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 | 15 | 53998158 | 53998158 | + | Missense_Mutation | SNP | A | A | T | TCGA-OR-A5KV-01A-11D-A29I-10 | TCGA-OR-A5KV-10A-01D-A29L-10 | g.chr15:53998158A>T | c.1068T>A | c.(1066-1068)gaT>gaA | p.D356E |
BLCA | 15 | 53907716 | 53907716 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZF-A9R9-01A-11D-A38G-08 | TCGA-ZF-A9R9-10A-01D-A38J-08 | g.chr15:53907716C>T | c.2687G>A | c.(2686-2688)cGa>cAa | p.R896Q |
BLCA | 15 | 53907946 | 53907946 | + | Silent | SNP | G | G | C | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr15:53907946G>C | c.2457C>G | c.(2455-2457)ctC>ctG | p.L819L |
BLCA | 15 | 53907975 | 53907975 | + | Missense_Mutation | SNP | C | C | A | TCGA-BT-A20V-01A-11D-A14W-08 | TCGA-BT-A20V-11A-11D-A14W-08 | g.chr15:53907975C>A | c.2428G>T | c.(2428-2430)Gat>Tat | p.D810Y |
BLCA | 15 | 53907989 | 53907989 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-E7-A7DV-01A-11D-A339-08 | TCGA-E7-A7DV-10A-01D-A339-08 | g.chr15:53907989C>T | c.2414G>A | c.(2413-2415)tGg>tAg | p.W805* |
BLCA | 15 | 53908141 | 53908141 | + | Silent | SNP | A | A | G | TCGA-2F-A9KR-01A-11D-A38G-08 | TCGA-2F-A9KR-10A-01D-A38J-08 | g.chr15:53908141A>G | c.2262T>C | c.(2260-2262)gaT>gaC | p.D754D |
BLCA | 15 | 53908309 | 53908309 | + | Silent | SNP | G | G | C | TCGA-BT-A0YX-01A-11D-A10S-08 | TCGA-BT-A0YX-10A-01D-A10S-08 | g.chr15:53908309G>C | c.2094C>G | c.(2092-2094)ctC>ctG | p.L698L |
BLCA | 15 | 53908364 | 53908364 | + | Missense_Mutation | SNP | T | T | A | TCGA-XF-A8HH-01A-11D-A38G-08 | TCGA-XF-A8HH-10A-01D-A38J-08 | g.chr15:53908364T>A | c.2039A>T | c.(2038-2040)cAt>cTt | p.H680L |
BLCA | 15 | 53957875 | 53957875 | + | Missense_Mutation | SNP | A | A | T | TCGA-ZF-A9R5-01A-12D-A42E-08 | TCGA-ZF-A9R5-10A-01D-A42H-08 | g.chr15:53957875A>T | c.1856T>A | c.(1855-1857)aTt>aAt | p.I619N |
BLCA | 15 | 53994342 | 53994342 | + | Missense_Mutation | SNP | C | C | T | TCGA-CF-A3MI-01A-11D-A20D-08 | TCGA-CF-A3MI-10A-01D-A20D-08 | g.chr15:53994342C>T | c.1558G>A | c.(1558-1560)Gag>Aag | p.E520K |
BLCA | 15 | 53998239 | 53998239 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZF-A9RC-01A-11D-A38G-08 | TCGA-ZF-A9RC-10A-01D-A38J-08 | g.chr15:53998239C>T | c.987G>A | c.(985-987)atG>atA | p.M329I |
BLCA | 15 | 54003115 | 54003115 | + | Missense_Mutation | SNP | C | C | T | TCGA-GC-A3I6-01A-11D-A20D-08 | TCGA-GC-A3I6-10A-01D-A20D-08 | g.chr15:54003115C>T | c.893G>A | c.(892-894)aGa>aAa | p.R298K |
BLCA | 15 | 54003547 | 54003547 | + | Silent | SNP | A | A | G | TCGA-BT-A3PJ-01A-21D-A21Z-08 | TCGA-BT-A3PJ-10A-01D-A21Z-08 | g.chr15:54003547A>G | c.843T>C | c.(841-843)taT>taC | p.Y281Y |
BLCA | 15 | 54003679 | 54003679 | + | Splice_Site | SNP | C | C | G | TCGA-K4-A54R-01A-11D-A26M-08 | TCGA-K4-A54R-10A-01D-A26K-08 | g.chr15:54003679C>G | | c.e8-1 | |
BLCA | 15 | 54005008 | 54005008 | + | Silent | SNP | A | A | C | TCGA-G2-AA3C-01A-21D-A391-08 | TCGA-G2-AA3C-10A-01D-A394-08 | g.chr15:54005008A>C | c.672T>G | c.(670-672)acT>acG | p.T224T |
BLCA | 15 | 54008834 | 54008834 | + | Silent | SNP | A | A | T | TCGA-H4-A2HQ-01A-11D-A17V-08 | TCGA-H4-A2HQ-10A-01D-A17V-08 | g.chr15:54008834A>T | c.309T>A | c.(307-309)gcT>gcA | p.A103A |
BRCA | 15 | 53815460 | 53815460 | + | Missense_Mutation | SNP | C | C | T | TCGA-C8-A26Y-01A-11D-A16D-09 | TCGA-C8-A26Y-10A-01D-A16D-09 | g.chr15:53815460C>T | c.3208G>A | c.(3208-3210)Gag>Aag | p.E1070K |
BRCA | 15 | 53889357 | 53889358 | + | Frame_Shift_Del | DEL | CA | CA | - | TCGA-C8-A1HN-01A-11D-A135-09 | TCGA-C8-A1HN-10A-01D-A135-09 | g.chr15:53889357_53889358delCA | c.3066_3067delTG | c.(3064-3069)tgtgagfs | p.CE1022fs |
BRCA | 15 | 53907842 | 53907842 | + | Missense_Mutation | SNP | A | A | T | TCGA-A1-A0SD-01A-11D-A10Y-09 | TCGA-A1-A0SD-10A-01D-A110-09 | g.chr15:53907842A>T | c.2561T>A | c.(2560-2562)aTa>aAa | p.I854K |
BRCA | 15 | 53907944 | 53907944 | + | Missense_Mutation | SNP | T | T | C | TCGA-A8-A083-01A-21W-A019-09 | TCGA-A8-A083-10A-01W-A021-09 | g.chr15:53907944T>C | c.2459A>G | c.(2458-2460)aAt>aGt | p.N820S |
BRCA | 15 | 53908000 | 53908000 | + | Silent | SNP | G | G | A | TCGA-EW-A1PB-01A-11D-A142-09 | TCGA-EW-A1PB-10A-01D-A142-09 | g.chr15:53908000G>A | c.2403C>T | c.(2401-2403)tgC>tgT | p.C801C |
BRCA | 15 | 53908085 | 53908085 | + | Missense_Mutation | SNP | T | T | G | TCGA-C8-A12X-01A-11D-A10Y-09 | TCGA-C8-A12X-10A-01D-A110-09 | g.chr15:53908085T>G | c.2318A>C | c.(2317-2319)aAg>aCg | p.K773T |
BRCA | 15 | 54003115 | 54003115 | + | Missense_Mutation | SNP | C | C | G | TCGA-GM-A3NW-01A-21D-A228-09 | TCGA-GM-A3NW-10A-01D-A22A-09 | g.chr15:54003115C>G | c.893G>C | c.(892-894)aGa>aCa | p.R298T |
BRCA | 15 | 54008807 | 54008807 | + | Silent | SNP | G | G | T | TCGA-LL-A441-01A-11D-A243-09 | TCGA-LL-A441-10A-01D-A243-09 | g.chr15:54008807G>T | c.336C>A | c.(334-336)atC>atA | p.I112I |
BRCA | 15 | 54015063 | 54015063 | + | Missense_Mutation | SNP | T | T | A | TCGA-E2-A1LA-01A-11D-A142-09 | TCGA-E2-A1LA-10A-01D-A142-09 | g.chr15:54015063T>A | c.196A>T | c.(196-198)Aca>Tca | p.T66S |
BRCA | 15 | 54015098 | 54015098 | + | Missense_Mutation | SNP | G | G | A | TCGA-C8-A12X-01A-11D-A10Y-09 | TCGA-C8-A12X-10A-01D-A110-09 | g.chr15:54015098G>A | c.161C>T | c.(160-162)gCg>gTg | p.A54V |
BRCA | 15 | 54015098 | 54015099 | + | Frame_Shift_Ins | INS | - | - | AATT | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr15:54015098_54015099insAATT | c.160_161insAATT | c.(160-162)gcgfs | p.A54fs |
BRCA | 15 | 54025194 | 54025194 | + | Splice_Site | SNP | C | C | T | TCGA-BH-A0HA-01A-11D-A12Q-09 | TCGA-BH-A0HA-11A-31D-A12Q-09 | g.chr15:54025194C>T | c.153G>A | c.(151-153)aaG>aaA | p.K51K |
BRCA | 15 | 54025259 | 54025259 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-A2-A259-01A-11D-A16D-09 | TCGA-A2-A259-10A-01D-A16D-09 | g.chr15:54025259G>A | c.88C>T | c.(88-90)Cga>Tga | p.R30* |
BRCA | 15 | 54025306 | 54025306 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-AO-A1KO-01A-31D-A188-09 | TCGA-AO-A1KO-10A-01D-A13O-09 | g.chr15:54025306delT | c.41delA | c.(40-42)aagfs | p.K14fs |
CESC | 15 | 53994468 | 53994468 | + | Missense_Mutation | SNP | C | C | A | TCGA-EK-A3GK-01A-11D-A20U-09 | TCGA-EK-A3GK-10A-01D-A20U-09 | g.chr15:53994468C>A | c.1432G>T | c.(1432-1434)Gac>Tac | p.D478Y |
CESC | 15 | 54003546 | 54003546 | + | Missense_Mutation | SNP | G | G | C | TCGA-EK-A2PL-01A-11D-A18J-09 | TCGA-EK-A2PL-10A-01D-A18J-09 | g.chr15:54003546G>C | c.844C>G | c.(844-846)Cag>Gag | p.Q282E |
CESC | 15 | 54003550 | 54003550 | + | Silent | SNP | G | G | A | TCGA-EK-A2RJ-01A-11D-A18J-09 | TCGA-EK-A2RJ-10A-01D-A18J-09 | g.chr15:54003550G>A | c.840C>T | c.(838-840)atC>atT | p.I280I |
COAD | 15 | 53889318 | 53889318 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr15:53889318C>A | c.3106G>T | c.(3106-3108)Gaa>Taa | p.E1036* |
COAD | 15 | 53889403 | 53889403 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr15:53889403T>C | c.3021A>G | c.(3019-3021)atA>atG | p.I1007M |
COAD | 15 | 53889439 | 53889439 | + | Silent | SNP | C | C | T | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chr15:53889439C>T | c.2985G>A | c.(2983-2985)gcG>gcA | p.A995A |
COAD | 15 | 53901721 | 53901721 | + | Missense_Mutation | SNP | G | G | C | TCGA-DM-A1D9-01A-11D-A152-10 | TCGA-DM-A1D9-10A-01D-A152-10 | g.chr15:53901721G>C | c.2941C>G | c.(2941-2943)Cag>Gag | p.Q981E |
COAD | 15 | 53905904 | 53905904 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr15:53905904T>C | c.2831A>G | c.(2830-2832)gAc>gGc | p.D944G |
COAD | 15 | 53907756 | 53907756 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3861-01A-01W-0995-10 | TCGA-AA-3861-10A-01W-0995-10 | g.chr15:53907756C>A | c.2647G>T | c.(2647-2649)Gga>Tga | p.G883* |
COAD | 15 | 53907819 | 53907819 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr15:53907819A>C | c.2584T>G | c.(2584-2586)Tta>Gta | p.L862V |
COAD | 15 | 53907944 | 53907944 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:53907944T>G | c.2459A>C | c.(2458-2460)aAt>aCt | p.N820T |
COAD | 15 | 53907949 | 53907949 | + | Silent | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:53907949G>A | c.2454C>T | c.(2452-2454)caC>caT | p.H818H |
COAD | 15 | 53908010 | 53908010 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr15:53908010A>C | c.2393T>G | c.(2392-2394)tTt>tGt | p.F798C |
COAD | 15 | 53908282 | 53908282 | + | Missense_Mutation | SNP | G | G | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:53908282G>T | c.2121C>A | c.(2119-2121)ttC>ttA | p.F707L |
COAD | 15 | 53908294 | 53908294 | + | Silent | SNP | A | A | C | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr15:53908294A>C | c.2109T>G | c.(2107-2109)tcT>tcG | p.S703S |
COAD | 15 | 53908348 | 53908348 | + | Silent | SNP | A | A | G | TCGA-AA-3516-01A-02W-0833-10 | TCGA-AA-3516-10A-01W-0833-10 | g.chr15:53908348A>G | c.2055T>C | c.(2053-2055)gaT>gaC | p.D685D |
COAD | 15 | 53957929 | 53957929 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr15:53957929C>T | c.1802G>A | c.(1801-1803)cGa>cAa | p.R601Q |
COAD | 15 | 53992052 | 53992052 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A017-01A-01W-A00E-09 | TCGA-AA-A017-10A-01W-A00E-09 | g.chr15:53992052G>A | c.1660C>T | c.(1660-1662)Cgg>Tgg | p.R554W |
COAD | 15 | 53992098 | 53992098 | + | Silent | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr15:53992098G>A | c.1614C>T | c.(1612-1614)tcC>tcT | p.S538S |
COAD | 15 | 53992110 | 53992110 | + | Silent | SNP | G | G | A | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr15:53992110G>A | c.1602C>T | c.(1600-1602)tgC>tgT | p.C534C |
COAD | 15 | 53998203 | 53998203 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:53998203G>T | c.1023C>A | c.(1021-1023)ttC>ttA | p.F341L |
COAD | 15 | 54005064 | 54005064 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr15:54005064C>A | c.616G>T | c.(616-618)Gaa>Taa | p.E206* |
COAD | 15 | 54006632 | 54006632 | + | Splice_Site | SNP | T | T | C | TCGA-AA-A00R-01A-01W-A005-10 | TCGA-AA-A00R-10A-01W-A005-10 | g.chr15:54006632T>C | c.590A>G | c.(589-591)cAg>cGg | p.Q197R |
COAD | 15 | 54008832 | 54008832 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-2672-01A-01W-0833-10 | TCGA-A6-2672-10A-01W-0833-10 | g.chr15:54008832G>A | c.311C>T | c.(310-312)aCa>aTa | p.T104I |
COAD | 15 | 54015028 | 54015028 | + | Silent | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:54015028C>T | c.231G>A | c.(229-231)caG>caA | p.Q77Q |
COAD | 15 | 54015068 | 54015068 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr15:54015068G>A | c.191C>T | c.(190-192)tCg>tTg | p.S64L |
COADREAD | 15 | 53809937 | 53809937 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:53809937G>T | c.3268C>A | c.(3268-3270)Cat>Aat | p.H1090N |
COADREAD | 15 | 53815457 | 53815457 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:53815457C>T | c.3211G>A | c.(3211-3213)Gac>Aac | p.D1071N |
COADREAD | 15 | 53889318 | 53889318 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr15:53889318C>A | c.3106G>T | c.(3106-3108)Gaa>Taa | p.E1036* |
COADREAD | 15 | 53889403 | 53889403 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr15:53889403T>C | c.3021A>G | c.(3019-3021)atA>atG | p.I1007M |
COADREAD | 15 | 53889439 | 53889439 | + | Silent | SNP | C | C | T | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chr15:53889439C>T | c.2985G>A | c.(2983-2985)gcG>gcA | p.A995A |
COADREAD | 15 | 53901721 | 53901721 | + | Missense_Mutation | SNP | G | G | C | TCGA-DM-A1D9-01A-11D-A152-10 | TCGA-DM-A1D9-10A-01D-A152-10 | g.chr15:53901721G>C | c.2941C>G | c.(2941-2943)Cag>Gag | p.Q981E |
COADREAD | 15 | 53905904 | 53905904 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr15:53905904T>C | c.2831A>G | c.(2830-2832)gAc>gGc | p.D944G |
COADREAD | 15 | 53907722 | 53907722 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:53907722G>T | c.2681C>A | c.(2680-2682)tCt>tAt | p.S894Y |
COADREAD | 15 | 53907756 | 53907756 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3861-01A-01W-0995-10 | TCGA-AA-3861-10A-01W-0995-10 | g.chr15:53907756C>A | c.2647G>T | c.(2647-2649)Gga>Tga | p.G883* |
COADREAD | 15 | 53907819 | 53907819 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr15:53907819A>C | c.2584T>G | c.(2584-2586)Tta>Gta | p.L862V |
COADREAD | 15 | 53907944 | 53907944 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:53907944T>G | c.2459A>C | c.(2458-2460)aAt>aCt | p.N820T |
COADREAD | 15 | 53907949 | 53907949 | + | Silent | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:53907949G>A | c.2454C>T | c.(2452-2454)caC>caT | p.H818H |
COADREAD | 15 | 53908010 | 53908010 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr15:53908010A>C | c.2393T>G | c.(2392-2394)tTt>tGt | p.F798C |
COADREAD | 15 | 53908282 | 53908282 | + | Missense_Mutation | SNP | G | G | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:53908282G>T | c.2121C>A | c.(2119-2121)ttC>ttA | p.F707L |
COADREAD | 15 | 53908294 | 53908294 | + | Silent | SNP | A | A | C | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr15:53908294A>C | c.2109T>G | c.(2107-2109)tcT>tcG | p.S703S |
COADREAD | 15 | 53908348 | 53908348 | + | Silent | SNP | A | A | G | TCGA-AA-3516-01A-02W-0833-10 | TCGA-AA-3516-10A-01W-0833-10 | g.chr15:53908348A>G | c.2055T>C | c.(2053-2055)gaT>gaC | p.D685D |
COADREAD | 15 | 53957929 | 53957929 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr15:53957929C>T | c.1802G>A | c.(1801-1803)cGa>cAa | p.R601Q |
COADREAD | 15 | 53957939 | 53957939 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:53957939C>A | c.1792G>T | c.(1792-1794)Gaa>Taa | p.E598* |
COADREAD | 15 | 53992052 | 53992052 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A017-01A-01W-A00E-09 | TCGA-AA-A017-10A-01W-A00E-09 | g.chr15:53992052G>A | c.1660C>T | c.(1660-1662)Cgg>Tgg | p.R554W |
COADREAD | 15 | 53992098 | 53992098 | + | Silent | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr15:53992098G>A | c.1614C>T | c.(1612-1614)tcC>tcT | p.S538S |
COADREAD | 15 | 53992110 | 53992110 | + | Silent | SNP | G | G | A | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr15:53992110G>A | c.1602C>T | c.(1600-1602)tgC>tgT | p.C534C |
COADREAD | 15 | 53997398 | 53997398 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:53997398C>A | c.1135G>T | c.(1135-1137)Gat>Tat | p.D379Y |
COADREAD | 15 | 53998203 | 53998203 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:53998203G>T | c.1023C>A | c.(1021-1023)ttC>ttA | p.F341L |
COADREAD | 15 | 54005064 | 54005064 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr15:54005064C>A | c.616G>T | c.(616-618)Gaa>Taa | p.E206* |
COADREAD | 15 | 54006632 | 54006632 | + | Splice_Site | SNP | T | T | C | TCGA-AA-A00R-01A-01W-A005-10 | TCGA-AA-A00R-10A-01W-A005-10 | g.chr15:54006632T>C | c.590A>G | c.(589-591)cAg>cGg | p.Q197R |
COADREAD | 15 | 54008832 | 54008832 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-2672-01A-01W-0833-10 | TCGA-A6-2672-10A-01W-0833-10 | g.chr15:54008832G>A | c.311C>T | c.(310-312)aCa>aTa | p.T104I |
COADREAD | 15 | 54015028 | 54015028 | + | Silent | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:54015028C>T | c.231G>A | c.(229-231)caG>caA | p.Q77Q |
COADREAD | 15 | 54015068 | 54015068 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr15:54015068G>A | c.191C>T | c.(190-192)tCg>tTg | p.S64L |
DLBC | 15 | 53997415 | 53997415 | + | Missense_Mutation | SNP | G | G | T | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr15:53997415G>T | c.1118C>A | c.(1117-1119)gCc>gAc | p.A373D |
DLBC | 15 | 54007512 | 54007512 | + | Missense_Mutation | SNP | C | C | A | TCGA-GR-7351-01A-11D-2210-10 | TCGA-GR-7351-10A-01D-2210-10 | g.chr15:54007512C>A | c.392G>T | c.(391-393)gGa>gTa | p.G131V |
ESCA | 15 | 53907630 | 53907630 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A43I-01A-11D-A247-09 | TCGA-L5-A43I-11A-11D-A247-09 | g.chr15:53907630C>T | c.2773G>A | c.(2773-2775)Gtt>Att | p.V925I |
ESCA | 15 | 53908157 | 53908157 | + | Missense_Mutation | SNP | C | C | G | TCGA-XP-A8T8-01A-11D-A36J-09 | TCGA-XP-A8T8-10A-01D-A36M-09 | g.chr15:53908157C>G | c.2246G>C | c.(2245-2247)aGc>aCc | p.S749T |
ESCA | 15 | 53908282 | 53908282 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A8NF-01A-11D-A37C-09 | TCGA-L5-A8NF-11A-11D-A37F-09 | g.chr15:53908282G>T | c.2121C>A | c.(2119-2121)ttC>ttA | p.F707L |
ESCA | 15 | 54003577 | 54003577 | + | Silent | SNP | G | G | A | TCGA-L5-A8NL-01A-12D-A37C-09 | TCGA-L5-A8NL-11A-12D-A37F-09 | g.chr15:54003577G>A | c.813C>T | c.(811-813)atC>atT | p.I271I |
ESCA | 15 | 54003588 | 54003588 | + | Missense_Mutation | SNP | T | T | C | TCGA-2H-A9GR-01A-12D-A37C-09 | TCGA-2H-A9GR-11A-11D-A37F-09 | g.chr15:54003588T>C | c.802A>G | c.(802-804)Aga>Gga | p.R268G |
GBM | 15 | 53889439 | 53889439 | + | Silent | SNP | C | C | T | TCGA-12-0688-01A-02D-1492-08 | TCGA-12-0688-10A-01D-1492-08 | g.chr15:53889439C>T | c.2985G>A | c.(2983-2985)gcG>gcA | p.A995A |
GBM | 15 | 53908374 | 53908374 | + | Missense_Mutation | SNP | C | C | T | TCGA-28-2499-01A-01D-1494-08 | TCGA-28-2499-10A-01D-1494-08 | g.chr15:53908374C>T | c.2029G>A | c.(2029-2031)Gtt>Att | p.V677I |
GBM | 15 | 53992060 | 53992060 | + | Missense_Mutation | SNP | A | A | T | TCGA-27-1833-01A-01W-0643-08 | TCGA-27-1833-10A-01W-0644-08 | g.chr15:53992060A>T | c.1652T>A | c.(1651-1653)cTg>cAg | p.L551Q |
GBM | 15 | 53994476 | 53994476 | + | Missense_Mutation | SNP | G | G | A | TCGA-06-2558-01A-01D-1494-08 | TCGA-06-2558-10A-01D-1494-08 | g.chr15:53994476G>A | c.1424C>T | c.(1423-1425)tCg>tTg | p.S475L |
GBM | 15 | 53998128 | 53998128 | + | Silent | SNP | A | A | G | TCGA-32-1991-01A-01D-1353-08 | TCGA-32-1991-10C-01D-1353-08 | g.chr15:53998128A>G | c.1098T>C | c.(1096-1098)ccT>ccC | p.P366P |
GBM | 15 | 53998200 | 53998200 | + | Silent | SNP | A | A | T | TCGA-02-0003-01A-01D-1490-08 | TCGA-02-0003-10A-01D-1490-08 | g.chr15:53998200A>T | c.1026T>A | c.(1024-1026)tcT>tcA | p.S342S |
GBMLGG | 15 | 53889439 | 53889439 | + | Silent | SNP | C | C | T | TCGA-12-0688-01A-02D-1492-08 | TCGA-12-0688-10A-01D-1492-08 | g.chr15:53889439C>T | c.2985G>A | c.(2983-2985)gcG>gcA | p.A995A |
GBMLGG | 15 | 53907678 | 53907678 | + | Missense_Mutation | SNP | A | A | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:53907678A>C | c.2725T>G | c.(2725-2727)Ttt>Gtt | p.F909V |
GBMLGG | 15 | 53907717 | 53907717 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-RY-A83Z-01A-11D-A36O-08 | TCGA-RY-A83Z-10A-01D-A367-08 | g.chr15:53907717G>A | c.2686C>T | c.(2686-2688)Cga>Tga | p.R896* |
GBMLGG | 15 | 53908182 | 53908182 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-A76R-01A-11D-A32B-08 | TCGA-DU-A76R-10A-01D-A329-08 | g.chr15:53908182C>T | c.2221G>A | c.(2221-2223)Gca>Aca | p.A741T |
GBMLGG | 15 | 53908374 | 53908374 | + | Missense_Mutation | SNP | C | C | T | TCGA-28-2499-01A-01D-1494-08 | TCGA-28-2499-10A-01D-1494-08 | g.chr15:53908374C>T | c.2029G>A | c.(2029-2031)Gtt>Att | p.V677I |
GBMLGG | 15 | 53957930 | 53957930 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:53957930G>A | c.1801C>T | c.(1801-1803)Cga>Tga | p.R601* |
GBMLGG | 15 | 53992060 | 53992060 | + | Missense_Mutation | SNP | A | A | T | TCGA-27-1833-01A-01W-0643-08 | TCGA-27-1833-10A-01W-0644-08 | g.chr15:53992060A>T | c.1652T>A | c.(1651-1653)cTg>cAg | p.L551Q |
GBMLGG | 15 | 53994476 | 53994476 | + | Missense_Mutation | SNP | G | G | A | TCGA-06-2558-01A-01D-1494-08 | TCGA-06-2558-10A-01D-1494-08 | g.chr15:53994476G>A | c.1424C>T | c.(1423-1425)tCg>tTg | p.S475L |
GBMLGG | 15 | 53998128 | 53998128 | + | Silent | SNP | A | A | G | TCGA-32-1991-01A-01D-1353-08 | TCGA-32-1991-10C-01D-1353-08 | g.chr15:53998128A>G | c.1098T>C | c.(1096-1098)ccT>ccC | p.P366P |
GBMLGG | 15 | 53998200 | 53998200 | + | Silent | SNP | A | A | T | TCGA-02-0003-01A-01D-1490-08 | TCGA-02-0003-10A-01D-1490-08 | g.chr15:53998200A>T | c.1026T>A | c.(1024-1026)tcT>tcA | p.S342S |
HNSC | 15 | 53809925 | 53809925 | + | Missense_Mutation | SNP | C | C | A | TCGA-CR-5248-01A-01D-2012-08 | TCGA-CR-5248-10A-01D-2013-08 | g.chr15:53809925C>A | c.3280G>T | c.(3280-3282)Gca>Tca | p.A1094S |
HNSC | 15 | 53815463 | 53815463 | + | Missense_Mutation | SNP | C | C | T | TCGA-MT-A67G-01A-11D-A30E-08 | TCGA-MT-A67G-10A-01D-A30H-08 | g.chr15:53815463C>T | c.3205G>A | c.(3205-3207)Gtg>Atg | p.V1069M |
HNSC | 15 | 53815478 | 53815478 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-5977-01A-11D-1683-08 | TCGA-CV-5977-11A-01D-1683-08 | g.chr15:53815478C>T | c.3190G>A | c.(3190-3192)Gca>Aca | p.A1064T |
HNSC | 15 | 53889325 | 53889325 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CN-6019-01A-11D-1683-08 | TCGA-CN-6019-10A-01D-1683-08 | g.chr15:53889325delC | c.3099delG | c.(3097-3099)tggfs | p.W1033fs |
HNSC | 15 | 53889435 | 53889435 | + | Missense_Mutation | SNP | C | C | A | TCGA-CN-A63T-01A-11D-A28R-08 | TCGA-CN-A63T-10A-01D-A28U-08 | g.chr15:53889435C>A | c.2989G>T | c.(2989-2991)Gtt>Ttt | p.V997F |
HNSC | 15 | 53889439 | 53889439 | + | Silent | SNP | C | C | T | TCGA-CR-6491-01A-11D-1870-08 | TCGA-CR-6491-10A-01D-1870-08 | g.chr15:53889439C>T | c.2985G>A | c.(2983-2985)gcG>gcA | p.A995A |
HNSC | 15 | 53889440 | 53889440 | + | Missense_Mutation | SNP | G | G | A | TCGA-QK-A6IH-01A-11D-A31L-08 | TCGA-QK-A6IH-10A-01D-A31J-08 | g.chr15:53889440G>A | c.2984C>T | c.(2983-2985)gCg>gTg | p.A995V |
HNSC | 15 | 53901735 | 53901735 | + | Missense_Mutation | SNP | G | G | A | TCGA-D6-6516-01A-11D-1870-08 | TCGA-D6-6516-10A-01D-1870-08 | g.chr15:53901735G>A | c.2927C>T | c.(2926-2928)tCc>tTc | p.S976F |
HNSC | 15 | 53905881 | 53905881 | + | Missense_Mutation | SNP | A | A | C | TCGA-CV-A460-01A-21D-A25D-08 | TCGA-CV-A460-10A-01D-A25E-08 | g.chr15:53905881A>C | c.2854T>G | c.(2854-2856)Tac>Gac | p.Y952D |
HNSC | 15 | 53907901 | 53907901 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-7261-01A-11D-2012-08 | TCGA-CV-7261-10A-01D-2013-08 | g.chr15:53907901C>G | c.2502G>C | c.(2500-2502)ttG>ttC | p.L834F |
HNSC | 15 | 53907993 | 53907993 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-5977-01A-11D-1683-08 | TCGA-CV-5977-11A-01D-1683-08 | g.chr15:53907993G>A | c.2410C>T | c.(2410-2412)Cca>Tca | p.P804S |
HNSC | 15 | 53908088 | 53908088 | + | Missense_Mutation | SNP | A | A | C | TCGA-QK-A8ZA-01A-11D-A391-08 | TCGA-QK-A8ZA-10A-01D-A394-08 | g.chr15:53908088A>C | c.2315T>G | c.(2314-2316)aTg>aGg | p.M772R |
HNSC | 15 | 53992035 | 53992035 | + | Silent | SNP | A | A | C | TCGA-CN-A63U-01A-11D-A30E-08 | TCGA-CN-A63U-10A-01D-A30H-08 | g.chr15:53992035A>C | c.1677T>G | c.(1675-1677)ccT>ccG | p.P559P |
HNSC | 15 | 53992089 | 53992089 | + | Silent | SNP | G | G | A | TCGA-CQ-7071-01A-12D-A30E-08 | TCGA-CQ-7071-10A-01D-A30H-08 | g.chr15:53992089G>A | c.1623C>T | c.(1621-1623)ctC>ctT | p.L541L |
HNSC | 15 | 53994481 | 53994481 | + | Silent | SNP | G | G | C | TCGA-CV-7414-01A-11D-2078-08 | TCGA-CV-7414-10A-01D-2078-08 | g.chr15:53994481G>C | c.1419C>G | c.(1417-1419)ctC>ctG | p.L473L |
HNSC | 15 | 53997322 | 53997322 | + | Missense_Mutation | SNP | G | G | C | TCGA-BA-A6DA-01A-31D-A31L-08 | TCGA-BA-A6DA-10A-01D-A31J-08 | g.chr15:53997322G>C | c.1211C>G | c.(1210-1212)aCt>aGt | p.T404S |
HNSC | 15 | 53998227 | 53998227 | + | Silent | SNP | T | T | C | TCGA-CV-6954-01A-11D-1912-08 | TCGA-CV-6954-10A-01D-1912-08 | g.chr15:53998227T>C | c.999A>G | c.(997-999)aaA>aaG | p.K333K |
HNSC | 15 | 54003099 | 54003099 | + | Silent | SNP | G | G | T | TCGA-CV-7440-01A-11D-2129-08 | TCGA-CV-7440-10A-01D-2129-08 | g.chr15:54003099G>T | c.909C>A | c.(907-909)acC>acA | p.T303T |
HNSC | 15 | 54006650 | 54006650 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-A45W-01A-11D-A25D-08 | TCGA-CV-A45W-10A-01D-A25E-08 | g.chr15:54006650G>A | c.572C>T | c.(571-573)tCa>tTa | p.S191L |
HNSC | 15 | 54025296 | 54025296 | + | Silent | SNP | G | G | A | TCGA-UF-A71E-01A-31D-A34J-08 | TCGA-UF-A71E-10B-01D-A34M-08 | g.chr15:54025296G>A | c.51C>T | c.(49-51)ccC>ccT | p.P17P |
KICH | 15 | 53908269 | 53908269 | + | Missense_Mutation | SNP | C | C | A | TCGA-KL-8339-01A-11D-2310-10 | TCGA-KL-8339-11A-01D-2310-10 | g.chr15:53908269C>A | c.2134G>T | c.(2134-2136)Gtc>Ttc | p.V712F |
KICH | 15 | 53997272 | 53997272 | + | Missense_Mutation | SNP | A | A | G | TCGA-KL-8342-01A-11D-2310-10 | TCGA-KL-8342-11A-01D-2310-10 | g.chr15:53997272A>G | c.1261T>C | c.(1261-1263)Tgt>Cgt | p.C421R |
KIPAN | 15 | 53815462 | 53815462 | + | Missense_Mutation | SNP | A | A | G | TCGA-HE-A5NL-01A-11D-A26P-10 | TCGA-HE-A5NL-10A-01D-A26P-10 | g.chr15:53815462A>G | c.3206T>C | c.(3205-3207)gTg>gCg | p.V1069A |
KIPAN | 15 | 53907852 | 53907852 | + | Missense_Mutation | SNP | T | T | C | TCGA-B0-5098-01A-01D-1421-08 | TCGA-B0-5098-11A-01D-1421-08 | g.chr15:53907852T>C | c.2551A>G | c.(2551-2553)Agt>Ggt | p.S851G |
KIPAN | 15 | 53907894 | 53907895 | + | Frame_Shift_Ins | INS | - | - | TTCAT | TCGA-CJ-4920-01A-01D-1429-08 | TCGA-CJ-4920-11A-01D-1429-08 | g.chr15:53907894_53907895insTTCAT | c.2508_2509insATGAA | c.(2506-2511)gaagatfs | p.D837fs |
KIPAN | 15 | 53908269 | 53908269 | + | Missense_Mutation | SNP | C | C | A | TCGA-KL-8339-01A-11D-2310-10 | TCGA-KL-8339-11A-01D-2310-10 | g.chr15:53908269C>A | c.2134G>T | c.(2134-2136)Gtc>Ttc | p.V712F |
KIPAN | 15 | 53908347 | 53908347 | + | Missense_Mutation | SNP | G | G | C | TCGA-BP-5007-01A-01D-1462-08 | TCGA-BP-5007-11A-01D-1462-08 | g.chr15:53908347G>C | c.2056C>G | c.(2056-2058)Ctg>Gtg | p.L686V |
KIPAN | 15 | 53957926 | 53957926 | + | Missense_Mutation | SNP | A | A | T | TCGA-B8-5159-01A-01D-1421-08 | TCGA-B8-5159-10A-01D-1421-08 | g.chr15:53957926A>T | c.1805T>A | c.(1804-1806)aTt>aAt | p.I602N |
KIPAN | 15 | 53997272 | 53997272 | + | Missense_Mutation | SNP | A | A | G | TCGA-KL-8342-01A-11D-2310-10 | TCGA-KL-8342-11A-01D-2310-10 | g.chr15:53997272A>G | c.1261T>C | c.(1261-1263)Tgt>Cgt | p.C421R |
KIPAN | 15 | 54025233 | 54025233 | + | Silent | SNP | C | C | T | TCGA-B0-5121-01A-02D-1421-08 | TCGA-B0-5121-11A-01D-1421-08 | g.chr15:54025233C>T | c.114G>A | c.(112-114)gaG>gaA | p.E38E |
KIRC | 15 | 53907852 | 53907852 | + | Missense_Mutation | SNP | T | T | C | TCGA-B0-5098-01A-01D-1421-08 | TCGA-B0-5098-11A-01D-1421-08 | g.chr15:53907852T>C | c.2551A>G | c.(2551-2553)Agt>Ggt | p.S851G |
KIRC | 15 | 53907894 | 53907895 | + | Frame_Shift_Ins | INS | - | - | TTCAT | TCGA-CJ-4920-01A-01D-1429-08 | TCGA-CJ-4920-11A-01D-1429-08 | g.chr15:53907894_53907895insTTCAT | c.2508_2509insATGAA | c.(2506-2511)gaagatfs | p.D837fs |
KIRC | 15 | 53908347 | 53908347 | + | Missense_Mutation | SNP | G | G | C | TCGA-BP-5007-01A-01D-1462-08 | TCGA-BP-5007-11A-01D-1462-08 | g.chr15:53908347G>C | c.2056C>G | c.(2056-2058)Ctg>Gtg | p.L686V |
KIRC | 15 | 53957926 | 53957926 | + | Missense_Mutation | SNP | A | A | T | TCGA-B8-5159-01A-01D-1421-08 | TCGA-B8-5159-10A-01D-1421-08 | g.chr15:53957926A>T | c.1805T>A | c.(1804-1806)aTt>aAt | p.I602N |
KIRC | 15 | 54025233 | 54025233 | + | Silent | SNP | C | C | T | TCGA-B0-5121-01A-02D-1421-08 | TCGA-B0-5121-11A-01D-1421-08 | g.chr15:54025233C>T | c.114G>A | c.(112-114)gaG>gaA | p.E38E |
KIRP | 15 | 53815462 | 53815462 | + | Missense_Mutation | SNP | A | A | G | TCGA-HE-A5NL-01A-11D-A26P-10 | TCGA-HE-A5NL-10A-01D-A26P-10 | g.chr15:53815462A>G | c.3206T>C | c.(3205-3207)gTg>gCg | p.V1069A |
LGG | 15 | 53907678 | 53907678 | + | Missense_Mutation | SNP | A | A | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:53907678A>C | c.2725T>G | c.(2725-2727)Ttt>Gtt | p.F909V |
LGG | 15 | 53907717 | 53907717 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-RY-A83Z-01A-11D-A36O-08 | TCGA-RY-A83Z-10A-01D-A367-08 | g.chr15:53907717G>A | c.2686C>T | c.(2686-2688)Cga>Tga | p.R896* |
LGG | 15 | 53908182 | 53908182 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-A76R-01A-11D-A32B-08 | TCGA-DU-A76R-10A-01D-A329-08 | g.chr15:53908182C>T | c.2221G>A | c.(2221-2223)Gca>Aca | p.A741T |
LGG | 15 | 53957930 | 53957930 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:53957930G>A | c.1801C>T | c.(1801-1803)Cga>Tga | p.R601* |
LIHC | 15 | 53992110 | 53992110 | + | Silent | SNP | G | G | A | TCGA-DD-AADD-01A-11D-A40R-10 | TCGA-DD-AADD-10A-01D-A40U-10 | g.chr15:53992110G>A | c.1602C>T | c.(1600-1602)tgC>tgT | p.C534C |
LIHC | 15 | 54003136 | 54003136 | + | Missense_Mutation | SNP | C | C | T | TCGA-ES-A2HT-01A-12D-A183-10 | TCGA-ES-A2HT-11A-11D-A183-10 | g.chr15:54003136C>T | c.872G>A | c.(871-873)aGc>aAc | p.S291N |
LIHC | 15 | 54004983 | 54004983 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-DD-A3A0-01A-11D-A20W-10 | TCGA-DD-A3A0-11A-11D-A20W-10 | g.chr15:54004983delA | c.697delT | c.(697-699)tctfs | p.S233fs |
LUAD | 15 | 53809911 | 53809911 | + | Silent | SNP | G | G | A | TCGA-44-7662-01A-11D-2063-08 | TCGA-44-7662-10A-01D-2063-08 | g.chr15:53809911G>A | c.3294C>T | c.(3292-3294)ccC>ccT | p.P1098P |
LUAD | 15 | 53889352 | 53889352 | + | Missense_Mutation | SNP | C | C | T | TCGA-49-4507-01A-01D-1265-08 | TCGA-49-4507-11A-01D-1265-08 | g.chr15:53889352C>T | c.3072G>A | c.(3070-3072)atG>atA | p.M1024I |
LUAD | 15 | 53889376 | 53889376 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-A4SU-01A-11D-A24P-08 | TCGA-44-A4SU-10A-01D-A24P-08 | g.chr15:53889376C>A | c.3048G>T | c.(3046-3048)atG>atT | p.M1016I |
LUAD | 15 | 53889379 | 53889379 | + | Silent | SNP | G | G | T | TCGA-17-Z003-01A-01W-0746-08 | TCGA-17-Z003-11A-01W-0746-08 | g.chr15:53889379G>T | c.3045C>A | c.(3043-3045)tcC>tcA | p.S1015S |
LUAD | 15 | 53905934 | 53905934 | + | Missense_Mutation | SNP | A | A | T | TCGA-17-Z055-01A-01W-0747-08 | TCGA-17-Z055-11A-01W-0747-08 | g.chr15:53905934A>T | c.2801T>A | c.(2800-2802)aTa>aAa | p.I934K |
LUAD | 15 | 53907714 | 53907714 | + | Missense_Mutation | SNP | C | C | G | TCGA-50-6592-01A-11D-1753-08 | TCGA-50-6592-11A-01D-1753-08 | g.chr15:53907714C>G | c.2689G>C | c.(2689-2691)Gag>Cag | p.E897Q |
LUAD | 15 | 53907791 | 53907791 | + | Missense_Mutation | SNP | G | G | A | TCGA-99-8033-01A-11D-2238-08 | TCGA-99-8033-10A-01D-2238-08 | g.chr15:53907791G>A | c.2612C>T | c.(2611-2613)tCa>tTa | p.S871L |
LUAD | 15 | 53907848 | 53907848 | + | Missense_Mutation | SNP | C | C | A | TCGA-78-7158-01A-11D-2036-08 | TCGA-78-7158-10A-01D-2036-08 | g.chr15:53907848C>A | c.2555G>T | c.(2554-2556)gGa>gTa | p.G852V |
LUAD | 15 | 53907849 | 53907849 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-78-7158-01A-11D-2036-08 | TCGA-78-7158-10A-01D-2036-08 | g.chr15:53907849C>A | c.2554G>T | c.(2554-2556)Gga>Tga | p.G852* |
LUAD | 15 | 53908067 | 53908067 | + | Missense_Mutation | SNP | T | T | G | TCGA-55-7907-01A-11D-2167-08 | TCGA-55-7907-10A-01D-2167-08 | g.chr15:53908067T>G | c.2336A>C | c.(2335-2337)cAg>cCg | p.Q779P |
LUAD | 15 | 53908074 | 53908074 | + | Missense_Mutation | SNP | T | T | C | TCGA-05-4424-01A-22D-1855-08 | TCGA-05-4424-10A-01D-1855-08 | g.chr15:53908074T>C | c.2329A>G | c.(2329-2331)Aaa>Gaa | p.K777E |
LUAD | 15 | 53908079 | 53908079 | + | Missense_Mutation | SNP | G | G | C | TCGA-95-7944-01A-11D-2184-08 | TCGA-95-7944-10A-01D-2184-08 | g.chr15:53908079G>C | c.2324C>G | c.(2323-2325)tCc>tGc | p.S775C |
LUAD | 15 | 53908228 | 53908228 | + | Silent | SNP | C | C | G | TCGA-99-8025-01A-11D-2238-08 | TCGA-99-8025-10A-01D-2238-08 | g.chr15:53908228C>G | c.2175G>C | c.(2173-2175)ctG>ctC | p.L725L |
LUAD | 15 | 53908296 | 53908296 | + | Missense_Mutation | SNP | A | A | G | TCGA-44-7660-01A-11D-2063-08 | TCGA-44-7660-10A-01D-2063-08 | g.chr15:53908296A>G | c.2107T>C | c.(2107-2109)Tct>Cct | p.S703P |
LUAD | 15 | 53992079 | 53992079 | + | Missense_Mutation | SNP | C | C | T | TCGA-78-7150-01A-21D-2036-08 | TCGA-78-7150-10A-01D-2036-08 | g.chr15:53992079C>T | c.1633G>A | c.(1633-1635)Gag>Aag | p.E545K |
LUAD | 15 | 53992106 | 53992106 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-8281-01A-11D-2284-08 | TCGA-86-8281-10A-01D-2284-08 | g.chr15:53992106C>A | c.1606G>T | c.(1606-1608)Gac>Tac | p.D536Y |
LUAD | 15 | 53992108 | 53992108 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4244-01A-01D-1105-08 | TCGA-05-4244-10A-01D-1105-08 | g.chr15:53992108C>A | c.1604G>T | c.(1603-1605)gGt>gTt | p.G535V |
LUAD | 15 | 53994371 | 53994371 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8614-01A-11D-2393-08 | TCGA-55-8614-10A-01D-2393-08 | g.chr15:53994371C>A | c.1529G>T | c.(1528-1530)gGt>gTt | p.G510V |
LUAD | 15 | 53994429 | 53994429 | + | Missense_Mutation | SNP | C | C | A | TCGA-91-8499-01A-11D-2393-08 | TCGA-91-8499-10A-01D-2393-08 | g.chr15:53994429C>A | c.1471G>T | c.(1471-1473)Gtg>Ttg | p.V491L |
LUAD | 15 | 53997389 | 53997389 | + | Missense_Mutation | SNP | C | C | T | TCGA-78-7220-01A-11D-2036-08 | TCGA-78-7220-10A-01D-2036-08 | g.chr15:53997389C>T | c.1144G>A | c.(1144-1146)Gat>Aat | p.D382N |
LUAD | 15 | 53997423 | 53997423 | + | Silent | SNP | T | T | A | TCGA-49-6743-01A-11D-1855-08 | TCGA-49-6743-11A-01D-1855-08 | g.chr15:53997423T>A | c.1110A>T | c.(1108-1110)ccA>ccT | p.P370P |
LUAD | 15 | 53998260 | 53998260 | + | Silent | SNP | A | A | T | TCGA-95-7039-01A-11D-1945-08 | TCGA-95-7039-10A-01D-1946-08 | g.chr15:53998260A>T | c.966T>A | c.(964-966)cgT>cgA | p.R322R |
LUAD | 15 | 54003555 | 54003555 | + | Missense_Mutation | SNP | A | A | T | TCGA-05-4432-01A-01D-1265-08 | TCGA-05-4432-10A-01D-1265-08 | g.chr15:54003555A>T | c.835T>A | c.(835-837)Tac>Aac | p.Y279N |
LUAD | 15 | 54003627 | 54003627 | + | Missense_Mutation | SNP | C | C | A | TCGA-53-A4EZ-01A-12D-A24P-08 | TCGA-53-A4EZ-10A-01D-A24P-08 | g.chr15:54003627C>A | c.763G>T | c.(763-765)Ggg>Tgg | p.G255W |
LUAD | 15 | 54007479 | 54007479 | + | Missense_Mutation | SNP | T | T | C | TCGA-05-4427-01A-21D-1855-08 | TCGA-05-4427-10A-01D-1855-08 | g.chr15:54007479T>C | c.425A>G | c.(424-426)aAa>aGa | p.K142R |
LUAD | 15 | 54007541 | 54007541 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-8672-01A-21D-2393-08 | TCGA-86-8672-10A-01D-2393-08 | g.chr15:54007541C>A | c.363G>T | c.(361-363)atG>atT | p.M121I |
LUAD | 15 | 54015037 | 54015037 | + | Missense_Mutation | SNP | G | G | C | TCGA-17-Z032-01A-01W-0746-08 | TCGA-17-Z032-11A-01W-0746-08 | g.chr15:54015037G>C | c.222C>G | c.(220-222)ttC>ttG | p.F74L |
LUAD | 15 | 54015097 | 54015097 | + | Silent | SNP | C | C | T | TCGA-05-4420-01A-01D-1265-08 | TCGA-05-4420-10A-01D-1265-08 | g.chr15:54015097C>T | c.162G>A | c.(160-162)gcG>gcA | p.A54A |
LUAD | 15 | 54025290 | 54025290 | + | Silent | SNP | G | G | A | TCGA-62-A46O-01A-11D-A24D-08 | TCGA-62-A46O-10A-01D-A24F-08 | g.chr15:54025290G>A | c.57C>T | c.(55-57)agC>agT | p.S19S |
LUSC | 15 | 53815464 | 53815464 | + | Missense_Mutation | SNP | G | G | C | TCGA-66-2782-01A-01D-1522-08 | TCGA-66-2782-11A-01D-1522-08 | g.chr15:53815464G>C | c.3204C>G | c.(3202-3204)gaC>gaG | p.D1068E |
LUSC | 15 | 53889379 | 53889379 | + | Silent | SNP | G | G | T | TCGA-46-3765-01A-01D-0983-08 | TCGA-46-3765-10A-01D-0983-08 | g.chr15:53889379G>T | c.3045C>A | c.(3043-3045)tcC>tcA | p.S1015S |
LUSC | 15 | 53907719 | 53907719 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-22-4613-01A-01D-1441-08 | TCGA-22-4613-11A-01D-1441-08 | g.chr15:53907719delA | c.2684delT | c.(2683-2685)ttgfs | p.L895fs |
LUSC | 15 | 53907738 | 53907738 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-34-2608-01A-02D-1522-08 | TCGA-34-2608-11A-01D-1522-08 | g.chr15:53907738C>A | c.2665G>T | c.(2665-2667)Gaa>Taa | p.E889* |
LUSC | 15 | 53907987 | 53907987 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-33-4582-01A-01D-1441-08 | TCGA-33-4582-11A-01D-1441-08 | g.chr15:53907987C>A | c.2416G>T | c.(2416-2418)Gga>Tga | p.G806* |
LUSC | 15 | 53908224 | 53908224 | + | Missense_Mutation | SNP | G | G | T | TCGA-22-5473-01A-01D-1632-08 | TCGA-22-5473-11A-11D-1632-08 | g.chr15:53908224G>T | c.2179C>A | c.(2179-2181)Ctg>Atg | p.L727M |
LUSC | 15 | 53908393 | 53908393 | + | Silent | SNP | C | C | T | TCGA-21-5784-01A-01D-1632-08 | TCGA-21-5784-10A-01D-1632-08 | g.chr15:53908393C>T | c.2010G>A | c.(2008-2010)gtG>gtA | p.V670V |
LUSC | 15 | 53908408 | 53908408 | + | Missense_Mutation | SNP | A | A | C | TCGA-66-2763-01A-01D-1522-08 | TCGA-66-2763-11A-01D-1522-08 | g.chr15:53908408A>C | c.1995T>G | c.(1993-1995)ttT>ttG | p.F665L |
LUSC | 15 | 53957876 | 53957876 | + | Missense_Mutation | SNP | T | T | A | TCGA-60-2724-01A-01D-1522-08 | TCGA-60-2724-11A-01D-1522-08 | g.chr15:53957876T>A | c.1855A>T | c.(1855-1857)Att>Ttt | p.I619F |
LUSC | 15 | 53992045 | 53992045 | + | Missense_Mutation | SNP | T | T | G | TCGA-66-2780-01A-01D-1522-08 | TCGA-66-2780-11A-01D-1522-08 | g.chr15:53992045T>G | c.1667A>C | c.(1666-1668)cAc>cCc | p.H556P |
LUSC | 15 | 53998163 | 53998163 | + | Missense_Mutation | SNP | G | G | T | TCGA-37-5819-01A-01D-1632-08 | TCGA-37-5819-10A-01D-1632-08 | g.chr15:53998163G>T | c.1063C>A | c.(1063-1065)Cct>Act | p.P355T |
LUSC | 15 | 54006673 | 54006673 | + | Missense_Mutation | SNP | C | C | A | TCGA-34-2596-01A-01D-1522-08 | TCGA-34-2596-11A-01D-1522-08 | g.chr15:54006673C>A | c.549G>T | c.(547-549)gaG>gaT | p.E183D |
LUSC | 15 | 54007474 | 54007474 | + | Missense_Mutation | SNP | A | A | T | TCGA-66-2786-01A-01D-1522-08 | TCGA-66-2786-11A-01D-1522-08 | g.chr15:54007474A>T | c.430T>A | c.(430-432)Ttg>Atg | p.L144M |
LUSC | 15 | 54007484 | 54007484 | + | Silent | SNP | A | A | G | TCGA-51-4079-01A-01D-1458-08 | TCGA-51-4079-11A-01D-1458-08 | g.chr15:54007484A>G | c.420T>C | c.(418-420)gaT>gaC | p.D140D |
LUSC | 15 | 54007544 | 54007544 | + | Silent | SNP | C | C | A | TCGA-21-5782-01A-01D-1632-08 | TCGA-21-5782-10A-01D-1632-08 | g.chr15:54007544C>A | c.360G>T | c.(358-360)cgG>cgT | p.R120R |
LUSC | 15 | 54025310 | 54025310 | + | Missense_Mutation | SNP | G | G | C | TCGA-22-5471-01A-01D-1632-08 | TCGA-22-5471-11A-01D-1632-08 | g.chr15:54025310G>C | c.37C>G | c.(37-39)Cag>Gag | p.Q13E |
OV | 15 | 54025238 | 54025238 | + | Missense_Mutation | SNP | G | G | T | TCGA-13-2061-01A-01D-1526-09 | TCGA-13-2061-10A-01D-1526-09 | g.chr15:54025238G>T | c.109C>A | c.(109-111)Caa>Aaa | p.Q37K |
PAAD | 15 | 53815426 | 53815426 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:53815426G>A | c.3242C>T | c.(3241-3243)tCt>tTt | p.S1081F |
PAAD | 15 | 53889435 | 53889435 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:53889435C>T | c.2989G>A | c.(2989-2991)Gtt>Att | p.V997I |
PAAD | 15 | 53908400 | 53908400 | + | Missense_Mutation | SNP | A | A | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:53908400A>G | c.2003T>C | c.(2002-2004)tTg>tCg | p.L668S |
PRAD | 15 | 53889439 | 53889439 | + | Silent | SNP | C | C | T | TCGA-EJ-A65D-01A-11D-A30E-08 | TCGA-EJ-A65D-10A-01D-A30H-08 | g.chr15:53889439C>T | c.2985G>A | c.(2983-2985)gcG>gcA | p.A995A |
PRAD | 15 | 53907788 | 53907788 | + | Missense_Mutation | SNP | T | T | C | TCGA-ZG-A8QW-01A-11D-A377-08 | TCGA-ZG-A8QW-10A-01D-A37A-08 | g.chr15:53907788T>C | c.2615A>G | c.(2614-2616)gAt>gGt | p.D872G |
PRAD | 15 | 53908404 | 53908404 | + | Missense_Mutation | SNP | C | C | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr15:53908404C>A | c.1999G>T | c.(1999-2001)Gtc>Ttc | p.V667F |
PRAD | 15 | 53992051 | 53992051 | + | Missense_Mutation | SNP | C | C | T | TCGA-G9-7525-01A-31D-2260-08 | TCGA-G9-7525-10A-01D-2260-08 | g.chr15:53992051C>T | c.1661G>A | c.(1660-1662)cGg>cAg | p.R554Q |
PRAD | 15 | 53998136 | 53998136 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr15:53998136C>T | c.1090G>A | c.(1090-1092)Ggt>Agt | p.G364S |
PRAD | 15 | 53998224 | 53998224 | + | Silent | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr15:53998224C>T | c.1002G>A | c.(1000-1002)gaG>gaA | p.E334E |
PRAD | 15 | 54006701 | 54006701 | + | Missense_Mutation | SNP | G | G | T | TCGA-EJ-5508-01A-02D-1576-08 | TCGA-EJ-5508-10A-01D-1577-08 | g.chr15:54006701G>T | c.521C>A | c.(520-522)tCt>tAt | p.S174Y |
PRAD | 15 | 54015097 | 54015097 | + | Silent | SNP | C | C | T | TCGA-YJ-A8SW-01A-11D-A377-08 | TCGA-YJ-A8SW-10A-01D-A37A-08 | g.chr15:54015097C>T | c.162G>A | c.(160-162)gcG>gcA | p.A54A |
PRAD | 15 | 54025336 | 54025336 | + | Missense_Mutation | SNP | G | G | T | TCGA-XQ-A8TA-01A-11D-A364-08 | TCGA-XQ-A8TA-10A-01D-A362-08 | g.chr15:54025336G>T | c.11C>A | c.(10-12)tCc>tAc | p.S4Y |
READ | 15 | 53809937 | 53809937 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:53809937G>T | c.3268C>A | c.(3268-3270)Cat>Aat | p.H1090N |
READ | 15 | 53815457 | 53815457 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:53815457C>T | c.3211G>A | c.(3211-3213)Gac>Aac | p.D1071N |
READ | 15 | 53907722 | 53907722 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:53907722G>T | c.2681C>A | c.(2680-2682)tCt>tAt | p.S894Y |
READ | 15 | 53957939 | 53957939 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:53957939C>A | c.1792G>T | c.(1792-1794)Gaa>Taa | p.E598* |
READ | 15 | 53997398 | 53997398 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:53997398C>A | c.1135G>T | c.(1135-1137)Gat>Tat | p.D379Y |
SARC | 15 | 53809908 | 53809908 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-DX-A8BP-01A-11D-A37C-09 | TCGA-DX-A8BP-10A-01D-A37F-09 | g.chr15:53809908G>T | c.3297C>A | c.(3295-3297)tgC>tgA | p.C1099* |
SARC | 15 | 53994475 | 53994475 | + | Silent | SNP | C | C | T | TCGA-QQ-A8VG-01A-11D-A37C-09 | TCGA-QQ-A8VG-10A-01D-A37F-09 | g.chr15:53994475C>T | c.1425G>A | c.(1423-1425)tcG>tcA | p.S475S |
SKCM | 15 | 53809900 | 53809900 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:53809900G>A | c.3305C>T | c.(3304-3306)tCt>tTt | p.S1102F |
SKCM | 15 | 53889321 | 53889321 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr15:53889321C>T | c.3103G>A | c.(3103-3105)Gaa>Aaa | p.E1035K |
SKCM | 15 | 53889321 | 53889321 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr15:53889321C>T | c.3103G>A | c.(3103-3105)Gaa>Aaa | p.E1035K |
SKCM | 15 | 53889401 | 53889401 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZR-06A-21D-A197-08 | TCGA-FS-A1ZR-10A-01D-A199-08 | g.chr15:53889401G>A | c.3023C>T | c.(3022-3024)cCc>cTc | p.P1008L |
SKCM | 15 | 53889421 | 53889421 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr15:53889421C>T | c.3003G>A | c.(3001-3003)atG>atA | p.M1001I |
SKCM | 15 | 53901721 | 53901721 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr15:53901721G>A | c.2941C>T | c.(2941-2943)Cag>Tag | p.Q981* |
SKCM | 15 | 53905868 | 53905868 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AF-06A-11D-A196-08 | TCGA-EE-A3AF-10A-01D-A198-08 | g.chr15:53905868C>T | c.2867G>A | c.(2866-2868)cGa>cAa | p.R956Q |
SKCM | 15 | 53907716 | 53907716 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr15:53907716C>T | c.2687G>A | c.(2686-2688)cGa>cAa | p.R896Q |
SKCM | 15 | 53907738 | 53907738 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A4U8-06A-11D-A32N-08 | TCGA-GN-A4U8-10B-01D-A32N-08 | g.chr15:53907738C>T | c.2665G>A | c.(2665-2667)Gaa>Aaa | p.E889K |
SKCM | 15 | 53907746 | 53907746 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:53907746C>T | c.2657G>A | c.(2656-2658)aGa>aAa | p.R886K |
SKCM | 15 | 53907760 | 53907760 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:53907760C>T | c.2643G>A | c.(2641-2643)caG>caA | p.Q881Q |
SKCM | 15 | 53907812 | 53907812 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AE-06A-11D-A196-08 | TCGA-EE-A3AE-10A-01D-A198-08 | g.chr15:53907812G>A | c.2591C>T | c.(2590-2592)tCc>tTc | p.S864F |
SKCM | 15 | 53908026 | 53908026 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3TU-06A-11D-A23B-08 | TCGA-FW-A3TU-10A-01D-A23B-08 | g.chr15:53908026C>T | c.2377G>A | c.(2377-2379)Gac>Aac | p.D793N |
SKCM | 15 | 53908078 | 53908078 | + | Silent | SNP | G | G | A | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr15:53908078G>A | c.2325C>T | c.(2323-2325)tcC>tcT | p.S775S |
SKCM | 15 | 53908079 | 53908079 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr15:53908079G>A | c.2324C>T | c.(2323-2325)tCc>tTc | p.S775F |
SKCM | 15 | 53908113 | 53908113 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19E-06A-11D-A197-08 | TCGA-ER-A19E-10A-01D-A199-08 | g.chr15:53908113C>T | c.2290G>A | c.(2290-2292)Gat>Aat | p.D764N |
SKCM | 15 | 53908161 | 53908161 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZP-06A-11D-A197-08 | TCGA-FS-A1ZP-10A-01D-A199-08 | g.chr15:53908161C>T | c.2242G>A | c.(2242-2244)Gaa>Aaa | p.E748K |
SKCM | 15 | 53908220 | 53908220 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:53908220C>T | c.2183G>A | c.(2182-2184)aGa>aAa | p.R728K |
SKCM | 15 | 53908292 | 53908292 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A267-06A-21D-A196-08 | TCGA-GN-A267-10A-01D-A198-08 | g.chr15:53908292G>A | c.2111C>T | c.(2110-2112)tCc>tTc | p.S704F |
SKCM | 15 | 53908365 | 53908365 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3MR-06A-11D-A21A-08 | TCGA-D3-A3MR-10A-01D-A21A-08 | g.chr15:53908365G>A | c.2038C>T | c.(2038-2040)Cat>Tat | p.H680Y |
SKCM | 15 | 53908382 | 53908382 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FS-A1ZM-06A-12D-A197-08 | TCGA-FS-A1ZM-10A-01D-A199-08 | g.chr15:53908382C>T | c.2021G>A | c.(2020-2022)tGg>tAg | p.W674* |
SKCM | 15 | 53957906 | 53957906 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr15:53957906C>T | c.1825G>A | c.(1825-1827)Gat>Aat | p.D609N |
SKCM | 15 | 53957929 | 53957929 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZT-06A-11D-A197-08 | TCGA-FS-A1ZT-10A-01D-A199-08 | g.chr15:53957929C>T | c.1802G>A | c.(1801-1803)cGa>cAa | p.R601Q |
SKCM | 15 | 53991959 | 53991959 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZQ-06A-11D-A197-08 | TCGA-FS-A1ZQ-10A-01D-A199-08 | g.chr15:53991959C>T | c.1753G>A | c.(1753-1755)Gaa>Aaa | p.E585K |
SKCM | 15 | 53992010 | 53992010 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr15:53992010C>T | c.1702G>A | c.(1702-1704)Gtt>Att | p.V568I |
SKCM | 15 | 53994417 | 53994417 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3TU-06A-11D-A23B-08 | TCGA-FW-A3TU-10A-01D-A23B-08 | g.chr15:53994417C>T | c.1483G>A | c.(1483-1485)Gat>Aat | p.D495N |
SKCM | 15 | 53997401 | 53997401 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:53997401G>A | c.1132C>T | c.(1132-1134)Caa>Taa | p.Q378* |
SKCM | 15 | 53998203 | 53998203 | + | Silent | SNP | G | G | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr15:53998203G>A | c.1023C>T | c.(1021-1023)ttC>ttT | p.F341F |
SKCM | 15 | 53998206 | 53998206 | + | Silent | SNP | A | A | T | TCGA-D3-A2J9-06A-11D-A196-08 | TCGA-D3-A2J9-10A-01D-A198-08 | g.chr15:53998206A>T | c.1020T>A | c.(1018-1020)ctT>ctA | p.L340L |
SKCM | 15 | 53998215 | 53998215 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-EE-A2GL-06A-11D-A196-08 | TCGA-EE-A2GL-10A-01D-A198-08 | g.chr15:53998215G>T | c.1011C>A | c.(1009-1011)taC>taA | p.Y337* |
SKCM | 15 | 53998248 | 53998248 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr15:53998248C>T | c.978G>A | c.(976-978)atG>atA | p.M326I |
SKCM | 15 | 54003658 | 54003658 | + | Missense_Mutation | SNP | A | A | T | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr15:54003658A>T | c.732T>A | c.(730-732)ttT>ttA | p.F244L |
SKCM | 15 | 54005060 | 54005060 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr15:54005060G>A | c.620C>T | c.(619-621)tCc>tTc | p.S207F |
SKCM | 15 | 54007449 | 54007449 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29B-06A-11D-A197-08 | TCGA-EE-A29B-10A-01D-A199-08 | g.chr15:54007449G>A | c.455C>T | c.(454-456)tCa>tTa | p.S152L |
SKCM | 15 | 54008826 | 54008826 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr15:54008826G>A | c.317C>T | c.(316-318)cCt>cTt | p.P106L |
SKCM | 15 | 54008862 | 54008862 | + | Missense_Mutation | SNP | A | A | C | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr15:54008862A>C | c.281T>G | c.(280-282)gTc>gGc | p.V94G |
SKCM | 15 | 54015068 | 54015068 | + | Missense_Mutation | SNP | G | G | A | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr15:54015068G>A | c.191C>T | c.(190-192)tCg>tTg | p.S64L |
SKCM | 15 | 54015097 | 54015097 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:54015097C>T | c.162G>A | c.(160-162)gcG>gcA | p.A54A |
SKCM | 15 | 54025254 | 54025254 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:54025254C>T | c.93G>A | c.(91-93)acG>acA | p.T31T |
SKCM | 15 | 54025313 | 54025313 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr15:54025313C>T | c.34G>A | c.(34-36)Gga>Aga | p.G12R |
SKCM | 15 | 54025314 | 54025314 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FS-A4F0-06A-11D-A24R-08 | TCGA-FS-A4F0-10A-01D-A24R-08 | g.chr15:54025314C>T | c.33G>A | c.(31-33)tgG>tgA | p.W11* |
SKCM | 15 | 54025336 | 54025336 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29S-06A-11D-A197-08 | TCGA-EE-A29S-10A-01D-A199-08 | g.chr15:54025336G>A | c.11C>T | c.(10-12)tCc>tTc | p.S4F |