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 | 11 | 1298324 | 1298324 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A2I4-01A-11D-A21A-08 | TCGA-DK-A2I4-10A-01D-A21A-08 | g.chr11:1298324C>T | c.770G>A | c.(769-771)cGa>cAa | p.R257Q |
BLCA | 11 | 1298402 | 1298402 | + | Missense_Mutation | SNP | T | T | C | TCGA-E7-A541-01A-11D-A26M-08 | TCGA-E7-A541-10A-01D-A26K-08 | g.chr11:1298402T>C | c.692A>G | c.(691-693)gAg>gGg | p.E231G |
BLCA | 11 | 1311560 | 1311560 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9SP-01A-11D-A391-08 | TCGA-XF-A9SP-10A-01D-A394-08 | g.chr11:1311560G>A | c.263C>T | c.(262-264)aCg>aTg | p.T88M |
CESC | 11 | 1298482 | 1298482 | + | Splice_Site | SNP | C | C | T | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr11:1298482C>T | c.612G>A | c.(610-612)ggG>ggA | p.G204G |
COAD | 11 | 1298380 | 1298380 | + | Missense_Mutation | SNP | C | C | A | TCGA-CM-4746-01A-01D-1408-10 | TCGA-CM-4746-10A-01D-1408-10 | g.chr11:1298380C>A | c.714G>T | c.(712-714)caG>caT | p.Q238H |
COAD | 11 | 1307253 | 1307253 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr11:1307253C>T | c.589G>A | c.(589-591)Gtt>Att | p.V197I |
COAD | 11 | 1311498 | 1311498 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr11:1311498G>A | c.325C>T | c.(325-327)Ccc>Tcc | p.P109S |
COAD | 11 | 1316949 | 1316949 | + | Missense_Mutation | SNP | C | C | T | TCGA-CK-4947-01B-11D-1650-10 | TCGA-CK-4947-10A-01D-1650-10 | g.chr11:1316949C>T | c.109G>A | c.(109-111)Gcc>Acc | p.A37T |
COAD | 11 | 1316984 | 1316984 | + | Missense_Mutation | SNP | G | G | A | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr11:1316984G>A | c.74C>T | c.(73-75)aCg>aTg | p.T25M |
COADREAD | 11 | 1298380 | 1298380 | + | Missense_Mutation | SNP | C | C | A | TCGA-CM-4746-01A-01D-1408-10 | TCGA-CM-4746-10A-01D-1408-10 | g.chr11:1298380C>A | c.714G>T | c.(712-714)caG>caT | p.Q238H |
COADREAD | 11 | 1307253 | 1307253 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr11:1307253C>T | c.589G>A | c.(589-591)Gtt>Att | p.V197I |
COADREAD | 11 | 1311498 | 1311498 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr11:1311498G>A | c.325C>T | c.(325-327)Ccc>Tcc | p.P109S |
COADREAD | 11 | 1316949 | 1316949 | + | Missense_Mutation | SNP | C | C | T | TCGA-CK-4947-01B-11D-1650-10 | TCGA-CK-4947-10A-01D-1650-10 | g.chr11:1316949C>T | c.109G>A | c.(109-111)Gcc>Acc | p.A37T |
COADREAD | 11 | 1316984 | 1316984 | + | Missense_Mutation | SNP | G | G | A | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr11:1316984G>A | c.74C>T | c.(73-75)aCg>aTg | p.T25M |
ESCA | 11 | 1307298 | 1307298 | + | Missense_Mutation | SNP | G | G | A | TCGA-JY-A6FD-01A-11D-A33E-09 | TCGA-JY-A6FD-10A-01D-A33H-09 | g.chr11:1307298G>A | c.544C>T | c.(544-546)Cca>Tca | p.P182S |
GBMLGG | 11 | 1298448 | 1298448 | + | Missense_Mutation | SNP | C | C | T | TCGA-FG-A4MU-01B-11D-A289-08 | TCGA-FG-A4MU-10A-01D-A289-08 | g.chr11:1298448C>T | c.646G>A | c.(646-648)Gtg>Atg | p.V216M |
HNSC | 11 | 1298422 | 1298422 | + | Silent | SNP | G | G | A | TCGA-UF-A71E-01A-31D-A34J-08 | TCGA-UF-A71E-10B-01D-A34M-08 | g.chr11:1298422G>A | c.672C>T | c.(670-672)aaC>aaT | p.N224N |
HNSC | 11 | 1309866 | 1309866 | + | Silent | SNP | G | G | A | TCGA-CQ-5323-01A-01D-1683-08 | TCGA-CQ-5323-10A-01D-1683-08 | g.chr11:1309866G>A | c.507C>T | c.(505-507)gtC>gtT | p.V169V |
HNSC | 11 | 1309868 | 1309868 | + | Missense_Mutation | SNP | C | C | T | TCGA-TN-A7HL-01A-11D-A34J-08 | TCGA-TN-A7HL-10A-01D-A34M-08 | g.chr11:1309868C>T | c.505G>A | c.(505-507)Gtc>Atc | p.V169I |
HNSC | 11 | 1310007 | 1310007 | + | Splice_Site | SNP | C | C | T | TCGA-IQ-A61I-01A-11D-A30E-08 | TCGA-IQ-A61I-10A-01D-A30H-08 | g.chr11:1310007C>T | | c.e4-1 | |
LGG | 11 | 1298448 | 1298448 | + | Missense_Mutation | SNP | C | C | T | TCGA-FG-A4MU-01B-11D-A289-08 | TCGA-FG-A4MU-10A-01D-A289-08 | g.chr11:1298448C>T | c.646G>A | c.(646-648)Gtg>Atg | p.V216M |
LIHC | 11 | 1309926 | 1309926 | + | Silent | SNP | G | G | A | TCGA-GJ-A9DB-01A-11D-A36X-10 | TCGA-GJ-A9DB-10A-01D-A370-10 | g.chr11:1309926G>A | c.447C>T | c.(445-447)gaC>gaT | p.D149D |
LUAD | 11 | 1298328 | 1298328 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-3918-01A-01D-1105-08 | TCGA-44-3918-11A-01D-1105-08 | g.chr11:1298328G>T | c.766C>A | c.(766-768)Cag>Aag | p.Q256K |
LUAD | 11 | 1298461 | 1298461 | + | Silent | SNP | G | G | A | TCGA-L9-A444-01A-21D-A24D-08 | TCGA-L9-A444-10A-01D-A24F-08 | g.chr11:1298461G>A | c.633C>T | c.(631-633)ccC>ccT | p.P211P |
LUAD | 11 | 1311491 | 1311491 | + | Missense_Mutation | SNP | C | C | T | TCGA-53-7624-01A-11D-2063-08 | TCGA-53-7624-10A-01D-2063-08 | g.chr11:1311491C>T | c.332G>A | c.(331-333)gGc>gAc | p.G111D |
LUAD | 11 | 1316878 | 1316878 | + | Silent | SNP | T | T | C | TCGA-91-6831-01A-11D-1855-08 | TCGA-91-6831-11A-02D-1855-08 | g.chr11:1316878T>C | c.180A>G | c.(178-180)gtA>gtG | p.V60V |
LUSC | 11 | 1311618 | 1311618 | + | Missense_Mutation | SNP | C | C | T | TCGA-18-3406-01A-01D-0983-08 | TCGA-18-3406-11A-01D-0983-08 | g.chr11:1311618C>T | c.205G>A | c.(205-207)Ggc>Agc | p.G69S |
SARC | 11 | 1311571 | 1311571 | + | Silent | SNP | C | C | T | TCGA-UE-A6QU-01A-12D-A32I-09 | TCGA-UE-A6QU-10B-01D-A32I-09 | g.chr11:1311571C>T | c.252G>A | c.(250-252)gcG>gcA | p.A84A |
SKCM | 11 | 1311530 | 1311530 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr11:1311530G>A | c.293C>T | c.(292-294)cCc>cTc | p.P98L |