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 | 15 | 76165889 | 76165889 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-AA6S-01A-21D-A391-08 | TCGA-DK-AA6S-10A-01D-A394-08 | g.chr15:76165889C>G | c.568C>G | c.(568-570)Caa>Gaa | p.Q190E |
BLCA | 15 | 76171500 | 76171500 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9T0-01A-11D-A391-08 | TCGA-XF-A9T0-10A-01D-A394-08 | g.chr15:76171500G>A | c.796G>A | c.(796-798)Gaa>Aaa | p.E266K |
BLCA | 15 | 76175762 | 76175762 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9T0-01A-11D-A391-08 | TCGA-XF-A9T0-10A-01D-A394-08 | g.chr15:76175762G>A | c.881G>A | c.(880-882)gGa>gAa | p.G294E |
BRCA | 15 | 76146749 | 76146749 | + | Missense_Mutation | SNP | C | C | T | TCGA-A8-A09B-01A-11W-A019-09 | TCGA-A8-A09B-10A-01W-A021-09 | g.chr15:76146749C>T | c.203C>T | c.(202-204)cCg>cTg | p.P68L |
BRCA | 15 | 76152225 | 76152225 | + | Missense_Mutation | SNP | C | C | G | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr15:76152225C>G | c.289C>G | c.(289-291)Cag>Gag | p.Q97E |
CESC | 15 | 76136055 | 76136055 | + | Missense_Mutation | SNP | C | C | G | TCGA-IR-A3LA-01A-11D-A22X-09 | TCGA-IR-A3LA-10A-01D-A22X-09 | g.chr15:76136055C>G | c.48C>G | c.(46-48)atC>atG | p.I16M |
CHOL | 15 | 76183298 | 76183298 | + | Missense_Mutation | SNP | G | G | A | TCGA-3X-AAVE-01A-11D-A417-09 | TCGA-3X-AAVE-10A-01D-A41A-09 | g.chr15:76183298G>A | c.972G>A | c.(970-972)atG>atA | p.M324I |
COAD | 15 | 76152223 | 76152223 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr15:76152223G>A | c.287G>A | c.(286-288)cGt>cAt | p.R96H |
COAD | 15 | 76152223 | 76152223 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:76152223G>A | c.287G>A | c.(286-288)cGt>cAt | p.R96H |
COAD | 15 | 76161348 | 76161348 | + | Silent | SNP | T | T | C | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr15:76161348T>C | c.444T>C | c.(442-444)gcT>gcC | p.A148A |
COADREAD | 15 | 76152223 | 76152223 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr15:76152223G>A | c.287G>A | c.(286-288)cGt>cAt | p.R96H |
COADREAD | 15 | 76152223 | 76152223 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr15:76152223G>A | c.287G>A | c.(286-288)cGt>cAt | p.R96H |
COADREAD | 15 | 76161348 | 76161348 | + | Silent | SNP | T | T | C | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr15:76161348T>C | c.444T>C | c.(442-444)gcT>gcC | p.A148A |
DLBC | 15 | 76161328 | 76161330 | + | In_Frame_Del | DEL | GAA | GAA | - | TCGA-GS-A9U3-01A-11D-A38X-10 | TCGA-GS-A9U3-10A-01D-A38X-10 | g.chr15:76161328_76161330delGAA | c.424_426delGAA | c.(424-426)gaadel | p.E146del |
GBMLGG | 15 | 76165893 | 76165893 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:76165893G>T | c.572G>T | c.(571-573)aGg>aTg | p.R191M |
HNSC | 15 | 76171514 | 76171514 | + | Silent | SNP | T | T | G | TCGA-CR-7402-01A-11D-2012-08 | TCGA-CR-7402-10A-01D-2013-08 | g.chr15:76171514T>G | c.810T>G | c.(808-810)ctT>ctG | p.L270L |
HNSC | 15 | 76183295 | 76183295 | + | Silent | SNP | C | C | T | TCGA-F7-A50J-01A-21D-A28R-08 | TCGA-F7-A50J-10A-01D-A28U-08 | g.chr15:76183295C>T | c.969C>T | c.(967-969)atC>atT | p.I323I |
LGG | 15 | 76165893 | 76165893 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:76165893G>T | c.572G>T | c.(571-573)aGg>aTg | p.R191M |
LIHC | 15 | 76152229 | 76152229 | + | Missense_Mutation | SNP | A | A | T | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr15:76152229A>T | c.293A>T | c.(292-294)cAa>cTa | p.Q98L |
LIHC | 15 | 76165791 | 76165791 | + | Missense_Mutation | SNP | A | A | G | TCGA-CC-A3M9-01A-11D-A20W-10 | TCGA-CC-A3M9-10A-01D-A20W-10 | g.chr15:76165791A>G | c.470A>G | c.(469-471)tAt>tGt | p.Y157C |
LIHC | 15 | 76183289 | 76183289 | + | Silent | SNP | G | G | C | TCGA-DD-AACZ-01A-11D-A40R-10 | TCGA-DD-AACZ-10A-01D-A40U-10 | g.chr15:76183289G>C | c.963G>C | c.(961-963)tcG>tcC | p.S321S |
LIHC | 15 | 76183352 | 76183352 | + | Silent | SNP | T | T | C | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr15:76183352T>C | c.1026T>C | c.(1024-1026)aaT>aaC | p.N342N |
LIHC | 15 | 76191767 | 76191767 | + | Splice_Site | SNP | G | G | A | TCGA-2Y-A9GZ-01A-11D-A38X-10 | TCGA-2Y-A9GZ-10A-01D-A38X-10 | g.chr15:76191767G>A | | c.e13-1 | |
LUAD | 15 | 76152291 | 76152291 | + | Missense_Mutation | SNP | G | G | C | TCGA-95-7043-01A-11D-1945-08 | TCGA-95-7043-10A-01D-1946-08 | g.chr15:76152291G>C | c.355G>C | c.(355-357)Gag>Cag | p.E119Q |
LUAD | 15 | 76161303 | 76161305 | + | In_Frame_Del | DEL | AGA | AGA | - | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr15:76161303_76161305delAGA | c.399_401delAGA | c.(397-402)acagaa>aca | p.E135del |
LUAD | 15 | 76165798 | 76165798 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-6982-01A-11D-1945-08 | TCGA-55-6982-11A-01D-1945-08 | g.chr15:76165798G>A | c.477G>A | c.(475-477)atG>atA | p.M159I |
LUAD | 15 | 76168529 | 76168529 | + | Splice_Site | SNP | G | G | T | TCGA-99-8028-01A-11D-2238-08 | TCGA-99-8028-10A-01D-2238-08 | g.chr15:76168529G>T | c.590G>T | c.(589-591)gGt>gTt | p.G197V |
LUAD | 15 | 76168549 | 76168549 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-50-5933-01A-11D-1753-08 | TCGA-50-5933-11A-01D-1753-08 | g.chr15:76168549C>T | c.610C>T | c.(610-612)Caa>Taa | p.Q204* |
LUAD | 15 | 76168613 | 76168613 | + | Splice_Site | SNP | G | G | A | TCGA-91-6829-01A-21D-1855-08 | TCGA-91-6829-11A-01D-1855-08 | g.chr15:76168613G>A | | c.e6+1 | |
LUSC | 15 | 76152255 | 76152255 | + | Missense_Mutation | SNP | T | T | C | TCGA-18-3408-01A-01D-0983-08 | TCGA-18-3408-11A-01D-0983-08 | g.chr15:76152255T>C | c.319T>C | c.(319-321)Tgc>Cgc | p.C107R |
OV | 15 | 76165768 | 76165768 | + | Splice_Site | SNP | G | G | T | TCGA-13-1501-01A-01W-0545-08 | TCGA-13-1501-10A-01W-0546-08 | g.chr15:76165768G>T | | c.e5-1 | |
OV | 15 | 76175727 | 76175727 | + | Silent | SNP | T | T | C | TCGA-29-2431-01A-01D-1526-09 | TCGA-29-2431-10A-01D-1526-09 | g.chr15:76175727T>C | c.846T>C | c.(844-846)ccT>ccC | p.P282P |
OV | 15 | 76191783 | 76191783 | + | Missense_Mutation | SNP | C | C | G | TCGA-25-1313-01A-01W-0492-08 | TCGA-25-1313-10A-01W-0492-08 | g.chr15:76191783C>G | c.1112C>G | c.(1111-1113)cCa>cGa | p.P371R |
SKCM | 15 | 76146731 | 76146731 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3TV-06A-11D-A23B-08 | TCGA-FW-A3TV-10A-01D-A23B-08 | g.chr15:76146731C>T | c.185C>T | c.(184-186)tCc>tTc | p.S62F |
SKCM | 15 | 76175716 | 76175716 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AC-06A-11D-A196-08 | TCGA-EE-A3AC-10A-01D-A198-08 | g.chr15:76175716C>T | c.835C>T | c.(835-837)Cca>Tca | p.P279S |
SKCM | 15 | 76175737 | 76175737 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr15:76175737C>T | c.856C>T | c.(856-858)Cga>Tga | p.R286* |
SKCM | 15 | 76191779 | 76191779 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A51R-06A-11D-A25O-08 | TCGA-D3-A51R-10A-01D-A25O-08 | g.chr15:76191779C>T | c.1108C>T | c.(1108-1110)Cct>Tct | p.P370S |