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 | 3 | 23250252 | 23250252 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-A9R9-01A-11D-A38G-08 | TCGA-ZF-A9R9-10A-01D-A38J-08 | g.chr3:23250252G>A | c.62G>A | c.(61-63)gGa>gAa | p.G21E |
COAD | 3 | 23250307 | 23250307 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr3:23250307G>T | c.117G>T | c.(115-117)aaG>aaT | p.K39N |
COAD | 3 | 23541134 | 23541134 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr3:23541134G>A | c.263G>A | c.(262-264)aGg>aAg | p.R88K |
COAD | 3 | 23541165 | 23541165 | + | Silent | SNP | C | C | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr3:23541165C>A | c.294C>A | c.(292-294)gtC>gtA | p.V98V |
COAD | 3 | 23574093 | 23574093 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr3:23574093G>A | c.409G>A | c.(409-411)Gtg>Atg | p.V137M |
COAD | 3 | 23631283 | 23631283 | + | Silent | SNP | C | C | T | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr3:23631283C>T | c.567C>T | c.(565-567)gaC>gaT | p.D189D |
COADREAD | 3 | 23250307 | 23250307 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr3:23250307G>T | c.117G>T | c.(115-117)aaG>aaT | p.K39N |
COADREAD | 3 | 23541106 | 23541106 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-4007-01A-01W-1073-09 | TCGA-AG-4007-10A-01W-1073-09 | g.chr3:23541106C>A | c.235C>A | c.(235-237)Ccc>Acc | p.P79T |
COADREAD | 3 | 23541134 | 23541134 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr3:23541134G>A | c.263G>A | c.(262-264)aGg>aAg | p.R88K |
COADREAD | 3 | 23541165 | 23541165 | + | Silent | SNP | C | C | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr3:23541165C>A | c.294C>A | c.(292-294)gtC>gtA | p.V98V |
COADREAD | 3 | 23574093 | 23574093 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr3:23574093G>A | c.409G>A | c.(409-411)Gtg>Atg | p.V137M |
COADREAD | 3 | 23631283 | 23631283 | + | Silent | SNP | C | C | T | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr3:23631283C>T | c.567C>T | c.(565-567)gaC>gaT | p.D189D |
HNSC | 3 | 23574161 | 23574161 | + | Silent | SNP | C | C | T | TCGA-KU-A6H7-01A-11D-A31L-08 | TCGA-KU-A6H7-10A-01D-A31J-08 | g.chr3:23574161C>T | c.477C>T | c.(475-477)tcC>tcT | p.S159S |
KIPAN | 3 | 23541185 | 23541185 | + | Missense_Mutation | SNP | T | T | C | TCGA-B0-5081-01A-01D-1462-08 | TCGA-B0-5081-11A-01D-1462-08 | g.chr3:23541185T>C | c.314T>C | c.(313-315)tTt>tCt | p.F105S |
KIRC | 3 | 23541185 | 23541185 | + | Missense_Mutation | SNP | T | T | C | TCGA-B0-5081-01A-01D-1462-08 | TCGA-B0-5081-11A-01D-1462-08 | g.chr3:23541185T>C | c.314T>C | c.(313-315)tTt>tCt | p.F105S |
LIHC | 3 | 23631290 | 23631290 | + | Missense_Mutation | SNP | G | G | A | TCGA-4R-AA8I-01A-11D-A382-10 | TCGA-4R-AA8I-10B-01D-A385-10 | g.chr3:23631290G>A | c.574G>A | c.(574-576)Gcc>Acc | p.A192T |
LUAD | 3 | 23250261 | 23250261 | + | Missense_Mutation | SNP | G | G | A | TCGA-44-7660-01A-11D-2063-08 | TCGA-44-7660-10A-01D-2063-08 | g.chr3:23250261G>A | c.71G>A | c.(70-72)cGt>cAt | p.R24H |
LUAD | 3 | 23250330 | 23250330 | + | Missense_Mutation | SNP | G | G | T | TCGA-75-6214-01A-41D-1945-08 | TCGA-75-6214-10A-01D-1946-08 | g.chr3:23250330G>T | c.140G>T | c.(139-141)aGc>aTc | p.S47I |
LUAD | 3 | 23574055 | 23574055 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z025-01A-01W-0746-08 | TCGA-17-Z025-11A-01W-0746-08 | g.chr3:23574055G>T | c.371G>T | c.(370-372)cGa>cTa | p.R124L |
LUAD | 3 | 23631271 | 23631271 | + | Missense_Mutation | SNP | A | A | C | TCGA-78-7167-01A-11D-2063-08 | TCGA-78-7167-11A-01D-2063-08 | g.chr3:23631271A>C | c.555A>C | c.(553-555)agA>agC | p.R185S |
LUSC | 3 | 23541127 | 23541127 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-37-5819-01A-01D-1632-08 | TCGA-37-5819-10A-01D-1632-08 | g.chr3:23541127G>T | c.256G>T | c.(256-258)Gaa>Taa | p.E86* |
LUSC | 3 | 23541139 | 23541139 | + | Missense_Mutation | SNP | A | A | T | TCGA-66-2765-01A-01D-1522-08 | TCGA-66-2765-11A-01D-1522-08 | g.chr3:23541139A>T | c.268A>T | c.(268-270)Act>Tct | p.T90S |
READ | 3 | 23541106 | 23541106 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-4007-01A-01W-1073-09 | TCGA-AG-4007-10A-01W-1073-09 | g.chr3:23541106C>A | c.235C>A | c.(235-237)Ccc>Acc | p.P79T |
SKCM | 3 | 23250196 | 23250196 | + | Silent | SNP | C | C | T | TCGA-EE-A2A5-06A-11D-A197-08 | TCGA-EE-A2A5-10A-01D-A199-08 | g.chr3:23250196C>T | c.6C>T | c.(4-6)tcC>tcT | p.S2S |
SKCM | 3 | 23250314 | 23250314 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:23250314G>A | c.124G>A | c.(124-126)Gag>Aag | p.E42K |
SKCM | 3 | 23541152 | 23541152 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:23541152C>T | c.281C>T | c.(280-282)cCc>cTc | p.P94L |
SKCM | 3 | 23574053 | 23574053 | + | Silent | SNP | C | C | T | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr3:23574053C>T | c.369C>T | c.(367-369)ttC>ttT | p.F123F |
SKCM | 3 | 23574054 | 23574054 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr3:23574054C>T | c.370C>T | c.(370-372)Cga>Tga | p.R124* |
SKCM | 3 | 23574145 | 23574145 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr3:23574145C>T | c.461C>T | c.(460-462)tCt>tTt | p.S154F |