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 | 68434308 | 68434308 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr15:68434308G>A | c.494G>A | c.(493-495)cGa>cAa | p.R165Q |
BLCA | 15 | 68466151 | 68466151 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-DK-AA6L-01A-11D-A391-08 | TCGA-DK-AA6L-10A-01D-A394-08 | g.chr15:68466151C>T | c.1090C>T | c.(1090-1092)Cag>Tag | p.Q364* |
BLCA | 15 | 68468819 | 68468819 | + | Missense_Mutation | SNP | G | G | C | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chr15:68468819G>C | c.1308G>C | c.(1306-1308)ttG>ttC | p.L436F |
BRCA | 15 | 68438931 | 68438931 | + | Missense_Mutation | SNP | G | G | T | TCGA-A2-A25A-01A-12D-A16D-09 | TCGA-A2-A25A-10A-01D-A16D-09 | g.chr15:68438931G>T | c.721G>T | c.(721-723)Gtg>Ttg | p.V241L |
BRCA | 15 | 68438944 | 68438944 | + | Missense_Mutation | SNP | G | G | T | TCGA-A2-A25A-01A-12D-A16D-09 | TCGA-A2-A25A-10A-01D-A16D-09 | g.chr15:68438944G>T | c.734G>T | c.(733-735)cGa>cTa | p.R245L |
BRCA | 15 | 68466118 | 68466118 | + | Missense_Mutation | SNP | C | C | T | TCGA-C8-A26Y-01A-11D-A16D-09 | TCGA-C8-A26Y-10A-01D-A16D-09 | g.chr15:68466118C>T | c.1057C>T | c.(1057-1059)Cat>Tat | p.H353Y |
COAD | 15 | 68378698 | 68378698 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr15:68378698G>A | c.79G>A | c.(79-81)Ggg>Agg | p.G27R |
COAD | 15 | 68378933 | 68378933 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3660-01A-01D-1719-10 | TCGA-AA-3660-11A-01D-1719-10 | g.chr15:68378933C>A | c.314C>A | c.(313-315)tCa>tAa | p.S105* |
COAD | 15 | 68379021 | 68379021 | + | Silent | SNP | G | G | A | TCGA-AA-A01S-01A-21W-A096-10 | TCGA-AA-A01S-11A-21W-A096-10 | g.chr15:68379021G>A | c.402G>A | c.(400-402)ccG>ccA | p.P134P |
COAD | 15 | 68434291 | 68434291 | + | Silent | SNP | C | C | T | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr15:68434291C>T | c.477C>T | c.(475-477)gaC>gaT | p.D159D |
COAD | 15 | 68434291 | 68434291 | + | Silent | SNP | C | C | T | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr15:68434291C>T | c.477C>T | c.(475-477)gaC>gaT | p.D159D |
COAD | 15 | 68445935 | 68445935 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr15:68445935C>T | c.836C>T | c.(835-837)tCc>tTc | p.S279F |
COAD | 15 | 68466101 | 68466101 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr15:68466101G>A | c.1040G>A | c.(1039-1041)cGg>cAg | p.R347Q |
COAD | 15 | 68468922 | 68468922 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:68468922G>T | c.1411G>T | c.(1411-1413)Gag>Tag | p.E471* |
COADREAD | 15 | 68378698 | 68378698 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr15:68378698G>A | c.79G>A | c.(79-81)Ggg>Agg | p.G27R |
COADREAD | 15 | 68378933 | 68378933 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3660-01A-01D-1719-10 | TCGA-AA-3660-11A-01D-1719-10 | g.chr15:68378933C>A | c.314C>A | c.(313-315)tCa>tAa | p.S105* |
COADREAD | 15 | 68379021 | 68379021 | + | Silent | SNP | G | G | A | TCGA-AA-A01S-01A-21W-A096-10 | TCGA-AA-A01S-11A-21W-A096-10 | g.chr15:68379021G>A | c.402G>A | c.(400-402)ccG>ccA | p.P134P |
COADREAD | 15 | 68434291 | 68434291 | + | Silent | SNP | C | C | T | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr15:68434291C>T | c.477C>T | c.(475-477)gaC>gaT | p.D159D |
COADREAD | 15 | 68434291 | 68434291 | + | Silent | SNP | C | C | T | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr15:68434291C>T | c.477C>T | c.(475-477)gaC>gaT | p.D159D |
COADREAD | 15 | 68445935 | 68445935 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr15:68445935C>T | c.836C>T | c.(835-837)tCc>tTc | p.S279F |
COADREAD | 15 | 68466101 | 68466101 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr15:68466101G>A | c.1040G>A | c.(1039-1041)cGg>cAg | p.R347Q |
COADREAD | 15 | 68468922 | 68468922 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:68468922G>T | c.1411G>T | c.(1411-1413)Gag>Tag | p.E471* |
COADREAD | 15 | 68468982 | 68468982 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr15:68468982A>C | c.1471A>C | c.(1471-1473)Aat>Cat | p.N491H |
DLBC | 15 | 68479959 | 68479959 | + | Missense_Mutation | SNP | T | T | C | TCGA-GR-7353-01A-11D-2210-10 | TCGA-GR-7353-10A-01D-2210-10 | g.chr15:68479959T>C | c.1742T>C | c.(1741-1743)tTc>tCc | p.F581S |
ESCA | 15 | 68434296 | 68434296 | + | Missense_Mutation | SNP | G | G | T | TCGA-2H-A9GI-01A-11D-A37C-09 | TCGA-2H-A9GI-11A-11D-A37F-09 | g.chr15:68434296G>T | c.482G>T | c.(481-483)aGt>aTt | p.S161I |
ESCA | 15 | 68438931 | 68438931 | + | Missense_Mutation | SNP | G | G | T | TCGA-IG-A3YA-01A-11D-A247-09 | TCGA-IG-A3YA-10A-01D-A247-09 | g.chr15:68438931G>T | c.721G>T | c.(721-723)Gtg>Ttg | p.V241L |
ESCA | 15 | 68438931 | 68438931 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr15:68438931G>T | c.721G>T | c.(721-723)Gtg>Ttg | p.V241L |
ESCA | 15 | 68438944 | 68438944 | + | Missense_Mutation | SNP | G | G | T | TCGA-IG-A3YA-01A-11D-A247-09 | TCGA-IG-A3YA-10A-01D-A247-09 | g.chr15:68438944G>T | c.734G>T | c.(733-735)cGa>cTa | p.R245L |
ESCA | 15 | 68438944 | 68438944 | + | Missense_Mutation | SNP | G | G | T | TCGA-IG-A4P3-01A-11D-A27G-09 | TCGA-IG-A4P3-10A-01D-A27G-09 | g.chr15:68438944G>T | c.734G>T | c.(733-735)cGa>cTa | p.R245L |
ESCA | 15 | 68438944 | 68438944 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A4OH-01A-11D-A27G-09 | TCGA-L5-A4OH-11A-11D-A27G-09 | g.chr15:68438944G>T | c.734G>T | c.(733-735)cGa>cTa | p.R245L |
ESCA | 15 | 68438944 | 68438944 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr15:68438944G>T | c.734G>T | c.(733-735)cGa>cTa | p.R245L |
GBM | 15 | 68468841 | 68468841 | + | Missense_Mutation | SNP | G | G | T | TCGA-06-0644-01A-02D-1492-08 | TCGA-06-0644-10A-01D-1492-08 | g.chr15:68468841G>T | c.1330G>T | c.(1330-1332)Gta>Tta | p.V444L |
GBMLGG | 15 | 68378743 | 68378743 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:68378743C>A | c.124C>A | c.(124-126)Ctg>Atg | p.L42M |
GBMLGG | 15 | 68468841 | 68468841 | + | Missense_Mutation | SNP | G | G | T | TCGA-06-0644-01A-02D-1492-08 | TCGA-06-0644-10A-01D-1492-08 | g.chr15:68468841G>T | c.1330G>T | c.(1330-1332)Gta>Tta | p.V444L |
GBMLGG | 15 | 68468894 | 68468894 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:68468894C>T | c.1383C>T | c.(1381-1383)gaC>gaT | p.D461D |
HNSC | 15 | 68479984 | 68479984 | + | Missense_Mutation | SNP | T | T | G | TCGA-BB-A5HY-01A-11D-A28R-08 | TCGA-BB-A5HY-10A-01D-A28U-08 | g.chr15:68479984T>G | c.1767T>G | c.(1765-1767)ttT>ttG | p.F589L |
KIPAN | 15 | 68434644 | 68434644 | + | Missense_Mutation | SNP | A | A | G | TCGA-A4-A5Y1-01A-11D-A28G-10 | TCGA-A4-A5Y1-11A-11D-A28G-10 | g.chr15:68434644A>G | c.571A>G | c.(571-573)Aaa>Gaa | p.K191E |
KIPAN | 15 | 68434675 | 68434675 | + | Splice_Site | SNP | G | G | A | TCGA-B0-5095-01A-01D-1421-08 | TCGA-B0-5095-11A-01D-1421-08 | g.chr15:68434675G>A | c.602G>A | c.(601-603)aGg>aAg | p.R201K |
KIPAN | 15 | 68445966 | 68445966 | + | Silent | SNP | C | C | T | TCGA-AK-3451-01A-02D-1251-10 | TCGA-AK-3451-10A-01D-1251-10 | g.chr15:68445966C>T | c.867C>T | c.(865-867)tcC>tcT | p.S289S |
KIPAN | 15 | 68457098 | 68457098 | + | Missense_Mutation | SNP | A | A | G | TCGA-CZ-4859-01A-02D-1429-08 | TCGA-CZ-4859-11A-01D-1429-08 | g.chr15:68457098A>G | c.964A>G | c.(964-966)Agt>Ggt | p.S322G |
KIPAN | 15 | 68479999 | 68479999 | + | Silent | SNP | T | T | C | TCGA-BQ-5876-01A-11D-1589-08 | TCGA-BQ-5876-11A-01D-1589-08 | g.chr15:68479999T>C | c.1782T>C | c.(1780-1782)agT>agC | p.S594S |
KIRC | 15 | 68434675 | 68434675 | + | Splice_Site | SNP | G | G | A | TCGA-B0-5095-01A-01D-1421-08 | TCGA-B0-5095-11A-01D-1421-08 | g.chr15:68434675G>A | c.602G>A | c.(601-603)aGg>aAg | p.R201K |
KIRC | 15 | 68445966 | 68445966 | + | Silent | SNP | C | C | T | TCGA-AK-3451-01A-02D-1251-10 | TCGA-AK-3451-10A-01D-1251-10 | g.chr15:68445966C>T | c.867C>T | c.(865-867)tcC>tcT | p.S289S |
KIRC | 15 | 68457098 | 68457098 | + | Missense_Mutation | SNP | A | A | G | TCGA-CZ-4859-01A-02D-1429-08 | TCGA-CZ-4859-11A-01D-1429-08 | g.chr15:68457098A>G | c.964A>G | c.(964-966)Agt>Ggt | p.S322G |
KIRP | 15 | 68434644 | 68434644 | + | Missense_Mutation | SNP | A | A | G | TCGA-A4-A5Y1-01A-11D-A28G-10 | TCGA-A4-A5Y1-11A-11D-A28G-10 | g.chr15:68434644A>G | c.571A>G | c.(571-573)Aaa>Gaa | p.K191E |
KIRP | 15 | 68479999 | 68479999 | + | Silent | SNP | T | T | C | TCGA-BQ-5876-01A-11D-1589-08 | TCGA-BQ-5876-11A-01D-1589-08 | g.chr15:68479999T>C | c.1782T>C | c.(1780-1782)agT>agC | p.S594S |
LGG | 15 | 68378743 | 68378743 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:68378743C>A | c.124C>A | c.(124-126)Ctg>Atg | p.L42M |
LGG | 15 | 68468894 | 68468894 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:68468894C>T | c.1383C>T | c.(1381-1383)gaC>gaT | p.D461D |
LUAD | 15 | 68378695 | 68378695 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-3918-01A-01D-1105-08 | TCGA-44-3918-11A-01D-1105-08 | g.chr15:68378695G>T | c.76G>T | c.(76-78)Gcc>Tcc | p.A26S |
LUAD | 15 | 68378698 | 68378698 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-80-5611-01A-01D-1625-08 | TCGA-80-5611-10A-01D-1625-08 | g.chr15:68378698delG | c.79delG | c.(79-81)gggfs | p.G27fs |
LUSC | 15 | 68378917 | 68378917 | + | Missense_Mutation | SNP | G | G | T | TCGA-46-3768-01A-01D-0983-08 | TCGA-46-3768-10A-01D-0983-08 | g.chr15:68378917G>T | c.298G>T | c.(298-300)Gat>Tat | p.D100Y |
LUSC | 15 | 68434669 | 68434669 | + | Missense_Mutation | SNP | A | A | C | TCGA-22-5492-01A-01D-1632-08 | TCGA-22-5492-11A-01D-1632-08 | g.chr15:68434669A>C | c.596A>C | c.(595-597)cAg>cCg | p.Q199P |
LUSC | 15 | 68468058 | 68468058 | + | Missense_Mutation | SNP | C | C | T | TCGA-56-6545-01A-11D-1817-08 | TCGA-56-6545-10A-01D-1817-08 | g.chr15:68468058C>T | c.1253C>T | c.(1252-1254)tCa>tTa | p.S418L |
LUSC | 15 | 68468068 | 68468068 | + | Missense_Mutation | SNP | A | A | T | TCGA-34-5231-01A-21D-1817-08 | TCGA-34-5231-10A-01D-1817-08 | g.chr15:68468068A>T | c.1263A>T | c.(1261-1263)gaA>gaT | p.E421D |
LUSC | 15 | 68479904 | 68479904 | + | Missense_Mutation | SNP | G | G | T | TCGA-63-5128-01A-01D-1441-08 | TCGA-63-5128-10A-01D-1441-08 | g.chr15:68479904G>T | c.1687G>T | c.(1687-1689)Gct>Tct | p.A563S |
OV | 15 | 68434291 | 68434291 | + | Silent | SNP | C | C | T | TCGA-23-1022-01A-02W-0488-09 | TCGA-23-1022-10A-01W-0488-09 | g.chr15:68434291C>T | c.477C>T | c.(475-477)gaC>gaT | p.D159D |
PAAD | 15 | 68379085 | 68379089 | + | Splice_Site | DEL | CTAGG | CTAGG | - | TCGA-3A-A9IV-01A-11D-A40W-08 | TCGA-3A-A9IV-10A-01D-A40W-08 | g.chr15:68379085_68379089delCTAGG | c.466_469delCTAGG | c.(466-471)ctaggc>gc | p.LG156fs |
PAAD | 15 | 68479934 | 68479934 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:68479934G>T | c.1717G>T | c.(1717-1719)Gac>Tac | p.D573Y |
PAAD | 15 | 68479978 | 68479978 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:68479978G>A | c.1761G>A | c.(1759-1761)caG>caA | p.Q587Q |
READ | 15 | 68468982 | 68468982 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr15:68468982A>C | c.1471A>C | c.(1471-1473)Aat>Cat | p.N491H |
SARC | 15 | 68446007 | 68446007 | + | Missense_Mutation | SNP | G | G | T | TCGA-QQ-A5V2-01A-11D-A32I-09 | TCGA-QQ-A5V2-10A-01D-A32I-09 | g.chr15:68446007G>T | c.908G>T | c.(907-909)aGg>aTg | p.R303M |
SARC | 15 | 68468089 | 68468089 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-WK-A8XX-01A-11D-A37C-09 | TCGA-WK-A8XX-10A-01D-A37F-09 | g.chr15:68468089delT | c.1284delT | c.(1282-1284)tctfs | p.S428fs |
SKCM | 15 | 68379016 | 68379016 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3MR-06A-11D-A21A-08 | TCGA-D3-A3MR-10A-01D-A21A-08 | g.chr15:68379016C>T | c.397C>T | c.(397-399)Cat>Tat | p.H133Y |
SKCM | 15 | 68434638 | 68434638 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2A6-06A-11D-A197-08 | TCGA-EE-A2A6-10A-01D-A199-08 | g.chr15:68434638G>A | c.565G>A | c.(565-567)Ggg>Agg | p.G189R |
SKCM | 15 | 68445979 | 68445979 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:68445979C>T | c.880C>T | c.(880-882)Ctt>Ttt | p.L294F |
SKCM | 15 | 68446018 | 68446018 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A5GL-06A-11D-A27K-08 | TCGA-D3-A5GL-10A-01D-A27N-08 | g.chr15:68446018C>T | c.919C>T | c.(919-921)Cat>Tat | p.H307Y |
SKCM | 15 | 68457092 | 68457092 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JB-06A-11D-A21A-08 | TCGA-EE-A3JB-10A-01D-A21A-08 | g.chr15:68457092C>T | c.958C>T | c.(958-960)Cca>Tca | p.P320S |
SKCM | 15 | 68457093 | 68457093 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JB-06A-11D-A21A-08 | TCGA-EE-A3JB-10A-01D-A21A-08 | g.chr15:68457093C>T | c.959C>T | c.(958-960)cCa>cTa | p.P320L |
SKCM | 15 | 68468991 | 68468991 | + | Splice_Site | SNP | G | G | A | TCGA-EE-A3JA-06A-11D-A20D-08 | TCGA-EE-A3JA-10A-01D-A20D-08 | g.chr15:68468991G>A | c.1480G>A | c.(1480-1482)Ggc>Agc | p.G494S |