50678573 RCCC C T Missense p.E14K c.40G>A 10 50740971 CM C T Missense p.G1410R c.4228G>A 10 50667115 STAD C T Missense p.G410S c.1228G>A 10 50732248 BLCA C T Missense p.G456E c.1367G>A 10 50732109 STAD C T Missense p.M713I c.2139G>A 10 50690763 GBM C T Missense p.R1221Q c.3662G>A 10 50678344 UCEC C T Missense p.R1404H c.4211G>A 10 50667132 MB C T Missense p.R1404H c.4211G>A 10 50667132 UCEC C T Missense p.R735Q c.2204G>A 10 50686482 PAAD C T Missense p.R767H c.2300G>A 10 50684343 BRCA C T Missense p.V127I c.379G>A 10 50740632 STAD C T Missense p.V780I c.2338G>A 10 50684305 COREAD C T Nonsense p.W835* c.2505G>A 10 50682166 CM C T Synonymous p.Q511Q c.1533G>A 10 50708736 HC G A Missense p.A1374V c.4121C>T 10 50667222 SCLC G A Missense p.P376L c.1127C>T 10 50732349 CM G A Missense p.P591S c.1771C>T 10 50701213 CM G A Missense p.P740L c.2219C>T 10 50686467 CM G A Missense p.P896S c.2686C>T 10 50681546 BRCA G A Missense p.S1139F c.3416C>T 10 50678590 COREAD G A Missense p.S1380L c.4139C>T 10 50667204 BRCA G A Missense p.S57F c.170C>T 10 50740841 CM G A Missense p.S708F c.2123C>T 10 50690779 CM G A Missense p.S813F c.2438C>T 10 50682233 BLCA G A Missense p.T144M c.431C>T 10 50738878 UCEC G A Nonsense p.Q343* c.1027C>T 10 50732449 HC G A Nonsense p.Q524* c.1570C>T 10 50708699 OV G A Nonsense p.R1467* c.4399C>T 10 50666944 PRAD G A Nonsense p.R612* c.1834C>T 10 50691550 CM G A Nonsense p.R735* c.2203C>T 10 50686483 STAD G A Synonymous p.F504F c.1512C>T 10 50713944 CM G A Synonymous p.F874F c.2622C>T 10 50681610 CM G A Synonymous p.L610L c.1828C>T 10 50691556 CM G A Synonymous p.L987L c.2959C>T 10 50679132 STAD G A Synonymous p.N807N c.2421C>T 10 50682250 STAD G A Synonymous p.S1381S c.4143C>T 10 50667200 LUAD G A Synonymous p.T667T c.2001C>T 10 50690901 CM G A Synonymous p.V1366V c.4098C>T 10 50667245 CM G C Missense p.E1119Q c.3355G>C 10 50678651 BRCA G C Missense p.P253R c.758C>G 10 50732718 LUAD G C Missense p.R1038T c.3113G>C 10 50678893 BRCA G C Missense p.R557G c.1669C>G 10 50708600 OV G C Missense p.S687W c.2060C>G 10 50690842 BLCA GG AT MultiAAMissense p.S121_R122delinsRC c.363_364delinsAT 10 50740647 CM G T Missense p.P1349Q c.4046C>A 10 50668435 LUAD G T Missense p.R652L c.1955G>T 10 50691429 COREAD G T Missense p.T1018K c.3053C>A 10 50679038 ESCA G T Nonsense p.S893* c.2678C>A 10 50681554 UCEC T A IntronicSNV . c.2829+22A>T 10 50680933 STAD T A Missense p.D1249V c.3746A>T 10 50678260 HNSC T A Missense p.L697F c.2091A>T 10 50690811 LUSC T A Missense p.L697F c.2091A>T 10 50690811 NSCLC T A Missense p.Q664L c.1991A>T 10 50691393 LUSC T A Missense p.Q706L c.2117A>T 10 50690785 LUAD T C 3-UTRSNV . c.4479+411A>G 10 50666453 HC T C Missense p.K1184E c.3550A>G 10 50678456 HNSC T C Missense p.K1359E c.4075A>G 10 50667268 GBM T C Missense p.K323R c.968A>G 10 50732508 THCA T C Missense p.K979E c.2935A>G 10 50679156 BRCA T C Missense p.Q1438R c.4313A>G 10 50667030 LGG T C Synonymous p.A1374A c.4122A>G 10 50667221 HNSC T C Synonymous p.T1135T c.3405A>G 10 50678601 LUSC T G Missense p.K1210T c.3629A>C 10 50678377 STAD