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 | 103907682 | 103907682 | + | Missense_Mutation | SNP | G | G | T | TCGA-E7-A5KF-01A-11D-A289-08 | TCGA-E7-A5KF-10A-01D-A289-08 | g.chr11:103907682G>T | c.132G>T | c.(130-132)gaG>gaT | p.E44D |
BLCA | 11 | 103907712 | 103907712 | + | Silent | SNP | C | C | T | TCGA-K4-A5RJ-01A-11D-A289-08 | TCGA-K4-A5RJ-10A-01D-A289-08 | g.chr11:103907712C>T | c.162C>T | c.(160-162)ctC>ctT | p.L54L |
BLCA | 11 | 103908030 | 103908030 | + | Silent | SNP | C | C | G | TCGA-C4-A0F6-01A-11D-A10S-08 | TCGA-C4-A0F6-10A-01D-A10S-08 | g.chr11:103908030C>G | c.480C>G | c.(478-480)ctC>ctG | p.L160L |
BLCA | 11 | 103908223 | 103908223 | + | Missense_Mutation | SNP | G | G | A | TCGA-2F-A9KT-01A-11D-A38G-08 | TCGA-2F-A9KT-10A-01D-A38J-08 | g.chr11:103908223G>A | c.673G>A | c.(673-675)Gaa>Aaa | p.E225K |
BLCA | 11 | 103908332 | 103908332 | + | Missense_Mutation | SNP | C | C | T | TCGA-K4-A5RH-01A-11D-A30E-08 | TCGA-K4-A5RH-10A-01D-A30H-08 | g.chr11:103908332C>T | c.782C>T | c.(781-783)tCg>tTg | p.S261L |
BLCA | 11 | 103908440 | 103908440 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-AA6R-01A-11D-A42E-08 | TCGA-DK-AA6R-10A-01D-A42H-08 | g.chr11:103908440G>C | c.890G>C | c.(889-891)aGa>aCa | p.R297T |
BLCA | 11 | 103908506 | 103908506 | + | Missense_Mutation | SNP | C | C | G | TCGA-G2-A2EJ-01A-11D-A17V-08 | TCGA-G2-A2EJ-10A-01D-A17V-08 | g.chr11:103908506C>G | c.956C>G | c.(955-957)tCc>tGc | p.S319C |
BLCA | 11 | 103908520 | 103908520 | + | Missense_Mutation | SNP | C | C | A | TCGA-E7-A3Y1-01A-11D-A22Z-08 | TCGA-E7-A3Y1-10A-01D-A22Z-08 | g.chr11:103908520C>A | c.970C>A | c.(970-972)Caa>Aaa | p.Q324K |
BLCA | 11 | 103908679 | 103908679 | + | Missense_Mutation | SNP | G | G | C | TCGA-G2-AA3C-01A-21D-A391-08 | TCGA-G2-AA3C-10A-01D-A394-08 | g.chr11:103908679G>C | c.1129G>C | c.(1129-1131)Gat>Cat | p.D377H |
BRCA | 11 | 103907556 | 103907556 | + | Silent | SNP | G | G | A | TCGA-E2-A1LB-01A-11D-A142-09 | TCGA-E2-A1LB-11A-22D-A142-09 | g.chr11:103907556G>A | c.6G>A | c.(4-6)ctG>ctA | p.L2L |
BRCA | 11 | 103907921 | 103907921 | + | Missense_Mutation | SNP | G | G | A | TCGA-EW-A1PB-01A-11D-A142-09 | TCGA-EW-A1PB-10A-01D-A142-09 | g.chr11:103907921G>A | c.371G>A | c.(370-372)cGg>cAg | p.R124Q |
BRCA | 11 | 103908037 | 103908037 | + | Missense_Mutation | SNP | C | C | T | TCGA-C8-A12T-01A-11D-A10Y-09 | TCGA-C8-A12T-10A-01D-A110-09 | g.chr11:103908037C>T | c.487C>T | c.(487-489)Cgc>Tgc | p.R163C |
BRCA | 11 | 103908260 | 103908260 | + | Missense_Mutation | SNP | G | G | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr11:103908260G>T | c.710G>T | c.(709-711)aGt>aTt | p.S237I |
BRCA | 11 | 103908332 | 103908332 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A204-01A-11D-A159-09 | TCGA-BH-A204-11A-53D-A159-09 | g.chr11:103908332C>T | c.782C>T | c.(781-783)tCg>tTg | p.S261L |
BRCA | 11 | 103908577 | 103908577 | + | Missense_Mutation | SNP | G | G | A | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr11:103908577G>A | c.1027G>A | c.(1027-1029)Gat>Aat | p.D343N |
CESC | 11 | 103908011 | 103908011 | + | Missense_Mutation | SNP | C | C | T | TCGA-EK-A2RJ-01A-11D-A18J-09 | TCGA-EK-A2RJ-10A-01D-A18J-09 | g.chr11:103908011C>T | c.461C>T | c.(460-462)cCc>cTc | p.P154L |
CESC | 11 | 103908368 | 103908368 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A1BI-01B-11D-A13W-08 | TCGA-C5-A1BI-10A-01D-A13W-08 | g.chr11:103908368C>T | c.818C>T | c.(817-819)gCc>gTc | p.A273V |
CHOL | 11 | 103908641 | 103908641 | + | Missense_Mutation | SNP | G | G | T | TCGA-ZD-A8I3-01A-11D-A417-09 | TCGA-ZD-A8I3-10A-01D-A41A-09 | g.chr11:103908641G>T | c.1091G>T | c.(1090-1092)gGa>gTa | p.G364V |
COAD | 11 | 103907571 | 103907571 | + | Silent | SNP | C | C | T | TCGA-D5-6898-01A-11D-1924-10 | TCGA-D5-6898-10A-01D-1924-10 | g.chr11:103907571C>T | c.21C>T | c.(19-21)tgC>tgT | p.C7C |
COAD | 11 | 103907586 | 103907586 | + | Silent | SNP | C | C | T | TCGA-G4-6306-01A-11D-1771-10 | TCGA-G4-6306-10A-01D-1771-10 | g.chr11:103907586C>T | c.36C>T | c.(34-36)ctC>ctT | p.L12L |
COAD | 11 | 103907674 | 103907674 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6715-01A-21D-1835-10 | TCGA-CA-6715-10A-01D-1835-10 | g.chr11:103907674G>A | c.124G>A | c.(124-126)Gtc>Atc | p.V42I |
COAD | 11 | 103907676 | 103907676 | + | Silent | SNP | C | C | T | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr11:103907676C>T | c.126C>T | c.(124-126)gtC>gtT | p.V42V |
COAD | 11 | 103907716 | 103907716 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr11:103907716G>A | c.166G>A | c.(166-168)Gag>Aag | p.E56K |
COAD | 11 | 103907731 | 103907731 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr11:103907731C>A | c.181C>A | c.(181-183)Ctg>Atg | p.L61M |
COAD | 11 | 103907742 | 103907742 | + | Silent | SNP | C | C | T | TCGA-CK-4947-01B-11D-1650-10 | TCGA-CK-4947-10A-01D-1650-10 | g.chr11:103907742C>T | c.192C>T | c.(190-192)taC>taT | p.Y64Y |
COAD | 11 | 103907810 | 103907810 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr11:103907810G>A | c.260G>A | c.(259-261)cGt>cAt | p.R87H |
COAD | 11 | 103907872 | 103907872 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A01P-01A-21W-A096-10 | TCGA-AA-A01P-11A-11W-A096-10 | g.chr11:103907872C>T | c.322C>T | c.(322-324)Cgt>Tgt | p.R108C |
COAD | 11 | 103907882 | 103907882 | + | Missense_Mutation | SNP | A | A | T | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr11:103907882A>T | c.332A>T | c.(331-333)cAc>cTc | p.H111L |
COAD | 11 | 103907902 | 103907902 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A02K-01A-21W-A096-10 | TCGA-AA-A02K-10A-01W-A096-10 | g.chr11:103907902C>T | c.352C>T | c.(352-354)Cgc>Tgc | p.R118C |
COAD | 11 | 103907979 | 103907979 | + | Silent | SNP | C | C | T | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr11:103907979C>T | c.429C>T | c.(427-429)ccC>ccT | p.P143P |
COAD | 11 | 103908038 | 103908038 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr11:103908038G>A | c.488G>A | c.(487-489)cGc>cAc | p.R163H |
COAD | 11 | 103908145 | 103908145 | + | Missense_Mutation | SNP | C | C | A | TCGA-F4-6855-01A-11D-1924-10 | TCGA-F4-6855-10A-01D-1924-10 | g.chr11:103908145C>A | c.595C>A | c.(595-597)Cgt>Agt | p.R199S |
COAD | 11 | 103908146 | 103908146 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3870-01A-01W-0995-10 | TCGA-AA-3870-10A-01W-0995-10 | g.chr11:103908146G>A | c.596G>A | c.(595-597)cGt>cAt | p.R199H |
COAD | 11 | 103908323 | 103908323 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr11:103908323T>C | c.773T>C | c.(772-774)tTt>tCt | p.F258S |
COAD | 11 | 103908374 | 103908374 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr11:103908374G>A | c.824G>A | c.(823-825)cGa>cAa | p.R275Q |
COAD | 11 | 103908374 | 103908374 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr11:103908374G>A | c.824G>A | c.(823-825)cGa>cAa | p.R275Q |
COAD | 11 | 103908452 | 103908452 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr11:103908452G>A | c.902G>A | c.(901-903)cGt>cAt | p.R301H |
COAD | 11 | 103908691 | 103908691 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr11:103908691G>T | c.1141G>T | c.(1141-1143)Gac>Tac | p.D381Y |
COAD | 11 | 103908700 | 103908700 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr11:103908700A>G | c.1150A>G | c.(1150-1152)Att>Gtt | p.I384V |
COAD | 11 | 103908728 | 103908728 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr11:103908728G>A | c.1178G>A | c.(1177-1179)cGa>cAa | p.R393Q |
COADREAD | 11 | 103907571 | 103907571 | + | Silent | SNP | C | C | T | TCGA-D5-6898-01A-11D-1924-10 | TCGA-D5-6898-10A-01D-1924-10 | g.chr11:103907571C>T | c.21C>T | c.(19-21)tgC>tgT | p.C7C |
COADREAD | 11 | 103907586 | 103907586 | + | Silent | SNP | C | C | T | TCGA-G4-6306-01A-11D-1771-10 | TCGA-G4-6306-10A-01D-1771-10 | g.chr11:103907586C>T | c.36C>T | c.(34-36)ctC>ctT | p.L12L |
COADREAD | 11 | 103907674 | 103907674 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6715-01A-21D-1835-10 | TCGA-CA-6715-10A-01D-1835-10 | g.chr11:103907674G>A | c.124G>A | c.(124-126)Gtc>Atc | p.V42I |
COADREAD | 11 | 103907676 | 103907676 | + | Silent | SNP | C | C | T | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr11:103907676C>T | c.126C>T | c.(124-126)gtC>gtT | p.V42V |
COADREAD | 11 | 103907716 | 103907716 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr11:103907716G>A | c.166G>A | c.(166-168)Gag>Aag | p.E56K |
COADREAD | 11 | 103907731 | 103907731 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr11:103907731C>A | c.181C>A | c.(181-183)Ctg>Atg | p.L61M |
COADREAD | 11 | 103907742 | 103907742 | + | Silent | SNP | C | C | T | TCGA-CK-4947-01B-11D-1650-10 | TCGA-CK-4947-10A-01D-1650-10 | g.chr11:103907742C>T | c.192C>T | c.(190-192)taC>taT | p.Y64Y |
COADREAD | 11 | 103907810 | 103907810 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr11:103907810G>A | c.260G>A | c.(259-261)cGt>cAt | p.R87H |
COADREAD | 11 | 103907872 | 103907872 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A01P-01A-21W-A096-10 | TCGA-AA-A01P-11A-11W-A096-10 | g.chr11:103907872C>T | c.322C>T | c.(322-324)Cgt>Tgt | p.R108C |
COADREAD | 11 | 103907882 | 103907882 | + | Missense_Mutation | SNP | A | A | T | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr11:103907882A>T | c.332A>T | c.(331-333)cAc>cTc | p.H111L |
COADREAD | 11 | 103907902 | 103907902 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A02K-01A-21W-A096-10 | TCGA-AA-A02K-10A-01W-A096-10 | g.chr11:103907902C>T | c.352C>T | c.(352-354)Cgc>Tgc | p.R118C |
COADREAD | 11 | 103907979 | 103907979 | + | Silent | SNP | C | C | T | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr11:103907979C>T | c.429C>T | c.(427-429)ccC>ccT | p.P143P |
COADREAD | 11 | 103908038 | 103908038 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr11:103908038G>A | c.488G>A | c.(487-489)cGc>cAc | p.R163H |
COADREAD | 11 | 103908145 | 103908145 | + | Missense_Mutation | SNP | C | C | A | TCGA-F4-6855-01A-11D-1924-10 | TCGA-F4-6855-10A-01D-1924-10 | g.chr11:103908145C>A | c.595C>A | c.(595-597)Cgt>Agt | p.R199S |
COADREAD | 11 | 103908146 | 103908146 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3870-01A-01W-0995-10 | TCGA-AA-3870-10A-01W-0995-10 | g.chr11:103908146G>A | c.596G>A | c.(595-597)cGt>cAt | p.R199H |
COADREAD | 11 | 103908323 | 103908323 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr11:103908323T>C | c.773T>C | c.(772-774)tTt>tCt | p.F258S |
COADREAD | 11 | 103908374 | 103908374 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr11:103908374G>A | c.824G>A | c.(823-825)cGa>cAa | p.R275Q |
COADREAD | 11 | 103908374 | 103908374 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr11:103908374G>A | c.824G>A | c.(823-825)cGa>cAa | p.R275Q |
COADREAD | 11 | 103908452 | 103908452 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr11:103908452G>A | c.902G>A | c.(901-903)cGt>cAt | p.R301H |
COADREAD | 11 | 103908679 | 103908679 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr11:103908679G>A | c.1129G>A | c.(1129-1131)Gat>Aat | p.D377N |
COADREAD | 11 | 103908691 | 103908691 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr11:103908691G>T | c.1141G>T | c.(1141-1143)Gac>Tac | p.D381Y |
COADREAD | 11 | 103908700 | 103908700 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr11:103908700A>G | c.1150A>G | c.(1150-1152)Att>Gtt | p.I384V |
COADREAD | 11 | 103908728 | 103908728 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr11:103908728G>A | c.1178G>A | c.(1177-1179)cGa>cAa | p.R393Q |
DLBC | 11 | 103908517 | 103908517 | + | Missense_Mutation | SNP | G | G | A | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr11:103908517G>A | c.967G>A | c.(967-969)Gat>Aat | p.D323N |
ESCA | 11 | 103908168 | 103908168 | + | Silent | SNP | G | G | T | TCGA-2H-A9GH-01A-11D-A37C-09 | TCGA-2H-A9GH-11A-11D-A37F-09 | g.chr11:103908168G>T | c.618G>T | c.(616-618)ctG>ctT | p.L206L |
ESCA | 11 | 103908222 | 103908222 | + | Missense_Mutation | SNP | A | A | T | TCGA-2H-A9GR-01A-12D-A37C-09 | TCGA-2H-A9GR-11A-11D-A37F-09 | g.chr11:103908222A>T | c.672A>T | c.(670-672)gaA>gaT | p.E224D |
ESCA | 11 | 103908556 | 103908556 | + | Missense_Mutation | SNP | C | C | T | TCGA-LN-A8HZ-01A-11D-A36J-09 | TCGA-LN-A8HZ-10A-01D-A36M-09 | g.chr11:103908556C>T | c.1006C>T | c.(1006-1008)Cgg>Tgg | p.R336W |
ESCA | 11 | 103908640 | 103908640 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-2H-A9GJ-01A-11D-A37C-09 | TCGA-2H-A9GJ-11A-11D-A37F-09 | g.chr11:103908640G>T | c.1090G>T | c.(1090-1092)Gga>Tga | p.G364* |
GBM | 11 | 103908056 | 103908056 | + | Missense_Mutation | SNP | A | A | C | TCGA-06-0192-01B-01W-0348-08 | TCGA-06-0192-10A-01W-0348-08 | g.chr11:103908056A>C | c.506A>C | c.(505-507)gAa>gCa | p.E169A |
GBM | 11 | 103908142 | 103908142 | + | Missense_Mutation | SNP | C | C | G | TCGA-28-2513-01A-01D-1494-08 | TCGA-28-2513-10A-01D-1494-08 | g.chr11:103908142C>G | c.592C>G | c.(592-594)Ctt>Gtt | p.L198V |
GBM | 11 | 103908618 | 103908618 | + | Silent | SNP | G | G | A | TCGA-74-6584-01A-11D-1845-08 | TCGA-74-6584-10A-01D-1845-08 | g.chr11:103908618G>A | c.1068G>A | c.(1066-1068)acG>acA | p.T356T |
GBMLGG | 11 | 103907867 | 103907867 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr11:103907867G>A | c.317G>A | c.(316-318)aGc>aAc | p.S106N |
GBMLGG | 11 | 103907873 | 103907873 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-7012-01A-11D-2024-08 | TCGA-DU-7012-10A-01D-2024-08 | g.chr11:103907873G>A | c.323G>A | c.(322-324)cGt>cAt | p.R108H |
GBMLGG | 11 | 103908056 | 103908056 | + | Missense_Mutation | SNP | A | A | C | TCGA-06-0192-01B-01W-0348-08 | TCGA-06-0192-10A-01W-0348-08 | g.chr11:103908056A>C | c.506A>C | c.(505-507)gAa>gCa | p.E169A |
GBMLGG | 11 | 103908142 | 103908142 | + | Missense_Mutation | SNP | C | C | G | TCGA-28-2513-01A-01D-1494-08 | TCGA-28-2513-10A-01D-1494-08 | g.chr11:103908142C>G | c.592C>G | c.(592-594)Ctt>Gtt | p.L198V |
GBMLGG | 11 | 103908169 | 103908169 | + | Missense_Mutation | SNP | G | G | C | TCGA-P5-A5EV-01A-11D-A27K-08 | TCGA-P5-A5EV-10A-01D-A27N-08 | g.chr11:103908169G>C | c.619G>C | c.(619-621)Gat>Cat | p.D207H |
GBMLGG | 11 | 103908442 | 103908442 | + | Missense_Mutation | SNP | A | A | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr11:103908442A>T | c.892A>T | c.(892-894)Att>Ttt | p.I298F |
GBMLGG | 11 | 103908618 | 103908618 | + | Silent | SNP | G | G | A | TCGA-74-6584-01A-11D-1845-08 | TCGA-74-6584-10A-01D-1845-08 | g.chr11:103908618G>A | c.1068G>A | c.(1066-1068)acG>acA | p.T356T |
GBMLGG | 11 | 103908727 | 103908727 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-E1-A7YN-01A-11D-A34A-08 | TCGA-E1-A7YN-10A-01D-A34A-08 | g.chr11:103908727C>T | c.1177C>T | c.(1177-1179)Cga>Tga | p.R393* |
HNSC | 11 | 103907963 | 103907963 | + | Missense_Mutation | SNP | A | A | G | TCGA-CV-7446-01A-11D-2229-08 | TCGA-CV-7446-10A-01D-2229-08 | g.chr11:103907963A>G | c.413A>G | c.(412-414)cAa>cGa | p.Q138R |
HNSC | 11 | 103908268 | 103908268 | + | Missense_Mutation | SNP | C | C | A | TCGA-HD-7229-01A-11D-2012-08 | TCGA-HD-7229-10A-01D-2013-08 | g.chr11:103908268C>A | c.718C>A | c.(718-720)Caa>Aaa | p.Q240K |
HNSC | 11 | 103908425 | 103908425 | + | Missense_Mutation | SNP | G | G | A | TCGA-BA-6871-01A-11D-1870-08 | TCGA-BA-6871-10A-01D-1870-08 | g.chr11:103908425G>A | c.875G>A | c.(874-876)gGa>gAa | p.G292E |
HNSC | 11 | 103908508 | 103908508 | + | Missense_Mutation | SNP | A | A | G | TCGA-CR-7402-01A-11D-2012-08 | TCGA-CR-7402-10A-01D-2013-08 | g.chr11:103908508A>G | c.958A>G | c.(958-960)Ata>Gta | p.I320V |
HNSC | 11 | 103908514 | 103908514 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-4723-01A-01D-1434-08 | TCGA-CN-4723-10A-01D-1434-08 | g.chr11:103908514G>A | c.964G>A | c.(964-966)Gag>Aag | p.E322K |
KICH | 11 | 103908145 | 103908145 | + | Missense_Mutation | SNP | C | C | T | TCGA-KO-8408-01A-11D-2310-10 | TCGA-KO-8408-11A-01D-2311-10 | g.chr11:103908145C>T | c.595C>T | c.(595-597)Cgt>Tgt | p.R199C |
KIPAN | 11 | 103907571 | 103907571 | + | Silent | SNP | C | C | T | TCGA-G7-A8LC-01A-11D-A35Z-10 | TCGA-G7-A8LC-10A-01D-A35Z-10 | g.chr11:103907571C>T | c.21C>T | c.(19-21)tgC>tgT | p.C7C |
KIPAN | 11 | 103908145 | 103908145 | + | Missense_Mutation | SNP | C | C | T | TCGA-KO-8408-01A-11D-2310-10 | TCGA-KO-8408-11A-01D-2311-10 | g.chr11:103908145C>T | c.595C>T | c.(595-597)Cgt>Tgt | p.R199C |
KIPAN | 11 | 103908554 | 103908554 | + | Missense_Mutation | SNP | T | T | C | TCGA-BP-4975-01A-01D-1462-08 | TCGA-BP-4975-11A-01D-1462-08 | g.chr11:103908554T>C | c.1004T>C | c.(1003-1005)cTc>cCc | p.L335P |
KIPAN | 11 | 103908556 | 103908556 | + | Missense_Mutation | SNP | C | C | T | TCGA-BP-4164-01A-02D-1386-10 | TCGA-BP-4164-11A-01D-1251-10 | g.chr11:103908556C>T | c.1006C>T | c.(1006-1008)Cgg>Tgg | p.R336W |
KIRC | 11 | 103908554 | 103908554 | + | Missense_Mutation | SNP | T | T | C | TCGA-BP-4975-01A-01D-1462-08 | TCGA-BP-4975-11A-01D-1462-08 | g.chr11:103908554T>C | c.1004T>C | c.(1003-1005)cTc>cCc | p.L335P |
KIRC | 11 | 103908556 | 103908556 | + | Missense_Mutation | SNP | C | C | T | TCGA-BP-4164-01A-02D-1386-10 | TCGA-BP-4164-11A-01D-1251-10 | g.chr11:103908556C>T | c.1006C>T | c.(1006-1008)Cgg>Tgg | p.R336W |
KIRP | 11 | 103907571 | 103907571 | + | Silent | SNP | C | C | T | TCGA-G7-A8LC-01A-11D-A35Z-10 | TCGA-G7-A8LC-10A-01D-A35Z-10 | g.chr11:103907571C>T | c.21C>T | c.(19-21)tgC>tgT | p.C7C |
LGG | 11 | 103907867 | 103907867 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr11:103907867G>A | c.317G>A | c.(316-318)aGc>aAc | p.S106N |
LGG | 11 | 103907873 | 103907873 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-7012-01A-11D-2024-08 | TCGA-DU-7012-10A-01D-2024-08 | g.chr11:103907873G>A | c.323G>A | c.(322-324)cGt>cAt | p.R108H |
LGG | 11 | 103908169 | 103908169 | + | Missense_Mutation | SNP | G | G | C | TCGA-P5-A5EV-01A-11D-A27K-08 | TCGA-P5-A5EV-10A-01D-A27N-08 | g.chr11:103908169G>C | c.619G>C | c.(619-621)Gat>Cat | p.D207H |
LGG | 11 | 103908442 | 103908442 | + | Missense_Mutation | SNP | A | A | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr11:103908442A>T | c.892A>T | c.(892-894)Att>Ttt | p.I298F |
LGG | 11 | 103908727 | 103908727 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-E1-A7YN-01A-11D-A34A-08 | TCGA-E1-A7YN-10A-01D-A34A-08 | g.chr11:103908727C>T | c.1177C>T | c.(1177-1179)Cga>Tga | p.R393* |
LIHC | 11 | 103908038 | 103908038 | + | Missense_Mutation | SNP | G | G | A | TCGA-CC-A5UE-01A-11D-A28X-10 | TCGA-CC-A5UE-10A-01D-A28X-10 | g.chr11:103908038G>A | c.488G>A | c.(487-489)cGc>cAc | p.R163H |
LIHC | 11 | 103908147 | 103908147 | + | Silent | SNP | T | T | C | TCGA-CC-A3MB-01A-11D-A20W-10 | TCGA-CC-A3MB-10A-01D-A20W-10 | g.chr11:103908147T>C | c.597T>C | c.(595-597)cgT>cgC | p.R199R |
LIHC | 11 | 103908223 | 103908223 | + | Missense_Mutation | SNP | G | G | C | TCGA-DD-AAE3-01A-11D-A40R-10 | TCGA-DD-AAE3-10A-01D-A40U-10 | g.chr11:103908223G>C | c.673G>C | c.(673-675)Gaa>Caa | p.E225Q |
LIHC | 11 | 103908253 | 103908253 | + | Missense_Mutation | SNP | C | C | A | TCGA-MI-A75G-01A-11D-A32G-10 | TCGA-MI-A75G-10A-01D-A32G-10 | g.chr11:103908253C>A | c.703C>A | c.(703-705)Ccc>Acc | p.P235T |
LIHC | 11 | 103908514 | 103908514 | + | Missense_Mutation | SNP | G | G | A | TCGA-DD-AADM-01A-11D-A40R-10 | TCGA-DD-AADM-10A-01D-A40U-10 | g.chr11:103908514G>A | c.964G>A | c.(964-966)Gag>Aag | p.E322K |
LUAD | 11 | 103907614 | 103907614 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-55-8208-01A-11D-2238-08 | TCGA-55-8208-10A-01D-2238-08 | g.chr11:103907614delA | c.64delA | c.(64-66)agcfs | p.S22fs |
LUAD | 11 | 103907619 | 103907619 | + | Silent | SNP | C | C | A | TCGA-55-8299-01A-11D-2284-08 | TCGA-55-8299-10B-01D-2323-08 | g.chr11:103907619C>A | c.69C>A | c.(67-69)ccC>ccA | p.P23P |
LUAD | 11 | 103907640 | 103907640 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-6593-01A-11D-1753-08 | TCGA-50-6593-11A-01D-1753-08 | g.chr11:103907640C>A | c.90C>A | c.(88-90)ttC>ttA | p.F30L |
LUAD | 11 | 103907653 | 103907653 | + | Missense_Mutation | SNP | G | G | A | TCGA-86-7954-01A-11D-2184-08 | TCGA-86-7954-10A-01D-2184-08 | g.chr11:103907653G>A | c.103G>A | c.(103-105)Gaa>Aaa | p.E35K |
LUAD | 11 | 103907700 | 103907700 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-8507-01A-11D-2393-08 | TCGA-55-8507-10A-01D-2393-08 | g.chr11:103907700G>A | c.150G>A | c.(148-150)atG>atA | p.M50I |
LUAD | 11 | 103907704 | 103907704 | + | Silent | SNP | C | C | A | TCGA-64-5774-01A-01D-1625-08 | TCGA-64-5774-10A-01D-1625-08 | g.chr11:103907704C>A | c.154C>A | c.(154-156)Cga>Aga | p.R52R |
LUAD | 11 | 103907790 | 103907790 | + | Silent | SNP | G | G | T | TCGA-NJ-A4YF-01A-12D-A25L-08 | TCGA-NJ-A4YF-10A-01D-A25L-08 | g.chr11:103907790G>T | c.240G>T | c.(238-240)gtG>gtT | p.V80V |
LUAD | 11 | 103907842 | 103907842 | + | Missense_Mutation | SNP | G | G | A | TCGA-78-7158-01A-11D-2036-08 | TCGA-78-7158-10A-01D-2036-08 | g.chr11:103907842G>A | c.292G>A | c.(292-294)Ggc>Agc | p.G98S |
LUAD | 11 | 103907855 | 103907855 | + | Missense_Mutation | SNP | C | C | A | TCGA-95-7043-01A-11D-1945-08 | TCGA-95-7043-10A-01D-1946-08 | g.chr11:103907855C>A | c.305C>A | c.(304-306)cCt>cAt | p.P102H |
LUAD | 11 | 103907872 | 103907872 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr11:103907872C>A | c.322C>A | c.(322-324)Cgt>Agt | p.R108S |
LUAD | 11 | 103907872 | 103907872 | + | Missense_Mutation | SNP | C | C | G | TCGA-78-7148-01A-11D-2036-08 | TCGA-78-7148-10A-01D-2036-08 | g.chr11:103907872C>G | c.322C>G | c.(322-324)Cgt>Ggt | p.R108G |
LUAD | 11 | 103907912 | 103907912 | + | Missense_Mutation | SNP | C | C | T | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr11:103907912C>T | c.362C>T | c.(361-363)gCt>gTt | p.A121V |
LUAD | 11 | 103908003 | 103908003 | + | Silent | SNP | C | C | A | TCGA-17-Z005-01A-01W-0746-08 | TCGA-17-Z005-11A-01W-0746-08 | g.chr11:103908003C>A | c.453C>A | c.(451-453)ctC>ctA | p.L151L |
LUAD | 11 | 103908012 | 103908012 | + | Silent | SNP | C | C | A | TCGA-64-5781-01A-01D-1625-08 | TCGA-64-5781-10A-01D-1625-08 | g.chr11:103908012C>A | c.462C>A | c.(460-462)ccC>ccA | p.P154P |
LUAD | 11 | 103908038 | 103908038 | + | Missense_Mutation | SNP | G | G | T | TCGA-05-4382-01A-01D-1931-08 | TCGA-05-4382-10A-01D-1265-08 | g.chr11:103908038G>T | c.488G>T | c.(487-489)cGc>cTc | p.R163L |
LUAD | 11 | 103908057 | 103908057 | + | Missense_Mutation | SNP | A | A | C | TCGA-49-6742-01A-11D-1855-08 | TCGA-49-6742-11A-01D-1855-08 | g.chr11:103908057A>C | c.507A>C | c.(505-507)gaA>gaC | p.E169D |
LUAD | 11 | 103908104 | 103908104 | + | Missense_Mutation | SNP | A | A | G | TCGA-17-Z009-01A-01W-0746-08 | TCGA-17-Z009-11A-01W-0746-08 | g.chr11:103908104A>G | c.554A>G | c.(553-555)gAg>gGg | p.E185G |
LUAD | 11 | 103908164 | 103908164 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr11:103908164C>A | c.614C>A | c.(613-615)cCa>cAa | p.P205Q |
LUAD | 11 | 103908255 | 103908255 | + | Silent | SNP | C | C | A | TCGA-64-1676-01A-01D-0969-08 | TCGA-64-1676-10A-01D-0969-08 | g.chr11:103908255C>A | c.705C>A | c.(703-705)ccC>ccA | p.P235P |
LUAD | 11 | 103908282 | 103908282 | + | Silent | SNP | C | C | G | TCGA-49-4487-01A-21D-1855-08 | TCGA-49-4487-11A-01D-1855-08 | g.chr11:103908282C>G | c.732C>G | c.(730-732)ctC>ctG | p.L244L |
LUAD | 11 | 103908338 | 103908338 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-6594-01A-11D-1753-08 | TCGA-50-6594-11A-01D-1753-08 | g.chr11:103908338C>A | c.788C>A | c.(787-789)gCc>gAc | p.A263D |
LUAD | 11 | 103908369 | 103908369 | + | Silent | SNP | C | C | A | TCGA-64-1679-01A-21D-2063-08 | TCGA-64-1679-10A-01D-2063-08 | g.chr11:103908369C>A | c.819C>A | c.(817-819)gcC>gcA | p.A273A |
LUAD | 11 | 103908410 | 103908410 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr11:103908410C>A | c.860C>A | c.(859-861)gCt>gAt | p.A287D |
LUAD | 11 | 103908471 | 103908471 | + | Silent | SNP | T | T | A | TCGA-55-7283-01A-11D-2036-08 | TCGA-55-7283-10A-01D-2036-08 | g.chr11:103908471T>A | c.921T>A | c.(919-921)atT>atA | p.I307I |
LUAD | 11 | 103908544 | 103908544 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-6144-01A-11D-1753-08 | TCGA-44-6144-10A-01D-1753-08 | g.chr11:103908544C>A | c.994C>A | c.(994-996)Cta>Ata | p.L332I |
LUAD | 11 | 103908684 | 103908684 | + | Missense_Mutation | SNP | G | G | T | TCGA-67-3771-01A-01D-1040-01 | TCGA-67-3771-10A-01D-1040-01 | g.chr11:103908684G>T | c.1134G>T | c.(1132-1134)gaG>gaT | p.E378D |
LUSC | 11 | 103907666 | 103907666 | + | Missense_Mutation | SNP | G | G | A | TCGA-60-2726-01A-01D-1522-08 | TCGA-60-2726-11A-01D-1522-08 | g.chr11:103907666G>A | c.116G>A | c.(115-117)aGa>aAa | p.R39K |
LUSC | 11 | 103907805 | 103907805 | + | Silent | SNP | A | A | G | TCGA-37-4135-01A-01D-1352-08 | TCGA-37-4135-10A-01D-1352-08 | g.chr11:103907805A>G | c.255A>G | c.(253-255)ccA>ccG | p.P85P |
LUSC | 11 | 103908027 | 103908027 | + | Silent | SNP | G | G | A | TCGA-18-4083-01A-01D-1352-08 | TCGA-18-4083-11A-01D-1352-08 | g.chr11:103908027G>A | c.477G>A | c.(475-477)ctG>ctA | p.L159L |
LUSC | 11 | 103908335 | 103908335 | + | Missense_Mutation | SNP | G | G | T | TCGA-43-2578-01A-01D-1522-08 | TCGA-43-2578-11A-01D-1522-08 | g.chr11:103908335G>T | c.785G>T | c.(784-786)gGc>gTc | p.G262V |
LUSC | 11 | 103908395 | 103908395 | + | Missense_Mutation | SNP | T | T | G | TCGA-22-5491-01A-01D-1632-08 | TCGA-22-5491-11A-01D-1632-08 | g.chr11:103908395T>G | c.845T>G | c.(844-846)gTg>gGg | p.V282G |
LUSC | 11 | 103908634 | 103908634 | + | Missense_Mutation | SNP | C | C | T | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr11:103908634C>T | c.1084C>T | c.(1084-1086)Cct>Tct | p.P362S |
LUSC | 11 | 103908673 | 103908673 | + | Missense_Mutation | SNP | G | G | A | TCGA-33-4566-01A-01D-1441-08 | TCGA-33-4566-11A-01D-1441-08 | g.chr11:103908673G>A | c.1123G>A | c.(1123-1125)Ggg>Agg | p.G375R |
PAAD | 11 | 103907738 | 103907738 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr11:103907738C>T | c.188C>T | c.(187-189)tCc>tTc | p.S63F |
PAAD | 11 | 103908400 | 103908400 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr11:103908400C>T | c.850C>T | c.(850-852)Cga>Tga | p.R284* |
PRAD | 11 | 103907873 | 103907873 | + | Missense_Mutation | SNP | G | G | A | TCGA-HC-8265-01A-11D-2260-08 | TCGA-HC-8265-10A-01D-2260-08 | g.chr11:103907873G>A | c.323G>A | c.(322-324)cGt>cAt | p.R108H |
PRAD | 11 | 103908337 | 103908337 | + | Missense_Mutation | SNP | G | G | A | TCGA-EJ-A7NN-01A-11D-A33T-08 | TCGA-EJ-A7NN-10A-01D-A33W-08 | g.chr11:103908337G>A | c.787G>A | c.(787-789)Gcc>Acc | p.A263T |
PRAD | 11 | 103908404 | 103908404 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr11:103908404G>A | c.854G>A | c.(853-855)cGg>cAg | p.R285Q |
READ | 11 | 103908679 | 103908679 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr11:103908679G>A | c.1129G>A | c.(1129-1131)Gat>Aat | p.D377N |
SARC | 11 | 103908223 | 103908223 | + | Missense_Mutation | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr11:103908223G>A | c.673G>A | c.(673-675)Gaa>Aaa | p.E225K |
SARC | 11 | 103908420 | 103908420 | + | Silent | SNP | T | T | C | TCGA-DX-AB2H-01A-11D-A38Z-09 | TCGA-DX-AB2H-10A-01D-A38Z-09 | g.chr11:103908420T>C | c.870T>C | c.(868-870)gcT>gcC | p.A290A |
SKCM | 11 | 103907685 | 103907685 | + | Silent | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr11:103907685C>T | c.135C>T | c.(133-135)atC>atT | p.I45I |
SKCM | 11 | 103907691 | 103907691 | + | Silent | SNP | C | C | T | TCGA-DA-A1HW-06A-11D-A19A-08 | TCGA-DA-A1HW-10A-01D-A19A-08 | g.chr11:103907691C>T | c.141C>T | c.(139-141)atC>atT | p.I47I |
SKCM | 11 | 103907695 | 103907695 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr11:103907695C>T | c.145C>T | c.(145-147)Cac>Tac | p.H49Y |
SKCM | 11 | 103907782 | 103907782 | + | Missense_Mutation | SNP | G | G | A | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr11:103907782G>A | c.232G>A | c.(232-234)Gac>Aac | p.D78N |
SKCM | 11 | 103907792 | 103907792 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr11:103907792G>A | c.242G>A | c.(241-243)gGa>gAa | p.G81E |
SKCM | 11 | 103907797 | 103907797 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr11:103907797C>T | c.247C>T | c.(247-249)Cgg>Tgg | p.R83W |
SKCM | 11 | 103907887 | 103907887 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr11:103907887G>A | c.337G>A | c.(337-339)Gga>Aga | p.G113R |
SKCM | 11 | 103907979 | 103907979 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr11:103907979C>T | c.429C>T | c.(427-429)ccC>ccT | p.P143P |
SKCM | 11 | 103908010 | 103908010 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr11:103908010C>T | c.460C>T | c.(460-462)Ccc>Tcc | p.P154S |
SKCM | 11 | 103908033 | 103908033 | + | Silent | SNP | G | G | A | TCGA-FW-A3TU-06A-11D-A23B-08 | TCGA-FW-A3TU-10A-01D-A23B-08 | g.chr11:103908033G>A | c.483G>A | c.(481-483)aaG>aaA | p.K161K |
SKCM | 11 | 103908034 | 103908034 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3C8-06A-12D-A19A-08 | TCGA-D3-A3C8-10A-01D-A19A-08 | g.chr11:103908034G>A | c.484G>A | c.(484-486)Gaa>Aaa | p.E162K |
SKCM | 11 | 103908034 | 103908034 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3TU-06A-11D-A23B-08 | TCGA-FW-A3TU-10A-01D-A23B-08 | g.chr11:103908034G>A | c.484G>A | c.(484-486)Gaa>Aaa | p.E162K |
SKCM | 11 | 103908105 | 103908105 | + | Silent | SNP | G | G | A | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr11:103908105G>A | c.555G>A | c.(553-555)gaG>gaA | p.E185E |
SKCM | 11 | 103908115 | 103908115 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr11:103908115G>A | c.565G>A | c.(565-567)Gaa>Aaa | p.E189K |
SKCM | 11 | 103908168 | 103908168 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr11:103908168G>A | c.618G>A | c.(616-618)ctG>ctA | p.L206L |
SKCM | 11 | 103908172 | 103908172 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3J4-06A-11D-A20D-08 | TCGA-EE-A3J4-10A-01D-A20D-08 | g.chr11:103908172C>T | c.622C>T | c.(622-624)Cgg>Tgg | p.R208W |
SKCM | 11 | 103908174 | 103908174 | + | Silent | SNP | G | G | A | TCGA-D3-A3C7-06A-11D-A196-08 | TCGA-D3-A3C7-10A-01D-A198-08 | g.chr11:103908174G>A | c.624G>A | c.(622-624)cgG>cgA | p.R208R |
SKCM | 11 | 103908196 | 103908196 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JH-06A-11D-A21A-08 | TCGA-EE-A3JH-10A-01D-A21A-08 | g.chr11:103908196G>A | c.646G>A | c.(646-648)Gag>Aag | p.E216K |
SKCM | 11 | 103908311 | 103908311 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr11:103908311C>T | c.761C>T | c.(760-762)cCt>cTt | p.P254L |
SKCM | 11 | 103908370 | 103908370 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr11:103908370G>A | c.820G>A | c.(820-822)Gag>Aag | p.E274K |
SKCM | 11 | 103908478 | 103908478 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A2JN-06A-11D-A196-08 | TCGA-D3-A2JN-10A-01D-A198-08 | g.chr11:103908478G>A | c.928G>A | c.(928-930)Gaa>Aaa | p.E310K |
SKCM | 11 | 103908641 | 103908641 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr11:103908641G>A | c.1091G>A | c.(1090-1092)gGa>gAa | p.G364E |
SKCM | 11 | 103908686 | 103908686 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr11:103908686C>T | c.1136C>T | c.(1135-1137)tCt>tTt | p.S379F |
SKCM | 11 | 103908697 | 103908697 | + | Missense_Mutation | SNP | G | G | A | TCGA-RP-A693-06A-13D-A30X-08 | TCGA-RP-A693-10A-01D-A30X-08 | g.chr11:103908697G>A | c.1147G>A | c.(1147-1149)Gaa>Aaa | p.E383K |
SKCM | 11 | 103908728 | 103908728 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr11:103908728G>A | c.1178G>A | c.(1177-1179)cGa>cAa | p.R393Q |