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 | 11 | 113934100 | 113934100 | + | Missense_Mutation | SNP | G | G | C | TCGA-KQ-A41P-01A-12D-A339-08 | TCGA-KQ-A41P-10F-01D-A339-08 | g.chr11:113934100G>C | c.78G>C | c.(76-78)caG>caC | p.Q26H |
BLCA | 11 | 113934211 | 113934211 | + | Silent | SNP | C | C | T | TCGA-XF-AAMG-01A-11D-A42E-08 | TCGA-XF-AAMG-10A-01D-A42H-08 | g.chr11:113934211C>T | c.189C>T | c.(187-189)ttC>ttT | p.F63F |
BLCA | 11 | 113934320 | 113934320 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-AA71-01A-31D-A391-08 | TCGA-DK-AA71-10A-01D-A394-08 | g.chr11:113934320G>C | c.298G>C | c.(298-300)Gat>Cat | p.D100H |
BLCA | 11 | 113934410 | 113934410 | + | Missense_Mutation | SNP | G | G | A | TCGA-K4-A5RI-01A-11D-A289-08 | TCGA-K4-A5RI-10A-01D-A289-08 | g.chr11:113934410G>A | c.388G>A | c.(388-390)Gac>Aac | p.D130N |
BLCA | 11 | 113934475 | 113934475 | + | Silent | SNP | G | G | A | TCGA-ZF-A9R4-01A-11D-A38G-08 | TCGA-ZF-A9R4-10A-01D-A38J-08 | g.chr11:113934475G>A | c.453G>A | c.(451-453)cgG>cgA | p.R151R |
BLCA | 11 | 113934854 | 113934854 | + | Missense_Mutation | SNP | G | G | C | TCGA-G2-A2EO-01A-11D-A17V-08 | TCGA-G2-A2EO-11A-21D-A17V-08 | g.chr11:113934854G>C | c.832G>C | c.(832-834)Gag>Cag | p.E278Q |
BLCA | 11 | 113935159 | 113935159 | + | Silent | SNP | C | C | T | TCGA-FD-A43P-01A-31D-A23U-08 | TCGA-FD-A43P-10A-01D-A23U-08 | g.chr11:113935159C>T | c.1137C>T | c.(1135-1137)ttC>ttT | p.F379F |
BRCA | 11 | 113934294 | 113934294 | + | Missense_Mutation | SNP | C | C | T | TCGA-C8-A12T-01A-11D-A10Y-09 | TCGA-C8-A12T-10A-01D-A110-09 | g.chr11:113934294C>T | c.272C>T | c.(271-273)aCg>aTg | p.T91M |
BRCA | 11 | 113935031 | 113935031 | + | Missense_Mutation | SNP | T | T | G | TCGA-A8-A09I-01A-22W-A050-09 | TCGA-A8-A09I-10A-01W-A055-09 | g.chr11:113935031T>G | c.1009T>G | c.(1009-1011)Ttg>Gtg | p.L337V |
BRCA | 11 | 113935219 | 113935219 | + | Silent | SNP | C | C | T | TCGA-D8-A1Y1-01A-21D-A14K-09 | TCGA-D8-A1Y1-10A-01D-A14K-09 | g.chr11:113935219C>T | c.1197C>T | c.(1195-1197)agC>agT | p.S399S |
BRCA | 11 | 113935256 | 113935256 | + | Missense_Mutation | SNP | G | G | A | TCGA-A8-A06Q-01A-11W-A050-09 | TCGA-A8-A06Q-10A-01W-A055-09 | g.chr11:113935256G>A | c.1234G>A | c.(1234-1236)Gag>Aag | p.E412K |
BRCA | 11 | 114121049 | 114121049 | + | Splice_Site | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr11:114121049T>G | c.1794T>G | c.(1792-1794)ggT>ggG | p.G598G |
CESC | 11 | 113934839 | 113934839 | + | Missense_Mutation | SNP | G | G | A | TCGA-EK-A2RB-01A-11D-A18J-09 | TCGA-EK-A2RB-10A-01D-A18J-09 | g.chr11:113934839G>A | c.817G>A | c.(817-819)Gag>Aag | p.E273K |
CESC | 11 | 113934923 | 113934923 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A7CG-01A-11D-A32I-09 | TCGA-C5-A7CG-10A-01D-A32I-09 | g.chr11:113934923G>A | c.901G>A | c.(901-903)Gag>Aag | p.E301K |
CESC | 11 | 113935017 | 113935017 | + | Missense_Mutation | SNP | G | G | T | TCGA-EK-A2PM-01A-11D-A18J-09 | TCGA-EK-A2PM-10A-01D-A18J-09 | g.chr11:113935017G>T | c.995G>T | c.(994-996)gGc>gTc | p.G332V |
CESC | 11 | 114113003 | 114113003 | + | Missense_Mutation | SNP | G | G | C | TCGA-FU-A3WB-01A-11D-A22X-09 | TCGA-FU-A3WB-10A-01D-A22X-09 | g.chr11:114113003G>C | c.1568G>C | c.(1567-1569)tGc>tCc | p.C523S |
CHOL | 11 | 114121244 | 114121244 | + | Silent | SNP | A | A | T | TCGA-W5-AA39-01A-11D-A417-09 | TCGA-W5-AA39-10A-01D-A41A-09 | g.chr11:114121244A>T | c.1989A>T | c.(1987-1989)atA>atT | p.I663I |
COAD | 11 | 113934034 | 113934034 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr11:113934034delA | c.12delA | c.(10-12)acafs | p.T4fs |
COAD | 11 | 113934279 | 113934279 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr11:113934279A>G | c.257A>G | c.(256-258)tAt>tGt | p.Y86C |
COAD | 11 | 113934294 | 113934294 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr11:113934294C>T | c.272C>T | c.(271-273)aCg>aTg | p.T91M |
COAD | 11 | 113934368 | 113934368 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr11:113934368G>A | c.346G>A | c.(346-348)Gaa>Aaa | p.E116K |
COAD | 11 | 113934870 | 113934870 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr11:113934870C>T | c.848C>T | c.(847-849)cCg>cTg | p.P283L |
COAD | 11 | 113935069 | 113935069 | + | Silent | SNP | G | G | A | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr11:113935069G>A | c.1047G>A | c.(1045-1047)ccG>ccA | p.P349P |
COAD | 11 | 113935103 | 113935103 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3994-01A-01W-1073-09 | TCGA-AA-3994-10A-01W-1073-09 | g.chr11:113935103G>T | c.1081G>T | c.(1081-1083)Gcc>Tcc | p.A361S |
COAD | 11 | 113935122 | 113935122 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr11:113935122A>C | c.1100A>C | c.(1099-1101)gAc>gCc | p.D367A |
COAD | 11 | 114027087 | 114027087 | + | Missense_Mutation | SNP | G | G | A | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr11:114027087G>A | c.1297G>A | c.(1297-1299)Ggg>Agg | p.G433R |
COAD | 11 | 114057674 | 114057674 | + | Splice_Site | SNP | C | C | T | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr11:114057674C>T | c.1367C>T | c.(1366-1368)gCg>gTg | p.A456V |
COAD | 11 | 114057705 | 114057705 | + | Silent | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr11:114057705C>T | c.1398C>T | c.(1396-1398)tgC>tgT | p.C466C |
COAD | 11 | 114112919 | 114112920 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr11:114112919_114112920insT | c.1484_1485insT | c.(1483-1488)tgtgggfs | p.G496fs |
COAD | 11 | 114117945 | 114117945 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr11:114117945C>A | c.1650C>A | c.(1648-1650)ttC>ttA | p.F550L |
COAD | 11 | 114118068 | 114118068 | + | Silent | SNP | G | G | A | TCGA-AA-3955-01A-02W-0995-10 | TCGA-AA-3955-10A-01W-0995-10 | g.chr11:114118068G>A | c.1773G>A | c.(1771-1773)acG>acA | p.T591T |
COAD | 11 | 114121125 | 114121125 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6922-01A-11D-1924-10 | TCGA-D5-6922-10A-01D-1924-10 | g.chr11:114121125C>T | c.1870C>T | c.(1870-1872)Cac>Tac | p.H624Y |
COAD | 11 | 114121253 | 114121253 | + | Silent | SNP | G | G | A | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr11:114121253G>A | c.1998G>A | c.(1996-1998)acG>acA | p.T666T |
COADREAD | 11 | 113934034 | 113934034 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr11:113934034delA | c.12delA | c.(10-12)acafs | p.T4fs |
COADREAD | 11 | 113934279 | 113934279 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr11:113934279A>G | c.257A>G | c.(256-258)tAt>tGt | p.Y86C |
COADREAD | 11 | 113934294 | 113934294 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr11:113934294C>T | c.272C>T | c.(271-273)aCg>aTg | p.T91M |
COADREAD | 11 | 113934368 | 113934368 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr11:113934368G>A | c.346G>A | c.(346-348)Gaa>Aaa | p.E116K |
COADREAD | 11 | 113934842 | 113934842 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr11:113934842G>T | c.820G>T | c.(820-822)Gaa>Taa | p.E274* |
COADREAD | 11 | 113934870 | 113934870 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr11:113934870C>T | c.848C>T | c.(847-849)cCg>cTg | p.P283L |
COADREAD | 11 | 113935069 | 113935069 | + | Silent | SNP | G | G | A | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr11:113935069G>A | c.1047G>A | c.(1045-1047)ccG>ccA | p.P349P |
COADREAD | 11 | 113935103 | 113935103 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3994-01A-01W-1073-09 | TCGA-AA-3994-10A-01W-1073-09 | g.chr11:113935103G>T | c.1081G>T | c.(1081-1083)Gcc>Tcc | p.A361S |
COADREAD | 11 | 113935122 | 113935122 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr11:113935122A>C | c.1100A>C | c.(1099-1101)gAc>gCc | p.D367A |
COADREAD | 11 | 114027087 | 114027087 | + | Missense_Mutation | SNP | G | G | A | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr11:114027087G>A | c.1297G>A | c.(1297-1299)Ggg>Agg | p.G433R |
COADREAD | 11 | 114057674 | 114057674 | + | Splice_Site | SNP | C | C | T | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr11:114057674C>T | c.1367C>T | c.(1366-1368)gCg>gTg | p.A456V |
COADREAD | 11 | 114057705 | 114057705 | + | Silent | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr11:114057705C>T | c.1398C>T | c.(1396-1398)tgC>tgT | p.C466C |
COADREAD | 11 | 114057719 | 114057719 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr11:114057719C>T | c.1412C>T | c.(1411-1413)tCg>tTg | p.S471L |
COADREAD | 11 | 114112919 | 114112920 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr11:114112919_114112920insT | c.1484_1485insT | c.(1483-1488)tgtgggfs | p.G496fs |
COADREAD | 11 | 114112927 | 114112927 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3726-01A-02W-0899-10 | TCGA-AG-3726-10A-01W-0901-10 | g.chr11:114112927C>T | c.1492C>T | c.(1492-1494)Cgc>Tgc | p.R498C |
COADREAD | 11 | 114112956 | 114112956 | + | Silent | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr11:114112956G>A | c.1521G>A | c.(1519-1521)caG>caA | p.Q507Q |
COADREAD | 11 | 114117945 | 114117945 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr11:114117945C>A | c.1650C>A | c.(1648-1650)ttC>ttA | p.F550L |
COADREAD | 11 | 114118068 | 114118068 | + | Silent | SNP | G | G | A | TCGA-AA-3955-01A-02W-0995-10 | TCGA-AA-3955-10A-01W-0995-10 | g.chr11:114118068G>A | c.1773G>A | c.(1771-1773)acG>acA | p.T591T |
COADREAD | 11 | 114121125 | 114121125 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6922-01A-11D-1924-10 | TCGA-D5-6922-10A-01D-1924-10 | g.chr11:114121125C>T | c.1870C>T | c.(1870-1872)Cac>Tac | p.H624Y |
COADREAD | 11 | 114121253 | 114121253 | + | Silent | SNP | G | G | A | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr11:114121253G>A | c.1998G>A | c.(1996-1998)acG>acA | p.T666T |
DLBC | 11 | 114027086 | 114027086 | + | Silent | SNP | C | C | T | TCGA-GS-A9TZ-01A-11D-A38X-10 | TCGA-GS-A9TZ-10A-01D-A38X-10 | g.chr11:114027086C>T | c.1296C>T | c.(1294-1296)taC>taT | p.Y432Y |
DLBC | 11 | 114118019 | 114118019 | + | Missense_Mutation | SNP | A | A | G | TCGA-GR-7351-01A-11D-2210-10 | TCGA-GR-7351-10A-01D-2210-10 | g.chr11:114118019A>G | c.1724A>G | c.(1723-1725)gAg>gGg | p.E575G |
DLBC | 11 | 114121182 | 114121182 | + | Missense_Mutation | SNP | T | T | A | TCGA-G8-6914-01A-11D-2210-10 | TCGA-G8-6914-14A-01D-2210-10 | g.chr11:114121182T>A | c.1927T>A | c.(1927-1929)Tcc>Acc | p.S643T |
ESCA | 11 | 113934619 | 113934619 | + | Silent | SNP | C | C | A | TCGA-LN-A8I0-01A-11D-A36J-09 | TCGA-LN-A8I0-10A-01D-A36M-09 | g.chr11:113934619C>A | c.597C>A | c.(595-597)acC>acA | p.T199T |
ESCA | 11 | 113935103 | 113935103 | + | Missense_Mutation | SNP | G | G | A | TCGA-LN-A4A6-01A-11D-A27G-09 | TCGA-LN-A4A6-10A-01D-A27G-09 | g.chr11:113935103G>A | c.1081G>A | c.(1081-1083)Gcc>Acc | p.A361T |
ESCA | 11 | 114027093 | 114027093 | + | Missense_Mutation | SNP | G | G | A | TCGA-LN-A49S-01A-11D-A247-09 | TCGA-LN-A49S-10A-01D-A247-09 | g.chr11:114027093G>A | c.1303G>A | c.(1303-1305)Gag>Aag | p.E435K |
ESCA | 11 | 114112974 | 114112974 | + | Silent | SNP | G | G | A | TCGA-L5-A4OT-01A-11D-A28B-09 | TCGA-L5-A4OT-11A-11D-A28E-09 | g.chr11:114112974G>A | c.1539G>A | c.(1537-1539)gcG>gcA | p.A513A |
ESCA | 11 | 114118002 | 114118002 | + | Silent | SNP | G | G | A | TCGA-R6-A8W8-01B-11D-A37C-09 | TCGA-R6-A8W8-10A-01D-A37F-09 | g.chr11:114118002G>A | c.1707G>A | c.(1705-1707)acG>acA | p.T569T |
ESCA | 11 | 114118040 | 114118040 | + | Missense_Mutation | SNP | A | A | C | TCGA-R6-A8W8-01B-11D-A37C-09 | TCGA-R6-A8W8-10A-01D-A37F-09 | g.chr11:114118040A>C | c.1745A>C | c.(1744-1746)aAg>aCg | p.K582T |
ESCA | 11 | 114118040 | 114118040 | + | Missense_Mutation | SNP | A | A | G | TCGA-L5-A43E-01A-11D-A247-09 | TCGA-L5-A43E-10A-01D-A247-09 | g.chr11:114118040A>G | c.1745A>G | c.(1744-1746)aAg>aGg | p.K582R |
GBMLGG | 11 | 114112981 | 114112981 | + | Missense_Mutation | SNP | C | C | T | TCGA-DH-A7US-01A-11D-A33T-08 | TCGA-DH-A7US-10A-01D-A33W-08 | g.chr11:114112981C>T | c.1546C>T | c.(1546-1548)Cgc>Tgc | p.R516C |
GBMLGG | 11 | 114121089 | 114121089 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr11:114121089C>T | c.1834C>T | c.(1834-1836)Cgg>Tgg | p.R612W |
HNSC | 11 | 113934355 | 113934355 | + | Silent | SNP | C | C | A | TCGA-CV-A6JM-01A-11D-A31L-08 | TCGA-CV-A6JM-10A-01D-A31J-08 | g.chr11:113934355C>A | c.333C>A | c.(331-333)atC>atA | p.I111I |
HNSC | 11 | 113934661 | 113934661 | + | Silent | SNP | C | C | G | TCGA-CR-7402-01A-11D-2012-08 | TCGA-CR-7402-10A-01D-2013-08 | g.chr11:113934661C>G | c.639C>G | c.(637-639)ctC>ctG | p.L213L |
HNSC | 11 | 113934865 | 113934865 | + | Silent | SNP | G | G | T | TCGA-CQ-7068-01A-11D-2078-08 | TCGA-CQ-7068-10A-01D-2078-08 | g.chr11:113934865G>T | c.843G>T | c.(841-843)ggG>ggT | p.G281G |
HNSC | 11 | 113934906 | 113934906 | + | Missense_Mutation | SNP | T | T | A | TCGA-CV-A45W-01A-11D-A25D-08 | TCGA-CV-A45W-10A-01D-A25E-08 | g.chr11:113934906T>A | c.884T>A | c.(883-885)cTa>cAa | p.L295Q |
HNSC | 11 | 113935271 | 113935271 | + | Missense_Mutation | SNP | G | G | A | TCGA-CR-6472-01A-11D-1870-08 | TCGA-CR-6472-10A-01D-1870-08 | g.chr11:113935271G>A | c.1249G>A | c.(1249-1251)Gag>Aag | p.E417K |
HNSC | 11 | 114027108 | 114027108 | + | Silent | SNP | C | C | A | TCGA-CR-7398-01A-11D-2012-08 | TCGA-CR-7398-10A-01D-2013-08 | g.chr11:114027108C>A | c.1318C>A | c.(1318-1320)Cgg>Agg | p.R440R |
HNSC | 11 | 114027138 | 114027138 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-5374-01A-01D-1434-08 | TCGA-CN-5374-10A-01D-1434-08 | g.chr11:114027138C>T | c.1348C>T | c.(1348-1350)Cac>Tac | p.H450Y |
HNSC | 11 | 114113009 | 114113009 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-A6JU-01A-11D-A31L-08 | TCGA-CV-A6JU-10A-01D-A31J-08 | g.chr11:114113009G>A | c.1574G>A | c.(1573-1575)cGc>cAc | p.R525H |
HNSC | 11 | 114117978 | 114117978 | + | Silent | SNP | C | C | A | TCGA-UF-A71D-01A-12D-A34J-08 | TCGA-UF-A71D-10B-01D-A34M-08 | g.chr11:114117978C>A | c.1683C>A | c.(1681-1683)ctC>ctA | p.L561L |
HNSC | 11 | 114121062 | 114121062 | + | Missense_Mutation | SNP | G | G | C | TCGA-CR-6472-01A-11D-1870-08 | TCGA-CR-6472-10A-01D-1870-08 | g.chr11:114121062G>C | c.1807G>C | c.(1807-1809)Gag>Cag | p.E603Q |
HNSC | 11 | 114121088 | 114121088 | + | Silent | SNP | C | C | A | TCGA-CV-A461-01A-41D-A25Y-08 | TCGA-CV-A461-10A-01D-A25Y-08 | g.chr11:114121088C>A | c.1833C>A | c.(1831-1833)tcC>tcA | p.S611S |
HNSC | 11 | 114121202 | 114121202 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-4742-01A-02D-1512-08 | TCGA-CN-4742-10A-01D-1512-08 | g.chr11:114121202G>A | c.1947G>A | c.(1945-1947)atG>atA | p.M649I |
KICH | 11 | 113934295 | 113934295 | + | Silent | SNP | G | G | T | TCGA-KL-8326-01A-11D-2310-10 | TCGA-KL-8326-11A-01D-2310-10 | g.chr11:113934295G>T | c.273G>T | c.(271-273)acG>acT | p.T91T |
KIPAN | 11 | 113934295 | 113934295 | + | Silent | SNP | G | G | T | TCGA-KL-8326-01A-11D-2310-10 | TCGA-KL-8326-11A-01D-2310-10 | g.chr11:113934295G>T | c.273G>T | c.(271-273)acG>acT | p.T91T |
KIPAN | 11 | 113934420 | 113934420 | + | Missense_Mutation | SNP | C | C | T | TCGA-B8-4143-01A-01D-1806-10 | TCGA-B8-4143-11A-01D-1251-10 | g.chr11:113934420C>T | c.398C>T | c.(397-399)aCg>aTg | p.T133M |
KIRC | 11 | 113934420 | 113934420 | + | Missense_Mutation | SNP | C | C | T | TCGA-B8-4143-01A-01D-1806-10 | TCGA-B8-4143-11A-01D-1251-10 | g.chr11:113934420C>T | c.398C>T | c.(397-399)aCg>aTg | p.T133M |
LGG | 11 | 114112981 | 114112981 | + | Missense_Mutation | SNP | C | C | T | TCGA-DH-A7US-01A-11D-A33T-08 | TCGA-DH-A7US-10A-01D-A33W-08 | g.chr11:114112981C>T | c.1546C>T | c.(1546-1548)Cgc>Tgc | p.R516C |
LGG | 11 | 114121089 | 114121089 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr11:114121089C>T | c.1834C>T | c.(1834-1836)Cgg>Tgg | p.R612W |
LIHC | 11 | 113934393 | 113934393 | + | Missense_Mutation | SNP | C | C | A | TCGA-DD-AAE8-01A-11D-A40R-10 | TCGA-DD-AAE8-10A-01D-A40U-10 | g.chr11:113934393C>A | c.371C>A | c.(370-372)aCc>aAc | p.T124N |
LIHC | 11 | 114112895 | 114112895 | + | Missense_Mutation | SNP | A | A | G | TCGA-BC-A3KF-01A-11D-A20W-10 | TCGA-BC-A3KF-10A-01D-A20W-10 | g.chr11:114112895A>G | c.1460A>G | c.(1459-1461)gAc>gGc | p.D487G |
LIHC | 11 | 114113007 | 114113007 | + | Silent | SNP | C | C | T | TCGA-G3-A3CK-01A-11D-A20W-10 | TCGA-G3-A3CK-10A-01D-A20W-10 | g.chr11:114113007C>T | c.1572C>T | c.(1570-1572)aaC>aaT | p.N524N |
LUAD | 11 | 113934272 | 113934272 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-6968-01A-11D-1945-08 | TCGA-55-6968-11A-01D-1945-08 | g.chr11:113934272C>G | c.250C>G | c.(250-252)Ctg>Gtg | p.L84V |
LUAD | 11 | 113934379 | 113934379 | + | Silent | SNP | G | G | A | TCGA-86-7955-01A-11D-2184-08 | TCGA-86-7955-10A-01D-2184-08 | g.chr11:113934379G>A | c.357G>A | c.(355-357)ctG>ctA | p.L119L |
LUAD | 11 | 113934449 | 113934449 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-MN-A4N4-01A-12D-A24P-08 | TCGA-MN-A4N4-10A-01D-A24P-08 | g.chr11:113934449G>T | c.427G>T | c.(427-429)Gag>Tag | p.E143* |
LUAD | 11 | 113934619 | 113934619 | + | Silent | SNP | C | C | A | TCGA-78-7536-01A-11D-2063-08 | TCGA-78-7536-10A-01D-2063-08 | g.chr11:113934619C>A | c.597C>A | c.(595-597)acC>acA | p.T199T |
LUAD | 11 | 113934732 | 113934732 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-3918-01A-01D-1105-08 | TCGA-44-3918-11A-01D-1105-08 | g.chr11:113934732G>T | c.710G>T | c.(709-711)gGg>gTg | p.G237V |
LUAD | 11 | 113934754 | 113934754 | + | Missense_Mutation | SNP | G | G | C | TCGA-62-A46O-01A-11D-A24D-08 | TCGA-62-A46O-10A-01D-A24F-08 | g.chr11:113934754G>C | c.732G>C | c.(730-732)gaG>gaC | p.E244D |
LUAD | 11 | 113935030 | 113935030 | + | Silent | SNP | G | G | C | TCGA-50-7109-01A-11D-2036-08 | TCGA-50-7109-11A-01D-2036-08 | g.chr11:113935030G>C | c.1008G>C | c.(1006-1008)gtG>gtC | p.V336V |
LUAD | 11 | 113935185 | 113935186 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-69-7973-01A-11D-2184-08 | TCGA-69-7973-10A-01D-2184-08 | g.chr11:113935185_113935186insG | c.1163_1164insG | c.(1162-1167)ctggggfs | p.LG388fs |
LUAD | 11 | 113935191 | 113935191 | + | Missense_Mutation | SNP | A | A | T | TCGA-MN-A4N1-01A-11D-A24P-08 | TCGA-MN-A4N1-10A-01D-A24P-08 | g.chr11:113935191A>T | c.1169A>T | c.(1168-1170)gAg>gTg | p.E390V |
LUAD | 11 | 114112944 | 114112944 | + | Missense_Mutation | SNP | C | C | G | TCGA-91-A4BC-01A-11D-A24D-08 | TCGA-91-A4BC-10A-01D-A24F-08 | g.chr11:114112944C>G | c.1509C>G | c.(1507-1509)agC>agG | p.S503R |
LUAD | 11 | 114113009 | 114113009 | + | Missense_Mutation | SNP | G | G | C | TCGA-NJ-A4YQ-01A-11D-A25L-08 | TCGA-NJ-A4YQ-10A-01D-A25L-08 | g.chr11:114113009G>C | c.1574G>C | c.(1573-1575)cGc>cCc | p.R525P |
LUAD | 11 | 114113048 | 114113048 | + | Missense_Mutation | SNP | G | G | T | TCGA-67-3773-01A-01D-1040-01 | TCGA-67-3773-10A-01D-1489-08 | g.chr11:114113048G>T | c.1613G>T | c.(1612-1614)cGc>cTc | p.R538L |
LUAD | 11 | 114121118 | 114121118 | + | Silent | SNP | G | G | T | TCGA-17-Z057-01A-01W-0747-08 | TCGA-17-Z057-11A-01W-0747-08 | g.chr11:114121118G>T | c.1863G>T | c.(1861-1863)ctG>ctT | p.L621L |
LUSC | 11 | 113934218 | 113934218 | + | Missense_Mutation | SNP | A | A | G | TCGA-63-5131-01A-01D-1441-08 | TCGA-63-5131-10A-01D-1441-08 | g.chr11:113934218A>G | c.196A>G | c.(196-198)Aat>Gat | p.N66D |
LUSC | 11 | 113934591 | 113934591 | + | Missense_Mutation | SNP | C | C | T | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr11:113934591C>T | c.569C>T | c.(568-570)tCa>tTa | p.S190L |
LUSC | 11 | 114112921 | 114112921 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chr11:114112921delG | c.1486delG | c.(1486-1488)gggfs | p.G496fs |
LUSC | 11 | 114113012 | 114113012 | + | Missense_Mutation | SNP | C | C | A | TCGA-37-4141-01A-02D-1352-08 | TCGA-37-4141-10A-01D-1352-08 | g.chr11:114113012C>A | c.1577C>A | c.(1576-1578)aCc>aAc | p.T526N |
LUSC | 11 | 114121138 | 114121138 | + | Missense_Mutation | SNP | C | C | T | TCGA-37-3783-01A-01D-1267-08 | TCGA-37-3783-10A-01D-1267-08 | g.chr11:114121138C>T | c.1883C>T | c.(1882-1884)tCg>tTg | p.S628L |
LUSC | 11 | 114121265 | 114121265 | + | Silent | SNP | G | G | T | TCGA-33-4566-01A-01D-1441-08 | TCGA-33-4566-11A-01D-1441-08 | g.chr11:114121265G>T | c.2010G>T | c.(2008-2010)ctG>ctT | p.L670L |
OV | 11 | 113934217 | 113934217 | + | Silent | SNP | C | C | T | TCGA-10-0927-01A-02W-0419-10 | TCGA-10-0927-11A-01W-0419-10 | g.chr11:113934217C>T | c.195C>T | c.(193-195)cgC>cgT | p.R65R |
OV | 11 | 113934832 | 113934832 | + | Missense_Mutation | SNP | C | C | A | TCGA-24-1417-01A-01W-0549-09 | TCGA-24-1417-10A-01W-0549-09 | g.chr11:113934832C>A | c.810C>A | c.(808-810)gaC>gaA | p.D270E |
PAAD | 11 | 113934573 | 113934573 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr11:113934573G>A | c.551G>A | c.(550-552)aGc>aAc | p.S184N |
PAAD | 11 | 114027126 | 114027126 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-AAUO-01A-12D-A38G-08 | TCGA-IB-AAUO-10A-01D-A38J-08 | g.chr11:114027126C>T | c.1336C>T | c.(1336-1338)Cgg>Tgg | p.R446W |
PRAD | 11 | 114112945 | 114112945 | + | Missense_Mutation | SNP | G | G | A | TCGA-YL-A8HJ-01A-11D-A364-08 | TCGA-YL-A8HJ-10A-01D-A362-08 | g.chr11:114112945G>A | c.1510G>A | c.(1510-1512)Gca>Aca | p.A504T |
PRAD | 11 | 114113039 | 114113039 | + | Missense_Mutation | SNP | G | G | A | TCGA-HC-A48F-01A-11D-A257-08 | TCGA-HC-A48F-10A-01D-A25A-08 | g.chr11:114113039G>A | c.1604G>A | c.(1603-1605)cGc>cAc | p.R535H |
PRAD | 11 | 114118039 | 114118039 | + | Missense_Mutation | SNP | A | A | G | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr11:114118039A>G | c.1744A>G | c.(1744-1746)Aag>Gag | p.K582E |
READ | 11 | 113934842 | 113934842 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr11:113934842G>T | c.820G>T | c.(820-822)Gaa>Taa | p.E274* |
READ | 11 | 114057719 | 114057719 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr11:114057719C>T | c.1412C>T | c.(1411-1413)tCg>tTg | p.S471L |
READ | 11 | 114112927 | 114112927 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3726-01A-02W-0899-10 | TCGA-AG-3726-10A-01W-0901-10 | g.chr11:114112927C>T | c.1492C>T | c.(1492-1494)Cgc>Tgc | p.R498C |
READ | 11 | 114112956 | 114112956 | + | Silent | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr11:114112956G>A | c.1521G>A | c.(1519-1521)caG>caA | p.Q507Q |
SARC | 11 | 113934249 | 113934249 | + | Missense_Mutation | SNP | C | C | T | TCGA-KD-A5QT-01A-11D-A27P-09 | TCGA-KD-A5QT-10A-01D-A27P-09 | g.chr11:113934249C>T | c.227C>T | c.(226-228)tCg>tTg | p.S76L |
SKCM | 11 | 113934125 | 113934125 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr11:113934125G>A | c.103G>A | c.(103-105)Gat>Aat | p.D35N |
SKCM | 11 | 113934214 | 113934214 | + | Silent | SNP | C | C | T | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr11:113934214C>T | c.192C>T | c.(190-192)caC>caT | p.H64H |
SKCM | 11 | 113934445 | 113934445 | + | Silent | SNP | G | G | T | TCGA-GN-A26D-06A-11D-A19A-08 | TCGA-GN-A26D-10A-01D-A19A-08 | g.chr11:113934445G>T | c.423G>T | c.(421-423)ggG>ggT | p.G141G |
SKCM | 11 | 113934493 | 113934493 | + | Silent | SNP | C | C | T | TCGA-D3-A1Q6-06A-11D-A196-08 | TCGA-D3-A1Q6-10A-01D-A198-08 | g.chr11:113934493C>T | c.471C>T | c.(469-471)ttC>ttT | p.F157F |
SKCM | 11 | 113934508 | 113934508 | + | Silent | SNP | C | C | T | TCGA-FR-A3YO-06A-11D-A23B-08 | TCGA-FR-A3YO-10A-01D-A23B-08 | g.chr11:113934508C>T | c.486C>T | c.(484-486)tcC>tcT | p.S162S |
SKCM | 11 | 113934559 | 113934559 | + | Silent | SNP | C | C | T | TCGA-ER-A19E-06A-11D-A197-08 | TCGA-ER-A19E-10A-01D-A199-08 | g.chr11:113934559C>T | c.537C>T | c.(535-537)ccC>ccT | p.P179P |
SKCM | 11 | 113934564 | 113934564 | + | Missense_Mutation | SNP | T | T | G | TCGA-RP-A695-06A-11D-A30X-08 | TCGA-RP-A695-10A-01D-A30X-08 | g.chr11:113934564T>G | c.542T>G | c.(541-543)gTg>gGg | p.V181G |
SKCM | 11 | 113934657 | 113934657 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr11:113934657C>T | c.635C>T | c.(634-636)tCt>tTt | p.S212F |
SKCM | 11 | 113934796 | 113934796 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr11:113934796G>A | c.774G>A | c.(772-774)ggG>ggA | p.G258G |
SKCM | 11 | 113934823 | 113934823 | + | Silent | SNP | G | G | A | TCGA-EE-A2GN-06A-11D-A196-08 | TCGA-EE-A2GN-10A-01D-A198-08 | g.chr11:113934823G>A | c.801G>A | c.(799-801)ggG>ggA | p.G267G |
SKCM | 11 | 113934842 | 113934842 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr11:113934842G>A | c.820G>A | c.(820-822)Gaa>Aaa | p.E274K |
SKCM | 11 | 113934891 | 113934891 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr11:113934891C>T | c.869C>T | c.(868-870)aCc>aTc | p.T290I |
SKCM | 11 | 113935071 | 113935071 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr11:113935071C>T | c.1049C>T | c.(1048-1050)tCt>tTt | p.S350F |
SKCM | 11 | 113935271 | 113935271 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr11:113935271G>A | c.1249G>A | c.(1249-1251)Gag>Aag | p.E417K |
SKCM | 11 | 114027098 | 114027098 | + | Silent | SNP | C | C | T | TCGA-EE-A2GJ-06A-11D-A196-08 | TCGA-EE-A2GJ-10A-01D-A198-08 | g.chr11:114027098C>T | c.1308C>T | c.(1306-1308)ctC>ctT | p.L436L |
SKCM | 11 | 114112908 | 114112908 | + | Silent | SNP | C | C | T | TCGA-EE-A2MQ-06A-11D-A197-08 | TCGA-EE-A2MQ-10A-01D-A199-08 | g.chr11:114112908C>T | c.1473C>T | c.(1471-1473)ttC>ttT | p.F491F |
SKCM | 11 | 114113047 | 114113047 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr11:114113047C>T | c.1612C>T | c.(1612-1614)Cgc>Tgc | p.R538C |
SKCM | 11 | 114118013 | 114118013 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A1Q6-06A-11D-A196-08 | TCGA-D3-A1Q6-10A-01D-A198-08 | g.chr11:114118013C>T | c.1718C>T | c.(1717-1719)cCc>cTc | p.P573L |
SKCM | 11 | 114121090 | 114121090 | + | Missense_Mutation | SNP | G | G | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr11:114121090G>T | c.1835G>T | c.(1834-1836)cGg>cTg | p.R612L |
SKCM | 11 | 114121132 | 114121132 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr11:114121132G>A | c.1877G>A | c.(1876-1878)gGc>gAc | p.G626D |
SKCM | 11 | 114121168 | 114121168 | + | Missense_Mutation | SNP | A | A | G | TCGA-ER-A19B-06A-11D-A196-08 | TCGA-ER-A19B-10A-01D-A198-08 | g.chr11:114121168A>G | c.1913A>G | c.(1912-1914)tAc>tGc | p.Y638C |
SKCM | 11 | 114121187 | 114121187 | + | Silent | SNP | C | C | T | TCGA-EE-A2GJ-06A-11D-A196-08 | TCGA-EE-A2GJ-10A-01D-A198-08 | g.chr11:114121187C>T | c.1932C>T | c.(1930-1932)tcC>tcT | p.S644S |