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 | 8 | 124516888 | 124516888 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A3X1-01A-12D-A22Z-08 | TCGA-DK-A3X1-10A-01D-A22Z-08 | g.chr8:124516888C>G | c.934G>C | c.(934-936)Gat>Cat | p.D312H |
BLCA | 8 | 124525536 | 124525536 | + | Missense_Mutation | SNP | C | C | T | TCGA-UY-A9PD-01A-11D-A38G-08 | TCGA-UY-A9PD-10A-01D-A38J-08 | g.chr8:124525536C>T | c.553G>A | c.(553-555)Ggc>Agc | p.G185S |
BLCA | 8 | 124525576 | 124525576 | + | Silent | SNP | C | C | T | TCGA-ZF-A9RC-01A-11D-A38G-08 | TCGA-ZF-A9RC-10A-01D-A38J-08 | g.chr8:124525576C>T | c.513G>A | c.(511-513)caG>caA | p.Q171Q |
BLCA | 8 | 124553195 | 124553195 | + | Silent | SNP | G | G | A | TCGA-KQ-A41R-01A-21D-A34U-08 | TCGA-KQ-A41R-10G-01D-A34X-08 | g.chr8:124553195G>A | c.60C>T | c.(58-60)gaC>gaT | p.D20D |
BRCA | 8 | 124518725 | 124518725 | + | Silent | SNP | G | G | T | TCGA-B6-A0I1-01A-11D-A21Q-09 | TCGA-B6-A0I1-10A-01D-A21Q-09 | g.chr8:124518725G>T | c.741C>A | c.(739-741)gtC>gtA | p.V247V |
BRCA | 8 | 124526556 | 124526556 | + | Silent | SNP | T | T | C | TCGA-D8-A1JC-01A-11D-A13L-09 | TCGA-D8-A1JC-10A-01D-A13O-09 | g.chr8:124526556T>C | c.390A>G | c.(388-390)gcA>gcG | p.A130A |
BRCA | 8 | 124544170 | 124544170 | + | Missense_Mutation | SNP | G | G | C | TCGA-EW-A1J5-01A-11D-A13L-09 | TCGA-EW-A1J5-10A-01D-A13O-09 | g.chr8:124544170G>C | c.340C>G | c.(340-342)Ctg>Gtg | p.L114V |
CESC | 8 | 124516928 | 124516928 | + | Missense_Mutation | SNP | G | G | C | TCGA-WL-A834-01A-11D-A351-09 | TCGA-WL-A834-10A-01D-A351-09 | g.chr8:124516928G>C | c.894C>G | c.(892-894)ttC>ttG | p.F298L |
COAD | 8 | 124515668 | 124515668 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6898-01A-11D-1924-10 | TCGA-D5-6898-10A-01D-1924-10 | g.chr8:124515668T>C | c.1013A>G | c.(1012-1014)gAg>gGg | p.E338G |
COAD | 8 | 124518759 | 124518759 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr8:124518759A>G | c.707T>C | c.(706-708)aTc>aCc | p.I236T |
COAD | 8 | 124525479 | 124525479 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr8:124525479G>T | c.610C>A | c.(610-612)Ctc>Atc | p.L204I |
COAD | 8 | 124525494 | 124525494 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr8:124525494G>A | c.595C>T | c.(595-597)Cgg>Tgg | p.R199W |
COAD | 8 | 124525568 | 124525568 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-A00E-01A-01W-A005-10 | TCGA-AA-A00E-10A-01W-A005-10 | g.chr8:124525568T>C | c.521A>G | c.(520-522)tAc>tGc | p.Y174C |
COAD | 8 | 124544146 | 124544146 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr8:124544146C>T | c.364G>A | c.(364-366)Gtg>Atg | p.V122M |
COAD | 8 | 124545463 | 124545464 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr8:124545463_124545464insT | c.246_247insA | c.(244-249)aaatggfs | p.W83fs |
COADREAD | 8 | 124515668 | 124515668 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6898-01A-11D-1924-10 | TCGA-D5-6898-10A-01D-1924-10 | g.chr8:124515668T>C | c.1013A>G | c.(1012-1014)gAg>gGg | p.E338G |
COADREAD | 8 | 124516969 | 124516969 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:124516969G>T | c.853C>A | c.(853-855)Ctg>Atg | p.L285M |
COADREAD | 8 | 124518759 | 124518759 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr8:124518759A>G | c.707T>C | c.(706-708)aTc>aCc | p.I236T |
COADREAD | 8 | 124525479 | 124525479 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr8:124525479G>T | c.610C>A | c.(610-612)Ctc>Atc | p.L204I |
COADREAD | 8 | 124525494 | 124525494 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr8:124525494G>A | c.595C>T | c.(595-597)Cgg>Tgg | p.R199W |
COADREAD | 8 | 124525568 | 124525568 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-A00E-01A-01W-A005-10 | TCGA-AA-A00E-10A-01W-A005-10 | g.chr8:124525568T>C | c.521A>G | c.(520-522)tAc>tGc | p.Y174C |
COADREAD | 8 | 124544146 | 124544146 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr8:124544146C>T | c.364G>A | c.(364-366)Gtg>Atg | p.V122M |
COADREAD | 8 | 124545463 | 124545464 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr8:124545463_124545464insT | c.246_247insA | c.(244-249)aaatggfs | p.W83fs |
GBM | 8 | 124518764 | 124518764 | + | Silent | SNP | C | C | T | TCGA-06-0130-01A-01D-1490-08 | TCGA-06-0130-10A-01D-1490-08 | g.chr8:124518764C>T | c.702G>A | c.(700-702)ctG>ctA | p.L234L |
GBMLGG | 8 | 124518764 | 124518764 | + | Silent | SNP | C | C | T | TCGA-06-0130-01A-01D-1490-08 | TCGA-06-0130-10A-01D-1490-08 | g.chr8:124518764C>T | c.702G>A | c.(700-702)ctG>ctA | p.L234L |
HNSC | 8 | 124515703 | 124515703 | + | Splice_Site | SNP | C | C | A | TCGA-UF-A7JV-01A-11D-A34J-08 | TCGA-UF-A7JV-10A-01D-A34M-08 | g.chr8:124515703C>A | | c.e9-1 | |
HNSC | 8 | 124526525 | 124526525 | + | Missense_Mutation | SNP | C | C | T | TCGA-CX-7086-01A-11D-2078-08 | TCGA-CX-7086-10D-01D-2078-08 | g.chr8:124526525C>T | c.421G>A | c.(421-423)Gcc>Acc | p.A141T |
LIHC | 8 | 124553194 | 124553194 | + | Missense_Mutation | SNP | C | C | T | TCGA-CC-A7IJ-01A-11D-A33Q-10 | TCGA-CC-A7IJ-10A-01D-A33Q-10 | g.chr8:124553194C>T | c.61G>A | c.(61-63)Ggc>Agc | p.G21S |
LUAD | 8 | 124546959 | 124546959 | + | Missense_Mutation | SNP | C | C | T | TCGA-44-7669-01A-21D-2063-08 | TCGA-44-7669-10A-01D-2063-08 | g.chr8:124546959C>T | c.212G>A | c.(211-213)aGc>aAc | p.S71N |
LUSC | 8 | 124546943 | 124546943 | + | Splice_Site | SNP | C | C | A | TCGA-85-6561-01A-11D-1817-08 | TCGA-85-6561-10A-01D-1817-08 | g.chr8:124546943C>A | c.228G>T | c.(226-228)caG>caT | p.Q76H |
LUSC | 8 | 124547001 | 124547001 | + | Missense_Mutation | SNP | T | T | C | TCGA-22-5473-01A-01D-1632-08 | TCGA-22-5473-11A-11D-1632-08 | g.chr8:124547001T>C | c.170A>G | c.(169-171)tAt>tGt | p.Y57C |
LUSC | 8 | 124553144 | 124553144 | + | Silent | SNP | G | G | A | TCGA-33-4583-01A-01D-1441-08 | TCGA-33-4583-11A-01D-1441-08 | g.chr8:124553144G>A | c.111C>T | c.(109-111)ctC>ctT | p.L37L |
LUSC | 8 | 124553156 | 124553156 | + | Silent | SNP | G | G | A | TCGA-37-3783-01A-01D-1267-08 | TCGA-37-3783-10A-01D-1267-08 | g.chr8:124553156G>A | c.99C>T | c.(97-99)ttC>ttT | p.F33F |
PCPG | 8 | 124526522 | 124526522 | + | Missense_Mutation | SNP | G | G | C | TCGA-QR-A705-01A-11D-A35D-08 | TCGA-QR-A705-10A-01D-A35B-08 | g.chr8:124526522G>C | c.424C>G | c.(424-426)Caa>Gaa | p.Q142E |
PRAD | 8 | 124547022 | 124547022 | + | Missense_Mutation | SNP | T | T | G | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr8:124547022T>G | c.149A>C | c.(148-150)aAt>aCt | p.N50T |
READ | 8 | 124516969 | 124516969 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:124516969G>T | c.853C>A | c.(853-855)Ctg>Atg | p.L285M |
SKCM | 8 | 124518738 | 124518738 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JL-06A-11D-A196-08 | TCGA-D3-A2JL-10A-01D-A198-08 | g.chr8:124518738C>T | c.728G>A | c.(727-729)gGg>gAg | p.G243E |
SKCM | 8 | 124518793 | 124518793 | + | Missense_Mutation | SNP | A | A | G | TCGA-EB-A5UL-06A-11D-A30X-08 | TCGA-EB-A5UL-10A-01D-A30X-08 | g.chr8:124518793A>G | c.673T>C | c.(673-675)Ttc>Ctc | p.F225L |
SKCM | 8 | 124518802 | 124518802 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A19N-06A-11D-A197-08 | TCGA-ER-A19N-10A-01D-A199-08 | g.chr8:124518802C>T | c.664G>A | c.(664-666)Ggc>Agc | p.G222S |
SKCM | 8 | 124553147 | 124553147 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr8:124553147G>A | c.108C>T | c.(106-108)gaC>gaT | p.D36D |
SKCM | 8 | 124553243 | 124553243 | + | Silent | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr8:124553243G>A | c.12C>T | c.(10-12)ctC>ctT | p.L4L |
SKCM | 8 | 124553245 | 124553245 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr8:124553245G>A | c.10C>T | c.(10-12)Ctc>Ttc | p.L4F |