Mutation - TCGA |
Type | Chromosome | Start Position | End Position | Strand | Variant Classification | Variant Type | Reference Allele | Tumor_seq Allele 1 | Tumor_seq Allele 2 | Tumor Sample Barcode | Matched Norm Sample Barcode | Genome Change | cDNA Change | Codon Change | Protein Change |
BLCA | 10 | 105361657 | 105361657 | + | Silent | SNP | A | A | G | TCGA-DK-A1AD-01A-11D-A13W-08 | TCGA-DK-A1AD-10A-01D-A13W-08 | g.chr10:105361657A>G | c.3318T>C | c.(3316-3318)aaT>aaC | p.N1106N |
BLCA | 10 | 105361888 | 105361888 | + | Silent | SNP | C | C | T | TCGA-XF-AAMX-01A-11D-A42E-08 | TCGA-XF-AAMX-10A-01D-A42H-08 | g.chr10:105361888C>T | c.3087G>A | c.(3085-3087)aaG>aaA | p.K1029K |
BLCA | 10 | 105362460 | 105362460 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-K4-A6FZ-01A-11D-A31L-08 | TCGA-K4-A6FZ-10A-01D-A31J-08 | g.chr10:105362460C>A | c.2515G>T | c.(2515-2517)Gaa>Taa | p.E839* |
BLCA | 10 | 105362583 | 105362583 | + | Missense_Mutation | SNP | C | C | T | TCGA-K4-A54R-01A-11D-A26M-08 | TCGA-K4-A54R-10A-01D-A26K-08 | g.chr10:105362583C>T | c.2392G>A | c.(2392-2394)Gag>Aag | p.E798K |
BLCA | 10 | 105372779 | 105372780 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-DK-A1A6-01A-11D-A13W-08 | TCGA-DK-A1A6-10A-01D-A13W-08 | g.chr10:105372779_105372780insG | c.1088_1089insC | c.(1087-1089)ccafs | p.P363fs |
BLCA | 10 | 105420777 | 105420777 | + | Missense_Mutation | SNP | C | C | T | TCGA-4Z-AA87-01A-11D-A391-08 | TCGA-4Z-AA87-10A-01D-A394-08 | g.chr10:105420777C>T | c.568G>A | c.(568-570)Ggg>Agg | p.G190R |
BLCA | 10 | 105420847 | 105420847 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-A9SK-01A-11D-A42E-08 | TCGA-XF-A9SK-10A-01D-A42H-08 | g.chr10:105420847C>T | c.498G>A | c.(496-498)atG>atA | p.M166I |
BLCA | 10 | 105495508 | 105495508 | + | Silent | SNP | G | G | T | TCGA-CF-A1HS-01A-11D-A13W-08 | TCGA-CF-A1HS-10A-01D-A13W-08 | g.chr10:105495508G>T | c.288C>A | c.(286-288)ccC>ccA | p.P96P |
BLCA | 10 | 105495534 | 105495534 | + | Missense_Mutation | SNP | C | C | A | TCGA-FJ-A3ZE-01A-11D-A23M-08 | TCGA-FJ-A3ZE-10A-01D-A23K-08 | g.chr10:105495534C>A | c.262G>T | c.(262-264)Gac>Tac | p.D88Y |
BLCA | 10 | 105561083 | 105561083 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A7XN-01A-11D-A34U-08 | TCGA-E7-A7XN-10A-01D-A34X-08 | g.chr10:105561083G>A | c.110C>T | c.(109-111)tCc>tTc | p.S37F |
BRCA | 10 | 105362404 | 105362404 | + | Silent | SNP | C | C | T | TCGA-A8-A09E-01A-11W-A019-09 | TCGA-A8-A09E-10A-01W-A021-09 | g.chr10:105362404C>T | c.2571G>A | c.(2569-2571)tcG>tcA | p.S857S |
BRCA | 10 | 105362470 | 105362470 | + | Missense_Mutation | SNP | C | C | G | TCGA-D8-A1JA-01A-11D-A13L-09 | TCGA-D8-A1JA-10A-01W-A14R-09 | g.chr10:105362470C>G | c.2505G>C | c.(2503-2505)aaG>aaC | p.K835N |
BRCA | 10 | 105363029 | 105363029 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-A8-A08B-01A-11W-A019-09 | TCGA-A8-A08B-10A-01W-A021-09 | g.chr10:105363029G>T | c.1946C>A | c.(1945-1947)tCg>tAg | p.S649* |
BRCA | 10 | 105372651 | 105372651 | + | Missense_Mutation | SNP | G | G | C | TCGA-AC-A2B8-01A-11D-A17D-09 | TCGA-AC-A2B8-10A-01D-A17D-09 | g.chr10:105372651G>C | c.1217C>G | c.(1216-1218)tCt>tGt | p.S406C |
BRCA | 10 | 105372694 | 105372694 | + | Missense_Mutation | SNP | C | C | T | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr10:105372694C>T | c.1174G>A | c.(1174-1176)Gtg>Atg | p.V392M |
BRCA | 10 | 105372948 | 105372948 | + | Splice_Site | SNP | C | C | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr10:105372948C>T | | c.e12-1 | |
BRCA | 10 | 105377012 | 105377012 | + | Missense_Mutation | SNP | C | C | G | TCGA-C8-A12T-01A-11D-A10Y-09 | TCGA-C8-A12T-10A-01D-A110-09 | g.chr10:105377012C>G | c.862G>C | c.(862-864)Gag>Cag | p.E288Q |
CHOL | 10 | 105526913 | 105526913 | + | Missense_Mutation | SNP | A | A | T | TCGA-W5-AA31-01A-11D-A417-09 | TCGA-W5-AA31-10A-01D-A41A-09 | g.chr10:105526913A>T | c.168T>A | c.(166-168)gaT>gaA | p.D56E |
COAD | 10 | 105361585 | 105361585 | + | Silent | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr10:105361585C>T | c.3390G>A | c.(3388-3390)gaG>gaA | p.E1130E |
COAD | 10 | 105361689 | 105361689 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr10:105361689delC | c.3286delG | c.(3286-3288)gtgfs | p.V1096fs |
COAD | 10 | 105361771 | 105361771 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr10:105361771G>T | c.3204C>A | c.(3202-3204)ttC>ttA | p.F1068L |
COAD | 10 | 105361934 | 105361934 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A02J-01A-01W-A00E-09 | TCGA-AA-A02J-10A-01W-A00E-09 | g.chr10:105361934C>T | c.3041G>A | c.(3040-3042)cGg>cAg | p.R1014Q |
COAD | 10 | 105362068 | 105362068 | + | Missense_Mutation | SNP | C | C | A | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr10:105362068C>A | c.2907G>T | c.(2905-2907)agG>agT | p.R969S |
COAD | 10 | 105362228 | 105362228 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3854-01A-01W-0900-09 | TCGA-AA-3854-10A-01W-0900-09 | g.chr10:105362228C>T | c.2747G>A | c.(2746-2748)gGc>gAc | p.G916D |
COAD | 10 | 105363372 | 105363372 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6654-01A-21D-1835-10 | TCGA-A6-6654-10A-01D-1835-10 | g.chr10:105363372C>T | c.1603G>A | c.(1603-1605)Gag>Aag | p.E535K |
COAD | 10 | 105363391 | 105363391 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr10:105363391delG | c.1584delC | c.(1582-1584)cccfs | p.P528fs |
COAD | 10 | 105363391 | 105363391 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr10:105363391delG | c.1584delC | c.(1582-1584)cccfs | p.P528fs |
COAD | 10 | 105363438 | 105363438 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3875-01A-01W-0900-09 | TCGA-AA-3875-10A-01W-0902-09 | g.chr10:105363438G>A | c.1537C>T | c.(1537-1539)Cgc>Tgc | p.R513C |
COAD | 10 | 105363470 | 105363470 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr10:105363470A>G | c.1505T>C | c.(1504-1506)aTc>aCc | p.I502T |
COAD | 10 | 105365574 | 105365574 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr10:105365574C>T | c.1409G>A | c.(1408-1410)cGg>cAg | p.R470Q |
COAD | 10 | 105372696 | 105372696 | + | Missense_Mutation | SNP | G | G | T | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr10:105372696G>T | c.1172C>A | c.(1171-1173)gCc>gAc | p.A391D |
COAD | 10 | 105372744 | 105372744 | + | Missense_Mutation | SNP | T | T | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr10:105372744T>G | c.1124A>C | c.(1123-1125)aAg>aCg | p.K375T |
COAD | 10 | 105372924 | 105372924 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr10:105372924G>A | c.944C>T | c.(943-945)gCg>gTg | p.A315V |
COAD | 10 | 105420830 | 105420830 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr10:105420830A>G | c.515T>C | c.(514-516)gTg>gCg | p.V172A |
COAD | 10 | 105420859 | 105420859 | + | Silent | SNP | G | G | T | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr10:105420859G>T | c.486C>A | c.(484-486)acC>acA | p.T162T |
COAD | 10 | 105484119 | 105484119 | + | Splice_Site | SNP | C | C | T | TCGA-D5-5538-01A-01D-1650-10 | TCGA-D5-5538-10A-02D-1650-10 | g.chr10:105484119C>T | c.307G>A | c.(307-309)Gca>Aca | p.A103T |
COADREAD | 10 | 105361585 | 105361585 | + | Silent | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr10:105361585C>T | c.3390G>A | c.(3388-3390)gaG>gaA | p.E1130E |
COADREAD | 10 | 105361689 | 105361689 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr10:105361689delC | c.3286delG | c.(3286-3288)gtgfs | p.V1096fs |
COADREAD | 10 | 105361771 | 105361771 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr10:105361771G>T | c.3204C>A | c.(3202-3204)ttC>ttA | p.F1068L |
COADREAD | 10 | 105361934 | 105361934 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A02J-01A-01W-A00E-09 | TCGA-AA-A02J-10A-01W-A00E-09 | g.chr10:105361934C>T | c.3041G>A | c.(3040-3042)cGg>cAg | p.R1014Q |
COADREAD | 10 | 105362068 | 105362068 | + | Missense_Mutation | SNP | C | C | A | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr10:105362068C>A | c.2907G>T | c.(2905-2907)agG>agT | p.R969S |
COADREAD | 10 | 105362228 | 105362228 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3854-01A-01W-0900-09 | TCGA-AA-3854-10A-01W-0900-09 | g.chr10:105362228C>T | c.2747G>A | c.(2746-2748)gGc>gAc | p.G916D |
COADREAD | 10 | 105363372 | 105363372 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6654-01A-21D-1835-10 | TCGA-A6-6654-10A-01D-1835-10 | g.chr10:105363372C>T | c.1603G>A | c.(1603-1605)Gag>Aag | p.E535K |
COADREAD | 10 | 105363391 | 105363391 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr10:105363391delG | c.1584delC | c.(1582-1584)cccfs | p.P528fs |
COADREAD | 10 | 105363391 | 105363391 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr10:105363391delG | c.1584delC | c.(1582-1584)cccfs | p.P528fs |
COADREAD | 10 | 105363438 | 105363438 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3875-01A-01W-0900-09 | TCGA-AA-3875-10A-01W-0902-09 | g.chr10:105363438G>A | c.1537C>T | c.(1537-1539)Cgc>Tgc | p.R513C |
COADREAD | 10 | 105363470 | 105363470 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr10:105363470A>G | c.1505T>C | c.(1504-1506)aTc>aCc | p.I502T |
COADREAD | 10 | 105365574 | 105365574 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr10:105365574C>T | c.1409G>A | c.(1408-1410)cGg>cAg | p.R470Q |
COADREAD | 10 | 105372696 | 105372696 | + | Missense_Mutation | SNP | G | G | T | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr10:105372696G>T | c.1172C>A | c.(1171-1173)gCc>gAc | p.A391D |
COADREAD | 10 | 105372744 | 105372744 | + | Missense_Mutation | SNP | T | T | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr10:105372744T>G | c.1124A>C | c.(1123-1125)aAg>aCg | p.K375T |
COADREAD | 10 | 105372924 | 105372924 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr10:105372924G>A | c.944C>T | c.(943-945)gCg>gTg | p.A315V |
COADREAD | 10 | 105420830 | 105420830 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr10:105420830A>G | c.515T>C | c.(514-516)gTg>gCg | p.V172A |
COADREAD | 10 | 105420859 | 105420859 | + | Silent | SNP | G | G | T | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr10:105420859G>T | c.486C>A | c.(484-486)acC>acA | p.T162T |
COADREAD | 10 | 105484119 | 105484119 | + | Splice_Site | SNP | C | C | T | TCGA-D5-5538-01A-01D-1650-10 | TCGA-D5-5538-10A-02D-1650-10 | g.chr10:105484119C>T | c.307G>A | c.(307-309)Gca>Aca | p.A103T |
COADREAD | 10 | 105526904 | 105526904 | + | Silent | SNP | G | G | A | TCGA-AG-4005-01A-01W-1073-09 | TCGA-AG-4005-10A-01W-1073-09 | g.chr10:105526904G>A | c.177C>T | c.(175-177)ccC>ccT | p.P59P |
DLBC | 10 | 105362350 | 105362350 | + | Silent | SNP | G | G | A | TCGA-GS-A9TV-01A-11D-A382-10 | TCGA-GS-A9TV-10A-01D-A385-10 | g.chr10:105362350G>A | c.2625C>T | c.(2623-2625)agC>agT | p.S875S |
ESCA | 10 | 105362131 | 105362131 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr10:105362131delG | c.2844delC | c.(2842-2844)cccfs | p.P948fs |
ESCA | 10 | 105362805 | 105362805 | + | Missense_Mutation | SNP | A | A | G | TCGA-L5-A4OJ-01A-11D-A27G-09 | TCGA-L5-A4OJ-11A-12D-A27G-09 | g.chr10:105362805A>G | c.2170T>C | c.(2170-2172)Tcg>Ccg | p.S724P |
ESCA | 10 | 105386873 | 105386873 | + | Missense_Mutation | SNP | C | C | T | TCGA-LN-A8I1-01A-11D-A36J-09 | TCGA-LN-A8I1-10A-01D-A36M-09 | g.chr10:105386873C>T | c.691G>A | c.(691-693)Gac>Aac | p.D231N |
ESCA | 10 | 105386894 | 105386894 | + | Missense_Mutation | SNP | T | T | A | TCGA-IG-A97I-01A-11D-A387-09 | TCGA-IG-A97I-10A-01D-A38A-09 | g.chr10:105386894T>A | c.670A>T | c.(670-672)Aat>Tat | p.N224Y |
GBMLGG | 10 | 105361942 | 105361942 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:105361942G>A | c.3033C>T | c.(3031-3033)ggC>ggT | p.G1011G |
GBMLGG | 10 | 105362350 | 105362350 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:105362350G>A | c.2625C>T | c.(2623-2625)agC>agT | p.S875S |
GBMLGG | 10 | 105362427 | 105362427 | + | Missense_Mutation | SNP | C | C | T | TCGA-FG-A70Y-01A-12D-A34J-08 | TCGA-FG-A70Y-10B-01D-A34M-08 | g.chr10:105362427C>T | c.2548G>A | c.(2548-2550)Gcc>Acc | p.A850T |
GBMLGG | 10 | 105362637 | 105362637 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:105362637G>A | c.2338C>T | c.(2338-2340)Cgc>Tgc | p.R780C |
GBMLGG | 10 | 105377025 | 105377025 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:105377025G>A | c.849C>T | c.(847-849)gaC>gaT | p.D283D |
HNSC | 10 | 105361946 | 105361946 | + | Missense_Mutation | SNP | C | C | T | TCGA-BA-A6DA-01A-31D-A31L-08 | TCGA-BA-A6DA-10A-01D-A31J-08 | g.chr10:105361946C>T | c.3029G>A | c.(3028-3030)cGa>cAa | p.R1010Q |
HNSC | 10 | 105362339 | 105362339 | + | Missense_Mutation | SNP | T | T | A | TCGA-CN-6997-01A-11D-2012-08 | TCGA-CN-6997-10A-01D-2013-08 | g.chr10:105362339T>A | c.2636A>T | c.(2635-2637)tAt>tTt | p.Y879F |
HNSC | 10 | 105362410 | 105362410 | + | Silent | SNP | C | C | T | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr10:105362410C>T | c.2565G>A | c.(2563-2565)caG>caA | p.Q855Q |
HNSC | 10 | 105362544 | 105362544 | + | Missense_Mutation | SNP | G | G | A | TCGA-D6-6516-01A-11D-1870-08 | TCGA-D6-6516-10A-01D-1870-08 | g.chr10:105362544G>A | c.2431C>T | c.(2431-2433)Ccc>Tcc | p.P811S |
HNSC | 10 | 105362799 | 105362799 | + | Missense_Mutation | SNP | C | C | T | TCGA-UF-A7JK-01A-11D-A34J-08 | TCGA-UF-A7JK-10A-01D-A34M-08 | g.chr10:105362799C>T | c.2176G>A | c.(2176-2178)Gca>Aca | p.A726T |
HNSC | 10 | 105362864 | 105362864 | + | Missense_Mutation | SNP | G | G | C | TCGA-CN-A63W-01A-11D-A30E-08 | TCGA-CN-A63W-10A-01D-A30H-08 | g.chr10:105362864G>C | c.2111C>G | c.(2110-2112)tCt>tGt | p.S704C |
HNSC | 10 | 105362870 | 105362870 | + | Missense_Mutation | SNP | G | G | T | TCGA-F7-A623-01A-11D-A28R-08 | TCGA-F7-A623-10A-01D-A28U-08 | g.chr10:105362870G>T | c.2105C>A | c.(2104-2106)tCc>tAc | p.S702Y |
HNSC | 10 | 105362900 | 105362900 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-CR-7386-01A-11D-2012-08 | TCGA-CR-7386-10A-01D-2013-08 | g.chr10:105362900G>C | c.2075C>G | c.(2074-2076)tCa>tGa | p.S692* |
HNSC | 10 | 105363339 | 105363339 | + | Missense_Mutation | SNP | C | C | G | TCGA-D6-A74Q-01A-11D-A34J-08 | TCGA-D6-A74Q-10A-02D-A34M-08 | g.chr10:105363339C>G | c.1636G>C | c.(1636-1638)Gac>Cac | p.D546H |
HNSC | 10 | 105363391 | 105363391 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr10:105363391delG | c.1584delC | c.(1582-1584)cccfs | p.P528fs |
HNSC | 10 | 105363403 | 105363403 | + | Silent | SNP | C | C | T | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr10:105363403C>T | c.1572G>A | c.(1570-1572)ccG>ccA | p.P524P |
HNSC | 10 | 105363418 | 105363418 | + | Silent | SNP | C | C | T | TCGA-CV-A6JM-01A-11D-A31L-08 | TCGA-CV-A6JM-10A-01D-A31J-08 | g.chr10:105363418C>T | c.1557G>A | c.(1555-1557)cgG>cgA | p.R519R |
HNSC | 10 | 105386929 | 105386929 | + | Missense_Mutation | SNP | T | T | A | TCGA-UF-A7JD-01A-11D-A34J-08 | TCGA-UF-A7JD-10A-01D-A34M-08 | g.chr10:105386929T>A | c.635A>T | c.(634-636)cAg>cTg | p.Q212L |
KICH | 10 | 105362429 | 105362429 | + | Missense_Mutation | SNP | C | C | T | TCGA-KL-8333-01A-11D-2310-10 | TCGA-KL-8333-11A-01D-2310-10 | g.chr10:105362429C>T | c.2546G>A | c.(2545-2547)aGc>aAc | p.S849N |
KIPAN | 10 | 105362429 | 105362429 | + | Missense_Mutation | SNP | C | C | T | TCGA-KL-8333-01A-11D-2310-10 | TCGA-KL-8333-11A-01D-2310-10 | g.chr10:105362429C>T | c.2546G>A | c.(2545-2547)aGc>aAc | p.S849N |
LGG | 10 | 105361942 | 105361942 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:105361942G>A | c.3033C>T | c.(3031-3033)ggC>ggT | p.G1011G |
LGG | 10 | 105362350 | 105362350 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:105362350G>A | c.2625C>T | c.(2623-2625)agC>agT | p.S875S |
LGG | 10 | 105362427 | 105362427 | + | Missense_Mutation | SNP | C | C | T | TCGA-FG-A70Y-01A-12D-A34J-08 | TCGA-FG-A70Y-10B-01D-A34M-08 | g.chr10:105362427C>T | c.2548G>A | c.(2548-2550)Gcc>Acc | p.A850T |
LGG | 10 | 105362637 | 105362637 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:105362637G>A | c.2338C>T | c.(2338-2340)Cgc>Tgc | p.R780C |
LGG | 10 | 105377025 | 105377025 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:105377025G>A | c.849C>T | c.(847-849)gaC>gaT | p.D283D |
LIHC | 10 | 105361743 | 105361743 | + | Missense_Mutation | SNP | C | C | T | TCGA-5C-A9VH-01A-11D-A36X-10 | TCGA-5C-A9VH-10A-01D-A370-10 | g.chr10:105361743C>T | c.3232G>A | c.(3232-3234)Gtc>Atc | p.V1078I |
LIHC | 10 | 105362908 | 105362908 | + | Silent | SNP | G | G | T | TCGA-K7-A5RF-01A-11D-A28X-10 | TCGA-K7-A5RF-10B-01D-A28X-10 | g.chr10:105362908G>T | c.2067C>A | c.(2065-2067)tcC>tcA | p.S689S |
LUAD | 10 | 105362061 | 105362061 | + | Missense_Mutation | SNP | C | C | A | TCGA-64-5781-01A-01D-1625-08 | TCGA-64-5781-10A-01D-1625-08 | g.chr10:105362061C>A | c.2914G>T | c.(2914-2916)Gtg>Ttg | p.V972L |
LUAD | 10 | 105362155 | 105362155 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z018-01A-01W-0746-08 | TCGA-17-Z018-11A-01W-0746-08 | g.chr10:105362155G>T | c.2820C>A | c.(2818-2820)aaC>aaA | p.N940K |
LUAD | 10 | 105362386 | 105362386 | + | Silent | SNP | C | C | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr10:105362386C>A | c.2589G>T | c.(2587-2589)gcG>gcT | p.A863A |
LUAD | 10 | 105362429 | 105362429 | + | Missense_Mutation | SNP | C | C | G | TCGA-91-6828-01A-11D-1855-08 | TCGA-91-6828-10A-01D-1855-08 | g.chr10:105362429C>G | c.2546G>C | c.(2545-2547)aGc>aCc | p.S849T |
LUAD | 10 | 105362444 | 105362444 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z026-01A-01W-0746-08 | TCGA-17-Z026-11A-01W-0746-08 | g.chr10:105362444G>A | c.2531C>T | c.(2530-2532)tCg>tTg | p.S844L |
LUAD | 10 | 105362704 | 105362704 | + | Silent | SNP | C | C | T | TCGA-75-6207-01A-11D-1753-08 | TCGA-75-6207-10A-01D-1753-08 | g.chr10:105362704C>T | c.2271G>A | c.(2269-2271)cgG>cgA | p.R757R |
LUAD | 10 | 105362730 | 105362732 | + | In_Frame_Del | DEL | AGG | AGG | - | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr10:105362730_105362732delAGG | c.2243_2245delCCT | c.(2242-2247)tcctgt>tgt | p.S748del |
LUAD | 10 | 105362787 | 105362787 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-6968-01A-11D-1945-08 | TCGA-55-6968-11A-01D-1945-08 | g.chr10:105362787C>A | c.2188G>T | c.(2188-2190)Ggc>Tgc | p.G730C |
LUAD | 10 | 105363225 | 105363225 | + | Missense_Mutation | SNP | T | T | A | TCGA-91-6835-01A-11D-1855-08 | TCGA-91-6835-11A-01D-1855-08 | g.chr10:105363225T>A | c.1750A>T | c.(1750-1752)Agg>Tgg | p.R584W |
LUAD | 10 | 105363419 | 105363419 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr10:105363419C>A | c.1556G>T | c.(1555-1557)cGg>cTg | p.R519L |
LUAD | 10 | 105365603 | 105365603 | + | Silent | SNP | C | C | T | TCGA-55-6969-01A-11D-1945-08 | TCGA-55-6969-11A-01D-1945-08 | g.chr10:105365603C>T | c.1380G>A | c.(1378-1380)caG>caA | p.Q460Q |
LUAD | 10 | 105365611 | 105365611 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-44-7662-01A-11D-2063-08 | TCGA-44-7662-10A-01D-2063-08 | g.chr10:105365611C>A | c.1372G>T | c.(1372-1374)Gaa>Taa | p.E458* |
LUAD | 10 | 105372657 | 105372657 | + | Missense_Mutation | SNP | T | T | A | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr10:105372657T>A | c.1211A>T | c.(1210-1212)cAg>cTg | p.Q404L |
LUAD | 10 | 105484119 | 105484119 | + | Splice_Site | SNP | C | C | G | TCGA-44-8117-01A-11D-2238-08 | TCGA-44-8117-10A-01D-2238-08 | g.chr10:105484119C>G | c.307G>C | c.(307-309)Gca>Cca | p.A103P |
LUSC | 10 | 105361813 | 105361813 | + | Silent | SNP | G | G | A | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr10:105361813G>A | c.3162C>T | c.(3160-3162)ccC>ccT | p.P1054P |
LUSC | 10 | 105362464 | 105362464 | + | Missense_Mutation | SNP | T | T | G | TCGA-63-5128-01A-01D-1441-08 | TCGA-63-5128-10A-01D-1441-08 | g.chr10:105362464T>G | c.2511A>C | c.(2509-2511)gaA>gaC | p.E837D |
LUSC | 10 | 105362496 | 105362496 | + | Missense_Mutation | SNP | C | C | T | TCGA-63-5128-01A-01D-1441-08 | TCGA-63-5128-10A-01D-1441-08 | g.chr10:105362496C>T | c.2479G>A | c.(2479-2481)Gcc>Acc | p.A827T |
LUSC | 10 | 105363329 | 105363329 | + | Missense_Mutation | SNP | C | C | T | TCGA-34-2600-01A-01D-1522-08 | TCGA-34-2600-11A-01D-1522-08 | g.chr10:105363329C>T | c.1646G>A | c.(1645-1647)cGg>cAg | p.R549Q |
LUSC | 10 | 105372887 | 105372887 | + | Silent | SNP | C | C | A | TCGA-18-3411-01A-01D-0983-08 | TCGA-18-3411-11A-01D-0983-08 | g.chr10:105372887C>A | c.981G>T | c.(979-981)ctG>ctT | p.L327L |
LUSC | 10 | 105484070 | 105484070 | + | Missense_Mutation | SNP | C | C | G | TCGA-60-2713-01A-01D-1522-08 | TCGA-60-2713-11A-01D-1522-08 | g.chr10:105484070C>G | c.356G>C | c.(355-357)cGg>cCg | p.R119P |
OV | 10 | 105361944 | 105361944 | + | Missense_Mutation | SNP | C | C | G | TCGA-23-2649-01A-01D-1526-09 | TCGA-23-2649-10A-01D-1526-09 | g.chr10:105361944C>G | c.3031G>C | c.(3031-3033)Ggc>Cgc | p.G1011R |
OV | 10 | 105362427 | 105362427 | + | Missense_Mutation | SNP | C | C | T | TCGA-09-1674-01A-01W-0633-09 | TCGA-09-1674-10A-01W-0633-09 | g.chr10:105362427C>T | c.2548G>A | c.(2548-2550)Gcc>Acc | p.A850T |
PAAD | 10 | 105362124 | 105362124 | + | Missense_Mutation | SNP | A | A | G | TCGA-IB-A5SQ-01A-11D-A32N-08 | TCGA-IB-A5SQ-10A-01D-A32N-08 | g.chr10:105362124A>G | c.2851T>C | c.(2851-2853)Tcc>Ccc | p.S951P |
PAAD | 10 | 105362601 | 105362601 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr10:105362601G>T | c.2374C>A | c.(2374-2376)Ctc>Atc | p.L792I |
PAAD | 10 | 105362640 | 105362640 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr10:105362640G>A | c.2335C>T | c.(2335-2337)Cgg>Tgg | p.R779W |
PAAD | 10 | 105362640 | 105362640 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-AAUU-01A-11D-A377-08 | TCGA-IB-AAUU-10A-01D-A37A-08 | g.chr10:105362640G>A | c.2335C>T | c.(2335-2337)Cgg>Tgg | p.R779W |
PAAD | 10 | 105362640 | 105362640 | + | Missense_Mutation | SNP | G | G | A | TCGA-LB-A7SX-01A-11D-A33T-08 | TCGA-LB-A7SX-10A-01D-A33W-08 | g.chr10:105362640G>A | c.2335C>T | c.(2335-2337)Cgg>Tgg | p.R779W |
PAAD | 10 | 105362849 | 105362851 | + | In_Frame_Del | DEL | GAG | GAG | - | TCGA-IB-AAUP-01A-11D-A377-08 | TCGA-IB-AAUP-10A-01D-A37A-08 | g.chr10:105362849_105362851delGAG | c.2124_2126delCTC | c.(2122-2127)tcctct>tct | p.708_709SS>S |
PAAD | 10 | 105363058 | 105363058 | + | Silent | SNP | G | G | A | TCGA-2L-AAQA-01A-21D-A38G-08 | TCGA-2L-AAQA-11A-11D-A38J-08 | g.chr10:105363058G>A | c.1917C>T | c.(1915-1917)tcC>tcT | p.S639S |
PAAD | 10 | 105363099 | 105363099 | + | Missense_Mutation | SNP | G | G | A | TCGA-2L-AAQI-01A-12D-A397-08 | TCGA-2L-AAQI-11A-11D-A39A-08 | g.chr10:105363099G>A | c.1876C>T | c.(1876-1878)Cgg>Tgg | p.R626W |
PAAD | 10 | 105363099 | 105363099 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-A6UG-01A-32D-A33T-08 | TCGA-IB-A6UG-10A-01D-A33W-08 | g.chr10:105363099G>A | c.1876C>T | c.(1876-1878)Cgg>Tgg | p.R626W |
PAAD | 10 | 105363480 | 105363480 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr10:105363480C>T | c.1495G>A | c.(1495-1497)Gca>Aca | p.A499T |
PAAD | 10 | 105372695 | 105372695 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr10:105372695G>A | c.1173C>T | c.(1171-1173)gcC>gcT | p.A391A |
PRAD | 10 | 105361687 | 105361687 | + | Silent | SNP | C | C | A | TCGA-EJ-7783-01A-11D-2114-08 | TCGA-EJ-7783-10A-01D-2114-08 | g.chr10:105361687C>A | c.3288G>T | c.(3286-3288)gtG>gtT | p.V1096V |
PRAD | 10 | 105362575 | 105362575 | + | Silent | SNP | C | C | T | TCGA-KK-A59V-01A-11D-A29Q-08 | TCGA-KK-A59V-11A-11D-A29Q-08 | g.chr10:105362575C>T | c.2400G>A | c.(2398-2400)tcG>tcA | p.S800S |
PRAD | 10 | 105372694 | 105372694 | + | Missense_Mutation | SNP | C | C | T | TCGA-KK-A7AP-01A-12D-A33T-08 | TCGA-KK-A7AP-11A-21D-A33W-08 | g.chr10:105372694C>T | c.1174G>A | c.(1174-1176)Gtg>Atg | p.V392M |
READ | 10 | 105526904 | 105526904 | + | Silent | SNP | G | G | A | TCGA-AG-4005-01A-01W-1073-09 | TCGA-AG-4005-10A-01W-1073-09 | g.chr10:105526904G>A | c.177C>T | c.(175-177)ccC>ccT | p.P59P |
SKCM | 10 | 105361807 | 105361807 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:105361807G>A | c.3168C>T | c.(3166-3168)tcC>tcT | p.S1056S |
SKCM | 10 | 105361947 | 105361947 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr10:105361947G>A | c.3028C>T | c.(3028-3030)Cga>Tga | p.R1010* |
SKCM | 10 | 105362047 | 105362047 | + | Silent | SNP | C | C | A | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr10:105362047C>A | c.2928G>T | c.(2926-2928)gcG>gcT | p.A976A |
SKCM | 10 | 105362473 | 105362473 | + | Silent | SNP | G | G | A | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr10:105362473G>A | c.2502C>T | c.(2500-2502)acC>acT | p.T834T |
SKCM | 10 | 105362500 | 105362500 | + | Silent | SNP | G | G | A | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr10:105362500G>A | c.2475C>T | c.(2473-2475)ctC>ctT | p.L825L |
SKCM | 10 | 105362514 | 105362514 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A4U4-06A-11D-A32N-08 | TCGA-GN-A4U4-10B-01D-A32N-08 | g.chr10:105362514C>T | c.2461G>A | c.(2461-2463)Gac>Aac | p.D821N |
SKCM | 10 | 105362802 | 105362802 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr10:105362802C>T | c.2173G>A | c.(2173-2175)Gac>Aac | p.D725N |
SKCM | 10 | 105363294 | 105363294 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A19G-06A-11D-A196-08 | TCGA-ER-A19G-10A-01D-A198-08 | g.chr10:105363294G>A | c.1681C>T | c.(1681-1683)Cct>Tct | p.P561S |
SKCM | 10 | 105372776 | 105372776 | + | Silent | SNP | G | G | A | TCGA-ER-A42L-06A-11D-A24R-08 | TCGA-ER-A42L-10A-01D-A24R-08 | g.chr10:105372776G>A | c.1092C>T | c.(1090-1092)gcC>gcT | p.A364A |
SKCM | 10 | 105386856 | 105386856 | + | Silent | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr10:105386856C>T | c.708G>A | c.(706-708)aaG>aaA | p.K236K |
SKCM | 10 | 105386875 | 105386875 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:105386875G>A | c.689C>T | c.(688-690)tCc>tTc | p.S230F |
SKCM | 10 | 105386875 | 105386875 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:105386875G>A | c.689C>T | c.(688-690)tCc>tTc | p.S230F |
SKCM | 10 | 105484080 | 105484080 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1IC-06A-11D-A197-08 | TCGA-DA-A1IC-10A-01D-A199-08 | g.chr10:105484080C>T | c.346G>A | c.(346-348)Gaa>Aaa | p.E116K |
SKCM | 10 | 105484080 | 105484080 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:105484080C>T | c.346G>A | c.(346-348)Gaa>Aaa | p.E116K |
SKCM | 10 | 105561083 | 105561083 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A51E-06A-11D-A25O-08 | TCGA-D3-A51E-10A-01D-A25O-08 | g.chr10:105561083G>A | c.110C>T | c.(109-111)tCc>tTc | p.S37F |