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 | 13 | 114112384 | 114112384 | + | Missense_Mutation | SNP | G | G | T | TCGA-OR-A5JT-01A-11D-A29I-10 | TCGA-OR-A5JT-10A-01D-A29L-10 | g.chr13:114112384G>T | c.740C>A | c.(739-741)gCa>gAa | p.A247E |
BLCA | 13 | 114134912 | 114134912 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-A9ST-01A-11D-A42E-08 | TCGA-XF-A9ST-10A-01D-A42H-08 | g.chr13:114134912G>C | c.367C>G | c.(367-369)Cta>Gta | p.L123V |
BLCA | 13 | 114134914 | 114134914 | + | Missense_Mutation | SNP | A | A | G | TCGA-UY-A8OB-01A-12D-A42E-08 | TCGA-UY-A8OB-11A-12D-A42H-08 | g.chr13:114134914A>G | c.365T>C | c.(364-366)tTt>tCt | p.F122S |
BLCA | 13 | 114135050 | 114135050 | + | Missense_Mutation | SNP | C | C | T | TCGA-S5-A6DX-01A-11D-A31L-08 | TCGA-S5-A6DX-10A-01D-A31J-08 | g.chr13:114135050C>T | c.229G>A | c.(229-231)Gat>Aat | p.D77N |
BLCA | 13 | 114138204 | 114138204 | + | Silent | SNP | C | C | T | TCGA-XF-AAMF-01A-21D-A42E-08 | TCGA-XF-AAMF-10A-01D-A42H-08 | g.chr13:114138204C>T | c.171G>A | c.(169-171)cgG>cgA | p.R57R |
BLCA | 13 | 114138263 | 114138263 | + | Missense_Mutation | SNP | C | C | G | TCGA-BT-A42E-01A-11D-A23U-08 | TCGA-BT-A42E-10A-01D-A23U-08 | g.chr13:114138263C>G | c.112G>C | c.(112-114)Gac>Cac | p.D38H |
BLCA | 13 | 114138283 | 114138283 | + | Missense_Mutation | SNP | G | G | A | TCGA-YC-A9TC-01A-22D-A391-08 | TCGA-YC-A9TC-10A-01D-A394-08 | g.chr13:114138283G>A | c.92C>T | c.(91-93)aCg>aTg | p.T31M |
BLCA | 13 | 114138370 | 114138370 | + | Splice_Site | SNP | T | T | C | TCGA-GC-A3RD-01A-12D-A22Z-08 | TCGA-GC-A3RD-10B-01D-A22Z-08 | g.chr13:114138370T>C | c.5A>G | c.(4-6)cAt>cGt | p.H2R |
BRCA | 13 | 114112365 | 114112365 | + | Silent | SNP | A | A | C | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr13:114112365A>C | c.759T>G | c.(757-759)ggT>ggG | p.G253G |
BRCA | 13 | 114128499 | 114128499 | + | Missense_Mutation | SNP | A | A | G | TCGA-C8-A130-01A-31D-A10Y-09 | TCGA-C8-A130-10A-01D-A110-09 | g.chr13:114128499A>G | c.460T>C | c.(460-462)Ttt>Ctt | p.F154L |
BRCA | 13 | 114138226 | 114138226 | + | Missense_Mutation | SNP | G | G | A | TCGA-B6-A0RO-01A-22D-A099-09 | TCGA-B6-A0RO-10A-01D-A099-09 | g.chr13:114138226G>A | c.149C>T | c.(148-150)tCg>tTg | p.S50L |
BRCA | 13 | 114138363 | 114138363 | + | Silent | SNP | A | A | G | TCGA-D8-A1XK-01A-21D-A14K-09 | TCGA-D8-A1XK-10A-01D-A14K-09 | g.chr13:114138363A>G | c.12T>C | c.(10-12)ctT>ctC | p.L4L |
COAD | 13 | 114113636 | 114113636 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6678-01A-11D-1835-10 | TCGA-CM-6678-10A-01D-1835-10 | g.chr13:114113636C>T | c.691G>A | c.(691-693)Gat>Aat | p.D231N |
COAD | 13 | 114128489 | 114128489 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr13:114128489A>C | c.470T>G | c.(469-471)tTt>tGt | p.F157C |
COADREAD | 13 | 114113636 | 114113636 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6678-01A-11D-1835-10 | TCGA-CM-6678-10A-01D-1835-10 | g.chr13:114113636C>T | c.691G>A | c.(691-693)Gat>Aat | p.D231N |
COADREAD | 13 | 114128489 | 114128489 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr13:114128489A>C | c.470T>G | c.(469-471)tTt>tGt | p.F157C |
GBMLGG | 13 | 114135036 | 114135036 | + | Silent | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr13:114135036A>G | c.243T>C | c.(241-243)atT>atC | p.I81I |
HNSC | 13 | 114112358 | 114112358 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-5436-01A-01D-1512-08 | TCGA-CV-5436-10A-01D-1870-08 | g.chr13:114112358G>A | c.766C>T | c.(766-768)Cgc>Tgc | p.R256C |
LGG | 13 | 114135036 | 114135036 | + | Silent | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr13:114135036A>G | c.243T>C | c.(241-243)atT>atC | p.I81I |
LIHC | 13 | 114112422 | 114112422 | + | Splice_Site | SNP | T | T | C | TCGA-CC-A3MA-01A-11D-A20W-10 | TCGA-CC-A3MA-10A-01D-A20W-10 | g.chr13:114112422T>C | c.702A>G | c.(700-702)ggA>ggG | p.G234G |
LUAD | 13 | 114128538 | 114128538 | + | Silent | SNP | G | G | A | TCGA-17-Z032-01A-01W-0746-08 | TCGA-17-Z032-11A-01W-0746-08 | g.chr13:114128538G>A | c.421C>T | c.(421-423)Ctg>Ttg | p.L141L |
LUAD | 13 | 114134923 | 114134923 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8614-01A-11D-2393-08 | TCGA-55-8614-10A-01D-2393-08 | g.chr13:114134923C>T | c.356G>A | c.(355-357)aGa>aAa | p.R119K |
LUAD | 13 | 114138335 | 114138335 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-78-7167-01A-11D-2063-08 | TCGA-78-7167-11A-01D-2063-08 | g.chr13:114138335G>A | c.40C>T | c.(40-42)Cag>Tag | p.Q14* |
LUSC | 13 | 114112392 | 114112392 | + | Silent | SNP | T | T | C | TCGA-34-5927-01A-11D-1817-08 | TCGA-34-5927-10A-01D-1817-08 | g.chr13:114112392T>C | c.732A>G | c.(730-732)gtA>gtG | p.V244V |
LUSC | 13 | 114138238 | 114138238 | + | Missense_Mutation | SNP | T | T | C | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr13:114138238T>C | c.137A>G | c.(136-138)cAa>cGa | p.Q46R |
PRAD | 13 | 114112358 | 114112358 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr13:114112358G>A | c.766C>T | c.(766-768)Cgc>Tgc | p.R256C |
PRAD | 13 | 114128477 | 114128477 | + | Missense_Mutation | SNP | G | G | A | TCGA-YL-A9WX-01A-21D-A41K-08 | TCGA-YL-A9WX-10A-01D-A41N-08 | g.chr13:114128477G>A | c.482C>T | c.(481-483)aCc>aTc | p.T161I |