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 | 28101442 | 28101442 | + | Nonstop_Mutation | SNP | C | C | G | TCGA-G2-AA3B-01A-11D-A391-08 | TCGA-G2-AA3B-10A-01D-A394-08 | g.chr10:28101442C>G | c.3134G>C | c.(3133-3135)tGa>tCa | p.*1045S |
BLCA | 10 | 28151397 | 28151397 | + | Missense_Mutation | SNP | C | C | A | TCGA-BT-A3PJ-01A-21D-A21Z-08 | TCGA-BT-A3PJ-10A-01D-A21Z-08 | g.chr10:28151397C>A | c.2765G>T | c.(2764-2766)gGa>gTa | p.G922V |
BLCA | 10 | 28151455 | 28151455 | + | Missense_Mutation | SNP | C | C | T | TCGA-BT-A0YX-01A-11D-A10S-08 | TCGA-BT-A0YX-10A-01D-A10S-08 | g.chr10:28151455C>T | c.2707G>A | c.(2707-2709)Gct>Act | p.A903T |
BLCA | 10 | 28196616 | 28196616 | + | Silent | SNP | G | G | C | TCGA-FD-A3SM-01A-11D-A22Z-08 | TCGA-FD-A3SM-10A-01D-A22Z-08 | g.chr10:28196616G>C | c.2586C>G | c.(2584-2586)ctC>ctG | p.L862L |
BLCA | 10 | 28229527 | 28229527 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZF-AA51-01A-21D-A391-08 | TCGA-ZF-AA51-10A-01D-A394-08 | g.chr10:28229527G>C | c.1951C>G | c.(1951-1953)Cca>Gca | p.P651A |
BLCA | 10 | 28233160 | 28233160 | + | Silent | SNP | G | G | A | TCGA-GU-AATQ-01A-11D-A391-08 | TCGA-GU-AATQ-10A-01D-A394-08 | g.chr10:28233160G>A | c.1734C>T | c.(1732-1734)atC>atT | p.I578I |
BLCA | 10 | 28233216 | 28233216 | + | Missense_Mutation | SNP | C | C | A | TCGA-ZF-A9R5-01A-12D-A42E-08 | TCGA-ZF-A9R5-10A-01D-A42H-08 | g.chr10:28233216C>A | c.1678G>T | c.(1678-1680)Gcg>Tcg | p.A560S |
BLCA | 10 | 28273125 | 28273125 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A1AB-01A-11D-A13W-08 | TCGA-DK-A1AB-10A-01D-A13W-08 | g.chr10:28273125C>G | c.670G>C | c.(670-672)Gaa>Caa | p.E224Q |
BLCA | 10 | 28276464 | 28276464 | + | Missense_Mutation | SNP | G | G | C | TCGA-GV-A3JX-01A-11D-A20D-08 | TCGA-GV-A3JX-10A-01D-A20D-08 | g.chr10:28276464G>C | c.233C>G | c.(232-234)aCa>aGa | p.T78R |
BLCA | 10 | 28283854 | 28283854 | + | Missense_Mutation | SNP | A | A | G | TCGA-UY-A78K-01A-11D-A339-08 | TCGA-UY-A78K-10A-01D-A339-08 | g.chr10:28283854A>G | c.218T>C | c.(217-219)gTt>gCt | p.V73A |
BLCA | 10 | 28283955 | 28283955 | + | Silent | SNP | C | C | T | TCGA-UY-A9PF-01A-11D-A38G-08 | TCGA-UY-A9PF-10A-01D-A38J-08 | g.chr10:28283955C>T | c.117G>A | c.(115-117)gaG>gaA | p.E39E |
BRCA | 10 | 28196616 | 28196616 | + | Silent | SNP | G | G | A | TCGA-D8-A1JA-01A-11D-A13L-09 | TCGA-D8-A1JA-10A-01W-A14R-09 | g.chr10:28196616G>A | c.2586C>T | c.(2584-2586)ctC>ctT | p.L862L |
BRCA | 10 | 28229609 | 28229609 | + | Silent | SNP | C | C | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr10:28229609C>T | c.1869G>A | c.(1867-1869)acG>acA | p.T623T |
BRCA | 10 | 28250537 | 28250537 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-AO-A03M-01B-11D-A10M-09 | TCGA-AO-A03M-10A-01D-A10M-09 | g.chr10:28250537G>C | c.1346C>G | c.(1345-1347)tCa>tGa | p.S449* |
BRCA | 10 | 28250550 | 28250550 | + | Missense_Mutation | SNP | C | C | A | TCGA-EW-A1OV-01A-11D-A142-09 | TCGA-EW-A1OV-10A-01D-A142-09 | g.chr10:28250550C>A | c.1333G>T | c.(1333-1335)Gca>Tca | p.A445S |
BRCA | 10 | 28257852 | 28257852 | + | Splice_Site | SNP | C | C | T | TCGA-AO-A12E-01A-11D-A10M-09 | TCGA-AO-A12E-10A-01D-A10M-09 | g.chr10:28257852C>T | c.1238G>A | c.(1237-1239)cGg>cAg | p.R413Q |
BRCA | 10 | 28260103 | 28260103 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AN-A0AK-01A-21W-A019-09 | TCGA-AN-A0AK-10A-01W-A021-09 | g.chr10:28260103C>T | c.1076G>A | c.(1075-1077)tGg>tAg | p.W359* |
BRCA | 10 | 28270402 | 28270402 | + | Missense_Mutation | SNP | G | G | C | TCGA-AR-A2LE-01A-11D-A17W-09 | TCGA-AR-A2LE-10A-01D-A17W-09 | g.chr10:28270402G>C | c.929C>G | c.(928-930)tCt>tGt | p.S310C |
BRCA | 10 | 28273951 | 28273951 | + | Missense_Mutation | SNP | G | G | A | TCGA-A2-A04W-01A-31D-A10Y-09 | TCGA-A2-A04W-10A-01D-A110-09 | g.chr10:28273951G>A | c.572C>T | c.(571-573)tCa>tTa | p.S191L |
CESC | 10 | 28151524 | 28151524 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A3HD-01B-11D-A20U-09 | TCGA-C5-A3HD-10A-01D-A20U-09 | g.chr10:28151524C>T | c.2638G>A | c.(2638-2640)Gtt>Att | p.V880I |
CESC | 10 | 28233243 | 28233243 | + | Missense_Mutation | SNP | G | G | C | TCGA-JX-A3Q0-01A-11D-A21Q-09 | TCGA-JX-A3Q0-10A-01D-A21Q-09 | g.chr10:28233243G>C | c.1651C>G | c.(1651-1653)Cta>Gta | p.L551V |
CESC | 10 | 28250635 | 28250635 | + | Silent | SNP | A | A | C | TCGA-FU-A3NI-01A-11D-A21Q-09 | TCGA-FU-A3NI-10A-01D-A21Q-09 | g.chr10:28250635A>C | c.1248T>G | c.(1246-1248)gcT>gcG | p.A416A |
CESC | 10 | 28273115 | 28273115 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-Q1-A5R2-01A-11D-A28B-09 | TCGA-Q1-A5R2-10A-01D-A28E-09 | g.chr10:28273115G>C | c.680C>G | c.(679-681)tCa>tGa | p.S227* |
CESC | 10 | 28273994 | 28273994 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-Q1-A73P-01A-11D-A32I-09 | TCGA-Q1-A73P-10B-01D-A32I-09 | g.chr10:28273994G>A | c.529C>T | c.(529-531)Caa>Taa | p.Q177* |
CESC | 10 | 28283895 | 28283895 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr10:28283895C>T | c.177G>A | c.(175-177)tgG>tgA | p.W59* |
CESC | 10 | 28283975 | 28283975 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr10:28283975C>A | c.97G>T | c.(97-99)Gaa>Taa | p.E33* |
CHOL | 10 | 28196701 | 28196701 | + | Missense_Mutation | SNP | A | A | G | TCGA-W5-AA39-01A-11D-A417-09 | TCGA-W5-AA39-10A-01D-A41A-09 | g.chr10:28196701A>G | c.2501T>C | c.(2500-2502)aTt>aCt | p.I834T |
COAD | 10 | 28101481 | 28101481 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr10:28101481C>T | c.3095G>A | c.(3094-3096)cGc>cAc | p.R1032H |
COAD | 10 | 28101549 | 28101549 | + | Silent | SNP | T | T | C | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr10:28101549T>C | c.3027A>G | c.(3025-3027)ctA>ctG | p.L1009L |
COAD | 10 | 28149641 | 28149641 | + | Silent | SNP | G | G | A | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr10:28149641G>A | c.2934C>T | c.(2932-2934)aaC>aaT | p.N978N |
COAD | 10 | 28149667 | 28149667 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr10:28149667G>A | c.2908C>T | c.(2908-2910)Cgt>Tgt | p.R970C |
COAD | 10 | 28149710 | 28149710 | + | Silent | SNP | A | A | G | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr10:28149710A>G | c.2865T>C | c.(2863-2865)aaT>aaC | p.N955N |
COAD | 10 | 28151370 | 28151370 | + | Missense_Mutation | SNP | G | G | T | TCGA-D5-6529-01A-11D-1771-10 | TCGA-D5-6529-10A-01D-1771-10 | g.chr10:28151370G>T | c.2792C>A | c.(2791-2793)gCa>gAa | p.A931E |
COAD | 10 | 28151442 | 28151442 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr10:28151442T>C | c.2720A>G | c.(2719-2721)aAc>aGc | p.N907S |
COAD | 10 | 28196631 | 28196631 | + | Silent | SNP | G | G | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr10:28196631G>A | c.2571C>T | c.(2569-2571)agC>agT | p.S857S |
COAD | 10 | 28196645 | 28196645 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr10:28196645C>A | c.2557G>T | c.(2557-2559)Gac>Tac | p.D853Y |
COAD | 10 | 28224033 | 28224033 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3516-01A-02W-0833-10 | TCGA-AA-3516-10A-01W-0833-10 | g.chr10:28224033G>A | c.2401C>T | c.(2401-2403)Cca>Tca | p.P801S |
COAD | 10 | 28224054 | 28224054 | + | Missense_Mutation | SNP | G | G | A | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr10:28224054G>A | c.2380C>T | c.(2380-2382)Cgg>Tgg | p.R794W |
COAD | 10 | 28228874 | 28228874 | + | Silent | SNP | A | A | G | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chr10:28228874A>G | c.2049T>C | c.(2047-2049)aaT>aaC | p.N683N |
COAD | 10 | 28229562 | 28229562 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3549-01A-02W-0831-10 | TCGA-AA-3549-10A-01W-0831-10 | g.chr10:28229562C>T | c.1916G>A | c.(1915-1917)cGg>cAg | p.R639Q |
COAD | 10 | 28229687 | 28229687 | + | Silent | SNP | C | C | T | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr10:28229687C>T | c.1791G>A | c.(1789-1791)tcG>tcA | p.S597S |
COAD | 10 | 28229731 | 28229731 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr10:28229731C>T | c.1747G>A | c.(1747-1749)Gct>Act | p.A583T |
COAD | 10 | 28233250 | 28233250 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3968-01A-01W-0995-10 | TCGA-AA-3968-10A-01W-0995-10 | g.chr10:28233250G>T | c.1644C>A | c.(1642-1644)caC>caA | p.H548Q |
COAD | 10 | 28233310 | 28233310 | + | Silent | SNP | T | T | C | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr10:28233310T>C | c.1584A>G | c.(1582-1584)agA>agG | p.R528R |
COAD | 10 | 28250542 | 28250542 | + | Silent | SNP | C | C | T | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr10:28250542C>T | c.1341G>A | c.(1339-1341)ttG>ttA | p.L447L |
COAD | 10 | 28270406 | 28270406 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr10:28270406T>C | c.925A>G | c.(925-927)Atg>Gtg | p.M309V |
COAD | 10 | 28272839 | 28272839 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr10:28272839A>G | c.752T>C | c.(751-753)cTg>cCg | p.L251P |
COAD | 10 | 28272885 | 28272885 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr10:28272885G>A | c.706C>T | c.(706-708)Cga>Tga | p.R236* |
COAD | 10 | 28273218 | 28273218 | + | Splice_Site | SNP | C | C | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr10:28273218C>A | c.577G>T | c.(577-579)Gaa>Taa | p.E193* |
COAD | 10 | 28274002 | 28274002 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr10:28274002A>C | c.521T>G | c.(520-522)cTg>cGg | p.L174R |
COAD | 10 | 28283956 | 28283956 | + | Missense_Mutation | SNP | T | T | C | TCGA-CA-6716-01A-11D-1835-10 | TCGA-CA-6716-10A-01D-1835-10 | g.chr10:28283956T>C | c.116A>G | c.(115-117)gAg>gGg | p.E39G |
COAD | 10 | 28284008 | 28284008 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr10:28284008C>T | c.64G>A | c.(64-66)Gaa>Aaa | p.E22K |
COAD | 10 | 28284017 | 28284017 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr10:28284017C>A | c.55G>T | c.(55-57)Gga>Tga | p.G19* |
COAD | 10 | 28284046 | 28284046 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-3808-01A-01W-0995-10 | TCGA-A6-3808-11A-01W-0995-10 | g.chr10:28284046G>A | c.26C>T | c.(25-27)aCg>aTg | p.T9M |
COADREAD | 10 | 28101481 | 28101481 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr10:28101481C>T | c.3095G>A | c.(3094-3096)cGc>cAc | p.R1032H |
COADREAD | 10 | 28101549 | 28101549 | + | Silent | SNP | T | T | C | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr10:28101549T>C | c.3027A>G | c.(3025-3027)ctA>ctG | p.L1009L |
COADREAD | 10 | 28149641 | 28149641 | + | Silent | SNP | G | G | A | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr10:28149641G>A | c.2934C>T | c.(2932-2934)aaC>aaT | p.N978N |
COADREAD | 10 | 28149667 | 28149667 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr10:28149667G>A | c.2908C>T | c.(2908-2910)Cgt>Tgt | p.R970C |
COADREAD | 10 | 28149710 | 28149710 | + | Silent | SNP | A | A | G | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr10:28149710A>G | c.2865T>C | c.(2863-2865)aaT>aaC | p.N955N |
COADREAD | 10 | 28151370 | 28151370 | + | Missense_Mutation | SNP | G | G | T | TCGA-D5-6529-01A-11D-1771-10 | TCGA-D5-6529-10A-01D-1771-10 | g.chr10:28151370G>T | c.2792C>A | c.(2791-2793)gCa>gAa | p.A931E |
COADREAD | 10 | 28151422 | 28151422 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr10:28151422T>G | c.2740A>C | c.(2740-2742)Aat>Cat | p.N914H |
COADREAD | 10 | 28151442 | 28151442 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr10:28151442T>C | c.2720A>G | c.(2719-2721)aAc>aGc | p.N907S |
COADREAD | 10 | 28196631 | 28196631 | + | Silent | SNP | G | G | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr10:28196631G>A | c.2571C>T | c.(2569-2571)agC>agT | p.S857S |
COADREAD | 10 | 28196645 | 28196645 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr10:28196645C>A | c.2557G>T | c.(2557-2559)Gac>Tac | p.D853Y |
COADREAD | 10 | 28224033 | 28224033 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3516-01A-02W-0833-10 | TCGA-AA-3516-10A-01W-0833-10 | g.chr10:28224033G>A | c.2401C>T | c.(2401-2403)Cca>Tca | p.P801S |
COADREAD | 10 | 28224054 | 28224054 | + | Missense_Mutation | SNP | G | G | A | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr10:28224054G>A | c.2380C>T | c.(2380-2382)Cgg>Tgg | p.R794W |
COADREAD | 10 | 28228874 | 28228874 | + | Silent | SNP | A | A | G | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chr10:28228874A>G | c.2049T>C | c.(2047-2049)aaT>aaC | p.N683N |
COADREAD | 10 | 28229554 | 28229554 | + | Missense_Mutation | SNP | T | T | C | TCGA-DC-5337-01A-01D-1657-10 | TCGA-DC-5337-10A-01D-1657-10 | g.chr10:28229554T>C | c.1924A>G | c.(1924-1926)Aag>Gag | p.K642E |
COADREAD | 10 | 28229562 | 28229562 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3549-01A-02W-0831-10 | TCGA-AA-3549-10A-01W-0831-10 | g.chr10:28229562C>T | c.1916G>A | c.(1915-1917)cGg>cAg | p.R639Q |
COADREAD | 10 | 28229687 | 28229687 | + | Silent | SNP | C | C | T | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr10:28229687C>T | c.1791G>A | c.(1789-1791)tcG>tcA | p.S597S |
COADREAD | 10 | 28229731 | 28229731 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr10:28229731C>T | c.1747G>A | c.(1747-1749)Gct>Act | p.A583T |
COADREAD | 10 | 28233250 | 28233250 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3968-01A-01W-0995-10 | TCGA-AA-3968-10A-01W-0995-10 | g.chr10:28233250G>T | c.1644C>A | c.(1642-1644)caC>caA | p.H548Q |
COADREAD | 10 | 28233310 | 28233310 | + | Silent | SNP | T | T | C | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr10:28233310T>C | c.1584A>G | c.(1582-1584)agA>agG | p.R528R |
COADREAD | 10 | 28250542 | 28250542 | + | Silent | SNP | C | C | T | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr10:28250542C>T | c.1341G>A | c.(1339-1341)ttG>ttA | p.L447L |
COADREAD | 10 | 28260161 | 28260161 | + | Missense_Mutation | SNP | G | G | A | TCGA-AF-5654-01A-01D-1657-10 | TCGA-AF-5654-10A-01D-1657-10 | g.chr10:28260161G>A | c.1018C>T | c.(1018-1020)Cgc>Tgc | p.R340C |
COADREAD | 10 | 28270406 | 28270406 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr10:28270406T>C | c.925A>G | c.(925-927)Atg>Gtg | p.M309V |
COADREAD | 10 | 28272839 | 28272839 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr10:28272839A>G | c.752T>C | c.(751-753)cTg>cCg | p.L251P |
COADREAD | 10 | 28272885 | 28272885 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr10:28272885G>A | c.706C>T | c.(706-708)Cga>Tga | p.R236* |
COADREAD | 10 | 28273218 | 28273218 | + | Splice_Site | SNP | C | C | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr10:28273218C>A | c.577G>T | c.(577-579)Gaa>Taa | p.E193* |
COADREAD | 10 | 28274002 | 28274002 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr10:28274002A>C | c.521T>G | c.(520-522)cTg>cGg | p.L174R |
COADREAD | 10 | 28274019 | 28274019 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-3605-01A-01W-0833-10 | TCGA-AG-3605-10A-01W-0833-10 | g.chr10:28274019C>A | c.504G>T | c.(502-504)aaG>aaT | p.K168N |
COADREAD | 10 | 28283956 | 28283956 | + | Missense_Mutation | SNP | T | T | C | TCGA-CA-6716-01A-11D-1835-10 | TCGA-CA-6716-10A-01D-1835-10 | g.chr10:28283956T>C | c.116A>G | c.(115-117)gAg>gGg | p.E39G |
COADREAD | 10 | 28284008 | 28284008 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr10:28284008C>T | c.64G>A | c.(64-66)Gaa>Aaa | p.E22K |
COADREAD | 10 | 28284017 | 28284017 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr10:28284017C>A | c.55G>T | c.(55-57)Gga>Tga | p.G19* |
COADREAD | 10 | 28284046 | 28284046 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-3808-01A-01W-0995-10 | TCGA-A6-3808-11A-01W-0995-10 | g.chr10:28284046G>A | c.26C>T | c.(25-27)aCg>aTg | p.T9M |
ESCA | 10 | 28149697 | 28149697 | + | Missense_Mutation | SNP | C | C | A | TCGA-JY-A6FB-01A-11D-A33E-09 | TCGA-JY-A6FB-10A-01D-A33H-09 | g.chr10:28149697C>A | c.2878G>T | c.(2878-2880)Ggt>Tgt | p.G960C |
ESCA | 10 | 28151508 | 28151508 | + | Missense_Mutation | SNP | A | A | G | TCGA-L5-A8NG-01A-11D-A37C-09 | TCGA-L5-A8NG-11A-11D-A37F-09 | g.chr10:28151508A>G | c.2654T>C | c.(2653-2655)cTt>cCt | p.L885P |
ESCA | 10 | 28196695 | 28196695 | + | Missense_Mutation | SNP | C | C | T | TCGA-LN-A49K-01A-11D-A247-09 | TCGA-LN-A49K-10A-01D-A247-09 | g.chr10:28196695C>T | c.2507G>A | c.(2506-2508)cGc>cAc | p.R836H |
ESCA | 10 | 28224072 | 28224072 | + | Missense_Mutation | SNP | C | C | T | TCGA-Q9-A6FU-01A-11D-A31U-09 | TCGA-Q9-A6FU-10A-01D-A31U-09 | g.chr10:28224072C>T | c.2362G>A | c.(2362-2364)Gaa>Aaa | p.E788K |
ESCA | 10 | 28229562 | 28229562 | + | Missense_Mutation | SNP | C | C | T | TCGA-LN-A49V-01A-11D-A247-09 | TCGA-LN-A49V-10A-01D-A247-09 | g.chr10:28229562C>T | c.1916G>A | c.(1915-1917)cGg>cAg | p.R639Q |
ESCA | 10 | 28233164 | 28233164 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr10:28233164delC | c.1730delG | c.(1729-1731)ggtfs | p.G577fs |
ESCA | 10 | 28250550 | 28250550 | + | Missense_Mutation | SNP | C | C | A | TCGA-L5-A4OJ-01A-11D-A27G-09 | TCGA-L5-A4OJ-11A-12D-A27G-09 | g.chr10:28250550C>A | c.1333G>T | c.(1333-1335)Gca>Tca | p.A445S |
ESCA | 10 | 28270417 | 28270417 | + | Missense_Mutation | SNP | A | A | C | TCGA-R6-A6Y2-01B-11D-A33E-09 | TCGA-R6-A6Y2-10A-01D-A33H-09 | g.chr10:28270417A>C | c.914T>G | c.(913-915)tTt>tGt | p.F305C |
ESCA | 10 | 28270509 | 28270509 | + | Silent | SNP | G | G | T | TCGA-IG-A4P3-01A-11D-A27G-09 | TCGA-IG-A4P3-10A-01D-A27G-09 | g.chr10:28270509G>T | c.822C>A | c.(820-822)ggC>ggA | p.G274G |
GBM | 10 | 28228843 | 28228843 | + | Missense_Mutation | SNP | C | C | T | TCGA-28-5209-01A-01D-1486-08 | TCGA-28-5209-10A-01D-1486-08 | g.chr10:28228843C>T | c.2080G>A | c.(2080-2082)Gcc>Acc | p.A694T |
GBM | 10 | 28229528 | 28229528 | + | Missense_Mutation | SNP | A | A | C | TCGA-06-0174-01A-01D-1491-08 | TCGA-06-0174-10B-01D-1491-08 | g.chr10:28229528A>C | c.1950T>G | c.(1948-1950)atT>atG | p.I650M |
GBM | 10 | 28229643 | 28229643 | + | Missense_Mutation | SNP | G | G | T | TCGA-19-2625-01A-01D-1495-08 | TCGA-19-2625-10A-01D-1495-08 | g.chr10:28229643G>T | c.1835C>A | c.(1834-1836)gCa>gAa | p.A612E |
GBM | 10 | 28283881 | 28283881 | + | Missense_Mutation | SNP | G | G | A | TCGA-32-4211-01A-01D-1353-08 | TCGA-32-4211-10A-01D-1353-08 | g.chr10:28283881G>A | c.191C>T | c.(190-192)gCg>gTg | p.A64V |
GBMLGG | 10 | 28151500 | 28151500 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:28151500T>C | c.2662A>G | c.(2662-2664)Aat>Gat | p.N888D |
GBMLGG | 10 | 28196637 | 28196637 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:28196637C>T | c.2565G>A | c.(2563-2565)aaG>aaA | p.K855K |
GBMLGG | 10 | 28228843 | 28228843 | + | Missense_Mutation | SNP | C | C | T | TCGA-28-5209-01A-01D-1486-08 | TCGA-28-5209-10A-01D-1486-08 | g.chr10:28228843C>T | c.2080G>A | c.(2080-2082)Gcc>Acc | p.A694T |
GBMLGG | 10 | 28229528 | 28229528 | + | Missense_Mutation | SNP | A | A | C | TCGA-06-0174-01A-01D-1491-08 | TCGA-06-0174-10B-01D-1491-08 | g.chr10:28229528A>C | c.1950T>G | c.(1948-1950)atT>atG | p.I650M |
GBMLGG | 10 | 28229643 | 28229643 | + | Missense_Mutation | SNP | G | G | T | TCGA-19-2625-01A-01D-1495-08 | TCGA-19-2625-10A-01D-1495-08 | g.chr10:28229643G>T | c.1835C>A | c.(1834-1836)gCa>gAa | p.A612E |
GBMLGG | 10 | 28233780 | 28233780 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:28233780T>C | c.1498A>G | c.(1498-1500)Ata>Gta | p.I500V |
GBMLGG | 10 | 28260120 | 28260120 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:28260120C>A | c.1059G>T | c.(1057-1059)aaG>aaT | p.K353N |
GBMLGG | 10 | 28283881 | 28283881 | + | Missense_Mutation | SNP | G | G | A | TCGA-32-4211-01A-01D-1353-08 | TCGA-32-4211-10A-01D-1353-08 | g.chr10:28283881G>A | c.191C>T | c.(190-192)gCg>gTg | p.A64V |
HNSC | 10 | 28149713 | 28149713 | + | Silent | SNP | C | C | T | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr10:28149713C>T | c.2862G>A | c.(2860-2862)agG>agA | p.R954R |
HNSC | 10 | 28149714 | 28149714 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr10:28149714C>T | c.2861G>A | c.(2860-2862)aGg>aAg | p.R954K |
HNSC | 10 | 28151364 | 28151364 | + | Splice_Site | SNP | G | G | C | TCGA-CN-6995-01A-31D-2012-08 | TCGA-CN-6995-10A-01D-2013-08 | g.chr10:28151364G>C | c.2798C>G | c.(2797-2799)aCa>aGa | p.T933R |
HNSC | 10 | 28151401 | 28151401 | + | Missense_Mutation | SNP | G | G | A | TCGA-BB-4227-01A-01D-1870-08 | TCGA-BB-4227-10A-01D-1870-08 | g.chr10:28151401G>A | c.2761C>T | c.(2761-2763)Cat>Tat | p.H921Y |
HNSC | 10 | 28151529 | 28151529 | + | Missense_Mutation | SNP | G | G | T | TCGA-BB-4227-01A-01D-1870-08 | TCGA-BB-4227-10A-01D-1870-08 | g.chr10:28151529G>T | c.2633C>A | c.(2632-2634)tCc>tAc | p.S878Y |
HNSC | 10 | 28196653 | 28196653 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-6956-01A-21D-2012-08 | TCGA-CV-6956-10A-01D-2013-08 | g.chr10:28196653G>A | c.2549C>T | c.(2548-2550)cCt>cTt | p.P850L |
HNSC | 10 | 28228887 | 28228887 | + | Missense_Mutation | SNP | A | A | G | TCGA-CR-7376-01A-11D-2129-08 | TCGA-CR-7376-10A-01D-2129-08 | g.chr10:28228887A>G | c.2036T>C | c.(2035-2037)gTc>gCc | p.V679A |
HNSC | 10 | 28229719 | 28229719 | + | Missense_Mutation | SNP | A | A | T | TCGA-CX-7085-01A-21D-2012-08 | TCGA-CX-7085-10A-01D-2013-08 | g.chr10:28229719A>T | c.1759T>A | c.(1759-1761)Tgt>Agt | p.C587S |
HNSC | 10 | 28233203 | 28233203 | + | Missense_Mutation | SNP | T | T | A | TCGA-P3-A6T6-01A-11D-A34J-08 | TCGA-P3-A6T6-10A-01D-A34M-08 | g.chr10:28233203T>A | c.1691A>T | c.(1690-1692)aAg>aTg | p.K564M |
HNSC | 10 | 28250520 | 28250520 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CV-A45Q-01A-11D-A24D-08 | TCGA-CV-A45Q-10A-01D-A24F-08 | g.chr10:28250520G>A | c.1363C>T | c.(1363-1365)Cag>Tag | p.Q455* |
HNSC | 10 | 28250550 | 28250550 | + | Missense_Mutation | SNP | C | C | A | TCGA-D6-A6EK-01A-11D-A31L-08 | TCGA-D6-A6EK-10A-01D-A31J-08 | g.chr10:28250550C>A | c.1333G>T | c.(1333-1335)Gca>Tca | p.A445S |
HNSC | 10 | 28270429 | 28270429 | + | Missense_Mutation | SNP | T | T | C | TCGA-CV-6962-01A-11D-1912-08 | TCGA-CV-6962-10A-01D-1912-08 | g.chr10:28270429T>C | c.902A>G | c.(901-903)aAa>aGa | p.K301R |
HNSC | 10 | 28272787 | 28272787 | + | Silent | SNP | T | T | A | TCGA-CQ-6221-01A-11D-2078-08 | TCGA-CQ-6221-10A-01D-2078-08 | g.chr10:28272787T>A | c.804A>T | c.(802-804)ggA>ggT | p.G268G |
HNSC | 10 | 28272826 | 28272826 | + | Silent | SNP | G | G | A | TCGA-F7-8298-01A-11D-2394-08 | TCGA-F7-8298-10A-01D-2394-08 | g.chr10:28272826G>A | c.765C>T | c.(763-765)caC>caT | p.H255H |
HNSC | 10 | 28283901 | 28283901 | + | Silent | SNP | A | A | T | TCGA-MZ-A5BI-01A-31D-A34J-08 | TCGA-MZ-A5BI-10C-01D-A34M-08 | g.chr10:28283901A>T | c.171T>A | c.(169-171)ctT>ctA | p.L57L |
HNSC | 10 | 28284017 | 28284017 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-BA-4076-01A-01D-1434-08 | TCGA-BA-4076-10A-01D-1434-08 | g.chr10:28284017C>A | c.55G>T | c.(55-57)Gga>Tga | p.G19* |
KIPAN | 10 | 28149666 | 28149666 | + | Missense_Mutation | SNP | C | C | G | TCGA-B0-5712-01A-11D-1669-08 | TCGA-B0-5712-11A-01D-1669-08 | g.chr10:28149666C>G | c.2909G>C | c.(2908-2910)cGt>cCt | p.R970P |
KIPAN | 10 | 28229610 | 28229610 | + | Missense_Mutation | SNP | G | G | A | TCGA-B0-5691-01A-11D-1534-10 | TCGA-B0-5691-11A-01D-1534-10 | g.chr10:28229610G>A | c.1868C>T | c.(1867-1869)aCg>aTg | p.T623M |
KIPAN | 10 | 28233812 | 28233812 | + | Missense_Mutation | SNP | G | G | T | TCGA-A3-3367-01A-02D-1421-08 | TCGA-A3-3367-11A-01D-1421-08 | g.chr10:28233812G>T | c.1466C>A | c.(1465-1467)gCc>gAc | p.A489D |
KIPAN | 10 | 28250531 | 28250532 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-B0-5094-01A-01D-1421-08 | TCGA-B0-5094-11A-01D-1421-08 | g.chr10:28250531_28250532insA | c.1351_1352insT | c.(1351-1353)tatfs | p.Y451fs |
KIPAN | 10 | 28257893 | 28257893 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-B9-4114-01A-01D-1252-08 | TCGA-B9-4114-10A-01D-1252-08 | g.chr10:28257893delT | c.1197delA | c.(1195-1197)aaafs | p.K399fs |
KIPAN | 10 | 28270411 | 28270411 | + | Missense_Mutation | SNP | T | T | G | TCGA-BP-5185-01A-01D-1429-08 | TCGA-BP-5185-11A-01D-1429-08 | g.chr10:28270411T>G | c.920A>C | c.(919-921)gAa>gCa | p.E307A |
KIPAN | 10 | 28270470 | 28270470 | + | Silent | SNP | T | T | C | TCGA-DW-7840-01A-11D-2136-08 | TCGA-DW-7840-10A-01D-2136-08 | g.chr10:28270470T>C | c.861A>G | c.(859-861)aaA>aaG | p.K287K |
KIPAN | 10 | 28274097 | 28274097 | + | Silent | SNP | A | A | G | TCGA-CZ-5467-01A-01D-1501-10 | TCGA-CZ-5467-11A-01D-1501-10 | g.chr10:28274097A>G | c.426T>C | c.(424-426)aaT>aaC | p.N142N |
KIRC | 10 | 28149666 | 28149666 | + | Missense_Mutation | SNP | C | C | G | TCGA-B0-5712-01A-11D-1669-08 | TCGA-B0-5712-11A-01D-1669-08 | g.chr10:28149666C>G | c.2909G>C | c.(2908-2910)cGt>cCt | p.R970P |
KIRC | 10 | 28229610 | 28229610 | + | Missense_Mutation | SNP | G | G | A | TCGA-B0-5691-01A-11D-1534-10 | TCGA-B0-5691-11A-01D-1534-10 | g.chr10:28229610G>A | c.1868C>T | c.(1867-1869)aCg>aTg | p.T623M |
KIRC | 10 | 28233812 | 28233812 | + | Missense_Mutation | SNP | G | G | T | TCGA-A3-3367-01A-02D-1421-08 | TCGA-A3-3367-11A-01D-1421-08 | g.chr10:28233812G>T | c.1466C>A | c.(1465-1467)gCc>gAc | p.A489D |
KIRC | 10 | 28250531 | 28250532 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-B0-5094-01A-01D-1421-08 | TCGA-B0-5094-11A-01D-1421-08 | g.chr10:28250531_28250532insA | c.1351_1352insT | c.(1351-1353)tatfs | p.Y451fs |
KIRC | 10 | 28270411 | 28270411 | + | Missense_Mutation | SNP | T | T | G | TCGA-BP-5185-01A-01D-1429-08 | TCGA-BP-5185-11A-01D-1429-08 | g.chr10:28270411T>G | c.920A>C | c.(919-921)gAa>gCa | p.E307A |
KIRC | 10 | 28274097 | 28274097 | + | Silent | SNP | A | A | G | TCGA-CZ-5467-01A-01D-1501-10 | TCGA-CZ-5467-11A-01D-1501-10 | g.chr10:28274097A>G | c.426T>C | c.(424-426)aaT>aaC | p.N142N |
KIRP | 10 | 28257893 | 28257893 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-B9-4114-01A-01D-1252-08 | TCGA-B9-4114-10A-01D-1252-08 | g.chr10:28257893delT | c.1197delA | c.(1195-1197)aaafs | p.K399fs |
KIRP | 10 | 28270470 | 28270470 | + | Silent | SNP | T | T | C | TCGA-DW-7840-01A-11D-2136-08 | TCGA-DW-7840-10A-01D-2136-08 | g.chr10:28270470T>C | c.861A>G | c.(859-861)aaA>aaG | p.K287K |
LGG | 10 | 28151500 | 28151500 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:28151500T>C | c.2662A>G | c.(2662-2664)Aat>Gat | p.N888D |
LGG | 10 | 28196637 | 28196637 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:28196637C>T | c.2565G>A | c.(2563-2565)aaG>aaA | p.K855K |
LGG | 10 | 28233780 | 28233780 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:28233780T>C | c.1498A>G | c.(1498-1500)Ata>Gta | p.I500V |
LGG | 10 | 28260120 | 28260120 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:28260120C>A | c.1059G>T | c.(1057-1059)aaG>aaT | p.K353N |
LIHC | 10 | 28224053 | 28224053 | + | Missense_Mutation | SNP | C | C | A | TCGA-UB-AA0U-01A-11D-A382-10 | TCGA-UB-AA0U-10A-01D-A385-10 | g.chr10:28224053C>A | c.2381G>T | c.(2380-2382)cGg>cTg | p.R794L |
LIHC | 10 | 28228827 | 28228827 | + | Splice_Site | SNP | T | T | C | TCGA-5R-AAAM-01A-12D-A40R-10 | TCGA-5R-AAAM-10A-01D-A40U-10 | g.chr10:28228827T>C | c.2096A>G | c.(2095-2097)cAg>cGg | p.Q699R |
LIHC | 10 | 28276331 | 28276331 | + | Silent | SNP | G | G | T | TCGA-DD-AAEE-01A-11D-A40R-10 | TCGA-DD-AAEE-10A-01D-A40U-10 | g.chr10:28276331G>T | c.366C>A | c.(364-366)gcC>gcA | p.A122A |
LUAD | 10 | 28149741 | 28149741 | + | Missense_Mutation | SNP | G | G | C | TCGA-86-6851-01A-11D-1945-08 | TCGA-86-6851-10A-01D-1946-08 | g.chr10:28149741G>C | c.2834C>G | c.(2833-2835)gCt>gGt | p.A945G |
LUAD | 10 | 28224001 | 28224001 | + | Missense_Mutation | SNP | T | T | A | TCGA-50-5946-01A-11D-1753-08 | TCGA-50-5946-10A-01D-1753-08 | g.chr10:28224001T>A | c.2433A>T | c.(2431-2433)caA>caT | p.Q811H |
LUAD | 10 | 28224177 | 28224177 | + | Silent | SNP | G | G | T | TCGA-55-A492-01A-11D-A24D-08 | TCGA-55-A492-10A-01D-A24F-08 | g.chr10:28224177G>T | c.2257C>A | c.(2257-2259)Cgg>Agg | p.R753R |
LUAD | 10 | 28225785 | 28225785 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-A491-01A-11D-A24D-08 | TCGA-55-A491-10A-01D-A24F-08 | g.chr10:28225785C>T | c.2122G>A | c.(2122-2124)Gac>Aac | p.D708N |
LUAD | 10 | 28228927 | 28228927 | + | Missense_Mutation | SNP | G | G | A | TCGA-50-5933-01A-11D-1753-08 | TCGA-50-5933-11A-01D-1753-08 | g.chr10:28228927G>A | c.1996C>T | c.(1996-1998)Cgg>Tgg | p.R666W |
LUAD | 10 | 28233166 | 28233166 | + | Silent | SNP | C | C | T | TCGA-55-A4DF-01A-11D-A24D-08 | TCGA-55-A4DF-10A-01D-A24F-08 | g.chr10:28233166C>T | c.1728G>A | c.(1726-1728)ggG>ggA | p.G576G |
LUAD | 10 | 28233185 | 28233185 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-6642-01A-11D-1855-08 | TCGA-55-6642-11A-01D-1855-08 | g.chr10:28233185C>T | c.1709G>A | c.(1708-1710)cGg>cAg | p.R570Q |
LUAD | 10 | 28233208 | 28233208 | + | Silent | SNP | A | A | T | TCGA-91-6848-01A-11D-1945-08 | TCGA-91-6848-11A-01D-1945-08 | g.chr10:28233208A>T | c.1686T>A | c.(1684-1686)gtT>gtA | p.V562V |
LUAD | 10 | 28233214 | 28233214 | + | Silent | SNP | C | C | T | TCGA-78-8662-01A-11D-2393-08 | TCGA-78-8662-10A-01D-2393-08 | g.chr10:28233214C>T | c.1680G>A | c.(1678-1680)gcG>gcA | p.A560A |
LUAD | 10 | 28233798 | 28233798 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-44-7667-01A-31D-2063-08 | TCGA-44-7667-10A-01D-2063-08 | g.chr10:28233798C>A | c.1480G>T | c.(1480-1482)Gga>Tga | p.G494* |
LUAD | 10 | 28250547 | 28250547 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-8511-01A-11D-2393-08 | TCGA-55-8511-10A-01D-2393-08 | g.chr10:28250547C>G | c.1336G>C | c.(1336-1338)Gat>Cat | p.D446H |
LUAD | 10 | 28260203 | 28260203 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-91-A4BC-01A-11D-A24D-08 | TCGA-91-A4BC-10A-01D-A24F-08 | g.chr10:28260203G>A | c.976C>T | c.(976-978)Cag>Tag | p.Q326* |
LUAD | 10 | 28260243 | 28260243 | + | Splice_Site | SNP | C | C | A | TCGA-55-1592-01A-01D-0969-08 | TCGA-55-1592-11A-01D-0969-08 | g.chr10:28260243C>A | | c.e8-1 | |
LUAD | 10 | 28273196 | 28273196 | + | Missense_Mutation | SNP | G | G | C | TCGA-MP-A4TF-01A-11D-A25L-08 | TCGA-MP-A4TF-10A-01D-A25L-08 | g.chr10:28273196G>C | c.599C>G | c.(598-600)aCg>aGg | p.T200R |
LUAD | 10 | 28276314 | 28276314 | + | Splice_Site | SNP | C | C | T | TCGA-44-7660-01A-11D-2063-08 | TCGA-44-7660-10A-01D-2063-08 | g.chr10:28276314C>T | | c.e3+1 | |
LUAD | 10 | 28276388 | 28276388 | + | Missense_Mutation | SNP | G | G | C | TCGA-17-Z026-01A-01W-0746-08 | TCGA-17-Z026-11A-01W-0746-08 | g.chr10:28276388G>C | c.309C>G | c.(307-309)agC>agG | p.S103R |
LUAD | 10 | 28276389 | 28276389 | + | Missense_Mutation | SNP | C | C | A | TCGA-NJ-A4YQ-01A-11D-A25L-08 | TCGA-NJ-A4YQ-10A-01D-A25L-08 | g.chr10:28276389C>A | c.308G>T | c.(307-309)aGc>aTc | p.S103I |
LUSC | 10 | 28151364 | 28151364 | + | Splice_Site | SNP | G | G | T | TCGA-43-6143-01A-11D-1817-08 | TCGA-43-6143-11A-01D-1817-08 | g.chr10:28151364G>T | c.2798C>A | c.(2797-2799)aCa>aAa | p.T933K |
LUSC | 10 | 28224093 | 28224093 | + | Missense_Mutation | SNP | C | C | T | TCGA-43-5668-01A-01D-1632-08 | TCGA-43-5668-11A-01D-1632-08 | g.chr10:28224093C>T | c.2341G>A | c.(2341-2343)Gga>Aga | p.G781R |
LUSC | 10 | 28225785 | 28225785 | + | Missense_Mutation | SNP | C | C | A | TCGA-21-1070-01A-01D-1521-08 | TCGA-21-1070-11A-01D-1521-08 | g.chr10:28225785C>A | c.2122G>T | c.(2122-2124)Gac>Tac | p.D708Y |
LUSC | 10 | 28228919 | 28228919 | + | Silent | SNP | T | T | A | TCGA-66-2795-01A-02D-0983-08 | TCGA-66-2795-11A-01D-0983-08 | g.chr10:28228919T>A | c.2004A>T | c.(2002-2004)gcA>gcT | p.A668A |
LUSC | 10 | 28229604 | 28229604 | + | Missense_Mutation | SNP | T | T | A | TCGA-22-5471-01A-01D-1632-08 | TCGA-22-5471-11A-01D-1632-08 | g.chr10:28229604T>A | c.1874A>T | c.(1873-1875)aAa>aTa | p.K625I |
LUSC | 10 | 28233220 | 28233220 | + | Silent | SNP | A | A | G | TCGA-66-2756-01A-01D-1522-08 | TCGA-66-2756-11A-01D-1522-08 | g.chr10:28233220A>G | c.1674T>C | c.(1672-1674)acT>acC | p.T558T |
LUSC | 10 | 28233361 | 28233361 | + | Splice_Site | SNP | C | C | A | TCGA-60-2726-01A-01D-1522-08 | TCGA-60-2726-11A-01D-1522-08 | g.chr10:28233361C>A | | c.e12-1 | |
LUSC | 10 | 28233794 | 28233794 | + | Missense_Mutation | SNP | C | C | A | TCGA-63-5128-01A-01D-1441-08 | TCGA-63-5128-10A-01D-1441-08 | g.chr10:28233794C>A | c.1484G>T | c.(1483-1485)gGc>gTc | p.G495V |
LUSC | 10 | 28233864 | 28233864 | + | Missense_Mutation | SNP | C | C | G | TCGA-60-2721-01A-01D-1522-08 | TCGA-60-2721-11A-01D-1522-08 | g.chr10:28233864C>G | c.1414G>C | c.(1414-1416)Gcg>Ccg | p.A472P |
LUSC | 10 | 28274056 | 28274056 | + | Missense_Mutation | SNP | T | T | A | TCGA-66-2783-01A-01D-1267-08 | TCGA-66-2783-11A-01D-1267-08 | g.chr10:28274056T>A | c.467A>T | c.(466-468)aAa>aTa | p.K156I |
OV | 10 | 28101521 | 28101521 | + | Missense_Mutation | SNP | C | C | A | TCGA-04-1338-01A-01W-0484-10 | TCGA-04-1338-11A-01W-0485-10 | g.chr10:28101521C>A | c.3055G>T | c.(3055-3057)Gat>Tat | p.D1019Y |
OV | 10 | 28149706 | 28149706 | + | Missense_Mutation | SNP | C | C | G | TCGA-04-1357-01A-01W-0492-08 | TCGA-04-1357-11A-01W-0492-08 | g.chr10:28149706C>G | c.2869G>C | c.(2869-2871)Gtg>Ctg | p.V957L |
OV | 10 | 28228876 | 28228876 | + | Missense_Mutation | SNP | T | T | A | TCGA-13-1483-01A-01W-0549-09 | TCGA-13-1483-10A-01W-0549-09 | g.chr10:28228876T>A | c.2047A>T | c.(2047-2049)Aat>Tat | p.N683Y |
OV | 10 | 28229687 | 28229687 | + | Silent | SNP | C | C | T | TCGA-36-2548-01A-01D-1526-09 | TCGA-36-2548-10A-01D-1526-09 | g.chr10:28229687C>T | c.1791G>A | c.(1789-1791)tcG>tcA | p.S597S |
OV | 10 | 28283956 | 28283956 | + | Missense_Mutation | SNP | T | T | G | TCGA-24-1614-01A-01W-0552-10 | TCGA-24-1614-10A-01W-0552-10 | g.chr10:28283956T>G | c.116A>C | c.(115-117)gAg>gCg | p.E39A |
PAAD | 10 | 28224123 | 28224123 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr10:28224123C>A | c.2311G>T | c.(2311-2313)Gaa>Taa | p.E771* |
PRAD | 10 | 28229592 | 28229592 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr10:28229592C>T | c.1886G>A | c.(1885-1887)cGc>cAc | p.R629H |
PRAD | 10 | 28272875 | 28272875 | + | Missense_Mutation | SNP | G | G | A | TCGA-KK-A59V-01A-11D-A29Q-08 | TCGA-KK-A59V-11A-11D-A29Q-08 | g.chr10:28272875G>A | c.716C>T | c.(715-717)cCg>cTg | p.P239L |
READ | 10 | 28151422 | 28151422 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr10:28151422T>G | c.2740A>C | c.(2740-2742)Aat>Cat | p.N914H |
READ | 10 | 28229554 | 28229554 | + | Missense_Mutation | SNP | T | T | C | TCGA-DC-5337-01A-01D-1657-10 | TCGA-DC-5337-10A-01D-1657-10 | g.chr10:28229554T>C | c.1924A>G | c.(1924-1926)Aag>Gag | p.K642E |
READ | 10 | 28260161 | 28260161 | + | Missense_Mutation | SNP | G | G | A | TCGA-AF-5654-01A-01D-1657-10 | TCGA-AF-5654-10A-01D-1657-10 | g.chr10:28260161G>A | c.1018C>T | c.(1018-1020)Cgc>Tgc | p.R340C |
READ | 10 | 28274019 | 28274019 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-3605-01A-01W-0833-10 | TCGA-AG-3605-10A-01W-0833-10 | g.chr10:28274019C>A | c.504G>T | c.(502-504)aaG>aaT | p.K168N |
SARC | 10 | 28233361 | 28233361 | + | Splice_Site | SNP | C | C | T | TCGA-DX-AB2E-01A-11D-A38Z-09 | TCGA-DX-AB2E-10A-01D-A38Z-09 | g.chr10:28233361C>T | | c.e12-1 | |
SARC | 10 | 28270465 | 28270465 | + | Missense_Mutation | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr10:28270465G>A | c.866C>T | c.(865-867)tCa>tTa | p.S289L |
SKCM | 10 | 28101451 | 28101451 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1I0-06A-11D-A20D-08 | TCGA-DA-A1I0-10B-01D-A20D-08 | g.chr10:28101451C>T | c.3125G>A | c.(3124-3126)aGa>aAa | p.R1042K |
SKCM | 10 | 28101452 | 28101452 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr10:28101452T>C | c.3124A>G | c.(3124-3126)Aga>Gga | p.R1042G |
SKCM | 10 | 28101482 | 28101482 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr10:28101482G>A | c.3094C>T | c.(3094-3096)Cgc>Tgc | p.R1032C |
SKCM | 10 | 28101489 | 28101489 | + | Silent | SNP | G | G | A | TCGA-D9-A148-06A-11D-A19A-08 | TCGA-D9-A148-10A-01D-A19A-08 | g.chr10:28101489G>A | c.3087C>T | c.(3085-3087)tcC>tcT | p.S1029S |
SKCM | 10 | 28101521 | 28101521 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1HV-06A-21D-A196-08 | TCGA-DA-A1HV-10A-01D-A198-08 | g.chr10:28101521C>T | c.3055G>A | c.(3055-3057)Gat>Aat | p.D1019N |
SKCM | 10 | 28101521 | 28101521 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:28101521C>T | c.3055G>A | c.(3055-3057)Gat>Aat | p.D1019N |
SKCM | 10 | 28149569 | 28149569 | + | Silent | SNP | C | C | T | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr10:28149569C>T | c.3006G>A | c.(3004-3006)gaG>gaA | p.E1002E |
SKCM | 10 | 28149605 | 28149605 | + | Silent | SNP | G | G | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr10:28149605G>A | c.2970C>T | c.(2968-2970)ctC>ctT | p.L990L |
SKCM | 10 | 28149619 | 28149619 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JO-06A-11D-A196-08 | TCGA-D3-A2JO-10A-01D-A198-08 | g.chr10:28149619C>T | c.2956G>A | c.(2956-2958)Gcc>Acc | p.A986T |
SKCM | 10 | 28149631 | 28149631 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MC-06A-12D-A197-08 | TCGA-EE-A2MC-10A-01D-A199-08 | g.chr10:28149631C>T | c.2944G>A | c.(2944-2946)Gcg>Acg | p.A982T |
SKCM | 10 | 28149675 | 28149675 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28149675G>A | c.2900C>T | c.(2899-2901)cCa>cTa | p.P967L |
SKCM | 10 | 28151401 | 28151401 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3TU-06A-11D-A23B-08 | TCGA-FW-A3TU-10A-01D-A23B-08 | g.chr10:28151401G>A | c.2761C>T | c.(2761-2763)Cat>Tat | p.H921Y |
SKCM | 10 | 28151489 | 28151489 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-DA-A1HY-06A-11D-A19A-08 | TCGA-DA-A1HY-10A-01D-A19A-08 | g.chr10:28151489delT | c.2673delA | c.(2671-2673)aaafs | p.K891fs |
SKCM | 10 | 28151526 | 28151526 | + | Missense_Mutation | SNP | A | A | T | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr10:28151526A>T | c.2636T>A | c.(2635-2637)tTt>tAt | p.F879Y |
SKCM | 10 | 28151542 | 28151542 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AE-06A-11D-A196-08 | TCGA-EE-A3AE-10A-01D-A198-08 | g.chr10:28151542C>T | c.2620G>A | c.(2620-2622)Gaa>Aaa | p.E874K |
SKCM | 10 | 28151543 | 28151543 | + | Silent | SNP | C | C | T | TCGA-EE-A29B-06A-11D-A197-08 | TCGA-EE-A29B-10A-01D-A199-08 | g.chr10:28151543C>T | c.2619G>A | c.(2617-2619)ggG>ggA | p.G873G |
SKCM | 10 | 28151544 | 28151544 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29B-06A-11D-A197-08 | TCGA-EE-A29B-10A-01D-A199-08 | g.chr10:28151544C>T | c.2618G>A | c.(2617-2619)gGg>gAg | p.G873E |
SKCM | 10 | 28151551 | 28151551 | + | Splice_Site | SNP | C | C | T | TCGA-EE-A20F-06A-21D-A196-08 | TCGA-EE-A20F-10A-01D-A198-08 | g.chr10:28151551C>T | c.2611G>A | c.(2611-2613)Gat>Aat | p.D871N |
SKCM | 10 | 28196592 | 28196592 | + | Splice_Site | SNP | C | C | T | TCGA-FS-A4F8-06A-11D-A25O-08 | TCGA-FS-A4F8-10B-01D-A25O-08 | g.chr10:28196592C>T | c.2610G>A | c.(2608-2610)aaG>aaA | p.K870K |
SKCM | 10 | 28196667 | 28196667 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr10:28196667G>A | c.2535C>T | c.(2533-2535)tcC>tcT | p.S845S |
SKCM | 10 | 28196681 | 28196681 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr10:28196681G>A | c.2521C>T | c.(2521-2523)Cgt>Tgt | p.R841C |
SKCM | 10 | 28196681 | 28196681 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr10:28196681G>A | c.2521C>T | c.(2521-2523)Cgt>Tgt | p.R841C |
SKCM | 10 | 28196706 | 28196706 | + | Splice_Site | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr10:28196706C>T | c.2496G>A | c.(2494-2496)atG>atA | p.M832I |
SKCM | 10 | 28223949 | 28223949 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A5GO-06A-12D-A27K-08 | TCGA-D3-A5GO-10A-01D-A27N-08 | g.chr10:28223949C>T | c.2485G>A | c.(2485-2487)Gaa>Aaa | p.E829K |
SKCM | 10 | 28223958 | 28223958 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:28223958C>T | c.2476G>A | c.(2476-2478)Gta>Ata | p.V826I |
SKCM | 10 | 28224012 | 28224012 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr10:28224012C>T | c.2422G>A | c.(2422-2424)Gga>Aga | p.G808R |
SKCM | 10 | 28224025 | 28224025 | + | Silent | SNP | C | C | T | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr10:28224025C>T | c.2409G>A | c.(2407-2409)gtG>gtA | p.V803V |
SKCM | 10 | 28224036 | 28224036 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr10:28224036G>A | c.2398C>T | c.(2398-2400)Caa>Taa | p.Q800* |
SKCM | 10 | 28224106 | 28224106 | + | Silent | SNP | C | C | T | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:28224106C>T | c.2328G>A | c.(2326-2328)gtG>gtA | p.V776V |
SKCM | 10 | 28224136 | 28224136 | + | Silent | SNP | T | T | G | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr10:28224136T>G | c.2298A>C | c.(2296-2298)acA>acC | p.T766T |
SKCM | 10 | 28224174 | 28224174 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:28224174C>T | c.2260G>A | c.(2260-2262)Gaa>Aaa | p.E754K |
SKCM | 10 | 28224181 | 28224181 | + | Splice_Site | SNP | C | C | T | TCGA-D3-A3C7-06A-11D-A196-08 | TCGA-D3-A3C7-10A-01D-A198-08 | g.chr10:28224181C>T | c.2253G>A | c.(2251-2253)aaG>aaA | p.K751K |
SKCM | 10 | 28225687 | 28225687 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-D3-A2JL-06A-11D-A196-08 | TCGA-D3-A2JL-10A-01D-A198-08 | g.chr10:28225687C>T | c.2220G>A | c.(2218-2220)tgG>tgA | p.W740* |
SKCM | 10 | 28225687 | 28225687 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr10:28225687C>T | c.2220G>A | c.(2218-2220)tgG>tgA | p.W740* |
SKCM | 10 | 28225697 | 28225697 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GH-06A-11D-A196-08 | TCGA-EE-A2GH-10A-01D-A198-08 | g.chr10:28225697C>T | c.2210G>A | c.(2209-2211)gGg>gAg | p.G737E |
SKCM | 10 | 28225752 | 28225752 | + | Missense_Mutation | SNP | A | A | C | TCGA-EE-A3AF-06A-11D-A196-08 | TCGA-EE-A3AF-10A-01D-A198-08 | g.chr10:28225752A>C | c.2155T>G | c.(2155-2157)Ttg>Gtg | p.L719V |
SKCM | 10 | 28225792 | 28225792 | + | Missense_Mutation | SNP | T | T | G | TCGA-EE-A2GJ-06A-11D-A196-08 | TCGA-EE-A2GJ-10A-01D-A198-08 | g.chr10:28225792T>G | c.2115A>C | c.(2113-2115)gaA>gaC | p.E705D |
SKCM | 10 | 28225794 | 28225794 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MG-06A-11D-A197-08 | TCGA-EE-A2MG-10A-01D-A199-08 | g.chr10:28225794C>T | c.2113G>A | c.(2113-2115)Gaa>Aaa | p.E705K |
SKCM | 10 | 28225794 | 28225794 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr10:28225794C>T | c.2113G>A | c.(2113-2115)Gaa>Aaa | p.E705K |
SKCM | 10 | 28225794 | 28225794 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr10:28225794C>T | c.2113G>A | c.(2113-2115)Gaa>Aaa | p.E705K |
SKCM | 10 | 28228901 | 28228901 | + | Silent | SNP | G | G | A | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr10:28228901G>A | c.2022C>T | c.(2020-2022)atC>atT | p.I674I |
SKCM | 10 | 28228904 | 28228904 | + | Silent | SNP | C | C | T | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr10:28228904C>T | c.2019G>A | c.(2017-2019)agG>agA | p.R673R |
SKCM | 10 | 28228936 | 28228936 | + | Splice_Site | SNP | C | C | T | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr10:28228936C>T | c.1987G>A | c.(1987-1989)Gaa>Aaa | p.E663K |
SKCM | 10 | 28229547 | 28229547 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr10:28229547G>A | c.1931C>T | c.(1930-1932)tCt>tTt | p.S644F |
SKCM | 10 | 28229561 | 28229561 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28229561C>T | c.1917G>A | c.(1915-1917)cgG>cgA | p.R639R |
SKCM | 10 | 28229653 | 28229653 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr10:28229653G>A | c.1825C>T | c.(1825-1827)Cgc>Tgc | p.R609C |
SKCM | 10 | 28229688 | 28229688 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1IA-06A-11D-A196-08 | TCGA-DA-A1IA-10A-01D-A198-08 | g.chr10:28229688G>A | c.1790C>T | c.(1789-1791)tCg>tTg | p.S597L |
SKCM | 10 | 28229730 | 28229730 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1I0-06A-11D-A20D-08 | TCGA-DA-A1I0-10B-01D-A20D-08 | g.chr10:28229730G>A | c.1748C>T | c.(1747-1749)gCt>gTt | p.A583V |
SKCM | 10 | 28229733 | 28229733 | + | Splice_Site | SNP | A | A | G | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28229733A>G | c.1745T>C | c.(1744-1746)gTt>gCt | p.V582A |
SKCM | 10 | 28233271 | 28233271 | + | Silent | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr10:28233271C>T | c.1623G>A | c.(1621-1623)gtG>gtA | p.V541V |
SKCM | 10 | 28233286 | 28233286 | + | Silent | SNP | G | G | A | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:28233286G>A | c.1608C>T | c.(1606-1608)ggC>ggT | p.G536G |
SKCM | 10 | 28233311 | 28233311 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MF-06A-11D-A21A-08 | TCGA-EE-A2MF-10B-01D-A21A-08 | g.chr10:28233311C>T | c.1583G>A | c.(1582-1584)aGa>aAa | p.R528K |
SKCM | 10 | 28233336 | 28233336 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A182-06A-11D-A196-08 | TCGA-EE-A182-10A-01D-A198-08 | g.chr10:28233336C>T | c.1558G>A | c.(1558-1560)Gaa>Aaa | p.E520K |
SKCM | 10 | 28233336 | 28233336 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:28233336C>T | c.1558G>A | c.(1558-1560)Gaa>Aaa | p.E520K |
SKCM | 10 | 28233336 | 28233336 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GD-06A-11D-A196-08 | TCGA-EE-A2GD-10A-01D-A198-08 | g.chr10:28233336C>T | c.1558G>A | c.(1558-1560)Gaa>Aaa | p.E520K |
SKCM | 10 | 28233806 | 28233806 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr10:28233806C>T | c.1472G>A | c.(1471-1473)aGa>aAa | p.R491K |
SKCM | 10 | 28233806 | 28233806 | + | Missense_Mutation | SNP | C | C | T | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr10:28233806C>T | c.1472G>A | c.(1471-1473)aGa>aAa | p.R491K |
SKCM | 10 | 28233854 | 28233854 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28233854G>A | c.1424C>T | c.(1423-1425)tCa>tTa | p.S475L |
SKCM | 10 | 28250509 | 28250509 | + | Silent | SNP | C | C | T | TCGA-FS-A4F8-06A-11D-A25O-08 | TCGA-FS-A4F8-10B-01D-A25O-08 | g.chr10:28250509C>T | c.1374G>A | c.(1372-1374)gtG>gtA | p.V458V |
SKCM | 10 | 28260045 | 28260045 | + | Silent | SNP | A | A | G | TCGA-ER-A19M-06A-61D-A23B-08 | TCGA-ER-A19M-10A-01D-A23B-08 | g.chr10:28260045A>G | c.1134T>C | c.(1132-1134)aaT>aaC | p.N378N |
SKCM | 10 | 28260126 | 28260126 | + | Silent | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr10:28260126C>T | c.1053G>A | c.(1051-1053)ctG>ctA | p.L351L |
SKCM | 10 | 28260161 | 28260161 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A183-06A-11D-A196-08 | TCGA-EE-A183-10A-01D-A198-08 | g.chr10:28260161G>A | c.1018C>T | c.(1018-1020)Cgc>Tgc | p.R340C |
SKCM | 10 | 28260179 | 28260179 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr10:28260179C>T | c.1000G>A | c.(1000-1002)Gaa>Aaa | p.E334K |
SKCM | 10 | 28260212 | 28260212 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28260212C>T | c.967G>A | c.(967-969)Gaa>Aaa | p.E323K |
SKCM | 10 | 28260241 | 28260241 | + | Splice_Site | SNP | C | C | T | TCGA-FW-A3TV-06A-11D-A23B-08 | TCGA-FW-A3TV-10A-01D-A23B-08 | g.chr10:28260241C>T | c.938G>A | c.(937-939)gGa>gAa | p.G313E |
SKCM | 10 | 28270414 | 28270414 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZE-06A-11D-A197-08 | TCGA-FS-A1ZE-10A-01D-A199-08 | g.chr10:28270414G>A | c.917C>T | c.(916-918)tCa>tTa | p.S306L |
SKCM | 10 | 28270426 | 28270426 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A51T-06A-11D-A25O-08 | TCGA-D3-A51T-10A-01D-A25O-08 | g.chr10:28270426G>A | c.905C>T | c.(904-906)tCa>tTa | p.S302L |
SKCM | 10 | 28270426 | 28270426 | + | Missense_Mutation | SNP | G | G | A | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr10:28270426G>A | c.905C>T | c.(904-906)tCa>tTa | p.S302L |
SKCM | 10 | 28270487 | 28270487 | + | Missense_Mutation | SNP | C | C | G | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr10:28270487C>G | c.844G>C | c.(844-846)Gtt>Ctt | p.V282L |
SKCM | 10 | 28270496 | 28270496 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A5GS-06A-11D-A27K-08 | TCGA-D3-A5GS-10A-01D-A27N-08 | g.chr10:28270496C>T | c.835G>A | c.(835-837)Gaa>Aaa | p.E279K |
SKCM | 10 | 28272774 | 28272774 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr10:28272774C>T | c.817G>A | c.(817-819)Ggt>Agt | p.G273S |
SKCM | 10 | 28272791 | 28272791 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZT-06A-11D-A197-08 | TCGA-FS-A1ZT-10A-01D-A199-08 | g.chr10:28272791C>T | c.800G>A | c.(799-801)gGa>gAa | p.G267E |
SKCM | 10 | 28272830 | 28272830 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JI-06A-11D-A21A-08 | TCGA-EE-A3JI-10A-01D-A21A-08 | g.chr10:28272830G>A | c.761C>T | c.(760-762)cCt>cTt | p.P254L |
SKCM | 10 | 28272835 | 28272835 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28272835C>T | c.756G>A | c.(754-756)gtG>gtA | p.V252V |
SKCM | 10 | 28272855 | 28272855 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MI-06A-11D-A197-08 | TCGA-EE-A2MI-10A-01D-A199-08 | g.chr10:28272855C>T | c.736G>A | c.(736-738)Gaa>Aaa | p.E246K |
SKCM | 10 | 28272861 | 28272861 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29R-06A-11D-A197-08 | TCGA-EE-A29R-10A-01D-A199-08 | g.chr10:28272861G>A | c.730C>T | c.(730-732)Cgt>Tgt | p.R244C |
SKCM | 10 | 28272861 | 28272861 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr10:28272861G>A | c.730C>T | c.(730-732)Cgt>Tgt | p.R244C |
SKCM | 10 | 28272878 | 28272878 | + | Missense_Mutation | SNP | G | G | A | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr10:28272878G>A | c.713C>T | c.(712-714)cCa>cTa | p.P238L |
SKCM | 10 | 28272885 | 28272885 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr10:28272885G>A | c.706C>T | c.(706-708)Cga>Tga | p.R236* |
SKCM | 10 | 28272896 | 28272896 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1HY-06A-11D-A19A-08 | TCGA-DA-A1HY-10A-01D-A19A-08 | g.chr10:28272896G>A | c.695C>T | c.(694-696)tCa>tTa | p.S232L |
SKCM | 10 | 28272896 | 28272896 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A4U8-06A-11D-A32N-08 | TCGA-GN-A4U8-10B-01D-A32N-08 | g.chr10:28272896G>A | c.695C>T | c.(694-696)tCa>tTa | p.S232L |
SKCM | 10 | 28272903 | 28272903 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A5GO-06A-12D-A27K-08 | TCGA-D3-A5GO-10A-01D-A27N-08 | g.chr10:28272903C>T | c.688G>A | c.(688-690)Gaa>Aaa | p.E230K |
SKCM | 10 | 28273125 | 28273125 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28273125C>T | c.670G>A | c.(670-672)Gaa>Aaa | p.E224K |
SKCM | 10 | 28273152 | 28273152 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr10:28273152C>T | c.643G>A | c.(643-645)Gga>Aga | p.G215R |
SKCM | 10 | 28273157 | 28273157 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr10:28273157C>T | c.638G>A | c.(637-639)gGa>gAa | p.G213E |
SKCM | 10 | 28273157 | 28273157 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr10:28273157C>T | c.638G>A | c.(637-639)gGa>gAa | p.G213E |
SKCM | 10 | 28273185 | 28273185 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr10:28273185C>T | c.610G>A | c.(610-612)Gat>Aat | p.D204N |
SKCM | 10 | 28273189 | 28273189 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28273189C>T | c.606G>A | c.(604-606)aaG>aaA | p.K202K |
SKCM | 10 | 28273212 | 28273212 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:28273212T>C | c.583A>G | c.(583-585)Agt>Ggt | p.S195G |
SKCM | 10 | 28273954 | 28273954 | + | Missense_Mutation | SNP | A | A | T | TCGA-FS-A1Z3-06A-11D-A197-08 | TCGA-FS-A1Z3-10A-01D-A199-08 | g.chr10:28273954A>T | c.569T>A | c.(568-570)aTt>aAt | p.I190N |
SKCM | 10 | 28273976 | 28273976 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28273976G>A | c.547C>T | c.(547-549)Ctc>Ttc | p.L183F |
SKCM | 10 | 28274109 | 28274109 | + | Silent | SNP | G | G | A | TCGA-EE-A3JI-06A-11D-A21A-08 | TCGA-EE-A3JI-10A-01D-A21A-08 | g.chr10:28274109G>A | c.414C>T | c.(412-414)ggC>ggT | p.G138G |
SKCM | 10 | 28276336 | 28276336 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A51R-06A-11D-A25O-08 | TCGA-D3-A51R-10A-01D-A25O-08 | g.chr10:28276336C>T | c.361G>A | c.(361-363)Gaa>Aaa | p.E121K |
SKCM | 10 | 28276346 | 28276346 | + | Silent | SNP | C | C | T | TCGA-FS-A1ZW-06A-12D-A197-08 | TCGA-FS-A1ZW-10A-01D-A199-08 | g.chr10:28276346C>T | c.351G>A | c.(349-351)ggG>ggA | p.G117G |
SKCM | 10 | 28276434 | 28276434 | + | Missense_Mutation | SNP | C | C | T | TCGA-OD-A75X-06A-12D-A32N-08 | TCGA-OD-A75X-10A-01D-A32N-08 | g.chr10:28276434C>T | c.263G>A | c.(262-264)gGa>gAa | p.G88E |
SKCM | 10 | 28283909 | 28283909 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr10:28283909C>T | c.163G>A | c.(163-165)Gaa>Aaa | p.E55K |
SKCM | 10 | 28283985 | 28283985 | + | Silent | SNP | C | C | T | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr10:28283985C>T | c.87G>A | c.(85-87)gcG>gcA | p.A29A |
SKCM | 10 | 28284003 | 28284003 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr10:28284003G>A | c.69C>T | c.(67-69)atC>atT | p.I23I |
SKCM | 10 | 28284008 | 28284008 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chr10:28284008C>T | c.64G>A | c.(64-66)Gaa>Aaa | p.E22K |
SKCM | 10 | 28284008 | 28284008 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1IA-06A-11D-A196-08 | TCGA-DA-A1IA-10A-01D-A198-08 | g.chr10:28284008C>T | c.64G>A | c.(64-66)Gaa>Aaa | p.E22K |
SKCM | 10 | 28284008 | 28284008 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MI-06A-11D-A197-08 | TCGA-EE-A2MI-10A-01D-A199-08 | g.chr10:28284008C>T | c.64G>A | c.(64-66)Gaa>Aaa | p.E22K |
SKCM | 10 | 28284008 | 28284008 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr10:28284008C>T | c.64G>A | c.(64-66)Gaa>Aaa | p.E22K |
SKCM | 10 | 28284008 | 28284008 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr10:28284008C>T | c.64G>A | c.(64-66)Gaa>Aaa | p.E22K |
SKCM | 10 | 28284008 | 28284008 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr10:28284008C>T | c.64G>A | c.(64-66)Gaa>Aaa | p.E22K |
SKCM | 10 | 28284008 | 28284008 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:28284008C>T | c.64G>A | c.(64-66)Gaa>Aaa | p.E22K |
SKCM | 10 | 28284054 | 28284054 | + | Silent | SNP | C | C | T | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr10:28284054C>T | c.18G>A | c.(16-18)agG>agA | p.R6R |