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 | 84228047 | 84228047 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZF-A9R9-01A-11D-A38G-08 | TCGA-ZF-A9R9-10A-01D-A38J-08 | g.chr15:84228047G>C | c.88G>C | c.(88-90)Gac>Cac | p.D30H |
BLCA | 15 | 84233946 | 84233946 | + | Missense_Mutation | SNP | C | C | A | TCGA-BT-A20T-01A-11D-A14W-08 | TCGA-BT-A20T-11A-11D-A14W-08 | g.chr15:84233946C>A | c.175C>A | c.(175-177)Cag>Aag | p.Q59K |
BLCA | 15 | 84237317 | 84237317 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr15:84237317C>T | c.224C>T | c.(223-225)tCg>tTg | p.S75L |
BLCA | 15 | 84286834 | 84286834 | + | Splice_Site | SNP | G | G | A | TCGA-S5-A6DX-01A-11D-A31L-08 | TCGA-S5-A6DX-10A-01D-A31J-08 | g.chr15:84286834G>A | c.839G>A | c.(838-840)gGt>gAt | p.G280D |
BLCA | 15 | 84286884 | 84286884 | + | Missense_Mutation | SNP | G | G | C | TCGA-S5-AA26-01A-11D-A38G-08 | TCGA-S5-AA26-10A-01D-A38J-08 | g.chr15:84286884G>C | c.889G>C | c.(889-891)Gag>Cag | p.E297Q |
BRCA | 15 | 84241415 | 84241415 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-C8-A27B-01A-11D-A167-09 | TCGA-C8-A27B-10A-01D-A167-09 | g.chr15:84241415C>T | c.430C>T | c.(430-432)Cag>Tag | p.Q144* |
COAD | 15 | 84116331 | 84116331 | + | Splice_Site | SNP | G | G | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:84116331G>T | | c.e1+1 | |
COAD | 15 | 84228059 | 84228059 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:84228059C>A | c.100C>A | c.(100-102)Ctt>Att | p.L34I |
COAD | 15 | 84237317 | 84237317 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:84237317C>T | c.224C>T | c.(223-225)tCg>tTg | p.S75L |
COAD | 15 | 84237326 | 84237326 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A01S-01A-21W-A096-10 | TCGA-AA-A01S-11A-21W-A096-10 | g.chr15:84237326G>A | c.233G>A | c.(232-234)cGa>cAa | p.R78Q |
COAD | 15 | 84245375 | 84245375 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr15:84245375A>C | c.506A>C | c.(505-507)gAt>gCt | p.D169A |
COAD | 15 | 84245389 | 84245389 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr15:84245389C>T | c.520C>T | c.(520-522)Cga>Tga | p.R174* |
COAD | 15 | 84245410 | 84245410 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr15:84245410G>A | c.541G>A | c.(541-543)Gaa>Aaa | p.E181K |
COAD | 15 | 84255835 | 84255835 | + | Missense_Mutation | SNP | T | T | C | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr15:84255835T>C | c.725T>C | c.(724-726)aTg>aCg | p.M242T |
COAD | 15 | 84257427 | 84257427 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr15:84257427T>C | c.742T>C | c.(742-744)Tcc>Ccc | p.S248P |
COAD | 15 | 84286945 | 84286945 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:84286945A>G | c.950A>G | c.(949-951)cAa>cGa | p.Q317R |
COADREAD | 15 | 84116331 | 84116331 | + | Splice_Site | SNP | G | G | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:84116331G>T | | c.e1+1 | |
COADREAD | 15 | 84228059 | 84228059 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:84228059C>A | c.100C>A | c.(100-102)Ctt>Att | p.L34I |
COADREAD | 15 | 84237317 | 84237317 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:84237317C>T | c.224C>T | c.(223-225)tCg>tTg | p.S75L |
COADREAD | 15 | 84237326 | 84237326 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A01S-01A-21W-A096-10 | TCGA-AA-A01S-11A-21W-A096-10 | g.chr15:84237326G>A | c.233G>A | c.(232-234)cGa>cAa | p.R78Q |
COADREAD | 15 | 84237364 | 84237364 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A026-01A-32W-A096-10 | TCGA-AG-A026-10A-01W-A096-10 | g.chr15:84237364G>A | c.271G>A | c.(271-273)Ggc>Agc | p.G91S |
COADREAD | 15 | 84237406 | 84237406 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-4001-01A-02W-1073-09 | TCGA-AG-4001-10A-01W-1073-09 | g.chr15:84237406G>T | c.313G>T | c.(313-315)Ggg>Tgg | p.G105W |
COADREAD | 15 | 84241320 | 84241320 | + | Missense_Mutation | SNP | A | A | G | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr15:84241320A>G | c.335A>G | c.(334-336)aAt>aGt | p.N112S |
COADREAD | 15 | 84241376 | 84241376 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:84241376C>A | c.391C>A | c.(391-393)Ctt>Att | p.L131I |
COADREAD | 15 | 84245375 | 84245375 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr15:84245375A>C | c.506A>C | c.(505-507)gAt>gCt | p.D169A |
COADREAD | 15 | 84245389 | 84245389 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr15:84245389C>T | c.520C>T | c.(520-522)Cga>Tga | p.R174* |
COADREAD | 15 | 84245410 | 84245410 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr15:84245410G>A | c.541G>A | c.(541-543)Gaa>Aaa | p.E181K |
COADREAD | 15 | 84255835 | 84255835 | + | Missense_Mutation | SNP | T | T | C | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr15:84255835T>C | c.725T>C | c.(724-726)aTg>aCg | p.M242T |
COADREAD | 15 | 84257427 | 84257427 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr15:84257427T>C | c.742T>C | c.(742-744)Tcc>Ccc | p.S248P |
COADREAD | 15 | 84286945 | 84286945 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr15:84286945A>G | c.950A>G | c.(949-951)cAa>cGa | p.Q317R |
COADREAD | 15 | 84286958 | 84286958 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:84286958C>A | c.963C>A | c.(961-963)aaC>aaA | p.N321K |
DLBC | 15 | 84287010 | 84287010 | + | Missense_Mutation | SNP | G | G | A | TCGA-FF-8041-01A-11D-2210-10 | TCGA-FF-8041-10A-01D-2210-10 | g.chr15:84287010G>A | c.1015G>A | c.(1015-1017)Gtg>Atg | p.V339M |
ESCA | 15 | 84237334 | 84237334 | + | Missense_Mutation | SNP | G | G | A | TCGA-JY-A93F-01A-21D-A37C-09 | TCGA-JY-A93F-10A-01D-A37F-09 | g.chr15:84237334G>A | c.241G>A | c.(241-243)Gtg>Atg | p.V81M |
ESCA | 15 | 84237360 | 84237360 | + | Silent | SNP | G | G | A | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr15:84237360G>A | c.267G>A | c.(265-267)acG>acA | p.T89T |
ESCA | 15 | 84245418 | 84245418 | + | Silent | SNP | C | C | T | TCGA-2H-A9GF-01A-11D-A37C-09 | TCGA-2H-A9GF-11A-11D-A37F-09 | g.chr15:84245418C>T | c.549C>T | c.(547-549)gtC>gtT | p.V183V |
ESCA | 15 | 84286908 | 84286908 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A43I-01A-11D-A247-09 | TCGA-L5-A43I-11A-11D-A247-09 | g.chr15:84286908G>A | c.913G>A | c.(913-915)Gga>Aga | p.G305R |
GBM | 15 | 84237359 | 84237359 | + | Missense_Mutation | SNP | C | C | T | TCGA-32-1979-01A-01D-1696-08 | TCGA-32-1979-10A-01D-1696-08 | g.chr15:84237359C>T | c.266C>T | c.(265-267)aCg>aTg | p.T89M |
GBM | 15 | 84245409 | 84245409 | + | Silent | SNP | C | C | T | TCGA-14-0813-01A-01W-0424-08 | TCGA-14-0813-10A-01W-0424-08 | g.chr15:84245409C>T | c.540C>T | c.(538-540)gaC>gaT | p.D180D |
GBM | 15 | 84257442 | 84257442 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-19-4068-01A-01D-1353-08 | TCGA-19-4068-10A-01D-1353-08 | g.chr15:84257442C>T | c.757C>T | c.(757-759)Cga>Tga | p.R253* |
GBMLGG | 15 | 84237359 | 84237359 | + | Missense_Mutation | SNP | C | C | T | TCGA-32-1979-01A-01D-1696-08 | TCGA-32-1979-10A-01D-1696-08 | g.chr15:84237359C>T | c.266C>T | c.(265-267)aCg>aTg | p.T89M |
GBMLGG | 15 | 84245409 | 84245409 | + | Silent | SNP | C | C | T | TCGA-14-0813-01A-01W-0424-08 | TCGA-14-0813-10A-01W-0424-08 | g.chr15:84245409C>T | c.540C>T | c.(538-540)gaC>gaT | p.D180D |
GBMLGG | 15 | 84257442 | 84257442 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-19-4068-01A-01D-1353-08 | TCGA-19-4068-10A-01D-1353-08 | g.chr15:84257442C>T | c.757C>T | c.(757-759)Cga>Tga | p.R253* |
GBMLGG | 15 | 84286924 | 84286924 | + | Missense_Mutation | SNP | A | A | G | TCGA-DB-5274-01A-01D-1468-08 | TCGA-DB-5274-10A-01D-1468-08 | g.chr15:84286924A>G | c.929A>G | c.(928-930)gAc>gGc | p.D310G |
HNSC | 15 | 84241361 | 84241361 | + | Missense_Mutation | SNP | G | G | A | TCGA-DQ-5625-01A-01D-1870-08 | TCGA-DQ-5625-10A-01D-1870-08 | g.chr15:84241361G>A | c.376G>A | c.(376-378)Gag>Aag | p.E126K |
HNSC | 15 | 84241424 | 84241424 | + | Missense_Mutation | SNP | C | C | G | TCGA-MZ-A7D7-01A-21D-A34J-08 | TCGA-MZ-A7D7-10A-01D-A34M-08 | g.chr15:84241424C>G | c.439C>G | c.(439-441)Caa>Gaa | p.Q147E |
HNSC | 15 | 84255793 | 84255793 | + | Missense_Mutation | SNP | A | A | T | TCGA-CN-6995-01A-31D-2012-08 | TCGA-CN-6995-10A-01D-2013-08 | g.chr15:84255793A>T | c.683A>T | c.(682-684)cAg>cTg | p.Q228L |
HNSC | 15 | 84286874 | 84286874 | + | Silent | SNP | C | C | G | TCGA-CR-7373-01A-11D-2012-08 | TCGA-CR-7373-10A-01D-2013-08 | g.chr15:84286874C>G | c.879C>G | c.(877-879)ctC>ctG | p.L293L |
KICH | 15 | 84286962 | 84286962 | + | Missense_Mutation | SNP | T | T | C | TCGA-KM-8476-01A-11D-2310-10 | TCGA-KM-8476-10A-01D-2311-10 | g.chr15:84286962T>C | c.967T>C | c.(967-969)Tat>Cat | p.Y323H |
KIPAN | 15 | 84228033 | 84228033 | + | Missense_Mutation | SNP | A | A | C | TCGA-UZ-A9PN-01A-11D-A382-10 | TCGA-UZ-A9PN-10A-01D-A385-10 | g.chr15:84228033A>C | c.74A>C | c.(73-75)gAa>gCa | p.E25A |
KIPAN | 15 | 84286962 | 84286962 | + | Missense_Mutation | SNP | T | T | C | TCGA-KM-8476-01A-11D-2310-10 | TCGA-KM-8476-10A-01D-2311-10 | g.chr15:84286962T>C | c.967T>C | c.(967-969)Tat>Cat | p.Y323H |
KIRP | 15 | 84228033 | 84228033 | + | Missense_Mutation | SNP | A | A | C | TCGA-UZ-A9PN-01A-11D-A382-10 | TCGA-UZ-A9PN-10A-01D-A385-10 | g.chr15:84228033A>C | c.74A>C | c.(73-75)gAa>gCa | p.E25A |
LGG | 15 | 84286924 | 84286924 | + | Missense_Mutation | SNP | A | A | G | TCGA-DB-5274-01A-01D-1468-08 | TCGA-DB-5274-10A-01D-1468-08 | g.chr15:84286924A>G | c.929A>G | c.(928-930)gAc>gGc | p.D310G |
LIHC | 15 | 84237305 | 84237305 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-AACY-01A-11D-A40R-10 | TCGA-DD-AACY-10A-01D-A40U-10 | g.chr15:84237305T>C | c.212T>C | c.(211-213)cTg>cCg | p.L71P |
LIHC | 15 | 84241337 | 84241337 | + | Missense_Mutation | SNP | G | G | C | TCGA-UB-A7MF-01A-11D-A33K-10 | TCGA-UB-A7MF-10A-01D-A33K-10 | g.chr15:84241337G>C | c.352G>C | c.(352-354)Ggt>Cgt | p.G118R |
LUAD | 15 | 84237364 | 84237364 | + | Missense_Mutation | SNP | G | G | A | TCGA-44-2656-01A-02D-0969-08 | TCGA-44-2656-10A-01D-0969-08 | g.chr15:84237364G>A | c.271G>A | c.(271-273)Ggc>Agc | p.G91S |
LUAD | 15 | 84237387 | 84237387 | + | Silent | SNP | G | G | C | TCGA-NJ-A4YQ-01A-11D-A25L-08 | TCGA-NJ-A4YQ-10A-01D-A25L-08 | g.chr15:84237387G>C | c.294G>C | c.(292-294)ctG>ctC | p.L98L |
LUAD | 15 | 84237394 | 84237394 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-2656-01A-02D-0969-08 | TCGA-44-2656-10A-01D-0969-08 | g.chr15:84237394G>T | c.301G>T | c.(301-303)Ggg>Tgg | p.G101W |
LUAD | 15 | 84237416 | 84237416 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-8358-01A-11D-2323-08 | TCGA-86-8358-10A-01D-2323-08 | g.chr15:84237416C>A | c.323C>A | c.(322-324)tCc>tAc | p.S108Y |
LUAD | 15 | 84237417 | 84237417 | + | Silent | SNP | C | C | A | TCGA-86-8358-01A-11D-2323-08 | TCGA-86-8358-10A-01D-2323-08 | g.chr15:84237417C>A | c.324C>A | c.(322-324)tcC>tcA | p.S108S |
LUAD | 15 | 84237419 | 84237419 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-38-4631-01A-01D-1753-08 | TCGA-38-4631-11A-01D-1753-08 | g.chr15:84237419delC | c.326delC | c.(325-327)accfs | p.T109fs |
LUAD | 15 | 84241444 | 84241444 | + | Missense_Mutation | SNP | G | G | C | TCGA-95-7039-01A-11D-1945-08 | TCGA-95-7039-10A-01D-1946-08 | g.chr15:84241444G>C | c.459G>C | c.(457-459)gaG>gaC | p.E153D |
LUAD | 15 | 84245390 | 84245390 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-3396-01A-01D-1553-08 | TCGA-44-3396-10A-01D-1265-08 | g.chr15:84245390G>T | c.521G>T | c.(520-522)cGa>cTa | p.R174L |
LUAD | 15 | 84245427 | 84245427 | + | Silent | SNP | G | G | T | TCGA-95-7039-01A-11D-1945-08 | TCGA-95-7039-10A-01D-1946-08 | g.chr15:84245427G>T | c.558G>T | c.(556-558)gcG>gcT | p.A186A |
LUAD | 15 | 84255752 | 84255752 | + | Missense_Mutation | SNP | G | G | T | TCGA-O1-A52J-01A-11D-A25L-08 | TCGA-O1-A52J-10A-01D-A25L-08 | g.chr15:84255752G>T | c.642G>T | c.(640-642)caG>caT | p.Q214H |
LUAD | 15 | 84255823 | 84255823 | + | Missense_Mutation | SNP | G | G | A | TCGA-49-4514-01A-21D-1855-08 | TCGA-49-4514-11A-01D-1855-08 | g.chr15:84255823G>A | c.713G>A | c.(712-714)aGc>aAc | p.S238N |
LUAD | 15 | 84257444 | 84257444 | + | Silent | SNP | A | A | T | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr15:84257444A>T | c.759A>T | c.(757-759)cgA>cgT | p.R253R |
LUAD | 15 | 84286886 | 84286886 | + | Silent | SNP | G | G | A | TCGA-91-6836-01A-21D-1855-08 | TCGA-91-6836-11A-01D-1855-08 | g.chr15:84286886G>A | c.891G>A | c.(889-891)gaG>gaA | p.E297E |
LUAD | 15 | 84286922 | 84286922 | + | Silent | SNP | G | G | A | TCGA-05-5425-01A-02D-1625-08 | TCGA-05-5425-10A-01D-1625-08 | g.chr15:84286922G>A | c.927G>A | c.(925-927)ggG>ggA | p.G309G |
LUSC | 15 | 84245363 | 84245363 | + | Missense_Mutation | SNP | G | G | T | TCGA-37-5819-01A-01D-1632-08 | TCGA-37-5819-10A-01D-1632-08 | g.chr15:84245363G>T | c.494G>T | c.(493-495)cGc>cTc | p.R165L |
OV | 15 | 84237359 | 84237359 | + | Missense_Mutation | SNP | C | C | T | TCGA-29-1702-01A-01W-0633-09 | TCGA-29-1702-10A-01W-0633-09 | g.chr15:84237359C>T | c.266C>T | c.(265-267)aCg>aTg | p.T89M |
PAAD | 15 | 84237341 | 84237341 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:84237341C>T | c.248C>T | c.(247-249)aCc>aTc | p.T83I |
PAAD | 15 | 84257442 | 84257442 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr15:84257442C>T | c.757C>T | c.(757-759)Cga>Tga | p.R253* |
READ | 15 | 84237364 | 84237364 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A026-01A-32W-A096-10 | TCGA-AG-A026-10A-01W-A096-10 | g.chr15:84237364G>A | c.271G>A | c.(271-273)Ggc>Agc | p.G91S |
READ | 15 | 84237406 | 84237406 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-4001-01A-02W-1073-09 | TCGA-AG-4001-10A-01W-1073-09 | g.chr15:84237406G>T | c.313G>T | c.(313-315)Ggg>Tgg | p.G105W |
READ | 15 | 84241320 | 84241320 | + | Missense_Mutation | SNP | A | A | G | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr15:84241320A>G | c.335A>G | c.(334-336)aAt>aGt | p.N112S |
READ | 15 | 84241376 | 84241376 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:84241376C>A | c.391C>A | c.(391-393)Ctt>Att | p.L131I |
READ | 15 | 84286958 | 84286958 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr15:84286958C>A | c.963C>A | c.(961-963)aaC>aaA | p.N321K |
SKCM | 15 | 84233937 | 84233937 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr15:84233937G>A | c.166G>A | c.(166-168)Gaa>Aaa | p.E56K |
SKCM | 15 | 84237342 | 84237342 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:84237342C>T | c.249C>T | c.(247-249)acC>acT | p.T83T |
SKCM | 15 | 84237407 | 84237407 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr15:84237407G>A | c.314G>A | c.(313-315)gGg>gAg | p.G105E |
SKCM | 15 | 84245343 | 84245343 | + | Silent | SNP | G | G | A | TCGA-ER-A19G-06A-11D-A196-08 | TCGA-ER-A19G-10A-01D-A198-08 | g.chr15:84245343G>A | c.474G>A | c.(472-474)ctG>ctA | p.L158L |
SKCM | 15 | 84245353 | 84245353 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr15:84245353G>A | c.484G>A | c.(484-486)Gaa>Aaa | p.E162K |
SKCM | 15 | 84245374 | 84245374 | + | Missense_Mutation | SNP | G | G | A | TCGA-FR-A69P-06A-21D-A30X-08 | TCGA-FR-A69P-10A-01D-A30X-08 | g.chr15:84245374G>A | c.505G>A | c.(505-507)Gat>Aat | p.D169N |
SKCM | 15 | 84245385 | 84245385 | + | Silent | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr15:84245385G>A | c.516G>A | c.(514-516)aaG>aaA | p.K172K |
SKCM | 15 | 84245413 | 84245413 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr15:84245413G>A | c.544G>A | c.(544-546)Gaa>Aaa | p.E182K |
SKCM | 15 | 84257427 | 84257427 | + | Missense_Mutation | SNP | T | T | A | TCGA-ER-A42L-06A-11D-A24R-08 | TCGA-ER-A42L-10A-01D-A24R-08 | g.chr15:84257427T>A | c.742T>A | c.(742-744)Tcc>Acc | p.S248T |
SKCM | 15 | 84257443 | 84257443 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A1Q4-06A-11D-A196-08 | TCGA-D3-A1Q4-10A-01D-A198-08 | g.chr15:84257443G>A | c.758G>A | c.(757-759)cGa>cAa | p.R253Q |
SKCM | 15 | 84257443 | 84257443 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:84257443G>A | c.758G>A | c.(757-759)cGa>cAa | p.R253Q |
SKCM | 15 | 84286846 | 84286846 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr15:84286846C>T | c.851C>T | c.(850-852)cCc>cTc | p.P284L |
SKCM | 15 | 84287021 | 84287021 | + | Silent | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr15:84287021C>T | c.1026C>T | c.(1024-1026)atC>atT | p.I342I |
SKCM | 15 | 84287021 | 84287021 | + | Silent | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr15:84287021C>T | c.1026C>T | c.(1024-1026)atC>atT | p.I342I |