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 | 6 | 83728704 | 83728704 | + | Missense_Mutation | SNP | C | C | T | TCGA-UY-A78K-01A-11D-A339-08 | TCGA-UY-A78K-10A-01D-A339-08 | g.chr6:83728704C>T | c.998G>A | c.(997-999)aGc>aAc | p.S333N |
BLCA | 6 | 83775419 | 83775419 | + | Missense_Mutation | SNP | C | C | T | TCGA-K4-A5RJ-01A-11D-A289-08 | TCGA-K4-A5RJ-10A-01D-A289-08 | g.chr6:83775419C>T | c.19G>A | c.(19-21)Gag>Aag | p.E7K |
BRCA | 6 | 83667047 | 83667047 | + | Missense_Mutation | SNP | C | C | T | TCGA-E2-A153-01A-12D-A12B-09 | TCGA-E2-A153-11A-31D-A12B-09 | g.chr6:83667047C>T | c.1133G>A | c.(1132-1134)cGt>cAt | p.R378H |
BRCA | 6 | 83728709 | 83728709 | + | Silent | SNP | G | G | A | TCGA-AR-A256-01A-11D-A167-09 | TCGA-AR-A256-10A-01D-A167-09 | g.chr6:83728709G>A | c.993C>T | c.(991-993)atC>atT | p.I331I |
BRCA | 6 | 83732240 | 83732240 | + | Missense_Mutation | SNP | G | G | T | TCGA-AC-A2QJ-01A-12D-A19Y-09 | TCGA-AC-A2QJ-11A-12D-A19Y-09 | g.chr6:83732240G>T | c.778C>A | c.(778-780)Cag>Aag | p.Q260K |
BRCA | 6 | 83767586 | 83767586 | + | Missense_Mutation | SNP | C | C | T | TCGA-A8-A06O-01A-11W-A019-09 | TCGA-A8-A06O-10A-01W-A021-09 | g.chr6:83767586C>T | c.233G>A | c.(232-234)gGa>gAa | p.G78E |
CESC | 6 | 83732175 | 83732175 | + | Missense_Mutation | SNP | G | G | C | TCGA-BI-A0VR-01A-11D-A10S-08 | TCGA-BI-A0VR-10A-01D-A10S-08 | g.chr6:83732175G>C | c.843C>G | c.(841-843)atC>atG | p.I281M |
CESC | 6 | 83767592 | 83767592 | + | Missense_Mutation | SNP | C | C | G | TCGA-EK-A3GK-01A-11D-A20U-09 | TCGA-EK-A3GK-10A-01D-A20U-09 | g.chr6:83767592C>G | c.227G>C | c.(226-228)gGa>gCa | p.G76A |
CHOL | 6 | 83667047 | 83667047 | + | Missense_Mutation | SNP | C | C | T | TCGA-W5-AA39-01A-11D-A417-09 | TCGA-W5-AA39-10A-01D-A41A-09 | g.chr6:83667047C>T | c.1133G>A | c.(1132-1134)cGt>cAt | p.R378H |
COAD | 6 | 83667051 | 83667051 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr6:83667051G>A | c.1129C>T | c.(1129-1131)Cgc>Tgc | p.R377C |
COAD | 6 | 83667114 | 83667114 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6625-01A-21D-1771-10 | TCGA-G4-6625-11A-01D-1771-10 | g.chr6:83667114C>T | c.1066G>A | c.(1066-1068)Gca>Aca | p.A356T |
COAD | 6 | 83733743 | 83733743 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr6:83733743A>G | c.682T>C | c.(682-684)Tat>Cat | p.Y228H |
COAD | 6 | 83754183 | 83754183 | + | Silent | SNP | C | C | T | TCGA-AA-3554-01A-01W-0833-10 | TCGA-AA-3554-10A-01W-0833-10 | g.chr6:83754183C>T | c.561G>A | c.(559-561)gaG>gaA | p.E187E |
COAD | 6 | 83754213 | 83754213 | + | Missense_Mutation | SNP | C | C | A | TCGA-F4-6703-01A-11D-1835-10 | TCGA-F4-6703-10A-01D-1835-10 | g.chr6:83754213C>A | c.531G>T | c.(529-531)tgG>tgT | p.W177C |
COAD | 6 | 83754351 | 83754351 | + | Silent | SNP | C | C | T | TCGA-AY-5543-01A-01D-1650-10 | TCGA-AY-5543-10A-01D-1650-10 | g.chr6:83754351C>T | c.393G>A | c.(391-393)ccG>ccA | p.P131P |
COAD | 6 | 83767641 | 83767641 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr6:83767641C>T | c.178G>A | c.(178-180)Gag>Aag | p.E60K |
COAD | 6 | 83767664 | 83767664 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00E-01A-01W-A005-10 | TCGA-AA-A00E-10A-01W-A005-10 | g.chr6:83767664C>T | c.155G>A | c.(154-156)tGc>tAc | p.C52Y |
COAD | 6 | 83767698 | 83767698 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-3809-01A-01W-0995-10 | TCGA-A6-3809-11A-01W-0995-10 | g.chr6:83767698G>A | c.121C>T | c.(121-123)Cca>Tca | p.P41S |
COADREAD | 6 | 83667051 | 83667051 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr6:83667051G>A | c.1129C>T | c.(1129-1131)Cgc>Tgc | p.R377C |
COADREAD | 6 | 83667113 | 83667113 | + | Missense_Mutation | SNP | G | G | T | TCGA-EI-6506-01A-11D-1733-10 | TCGA-EI-6506-10A-01D-1733-10 | g.chr6:83667113G>T | c.1067C>A | c.(1066-1068)gCa>gAa | p.A356E |
COADREAD | 6 | 83667114 | 83667114 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6625-01A-21D-1771-10 | TCGA-G4-6625-11A-01D-1771-10 | g.chr6:83667114C>T | c.1066G>A | c.(1066-1068)Gca>Aca | p.A356T |
COADREAD | 6 | 83733743 | 83733743 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr6:83733743A>G | c.682T>C | c.(682-684)Tat>Cat | p.Y228H |
COADREAD | 6 | 83754183 | 83754183 | + | Silent | SNP | C | C | T | TCGA-AA-3554-01A-01W-0833-10 | TCGA-AA-3554-10A-01W-0833-10 | g.chr6:83754183C>T | c.561G>A | c.(559-561)gaG>gaA | p.E187E |
COADREAD | 6 | 83754213 | 83754213 | + | Missense_Mutation | SNP | C | C | A | TCGA-F4-6703-01A-11D-1835-10 | TCGA-F4-6703-10A-01D-1835-10 | g.chr6:83754213C>A | c.531G>T | c.(529-531)tgG>tgT | p.W177C |
COADREAD | 6 | 83754351 | 83754351 | + | Silent | SNP | C | C | T | TCGA-AY-5543-01A-01D-1650-10 | TCGA-AY-5543-10A-01D-1650-10 | g.chr6:83754351C>T | c.393G>A | c.(391-393)ccG>ccA | p.P131P |
COADREAD | 6 | 83763888 | 83763888 | + | Missense_Mutation | SNP | C | C | G | TCGA-AG-3609-01A-02W-0833-10 | TCGA-AG-3609-10A-01W-0833-10 | g.chr6:83763888C>G | c.344G>C | c.(343-345)gGt>gCt | p.G115A |
COADREAD | 6 | 83767641 | 83767641 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr6:83767641C>T | c.178G>A | c.(178-180)Gag>Aag | p.E60K |
COADREAD | 6 | 83767664 | 83767664 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00E-01A-01W-A005-10 | TCGA-AA-A00E-10A-01W-A005-10 | g.chr6:83767664C>T | c.155G>A | c.(154-156)tGc>tAc | p.C52Y |
COADREAD | 6 | 83767698 | 83767698 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-3809-01A-01W-0995-10 | TCGA-A6-3809-11A-01W-0995-10 | g.chr6:83767698G>A | c.121C>T | c.(121-123)Cca>Tca | p.P41S |
ESCA | 6 | 83732246 | 83732246 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A88Z-01A-11D-A36J-09 | TCGA-L5-A88Z-11A-11D-A36M-09 | g.chr6:83732246G>T | c.772C>A | c.(772-774)Ctg>Atg | p.L258M |
ESCA | 6 | 83732251 | 83732251 | + | Missense_Mutation | SNP | T | T | C | TCGA-VR-AA7I-01A-11D-A403-09 | TCGA-VR-AA7I-10A-01D-A403-09 | g.chr6:83732251T>C | c.767A>G | c.(766-768)cAg>cGg | p.Q256R |
GBM | 6 | 83728822 | 83728822 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-06-0238-01A-02D-1492-08 | TCGA-06-0238-10A-01D-1492-08 | g.chr6:83728822delC | c.880delG | c.(880-882)gaafs | p.E294fs |
GBMLGG | 6 | 83667135 | 83667135 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:83667135G>T | c.1045C>A | c.(1045-1047)Cac>Aac | p.H349N |
GBMLGG | 6 | 83728822 | 83728822 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-06-0238-01A-02D-1492-08 | TCGA-06-0238-10A-01D-1492-08 | g.chr6:83728822delC | c.880delG | c.(880-882)gaafs | p.E294fs |
HNSC | 6 | 83748144 | 83748144 | + | Missense_Mutation | SNP | C | C | A | TCGA-P3-A6SX-01A-11D-A34J-08 | TCGA-P3-A6SX-10A-01D-A34M-08 | g.chr6:83748144C>A | c.658G>T | c.(658-660)Gtg>Ttg | p.V220L |
HNSC | 6 | 83748144 | 83748144 | + | Missense_Mutation | SNP | C | C | G | TCGA-BB-A5HZ-01A-21D-A28R-08 | TCGA-BB-A5HZ-10A-01D-A28U-08 | g.chr6:83748144C>G | c.658G>C | c.(658-660)Gtg>Ctg | p.V220L |
HNSC | 6 | 83767585 | 83767585 | + | Silent | SNP | T | T | G | TCGA-F7-7848-01A-11D-2129-08 | TCGA-F7-7848-10A-01D-2129-08 | g.chr6:83767585T>G | c.234A>C | c.(232-234)ggA>ggC | p.G78G |
KIPAN | 6 | 83767555 | 83767555 | + | Missense_Mutation | SNP | T | T | G | TCGA-P4-A5EB-01A-11D-A28G-10 | TCGA-P4-A5EB-11A-11D-A28G-10 | g.chr6:83767555T>G | c.264A>C | c.(262-264)aaA>aaC | p.K88N |
KIPAN | 6 | 83767689 | 83767689 | + | Missense_Mutation | SNP | G | G | A | TCGA-4A-A93X-01A-11D-A36X-10 | TCGA-4A-A93X-10A-01D-A370-10 | g.chr6:83767689G>A | c.130C>T | c.(130-132)Ctc>Ttc | p.L44F |
KIRP | 6 | 83767555 | 83767555 | + | Missense_Mutation | SNP | T | T | G | TCGA-P4-A5EB-01A-11D-A28G-10 | TCGA-P4-A5EB-11A-11D-A28G-10 | g.chr6:83767555T>G | c.264A>C | c.(262-264)aaA>aaC | p.K88N |
KIRP | 6 | 83767689 | 83767689 | + | Missense_Mutation | SNP | G | G | A | TCGA-4A-A93X-01A-11D-A36X-10 | TCGA-4A-A93X-10A-01D-A370-10 | g.chr6:83767689G>A | c.130C>T | c.(130-132)Ctc>Ttc | p.L44F |
LGG | 6 | 83667135 | 83667135 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:83667135G>T | c.1045C>A | c.(1045-1047)Cac>Aac | p.H349N |
LIHC | 6 | 83667146 | 83667146 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-A1EG-01A-11D-A20W-10 | TCGA-DD-A1EG-10A-01D-A20W-10 | g.chr6:83667146T>C | c.1034A>G | c.(1033-1035)gAc>gGc | p.D345G |
LIHC | 6 | 83728705 | 83728705 | + | Missense_Mutation | SNP | T | T | C | TCGA-BD-A3ER-01A-11D-A20W-10 | TCGA-BD-A3ER-11A-11D-A20W-10 | g.chr6:83728705T>C | c.997A>G | c.(997-999)Agc>Ggc | p.S333G |
LIHC | 6 | 83733743 | 83733743 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-DD-A39Y-01A-11D-A20W-10 | TCGA-DD-A39Y-11A-11D-A20W-10 | g.chr6:83733743delA | c.682delT | c.(682-684)tatfs | p.Y228fs |
LUAD | 6 | 83732221 | 83732221 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8094-01A-11D-2238-08 | TCGA-55-8094-10A-01D-2238-08 | g.chr6:83732221C>T | c.797G>A | c.(796-798)aGc>aAc | p.S266N |
LUAD | 6 | 83732233 | 83732233 | + | Missense_Mutation | SNP | G | G | C | TCGA-MP-A4TI-01A-21D-A24P-08 | TCGA-MP-A4TI-10A-01D-A24P-08 | g.chr6:83732233G>C | c.785C>G | c.(784-786)tCc>tGc | p.S262C |
LUAD | 6 | 83732261 | 83732261 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr6:83732261C>A | c.757G>T | c.(757-759)Gtg>Ttg | p.V253L |
LUAD | 6 | 83733734 | 83733734 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-49-6743-01A-11D-1855-08 | TCGA-49-6743-11A-01D-1855-08 | g.chr6:83733734C>A | c.691G>T | c.(691-693)Gag>Tag | p.E231* |
LUAD | 6 | 83733741 | 83733741 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-49-6743-01A-11D-1855-08 | TCGA-49-6743-11A-01D-1855-08 | g.chr6:83733741A>T | c.684T>A | c.(682-684)taT>taA | p.Y228* |
LUAD | 6 | 83748197 | 83748197 | + | Missense_Mutation | SNP | T | T | A | TCGA-05-4405-01A-21D-1855-08 | TCGA-05-4405-10A-01D-1855-08 | g.chr6:83748197T>A | c.605A>T | c.(604-606)aAg>aTg | p.K202M |
LUAD | 6 | 83767714 | 83767714 | + | Missense_Mutation | SNP | C | C | T | TCGA-49-6745-01A-11D-1855-08 | TCGA-49-6745-11A-01D-1855-08 | g.chr6:83767714C>T | c.105G>A | c.(103-105)atG>atA | p.M35I |
LUAD | 6 | 83775392 | 83775392 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-67-3773-01A-01D-1040-01 | TCGA-67-3773-10A-01D-1489-08 | g.chr6:83775392C>A | c.46G>T | c.(46-48)Gga>Tga | p.G16* |
LUSC | 6 | 83732255 | 83732255 | + | Missense_Mutation | SNP | C | C | T | TCGA-33-6737-01A-11D-1817-08 | TCGA-33-6737-11A-01D-1817-08 | g.chr6:83732255C>T | c.763G>A | c.(763-765)Gcc>Acc | p.A255T |
LUSC | 6 | 83748153 | 83748153 | + | Missense_Mutation | SNP | C | C | T | TCGA-60-2719-01A-01D-1522-08 | TCGA-60-2719-11A-01D-1522-08 | g.chr6:83748153C>T | c.649G>A | c.(649-651)Gga>Aga | p.G217R |
LUSC | 6 | 83748181 | 83748181 | + | Silent | SNP | T | T | C | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr6:83748181T>C | c.621A>G | c.(619-621)gtA>gtG | p.V207V |
LUSC | 6 | 83754351 | 83754351 | + | Silent | SNP | C | C | A | TCGA-85-6561-01A-11D-1817-08 | TCGA-85-6561-10A-01D-1817-08 | g.chr6:83754351C>A | c.393G>T | c.(391-393)ccG>ccT | p.P131P |
OV | 6 | 83667113 | 83667113 | + | Missense_Mutation | SNP | G | G | A | TCGA-61-2002-01A-01W-0722-08 | TCGA-61-2002-11A-01W-0722-08 | g.chr6:83667113G>A | c.1067C>T | c.(1066-1068)gCa>gTa | p.A356V |
PAAD | 6 | 83754249 | 83754249 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr6:83754249G>T | c.495C>A | c.(493-495)gaC>gaA | p.D165E |
READ | 6 | 83667113 | 83667113 | + | Missense_Mutation | SNP | G | G | T | TCGA-EI-6506-01A-11D-1733-10 | TCGA-EI-6506-10A-01D-1733-10 | g.chr6:83667113G>T | c.1067C>A | c.(1066-1068)gCa>gAa | p.A356E |
READ | 6 | 83763888 | 83763888 | + | Missense_Mutation | SNP | C | C | G | TCGA-AG-3609-01A-02W-0833-10 | TCGA-AG-3609-10A-01W-0833-10 | g.chr6:83763888C>G | c.344G>C | c.(343-345)gGt>gCt | p.G115A |
SARC | 6 | 83667038 | 83667038 | + | Missense_Mutation | SNP | G | G | A | TCGA-DX-AB2E-01A-11D-A38Z-09 | TCGA-DX-AB2E-10A-01D-A38Z-09 | g.chr6:83667038G>A | c.1142C>T | c.(1141-1143)tCc>tTc | p.S381F |
SKCM | 6 | 83667048 | 83667048 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1I4-06A-11D-A196-08 | TCGA-DA-A1I4-10A-01D-A198-08 | g.chr6:83667048G>A | c.1132C>T | c.(1132-1134)Cgt>Tgt | p.R378C |
SKCM | 6 | 83728787 | 83728787 | + | Silent | SNP | G | G | A | TCGA-D3-A5GO-06A-12D-A27K-08 | TCGA-D3-A5GO-10A-01D-A27N-08 | g.chr6:83728787G>A | c.915C>T | c.(913-915)ttC>ttT | p.F305F |
SKCM | 6 | 83728787 | 83728787 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr6:83728787G>A | c.915C>T | c.(913-915)ttC>ttT | p.F305F |
SKCM | 6 | 83728796 | 83728796 | + | Silent | SNP | G | G | A | TCGA-DA-A1IC-06A-11D-A197-08 | TCGA-DA-A1IC-10A-01D-A199-08 | g.chr6:83728796G>A | c.906C>T | c.(904-906)atC>atT | p.I302I |
SKCM | 6 | 83733701 | 83733701 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29N-06A-12D-A197-08 | TCGA-EE-A29N-10A-01D-A199-08 | g.chr6:83733701G>A | c.724C>T | c.(724-726)Cct>Tct | p.P242S |
SKCM | 6 | 83754240 | 83754240 | + | Silent | SNP | G | G | A | TCGA-EB-A5UL-06A-11D-A30X-08 | TCGA-EB-A5UL-10A-01D-A30X-08 | g.chr6:83754240G>A | c.504C>T | c.(502-504)ttC>ttT | p.F168F |