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 | 8 | 41790513 | 41790513 | + | Missense_Mutation | SNP | C | C | T | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chr8:41790513C>T | c.5225G>A | c.(5224-5226)gGc>gAc | p.G1742D |
ACC | 8 | 41791017 | 41791017 | + | Missense_Mutation | SNP | C | C | T | TCGA-OR-A5K9-01A-11D-A29I-10 | TCGA-OR-A5K9-11A-11D-A29L-10 | g.chr8:41791017C>T | c.4721G>A | c.(4720-4722)gGc>gAc | p.G1574D |
ACC | 8 | 41798484 | 41798484 | + | Missense_Mutation | SNP | C | C | T | TCGA-OR-A5JI-01A-11D-A29I-10 | TCGA-OR-A5JI-10A-01D-A29L-10 | g.chr8:41798484C>T | c.2915G>A | c.(2914-2916)cGc>cAc | p.R972H |
BLCA | 8 | 41789950 | 41789950 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A6B5-01A-11D-A31L-08 | TCGA-DK-A6B5-10A-01D-A31J-08 | g.chr8:41789950G>A | c.5788C>T | c.(5788-5790)Ccc>Tcc | p.P1930S |
BLCA | 8 | 41790517 | 41790517 | + | Missense_Mutation | SNP | C | C | A | TCGA-CU-A3YL-01A-11D-A22Z-08 | TCGA-CU-A3YL-10A-01D-A22Z-08 | g.chr8:41790517C>A | c.5221G>T | c.(5221-5223)Gcc>Tcc | p.A1741S |
BLCA | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-E7-A677-01A-11D-A30E-08 | TCGA-E7-A677-10A-01D-A30H-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
BLCA | 8 | 41790682 | 41790682 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-A9SM-01A-11D-A42E-08 | TCGA-XF-A9SM-10A-01D-A42H-08 | g.chr8:41790682G>C | c.5056C>G | c.(5056-5058)Cag>Gag | p.Q1686E |
BLCA | 8 | 41790872 | 41790872 | + | Missense_Mutation | SNP | G | G | C | TCGA-UY-A9PD-01A-11D-A38G-08 | TCGA-UY-A9PD-10A-01D-A38J-08 | g.chr8:41790872G>C | c.4866C>G | c.(4864-4866)agC>agG | p.S1622R |
BLCA | 8 | 41791111 | 41791111 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-AAML-01A-11D-A42E-08 | TCGA-XF-AAML-10A-01D-A42H-08 | g.chr8:41791111G>C | c.4627C>G | c.(4627-4629)Cag>Gag | p.Q1543E |
BLCA | 8 | 41791315 | 41791315 | + | Missense_Mutation | SNP | G | G | A | TCGA-4Z-AA7R-01A-11D-A391-08 | TCGA-4Z-AA7R-10A-01D-A394-08 | g.chr8:41791315G>A | c.4423C>T | c.(4423-4425)Cat>Tat | p.H1475Y |
BLCA | 8 | 41791399 | 41791399 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-AAN2-01A-11D-A42E-08 | TCGA-XF-AAN2-10A-01D-A42H-08 | g.chr8:41791399C>T | c.4339G>A | c.(4339-4341)Gag>Aag | p.E1447K |
BLCA | 8 | 41791525 | 41791525 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A2I6-01A-12D-A18F-08 | TCGA-DK-A2I6-10A-01D-A18F-08 | g.chr8:41791525C>T | c.4213G>A | c.(4213-4215)Gag>Aag | p.E1405K |
BLCA | 8 | 41792359 | 41792359 | + | Missense_Mutation | SNP | G | G | C | TCGA-E5-A2PC-01A-11D-A202-08 | TCGA-E5-A2PC-10B-01D-A202-08 | g.chr8:41792359G>C | c.3379C>G | c.(3379-3381)Ctt>Gtt | p.L1127V |
BLCA | 8 | 41794882 | 41794882 | + | Missense_Mutation | SNP | T | T | C | TCGA-CU-A0YR-01A-12D-A10S-08 | TCGA-CU-A0YR-10A-01D-A10S-08 | g.chr8:41794882T>C | c.3244A>G | c.(3244-3246)Aga>Gga | p.R1082G |
BLCA | 8 | 41798546 | 41798546 | + | Silent | SNP | G | G | C | TCGA-XF-A9SY-01A-21D-A42E-08 | TCGA-XF-A9SY-10A-01D-A42H-08 | g.chr8:41798546G>C | c.2853C>G | c.(2851-2853)ctC>ctG | p.L951L |
BLCA | 8 | 41798738 | 41798738 | + | Silent | SNP | G | G | A | TCGA-DK-A6B6-01A-11D-A30E-08 | TCGA-DK-A6B6-10A-01D-A30H-08 | g.chr8:41798738G>A | c.2661C>T | c.(2659-2661)ctC>ctT | p.L887L |
BLCA | 8 | 41800466 | 41800466 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-ZF-AA51-01A-21D-A391-08 | TCGA-ZF-AA51-10A-01D-A394-08 | g.chr8:41800466G>A | c.2281C>T | c.(2281-2283)Cag>Tag | p.Q761* |
BLCA | 8 | 41801321 | 41801321 | + | Missense_Mutation | SNP | G | G | C | TCGA-E7-A7DV-01A-11D-A339-08 | TCGA-E7-A7DV-10A-01D-A339-08 | g.chr8:41801321G>C | c.2173C>G | c.(2173-2175)Caa>Gaa | p.Q725E |
BLCA | 8 | 41832305 | 41832305 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-A9SY-01A-21D-A42E-08 | TCGA-XF-A9SY-10A-01D-A42H-08 | g.chr8:41832305C>T | c.1399G>A | c.(1399-1401)Gag>Aag | p.E467K |
BLCA | 8 | 41906066 | 41906066 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-A9SM-01A-11D-A42E-08 | TCGA-XF-A9SM-10A-01D-A42H-08 | g.chr8:41906066G>C | c.430C>G | c.(430-432)Cac>Gac | p.H144D |
BLCA | 8 | 41906179 | 41906179 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-AA74-01A-11D-A391-08 | TCGA-DK-AA74-10A-01D-A394-08 | g.chr8:41906179G>A | c.317C>T | c.(316-318)gCa>gTa | p.A106V |
BLCA | 8 | 41906295 | 41906295 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-E7-A7XN-01A-11D-A34U-08 | TCGA-E7-A7XN-10A-01D-A34X-08 | g.chr8:41906295delT | c.201delA | c.(199-201)ggafs | p.G67fs |
BLCA | 8 | 41906305 | 41906305 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-FD-A3SS-01A-12D-A22Z-08 | TCGA-FD-A3SS-10A-01D-A22Z-08 | g.chr8:41906305G>C | c.191C>G | c.(190-192)tCa>tGa | p.S64* |
BLCA | 8 | 41906383 | 41906383 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A5KF-01A-11D-A289-08 | TCGA-E7-A5KF-10A-01D-A289-08 | g.chr8:41906383G>A | c.113C>T | c.(112-114)tCa>tTa | p.S38L |
BRCA | 8 | 41790605 | 41790605 | + | Silent | SNP | G | G | A | TCGA-C8-A27B-01A-11D-A167-09 | TCGA-C8-A27B-10A-01D-A167-09 | g.chr8:41790605G>A | c.5133C>T | c.(5131-5133)ttC>ttT | p.F1711F |
BRCA | 8 | 41790653 | 41790653 | + | Silent | SNP | A | A | G | TCGA-D8-A3Z5-01A-41D-A243-09 | TCGA-D8-A3Z5-10A-01D-A243-09 | g.chr8:41790653A>G | c.5085T>C | c.(5083-5085)ccT>ccC | p.P1695P |
BRCA | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-D8-A3Z5-01A-41D-A243-09 | TCGA-D8-A3Z5-10A-01D-A243-09 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
BRCA | 8 | 41791830 | 41791830 | + | Missense_Mutation | SNP | T | T | C | TCGA-C8-A275-01A-21D-A16D-09 | TCGA-C8-A275-10A-01D-A16D-09 | g.chr8:41791830T>C | c.3908A>G | c.(3907-3909)gAt>gGt | p.D1303G |
BRCA | 8 | 41791871 | 41791873 | + | In_Frame_Del | DEL | CTC | CTC | - | TCGA-BH-A18G-01A-11D-A12B-09 | TCGA-BH-A18G-10A-01D-A12B-09 | g.chr8:41791871_41791873delCTC | c.3865_3867delGAG | c.(3865-3867)gagdel | p.E1289del |
BRCA | 8 | 41791980 | 41791980 | + | Missense_Mutation | SNP | G | G | A | TCGA-BH-A0B6-01A-11D-A19Y-09 | TCGA-BH-A0B6-10A-01D-A19Y-09 | g.chr8:41791980G>A | c.3758C>T | c.(3757-3759)tCt>tTt | p.S1253F |
BRCA | 8 | 41792232 | 41792232 | + | Missense_Mutation | SNP | C | C | T | TCGA-A8-A093-01A-11W-A019-09 | TCGA-A8-A093-10A-01W-A021-09 | g.chr8:41792232C>T | c.3506G>A | c.(3505-3507)cGa>cAa | p.R1169Q |
BRCA | 8 | 41798386 | 41798386 | + | Missense_Mutation | SNP | G | G | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr8:41798386G>T | c.3013C>A | c.(3013-3015)Ctc>Atc | p.L1005I |
BRCA | 8 | 41798588 | 41798588 | + | Missense_Mutation | SNP | C | C | G | TCGA-BH-A18P-01A-11D-A12B-09 | TCGA-BH-A18P-11A-43D-A12B-09 | g.chr8:41798588C>G | c.2811G>C | c.(2809-2811)aaG>aaC | p.K937N |
BRCA | 8 | 41834588 | 41834588 | + | Missense_Mutation | SNP | G | G | C | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr8:41834588G>C | c.1301C>G | c.(1300-1302)tCt>tGt | p.S434C |
BRCA | 8 | 41906162 | 41906162 | + | Missense_Mutation | SNP | C | C | G | TCGA-D8-A1JA-01A-11D-A13L-09 | TCGA-D8-A1JA-10A-01W-A14R-09 | g.chr8:41906162C>G | c.334G>C | c.(334-336)Gag>Cag | p.E112Q |
CESC | 8 | 41789766 | 41789766 | + | Missense_Mutation | SNP | C | C | T | TCGA-EA-A3HT-01A-61D-A21Q-09 | TCGA-EA-A3HT-10A-01D-A21Q-09 | g.chr8:41789766C>T | c.5972G>A | c.(5971-5973)gGc>gAc | p.G1991D |
CESC | 8 | 41790749 | 41790749 | + | Silent | SNP | C | C | T | TCGA-EA-A3HU-01A-11D-A20U-09 | TCGA-EA-A3HU-10B-01D-A20U-09 | g.chr8:41790749C>T | c.4989G>A | c.(4987-4989)ccG>ccA | p.P1663P |
CESC | 8 | 41798407 | 41798407 | + | Missense_Mutation | SNP | G | G | A | TCGA-MU-A51Y-01A-11D-A26G-09 | TCGA-MU-A51Y-10A-01D-A26G-09 | g.chr8:41798407G>A | c.2992C>T | c.(2992-2994)Cgg>Tgg | p.R998W |
CESC | 8 | 41798922 | 41798922 | + | Missense_Mutation | SNP | G | G | C | TCGA-JW-A5VI-01A-11D-A28B-09 | TCGA-JW-A5VI-10A-01D-A28E-09 | g.chr8:41798922G>C | c.2477C>G | c.(2476-2478)tCt>tGt | p.S826C |
CESC | 8 | 41906386 | 41906386 | + | Missense_Mutation | SNP | G | G | T | TCGA-C5-A1BK-01B-11D-A13W-08 | TCGA-C5-A1BK-10A-01D-A13W-08 | g.chr8:41906386G>T | c.110C>A | c.(109-111)tCt>tAt | p.S37Y |
CHOL | 8 | 41806877 | 41806877 | + | Missense_Mutation | SNP | G | G | T | TCGA-W5-AA2G-01A-11D-A417-09 | TCGA-W5-AA2G-10A-01D-A41A-09 | g.chr8:41806877G>T | c.1603C>A | c.(1603-1605)Ccc>Acc | p.P535T |
COAD | 8 | 41789773 | 41789773 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr8:41789773C>T | c.5965G>A | c.(5965-5967)Gct>Act | p.A1989T |
COAD | 8 | 41790016 | 41790016 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00A-01A-01W-A005-10 | TCGA-AA-A00A-10A-01W-A005-10 | g.chr8:41790016C>T | c.5722G>A | c.(5722-5724)Gcc>Acc | p.A1908T |
COAD | 8 | 41790054 | 41790054 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr8:41790054C>T | c.5684G>A | c.(5683-5685)cGt>cAt | p.R1895H |
COAD | 8 | 41790070 | 41790070 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4682-01B-01D-1408-10 | TCGA-AZ-4682-10A-01D-1408-10 | g.chr8:41790070C>T | c.5668G>A | c.(5668-5670)Gca>Aca | p.A1890T |
COAD | 8 | 41790493 | 41790493 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6625-01A-21D-1771-10 | TCGA-G4-6625-11A-01D-1771-10 | g.chr8:41790493C>T | c.5245G>A | c.(5245-5247)Gcc>Acc | p.A1749T |
COAD | 8 | 41790659 | 41790660 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr8:41790659_41790660insG | c.5078_5079insC | c.(5077-5079)ccafs | p.P1693fs |
COAD | 8 | 41790674 | 41790674 | + | Silent | SNP | C | C | T | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr8:41790674C>T | c.5064G>A | c.(5062-5064)caG>caA | p.Q1688Q |
COAD | 8 | 41791251 | 41791251 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr8:41791251G>A | c.4487C>T | c.(4486-4488)tCg>tTg | p.S1496L |
COAD | 8 | 41791311 | 41791311 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00A-01A-01W-A005-10 | TCGA-AA-A00A-10A-01W-A005-10 | g.chr8:41791311G>A | c.4427C>T | c.(4426-4428)gCg>gTg | p.A1476V |
COAD | 8 | 41792011 | 41792011 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr8:41792011delC | c.3727delG | c.(3727-3729)gatfs | p.D1243fs |
COAD | 8 | 41792145 | 41792145 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3989-01A-01W-0995-10 | TCGA-AA-3989-10A-01W-0999-10 | g.chr8:41792145G>A | c.3593C>T | c.(3592-3594)gCt>gTt | p.A1198V |
COAD | 8 | 41794925 | 41794925 | + | Silent | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr8:41794925G>A | c.3201C>T | c.(3199-3201)atC>atT | p.I1067I |
COAD | 8 | 41798469 | 41798469 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr8:41798469T>C | c.2930A>G | c.(2929-2931)gAc>gGc | p.D977G |
COAD | 8 | 41798484 | 41798484 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr8:41798484C>T | c.2915G>A | c.(2914-2916)cGc>cAc | p.R972H |
COAD | 8 | 41798487 | 41798487 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr8:41798487C>T | c.2912G>A | c.(2911-2913)cGt>cAt | p.R971H |
COAD | 8 | 41798495 | 41798495 | + | Silent | SNP | C | C | T | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr8:41798495C>T | c.2904G>A | c.(2902-2904)agG>agA | p.R968R |
COAD | 8 | 41798808 | 41798808 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chr8:41798808C>T | c.2591G>A | c.(2590-2592)cGg>cAg | p.R864Q |
COAD | 8 | 41798947 | 41798947 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A01Q-01A-01W-A005-10 | TCGA-AA-A01Q-10A-01W-A005-10 | g.chr8:41798947A>G | c.2452T>C | c.(2452-2454)Tct>Cct | p.S818P |
COAD | 8 | 41801475 | 41801475 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr8:41801475T>A | c.2019A>T | c.(2017-2019)gaA>gaT | p.E673D |
COAD | 8 | 41801475 | 41801475 | + | Silent | SNP | T | T | C | TCGA-AU-3779-01A-01D-1719-10 | TCGA-AU-3779-10A-01D-1719-10 | g.chr8:41801475T>C | c.2019A>G | c.(2017-2019)gaA>gaG | p.E673E |
COAD | 8 | 41801477 | 41801477 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr8:41801477C>A | c.2017G>T | c.(2017-2019)Gaa>Taa | p.E673* |
COAD | 8 | 41804115 | 41804115 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr8:41804115C>T | c.1990G>A | c.(1990-1992)Gat>Aat | p.D664N |
COAD | 8 | 41804115 | 41804115 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr8:41804115C>T | c.1990G>A | c.(1990-1992)Gat>Aat | p.D664N |
COAD | 8 | 41805417 | 41805417 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr8:41805417A>G | c.1754T>C | c.(1753-1755)gTg>gCg | p.V585A |
COAD | 8 | 41805417 | 41805417 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6303-01A-11D-1771-10 | TCGA-G4-6303-10A-01D-1771-10 | g.chr8:41805417A>G | c.1754T>C | c.(1753-1755)gTg>gCg | p.V585A |
COAD | 8 | 41812837 | 41812837 | + | Silent | SNP | G | G | A | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr8:41812837G>A | c.1575C>T | c.(1573-1575)tcC>tcT | p.S525S |
COAD | 8 | 41812840 | 41812840 | + | Silent | SNP | G | G | A | TCGA-F4-6807-01A-11D-1835-10 | TCGA-F4-6807-10A-01D-1835-10 | g.chr8:41812840G>A | c.1572C>T | c.(1570-1572)tcC>tcT | p.S524S |
COAD | 8 | 41832336 | 41832336 | + | Silent | SNP | A | A | G | TCGA-DM-A28K-01A-21D-A16V-10 | TCGA-DM-A28K-10A-01D-A16V-10 | g.chr8:41832336A>G | c.1368T>C | c.(1366-1368)aaT>aaC | p.N456N |
COAD | 8 | 41832337 | 41832337 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6607-01A-11D-1835-10 | TCGA-AZ-6607-11A-01D-1835-10 | g.chr8:41832337T>C | c.1367A>G | c.(1366-1368)aAt>aGt | p.N456S |
COAD | 8 | 41832337 | 41832337 | + | Missense_Mutation | SNP | T | T | C | TCGA-DM-A28E-01A-11D-A16V-10 | TCGA-DM-A28E-10A-01D-A16V-10 | g.chr8:41832337T>C | c.1367A>G | c.(1366-1368)aAt>aGt | p.N456S |
COAD | 8 | 41832337 | 41832337 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6315-01A-11D-1719-10 | TCGA-G4-6315-10A-01D-1720-10 | g.chr8:41832337T>C | c.1367A>G | c.(1366-1368)aAt>aGt | p.N456S |
COAD | 8 | 41834576 | 41834576 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr8:41834576C>T | c.1313G>A | c.(1312-1314)cGa>cAa | p.R438Q |
COAD | 8 | 41836162 | 41836162 | + | Silent | SNP | C | C | T | TCGA-CM-4746-01A-01D-1408-10 | TCGA-CM-4746-10A-01D-1408-10 | g.chr8:41836162C>T | c.1041G>A | c.(1039-1041)acG>acA | p.T347T |
COAD | 8 | 41836215 | 41836215 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr8:41836215G>A | c.988C>T | c.(988-990)Cgc>Tgc | p.R330C |
COAD | 8 | 41906260 | 41906260 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr8:41906260C>T | c.236G>A | c.(235-237)cGa>cAa | p.R79Q |
COAD | 8 | 41906365 | 41906365 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr8:41906365C>T | c.131G>A | c.(130-132)cGt>cAt | p.R44H |
COADREAD | 8 | 41789773 | 41789773 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr8:41789773C>T | c.5965G>A | c.(5965-5967)Gct>Act | p.A1989T |
COADREAD | 8 | 41790016 | 41790016 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00A-01A-01W-A005-10 | TCGA-AA-A00A-10A-01W-A005-10 | g.chr8:41790016C>T | c.5722G>A | c.(5722-5724)Gcc>Acc | p.A1908T |
COADREAD | 8 | 41790054 | 41790054 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr8:41790054C>T | c.5684G>A | c.(5683-5685)cGt>cAt | p.R1895H |
COADREAD | 8 | 41790070 | 41790070 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4682-01B-01D-1408-10 | TCGA-AZ-4682-10A-01D-1408-10 | g.chr8:41790070C>T | c.5668G>A | c.(5668-5670)Gca>Aca | p.A1890T |
COADREAD | 8 | 41790493 | 41790493 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6625-01A-21D-1771-10 | TCGA-G4-6625-11A-01D-1771-10 | g.chr8:41790493C>T | c.5245G>A | c.(5245-5247)Gcc>Acc | p.A1749T |
COADREAD | 8 | 41790573 | 41790573 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:41790573T>G | c.5165A>C | c.(5164-5166)gAa>gCa | p.E1722A |
COADREAD | 8 | 41790659 | 41790660 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr8:41790659_41790660insG | c.5078_5079insC | c.(5077-5079)ccafs | p.P1693fs |
COADREAD | 8 | 41790674 | 41790674 | + | Silent | SNP | C | C | T | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr8:41790674C>T | c.5064G>A | c.(5062-5064)caG>caA | p.Q1688Q |
COADREAD | 8 | 41791251 | 41791251 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr8:41791251G>A | c.4487C>T | c.(4486-4488)tCg>tTg | p.S1496L |
COADREAD | 8 | 41791311 | 41791311 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00A-01A-01W-A005-10 | TCGA-AA-A00A-10A-01W-A005-10 | g.chr8:41791311G>A | c.4427C>T | c.(4426-4428)gCg>gTg | p.A1476V |
COADREAD | 8 | 41791516 | 41791516 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:41791516C>T | c.4222G>A | c.(4222-4224)Gaa>Aaa | p.E1408K |
COADREAD | 8 | 41792011 | 41792011 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr8:41792011delC | c.3727delG | c.(3727-3729)gatfs | p.D1243fs |
COADREAD | 8 | 41792145 | 41792145 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3989-01A-01W-0995-10 | TCGA-AA-3989-10A-01W-0999-10 | g.chr8:41792145G>A | c.3593C>T | c.(3592-3594)gCt>gTt | p.A1198V |
COADREAD | 8 | 41794925 | 41794925 | + | Silent | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr8:41794925G>A | c.3201C>T | c.(3199-3201)atC>atT | p.I1067I |
COADREAD | 8 | 41798469 | 41798469 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr8:41798469T>C | c.2930A>G | c.(2929-2931)gAc>gGc | p.D977G |
COADREAD | 8 | 41798484 | 41798484 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr8:41798484C>T | c.2915G>A | c.(2914-2916)cGc>cAc | p.R972H |
COADREAD | 8 | 41798487 | 41798487 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr8:41798487C>T | c.2912G>A | c.(2911-2913)cGt>cAt | p.R971H |
COADREAD | 8 | 41798495 | 41798495 | + | Silent | SNP | C | C | T | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr8:41798495C>T | c.2904G>A | c.(2902-2904)agG>agA | p.R968R |
COADREAD | 8 | 41798808 | 41798808 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chr8:41798808C>T | c.2591G>A | c.(2590-2592)cGg>cAg | p.R864Q |
COADREAD | 8 | 41798926 | 41798926 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:41798926C>A | c.2473G>T | c.(2473-2475)Gat>Tat | p.D825Y |
COADREAD | 8 | 41798947 | 41798947 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A01Q-01A-01W-A005-10 | TCGA-AA-A01Q-10A-01W-A005-10 | g.chr8:41798947A>G | c.2452T>C | c.(2452-2454)Tct>Cct | p.S818P |
COADREAD | 8 | 41801475 | 41801475 | + | Missense_Mutation | SNP | T | T | A | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr8:41801475T>A | c.2019A>T | c.(2017-2019)gaA>gaT | p.E673D |
COADREAD | 8 | 41801475 | 41801475 | + | Silent | SNP | T | T | C | TCGA-AU-3779-01A-01D-1719-10 | TCGA-AU-3779-10A-01D-1719-10 | g.chr8:41801475T>C | c.2019A>G | c.(2017-2019)gaA>gaG | p.E673E |
COADREAD | 8 | 41801477 | 41801477 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr8:41801477C>A | c.2017G>T | c.(2017-2019)Gaa>Taa | p.E673* |
COADREAD | 8 | 41804115 | 41804115 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr8:41804115C>T | c.1990G>A | c.(1990-1992)Gat>Aat | p.D664N |
COADREAD | 8 | 41804115 | 41804115 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr8:41804115C>T | c.1990G>A | c.(1990-1992)Gat>Aat | p.D664N |
COADREAD | 8 | 41805417 | 41805417 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr8:41805417A>G | c.1754T>C | c.(1753-1755)gTg>gCg | p.V585A |
COADREAD | 8 | 41805417 | 41805417 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6303-01A-11D-1771-10 | TCGA-G4-6303-10A-01D-1771-10 | g.chr8:41805417A>G | c.1754T>C | c.(1753-1755)gTg>gCg | p.V585A |
COADREAD | 8 | 41806765 | 41806765 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:41806765C>A | c.1715G>T | c.(1714-1716)aGa>aTa | p.R572I |
COADREAD | 8 | 41812837 | 41812837 | + | Silent | SNP | G | G | A | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr8:41812837G>A | c.1575C>T | c.(1573-1575)tcC>tcT | p.S525S |
COADREAD | 8 | 41812840 | 41812840 | + | Silent | SNP | G | G | A | TCGA-F4-6807-01A-11D-1835-10 | TCGA-F4-6807-10A-01D-1835-10 | g.chr8:41812840G>A | c.1572C>T | c.(1570-1572)tcC>tcT | p.S524S |
COADREAD | 8 | 41832336 | 41832336 | + | Silent | SNP | A | A | G | TCGA-DM-A28K-01A-21D-A16V-10 | TCGA-DM-A28K-10A-01D-A16V-10 | g.chr8:41832336A>G | c.1368T>C | c.(1366-1368)aaT>aaC | p.N456N |
COADREAD | 8 | 41832337 | 41832337 | + | Missense_Mutation | SNP | T | T | C | TCGA-AZ-6607-01A-11D-1835-10 | TCGA-AZ-6607-11A-01D-1835-10 | g.chr8:41832337T>C | c.1367A>G | c.(1366-1368)aAt>aGt | p.N456S |
COADREAD | 8 | 41832337 | 41832337 | + | Missense_Mutation | SNP | T | T | C | TCGA-DM-A28E-01A-11D-A16V-10 | TCGA-DM-A28E-10A-01D-A16V-10 | g.chr8:41832337T>C | c.1367A>G | c.(1366-1368)aAt>aGt | p.N456S |
COADREAD | 8 | 41832337 | 41832337 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6315-01A-11D-1719-10 | TCGA-G4-6315-10A-01D-1720-10 | g.chr8:41832337T>C | c.1367A>G | c.(1366-1368)aAt>aGt | p.N456S |
COADREAD | 8 | 41832338 | 41832338 | + | Missense_Mutation | SNP | T | T | C | TCGA-DC-6681-01A-11D-1826-10 | TCGA-DC-6681-10A-01D-1826-10 | g.chr8:41832338T>C | c.1366A>G | c.(1366-1368)Aat>Gat | p.N456D |
COADREAD | 8 | 41834576 | 41834576 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr8:41834576C>T | c.1313G>A | c.(1312-1314)cGa>cAa | p.R438Q |
COADREAD | 8 | 41834819 | 41834819 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr8:41834819C>T | c.1070G>A | c.(1069-1071)cGa>cAa | p.R357Q |
COADREAD | 8 | 41836162 | 41836162 | + | Silent | SNP | C | C | T | TCGA-CM-4746-01A-01D-1408-10 | TCGA-CM-4746-10A-01D-1408-10 | g.chr8:41836162C>T | c.1041G>A | c.(1039-1041)acG>acA | p.T347T |
COADREAD | 8 | 41836215 | 41836215 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr8:41836215G>A | c.988C>T | c.(988-990)Cgc>Tgc | p.R330C |
COADREAD | 8 | 41906260 | 41906260 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr8:41906260C>T | c.236G>A | c.(235-237)cGa>cAa | p.R79Q |
COADREAD | 8 | 41906365 | 41906365 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3525-01A-02W-0833-10 | TCGA-AA-3525-10A-01W-0833-10 | g.chr8:41906365C>T | c.131G>A | c.(130-132)cGt>cAt | p.R44H |
DLBC | 8 | 41790866 | 41790866 | + | Silent | SNP | G | G | C | TCGA-G8-6325-01A-11D-2210-10 | TCGA-G8-6325-10A-01D-2210-10 | g.chr8:41790866G>C | c.4872C>G | c.(4870-4872)gtC>gtG | p.V1624V |
DLBC | 8 | 41834600 | 41834600 | + | Missense_Mutation | SNP | A | A | G | TCGA-VB-A8QN-01A-11D-A382-10 | TCGA-VB-A8QN-10A-01D-A385-10 | g.chr8:41834600A>G | c.1289T>C | c.(1288-1290)gTg>gCg | p.V430A |
ESCA | 8 | 41790300 | 41790300 | + | Missense_Mutation | SNP | G | G | T | TCGA-RE-A7BO-01A-11D-A33E-09 | TCGA-RE-A7BO-10A-01D-A33H-09 | g.chr8:41790300G>T | c.5438C>A | c.(5437-5439)cCc>cAc | p.P1813H |
ESCA | 8 | 41791382 | 41791382 | + | Silent | SNP | C | C | T | TCGA-IG-A7DP-01A-31D-A33E-09 | TCGA-IG-A7DP-10A-01D-A33H-09 | g.chr8:41791382C>T | c.4356G>A | c.(4354-4356)gcG>gcA | p.A1452A |
ESCA | 8 | 41791588 | 41791588 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr8:41791588C>T | c.4150G>A | c.(4150-4152)Gtg>Atg | p.V1384M |
ESCA | 8 | 41792007 | 41792007 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A88W-01A-11D-A351-09 | TCGA-L5-A88W-11A-11D-A351-09 | g.chr8:41792007G>A | c.3731C>T | c.(3730-3732)gCa>gTa | p.A1244V |
ESCA | 8 | 41798620 | 41798620 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A4OW-01A-11D-A28B-09 | TCGA-L5-A4OW-11A-11D-A28E-09 | g.chr8:41798620G>A | c.2779C>T | c.(2779-2781)Cca>Tca | p.P927S |
ESCA | 8 | 41800501 | 41800501 | + | Missense_Mutation | SNP | C | C | T | TCGA-JY-A93D-01A-11D-A387-09 | TCGA-JY-A93D-10A-01D-A38A-09 | g.chr8:41800501C>T | c.2246G>A | c.(2245-2247)cGg>cAg | p.R749Q |
ESCA | 8 | 41806773 | 41806773 | + | Silent | SNP | C | C | T | TCGA-LN-A4A9-01A-11D-A28B-09 | TCGA-LN-A4A9-10A-01D-A28E-09 | g.chr8:41806773C>T | c.1707G>A | c.(1705-1707)gaG>gaA | p.E569E |
ESCA | 8 | 41836217 | 41836217 | + | Missense_Mutation | SNP | C | C | T | TCGA-XP-A8T6-01A-11D-A36J-09 | TCGA-XP-A8T6-10A-01D-A36M-09 | g.chr8:41836217C>T | c.986G>A | c.(985-987)cGg>cAg | p.R329Q |
ESCA | 8 | 41836223 | 41836223 | + | Missense_Mutation | SNP | A | A | G | TCGA-L5-A88S-01A-11D-A36J-09 | TCGA-L5-A88S-11A-21D-A36M-09 | g.chr8:41836223A>G | c.980T>C | c.(979-981)aTa>aCa | p.I327T |
ESCA | 8 | 41838370 | 41838370 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A8NF-01A-11D-A37C-09 | TCGA-L5-A8NF-11A-11D-A37F-09 | g.chr8:41838370G>A | c.901C>T | c.(901-903)Cca>Tca | p.P301S |
ESCA | 8 | 41838388 | 41838388 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr8:41838388G>T | c.883C>A | c.(883-885)Ccg>Acg | p.P295T |
GBMLGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-HT-7477-01B-11D-A289-08 | TCGA-HT-7477-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
GBMLGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-HT-8015-01B-11D-A289-08 | TCGA-HT-8015-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
GBMLGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-HT-8111-01A-11D-2395-08 | TCGA-HT-8111-10A-01D-2396-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
GBMLGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-HT-A5R5-01A-11D-A289-08 | TCGA-HT-A5R5-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
GBMLGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-HT-A5RA-01A-11D-A289-08 | TCGA-HT-A5RA-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
GBMLGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-P5-A5F0-01A-11D-A289-08 | TCGA-P5-A5F0-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
GBMLGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-P5-A5F1-01A-11D-A289-08 | TCGA-P5-A5F1-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
GBMLGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-P5-A5F2-01A-11D-A289-08 | TCGA-P5-A5F2-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
GBMLGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-P5-A5F4-01A-11D-A289-08 | TCGA-P5-A5F4-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
GBMLGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-P5-A5F6-01A-11D-A289-08 | TCGA-P5-A5F6-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
GBMLGG | 8 | 41791219 | 41791219 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:41791219T>C | c.4519A>G | c.(4519-4521)Agt>Ggt | p.S1507G |
GBMLGG | 8 | 41791277 | 41791277 | + | Missense_Mutation | SNP | C | C | A | TCGA-S9-A6U0-01A-12D-A32B-08 | TCGA-S9-A6U0-10A-01D-A329-08 | g.chr8:41791277C>A | c.4461G>T | c.(4459-4461)caG>caT | p.Q1487H |
GBMLGG | 8 | 41798681 | 41798681 | + | Silent | SNP | T | T | C | TCGA-HT-A74K-01A-11D-A32B-08 | TCGA-HT-A74K-10A-01D-A329-08 | g.chr8:41798681T>C | c.2718A>G | c.(2716-2718)tcA>tcG | p.S906S |
GBMLGG | 8 | 41839368 | 41839368 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:41839368C>A | c.814G>T | c.(814-816)Ggc>Tgc | p.G272C |
HNSC | 8 | 41791310 | 41791310 | + | Silent | SNP | C | C | T | TCGA-CN-6994-01A-11D-1912-08 | TCGA-CN-6994-10A-01D-1912-08 | g.chr8:41791310C>T | c.4428G>A | c.(4426-4428)gcG>gcA | p.A1476A |
HNSC | 8 | 41791507 | 41791507 | + | Missense_Mutation | SNP | C | C | G | TCGA-CR-7371-01A-11D-2012-08 | TCGA-CR-7371-10A-01D-2013-08 | g.chr8:41791507C>G | c.4231G>C | c.(4231-4233)Gag>Cag | p.E1411Q |
HNSC | 8 | 41791631 | 41791631 | + | Silent | SNP | G | G | A | TCGA-CV-6953-01A-11D-1912-08 | TCGA-CV-6953-10A-01D-1912-08 | g.chr8:41791631G>A | c.4107C>T | c.(4105-4107)acC>acT | p.T1369T |
HNSC | 8 | 41791962 | 41791962 | + | Missense_Mutation | SNP | T | T | C | TCGA-IQ-A6SH-01A-12D-A34J-08 | TCGA-IQ-A6SH-10A-01D-A34M-08 | g.chr8:41791962T>C | c.3776A>G | c.(3775-3777)aAt>aGt | p.N1259S |
HNSC | 8 | 41792081 | 41792081 | + | Silent | SNP | T | T | C | TCGA-CR-7374-01A-11D-2012-08 | TCGA-CR-7374-10A-01D-2013-08 | g.chr8:41792081T>C | c.3657A>G | c.(3655-3657)ctA>ctG | p.L1219L |
HNSC | 8 | 41792294 | 41792294 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CN-4731-01A-01D-1434-08 | TCGA-CN-4731-10A-01D-1434-08 | g.chr8:41792294delC | c.3444delG | c.(3442-3444)aagfs | p.K1150fs |
HNSC | 8 | 41798569 | 41798569 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CN-5369-01A-01D-1434-08 | TCGA-CN-5369-10A-01D-1434-08 | g.chr8:41798569delC | c.2830delG | c.(2830-2832)gttfs | p.V944fs |
HNSC | 8 | 41798738 | 41798738 | + | Silent | SNP | G | G | C | TCGA-CR-7371-01A-11D-2012-08 | TCGA-CR-7371-10A-01D-2013-08 | g.chr8:41798738G>C | c.2661C>G | c.(2659-2661)ctC>ctG | p.L887L |
HNSC | 8 | 41798814 | 41798814 | + | Missense_Mutation | SNP | G | G | A | TCGA-D6-6516-01A-11D-1870-08 | TCGA-D6-6516-10A-01D-1870-08 | g.chr8:41798814G>A | c.2585C>T | c.(2584-2586)cCa>cTa | p.P862L |
HNSC | 8 | 41798870 | 41798870 | + | Silent | SNP | A | A | G | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr8:41798870A>G | c.2529T>C | c.(2527-2529)tcT>tcC | p.S843S |
HNSC | 8 | 41801352 | 41801352 | + | Missense_Mutation | SNP | C | C | G | TCGA-UF-A7JT-01A-11D-A34J-08 | TCGA-UF-A7JT-10A-01D-A34M-08 | g.chr8:41801352C>G | c.2142G>C | c.(2140-2142)aaG>aaC | p.K714N |
HNSC | 8 | 41836253 | 41836253 | + | Missense_Mutation | SNP | C | C | G | TCGA-CR-7364-01A-11D-2012-08 | TCGA-CR-7364-10A-01D-2013-08 | g.chr8:41836253C>G | c.950G>C | c.(949-951)cGa>cCa | p.R317P |
HNSC | 8 | 41839364 | 41839364 | + | Missense_Mutation | SNP | T | T | C | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr8:41839364T>C | c.818A>G | c.(817-819)aAa>aGa | p.K273R |
KIPAN | 8 | 41790172 | 41790172 | + | Missense_Mutation | SNP | A | A | G | TCGA-2K-A9WE-01A-11D-A382-10 | TCGA-2K-A9WE-10A-01D-A385-10 | g.chr8:41790172A>G | c.5566T>C | c.(5566-5568)Tcc>Ccc | p.S1856P |
KIPAN | 8 | 41790405 | 41790405 | + | Missense_Mutation | SNP | G | G | T | TCGA-BP-5181-01A-01D-1429-08 | TCGA-BP-5181-11A-01D-1429-08 | g.chr8:41790405G>T | c.5333C>A | c.(5332-5334)aCt>aAt | p.T1778N |
KIPAN | 8 | 41791800 | 41791800 | + | Missense_Mutation | SNP | T | T | C | TCGA-BP-4167-01A-02D-1386-10 | TCGA-BP-4167-11A-01D-1251-10 | g.chr8:41791800T>C | c.3938A>G | c.(3937-3939)gAc>gGc | p.D1313G |
KIPAN | 8 | 41791942 | 41791942 | + | Missense_Mutation | SNP | T | T | G | TCGA-DW-7837-01A-11D-2136-08 | TCGA-DW-7837-10A-01D-2136-08 | g.chr8:41791942T>G | c.3796A>C | c.(3796-3798)Aag>Cag | p.K1266Q |
KIPAN | 8 | 41792289 | 41792289 | + | Missense_Mutation | SNP | T | T | G | TCGA-CZ-4853-01A-01D-1429-08 | TCGA-CZ-4853-11A-01D-1429-08 | g.chr8:41792289T>G | c.3449A>C | c.(3448-3450)aAg>aCg | p.K1150T |
KIPAN | 8 | 41794928 | 41794928 | + | Missense_Mutation | SNP | C | C | A | TCGA-B9-5155-01A-01D-1589-08 | TCGA-B9-5155-10A-01D-1589-08 | g.chr8:41794928C>A | c.3198G>T | c.(3196-3198)gaG>gaT | p.E1066D |
KIPAN | 8 | 41794945 | 41794945 | + | Missense_Mutation | SNP | A | A | T | TCGA-HE-A5NK-01A-11D-A26P-10 | TCGA-HE-A5NK-10A-01D-A26P-10 | g.chr8:41794945A>T | c.3181T>A | c.(3181-3183)Tta>Ata | p.L1061I |
KIPAN | 8 | 41801275 | 41801275 | + | Missense_Mutation | SNP | C | C | A | TCGA-BP-4177-01A-02D-1421-08 | TCGA-BP-4177-11A-01D-1421-08 | g.chr8:41801275C>A | c.2219G>T | c.(2218-2220)cGt>cTt | p.R740L |
KIPAN | 8 | 41804117 | 41804117 | + | Missense_Mutation | SNP | A | A | G | TCGA-B0-5710-01A-11D-1669-08 | TCGA-B0-5710-11A-01D-1669-08 | g.chr8:41804117A>G | c.1988T>C | c.(1987-1989)aTc>aCc | p.I663T |
KIPAN | 8 | 41836161 | 41836161 | + | Splice_Site | DEL | C | C | - | TCGA-BQ-7046-01A-11D-1961-08 | TCGA-BQ-7046-11A-01D-1961-08 | g.chr8:41836161delC | c.1042delG | c.(1042-1044)gta>ta | p.V348fs |
KIPAN | 8 | 41836218 | 41836218 | + | Missense_Mutation | SNP | G | G | A | TCGA-B0-5099-01A-01D-1421-08 | TCGA-B0-5099-11A-01D-1421-08 | g.chr8:41836218G>A | c.985C>T | c.(985-987)Cgg>Tgg | p.R329W |
KIPAN | 8 | 41906305 | 41906305 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-2Z-A9J2-01A-11D-A382-10 | TCGA-2Z-A9J2-10A-01D-A385-10 | g.chr8:41906305G>T | c.191C>A | c.(190-192)tCa>tAa | p.S64* |
KIRC | 8 | 41790405 | 41790405 | + | Missense_Mutation | SNP | G | G | T | TCGA-BP-5181-01A-01D-1429-08 | TCGA-BP-5181-11A-01D-1429-08 | g.chr8:41790405G>T | c.5333C>A | c.(5332-5334)aCt>aAt | p.T1778N |
KIRC | 8 | 41791800 | 41791800 | + | Missense_Mutation | SNP | T | T | C | TCGA-BP-4167-01A-02D-1386-10 | TCGA-BP-4167-11A-01D-1251-10 | g.chr8:41791800T>C | c.3938A>G | c.(3937-3939)gAc>gGc | p.D1313G |
KIRC | 8 | 41792289 | 41792289 | + | Missense_Mutation | SNP | T | T | G | TCGA-CZ-4853-01A-01D-1429-08 | TCGA-CZ-4853-11A-01D-1429-08 | g.chr8:41792289T>G | c.3449A>C | c.(3448-3450)aAg>aCg | p.K1150T |
KIRC | 8 | 41801275 | 41801275 | + | Missense_Mutation | SNP | C | C | A | TCGA-BP-4177-01A-02D-1421-08 | TCGA-BP-4177-11A-01D-1421-08 | g.chr8:41801275C>A | c.2219G>T | c.(2218-2220)cGt>cTt | p.R740L |
KIRC | 8 | 41804117 | 41804117 | + | Missense_Mutation | SNP | A | A | G | TCGA-B0-5710-01A-11D-1669-08 | TCGA-B0-5710-11A-01D-1669-08 | g.chr8:41804117A>G | c.1988T>C | c.(1987-1989)aTc>aCc | p.I663T |
KIRC | 8 | 41836218 | 41836218 | + | Missense_Mutation | SNP | G | G | A | TCGA-B0-5099-01A-01D-1421-08 | TCGA-B0-5099-11A-01D-1421-08 | g.chr8:41836218G>A | c.985C>T | c.(985-987)Cgg>Tgg | p.R329W |
KIRP | 8 | 41790172 | 41790172 | + | Missense_Mutation | SNP | A | A | G | TCGA-2K-A9WE-01A-11D-A382-10 | TCGA-2K-A9WE-10A-01D-A385-10 | g.chr8:41790172A>G | c.5566T>C | c.(5566-5568)Tcc>Ccc | p.S1856P |
KIRP | 8 | 41791942 | 41791942 | + | Missense_Mutation | SNP | T | T | G | TCGA-DW-7837-01A-11D-2136-08 | TCGA-DW-7837-10A-01D-2136-08 | g.chr8:41791942T>G | c.3796A>C | c.(3796-3798)Aag>Cag | p.K1266Q |
KIRP | 8 | 41794928 | 41794928 | + | Missense_Mutation | SNP | C | C | A | TCGA-B9-5155-01A-01D-1589-08 | TCGA-B9-5155-10A-01D-1589-08 | g.chr8:41794928C>A | c.3198G>T | c.(3196-3198)gaG>gaT | p.E1066D |
KIRP | 8 | 41794945 | 41794945 | + | Missense_Mutation | SNP | A | A | T | TCGA-HE-A5NK-01A-11D-A26P-10 | TCGA-HE-A5NK-10A-01D-A26P-10 | g.chr8:41794945A>T | c.3181T>A | c.(3181-3183)Tta>Ata | p.L1061I |
KIRP | 8 | 41836161 | 41836161 | + | Splice_Site | DEL | C | C | - | TCGA-BQ-7046-01A-11D-1961-08 | TCGA-BQ-7046-11A-01D-1961-08 | g.chr8:41836161delC | c.1042delG | c.(1042-1044)gta>ta | p.V348fs |
KIRP | 8 | 41906305 | 41906305 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-2Z-A9J2-01A-11D-A382-10 | TCGA-2Z-A9J2-10A-01D-A385-10 | g.chr8:41906305G>T | c.191C>A | c.(190-192)tCa>tAa | p.S64* |
LGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-HT-7477-01B-11D-A289-08 | TCGA-HT-7477-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-HT-8015-01B-11D-A289-08 | TCGA-HT-8015-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-HT-8111-01A-11D-2395-08 | TCGA-HT-8111-10A-01D-2396-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-HT-A5R5-01A-11D-A289-08 | TCGA-HT-A5R5-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-HT-A5RA-01A-11D-A289-08 | TCGA-HT-A5RA-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-P5-A5F0-01A-11D-A289-08 | TCGA-P5-A5F0-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-P5-A5F1-01A-11D-A289-08 | TCGA-P5-A5F1-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-P5-A5F2-01A-11D-A289-08 | TCGA-P5-A5F2-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-P5-A5F4-01A-11D-A289-08 | TCGA-P5-A5F4-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LGG | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-P5-A5F6-01A-11D-A289-08 | TCGA-P5-A5F6-10A-01D-A289-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LGG | 8 | 41791219 | 41791219 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:41791219T>C | c.4519A>G | c.(4519-4521)Agt>Ggt | p.S1507G |
LGG | 8 | 41791277 | 41791277 | + | Missense_Mutation | SNP | C | C | A | TCGA-S9-A6U0-01A-12D-A32B-08 | TCGA-S9-A6U0-10A-01D-A329-08 | g.chr8:41791277C>A | c.4461G>T | c.(4459-4461)caG>caT | p.Q1487H |
LGG | 8 | 41798681 | 41798681 | + | Silent | SNP | T | T | C | TCGA-HT-A74K-01A-11D-A32B-08 | TCGA-HT-A74K-10A-01D-A329-08 | g.chr8:41798681T>C | c.2718A>G | c.(2716-2718)tcA>tcG | p.S906S |
LGG | 8 | 41839368 | 41839368 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr8:41839368C>A | c.814G>T | c.(814-816)Ggc>Tgc | p.G272C |
LIHC | 8 | 41790607 | 41790607 | + | Missense_Mutation | SNP | A | A | G | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chr8:41790607A>G | c.5131T>C | c.(5131-5133)Ttc>Ctc | p.F1711L |
LIHC | 8 | 41791422 | 41791422 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-A119-01A-11D-A12Z-10 | TCGA-DD-A119-10A-01D-A12Z-10 | g.chr8:41791422T>C | c.4316A>G | c.(4315-4317)cAt>cGt | p.H1439R |
LIHC | 8 | 41791551 | 41791551 | + | Missense_Mutation | SNP | T | T | C | TCGA-CC-A3MB-01A-11D-A20W-10 | TCGA-CC-A3MB-10A-01D-A20W-10 | g.chr8:41791551T>C | c.4187A>G | c.(4186-4188)cAc>cGc | p.H1396R |
LIHC | 8 | 41791683 | 41791683 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chr8:41791683delA | c.4055delT | c.(4054-4056)ttafs | p.L1352fs |
LIHC | 8 | 41792228 | 41792228 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chr8:41792228delT | c.3510delA | c.(3508-3510)aaafs | p.K1170fs |
LIHC | 8 | 41794799 | 41794799 | + | Missense_Mutation | SNP | T | T | A | TCGA-DD-A119-01A-11D-A12Z-10 | TCGA-DD-A119-10A-01D-A12Z-10 | g.chr8:41794799T>A | c.3327A>T | c.(3325-3327)gaA>gaT | p.E1109D |
LIHC | 8 | 41798614 | 41798614 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DD-AAE6-01A-11D-A40R-10 | TCGA-DD-AAE6-10A-01D-A40U-10 | g.chr8:41798614G>A | c.2785C>T | c.(2785-2787)Cag>Tag | p.Q929* |
LIHC | 8 | 41805294 | 41805294 | + | Missense_Mutation | SNP | C | C | A | TCGA-DD-AAD1-01A-11D-A40R-10 | TCGA-DD-AAD1-10A-01D-A40U-10 | g.chr8:41805294C>A | c.1877G>T | c.(1876-1878)tGc>tTc | p.C626F |
LIHC | 8 | 41812897 | 41812897 | + | Silent | SNP | T | T | C | TCGA-WX-AA46-01A-11D-A38X-10 | TCGA-WX-AA46-10A-01D-A38X-10 | g.chr8:41812897T>C | c.1515A>G | c.(1513-1515)caA>caG | p.Q505Q |
LIHC | 8 | 41832291 | 41832291 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-DD-A39Y-01A-11D-A20W-10 | TCGA-DD-A39Y-11A-11D-A20W-10 | g.chr8:41832291delA | c.1413delT | c.(1411-1413)tttfs | p.F471fs |
LIHC | 8 | 41905925 | 41905925 | + | Missense_Mutation | SNP | C | C | A | TCGA-DD-AADM-01A-11D-A40R-10 | TCGA-DD-AADM-10A-01D-A40U-10 | g.chr8:41905925C>A | c.571G>T | c.(571-573)Gtg>Ttg | p.V191L |
LIHC | 8 | 41906233 | 41906233 | + | Missense_Mutation | SNP | T | T | A | TCGA-DD-AADP-01A-11D-A38X-10 | TCGA-DD-AADP-10A-01D-A38X-10 | g.chr8:41906233T>A | c.263A>T | c.(262-264)cAt>cTt | p.H88L |
LIHC | 8 | 41906387 | 41906387 | + | Missense_Mutation | SNP | A | A | G | TCGA-ES-A2HT-01A-12D-A183-10 | TCGA-ES-A2HT-11A-11D-A183-10 | g.chr8:41906387A>G | c.109T>C | c.(109-111)Tct>Cct | p.S37P |
LUAD | 8 | 41789903 | 41789903 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z057-01A-01W-0747-08 | TCGA-17-Z057-11A-01W-0747-08 | g.chr8:41789903C>A | c.5835G>T | c.(5833-5835)caG>caT | p.Q1945H |
LUAD | 8 | 41790299 | 41790299 | + | Silent | SNP | G | G | A | TCGA-75-6214-01A-41D-1945-08 | TCGA-75-6214-10A-01D-1946-08 | g.chr8:41790299G>A | c.5439C>T | c.(5437-5439)ccC>ccT | p.P1813P |
LUAD | 8 | 41790452 | 41790452 | + | Silent | SNP | G | G | A | TCGA-17-Z028-01A-01W-0746-08 | TCGA-17-Z028-11A-01W-0746-08 | g.chr8:41790452G>A | c.5286C>T | c.(5284-5286)acC>acT | p.T1762T |
LUAD | 8 | 41790583 | 41790583 | + | Missense_Mutation | SNP | C | C | T | TCGA-NJ-A4YP-01A-11D-A25L-08 | TCGA-NJ-A4YP-10A-01D-A25L-08 | g.chr8:41790583C>T | c.5155G>A | c.(5155-5157)Gag>Aag | p.E1719K |
LUAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-78-8662-01A-11D-2393-08 | TCGA-78-8662-10A-01D-2393-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LUAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-86-8672-01A-21D-2393-08 | TCGA-86-8672-10A-01D-2393-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LUAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-86-8673-01A-11D-2393-08 | TCGA-86-8673-10A-01D-2393-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LUAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-97-8547-01A-11D-2393-08 | TCGA-97-8547-10A-01D-2393-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
LUAD | 8 | 41791195 | 41791195 | + | Missense_Mutation | SNP | C | C | T | TCGA-86-8056-01A-11D-2238-08 | TCGA-86-8056-10A-01D-2238-08 | g.chr8:41791195C>T | c.4543G>A | c.(4543-4545)Gaa>Aaa | p.E1515K |
LUAD | 8 | 41791382 | 41791382 | + | Silent | SNP | C | C | A | TCGA-49-4494-01A-01D-1265-08 | TCGA-49-4494-11A-01D-1265-08 | g.chr8:41791382C>A | c.4356G>T | c.(4354-4356)gcG>gcT | p.A1452A |
LUAD | 8 | 41791408 | 41791408 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-49-6745-01A-11D-1855-08 | TCGA-49-6745-11A-01D-1855-08 | g.chr8:41791408G>A | c.4330C>T | c.(4330-4332)Cag>Tag | p.Q1444* |
LUAD | 8 | 41791420 | 41791420 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-78-7149-01A-11D-2036-08 | TCGA-78-7149-10A-01D-2036-08 | g.chr8:41791420C>A | c.4318G>T | c.(4318-4320)Gag>Tag | p.E1440* |
LUAD | 8 | 41791426 | 41791426 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-L9-A444-01A-21D-A24D-08 | TCGA-L9-A444-10A-01D-A24F-08 | g.chr8:41791426C>A | c.4312G>T | c.(4312-4314)Gag>Tag | p.E1438* |
LUAD | 8 | 41791831 | 41791831 | + | Missense_Mutation | SNP | C | C | A | TCGA-62-8399-01A-21D-2323-08 | TCGA-62-8399-10A-01D-2323-08 | g.chr8:41791831C>A | c.3907G>T | c.(3907-3909)Gat>Tat | p.D1303Y |
LUAD | 8 | 41792282 | 41792282 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-50-5941-01A-11D-1753-08 | TCGA-50-5941-10A-01D-1753-08 | g.chr8:41792282C>T | c.3456G>A | c.(3454-3456)tgG>tgA | p.W1152* |
LUAD | 8 | 41792359 | 41792359 | + | Missense_Mutation | SNP | G | G | A | TCGA-97-7941-01A-11D-2184-08 | TCGA-97-7941-10A-01D-2184-08 | g.chr8:41792359G>A | c.3379C>T | c.(3379-3381)Ctt>Ttt | p.L1127F |
LUAD | 8 | 41794835 | 41794835 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-7667-01A-31D-2063-08 | TCGA-44-7667-10A-01D-2063-08 | g.chr8:41794835C>A | c.3291G>T | c.(3289-3291)caG>caT | p.Q1097H |
LUAD | 8 | 41805339 | 41805339 | + | Missense_Mutation | SNP | T | T | A | TCGA-69-A59K-01A-11D-A25L-08 | TCGA-69-A59K-10A-01D-A25L-08 | g.chr8:41805339T>A | c.1832A>T | c.(1831-1833)gAg>gTg | p.E611V |
LUAD | 8 | 41812836 | 41812836 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8511-01A-11D-2393-08 | TCGA-55-8511-10A-01D-2393-08 | g.chr8:41812836G>T | c.1576C>A | c.(1576-1578)Cca>Aca | p.P526T |
LUAD | 8 | 41834584 | 41834584 | + | Silent | SNP | C | C | T | TCGA-67-3771-01A-01D-1040-01 | TCGA-67-3771-10A-01D-1040-01 | g.chr8:41834584C>T | c.1305G>A | c.(1303-1305)gaG>gaA | p.E435E |
LUAD | 8 | 41836245 | 41836245 | + | Silent | SNP | G | G | A | TCGA-MP-A4T4-01A-11D-A25L-08 | TCGA-MP-A4T4-10A-01D-A25L-08 | g.chr8:41836245G>A | c.958C>T | c.(958-960)Cta>Tta | p.L320L |
LUAD | 8 | 41836297 | 41836297 | + | Splice_Site | SNP | T | T | A | TCGA-50-5049-01A-01D-1625-08 | TCGA-50-5049-10A-01D-1625-08 | g.chr8:41836297T>A | | c.e7-2 | |
LUAD | 8 | 41839446 | 41839446 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-8616-01A-11D-2393-08 | TCGA-55-8616-10A-01D-2393-08 | g.chr8:41839446G>C | c.736C>G | c.(736-738)Cct>Gct | p.P246A |
LUAD | 8 | 41906267 | 41906267 | + | Missense_Mutation | SNP | G | G | C | TCGA-MP-A4TA-01A-21D-A24P-08 | TCGA-MP-A4TA-10A-01D-A24P-08 | g.chr8:41906267G>C | c.229C>G | c.(229-231)Cct>Gct | p.P77A |
LUSC | 8 | 41790175 | 41790175 | + | Missense_Mutation | SNP | T | T | A | TCGA-39-5031-01A-01D-1441-08 | TCGA-39-5031-11A-01D-1441-08 | g.chr8:41790175T>A | c.5563A>T | c.(5563-5565)Att>Ttt | p.I1855F |
LUSC | 8 | 41791206 | 41791206 | + | Missense_Mutation | SNP | T | T | A | TCGA-56-6545-01A-11D-1817-08 | TCGA-56-6545-10A-01D-1817-08 | g.chr8:41791206T>A | c.4532A>T | c.(4531-4533)cAg>cTg | p.Q1511L |
LUSC | 8 | 41792162 | 41792162 | + | Silent | SNP | G | G | A | TCGA-85-6560-01A-11D-1817-08 | TCGA-85-6560-10A-01D-1817-08 | g.chr8:41792162G>A | c.3576C>T | c.(3574-3576)atC>atT | p.I1192I |
LUSC | 8 | 41798403 | 41798403 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-34-2600-01A-01D-1522-08 | TCGA-34-2600-11A-01D-1522-08 | g.chr8:41798403G>C | c.2996C>G | c.(2995-2997)tCa>tGa | p.S999* |
LUSC | 8 | 41798770 | 41798770 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-60-2720-01A-01D-1522-08 | TCGA-60-2720-11A-01D-1522-08 | g.chr8:41798770C>A | c.2629G>T | c.(2629-2631)Gaa>Taa | p.E877* |
LUSC | 8 | 41800488 | 41800488 | + | Silent | SNP | G | G | A | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr8:41800488G>A | c.2259C>T | c.(2257-2259)atC>atT | p.I753I |
LUSC | 8 | 41804152 | 41804152 | + | Silent | SNP | A | A | C | TCGA-46-3765-01A-01D-0983-08 | TCGA-46-3765-10A-01D-0983-08 | g.chr8:41804152A>C | c.1953T>G | c.(1951-1953)ccT>ccG | p.P651P |
LUSC | 8 | 41806877 | 41806877 | + | Missense_Mutation | SNP | G | G | A | TCGA-18-5592-01A-01D-1632-08 | TCGA-18-5592-11A-11D-1632-08 | g.chr8:41806877G>A | c.1603C>T | c.(1603-1605)Ccc>Tcc | p.P535S |
LUSC | 8 | 41834527 | 41834527 | + | Splice_Site | SNP | T | T | A | TCGA-33-4586-01A-01D-1441-08 | TCGA-33-4586-11A-01D-1441-08 | g.chr8:41834527T>A | c.1362A>T | c.(1360-1362)acA>acT | p.T454T |
LUSC | 8 | 41834549 | 41834549 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr8:41834549G>C | c.1340C>G | c.(1339-1341)tCa>tGa | p.S447* |
LUSC | 8 | 41834699 | 41834699 | + | Missense_Mutation | SNP | T | T | C | TCGA-33-4582-01A-01D-1441-08 | TCGA-33-4582-11A-01D-1441-08 | g.chr8:41834699T>C | c.1190A>G | c.(1189-1191)aAt>aGt | p.N397S |
LUSC | 8 | 41834781 | 41834781 | + | Missense_Mutation | SNP | G | G | A | TCGA-22-5477-01A-01D-1632-08 | TCGA-22-5477-11A-11D-1632-08 | g.chr8:41834781G>A | c.1108C>T | c.(1108-1110)Ctt>Ttt | p.L370F |
LUSC | 8 | 41834802 | 41834802 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr8:41834802C>A | c.1087G>T | c.(1087-1089)Ggt>Tgt | p.G363C |
LUSC | 8 | 41838388 | 41838388 | + | Missense_Mutation | SNP | G | G | C | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr8:41838388G>C | c.883C>G | c.(883-885)Ccg>Gcg | p.P295A |
LUSC | 8 | 41845059 | 41845059 | + | Missense_Mutation | SNP | A | A | G | TCGA-18-3408-01A-01D-0983-08 | TCGA-18-3408-11A-01D-0983-08 | g.chr8:41845059A>G | c.623T>C | c.(622-624)aTc>aCc | p.I208T |
OV | 8 | 41791477 | 41791477 | + | Missense_Mutation | SNP | C | C | G | TCGA-61-1727-01A-01W-0639-09 | TCGA-61-1727-11A-01W-0639-09 | g.chr8:41791477C>G | c.4261G>C | c.(4261-4263)Gat>Cat | p.D1421H |
OV | 8 | 41792211 | 41792211 | + | Missense_Mutation | SNP | C | C | G | TCGA-23-2645-01A-01W-1091-09 | TCGA-23-2645-10A-01W-1091-09 | g.chr8:41792211C>G | c.3527G>C | c.(3526-3528)aGt>aCt | p.S1176T |
OV | 8 | 41801475 | 41801475 | + | Missense_Mutation | SNP | T | T | G | TCGA-13-0714-01A-01W-0370-10 | TCGA-13-0714-10B-01W-0370-10 | g.chr8:41801475T>G | c.2019A>C | c.(2017-2019)gaA>gaC | p.E673D |
OV | 8 | 41805418 | 41805418 | + | Missense_Mutation | SNP | C | C | T | TCGA-09-2049-01D-01W-0799-08 | TCGA-09-2049-10A-01W-0799-08 | g.chr8:41805418C>T | c.1753G>A | c.(1753-1755)Gtg>Atg | p.V585M |
OV | 8 | 41832337 | 41832337 | + | Missense_Mutation | SNP | T | T | C | TCGA-13-0904-01A-02W-0420-08 | TCGA-13-0904-10A-01D-0399-08 | g.chr8:41832337T>C | c.1367A>G | c.(1366-1368)aAt>aGt | p.N456S |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-2L-AAQI-01A-12D-A397-08 | TCGA-2L-AAQI-11A-11D-A39A-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-2L-AAQJ-01A-12D-A397-08 | TCGA-2L-AAQJ-11A-11D-A39A-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-3A-A9IB-01A-21D-A397-08 | TCGA-3A-A9IB-10A-01D-A39A-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-3A-A9IH-01A-12D-A397-08 | TCGA-3A-A9IH-10A-01D-A39A-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-3A-A9IS-01A-21D-A397-08 | TCGA-3A-A9IS-10A-01D-A39A-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-3A-A9IU-01A-11D-A397-08 | TCGA-3A-A9IU-10A-01D-A39A-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-FB-AAPS-01A-12D-A397-08 | TCGA-FB-AAPS-11A-11D-A39A-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-HV-AA8X-01A-11D-A397-08 | TCGA-HV-AA8X-10A-01D-A39A-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-IB-8126-01A-11D-2396-08 | TCGA-IB-8126-10A-01D-2396-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-RB-AA9M-01A-11D-A397-08 | TCGA-RB-AA9M-10A-01D-A39A-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-US-A77G-01A-11D-A32N-08 | TCGA-US-A77G-11A-11D-A32N-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-US-A77J-01A-11D-A32N-08 | TCGA-US-A77J-11A-11D-A32N-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41790659 | 41790659 | + | Silent | SNP | T | T | G | TCGA-XD-AAUL-01A-21D-A397-08 | TCGA-XD-AAUL-10A-01D-A39A-08 | g.chr8:41790659T>G | c.5079A>C | c.(5077-5079)ccA>ccC | p.P1693P |
PAAD | 8 | 41791219 | 41791219 | + | Missense_Mutation | SNP | T | T | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr8:41791219T>G | c.4519A>C | c.(4519-4521)Agt>Cgt | p.S1507R |
PAAD | 8 | 41794801 | 41794801 | + | Missense_Mutation | SNP | C | C | T | TCGA-H8-A6C1-01A-11D-A32N-08 | TCGA-H8-A6C1-10A-01D-A32N-08 | g.chr8:41794801C>T | c.3325G>A | c.(3325-3327)Gaa>Aaa | p.E1109K |
PAAD | 8 | 41834718 | 41834718 | + | Missense_Mutation | SNP | C | C | G | TCGA-HZ-7918-01A-11D-2154-08 | TCGA-HZ-7918-10A-01D-2154-08 | g.chr8:41834718C>G | c.1171G>C | c.(1171-1173)Gac>Cac | p.D391H |
PCPG | 8 | 41792302 | 41792302 | + | Silent | SNP | A | A | G | TCGA-SA-A6C2-01A-11D-A35I-08 | TCGA-SA-A6C2-10A-01D-A35G-08 | g.chr8:41792302A>G | c.3436T>C | c.(3436-3438)Ttg>Ctg | p.L1146L |
PCPG | 8 | 41805396 | 41805396 | + | Missense_Mutation | SNP | T | T | A | TCGA-QR-A6GT-01A-11D-A35D-08 | TCGA-QR-A6GT-10A-01D-A35B-08 | g.chr8:41805396T>A | c.1775A>T | c.(1774-1776)aAc>aTc | p.N592I |
PRAD | 8 | 41790016 | 41790016 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr8:41790016C>T | c.5722G>A | c.(5722-5724)Gcc>Acc | p.A1908T |
PRAD | 8 | 41795087 | 41795087 | + | Splice_Site | SNP | C | C | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr8:41795087C>A | | c.e17-1 | |
PRAD | 8 | 41800403 | 41800403 | + | Missense_Mutation | SNP | A | A | C | TCGA-EJ-5504-01A-01D-1576-08 | TCGA-EJ-5504-10A-01D-1577-08 | g.chr8:41800403A>C | c.2344T>G | c.(2344-2346)Tcc>Gcc | p.S782A |
PRAD | 8 | 41801448 | 41801448 | + | Silent | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr8:41801448C>T | c.2046G>A | c.(2044-2046)ccG>ccA | p.P682P |
PRAD | 8 | 41836190 | 41836190 | + | Missense_Mutation | SNP | G | G | A | TCGA-QU-A6IO-01A-11D-A31L-08 | TCGA-QU-A6IO-10A-01D-A31J-08 | g.chr8:41836190G>A | c.1013C>T | c.(1012-1014)cCa>cTa | p.P338L |
PRAD | 8 | 41845068 | 41845068 | + | Missense_Mutation | SNP | G | G | A | TCGA-CH-5762-01A-11D-1576-08 | TCGA-CH-5762-11A-01D-1576-08 | g.chr8:41845068G>A | c.614C>T | c.(613-615)cCa>cTa | p.P205L |
PRAD | 8 | 41905902 | 41905902 | + | Missense_Mutation | SNP | C | C | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr8:41905902C>A | c.594G>T | c.(592-594)aaG>aaT | p.K198N |
READ | 8 | 41790573 | 41790573 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:41790573T>G | c.5165A>C | c.(5164-5166)gAa>gCa | p.E1722A |
READ | 8 | 41791516 | 41791516 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:41791516C>T | c.4222G>A | c.(4222-4224)Gaa>Aaa | p.E1408K |
READ | 8 | 41798926 | 41798926 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:41798926C>A | c.2473G>T | c.(2473-2475)Gat>Tat | p.D825Y |
READ | 8 | 41806765 | 41806765 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr8:41806765C>A | c.1715G>T | c.(1714-1716)aGa>aTa | p.R572I |
READ | 8 | 41832338 | 41832338 | + | Missense_Mutation | SNP | T | T | C | TCGA-DC-6681-01A-11D-1826-10 | TCGA-DC-6681-10A-01D-1826-10 | g.chr8:41832338T>C | c.1366A>G | c.(1366-1368)Aat>Gat | p.N456D |
READ | 8 | 41834819 | 41834819 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr8:41834819C>T | c.1070G>A | c.(1069-1071)cGa>cAa | p.R357Q |
SARC | 8 | 41834533 | 41834533 | + | Missense_Mutation | SNP | C | C | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr8:41834533C>A | c.1356G>T | c.(1354-1356)tgG>tgT | p.W452C |
SKCM | 8 | 41790311 | 41790311 | + | Silent | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr8:41790311G>A | c.5427C>T | c.(5425-5427)acC>acT | p.T1809T |
SKCM | 8 | 41790352 | 41790352 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr8:41790352G>A | c.5386C>T | c.(5386-5388)Cca>Tca | p.P1796S |
SKCM | 8 | 41790361 | 41790361 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr8:41790361G>A | c.5377C>T | c.(5377-5379)Cag>Tag | p.Q1793* |
SKCM | 8 | 41790402 | 41790402 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr8:41790402G>A | c.5336C>T | c.(5335-5337)tCc>tTc | p.S1779F |
SKCM | 8 | 41791256 | 41791256 | + | Silent | SNP | G | G | A | TCGA-GF-A4EO-06A-12D-A24R-08 | TCGA-GF-A4EO-10A-01D-A24R-08 | g.chr8:41791256G>A | c.4482C>T | c.(4480-4482)gtC>gtT | p.V1494V |
SKCM | 8 | 41791341 | 41791341 | + | Missense_Mutation | SNP | G | G | A | TCGA-RP-A694-06A-11D-A30X-08 | TCGA-RP-A694-10A-01D-A30X-08 | g.chr8:41791341G>A | c.4397C>T | c.(4396-4398)cCt>cTt | p.P1466L |
SKCM | 8 | 41791374 | 41791374 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3C7-06A-11D-A196-08 | TCGA-D3-A3C7-10A-01D-A198-08 | g.chr8:41791374G>A | c.4364C>T | c.(4363-4365)aCc>aTc | p.T1455I |
SKCM | 8 | 41791730 | 41791730 | + | Silent | SNP | G | G | A | TCGA-DA-A1HY-06A-11D-A19A-08 | TCGA-DA-A1HY-10A-01D-A19A-08 | g.chr8:41791730G>A | c.4008C>T | c.(4006-4008)ccC>ccT | p.P1336P |
SKCM | 8 | 41792152 | 41792152 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2ML-06A-11D-A197-08 | TCGA-EE-A2ML-10A-01D-A199-08 | g.chr8:41792152G>A | c.3586C>T | c.(3586-3588)Cct>Tct | p.P1196S |
SKCM | 8 | 41792152 | 41792152 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr8:41792152G>A | c.3586C>T | c.(3586-3588)Cct>Tct | p.P1196S |
SKCM | 8 | 41792157 | 41792157 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AC-06A-11D-A196-08 | TCGA-EE-A3AC-10A-01D-A198-08 | g.chr8:41792157G>A | c.3581C>T | c.(3580-3582)tCc>tTc | p.S1194F |
SKCM | 8 | 41792309 | 41792309 | + | Silent | SNP | G | G | T | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr8:41792309G>T | c.3429C>A | c.(3427-3429)tcC>tcA | p.S1143S |
SKCM | 8 | 41798675 | 41798675 | + | Silent | SNP | G | G | A | TCGA-D3-A2J7-06A-11D-A196-08 | TCGA-D3-A2J7-10A-01D-A198-08 | g.chr8:41798675G>A | c.2724C>T | c.(2722-2724)gcC>gcT | p.A908A |
SKCM | 8 | 41801318 | 41801318 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr8:41801318C>T | c.2176G>A | c.(2176-2178)Gac>Aac | p.D726N |
SKCM | 8 | 41801328 | 41801328 | + | Silent | SNP | G | G | A | TCGA-DA-A1HV-06A-21D-A196-08 | TCGA-DA-A1HV-10A-01D-A198-08 | g.chr8:41801328G>A | c.2166C>T | c.(2164-2166)atC>atT | p.I722I |
SKCM | 8 | 41801438 | 41801438 | + | Missense_Mutation | SNP | G | G | C | TCGA-ER-A3EV-06A-11D-A20D-08 | TCGA-ER-A3EV-10A-01D-A20D-08 | g.chr8:41801438G>C | c.2056C>G | c.(2056-2058)Ctg>Gtg | p.L686V |
SKCM | 8 | 41806783 | 41806783 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A4U8-06A-11D-A32N-08 | TCGA-GN-A4U8-10B-01D-A32N-08 | g.chr8:41806783G>A | c.1697C>T | c.(1696-1698)cCt>cTt | p.P566L |
SKCM | 8 | 41812837 | 41812837 | + | Silent | SNP | G | G | A | TCGA-D3-A2JH-06A-11D-A196-08 | TCGA-D3-A2JH-10A-01D-A198-08 | g.chr8:41812837G>A | c.1575C>T | c.(1573-1575)tcC>tcT | p.S525S |
SKCM | 8 | 41812901 | 41812901 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr8:41812901G>A | c.1511C>T | c.(1510-1512)cCa>cTa | p.P504L |
SKCM | 8 | 41832276 | 41832276 | + | Silent | SNP | G | G | A | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr8:41832276G>A | c.1428C>T | c.(1426-1428)atC>atT | p.I476I |
SKCM | 8 | 41834751 | 41834751 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr8:41834751C>T | c.1138G>A | c.(1138-1140)Gaa>Aaa | p.E380K |
SKCM | 8 | 41834788 | 41834788 | + | Missense_Mutation | SNP | T | T | A | TCGA-DA-A1I5-06A-11D-A197-08 | TCGA-DA-A1I5-10A-01D-A199-08 | g.chr8:41834788T>A | c.1101A>T | c.(1099-1101)aaA>aaT | p.K367N |
SKCM | 8 | 41834820 | 41834820 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EE-A2MM-06A-11D-A196-08 | TCGA-EE-A2MM-10A-01D-A198-08 | g.chr8:41834820G>A | c.1069C>T | c.(1069-1071)Cga>Tga | p.R357* |
SKCM | 8 | 41839448 | 41839448 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr8:41839448G>A | c.734C>T | c.(733-735)tCc>tTc | p.S245F |
SKCM | 8 | 41844996 | 41844996 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr8:41844996G>A | c.686C>T | c.(685-687)tCc>tTc | p.S229F |
SKCM | 8 | 41845064 | 41845064 | + | Silent | SNP | G | G | A | TCGA-RP-A693-06A-13D-A30X-08 | TCGA-RP-A693-10A-01D-A30X-08 | g.chr8:41845064G>A | c.618C>T | c.(616-618)atC>atT | p.I206I |
SKCM | 8 | 41906287 | 41906287 | + | Missense_Mutation | SNP | G | G | A | TCGA-FR-A3YO-06A-11D-A23B-08 | TCGA-FR-A3YO-10A-01D-A23B-08 | g.chr8:41906287G>A | c.209C>T | c.(208-210)tCc>tTc | p.S70F |
SKCM | 8 | 41906403 | 41906403 | + | Silent | SNP | C | C | T | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr8:41906403C>T | c.93G>A | c.(91-93)agG>agA | p.R31R |