Mutation - TCGA |
Type | Chromosome | Start Position | End Position | Strand | Variant Classification | Variant Type | Reference Allele | Tumor_seq Allele 1 | Tumor_seq Allele 2 | Tumor Sample Barcode | Matched Norm Sample Barcode | Genome Change | cDNA Change | Codon Change | Protein Change |
BLCA | 15 | 56130727 | 56130727 | + | Missense_Mutation | SNP | C | C | T | TCGA-BT-A0YX-01A-11D-A10S-08 | TCGA-BT-A0YX-10A-01D-A10S-08 | g.chr15:56130727C>T | c.3364G>A | c.(3364-3366)Gat>Aat | p.D1122N |
BLCA | 15 | 56132708 | 56132708 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-XF-AAN5-01A-11D-A42E-08 | TCGA-XF-AAN5-10A-01D-A42H-08 | g.chr15:56132708delG | c.3225delC | c.(3223-3225)ttcfs | p.F1075fs |
BLCA | 15 | 56132822 | 56132822 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-AAN5-01A-11D-A42E-08 | TCGA-XF-AAN5-10A-01D-A42H-08 | g.chr15:56132822G>C | c.3199C>G | c.(3199-3201)Cat>Gat | p.H1067D |
BLCA | 15 | 56132916 | 56132916 | + | Silent | SNP | A | A | G | TCGA-DK-AA6R-01A-11D-A42E-08 | TCGA-DK-AA6R-10A-01D-A42H-08 | g.chr15:56132916A>G | c.3105T>C | c.(3103-3105)taT>taC | p.Y1035Y |
BLCA | 15 | 56134328 | 56134328 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr15:56134328G>A | c.2899C>T | c.(2899-2901)Cgc>Tgc | p.R967C |
BLCA | 15 | 56144667 | 56144667 | + | Silent | SNP | T | T | G | TCGA-LC-A66R-01A-41D-A30E-08 | TCGA-LC-A66R-10A-01D-A30H-08 | g.chr15:56144667T>G | c.2358A>C | c.(2356-2358)gtA>gtC | p.V786V |
BLCA | 15 | 56152722 | 56152722 | + | Silent | SNP | G | G | T | TCGA-FJ-A3ZE-01A-11D-A23M-08 | TCGA-FJ-A3ZE-10A-01D-A23K-08 | g.chr15:56152722G>T | c.2100C>A | c.(2098-2100)gcC>gcA | p.A700A |
BLCA | 15 | 56155208 | 56155208 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-AAMG-01A-11D-A42E-08 | TCGA-XF-AAMG-10A-01D-A42H-08 | g.chr15:56155208G>C | c.1834C>G | c.(1834-1836)Cta>Gta | p.L612V |
BLCA | 15 | 56208209 | 56208209 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-E7-A7XN-01A-11D-A34U-08 | TCGA-E7-A7XN-10A-01D-A34X-08 | g.chr15:56208209G>C | c.821C>G | c.(820-822)tCa>tGa | p.S274* |
BLCA | 15 | 56208871 | 56208871 | + | Silent | SNP | G | G | A | TCGA-DK-AA76-01A-11D-A391-08 | TCGA-DK-AA76-10A-01D-A394-08 | g.chr15:56208871G>A | c.159C>T | c.(157-159)ccC>ccT | p.P53P |
BRCA | 15 | 56122768 | 56122768 | + | Missense_Mutation | SNP | C | C | A | TCGA-A8-A09Z-01A-11W-A019-09 | TCGA-A8-A09Z-10A-01W-A021-09 | g.chr15:56122768C>A | c.3801G>T | c.(3799-3801)caG>caT | p.Q1267H |
BRCA | 15 | 56126305 | 56126305 | + | Missense_Mutation | SNP | G | G | C | TCGA-A2-A3Y0-01A-11D-A23C-09 | TCGA-A2-A3Y0-10A-01D-A23C-09 | g.chr15:56126305G>C | c.3618C>G | c.(3616-3618)gaC>gaG | p.D1206E |
BRCA | 15 | 56140722 | 56140723 | + | Frame_Shift_Ins | INS | - | - | C | TCGA-B6-A0RE-01A-11W-A071-09 | TCGA-B6-A0RE-10A-01W-A071-09 | g.chr15:56140722_56140723insC | c.2736_2737insG | c.(2734-2739)aatcacfs | p.H913fs |
BRCA | 15 | 56141078 | 56141078 | + | Missense_Mutation | SNP | G | G | A | TCGA-E2-A1B1-01A-21D-A12Q-09 | TCGA-E2-A1B1-10A-01D-A12Q-09 | g.chr15:56141078G>A | c.2611C>T | c.(2611-2613)Cca>Tca | p.P871S |
BRCA | 15 | 56207669 | 56207669 | + | Missense_Mutation | SNP | C | C | T | TCGA-AR-A250-01A-31D-A167-09 | TCGA-AR-A250-10A-01D-A167-09 | g.chr15:56207669C>T | c.1361G>A | c.(1360-1362)cGa>cAa | p.R454Q |
BRCA | 15 | 56209009 | 56209009 | + | Silent | SNP | C | C | T | TCGA-D8-A1J8-01A-11D-A13L-09 | TCGA-D8-A1J8-10A-01D-A13O-09 | g.chr15:56209009C>T | c.21G>A | c.(19-21)ttG>ttA | p.L7L |
BRCA | 15 | 56216855 | 56216855 | + | Missense_Mutation | SNP | C | C | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr15:56216855C>T | c.280G>A | c.(280-282)Gaa>Aaa | p.E94K |
CESC | 15 | 56130719 | 56130719 | + | Missense_Mutation | SNP | T | T | G | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr15:56130719T>G | c.3372A>C | c.(3370-3372)gaA>gaC | p.E1124D |
CESC | 15 | 56152670 | 56152670 | + | Missense_Mutation | SNP | C | C | T | TCGA-UC-A7PF-01A-11D-A351-09 | TCGA-UC-A7PF-11A-31D-A351-09 | g.chr15:56152670C>T | c.2152G>A | c.(2152-2154)Gaa>Aaa | p.E718K |
CESC | 15 | 56155208 | 56155208 | + | Missense_Mutation | SNP | G | G | C | TCGA-C5-A1BM-01A-11D-A13W-08 | TCGA-C5-A1BM-10A-01D-A13W-08 | g.chr15:56155208G>C | c.1834C>G | c.(1834-1836)Cta>Gta | p.L612V |
CHOL | 15 | 56258687 | 56258687 | + | Missense_Mutation | SNP | C | C | T | TCGA-W5-AA2Q-01A-11D-A417-09 | TCGA-W5-AA2Q-10A-01D-A41A-09 | g.chr15:56258687C>T | c.103G>A | c.(103-105)Gat>Aat | p.D35N |
COAD | 15 | 56122189 | 56122189 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr15:56122189C>T | c.3866G>A | c.(3865-3867)cGc>cAc | p.R1289H |
COAD | 15 | 56134294 | 56134294 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:56134294C>A | c.2933G>T | c.(2932-2934)aGa>aTa | p.R978I |
COAD | 15 | 56134342 | 56134342 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:56134342A>C | c.2885T>G | c.(2884-2886)tTt>tGt | p.F962C |
COAD | 15 | 56140591 | 56140591 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:56140591C>A | c.2778G>T | c.(2776-2778)gaG>gaT | p.E926D |
COAD | 15 | 56144633 | 56144633 | + | Missense_Mutation | SNP | G | G | C | TCGA-A6-4105-01A-02D-1771-10 | TCGA-A6-4105-10A-01D-1771-10 | g.chr15:56144633G>C | c.2392C>G | c.(2392-2394)Ccc>Gcc | p.P798A |
COAD | 15 | 56144726 | 56144726 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:56144726A>G | c.2299T>C | c.(2299-2301)Tct>Cct | p.S767P |
COAD | 15 | 56148330 | 56148330 | + | Splice_Site | SNP | A | A | C | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr15:56148330A>C | c.2282T>G | c.(2281-2283)gTg>gGg | p.V761G |
COAD | 15 | 56155113 | 56155113 | + | Silent | SNP | A | A | G | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr15:56155113A>G | c.1929T>C | c.(1927-1929)ccT>ccC | p.P643P |
COAD | 15 | 56155114 | 56155114 | + | Missense_Mutation | SNP | G | G | T | TCGA-DM-A28K-01A-21D-A16V-10 | TCGA-DM-A28K-10A-01D-A16V-10 | g.chr15:56155114G>T | c.1928C>A | c.(1927-1929)cCt>cAt | p.P643H |
COAD | 15 | 56155152 | 56155152 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:56155152G>T | c.1890C>A | c.(1888-1890)aaC>aaA | p.N630K |
COAD | 15 | 56155179 | 56155179 | + | Silent | SNP | A | A | G | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr15:56155179A>G | c.1863T>C | c.(1861-1863)gaT>gaC | p.D621D |
COAD | 15 | 56155208 | 56155210 | + | In_Frame_Del | DEL | GAG | GAG | - | TCGA-CM-5348-01A-21D-1719-10 | TCGA-CM-5348-10A-01D-1719-10 | g.chr15:56155208_56155210delGAG | c.1832_1834delCTC | c.(1831-1836)cctcta>cta | p.P611del |
COAD | 15 | 56155239 | 56155239 | + | Silent | SNP | G | G | A | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr15:56155239G>A | c.1803C>T | c.(1801-1803)tgC>tgT | p.C601C |
COAD | 15 | 56155254 | 56155254 | + | Silent | SNP | T | T | C | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr15:56155254T>C | c.1788A>G | c.(1786-1788)caA>caG | p.Q596Q |
COAD | 15 | 56208381 | 56208381 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr15:56208381G>A | c.649C>T | c.(649-651)Cca>Tca | p.P217S |
COAD | 15 | 56208538 | 56208538 | + | Missense_Mutation | SNP | G | G | T | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr15:56208538G>T | c.492C>A | c.(490-492)agC>agA | p.S164R |
COAD | 15 | 56208549 | 56208549 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6532-01A-11D-1719-10 | TCGA-D5-6532-10A-01D-1719-10 | g.chr15:56208549A>G | c.481T>C | c.(481-483)Tct>Cct | p.S161P |
COAD | 15 | 56208643 | 56208643 | + | Silent | SNP | A | A | G | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr15:56208643A>G | c.387T>C | c.(385-387)gaT>gaC | p.D129D |
COAD | 15 | 56208812 | 56208812 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr15:56208812G>T | c.218C>A | c.(217-219)tCt>tAt | p.S73Y |
COAD | 15 | 56208835 | 56208835 | + | Silent | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr15:56208835G>A | c.195C>T | c.(193-195)aaC>aaT | p.N65N |
COAD | 15 | 56208895 | 56208895 | + | Silent | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr15:56208895G>A | c.135C>T | c.(133-135)aaC>aaT | p.N45N |
COAD | 15 | 56208961 | 56208961 | + | Silent | SNP | G | G | A | TCGA-D5-6927-01A-21D-1924-10 | TCGA-D5-6927-10A-01D-1924-10 | g.chr15:56208961G>A | c.69C>T | c.(67-69)tcC>tcT | p.S23S |
COAD | 15 | 56209013 | 56209013 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr15:56209013C>T | c.17G>A | c.(16-18)cGa>cAa | p.R6Q |
COAD | 15 | 56216855 | 56216855 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:56216855C>T | c.280G>A | c.(280-282)Gaa>Aaa | p.E94K |
COADREAD | 15 | 56122106 | 56122106 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:56122106C>A | c.3949G>T | c.(3949-3951)Gga>Tga | p.G1317* |
COADREAD | 15 | 56122189 | 56122189 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr15:56122189C>T | c.3866G>A | c.(3865-3867)cGc>cAc | p.R1289H |
COADREAD | 15 | 56134294 | 56134294 | + | Missense_Mutation | SNP | C | C | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:56134294C>A | c.2933G>T | c.(2932-2934)aGa>aTa | p.R978I |
COADREAD | 15 | 56134342 | 56134342 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:56134342A>C | c.2885T>G | c.(2884-2886)tTt>tGt | p.F962C |
COADREAD | 15 | 56140591 | 56140591 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:56140591C>A | c.2778G>T | c.(2776-2778)gaG>gaT | p.E926D |
COADREAD | 15 | 56144633 | 56144633 | + | Missense_Mutation | SNP | G | G | C | TCGA-A6-4105-01A-02D-1771-10 | TCGA-A6-4105-10A-01D-1771-10 | g.chr15:56144633G>C | c.2392C>G | c.(2392-2394)Ccc>Gcc | p.P798A |
COADREAD | 15 | 56144725 | 56144725 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:56144725G>T | c.2300C>A | c.(2299-2301)tCt>tAt | p.S767Y |
COADREAD | 15 | 56144726 | 56144726 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:56144726A>G | c.2299T>C | c.(2299-2301)Tct>Cct | p.S767P |
COADREAD | 15 | 56148330 | 56148330 | + | Splice_Site | SNP | A | A | C | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr15:56148330A>C | c.2282T>G | c.(2281-2283)gTg>gGg | p.V761G |
COADREAD | 15 | 56155113 | 56155113 | + | Silent | SNP | A | A | G | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr15:56155113A>G | c.1929T>C | c.(1927-1929)ccT>ccC | p.P643P |
COADREAD | 15 | 56155114 | 56155114 | + | Missense_Mutation | SNP | G | G | T | TCGA-DM-A28K-01A-21D-A16V-10 | TCGA-DM-A28K-10A-01D-A16V-10 | g.chr15:56155114G>T | c.1928C>A | c.(1927-1929)cCt>cAt | p.P643H |
COADREAD | 15 | 56155152 | 56155152 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:56155152G>T | c.1890C>A | c.(1888-1890)aaC>aaA | p.N630K |
COADREAD | 15 | 56155179 | 56155179 | + | Silent | SNP | A | A | G | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr15:56155179A>G | c.1863T>C | c.(1861-1863)gaT>gaC | p.D621D |
COADREAD | 15 | 56155208 | 56155210 | + | In_Frame_Del | DEL | GAG | GAG | - | TCGA-CM-5348-01A-21D-1719-10 | TCGA-CM-5348-10A-01D-1719-10 | g.chr15:56155208_56155210delGAG | c.1832_1834delCTC | c.(1831-1836)cctcta>cta | p.P611del |
COADREAD | 15 | 56155239 | 56155239 | + | Silent | SNP | G | G | A | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr15:56155239G>A | c.1803C>T | c.(1801-1803)tgC>tgT | p.C601C |
COADREAD | 15 | 56155254 | 56155254 | + | Silent | SNP | T | T | C | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr15:56155254T>C | c.1788A>G | c.(1786-1788)caA>caG | p.Q596Q |
COADREAD | 15 | 56161868 | 56161868 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:56161868C>A | c.1673G>T | c.(1672-1674)aGa>aTa | p.R558I |
COADREAD | 15 | 56207629 | 56207629 | + | Silent | SNP | G | G | A | TCGA-F5-6812-01A-11D-1826-10 | TCGA-F5-6812-10A-01D-1826-10 | g.chr15:56207629G>A | c.1401C>T | c.(1399-1401)tcC>tcT | p.S467S |
COADREAD | 15 | 56207960 | 56207960 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:56207960G>A | c.1070C>T | c.(1069-1071)tCg>tTg | p.S357L |
COADREAD | 15 | 56208381 | 56208381 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr15:56208381G>A | c.649C>T | c.(649-651)Cca>Tca | p.P217S |
COADREAD | 15 | 56208538 | 56208538 | + | Missense_Mutation | SNP | G | G | T | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr15:56208538G>T | c.492C>A | c.(490-492)agC>agA | p.S164R |
COADREAD | 15 | 56208549 | 56208549 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6532-01A-11D-1719-10 | TCGA-D5-6532-10A-01D-1719-10 | g.chr15:56208549A>G | c.481T>C | c.(481-483)Tct>Cct | p.S161P |
COADREAD | 15 | 56208643 | 56208643 | + | Silent | SNP | A | A | G | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr15:56208643A>G | c.387T>C | c.(385-387)gaT>gaC | p.D129D |
COADREAD | 15 | 56208812 | 56208812 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr15:56208812G>T | c.218C>A | c.(217-219)tCt>tAt | p.S73Y |
COADREAD | 15 | 56208835 | 56208835 | + | Silent | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr15:56208835G>A | c.195C>T | c.(193-195)aaC>aaT | p.N65N |
COADREAD | 15 | 56208895 | 56208895 | + | Silent | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr15:56208895G>A | c.135C>T | c.(133-135)aaC>aaT | p.N45N |
COADREAD | 15 | 56208961 | 56208961 | + | Silent | SNP | G | G | A | TCGA-D5-6927-01A-21D-1924-10 | TCGA-D5-6927-10A-01D-1924-10 | g.chr15:56208961G>A | c.69C>T | c.(67-69)tcC>tcT | p.S23S |
COADREAD | 15 | 56209013 | 56209013 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr15:56209013C>T | c.17G>A | c.(16-18)cGa>cAa | p.R6Q |
COADREAD | 15 | 56216855 | 56216855 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:56216855C>T | c.280G>A | c.(280-282)Gaa>Aaa | p.E94K |
DLBC | 15 | 56208006 | 56208006 | + | Missense_Mutation | SNP | G | G | A | TCGA-FA-A6HO-01A-11D-A31X-10 | TCGA-FA-A6HO-10A-01D-A31X-10 | g.chr15:56208006G>A | c.1024C>T | c.(1024-1026)Cgg>Tgg | p.R342W |
ESCA | 15 | 56122187 | 56122187 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr15:56122187G>T | c.3868C>A | c.(3868-3870)Ctg>Atg | p.L1290M |
ESCA | 15 | 56207921 | 56207921 | + | Missense_Mutation | SNP | G | G | C | TCGA-L5-A8NQ-01A-11D-A36J-09 | TCGA-L5-A8NQ-11A-11D-A36M-09 | g.chr15:56207921G>C | c.1109C>G | c.(1108-1110)tCt>tGt | p.S370C |
ESCA | 15 | 56208246 | 56208246 | + | Missense_Mutation | SNP | G | G | T | TCGA-Z6-AAPN-01A-11D-A403-09 | TCGA-Z6-AAPN-10A-01D-A403-09 | g.chr15:56208246G>T | c.784C>A | c.(784-786)Cgt>Agt | p.R262S |
GBM | 15 | 56132880 | 56132880 | + | Silent | SNP | G | G | A | TCGA-19-5955-01A-11D-1696-08 | TCGA-19-5955-11A-01D-1696-08 | g.chr15:56132880G>A | c.3141C>T | c.(3139-3141)aaC>aaT | p.N1047N |
GBM | 15 | 56207523 | 56207523 | + | Missense_Mutation | SNP | T | T | G | TCGA-76-6660-01A-11D-1845-08 | TCGA-76-6660-10A-01D-1845-08 | g.chr15:56207523T>G | c.1507A>C | c.(1507-1509)Agc>Cgc | p.S503R |
GBM | 15 | 56208834 | 56208834 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-0126-01A-01D-1490-08 | TCGA-06-0126-10A-01D-1490-08 | g.chr15:56208834C>T | c.196G>A | c.(196-198)Gtt>Att | p.V66I |
GBMLGG | 15 | 56130001 | 56130001 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:56130001C>T | c.3505G>A | c.(3505-3507)Gct>Act | p.A1169T |
GBMLGG | 15 | 56132818 | 56132818 | + | Missense_Mutation | SNP | C | C | T | TCGA-R8-A6MK-01A-11D-A32B-08 | TCGA-R8-A6MK-10A-01D-A329-08 | g.chr15:56132818C>T | c.3203G>A | c.(3202-3204)gGc>gAc | p.G1068D |
GBMLGG | 15 | 56132880 | 56132880 | + | Silent | SNP | G | G | A | TCGA-19-5955-01A-11D-1696-08 | TCGA-19-5955-11A-01D-1696-08 | g.chr15:56132880G>A | c.3141C>T | c.(3139-3141)aaC>aaT | p.N1047N |
GBMLGG | 15 | 56134228 | 56134228 | + | Missense_Mutation | SNP | T | T | C | TCGA-FG-5965-01B-11D-1893-08 | TCGA-FG-5965-10A-01D-1893-08 | g.chr15:56134228T>C | c.2999A>G | c.(2998-3000)aAg>aGg | p.K1000R |
GBMLGG | 15 | 56134236 | 56134236 | + | Silent | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:56134236A>G | c.2991T>C | c.(2989-2991)gaT>gaC | p.D997D |
GBMLGG | 15 | 56142778 | 56142778 | + | Missense_Mutation | SNP | G | G | A | TCGA-QH-A6X3-01A-21D-A32B-08 | TCGA-QH-A6X3-10B-01D-A329-08 | g.chr15:56142778G>A | c.2566C>T | c.(2566-2568)Cct>Tct | p.P856S |
GBMLGG | 15 | 56142924 | 56142924 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:56142924C>T | c.2420G>A | c.(2419-2421)aGt>aAt | p.S807N |
GBMLGG | 15 | 56155250 | 56155250 | + | Missense_Mutation | SNP | C | C | G | TCGA-E1-A7YE-01A-11D-A34A-08 | TCGA-E1-A7YE-10A-01D-A34A-08 | g.chr15:56155250C>G | c.1792G>C | c.(1792-1794)Gat>Cat | p.D598H |
GBMLGG | 15 | 56207523 | 56207523 | + | Missense_Mutation | SNP | T | T | G | TCGA-76-6660-01A-11D-1845-08 | TCGA-76-6660-10A-01D-1845-08 | g.chr15:56207523T>G | c.1507A>C | c.(1507-1509)Agc>Cgc | p.S503R |
GBMLGG | 15 | 56208601 | 56208601 | + | Missense_Mutation | SNP | A | A | C | TCGA-VM-A8CH-01A-12D-A36O-08 | TCGA-VM-A8CH-10A-01D-A367-08 | g.chr15:56208601A>C | c.429T>G | c.(427-429)agT>agG | p.S143R |
GBMLGG | 15 | 56208834 | 56208834 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-0126-01A-01D-1490-08 | TCGA-06-0126-10A-01D-1490-08 | g.chr15:56208834C>T | c.196G>A | c.(196-198)Gtt>Att | p.V66I |
HNSC | 15 | 56126259 | 56126259 | + | Missense_Mutation | SNP | G | G | C | TCGA-UF-A7JT-01A-11D-A34J-08 | TCGA-UF-A7JT-10A-01D-A34M-08 | g.chr15:56126259G>C | c.3664C>G | c.(3664-3666)Cag>Gag | p.Q1222E |
HNSC | 15 | 56130006 | 56130006 | + | Missense_Mutation | SNP | T | T | G | TCGA-CV-6939-01A-11D-1912-08 | TCGA-CV-6939-10A-01D-1912-08 | g.chr15:56130006T>G | c.3500A>C | c.(3499-3501)cAa>cCa | p.Q1167P |
HNSC | 15 | 56130375 | 56130375 | + | Missense_Mutation | SNP | G | G | C | TCGA-CR-7398-01A-11D-2012-08 | TCGA-CR-7398-10A-01D-2013-08 | g.chr15:56130375G>C | c.3388C>G | c.(3388-3390)Cat>Gat | p.H1130D |
HNSC | 15 | 56132818 | 56132818 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-5366-01A-01D-1434-08 | TCGA-CN-5366-10A-01D-1434-08 | g.chr15:56132818C>T | c.3203G>A | c.(3202-3204)gGc>gAc | p.G1068D |
HNSC | 15 | 56134138 | 56134138 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-7425-01A-11D-2078-08 | TCGA-CV-7425-10A-01D-2078-08 | g.chr15:56134138G>A | c.3089C>T | c.(3088-3090)tCt>tTt | p.S1030F |
HNSC | 15 | 56140620 | 56140620 | + | Silent | SNP | T | T | G | TCGA-BB-A6UO-01A-12D-A34J-08 | TCGA-BB-A6UO-10A-01D-A34M-08 | g.chr15:56140620T>G | c.2749A>C | c.(2749-2751)Aga>Cga | p.R917R |
HNSC | 15 | 56142797 | 56142797 | + | Silent | SNP | C | C | T | TCGA-CQ-5329-01A-01D-1683-08 | TCGA-CQ-5329-10A-01D-1683-08 | g.chr15:56142797C>T | c.2547G>A | c.(2545-2547)cgG>cgA | p.R849R |
HNSC | 15 | 56144728 | 56144728 | + | Missense_Mutation | SNP | G | G | A | TCGA-CR-7394-01A-11D-2012-08 | TCGA-CR-7394-10A-01D-2013-08 | g.chr15:56144728G>A | c.2297C>T | c.(2296-2298)tCa>tTa | p.S766L |
HNSC | 15 | 56152955 | 56152955 | + | Missense_Mutation | SNP | C | C | G | TCGA-BA-A6DA-01A-31D-A31L-08 | TCGA-BA-A6DA-10A-01D-A31J-08 | g.chr15:56152955C>G | c.1953G>C | c.(1951-1953)gaG>gaC | p.E651D |
HNSC | 15 | 56207863 | 56207863 | + | Silent | SNP | G | G | A | TCGA-CV-7095-01A-21D-2012-08 | TCGA-CV-7095-10A-01D-2013-08 | g.chr15:56207863G>A | c.1167C>T | c.(1165-1167)gaC>gaT | p.D389D |
KIPAN | 15 | 56126438 | 56126438 | + | Missense_Mutation | SNP | T | T | G | TCGA-CZ-4861-01A-01D-1373-10 | TCGA-CZ-4861-11A-01D-1373-10 | g.chr15:56126438T>G | c.3566A>C | c.(3565-3567)gAa>gCa | p.E1189A |
KIPAN | 15 | 56140568 | 56140568 | + | Splice_Site | DEL | A | A | - | TCGA-CJ-4897-01A-03D-1429-08 | TCGA-CJ-4897-11A-01D-1429-08 | g.chr15:56140568delA | | c.e13+1 | |
KIPAN | 15 | 56142779 | 56142779 | + | Silent | SNP | C | C | T | TCGA-2Z-A9JM-01A-12D-A42J-10 | TCGA-2Z-A9JM-10A-01D-A42M-10 | g.chr15:56142779C>T | c.2565G>A | c.(2563-2565)agG>agA | p.R855R |
KIPAN | 15 | 56207639 | 56207639 | + | Missense_Mutation | SNP | G | G | T | TCGA-GL-A4EM-01A-11D-A25F-10 | TCGA-GL-A4EM-10A-01D-A25F-10 | g.chr15:56207639G>T | c.1391C>A | c.(1390-1392)cCa>cAa | p.P464Q |
KIPAN | 15 | 56207684 | 56207684 | + | Missense_Mutation | SNP | T | T | C | TCGA-J7-A8I2-01A-12D-A35Z-10 | TCGA-J7-A8I2-10A-01D-A35Z-10 | g.chr15:56207684T>C | c.1346A>G | c.(1345-1347)aAc>aGc | p.N449S |
KIPAN | 15 | 56207818 | 56207818 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-SX-A71U-01A-12D-A33Q-10 | TCGA-SX-A71U-10A-01D-A33Q-10 | g.chr15:56207818delA | c.1212delT | c.(1210-1212)attfs | p.I404fs |
KIPAN | 15 | 56208025 | 56208025 | + | Silent | SNP | G | G | A | TCGA-CW-6093-01A-11D-1669-08 | TCGA-CW-6093-11A-01D-1669-08 | g.chr15:56208025G>A | c.1005C>T | c.(1003-1005)ccC>ccT | p.P335P |
KIPAN | 15 | 56208589 | 56208589 | + | Silent | SNP | A | A | G | TCGA-B0-5695-01A-11D-1534-10 | TCGA-B0-5695-11A-01D-1534-10 | g.chr15:56208589A>G | c.441T>C | c.(439-441)tgT>tgC | p.C147C |
KIPAN | 15 | 56208931 | 56208934 | + | Frame_Shift_Del | DEL | CATG | CATG | - | TCGA-A4-7734-01A-11D-2136-08 | TCGA-A4-7734-10A-01D-2136-08 | g.chr15:56208931_56208934delCATG | c.96_99delCATG | c.(94-99)cacatgfs | p.HM32fs |
KIPAN | 15 | 56208934 | 56208934 | + | Silent | SNP | G | G | A | TCGA-A4-7734-01A-11D-2136-08 | TCGA-A4-7734-10A-01D-2136-08 | g.chr15:56208934G>A | c.96C>T | c.(94-96)caC>caT | p.H32H |
KIRC | 15 | 56126438 | 56126438 | + | Missense_Mutation | SNP | T | T | G | TCGA-CZ-4861-01A-01D-1373-10 | TCGA-CZ-4861-11A-01D-1373-10 | g.chr15:56126438T>G | c.3566A>C | c.(3565-3567)gAa>gCa | p.E1189A |
KIRC | 15 | 56140568 | 56140568 | + | Splice_Site | DEL | A | A | - | TCGA-CJ-4897-01A-03D-1429-08 | TCGA-CJ-4897-11A-01D-1429-08 | g.chr15:56140568delA | | c.e13+1 | |
KIRC | 15 | 56208025 | 56208025 | + | Silent | SNP | G | G | A | TCGA-CW-6093-01A-11D-1669-08 | TCGA-CW-6093-11A-01D-1669-08 | g.chr15:56208025G>A | c.1005C>T | c.(1003-1005)ccC>ccT | p.P335P |
KIRC | 15 | 56208589 | 56208589 | + | Silent | SNP | A | A | G | TCGA-B0-5695-01A-11D-1534-10 | TCGA-B0-5695-11A-01D-1534-10 | g.chr15:56208589A>G | c.441T>C | c.(439-441)tgT>tgC | p.C147C |
KIRP | 15 | 56142779 | 56142779 | + | Silent | SNP | C | C | T | TCGA-2Z-A9JM-01A-12D-A42J-10 | TCGA-2Z-A9JM-10A-01D-A42M-10 | g.chr15:56142779C>T | c.2565G>A | c.(2563-2565)agG>agA | p.R855R |
KIRP | 15 | 56207639 | 56207639 | + | Missense_Mutation | SNP | G | G | T | TCGA-GL-A4EM-01A-11D-A25F-10 | TCGA-GL-A4EM-10A-01D-A25F-10 | g.chr15:56207639G>T | c.1391C>A | c.(1390-1392)cCa>cAa | p.P464Q |
KIRP | 15 | 56207684 | 56207684 | + | Missense_Mutation | SNP | T | T | C | TCGA-J7-A8I2-01A-12D-A35Z-10 | TCGA-J7-A8I2-10A-01D-A35Z-10 | g.chr15:56207684T>C | c.1346A>G | c.(1345-1347)aAc>aGc | p.N449S |
KIRP | 15 | 56207818 | 56207818 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-SX-A71U-01A-12D-A33Q-10 | TCGA-SX-A71U-10A-01D-A33Q-10 | g.chr15:56207818delA | c.1212delT | c.(1210-1212)attfs | p.I404fs |
KIRP | 15 | 56208931 | 56208934 | + | Frame_Shift_Del | DEL | CATG | CATG | - | TCGA-A4-7734-01A-11D-2136-08 | TCGA-A4-7734-10A-01D-2136-08 | g.chr15:56208931_56208934delCATG | c.96_99delCATG | c.(94-99)cacatgfs | p.HM32fs |
KIRP | 15 | 56208934 | 56208934 | + | Silent | SNP | G | G | A | TCGA-A4-7734-01A-11D-2136-08 | TCGA-A4-7734-10A-01D-2136-08 | g.chr15:56208934G>A | c.96C>T | c.(94-96)caC>caT | p.H32H |
LGG | 15 | 56130001 | 56130001 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:56130001C>T | c.3505G>A | c.(3505-3507)Gct>Act | p.A1169T |
LGG | 15 | 56132818 | 56132818 | + | Missense_Mutation | SNP | C | C | T | TCGA-R8-A6MK-01A-11D-A32B-08 | TCGA-R8-A6MK-10A-01D-A329-08 | g.chr15:56132818C>T | c.3203G>A | c.(3202-3204)gGc>gAc | p.G1068D |
LGG | 15 | 56134228 | 56134228 | + | Missense_Mutation | SNP | T | T | C | TCGA-FG-5965-01B-11D-1893-08 | TCGA-FG-5965-10A-01D-1893-08 | g.chr15:56134228T>C | c.2999A>G | c.(2998-3000)aAg>aGg | p.K1000R |
LGG | 15 | 56134236 | 56134236 | + | Silent | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:56134236A>G | c.2991T>C | c.(2989-2991)gaT>gaC | p.D997D |
LGG | 15 | 56142778 | 56142778 | + | Missense_Mutation | SNP | G | G | A | TCGA-QH-A6X3-01A-21D-A32B-08 | TCGA-QH-A6X3-10B-01D-A329-08 | g.chr15:56142778G>A | c.2566C>T | c.(2566-2568)Cct>Tct | p.P856S |
LGG | 15 | 56142924 | 56142924 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:56142924C>T | c.2420G>A | c.(2419-2421)aGt>aAt | p.S807N |
LGG | 15 | 56155250 | 56155250 | + | Missense_Mutation | SNP | C | C | G | TCGA-E1-A7YE-01A-11D-A34A-08 | TCGA-E1-A7YE-10A-01D-A34A-08 | g.chr15:56155250C>G | c.1792G>C | c.(1792-1794)Gat>Cat | p.D598H |
LGG | 15 | 56208601 | 56208601 | + | Missense_Mutation | SNP | A | A | C | TCGA-VM-A8CH-01A-12D-A36O-08 | TCGA-VM-A8CH-10A-01D-A367-08 | g.chr15:56208601A>C | c.429T>G | c.(427-429)agT>agG | p.S143R |
LIHC | 15 | 56125247 | 56125247 | + | Missense_Mutation | SNP | C | C | T | TCGA-ES-A2HS-01A-11D-A183-10 | TCGA-ES-A2HS-11A-11D-A183-10 | g.chr15:56125247C>T | c.3743G>A | c.(3742-3744)gGc>gAc | p.G1248D |
LIHC | 15 | 56207944 | 56207944 | + | Silent | SNP | T | T | C | TCGA-CC-A3MA-01A-11D-A20W-10 | TCGA-CC-A3MA-10A-01D-A20W-10 | g.chr15:56207944T>C | c.1086A>G | c.(1084-1086)agA>agG | p.R362R |
LUAD | 15 | 56126273 | 56126273 | + | Missense_Mutation | SNP | T | T | C | TCGA-78-7149-01A-11D-2036-08 | TCGA-78-7149-10A-01D-2036-08 | g.chr15:56126273T>C | c.3650A>G | c.(3649-3651)tAc>tGc | p.Y1217C |
LUAD | 15 | 56130727 | 56130727 | + | Missense_Mutation | SNP | C | C | T | TCGA-95-7039-01A-11D-1945-08 | TCGA-95-7039-10A-01D-1946-08 | g.chr15:56130727C>T | c.3364G>A | c.(3364-3366)Gat>Aat | p.D1122N |
LUAD | 15 | 56140574 | 56140574 | + | Missense_Mutation | SNP | C | C | A | TCGA-69-7980-01A-11D-2184-08 | TCGA-69-7980-10A-01D-2184-08 | g.chr15:56140574C>A | c.2795G>T | c.(2794-2796)gGa>gTa | p.G932V |
LUAD | 15 | 56140605 | 56140605 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr15:56140605C>A | c.2764G>T | c.(2764-2766)Gat>Tat | p.D922Y |
LUAD | 15 | 56140724 | 56140724 | + | Missense_Mutation | SNP | T | T | C | TCGA-44-2656-01A-02D-0969-08 | TCGA-44-2656-10A-01D-0969-08 | g.chr15:56140724T>C | c.2735A>G | c.(2734-2736)aAt>aGt | p.N912S |
LUAD | 15 | 56141027 | 56141027 | + | Missense_Mutation | SNP | A | A | C | TCGA-50-6591-01A-11D-1753-08 | TCGA-50-6591-11A-01D-1753-08 | g.chr15:56141027A>C | c.2662T>G | c.(2662-2664)Tcc>Gcc | p.S888A |
LUAD | 15 | 56142789 | 56142789 | + | Missense_Mutation | SNP | G | G | A | TCGA-69-A59K-01A-11D-A25L-08 | TCGA-69-A59K-10A-01D-A25L-08 | g.chr15:56142789G>A | c.2555C>T | c.(2554-2556)cCa>cTa | p.P852L |
LUAD | 15 | 56142806 | 56142806 | + | Missense_Mutation | SNP | C | C | A | TCGA-38-4631-01A-01D-1753-08 | TCGA-38-4631-11A-01D-1753-08 | g.chr15:56142806C>A | c.2538G>T | c.(2536-2538)tgG>tgT | p.W846C |
LUAD | 15 | 56142807 | 56142807 | + | Missense_Mutation | SNP | C | C | A | TCGA-38-4631-01A-01D-1753-08 | TCGA-38-4631-11A-01D-1753-08 | g.chr15:56142807C>A | c.2537G>T | c.(2536-2538)tGg>tTg | p.W846L |
LUAD | 15 | 56142862 | 56142862 | + | Missense_Mutation | SNP | C | C | A | TCGA-38-4625-01A-01D-1553-08 | TCGA-38-4625-11A-01D-1553-08 | g.chr15:56142862C>A | c.2482G>T | c.(2482-2484)Ggc>Tgc | p.G828C |
LUAD | 15 | 56207620 | 56207620 | + | Silent | SNP | G | G | A | TCGA-53-7624-01A-11D-2063-08 | TCGA-53-7624-10A-01D-2063-08 | g.chr15:56207620G>A | c.1410C>T | c.(1408-1410)tcC>tcT | p.S470S |
LUAD | 15 | 56207664 | 56207664 | + | Missense_Mutation | SNP | T | T | G | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr15:56207664T>G | c.1366A>C | c.(1366-1368)Agt>Cgt | p.S456R |
LUAD | 15 | 56208063 | 56208063 | + | Missense_Mutation | SNP | C | C | A | TCGA-MP-A4TI-01A-21D-A24P-08 | TCGA-MP-A4TI-10A-01D-A24P-08 | g.chr15:56208063C>A | c.967G>T | c.(967-969)Gtc>Ttc | p.V323F |
LUAD | 15 | 56208071 | 56208071 | + | Missense_Mutation | SNP | G | G | A | TCGA-95-7944-01A-11D-2184-08 | TCGA-95-7944-10A-01D-2184-08 | g.chr15:56208071G>A | c.959C>T | c.(958-960)tCa>tTa | p.S320L |
LUAD | 15 | 56208095 | 56208095 | + | Missense_Mutation | SNP | C | C | A | TCGA-64-1679-01A-21D-2063-08 | TCGA-64-1679-10A-01D-2063-08 | g.chr15:56208095C>A | c.935G>T | c.(934-936)gGc>gTc | p.G312V |
LUAD | 15 | 56243739 | 56243739 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-73-4677-01A-01D-1265-08 | TCGA-73-4677-11A-01D-1265-08 | g.chr15:56243739delA | c.168delT | c.(166-168)cttfs | p.L56fs |
LUSC | 15 | 56144621 | 56144621 | + | Splice_Site | SNP | C | C | T | TCGA-66-2786-01A-01D-1522-08 | TCGA-66-2786-11A-01D-1522-08 | g.chr15:56144621C>T | | c.e9+1 | |
LUSC | 15 | 56152937 | 56152937 | + | Silent | SNP | C | C | A | TCGA-63-5128-01A-01D-1441-08 | TCGA-63-5128-10A-01D-1441-08 | g.chr15:56152937C>A | c.1971G>T | c.(1969-1971)ctG>ctT | p.L657L |
OV | 15 | 56130801 | 56130801 | + | Splice_Site | SNP | T | T | C | TCGA-36-2537-01A-01D-1526-09 | TCGA-36-2537-10A-01D-1526-09 | g.chr15:56130801T>C | c.3290A>G | c.(3289-3291)gAt>gGt | p.D1097G |
OV | 15 | 56208548 | 56208548 | + | Missense_Mutation | SNP | G | G | T | TCGA-04-1331-01A-01W-0486-08 | TCGA-04-1331-10A-01W-0486-08 | g.chr15:56208548G>T | c.482C>A | c.(481-483)tCt>tAt | p.S161Y |
OV | 15 | 56208755 | 56208755 | + | Missense_Mutation | SNP | T | T | G | TCGA-30-1855-01A-01W-0639-09 | TCGA-30-1855-10A-01W-0639-09 | g.chr15:56208755T>G | c.275A>C | c.(274-276)cAg>cCg | p.Q92P |
PAAD | 15 | 56132913 | 56132913 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:56132913G>A | c.3108C>T | c.(3106-3108)acC>acT | p.T1036T |
PAAD | 15 | 56139215 | 56139215 | + | Missense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:56139215C>A | c.2817G>T | c.(2815-2817)agG>agT | p.R939S |
PCPG | 15 | 56142797 | 56142797 | + | Silent | SNP | C | C | T | TCGA-QR-A708-01A-11D-A35D-08 | TCGA-QR-A708-10A-01D-A35B-08 | g.chr15:56142797C>T | c.2547G>A | c.(2545-2547)cgG>cgA | p.R849R |
PRAD | 15 | 56126282 | 56126282 | + | Missense_Mutation | SNP | T | T | C | TCGA-YL-A8HO-01A-11D-A364-08 | TCGA-YL-A8HO-10A-01D-A362-08 | g.chr15:56126282T>C | c.3641A>G | c.(3640-3642)aAa>aGa | p.K1214R |
READ | 15 | 56122106 | 56122106 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:56122106C>A | c.3949G>T | c.(3949-3951)Gga>Tga | p.G1317* |
READ | 15 | 56144725 | 56144725 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:56144725G>T | c.2300C>A | c.(2299-2301)tCt>tAt | p.S767Y |
READ | 15 | 56161868 | 56161868 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:56161868C>A | c.1673G>T | c.(1672-1674)aGa>aTa | p.R558I |
READ | 15 | 56207629 | 56207629 | + | Silent | SNP | G | G | A | TCGA-F5-6812-01A-11D-1826-10 | TCGA-F5-6812-10A-01D-1826-10 | g.chr15:56207629G>A | c.1401C>T | c.(1399-1401)tcC>tcT | p.S467S |
READ | 15 | 56207960 | 56207960 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:56207960G>A | c.1070C>T | c.(1069-1071)tCg>tTg | p.S357L |
SARC | 15 | 56164658 | 56164658 | + | Missense_Mutation | SNP | A | A | G | TCGA-DX-AB32-01A-11D-A417-09 | TCGA-DX-AB32-10A-01D-A41A-09 | g.chr15:56164658A>G | c.1616T>C | c.(1615-1617)tTg>tCg | p.L539S |
SKCM | 15 | 56122119 | 56122119 | + | Silent | SNP | G | G | T | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr15:56122119G>T | c.3936C>A | c.(3934-3936)acC>acA | p.T1312T |
SKCM | 15 | 56130018 | 56130018 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GJ-06A-11D-A196-08 | TCGA-EE-A2GJ-10A-01D-A198-08 | g.chr15:56130018C>T | c.3488G>A | c.(3487-3489)cGa>cAa | p.R1163Q |
SKCM | 15 | 56141063 | 56141063 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr15:56141063G>A | c.2626C>T | c.(2626-2628)Cca>Tca | p.P876S |
SKCM | 15 | 56155176 | 56155176 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZB-06A-12D-A197-08 | TCGA-FS-A1ZB-10A-01D-A199-08 | g.chr15:56155176G>A | c.1866C>T | c.(1864-1866)atC>atT | p.I622I |
SKCM | 15 | 56155188 | 56155188 | + | Silent | SNP | C | C | T | TCGA-EE-A2GN-06A-11D-A196-08 | TCGA-EE-A2GN-10A-01D-A198-08 | g.chr15:56155188C>T | c.1854G>A | c.(1852-1854)gaG>gaA | p.E618E |
SKCM | 15 | 56207630 | 56207630 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:56207630G>A | c.1400C>T | c.(1399-1401)tCc>tTc | p.S467F |
SKCM | 15 | 56207725 | 56207725 | + | Silent | SNP | G | G | A | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr15:56207725G>A | c.1305C>T | c.(1303-1305)atC>atT | p.I435I |
SKCM | 15 | 56216890 | 56216890 | + | Missense_Mutation | SNP | G | G | A | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr15:56216890G>A | c.245C>T | c.(244-246)cCt>cTt | p.P82L |