| 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 |
|---|
| ACC | 6 | 43181477 | 43181477 | + | Missense_Mutation | SNP | C | C | G | TCGA-OR-A5L2-01A-11D-A30A-10 | TCGA-OR-A5L2-10A-01D-A30A-10 | g.chr6:43181477C>G | c.5515C>G | c.(5515-5517)Ccc>Gcc | p.P1839A |
| ACC | 6 | 43188511 | 43188511 | + | Silent | SNP | T | T | C | TCGA-OR-A5JH-01A-11D-A30A-10 | TCGA-OR-A5JH-10A-01D-A30A-10 | g.chr6:43188511T>C | c.6450T>C | c.(6448-6450)taT>taC | p.Y2150Y |
| BLCA | 6 | 43152208 | 43152208 | + | Missense_Mutation | SNP | G | G | C | TCGA-UY-A9PF-01A-11D-A38G-08 | TCGA-UY-A9PF-10A-01D-A38J-08 | g.chr6:43152208G>C | c.160G>C | c.(160-162)Ggt>Cgt | p.G54R |
| BLCA | 6 | 43152278 | 43152278 | + | Missense_Mutation | SNP | C | C | T | TCGA-BT-A3PK-01A-21D-A21Z-08 | TCGA-BT-A3PK-10A-01D-A21Z-08 | g.chr6:43152278C>T | c.230C>T | c.(229-231)cCt>cTt | p.P77L |
| BLCA | 6 | 43152561 | 43152561 | + | Silent | SNP | C | C | A | TCGA-E7-A5KE-01A-11D-A289-08 | TCGA-E7-A5KE-10A-01D-A289-08 | g.chr6:43152561C>A | c.513C>A | c.(511-513)ctC>ctA | p.L171L |
| BLCA | 6 | 43153711 | 43153711 | + | Missense_Mutation | SNP | T | T | C | TCGA-UY-A8OB-01A-12D-A42E-08 | TCGA-UY-A8OB-11A-12D-A42H-08 | g.chr6:43153711T>C | c.769T>C | c.(769-771)Ttc>Ctc | p.F257L |
| BLCA | 6 | 43154764 | 43154764 | + | Missense_Mutation | SNP | G | G | C | TCGA-2F-A9KO-01A-11D-A38G-08 | TCGA-2F-A9KO-11A-12D-A38J-08 | g.chr6:43154764G>C | c.1318G>C | c.(1318-1320)Gag>Cag | p.E440Q |
| BLCA | 6 | 43155601 | 43155601 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A20T-01A-11D-A14W-08 | TCGA-BT-A20T-11A-11D-A14W-08 | g.chr6:43155601G>A | c.1732G>A | c.(1732-1734)Gaa>Aaa | p.E578K |
| BLCA | 6 | 43155715 | 43155715 | + | Missense_Mutation | SNP | G | G | T | TCGA-4Z-AA81-01A-11D-A391-08 | TCGA-4Z-AA81-10A-01D-A394-08 | g.chr6:43155715G>T | c.1846G>T | c.(1846-1848)Gcc>Tcc | p.A616S |
| BLCA | 6 | 43156294 | 43156294 | + | Missense_Mutation | SNP | G | G | A | TCGA-C4-A0F7-01A-11D-A10S-08 | TCGA-C4-A0F7-10A-01D-A10S-08 | g.chr6:43156294G>A | c.2021G>A | c.(2020-2022)cGc>cAc | p.R674H |
| BLCA | 6 | 43156401 | 43156401 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-A1AB-01A-11D-A13W-08 | TCGA-DK-A1AB-10A-01D-A13W-08 | g.chr6:43156401G>C | c.2128G>C | c.(2128-2130)Gag>Cag | p.E710Q |
| BLCA | 6 | 43156452 | 43156452 | + | Splice_Site | SNP | A | A | C | TCGA-FD-A3N5-01A-11D-A21A-08 | TCGA-FD-A3N5-10A-01D-A21A-08 | g.chr6:43156452A>C | c.2179A>C | c.(2179-2181)Aga>Cga | p.R727R |
| BLCA | 6 | 43160845 | 43160845 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-AA4R-01A-11D-A38G-08 | TCGA-ZF-AA4R-10A-01D-A38J-08 | g.chr6:43160845G>A | c.2287G>A | c.(2287-2289)Gag>Aag | p.E763K |
| BLCA | 6 | 43160906 | 43160906 | + | Missense_Mutation | SNP | A | A | G | TCGA-LC-A66R-01A-41D-A30E-08 | TCGA-LC-A66R-10A-01D-A30H-08 | g.chr6:43160906A>G | c.2348A>G | c.(2347-2349)gAa>gGa | p.E783G |
| BLCA | 6 | 43163948 | 43163948 | + | Missense_Mutation | SNP | G | G | C | TCGA-UY-A78L-01A-12D-A339-08 | TCGA-UY-A78L-10A-01D-A339-08 | g.chr6:43163948G>C | c.2530G>C | c.(2530-2532)Gag>Cag | p.E844Q |
| BLCA | 6 | 43164002 | 43164002 | + | Splice_Site | SNP | G | G | T | TCGA-E5-A4TZ-01A-11D-A31L-08 | TCGA-E5-A4TZ-10B-01D-A31J-08 | g.chr6:43164002G>T | c.2584G>T | c.(2584-2586)Ggg>Tgg | p.G862W |
| BLCA | 6 | 43171253 | 43171253 | + | Silent | SNP | C | C | G | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr6:43171253C>G | c.3948C>G | c.(3946-3948)ctC>ctG | p.L1316L |
| BLCA | 6 | 43172787 | 43172787 | + | Silent | SNP | C | C | T | TCGA-G2-A2EO-01A-11D-A17V-08 | TCGA-G2-A2EO-11A-21D-A17V-08 | g.chr6:43172787C>T | c.4566C>T | c.(4564-4566)ttC>ttT | p.F1522F |
| BLCA | 6 | 43173108 | 43173108 | + | Silent | SNP | C | C | T | TCGA-K4-A83P-01A-11D-A34U-08 | TCGA-K4-A83P-10A-01D-A34X-08 | g.chr6:43173108C>T | c.4740C>T | c.(4738-4740)ccC>ccT | p.P1580P |
| BLCA | 6 | 43174208 | 43174208 | + | Silent | SNP | C | C | T | TCGA-BL-A13I-01A-11D-A13W-08 | TCGA-BL-A13I-11A-11D-A13W-08 | g.chr6:43174208C>T | c.5172C>T | c.(5170-5172)ttC>ttT | p.F1724F |
| BLCA | 6 | 43181188 | 43181188 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-A1AC-01A-11D-A13W-08 | TCGA-DK-A1AC-10A-01D-A13W-08 | g.chr6:43181188G>C | c.5371G>C | c.(5371-5373)Gag>Cag | p.E1791Q |
| BLCA | 6 | 43181255 | 43181255 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A3IQ-01A-31D-A20D-08 | TCGA-DK-A3IQ-10A-01D-A20D-08 | g.chr6:43181255C>T | c.5438C>T | c.(5437-5439)tCa>tTa | p.S1813L |
| BLCA | 6 | 43184043 | 43184043 | + | Missense_Mutation | SNP | G | G | C | TCGA-GU-A767-01A-11D-A32B-08 | TCGA-GU-A767-10A-01D-A329-08 | g.chr6:43184043G>C | c.6084G>C | c.(6082-6084)ttG>ttC | p.L2028F |
| BLCA | 6 | 43184229 | 43184229 | + | Missense_Mutation | SNP | C | C | G | TCGA-GU-A766-01A-11D-A32B-08 | TCGA-GU-A766-10A-01D-A329-08 | g.chr6:43184229C>G | c.6270C>G | c.(6268-6270)caC>caG | p.H2090Q |
| BLCA | 6 | 43188499 | 43188499 | + | Silent | SNP | C | C | G | TCGA-KQ-A41N-01A-11D-A339-08 | TCGA-KQ-A41N-10D-01D-A339-08 | g.chr6:43188499C>G | c.6438C>G | c.(6436-6438)ctC>ctG | p.L2146L |
| BLCA | 6 | 43189453 | 43189453 | + | Silent | SNP | C | C | T | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chr6:43189453C>T | c.6783C>T | c.(6781-6783)ttC>ttT | p.F2261F |
| BLCA | 6 | 43189468 | 43189468 | + | Silent | SNP | C | C | T | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chr6:43189468C>T | c.6798C>T | c.(6796-6798)ctC>ctT | p.L2266L |
| BLCA | 6 | 43190340 | 43190340 | + | Silent | SNP | C | C | T | TCGA-DK-A1AC-01A-11D-A13W-08 | TCGA-DK-A1AC-10A-01D-A13W-08 | g.chr6:43190340C>T | c.6993C>T | c.(6991-6993)ttC>ttT | p.F2331F |
| BLCA | 6 | 43190562 | 43190562 | + | Missense_Mutation | SNP | G | G | C | TCGA-K4-A54R-01A-11D-A26M-08 | TCGA-K4-A54R-10A-01D-A26K-08 | g.chr6:43190562G>C | c.7078G>C | c.(7078-7080)Gag>Cag | p.E2360Q |
| BLCA | 6 | 43191839 | 43191839 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZF-A9RM-01A-11D-A38G-08 | TCGA-ZF-A9RM-10A-01D-A38J-08 | g.chr6:43191839C>T | c.7291C>T | c.(7291-7293)Cgg>Tgg | p.R2431W |
| BLCA | 6 | 43191853 | 43191853 | + | Missense_Mutation | SNP | G | G | C | TCGA-G2-AA3B-01A-11D-A391-08 | TCGA-G2-AA3B-10A-01D-A394-08 | g.chr6:43191853G>C | c.7305G>C | c.(7303-7305)caG>caC | p.Q2435H |
| BRCA | 6 | 43153245 | 43153245 | + | Missense_Mutation | SNP | A | A | C | TCGA-E2-A15D-01A-11D-A10Y-09 | TCGA-E2-A15D-10A-01D-A110-09 | g.chr6:43153245A>C | c.647A>C | c.(646-648)cAg>cCg | p.Q216P |
| BRCA | 6 | 43155157 | 43155157 | + | Missense_Mutation | SNP | C | C | A | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr6:43155157C>A | c.1561C>A | c.(1561-1563)Ctt>Att | p.L521I |
| BRCA | 6 | 43155721 | 43155721 | + | Missense_Mutation | SNP | G | G | A | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr6:43155721G>A | c.1852G>A | c.(1852-1854)Gcc>Acc | p.A618T |
| BRCA | 6 | 43163849 | 43163849 | + | Missense_Mutation | SNP | A | A | C | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr6:43163849A>C | c.2431A>C | c.(2431-2433)Act>Cct | p.T811P |
| BRCA | 6 | 43167709 | 43167709 | + | Missense_Mutation | SNP | A | A | G | TCGA-EW-A1OZ-01A-11D-A142-09 | TCGA-EW-A1OZ-10A-01D-A142-09 | g.chr6:43167709A>G | c.3199A>G | c.(3199-3201)Atg>Gtg | p.M1067V |
| BRCA | 6 | 43170930 | 43170930 | + | Missense_Mutation | SNP | G | G | T | TCGA-HN-A2NL-01A-11D-A18P-09 | TCGA-HN-A2NL-10A-01D-A18P-09 | g.chr6:43170930G>T | c.3837G>T | c.(3835-3837)aaG>aaT | p.K1279N |
| BRCA | 6 | 43171720 | 43171720 | + | Missense_Mutation | SNP | C | C | G | TCGA-B6-A0RG-01A-11W-A071-09 | TCGA-B6-A0RG-10A-01W-A071-09 | g.chr6:43171720C>G | c.4154C>G | c.(4153-4155)tCt>tGt | p.S1385C |
| BRCA | 6 | 43172796 | 43172796 | + | Silent | SNP | T | T | C | TCGA-D8-A1XQ-01A-11D-A14K-09 | TCGA-D8-A1XQ-10A-01D-A14K-09 | g.chr6:43172796T>C | c.4575T>C | c.(4573-4575)gcT>gcC | p.A1525A |
| BRCA | 6 | 43188323 | 43188323 | + | Missense_Mutation | SNP | G | G | C | TCGA-E2-A1AZ-01A-11D-A12Q-09 | TCGA-E2-A1AZ-10A-01D-A12Q-09 | g.chr6:43188323G>C | c.6409G>C | c.(6409-6411)Gag>Cag | p.E2137Q |
| BRCA | 6 | 43191035 | 43191035 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A0AV-01A-31D-A10Y-09 | TCGA-BH-A0AV-10A-01D-A110-09 | g.chr6:43191035C>T | c.7184C>T | c.(7183-7185)tCc>tTc | p.S2395F |
| CESC | 6 | 43153911 | 43153911 | + | Silent | SNP | C | C | T | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr6:43153911C>T | c.969C>T | c.(967-969)ctC>ctT | p.L323L |
| CESC | 6 | 43153970 | 43153970 | + | Missense_Mutation | SNP | C | C | T | TCGA-EK-A2RK-01A-11D-A18J-09 | TCGA-EK-A2RK-10A-01D-A18J-09 | g.chr6:43153970C>T | c.1028C>T | c.(1027-1029)tCa>tTa | p.S343L |
| CESC | 6 | 43163825 | 43163825 | + | Missense_Mutation | SNP | G | G | A | TCGA-LP-A7HU-01A-11D-A33O-09 | TCGA-LP-A7HU-10A-01D-A33O-09 | g.chr6:43163825G>A | c.2407G>A | c.(2407-2409)Gtc>Atc | p.V803I |
| CESC | 6 | 43163948 | 43163948 | + | Missense_Mutation | SNP | G | G | C | TCGA-C5-A1BJ-01A-11D-A13W-08 | TCGA-C5-A1BJ-10A-01D-A13W-08 | g.chr6:43163948G>C | c.2530G>C | c.(2530-2532)Gag>Cag | p.E844Q |
| CESC | 6 | 43164388 | 43164388 | + | Missense_Mutation | SNP | C | C | T | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr6:43164388C>T | c.2591C>T | c.(2590-2592)tCt>tTt | p.S864F |
| CESC | 6 | 43182816 | 43182816 | + | Splice_Site | SNP | G | G | T | TCGA-EK-A2PL-01A-11D-A18J-09 | TCGA-EK-A2PL-10A-01D-A18J-09 | g.chr6:43182816G>T | | c.e30-1 | |
| CESC | 6 | 43184222 | 43184222 | + | Missense_Mutation | SNP | G | G | A | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr6:43184222G>A | c.6263G>A | c.(6262-6264)tGc>tAc | p.C2088Y |
| COAD | 6 | 43152355 | 43152355 | + | Missense_Mutation | SNP | G | G | T | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr6:43152355G>T | c.307G>T | c.(307-309)Gat>Tat | p.D103Y |
| COAD | 6 | 43152466 | 43152466 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr6:43152466G>A | c.418G>A | c.(418-420)Gcc>Acc | p.A140T |
| COAD | 6 | 43152469 | 43152469 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr6:43152469G>A | c.421G>A | c.(421-423)Gct>Act | p.A141T |
| COAD | 6 | 43152504 | 43152504 | + | Silent | SNP | C | C | T | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr6:43152504C>T | c.456C>T | c.(454-456)taC>taT | p.Y152Y |
| COAD | 6 | 43153283 | 43153283 | + | Silent | SNP | C | C | T | TCGA-AA-3833-01A-01W-0900-09 | TCGA-AA-3833-10A-01W-0900-09 | g.chr6:43153283C>T | c.685C>T | c.(685-687)Ctg>Ttg | p.L229L |
| COAD | 6 | 43154154 | 43154154 | + | Silent | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr6:43154154C>T | c.1212C>T | c.(1210-1212)ggC>ggT | p.G404G |
| COAD | 6 | 43154161 | 43154161 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr6:43154161C>T | c.1219C>T | c.(1219-1221)Cgg>Tgg | p.R407W |
| COAD | 6 | 43154738 | 43154738 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr6:43154738G>A | c.1292G>A | c.(1291-1293)tGg>tAg | p.W431* |
| COAD | 6 | 43154777 | 43154777 | + | Missense_Mutation | SNP | A | A | C | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr6:43154777A>C | c.1331A>C | c.(1330-1332)gAg>gCg | p.E444A |
| COAD | 6 | 43155480 | 43155480 | + | Silent | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr6:43155480C>A | c.1611C>A | c.(1609-1611)atC>atA | p.I537I |
| COAD | 6 | 43156293 | 43156293 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3831-01A-01W-0900-09 | TCGA-AA-3831-10A-01W-0900-09 | g.chr6:43156293C>T | c.2020C>T | c.(2020-2022)Cgc>Tgc | p.R674C |
| COAD | 6 | 43156416 | 43156416 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr6:43156416C>T | c.2143C>T | c.(2143-2145)Cgg>Tgg | p.R715W |
| COAD | 6 | 43160851 | 43160851 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr6:43160851C>T | c.2293C>T | c.(2293-2295)Cgg>Tgg | p.R765W |
| COAD | 6 | 43164381 | 43164381 | + | Splice_Site | SNP | A | A | G | TCGA-F4-6703-01A-11D-1835-10 | TCGA-F4-6703-10A-01D-1835-10 | g.chr6:43164381A>G | | c.e11-1 | |
| COAD | 6 | 43166400 | 43166400 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr6:43166400C>T | c.2857C>T | c.(2857-2859)Cga>Tga | p.R953* |
| COAD | 6 | 43166414 | 43166414 | + | Silent | SNP | G | G | T | TCGA-AA-3558-01A-01W-0831-10 | TCGA-AA-3558-10A-01W-0831-10 | g.chr6:43166414G>T | c.2871G>T | c.(2869-2871)ggG>ggT | p.G957G |
| COAD | 6 | 43166584 | 43166584 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr6:43166584C>A | c.3041C>A | c.(3040-3042)tCt>tAt | p.S1014Y |
| COAD | 6 | 43167758 | 43167758 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr6:43167758T>C | c.3248T>C | c.(3247-3249)aTc>aCc | p.I1083T |
| COAD | 6 | 43171202 | 43171202 | + | Silent | SNP | G | G | A | TCGA-G4-6304-01A-11D-1924-10 | TCGA-G4-6304-10A-01D-1924-10 | g.chr6:43171202G>A | c.3897G>A | c.(3895-3897)aaG>aaA | p.K1299K |
| COAD | 6 | 43172149 | 43172150 | + | Frame_Shift_Del | DEL | AG | AG | - | TCGA-A6-2676-01A-01W-0833-10 | TCGA-A6-2676-10A-01W-0833-10 | g.chr6:43172149_43172150delAG | c.4211_4212delAG | c.(4210-4212)cagfs | p.Q1404fs |
| COAD | 6 | 43172731 | 43172732 | + | Frame_Shift_Del | DEL | CT | CT | - | TCGA-CM-6675-01A-11D-1835-10 | TCGA-CM-6675-10A-01D-1835-10 | g.chr6:43172731_43172732delCT | c.4510_4511delCT | c.(4510-4512)ctcfs | p.L1504fs |
| COAD | 6 | 43173750 | 43173750 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr6:43173750A>G | c.4799A>G | c.(4798-4800)tAt>tGt | p.Y1600C |
| COAD | 6 | 43173780 | 43173780 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr6:43173780C>T | c.4829C>T | c.(4828-4830)tCg>tTg | p.S1610L |
| COAD | 6 | 43173837 | 43173837 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr6:43173837T>C | c.4886T>C | c.(4885-4887)cTc>cCc | p.L1629P |
| COAD | 6 | 43173885 | 43173885 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chr6:43173885G>A | c.4934G>A | c.(4933-4935)cGc>cAc | p.R1645H |
| COAD | 6 | 43174224 | 43174224 | + | Missense_Mutation | SNP | C | C | A | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr6:43174224C>A | c.5188C>A | c.(5188-5190)Cgt>Agt | p.R1730S |
| COAD | 6 | 43174224 | 43174224 | + | Missense_Mutation | SNP | C | C | A | TCGA-DM-A28G-01A-11D-A16V-10 | TCGA-DM-A28G-10A-01D-A16V-10 | g.chr6:43174224C>A | c.5188C>A | c.(5188-5190)Cgt>Agt | p.R1730S |
| COAD | 6 | 43174224 | 43174224 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6532-01A-11D-1719-10 | TCGA-D5-6532-10A-01D-1719-10 | g.chr6:43174224C>T | c.5188C>T | c.(5188-5190)Cgt>Tgt | p.R1730C |
| COAD | 6 | 43180994 | 43180994 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr6:43180994G>A | c.5320G>A | c.(5320-5322)Gtg>Atg | p.V1774M |
| COAD | 6 | 43181594 | 43181594 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr6:43181594C>T | c.5632C>T | c.(5632-5634)Cgt>Tgt | p.R1878C |
| COAD | 6 | 43183990 | 43183990 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6304-01A-11D-1924-10 | TCGA-G4-6304-10A-01D-1924-10 | g.chr6:43183990C>T | c.6031C>T | c.(6031-6033)Cgt>Tgt | p.R2011C |
| COAD | 6 | 43184132 | 43184132 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3662-01A-01D-1719-10 | TCGA-AA-3662-11A-01D-1719-10 | g.chr6:43184132A>C | c.6173A>C | c.(6172-6174)cAc>cCc | p.H2058P |
| COAD | 6 | 43188319 | 43188319 | + | Silent | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr6:43188319G>A | c.6405G>A | c.(6403-6405)tcG>tcA | p.S2135S |
| COAD | 6 | 43188604 | 43188604 | + | Silent | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr6:43188604C>T | c.6543C>T | c.(6541-6543)tgC>tgT | p.C2181C |
| COAD | 6 | 43189011 | 43189011 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-5660-01A-01D-1650-10 | TCGA-A6-5660-10A-01D-1650-10 | g.chr6:43189011G>A | c.6704G>A | c.(6703-6705)cGc>cAc | p.R2235H |
| COAD | 6 | 43189023 | 43189023 | + | Missense_Mutation | SNP | G | G | C | TCGA-DM-A1DA-01A-11D-A152-10 | TCGA-DM-A1DA-10A-01D-A152-10 | g.chr6:43189023G>C | c.6716G>C | c.(6715-6717)tGt>tCt | p.C2239S |
| COAD | 6 | 43190322 | 43190322 | + | Silent | SNP | G | G | A | TCGA-A6-3808-01A-01W-0995-10 | TCGA-A6-3808-11A-01W-0995-10 | g.chr6:43190322G>A | c.6975G>A | c.(6973-6975)ccG>ccA | p.P2325P |
| COAD | 6 | 43191033 | 43191033 | + | Silent | SNP | C | C | A | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr6:43191033C>A | c.7182C>A | c.(7180-7182)gcC>gcA | p.A2394A |
| COADREAD | 6 | 43152355 | 43152355 | + | Missense_Mutation | SNP | G | G | T | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr6:43152355G>T | c.307G>T | c.(307-309)Gat>Tat | p.D103Y |
| COADREAD | 6 | 43152466 | 43152466 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr6:43152466G>A | c.418G>A | c.(418-420)Gcc>Acc | p.A140T |
| COADREAD | 6 | 43152469 | 43152469 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr6:43152469G>A | c.421G>A | c.(421-423)Gct>Act | p.A141T |
| COADREAD | 6 | 43152504 | 43152504 | + | Silent | SNP | C | C | T | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr6:43152504C>T | c.456C>T | c.(454-456)taC>taT | p.Y152Y |
| COADREAD | 6 | 43153283 | 43153283 | + | Silent | SNP | C | C | T | TCGA-AA-3833-01A-01W-0900-09 | TCGA-AA-3833-10A-01W-0900-09 | g.chr6:43153283C>T | c.685C>T | c.(685-687)Ctg>Ttg | p.L229L |
| COADREAD | 6 | 43154154 | 43154154 | + | Silent | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr6:43154154C>T | c.1212C>T | c.(1210-1212)ggC>ggT | p.G404G |
| COADREAD | 6 | 43154161 | 43154161 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr6:43154161C>T | c.1219C>T | c.(1219-1221)Cgg>Tgg | p.R407W |
| COADREAD | 6 | 43154738 | 43154738 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr6:43154738G>A | c.1292G>A | c.(1291-1293)tGg>tAg | p.W431* |
| COADREAD | 6 | 43154777 | 43154777 | + | Missense_Mutation | SNP | A | A | C | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr6:43154777A>C | c.1331A>C | c.(1330-1332)gAg>gCg | p.E444A |
| COADREAD | 6 | 43155480 | 43155480 | + | Silent | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr6:43155480C>A | c.1611C>A | c.(1609-1611)atC>atA | p.I537I |
| COADREAD | 6 | 43156293 | 43156293 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3831-01A-01W-0900-09 | TCGA-AA-3831-10A-01W-0900-09 | g.chr6:43156293C>T | c.2020C>T | c.(2020-2022)Cgc>Tgc | p.R674C |
| COADREAD | 6 | 43156416 | 43156416 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr6:43156416C>T | c.2143C>T | c.(2143-2145)Cgg>Tgg | p.R715W |
| COADREAD | 6 | 43160851 | 43160851 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr6:43160851C>T | c.2293C>T | c.(2293-2295)Cgg>Tgg | p.R765W |
| COADREAD | 6 | 43164381 | 43164381 | + | Splice_Site | SNP | A | A | G | TCGA-F4-6703-01A-11D-1835-10 | TCGA-F4-6703-10A-01D-1835-10 | g.chr6:43164381A>G | | c.e11-1 | |
| COADREAD | 6 | 43164514 | 43164514 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr6:43164514G>T | c.2717G>T | c.(2716-2718)aGa>aTa | p.R906I |
| COADREAD | 6 | 43166400 | 43166400 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr6:43166400C>T | c.2857C>T | c.(2857-2859)Cga>Tga | p.R953* |
| COADREAD | 6 | 43166413 | 43166413 | + | Missense_Mutation | SNP | G | G | T | TCGA-AF-2691-01A-01W-0831-10 | TCGA-AF-2691-10A-01W-0831-10 | g.chr6:43166413G>T | c.2870G>T | c.(2869-2871)gGg>gTg | p.G957V |
| COADREAD | 6 | 43166414 | 43166414 | + | Silent | SNP | G | G | T | TCGA-AA-3558-01A-01W-0831-10 | TCGA-AA-3558-10A-01W-0831-10 | g.chr6:43166414G>T | c.2871G>T | c.(2869-2871)ggG>ggT | p.G957G |
| COADREAD | 6 | 43166584 | 43166584 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr6:43166584C>A | c.3041C>A | c.(3040-3042)tCt>tAt | p.S1014Y |
| COADREAD | 6 | 43167758 | 43167758 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr6:43167758T>C | c.3248T>C | c.(3247-3249)aTc>aCc | p.I1083T |
| COADREAD | 6 | 43171202 | 43171202 | + | Silent | SNP | G | G | A | TCGA-G4-6304-01A-11D-1924-10 | TCGA-G4-6304-10A-01D-1924-10 | g.chr6:43171202G>A | c.3897G>A | c.(3895-3897)aaG>aaA | p.K1299K |
| COADREAD | 6 | 43172149 | 43172150 | + | Frame_Shift_Del | DEL | AG | AG | - | TCGA-A6-2676-01A-01W-0833-10 | TCGA-A6-2676-10A-01W-0833-10 | g.chr6:43172149_43172150delAG | c.4211_4212delAG | c.(4210-4212)cagfs | p.Q1404fs |
| COADREAD | 6 | 43172731 | 43172732 | + | Frame_Shift_Del | DEL | CT | CT | - | TCGA-CM-6675-01A-11D-1835-10 | TCGA-CM-6675-10A-01D-1835-10 | g.chr6:43172731_43172732delCT | c.4510_4511delCT | c.(4510-4512)ctcfs | p.L1504fs |
| COADREAD | 6 | 43173750 | 43173750 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr6:43173750A>G | c.4799A>G | c.(4798-4800)tAt>tGt | p.Y1600C |
| COADREAD | 6 | 43173780 | 43173780 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr6:43173780C>T | c.4829C>T | c.(4828-4830)tCg>tTg | p.S1610L |
| COADREAD | 6 | 43173837 | 43173837 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr6:43173837T>C | c.4886T>C | c.(4885-4887)cTc>cCc | p.L1629P |
| COADREAD | 6 | 43173885 | 43173885 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chr6:43173885G>A | c.4934G>A | c.(4933-4935)cGc>cAc | p.R1645H |
| COADREAD | 6 | 43174224 | 43174224 | + | Missense_Mutation | SNP | C | C | A | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr6:43174224C>A | c.5188C>A | c.(5188-5190)Cgt>Agt | p.R1730S |
| COADREAD | 6 | 43174224 | 43174224 | + | Missense_Mutation | SNP | C | C | A | TCGA-DM-A28G-01A-11D-A16V-10 | TCGA-DM-A28G-10A-01D-A16V-10 | g.chr6:43174224C>A | c.5188C>A | c.(5188-5190)Cgt>Agt | p.R1730S |
| COADREAD | 6 | 43174224 | 43174224 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6532-01A-11D-1719-10 | TCGA-D5-6532-10A-01D-1719-10 | g.chr6:43174224C>T | c.5188C>T | c.(5188-5190)Cgt>Tgt | p.R1730C |
| COADREAD | 6 | 43180950 | 43180950 | + | Missense_Mutation | SNP | G | G | A | TCGA-F5-6465-01A-11D-1733-10 | TCGA-F5-6465-10A-01D-1733-10 | g.chr6:43180950G>A | c.5276G>A | c.(5275-5277)cGg>cAg | p.R1759Q |
| COADREAD | 6 | 43180994 | 43180994 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr6:43180994G>A | c.5320G>A | c.(5320-5322)Gtg>Atg | p.V1774M |
| COADREAD | 6 | 43181594 | 43181594 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr6:43181594C>T | c.5632C>T | c.(5632-5634)Cgt>Tgt | p.R1878C |
| COADREAD | 6 | 43183990 | 43183990 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6304-01A-11D-1924-10 | TCGA-G4-6304-10A-01D-1924-10 | g.chr6:43183990C>T | c.6031C>T | c.(6031-6033)Cgt>Tgt | p.R2011C |
| COADREAD | 6 | 43184132 | 43184132 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3662-01A-01D-1719-10 | TCGA-AA-3662-11A-01D-1719-10 | g.chr6:43184132A>C | c.6173A>C | c.(6172-6174)cAc>cCc | p.H2058P |
| COADREAD | 6 | 43184152 | 43184152 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr6:43184152G>A | c.6193G>A | c.(6193-6195)Gta>Ata | p.V2065I |
| COADREAD | 6 | 43188319 | 43188319 | + | Silent | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr6:43188319G>A | c.6405G>A | c.(6403-6405)tcG>tcA | p.S2135S |
| COADREAD | 6 | 43188604 | 43188604 | + | Silent | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr6:43188604C>T | c.6543C>T | c.(6541-6543)tgC>tgT | p.C2181C |
| COADREAD | 6 | 43189011 | 43189011 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-5660-01A-01D-1650-10 | TCGA-A6-5660-10A-01D-1650-10 | g.chr6:43189011G>A | c.6704G>A | c.(6703-6705)cGc>cAc | p.R2235H |
| COADREAD | 6 | 43189023 | 43189023 | + | Missense_Mutation | SNP | G | G | C | TCGA-DM-A1DA-01A-11D-A152-10 | TCGA-DM-A1DA-10A-01D-A152-10 | g.chr6:43189023G>C | c.6716G>C | c.(6715-6717)tGt>tCt | p.C2239S |
| COADREAD | 6 | 43190322 | 43190322 | + | Silent | SNP | G | G | A | TCGA-A6-3808-01A-01W-0995-10 | TCGA-A6-3808-11A-01W-0995-10 | g.chr6:43190322G>A | c.6975G>A | c.(6973-6975)ccG>ccA | p.P2325P |
| COADREAD | 6 | 43191033 | 43191033 | + | Silent | SNP | C | C | A | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr6:43191033C>A | c.7182C>A | c.(7180-7182)gcC>gcA | p.A2394A |
| DLBC | 6 | 43152366 | 43152366 | + | Silent | SNP | C | C | A | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr6:43152366C>A | c.318C>A | c.(316-318)ggC>ggA | p.G106G |
| DLBC | 6 | 43152366 | 43152366 | + | Silent | SNP | C | C | A | TCGA-G8-6326-01A-11D-2210-10 | TCGA-G8-6326-10A-01D-2210-10 | g.chr6:43152366C>A | c.318C>A | c.(316-318)ggC>ggA | p.G106G |
| DLBC | 6 | 43154017 | 43154017 | + | Missense_Mutation | SNP | C | C | G | TCGA-G8-6325-01A-11D-2210-10 | TCGA-G8-6325-10A-01D-2210-10 | g.chr6:43154017C>G | c.1075C>G | c.(1075-1077)Caa>Gaa | p.Q359E |
| DLBC | 6 | 43154064 | 43154064 | + | Silent | SNP | C | C | T | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr6:43154064C>T | c.1122C>T | c.(1120-1122)ggC>ggT | p.G374G |
| DLBC | 6 | 43174057 | 43174065 | + | Splice_Site | DEL | AGGAGGAAG | AGGAGGAAG | - | TCGA-G8-6907-01A-11D-2210-10 | TCGA-G8-6907-14A-01D-2210-10 | g.chr6:43174057_43174065delAGGAGGAAG | c.5022_5029delAGGAGGAAG | c.(5020-5031)gaaggaggaaga>gaga | p.GGR1675del |
| ESCA | 6 | 43152426 | 43152426 | + | Silent | SNP | G | G | A | TCGA-L5-A893-01A-11D-A36J-09 | TCGA-L5-A893-11A-21D-A36M-09 | g.chr6:43152426G>A | c.378G>A | c.(376-378)gcG>gcA | p.A126A |
| ESCA | 6 | 43154799 | 43154799 | + | Silent | SNP | G | G | T | TCGA-XP-A8T7-01A-11D-A36J-09 | TCGA-XP-A8T7-10A-01D-A36M-09 | g.chr6:43154799G>T | c.1353G>T | c.(1351-1353)gtG>gtT | p.V451V |
| ESCA | 6 | 43160940 | 43160940 | + | Silent | SNP | G | G | T | TCGA-IC-A6RE-01A-11D-A33E-09 | TCGA-IC-A6RE-10A-01D-A33H-09 | g.chr6:43160940G>T | c.2382G>T | c.(2380-2382)ggG>ggT | p.G794G |
| ESCA | 6 | 43164484 | 43164484 | + | Missense_Mutation | SNP | C | C | T | TCGA-2H-A9GL-01A-12D-A37C-09 | TCGA-2H-A9GL-11A-11D-A37F-09 | g.chr6:43164484C>T | c.2687C>T | c.(2686-2688)aCg>aTg | p.T896M |
| ESCA | 6 | 43168191 | 43168191 | + | Silent | SNP | C | C | T | TCGA-2H-A9GK-01A-11D-A37C-09 | TCGA-2H-A9GK-11A-11D-A37F-09 | g.chr6:43168191C>T | c.3402C>T | c.(3400-3402)atC>atT | p.I1134I |
| ESCA | 6 | 43172752 | 43172752 | + | Missense_Mutation | SNP | G | G | A | TCGA-R6-A8WG-01A-11D-A37C-09 | TCGA-R6-A8WG-10A-01D-A37F-09 | g.chr6:43172752G>A | c.4531G>A | c.(4531-4533)Gca>Aca | p.A1511T |
| ESCA | 6 | 43181534 | 43181534 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-R6-A6XQ-01B-11D-A33E-09 | TCGA-R6-A6XQ-10A-01D-A33H-09 | g.chr6:43181534G>T | c.5572G>T | c.(5572-5574)Gag>Tag | p.E1858* |
| ESCA | 6 | 43188266 | 43188266 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A8NN-01A-11D-A37C-09 | TCGA-L5-A8NN-11A-11D-A37F-09 | g.chr6:43188266G>T | c.6352G>T | c.(6352-6354)Gcc>Tcc | p.A2118S |
| ESCA | 6 | 43189490 | 43189490 | + | Missense_Mutation | SNP | A | A | G | TCGA-Q9-A6FW-01A-31D-A31U-09 | TCGA-Q9-A6FW-10A-01D-A31U-09 | g.chr6:43189490A>G | c.6820A>G | c.(6820-6822)Aaa>Gaa | p.K2274E |
| ESCA | 6 | 43190586 | 43190589 | + | Frame_Shift_Del | DEL | CAGA | CAGA | - | TCGA-ZR-A9CJ-01B-11D-A387-09 | TCGA-ZR-A9CJ-10A-01D-A38A-09 | g.chr6:43190586_43190589delCAGA | c.7102_7105delCAGA | c.(7102-7107)cagacafs | p.QT2368fs |
| GBM | 6 | 43160945 | 43160945 | + | Splice_Site | SNP | C | C | T | TCGA-76-6660-01A-11D-1845-08 | TCGA-76-6660-10A-01D-1845-08 | g.chr6:43160945C>T | c.2387C>T | c.(2386-2388)gCg>gTg | p.A796V |
| GBM | 6 | 43163923 | 43163923 | + | Silent | SNP | C | C | A | TCGA-12-0618-01A-01D-1492-08 | TCGA-12-0618-10A-01D-1492-08 | g.chr6:43163923C>A | c.2505C>A | c.(2503-2505)atC>atA | p.I835I |
| GBM | 6 | 43164484 | 43164484 | + | Missense_Mutation | SNP | C | C | A | TCGA-27-1838-01A-01D-1494-08 | TCGA-27-1838-10A-01D-1494-08 | g.chr6:43164484C>A | c.2687C>A | c.(2686-2688)aCg>aAg | p.T896K |
| GBM | 6 | 43181519 | 43181519 | + | Missense_Mutation | SNP | G | G | A | TCGA-06-5415-01A-01D-1486-08 | TCGA-06-5415-10A-01D-1486-08 | g.chr6:43181519G>A | c.5557G>A | c.(5557-5559)Gca>Aca | p.A1853T |
| GBMLGG | 6 | 43152296 | 43152296 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-A7T6-01A-11D-A33T-08 | TCGA-DU-A7T6-10A-01D-A33W-08 | g.chr6:43152296G>A | c.248G>A | c.(247-249)cGg>cAg | p.R83Q |
| GBMLGG | 6 | 43153263 | 43153263 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:43153263G>A | c.665G>A | c.(664-666)aGt>aAt | p.S222N |
| GBMLGG | 6 | 43160945 | 43160945 | + | Splice_Site | SNP | C | C | T | TCGA-76-6660-01A-11D-1845-08 | TCGA-76-6660-10A-01D-1845-08 | g.chr6:43160945C>T | c.2387C>T | c.(2386-2388)gCg>gTg | p.A796V |
| GBMLGG | 6 | 43163923 | 43163923 | + | Silent | SNP | C | C | A | TCGA-12-0618-01A-01D-1492-08 | TCGA-12-0618-10A-01D-1492-08 | g.chr6:43163923C>A | c.2505C>A | c.(2503-2505)atC>atA | p.I835I |
| GBMLGG | 6 | 43164484 | 43164484 | + | Missense_Mutation | SNP | C | C | A | TCGA-27-1838-01A-01D-1494-08 | TCGA-27-1838-10A-01D-1494-08 | g.chr6:43164484C>A | c.2687C>A | c.(2686-2688)aCg>aAg | p.T896K |
| GBMLGG | 6 | 43168246 | 43168246 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:43168246C>T | c.3457C>T | c.(3457-3459)Ctc>Ttc | p.L1153F |
| GBMLGG | 6 | 43171720 | 43171720 | + | Missense_Mutation | SNP | C | C | G | TCGA-DU-A5TY-01A-11D-A289-08 | TCGA-DU-A5TY-10A-01D-A289-08 | g.chr6:43171720C>G | c.4154C>G | c.(4153-4155)tCt>tGt | p.S1385C |
| GBMLGG | 6 | 43172550 | 43172550 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:43172550C>T | c.4404C>T | c.(4402-4404)agC>agT | p.S1468S |
| GBMLGG | 6 | 43181519 | 43181519 | + | Missense_Mutation | SNP | G | G | A | TCGA-06-5415-01A-01D-1486-08 | TCGA-06-5415-10A-01D-1486-08 | g.chr6:43181519G>A | c.5557G>A | c.(5557-5559)Gca>Aca | p.A1853T |
| GBMLGG | 6 | 43181530 | 43181530 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:43181530C>T | c.5568C>T | c.(5566-5568)aaC>aaT | p.N1856N |
| GBMLGG | 6 | 43190124 | 43190124 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:43190124C>T | c.6917C>T | c.(6916-6918)gCg>gTg | p.A2306V |
| HNSC | 6 | 43152214 | 43152214 | + | Missense_Mutation | SNP | G | G | A | TCGA-IQ-7630-01A-11D-2078-08 | TCGA-IQ-7630-10A-01D-2078-08 | g.chr6:43152214G>A | c.166G>A | c.(166-168)Gaa>Aaa | p.E56K |
| HNSC | 6 | 43152524 | 43152524 | + | Missense_Mutation | SNP | C | C | G | TCGA-P3-A6T7-01A-11D-A34J-08 | TCGA-P3-A6T7-10A-01D-A34M-08 | g.chr6:43152524C>G | c.476C>G | c.(475-477)aCt>aGt | p.T159S |
| HNSC | 6 | 43152613 | 43152613 | + | Missense_Mutation | SNP | A | A | G | TCGA-CN-4730-01A-01D-1434-08 | TCGA-CN-4730-10A-01D-1434-08 | g.chr6:43152613A>G | c.565A>G | c.(565-567)Atg>Gtg | p.M189V |
| HNSC | 6 | 43153816 | 43153816 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-A45P-01A-11D-A24D-08 | TCGA-CV-A45P-10A-01D-A24F-08 | g.chr6:43153816G>A | c.874G>A | c.(874-876)Gag>Aag | p.E292K |
| HNSC | 6 | 43153942 | 43153943 | + | Frame_Shift_Ins | INS | - | - | C | TCGA-BA-5555-01A-01D-1512-08 | TCGA-BA-5555-10A-01D-1512-08 | g.chr6:43153942_43153943insC | c.1000_1001insC | c.(1000-1002)accfs | p.T334fs |
| HNSC | 6 | 43154058 | 43154058 | + | Silent | SNP | T | T | C | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr6:43154058T>C | c.1116T>C | c.(1114-1116)cgT>cgC | p.R372R |
| HNSC | 6 | 43155036 | 43155036 | + | Silent | SNP | C | C | T | TCGA-CN-4729-01A-01D-1434-08 | TCGA-CN-4729-10A-01D-1434-08 | g.chr6:43155036C>T | c.1440C>T | c.(1438-1440)taC>taT | p.Y480Y |
| HNSC | 6 | 43155037 | 43155037 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-4729-01A-01D-1434-08 | TCGA-CN-4729-10A-01D-1434-08 | g.chr6:43155037C>T | c.1441C>T | c.(1441-1443)Ctc>Ttc | p.L481F |
| HNSC | 6 | 43170895 | 43170895 | + | Missense_Mutation | SNP | A | A | G | TCGA-BA-6869-01A-11D-1870-08 | TCGA-BA-6869-10A-01D-1870-08 | g.chr6:43170895A>G | c.3802A>G | c.(3802-3804)Aac>Gac | p.N1268D |
| HNSC | 6 | 43172163 | 43172163 | + | Missense_Mutation | SNP | C | C | T | TCGA-MT-A67F-01A-11D-A30E-08 | TCGA-MT-A67F-10A-01D-A30H-08 | g.chr6:43172163C>T | c.4225C>T | c.(4225-4227)Cgg>Tgg | p.R1409W |
| HNSC | 6 | 43172776 | 43172776 | + | Missense_Mutation | SNP | C | C | T | TCGA-CQ-A4CA-01A-11D-A25D-08 | TCGA-CQ-A4CA-10A-01D-A25E-08 | g.chr6:43172776C>T | c.4555C>T | c.(4555-4557)Cgg>Tgg | p.R1519W |
| HNSC | 6 | 43173028 | 43173028 | + | Missense_Mutation | SNP | G | G | A | TCGA-CQ-5334-01A-01D-1683-08 | TCGA-CQ-5334-10A-01D-1683-08 | g.chr6:43173028G>A | c.4660G>A | c.(4660-4662)Gac>Aac | p.D1554N |
| HNSC | 6 | 43173746 | 43173746 | + | Splice_Site | SNP | C | C | T | TCGA-QK-A8ZA-01A-11D-A391-08 | TCGA-QK-A8ZA-10A-01D-A394-08 | g.chr6:43173746C>T | c.4795C>T | c.(4795-4797)Cat>Tat | p.H1599Y |
| HNSC | 6 | 43182962 | 43182962 | + | Missense_Mutation | SNP | G | G | A | TCGA-CQ-7072-01A-21D-A30E-08 | TCGA-CQ-7072-10A-01D-A30H-08 | g.chr6:43182962G>A | c.5834G>A | c.(5833-5835)cGg>cAg | p.R1945Q |
| HNSC | 6 | 43189000 | 43189000 | + | Silent | SNP | C | C | T | TCGA-CR-7369-01A-11D-2129-08 | TCGA-CR-7369-10A-01D-2129-08 | g.chr6:43189000C>T | c.6693C>T | c.(6691-6693)ctC>ctT | p.L2231L |
| KICH | 6 | 43164505 | 43164505 | + | Missense_Mutation | SNP | T | T | C | TCGA-KN-8428-01A-11D-2310-10 | TCGA-KN-8428-11A-01D-2311-10 | g.chr6:43164505T>C | c.2708T>C | c.(2707-2709)aTa>aCa | p.I903T |
| KIPAN | 6 | 43153712 | 43153713 | + | Missense_Mutation | DNP | TC | TC | CT | TCGA-A4-8517-01A-11D-2396-08 | TCGA-A4-8517-10A-01D-2396-08 | g.chr6:43153712_43153713TC>CT | c.770_771TC>CT | c.(769-771)tTC>tCT | p.F257S |
| KIPAN | 6 | 43153719 | 43153719 | + | Silent | SNP | G | G | A | TCGA-B8-5163-01A-01D-1421-08 | TCGA-B8-5163-10A-01D-1421-08 | g.chr6:43153719G>A | c.777G>A | c.(775-777)ttG>ttA | p.L259L |
| KIPAN | 6 | 43155541 | 43155541 | + | Missense_Mutation | SNP | A | A | G | TCGA-P4-A5EB-01A-11D-A28G-10 | TCGA-P4-A5EB-11A-11D-A28G-10 | g.chr6:43155541A>G | c.1672A>G | c.(1672-1674)Agc>Ggc | p.S558G |
| KIPAN | 6 | 43156328 | 43156328 | + | Silent | SNP | G | G | T | TCGA-BP-4965-01A-01D-1462-08 | TCGA-BP-4965-11A-01D-1462-08 | g.chr6:43156328G>T | c.2055G>T | c.(2053-2055)gtG>gtT | p.V685V |
| KIPAN | 6 | 43164505 | 43164505 | + | Missense_Mutation | SNP | T | T | C | TCGA-KN-8428-01A-11D-2310-10 | TCGA-KN-8428-11A-01D-2311-10 | g.chr6:43164505T>C | c.2708T>C | c.(2707-2709)aTa>aCa | p.I903T |
| KIPAN | 6 | 43170869 | 43170869 | + | Missense_Mutation | SNP | G | G | T | TCGA-B0-5106-01A-01D-1421-08 | TCGA-B0-5106-11A-01D-1421-08 | g.chr6:43170869G>T | c.3776G>T | c.(3775-3777)aGc>aTc | p.S1259I |
| KIPAN | 6 | 43173114 | 43173114 | + | Missense_Mutation | SNP | G | G | A | TCGA-CJ-6032-01A-11D-1669-08 | TCGA-CJ-6032-11A-01D-1669-08 | g.chr6:43173114G>A | c.4746G>A | c.(4744-4746)atG>atA | p.M1582I |
| KIPAN | 6 | 43174214 | 43174214 | + | Missense_Mutation | SNP | T | T | G | TCGA-AK-3428-01A-02D-1361-10 | TCGA-AK-3428-10A-01D-1361-10 | g.chr6:43174214T>G | c.5178T>G | c.(5176-5178)gaT>gaG | p.D1726E |
| KIPAN | 6 | 43174214 | 43174214 | + | Missense_Mutation | SNP | T | T | G | TCGA-B0-4697-01A-01D-1361-10 | TCGA-B0-4697-11A-01D-1361-10 | g.chr6:43174214T>G | c.5178T>G | c.(5176-5178)gaT>gaG | p.D1726E |
| KIPAN | 6 | 43174215 | 43174215 | + | Missense_Mutation | SNP | G | G | A | TCGA-AK-3460-01A-02D-1361-10 | TCGA-AK-3460-10A-01D-1361-10 | g.chr6:43174215G>A | c.5179G>A | c.(5179-5181)Gcc>Acc | p.A1727T |
| KIPAN | 6 | 43182827 | 43182827 | + | Missense_Mutation | SNP | C | C | A | TCGA-BP-4761-01A-01D-1366-10 | TCGA-BP-4761-11A-01D-1366-10 | g.chr6:43182827C>A | c.5699C>A | c.(5698-5700)gCc>gAc | p.A1900D |
| KIPAN | 6 | 43184050 | 43184050 | + | Missense_Mutation | SNP | T | T | C | TCGA-B1-A47M-01A-11D-A25F-10 | TCGA-B1-A47M-10A-01D-A25F-10 | g.chr6:43184050T>C | c.6091T>C | c.(6091-6093)Tcc>Ccc | p.S2031P |
| KIPAN | 6 | 43188337 | 43188337 | + | Splice_Site | SNP | G | G | A | TCGA-CZ-5457-01A-01D-1501-10 | TCGA-CZ-5457-11A-01D-1501-10 | g.chr6:43188337G>A | c.6423G>A | c.(6421-6423)aaG>aaA | p.K2141K |
| KIRC | 6 | 43153719 | 43153719 | + | Silent | SNP | G | G | A | TCGA-B8-5163-01A-01D-1421-08 | TCGA-B8-5163-10A-01D-1421-08 | g.chr6:43153719G>A | c.777G>A | c.(775-777)ttG>ttA | p.L259L |
| KIRC | 6 | 43156328 | 43156328 | + | Silent | SNP | G | G | T | TCGA-BP-4965-01A-01D-1462-08 | TCGA-BP-4965-11A-01D-1462-08 | g.chr6:43156328G>T | c.2055G>T | c.(2053-2055)gtG>gtT | p.V685V |
| KIRC | 6 | 43170869 | 43170869 | + | Missense_Mutation | SNP | G | G | T | TCGA-B0-5106-01A-01D-1421-08 | TCGA-B0-5106-11A-01D-1421-08 | g.chr6:43170869G>T | c.3776G>T | c.(3775-3777)aGc>aTc | p.S1259I |
| KIRC | 6 | 43173114 | 43173114 | + | Missense_Mutation | SNP | G | G | A | TCGA-CJ-6032-01A-11D-1669-08 | TCGA-CJ-6032-11A-01D-1669-08 | g.chr6:43173114G>A | c.4746G>A | c.(4744-4746)atG>atA | p.M1582I |
| KIRC | 6 | 43174214 | 43174214 | + | Missense_Mutation | SNP | T | T | G | TCGA-AK-3428-01A-02D-1361-10 | TCGA-AK-3428-10A-01D-1361-10 | g.chr6:43174214T>G | c.5178T>G | c.(5176-5178)gaT>gaG | p.D1726E |
| KIRC | 6 | 43174214 | 43174214 | + | Missense_Mutation | SNP | T | T | G | TCGA-B0-4697-01A-01D-1361-10 | TCGA-B0-4697-11A-01D-1361-10 | g.chr6:43174214T>G | c.5178T>G | c.(5176-5178)gaT>gaG | p.D1726E |
| KIRC | 6 | 43174215 | 43174215 | + | Missense_Mutation | SNP | G | G | A | TCGA-AK-3460-01A-02D-1361-10 | TCGA-AK-3460-10A-01D-1361-10 | g.chr6:43174215G>A | c.5179G>A | c.(5179-5181)Gcc>Acc | p.A1727T |
| KIRC | 6 | 43182827 | 43182827 | + | Missense_Mutation | SNP | C | C | A | TCGA-BP-4761-01A-01D-1366-10 | TCGA-BP-4761-11A-01D-1366-10 | g.chr6:43182827C>A | c.5699C>A | c.(5698-5700)gCc>gAc | p.A1900D |
| KIRC | 6 | 43188337 | 43188337 | + | Splice_Site | SNP | G | G | A | TCGA-CZ-5457-01A-01D-1501-10 | TCGA-CZ-5457-11A-01D-1501-10 | g.chr6:43188337G>A | c.6423G>A | c.(6421-6423)aaG>aaA | p.K2141K |
| KIRP | 6 | 43153712 | 43153713 | + | Missense_Mutation | DNP | TC | TC | CT | TCGA-A4-8517-01A-11D-2396-08 | TCGA-A4-8517-10A-01D-2396-08 | g.chr6:43153712_43153713TC>CT | c.770_771TC>CT | c.(769-771)tTC>tCT | p.F257S |
| KIRP | 6 | 43155541 | 43155541 | + | Missense_Mutation | SNP | A | A | G | TCGA-P4-A5EB-01A-11D-A28G-10 | TCGA-P4-A5EB-11A-11D-A28G-10 | g.chr6:43155541A>G | c.1672A>G | c.(1672-1674)Agc>Ggc | p.S558G |
| KIRP | 6 | 43184050 | 43184050 | + | Missense_Mutation | SNP | T | T | C | TCGA-B1-A47M-01A-11D-A25F-10 | TCGA-B1-A47M-10A-01D-A25F-10 | g.chr6:43184050T>C | c.6091T>C | c.(6091-6093)Tcc>Ccc | p.S2031P |
| LAML | 6 | 43166449 | 43166449 | + | Missense_Mutation | SNP | G | G | A | TCGA-AB-2891-03A-01W-0733-08 | TCGA-AB-2891-11A-01W-0732-08 | g.chr6:43166449G>A | c.2906G>A | c.(2905-2907)cGt>cAt | p.R969H |
| LGG | 6 | 43152296 | 43152296 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-A7T6-01A-11D-A33T-08 | TCGA-DU-A7T6-10A-01D-A33W-08 | g.chr6:43152296G>A | c.248G>A | c.(247-249)cGg>cAg | p.R83Q |
| LGG | 6 | 43153263 | 43153263 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:43153263G>A | c.665G>A | c.(664-666)aGt>aAt | p.S222N |
| LGG | 6 | 43168246 | 43168246 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:43168246C>T | c.3457C>T | c.(3457-3459)Ctc>Ttc | p.L1153F |
| LGG | 6 | 43171720 | 43171720 | + | Missense_Mutation | SNP | C | C | G | TCGA-DU-A5TY-01A-11D-A289-08 | TCGA-DU-A5TY-10A-01D-A289-08 | g.chr6:43171720C>G | c.4154C>G | c.(4153-4155)tCt>tGt | p.S1385C |
| LGG | 6 | 43172550 | 43172550 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:43172550C>T | c.4404C>T | c.(4402-4404)agC>agT | p.S1468S |
| LGG | 6 | 43181530 | 43181530 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:43181530C>T | c.5568C>T | c.(5566-5568)aaC>aaT | p.N1856N |
| LGG | 6 | 43190124 | 43190124 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr6:43190124C>T | c.6917C>T | c.(6916-6918)gCg>gTg | p.A2306V |
| LIHC | 6 | 43153266 | 43153266 | + | Missense_Mutation | SNP | G | G | A | TCGA-DD-A1EB-01A-11D-A12Z-10 | TCGA-DD-A1EB-10A-01D-A12Z-10 | g.chr6:43153266G>A | c.668G>A | c.(667-669)cGc>cAc | p.R223H |
| LIHC | 6 | 43153709 | 43153709 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-A39X-01A-11D-A20W-10 | TCGA-DD-A39X-11A-11D-A20W-10 | g.chr6:43153709T>C | c.767T>C | c.(766-768)cTt>cCt | p.L256P |
| LIHC | 6 | 43155009 | 43155009 | + | Silent | SNP | T | T | A | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr6:43155009T>A | c.1413T>A | c.(1411-1413)ccT>ccA | p.P471P |
| LIHC | 6 | 43155101 | 43155101 | + | Missense_Mutation | SNP | T | T | C | TCGA-CC-A7IH-01A-11D-A33K-10 | TCGA-CC-A7IH-10A-01D-A33K-10 | g.chr6:43155101T>C | c.1505T>C | c.(1504-1506)cTg>cCg | p.L502P |
| LIHC | 6 | 43160821 | 43160821 | + | Missense_Mutation | SNP | C | C | T | TCGA-RC-A7S9-01A-11D-A33Q-10 | TCGA-RC-A7S9-10A-02D-A33Q-10 | g.chr6:43160821C>T | c.2263C>T | c.(2263-2265)Ctt>Ttt | p.L755F |
| LIHC | 6 | 43160940 | 43160940 | + | Silent | SNP | G | G | A | TCGA-DD-AACI-01A-11D-A40R-10 | TCGA-DD-AACI-10A-01D-A40U-10 | g.chr6:43160940G>A | c.2382G>A | c.(2380-2382)ggG>ggA | p.G794G |
| LIHC | 6 | 43166474 | 43166474 | + | Silent | SNP | C | C | A | TCGA-HP-A5MZ-01A-21D-A27I-10 | TCGA-HP-A5MZ-10A-01D-A27I-10 | g.chr6:43166474C>A | c.2931C>A | c.(2929-2931)ccC>ccA | p.P977P |
| LIHC | 6 | 43172484 | 43172484 | + | Splice_Site | SNP | A | A | C | TCGA-WQ-A9G7-01A-11D-A36X-10 | TCGA-WQ-A9G7-10A-01D-A370-10 | g.chr6:43172484A>C | | c.e22-1 | |
| LIHC | 6 | 43172517 | 43172517 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-DD-A1EG-01A-11D-A20W-10 | TCGA-DD-A1EG-10A-01D-A20W-10 | g.chr6:43172517delC | c.4371delC | c.(4369-4371)agcfs | p.S1457fs |
| LIHC | 6 | 43172740 | 43172740 | + | Missense_Mutation | SNP | C | C | G | TCGA-ED-A7PX-01A-51D-A34Z-10 | TCGA-ED-A7PX-10A-01D-A34Z-10 | g.chr6:43172740C>G | c.4519C>G | c.(4519-4521)Cac>Gac | p.H1507D |
| LIHC | 6 | 43181019 | 43181022 | + | Frame_Shift_Del | DEL | TCAA | TCAA | - | TCGA-FV-A495-01A-11D-A25V-10 | TCGA-FV-A495-10A-01D-A25V-10 | g.chr6:43181019_43181022delTCAA | c.5345_5348delTCAA | c.(5344-5349)ttcaatfs | p.FN1782fs |
| LIHC | 6 | 43182826 | 43182827 | + | Missense_Mutation | DNP | GC | GC | TT | TCGA-DD-AACI-01A-11D-A40R-10 | TCGA-DD-AACI-10A-01D-A40U-10 | g.chr6:43182826_43182827GC>TT | c.5698_5699GC>TT | c.(5698-5700)GCc>TTc | p.A1900F |
| LIHC | 6 | 43183025 | 43183025 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-A39Z-01A-11D-A20W-10 | TCGA-DD-A39Z-11A-21D-A20W-10 | g.chr6:43183025T>C | c.5897T>C | c.(5896-5898)gTc>gCc | p.V1966A |
| LIHC | 6 | 43190596 | 43190596 | + | Missense_Mutation | SNP | A | A | G | TCGA-4R-AA8I-01A-11D-A382-10 | TCGA-4R-AA8I-10B-01D-A385-10 | g.chr6:43190596A>G | c.7112A>G | c.(7111-7113)aAc>aGc | p.N2371S |
| LIHC | 6 | 43192000 | 43192000 | + | Silent | SNP | C | C | A | TCGA-WQ-A9G7-01A-11D-A36X-10 | TCGA-WQ-A9G7-10A-01D-A370-10 | g.chr6:43192000C>A | c.7371C>A | c.(7369-7371)tcC>tcA | p.S2457S |
| LIHC | 6 | 43192005 | 43192005 | + | Missense_Mutation | SNP | G | G | T | TCGA-ZS-A9CF-01A-11D-A382-10 | TCGA-ZS-A9CF-10A-01D-A385-10 | g.chr6:43192005G>T | c.7376G>T | c.(7375-7377)gGg>gTg | p.G2459V |
| LUAD | 6 | 43152140 | 43152140 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z055-01A-01W-0747-08 | TCGA-17-Z055-11A-01W-0747-08 | g.chr6:43152140G>A | c.92G>A | c.(91-93)gGg>gAg | p.G31E |
| LUAD | 6 | 43152183 | 43152183 | + | Silent | SNP | G | G | A | TCGA-17-Z028-01A-01W-0746-08 | TCGA-17-Z028-11A-01W-0746-08 | g.chr6:43152183G>A | c.135G>A | c.(133-135)ctG>ctA | p.L45L |
| LUAD | 6 | 43152229 | 43152229 | + | Missense_Mutation | SNP | G | G | C | TCGA-17-Z028-01A-01W-0746-08 | TCGA-17-Z028-11A-01W-0746-08 | g.chr6:43152229G>C | c.181G>C | c.(181-183)Gag>Cag | p.E61Q |
| LUAD | 6 | 43152288 | 43152288 | + | Missense_Mutation | SNP | A | A | T | TCGA-73-4668-01A-01D-1265-08 | TCGA-73-4668-11A-01D-1265-08 | g.chr6:43152288A>T | c.240A>T | c.(238-240)ttA>ttT | p.L80F |
| LUAD | 6 | 43152373 | 43152373 | + | Missense_Mutation | SNP | G | G | A | TCGA-78-7149-01A-11D-2036-08 | TCGA-78-7149-10A-01D-2036-08 | g.chr6:43152373G>A | c.325G>A | c.(325-327)Gaa>Aaa | p.E109K |
| LUAD | 6 | 43152442 | 43152442 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z028-01A-01W-0746-08 | TCGA-17-Z028-11A-01W-0746-08 | g.chr6:43152442G>A | c.394G>A | c.(394-396)Gaa>Aaa | p.E132K |
| LUAD | 6 | 43152449 | 43152449 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z028-01A-01W-0746-08 | TCGA-17-Z028-11A-01W-0746-08 | g.chr6:43152449G>A | c.401G>A | c.(400-402)gGg>gAg | p.G134E |
| LUAD | 6 | 43152637 | 43152637 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z028-01A-01W-0746-08 | TCGA-17-Z028-11A-01W-0746-08 | g.chr6:43152637G>T | c.589G>T | c.(589-591)Gat>Tat | p.D197Y |
| LUAD | 6 | 43154012 | 43154012 | + | Missense_Mutation | SNP | G | G | A | TCGA-44-7660-01A-11D-2063-08 | TCGA-44-7660-10A-01D-2063-08 | g.chr6:43154012G>A | c.1070G>A | c.(1069-1071)aGa>aAa | p.R357K |
| LUAD | 6 | 43154105 | 43154105 | + | Missense_Mutation | SNP | G | G | A | TCGA-44-8120-01A-11D-2238-08 | TCGA-44-8120-10A-01D-2238-08 | g.chr6:43154105G>A | c.1163G>A | c.(1162-1164)cGa>cAa | p.R388Q |
| LUAD | 6 | 43154806 | 43154806 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-7728-01A-11D-2184-08 | TCGA-55-7728-10A-01D-2184-08 | g.chr6:43154806G>T | c.1360G>T | c.(1360-1362)Ggg>Tgg | p.G454W |
| LUAD | 6 | 43155093 | 43155093 | + | Missense_Mutation | SNP | G | G | T | TCGA-78-8640-01A-11D-2393-08 | TCGA-78-8640-11A-01D-2393-08 | g.chr6:43155093G>T | c.1497G>T | c.(1495-1497)tgG>tgT | p.W499C |
| LUAD | 6 | 43155663 | 43155663 | + | Silent | SNP | C | C | G | TCGA-78-7156-01A-11D-2036-08 | TCGA-78-7156-10A-01D-2036-08 | g.chr6:43155663C>G | c.1794C>G | c.(1792-1794)tcC>tcG | p.S598S |
| LUAD | 6 | 43164002 | 43164002 | + | Splice_Site | SNP | G | G | T | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr6:43164002G>T | c.2584G>T | c.(2584-2586)Ggg>Tgg | p.G862W |
| LUAD | 6 | 43164573 | 43164573 | + | Missense_Mutation | SNP | G | G | C | TCGA-86-8278-01A-11D-2284-08 | TCGA-86-8278-10A-01D-2284-08 | g.chr6:43164573G>C | c.2776G>C | c.(2776-2778)Gag>Cag | p.E926Q |
| LUAD | 6 | 43167690 | 43167690 | + | Silent | SNP | C | C | T | TCGA-44-7660-01A-11D-2063-08 | TCGA-44-7660-10A-01D-2063-08 | g.chr6:43167690C>T | c.3180C>T | c.(3178-3180)ttC>ttT | p.F1060F |
| LUAD | 6 | 43167711 | 43167711 | + | Missense_Mutation | SNP | G | G | A | TCGA-49-6743-01A-11D-1855-08 | TCGA-49-6743-11A-01D-1855-08 | g.chr6:43167711G>A | c.3201G>A | c.(3199-3201)atG>atA | p.M1067I |
| LUAD | 6 | 43167829 | 43167829 | + | Missense_Mutation | SNP | G | G | C | TCGA-49-6743-01A-11D-1855-08 | TCGA-49-6743-11A-01D-1855-08 | g.chr6:43167829G>C | c.3319G>C | c.(3319-3321)Gag>Cag | p.E1107Q |
| LUAD | 6 | 43171224 | 43171224 | + | Missense_Mutation | SNP | C | C | T | TCGA-78-7153-01A-11D-2036-08 | TCGA-78-7153-10A-01D-2036-08 | g.chr6:43171224C>T | c.3919C>T | c.(3919-3921)Cgg>Tgg | p.R1307W |
| LUAD | 6 | 43171614 | 43171614 | + | Missense_Mutation | SNP | G | G | A | TCGA-44-A47A-01A-21D-A24D-08 | TCGA-44-A47A-10A-01D-A24F-08 | g.chr6:43171614G>A | c.4048G>A | c.(4048-4050)Gag>Aag | p.E1350K |
| LUAD | 6 | 43171718 | 43171718 | + | Silent | SNP | C | C | T | TCGA-97-7937-01A-11D-2167-08 | TCGA-97-7937-10A-01D-2167-08 | g.chr6:43171718C>T | c.4152C>T | c.(4150-4152)acC>acT | p.T1384T |
| LUAD | 6 | 43172512 | 43172512 | + | Missense_Mutation | SNP | C | C | T | TCGA-67-4679-01B-01D-1753-08 | TCGA-67-4679-10A-01D-1753-08 | g.chr6:43172512C>T | c.4366C>T | c.(4366-4368)Cgg>Tgg | p.R1456W |
| LUAD | 6 | 43181476 | 43181476 | + | Silent | SNP | G | G | A | TCGA-NJ-A55A-01A-11D-A25L-08 | TCGA-NJ-A55A-10A-01D-A25L-08 | g.chr6:43181476G>A | c.5514G>A | c.(5512-5514)ggG>ggA | p.G1838G |
| LUAD | 6 | 43182863 | 43182863 | + | Missense_Mutation | SNP | G | G | T | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr6:43182863G>T | c.5735G>T | c.(5734-5736)gGc>gTc | p.G1912V |
| LUAD | 6 | 43190077 | 43190077 | + | Missense_Mutation | SNP | G | G | C | TCGA-17-Z026-01A-01W-0746-08 | TCGA-17-Z026-11A-01W-0746-08 | g.chr6:43190077G>C | c.6870G>C | c.(6868-6870)gaG>gaC | p.E2290D |
| LUAD | 6 | 43191089 | 43191089 | + | Missense_Mutation | SNP | G | G | T | TCGA-78-7162-01A-21D-2063-08 | TCGA-78-7162-11A-01D-2063-08 | g.chr6:43191089G>T | c.7238G>T | c.(7237-7239)cGg>cTg | p.R2413L |
| LUSC | 6 | 43153205 | 43153205 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr6:43153205C>G | c.607C>G | c.(607-609)Cac>Gac | p.H203D |
| LUSC | 6 | 43153813 | 43153813 | + | Missense_Mutation | SNP | A | A | G | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr6:43153813A>G | c.871A>G | c.(871-873)Aga>Gga | p.R291G |
| LUSC | 6 | 43155591 | 43155591 | + | Silent | SNP | G | G | A | TCGA-66-2795-01A-02D-0983-08 | TCGA-66-2795-11A-01D-0983-08 | g.chr6:43155591G>A | c.1722G>A | c.(1720-1722)ctG>ctA | p.L574L |
| LUSC | 6 | 43155792 | 43155792 | + | Silent | SNP | G | G | T | TCGA-22-5473-01A-01D-1632-08 | TCGA-22-5473-11A-11D-1632-08 | g.chr6:43155792G>T | c.1923G>T | c.(1921-1923)ctG>ctT | p.L641L |
| LUSC | 6 | 43156308 | 43156308 | + | Missense_Mutation | SNP | C | C | G | TCGA-60-2698-01A-01D-1522-08 | TCGA-60-2698-11A-01D-1522-08 | g.chr6:43156308C>G | c.2035C>G | c.(2035-2037)Cag>Gag | p.Q679E |
| LUSC | 6 | 43163986 | 43163986 | + | Silent | SNP | G | G | A | TCGA-22-5491-01A-01D-1632-08 | TCGA-22-5491-11A-01D-1632-08 | g.chr6:43163986G>A | c.2568G>A | c.(2566-2568)ctG>ctA | p.L856L |
| LUSC | 6 | 43172102 | 43172102 | + | Silent | SNP | G | G | T | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr6:43172102G>T | c.4164G>T | c.(4162-4164)gcG>gcT | p.A1388A |
| LUSC | 6 | 43172777 | 43172777 | + | Missense_Mutation | SNP | G | G | C | TCGA-22-4593-01A-21D-1817-08 | TCGA-22-4593-11A-01D-1817-08 | g.chr6:43172777G>C | c.4556G>C | c.(4555-4557)cGg>cCg | p.R1519P |
| LUSC | 6 | 43181259 | 43181259 | + | Silent | SNP | G | G | T | TCGA-22-4599-01A-01D-1441-08 | TCGA-22-4599-11A-01D-1441-08 | g.chr6:43181259G>T | c.5442G>T | c.(5440-5442)ggG>ggT | p.G1814G |
| LUSC | 6 | 43188302 | 43188302 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2768-01A-01D-1522-08 | TCGA-66-2768-11A-01D-1522-08 | g.chr6:43188302C>A | c.6388C>A | c.(6388-6390)Cgt>Agt | p.R2130S |
| LUSC | 6 | 43189039 | 43189039 | + | Silent | SNP | G | G | A | TCGA-18-4083-01A-01D-1352-08 | TCGA-18-4083-11A-01D-1352-08 | g.chr6:43189039G>A | c.6732G>A | c.(6730-6732)gaG>gaA | p.E2244E |
| LUSC | 6 | 43189468 | 43189468 | + | Silent | SNP | C | C | G | TCGA-21-1078-01A-01D-1521-08 | TCGA-21-1078-11A-01D-1521-08 | g.chr6:43189468C>G | c.6798C>G | c.(6796-6798)ctC>ctG | p.L2266L |
| LUSC | 6 | 43190375 | 43190375 | + | Missense_Mutation | SNP | G | G | A | TCGA-39-5030-01A-01D-1441-08 | TCGA-39-5030-11A-01D-1441-08 | g.chr6:43190375G>A | c.7028G>A | c.(7027-7029)cGg>cAg | p.R2343Q |
| LUSC | 6 | 43190552 | 43190552 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-60-2719-01A-01D-1522-08 | TCGA-60-2719-11A-01D-1522-08 | g.chr6:43190552delC | c.7068delC | c.(7066-7068)agcfs | p.S2356fs |
| OV | 6 | 43152469 | 43152469 | + | Missense_Mutation | SNP | G | G | A | TCGA-09-2045-01A-01W-0799-08 | TCGA-09-2045-11A-01W-0799-08 | g.chr6:43152469G>A | c.421G>A | c.(421-423)Gct>Act | p.A141T |
| OV | 6 | 43154024 | 43154024 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-23-1111-01A-01W-0639-09 | TCGA-23-1111-10C-01W-0639-09 | g.chr6:43154024G>A | c.1082G>A | c.(1081-1083)tGg>tAg | p.W361* |
| OV | 6 | 43154085 | 43154085 | + | Missense_Mutation | SNP | G | G | C | TCGA-23-2078-01A-01W-0722-08 | TCGA-23-2078-10A-01W-0722-08 | g.chr6:43154085G>C | c.1143G>C | c.(1141-1143)caG>caC | p.Q381H |
| OV | 6 | 43167739 | 43167739 | + | Missense_Mutation | SNP | T | T | G | TCGA-30-1855-01A-01W-0639-09 | TCGA-30-1855-10A-01W-0639-09 | g.chr6:43167739T>G | c.3229T>G | c.(3229-3231)Tgc>Ggc | p.C1077G |
| OV | 6 | 43174143 | 43174143 | + | Missense_Mutation | SNP | C | C | T | TCGA-59-2352-01A-01W-0799-08 | TCGA-59-2352-10A-01W-0800-08 | g.chr6:43174143C>T | c.5107C>T | c.(5107-5109)Cgc>Tgc | p.R1703C |
| OV | 6 | 43174215 | 43174215 | + | Missense_Mutation | SNP | G | G | T | TCGA-59-2352-01A-01W-0799-08 | TCGA-59-2352-10A-01W-0800-08 | g.chr6:43174215G>T | c.5179G>T | c.(5179-5181)Gcc>Tcc | p.A1727S |
| OV | 6 | 43174224 | 43174224 | + | Missense_Mutation | SNP | C | C | T | TCGA-24-2288-01A-01W-0799-08 | TCGA-24-2288-10A-01W-0799-08 | g.chr6:43174224C>T | c.5188C>T | c.(5188-5190)Cgt>Tgt | p.R1730C |
| PAAD | 6 | 43152468 | 43152468 | + | Silent | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr6:43152468C>T | c.420C>T | c.(418-420)gcC>gcT | p.A140A |
| PAAD | 6 | 43155033 | 43155033 | + | Silent | SNP | G | G | A | TCGA-IB-A5SP-01A-11D-A32N-08 | TCGA-IB-A5SP-10A-01D-A32N-08 | g.chr6:43155033G>A | c.1437G>A | c.(1435-1437)ccG>ccA | p.P479P |
| PAAD | 6 | 43155466 | 43155466 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr6:43155466G>A | c.1597G>A | c.(1597-1599)Gcc>Acc | p.A533T |
| PAAD | 6 | 43164434 | 43164434 | + | Silent | SNP | C | C | T | TCGA-HZ-A77O-01A-11D-A33T-08 | TCGA-HZ-A77O-10A-01D-A33W-08 | g.chr6:43164434C>T | c.2637C>T | c.(2635-2637)tgC>tgT | p.C879C |
| PAAD | 6 | 43171608 | 43171608 | + | Missense_Mutation | SNP | C | C | T | TCGA-F2-A8YN-01A-11D-A377-08 | TCGA-F2-A8YN-10A-01D-A37A-08 | g.chr6:43171608C>T | c.4042C>T | c.(4042-4044)Cgc>Tgc | p.R1348C |
| PAAD | 6 | 43171608 | 43171608 | + | Missense_Mutation | SNP | C | C | T | TCGA-LB-A8F3-01A-11D-A36O-08 | TCGA-LB-A8F3-10A-01D-A367-08 | g.chr6:43171608C>T | c.4042C>T | c.(4042-4044)Cgc>Tgc | p.R1348C |
| PAAD | 6 | 43182887 | 43182887 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr6:43182887C>T | c.5759C>T | c.(5758-5760)gCc>gTc | p.A1920V |
| PCPG | 6 | 43167852 | 43167852 | + | Silent | SNP | C | C | T | TCGA-RW-A685-01A-11D-A35D-08 | TCGA-RW-A685-10A-01D-A35B-08 | g.chr6:43167852C>T | c.3342C>T | c.(3340-3342)ctC>ctT | p.L1114L |
| PRAD | 6 | 43160785 | 43160785 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr6:43160785G>A | c.2227G>A | c.(2227-2229)Gga>Aga | p.G743R |
| PRAD | 6 | 43171608 | 43171608 | + | Missense_Mutation | SNP | C | C | T | TCGA-VP-A87B-01A-11D-A34U-08 | TCGA-VP-A87B-10A-01D-A34X-08 | g.chr6:43171608C>T | c.4042C>T | c.(4042-4044)Cgc>Tgc | p.R1348C |
| PRAD | 6 | 43172186 | 43172186 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr6:43172186G>A | c.4248G>A | c.(4246-4248)gcG>gcA | p.A1416A |
| PRAD | 6 | 43173002 | 43173002 | + | Splice_Site | DEL | T | T | - | TCGA-EJ-A7NJ-01A-22D-A34U-08 | TCGA-EJ-A7NJ-10A-01D-A34X-08 | g.chr6:43173002delT | c.4634delT | c.(4633-4635)atg>ag | p.M1545fs |
| PRAD | 6 | 43182853 | 43182853 | + | Missense_Mutation | SNP | G | G | C | TCGA-XJ-A83H-01A-11D-A34U-08 | TCGA-XJ-A83H-10A-01D-A34X-08 | g.chr6:43182853G>C | c.5725G>C | c.(5725-5727)Gga>Cga | p.G1909R |
| READ | 6 | 43164514 | 43164514 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr6:43164514G>T | c.2717G>T | c.(2716-2718)aGa>aTa | p.R906I |
| READ | 6 | 43166413 | 43166413 | + | Missense_Mutation | SNP | G | G | T | TCGA-AF-2691-01A-01W-0831-10 | TCGA-AF-2691-10A-01W-0831-10 | g.chr6:43166413G>T | c.2870G>T | c.(2869-2871)gGg>gTg | p.G957V |
| READ | 6 | 43180950 | 43180950 | + | Missense_Mutation | SNP | G | G | A | TCGA-F5-6465-01A-11D-1733-10 | TCGA-F5-6465-10A-01D-1733-10 | g.chr6:43180950G>A | c.5276G>A | c.(5275-5277)cGg>cAg | p.R1759Q |
| READ | 6 | 43184152 | 43184152 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr6:43184152G>A | c.6193G>A | c.(6193-6195)Gta>Ata | p.V2065I |
| SARC | 6 | 43152478 | 43152478 | + | Missense_Mutation | SNP | C | C | T | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr6:43152478C>T | c.430C>T | c.(430-432)Cac>Tac | p.H144Y |
| SARC | 6 | 43154707 | 43154707 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-Z4-A9VC-01A-11D-A37C-09 | TCGA-Z4-A9VC-10A-01D-A37F-09 | g.chr6:43154707C>T | c.1261C>T | c.(1261-1263)Cag>Tag | p.Q421* |
| SKCM | 6 | 43152353 | 43152353 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3BZ-06A-12D-A196-08 | TCGA-D3-A3BZ-10A-01D-A198-08 | g.chr6:43152353G>A | c.305G>A | c.(304-306)cGa>cAa | p.R102Q |
| SKCM | 6 | 43153697 | 43153697 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr6:43153697C>T | c.755C>T | c.(754-756)cCa>cTa | p.P252L |
| SKCM | 6 | 43153716 | 43153716 | + | Silent | SNP | C | C | T | TCGA-EE-A3AD-06A-11D-A196-08 | TCGA-EE-A3AD-10A-01D-A198-08 | g.chr6:43153716C>T | c.774C>T | c.(772-774)tcC>tcT | p.S258S |
| SKCM | 6 | 43153745 | 43153745 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr6:43153745C>T | c.803C>T | c.(802-804)tCc>tTc | p.S268F |
| SKCM | 6 | 43153772 | 43153772 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2ML-06A-11D-A197-08 | TCGA-EE-A2ML-10A-01D-A199-08 | g.chr6:43153772C>T | c.830C>T | c.(829-831)cCa>cTa | p.P277L |
| SKCM | 6 | 43153909 | 43153909 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A1QB-06A-11D-A19A-08 | TCGA-D3-A1QB-10A-01D-A19A-08 | g.chr6:43153909C>T | c.967C>T | c.(967-969)Ctc>Ttc | p.L323F |
| SKCM | 6 | 43153911 | 43153911 | + | Silent | SNP | C | C | T | TCGA-D3-A1QB-06A-11D-A19A-08 | TCGA-D3-A1QB-10A-01D-A19A-08 | g.chr6:43153911C>T | c.969C>T | c.(967-969)ctC>ctT | p.L323L |
| SKCM | 6 | 43154031 | 43154031 | + | Silent | SNP | C | C | T | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr6:43154031C>T | c.1089C>T | c.(1087-1089)ttC>ttT | p.F363F |
| SKCM | 6 | 43155482 | 43155482 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MC-06A-12D-A197-08 | TCGA-EE-A2MC-10A-01D-A199-08 | g.chr6:43155482C>T | c.1613C>T | c.(1612-1614)tCt>tTt | p.S538F |
| SKCM | 6 | 43155488 | 43155488 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GD-06A-11D-A196-08 | TCGA-EE-A2GD-10A-01D-A198-08 | g.chr6:43155488C>T | c.1619C>T | c.(1618-1620)tCc>tTc | p.S540F |
| SKCM | 6 | 43155681 | 43155681 | + | Silent | SNP | C | C | T | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr6:43155681C>T | c.1812C>T | c.(1810-1812)ttC>ttT | p.F604F |
| SKCM | 6 | 43156281 | 43156281 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A19E-06A-11D-A197-08 | TCGA-ER-A19E-10A-01D-A199-08 | g.chr6:43156281G>A | c.2008G>A | c.(2008-2010)Ggt>Agt | p.G670S |
| SKCM | 6 | 43156451 | 43156451 | + | Silent | SNP | G | G | A | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr6:43156451G>A | c.2178G>A | c.(2176-2178)ctG>ctA | p.L726L |
| SKCM | 6 | 43163840 | 43163840 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr6:43163840G>A | c.2422G>A | c.(2422-2424)Gag>Aag | p.E808K |
| SKCM | 6 | 43163916 | 43163916 | + | Missense_Mutation | SNP | C | C | G | TCGA-GN-A4U7-06A-21D-A32N-08 | TCGA-GN-A4U7-10B-01D-A32N-08 | g.chr6:43163916C>G | c.2498C>G | c.(2497-2499)gCc>gGc | p.A833G |
| SKCM | 6 | 43163917 | 43163917 | + | Silent | SNP | C | C | T | TCGA-GN-A4U7-06A-21D-A32N-08 | TCGA-GN-A4U7-10B-01D-A32N-08 | g.chr6:43163917C>T | c.2499C>T | c.(2497-2499)gcC>gcT | p.A833A |
| SKCM | 6 | 43164398 | 43164398 | + | Silent | SNP | G | G | A | TCGA-GN-A267-06A-21D-A196-08 | TCGA-GN-A267-10A-01D-A198-08 | g.chr6:43164398G>A | c.2601G>A | c.(2599-2601)gcG>gcA | p.A867A |
| SKCM | 6 | 43164422 | 43164422 | + | Silent | SNP | C | C | T | TCGA-EE-A2MC-06A-12D-A197-08 | TCGA-EE-A2MC-10A-01D-A199-08 | g.chr6:43164422C>T | c.2625C>T | c.(2623-2625)aaC>aaT | p.N875N |
| SKCM | 6 | 43164546 | 43164546 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr6:43164546C>T | c.2749C>T | c.(2749-2751)Ctc>Ttc | p.L917F |
| SKCM | 6 | 43166404 | 43166404 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr6:43166404C>T | c.2861C>T | c.(2860-2862)tCc>tTc | p.S954F |
| SKCM | 6 | 43167691 | 43167691 | + | Silent | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr6:43167691C>T | c.3181C>T | c.(3181-3183)Cta>Tta | p.L1061L |
| SKCM | 6 | 43167862 | 43167862 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29C-06A-21D-A197-08 | TCGA-EE-A29C-10A-01D-A199-08 | g.chr6:43167862C>T | c.3352C>T | c.(3352-3354)Ctc>Ttc | p.L1118F |
| SKCM | 6 | 43168531 | 43168531 | + | Silent | SNP | C | C | T | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr6:43168531C>T | c.3606C>T | c.(3604-3606)tcC>tcT | p.S1202S |
| SKCM | 6 | 43170918 | 43170918 | + | Silent | SNP | G | G | A | TCGA-D3-A51R-06A-11D-A25O-08 | TCGA-D3-A51R-10A-01D-A25O-08 | g.chr6:43170918G>A | c.3825G>A | c.(3823-3825)caG>caA | p.Q1275Q |
| SKCM | 6 | 43171673 | 43171673 | + | Silent | SNP | G | G | A | TCGA-EE-A3AB-06A-11D-A196-08 | TCGA-EE-A3AB-10A-01D-A198-08 | g.chr6:43171673G>A | c.4107G>A | c.(4105-4107)aaG>aaA | p.K1369K |
| SKCM | 6 | 43172271 | 43172271 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3C8-06A-12D-A19A-08 | TCGA-D3-A3C8-10A-01D-A19A-08 | g.chr6:43172271C>T | c.4333C>T | c.(4333-4335)Cgg>Tgg | p.R1445W |
| SKCM | 6 | 43172719 | 43172719 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr6:43172719C>T | c.4498C>T | c.(4498-4500)Cgt>Tgt | p.R1500C |
| SKCM | 6 | 43173000 | 43173000 | + | Splice_Site | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr6:43173000G>A | | c.e24-1 | |
| SKCM | 6 | 43173766 | 43173766 | + | Silent | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr6:43173766C>T | c.4815C>T | c.(4813-4815)ctC>ctT | p.L1605L |
| SKCM | 6 | 43173896 | 43173896 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr6:43173896C>T | c.4945C>T | c.(4945-4947)Ctc>Ttc | p.L1649F |
| SKCM | 6 | 43173928 | 43173928 | + | Silent | SNP | C | C | T | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr6:43173928C>T | c.4977C>T | c.(4975-4977)ttC>ttT | p.F1659F |
| SKCM | 6 | 43181465 | 43181465 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A149-06A-11D-A196-08 | TCGA-D9-A149-10A-01D-A198-08 | g.chr6:43181465C>T | c.5503C>T | c.(5503-5505)Cat>Tat | p.H1835Y |
| SKCM | 6 | 43181575 | 43181575 | + | Silent | SNP | C | C | T | TCGA-FS-A1ZC-06A-11D-A197-08 | TCGA-FS-A1ZC-10A-01D-A199-08 | g.chr6:43181575C>T | c.5613C>T | c.(5611-5613)ctC>ctT | p.L1871L |
| SKCM | 6 | 43181615 | 43181615 | + | Missense_Mutation | SNP | G | G | A | TCGA-D9-A3Z3-06A-11D-A23B-08 | TCGA-D9-A3Z3-10A-01D-A23B-08 | g.chr6:43181615G>A | c.5653G>A | c.(5653-5655)Gaa>Aaa | p.E1885K |
| SKCM | 6 | 43182949 | 43182949 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A4U9-06A-11D-A32N-08 | TCGA-GN-A4U9-10B-01D-A32N-08 | g.chr6:43182949C>T | c.5821C>T | c.(5821-5823)Cgg>Tgg | p.R1941W |
| SKCM | 6 | 43184064 | 43184064 | + | Silent | SNP | T | T | A | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr6:43184064T>A | c.6105T>A | c.(6103-6105)gcT>gcA | p.A2035A |
| SKCM | 6 | 43184184 | 43184184 | + | Missense_Mutation | SNP | C | C | A | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr6:43184184C>A | c.6225C>A | c.(6223-6225)agC>agA | p.S2075R |
| SKCM | 6 | 43184185 | 43184185 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr6:43184185C>T | c.6226C>T | c.(6226-6228)Ccc>Tcc | p.P2076S |
| SKCM | 6 | 43188298 | 43188298 | + | Silent | SNP | C | C | T | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr6:43188298C>T | c.6384C>T | c.(6382-6384)ttC>ttT | p.F2128F |
| SKCM | 6 | 43188593 | 43188593 | + | Missense_Mutation | SNP | G | G | C | TCGA-D3-A2JA-06A-11D-A196-08 | TCGA-D3-A2JA-10A-01D-A198-08 | g.chr6:43188593G>C | c.6532G>C | c.(6532-6534)Ggg>Cgg | p.G2178R |