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 | 14 | 24686377 | 24686377 | + | Missense_Mutation | SNP | G | G | A | TCGA-K4-A6FZ-01A-11D-A31L-08 | TCGA-K4-A6FZ-10A-01D-A31J-08 | g.chr14:24686377G>A | c.202C>T | c.(202-204)Cac>Tac | p.H68Y |
BLCA | 14 | 24687356 | 24687356 | + | Silent | SNP | G | G | A | TCGA-H4-A2HQ-01A-11D-A17V-08 | TCGA-H4-A2HQ-10A-01D-A17V-08 | g.chr14:24687356G>A | c.132C>T | c.(130-132)atC>atT | p.I44I |
BLCA | 14 | 24687622 | 24687622 | + | Missense_Mutation | SNP | C | C | T | TCGA-UY-A8OB-01A-12D-A42E-08 | TCGA-UY-A8OB-11A-12D-A42H-08 | g.chr14:24687622C>T | c.34G>A | c.(34-36)Gag>Aag | p.E12K |
BRCA | 14 | 24687410 | 24687410 | + | Missense_Mutation | SNP | G | G | C | TCGA-A2-A0YK-01A-22D-A117-09 | TCGA-A2-A0YK-10A-01D-A117-09 | g.chr14:24687410G>C | c.78C>G | c.(76-78)atC>atG | p.I26M |
COADREAD | 14 | 24687414 | 24687414 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr14:24687414C>T | c.74G>A | c.(73-75)cGa>cAa | p.R25Q |
ESCA | 14 | 24686403 | 24686403 | + | Missense_Mutation | SNP | T | T | A | TCGA-LN-A9FP-01A-31D-A387-09 | TCGA-LN-A9FP-10A-01D-A38A-09 | g.chr14:24686403T>A | c.176A>T | c.(175-177)tAc>tTc | p.Y59F |
ESCA | 14 | 24687342 | 24687342 | + | Missense_Mutation | SNP | T | T | C | TCGA-LN-A49U-01A-31D-A27G-09 | TCGA-LN-A49U-10A-01D-A27G-09 | g.chr14:24687342T>C | c.146A>G | c.(145-147)cAg>cGg | p.Q49R |
GBMLGG | 14 | 24687634 | 24687634 | + | Silent | SNP | G | G | A | TCGA-RY-A840-01A-11D-A36O-08 | TCGA-RY-A840-10A-01D-A367-08 | g.chr14:24687634G>A | c.22C>T | c.(22-24)Ctg>Ttg | p.L8L |
HNSC | 14 | 24686415 | 24686415 | + | Missense_Mutation | SNP | G | G | C | TCGA-DQ-5625-01A-01D-1870-08 | TCGA-DQ-5625-10A-01D-1870-08 | g.chr14:24686415G>C | c.164C>G | c.(163-165)aCa>aGa | p.T55R |
HNSC | 14 | 24687636 | 24687636 | + | Splice_Site | SNP | G | G | A | TCGA-UF-A719-01A-12D-A34J-08 | TCGA-UF-A719-10A-01D-A34M-08 | g.chr14:24687636G>A | c.20C>T | c.(19-21)aCg>aTg | p.T7M |
LGG | 14 | 24687634 | 24687634 | + | Silent | SNP | G | G | A | TCGA-RY-A840-01A-11D-A36O-08 | TCGA-RY-A840-10A-01D-A367-08 | g.chr14:24687634G>A | c.22C>T | c.(22-24)Ctg>Ttg | p.L8L |
LUAD | 14 | 24687414 | 24687414 | + | Missense_Mutation | SNP | C | C | T | TCGA-05-4403-01A-01D-1265-08 | TCGA-05-4403-10A-01D-1265-08 | g.chr14:24687414C>T | c.74G>A | c.(73-75)cGa>cAa | p.R25Q |
LUAD | 14 | 24687421 | 24687421 | + | Splice_Site | SNP | C | C | T | TCGA-05-4433-01A-22D-1855-08 | TCGA-05-4433-10A-01D-1855-08 | g.chr14:24687421C>T | c.67G>A | c.(67-69)Gtg>Atg | p.V23M |
READ | 14 | 24687414 | 24687414 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr14:24687414C>T | c.74G>A | c.(73-75)cGa>cAa | p.R25Q |