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 | 62631383 | 62631383 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-AAMY-01A-11D-A42E-08 | TCGA-XF-AAMY-10A-01D-A42H-08 | g.chr10:62631383G>A | c.1948C>T | c.(1948-1950)Cgc>Tgc | p.R650C |
BLCA | 10 | 62631954 | 62631954 | + | Missense_Mutation | SNP | G | G | A | TCGA-BT-A2LB-01A-11D-A18F-08 | TCGA-BT-A2LB-10A-01D-A18F-08 | g.chr10:62631954G>A | c.1910C>T | c.(1909-1911)tCa>tTa | p.S637L |
BLCA | 10 | 62634778 | 62634778 | + | Silent | SNP | C | C | T | TCGA-ZF-A9R4-01A-11D-A38G-08 | TCGA-ZF-A9R4-10A-01D-A38J-08 | g.chr10:62634778C>T | c.1749G>A | c.(1747-1749)ttG>ttA | p.L583L |
BLCA | 10 | 62637763 | 62637763 | + | Silent | SNP | G | G | C | TCGA-DK-AA71-01A-31D-A391-08 | TCGA-DK-AA71-10A-01D-A394-08 | g.chr10:62637763G>C | c.1629C>G | c.(1627-1629)ctC>ctG | p.L543L |
BLCA | 10 | 62645942 | 62645942 | + | Silent | SNP | C | C | T | TCGA-SY-A9G0-01A-12D-A38G-08 | TCGA-SY-A9G0-10A-01D-A38J-08 | g.chr10:62645942C>T | c.1503G>A | c.(1501-1503)ccG>ccA | p.P501P |
BLCA | 10 | 62648858 | 62648858 | + | Missense_Mutation | SNP | C | C | G | TCGA-E7-A7XN-01A-11D-A34U-08 | TCGA-E7-A7XN-10A-01D-A34X-08 | g.chr10:62648858C>G | c.568G>C | c.(568-570)Gtg>Ctg | p.V190L |
BLCA | 10 | 62648934 | 62648934 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A43X-01A-11D-A23U-08 | TCGA-FD-A43X-10A-01D-A23U-08 | g.chr10:62648934C>G | c.492G>C | c.(490-492)aaG>aaC | p.K164N |
BLCA | 10 | 62670660 | 62670660 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZF-AA51-01A-21D-A391-08 | TCGA-ZF-AA51-10A-01D-A394-08 | g.chr10:62670660C>T | c.281G>A | c.(280-282)cGc>cAc | p.R94H |
BRCA | 10 | 62648543 | 62648543 | + | Silent | SNP | G | G | A | TCGA-BH-A0HF-01A-11W-A071-09 | TCGA-BH-A0HF-10A-01W-A071-09 | g.chr10:62648543G>A | c.883C>T | c.(883-885)Ctg>Ttg | p.L295L |
BRCA | 10 | 62671216 | 62671216 | + | Missense_Mutation | SNP | G | G | A | TCGA-A2-A1FZ-01A-51D-A17G-09 | TCGA-A2-A1FZ-10A-01D-A14G-09 | g.chr10:62671216G>A | c.85C>T | c.(85-87)Cgc>Tgc | p.R29C |
CESC | 10 | 62632020 | 62632020 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-C5-A1BK-01B-11D-A13W-08 | TCGA-C5-A1BK-10A-01D-A13W-08 | g.chr10:62632020C>T | c.1844G>A | c.(1843-1845)tGg>tAg | p.W615* |
CHOL | 10 | 62648582 | 62648582 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZU-A8S4-01A-11D-A417-09 | TCGA-ZU-A8S4-10A-01D-A41A-09 | g.chr10:62648582G>C | c.844C>G | c.(844-846)Cga>Gga | p.R282G |
COAD | 10 | 62631970 | 62631970 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6782-01A-11D-1835-10 | TCGA-A6-6782-10A-01D-1835-10 | g.chr10:62631970G>A | c.1894C>T | c.(1894-1896)Cgt>Tgt | p.R632C |
COAD | 10 | 62631980 | 62631980 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr10:62631980G>T | c.1884C>A | c.(1882-1884)tgC>tgA | p.C628* |
COAD | 10 | 62632024 | 62632024 | + | Missense_Mutation | SNP | C | C | T | TCGA-AY-6386-01A-21D-1719-10 | TCGA-AY-6386-10A-01D-1719-10 | g.chr10:62632024C>T | c.1840G>A | c.(1840-1842)Gcc>Acc | p.A614T |
COAD | 10 | 62634770 | 62634770 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr10:62634770G>A | c.1757C>T | c.(1756-1758)gCc>gTc | p.A586V |
COAD | 10 | 62634791 | 62634791 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr10:62634791G>A | c.1736C>T | c.(1735-1737)gCc>gTc | p.A579V |
COAD | 10 | 62647977 | 62647977 | + | Silent | SNP | C | C | T | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr10:62647977C>T | c.1449G>A | c.(1447-1449)acG>acA | p.T483T |
COAD | 10 | 62648035 | 62648035 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3519-01A-02W-0831-10 | TCGA-AA-3519-10A-01W-0831-10 | g.chr10:62648035G>A | c.1391C>T | c.(1390-1392)aCg>aTg | p.T464M |
COAD | 10 | 62648343 | 62648343 | + | Silent | SNP | G | G | A | TCGA-AA-3660-01A-01D-1719-10 | TCGA-AA-3660-11A-01D-1719-10 | g.chr10:62648343G>A | c.1083C>T | c.(1081-1083)gcC>gcT | p.A361A |
COAD | 10 | 62648478 | 62648478 | + | Missense_Mutation | SNP | C | C | G | TCGA-F4-6460-01A-11D-1771-10 | TCGA-F4-6460-10B-01D-1771-10 | g.chr10:62648478C>G | c.948G>C | c.(946-948)caG>caC | p.Q316H |
COAD | 10 | 62671217 | 62671217 | + | Silent | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr10:62671217C>T | c.84G>A | c.(82-84)acG>acA | p.T28T |
COAD | 10 | 62671289 | 62671289 | + | Silent | SNP | G | G | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr10:62671289G>A | c.12C>T | c.(10-12)gaC>gaT | p.D4D |
COADREAD | 10 | 62631970 | 62631970 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6782-01A-11D-1835-10 | TCGA-A6-6782-10A-01D-1835-10 | g.chr10:62631970G>A | c.1894C>T | c.(1894-1896)Cgt>Tgt | p.R632C |
COADREAD | 10 | 62631980 | 62631980 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr10:62631980G>T | c.1884C>A | c.(1882-1884)tgC>tgA | p.C628* |
COADREAD | 10 | 62632024 | 62632024 | + | Missense_Mutation | SNP | C | C | T | TCGA-AY-6386-01A-21D-1719-10 | TCGA-AY-6386-10A-01D-1719-10 | g.chr10:62632024C>T | c.1840G>A | c.(1840-1842)Gcc>Acc | p.A614T |
COADREAD | 10 | 62634763 | 62634763 | + | Silent | SNP | C | C | T | TCGA-AG-A01W-01A-21W-A096-10 | TCGA-AG-A01W-11A-11W-A096-10 | g.chr10:62634763C>T | c.1764G>A | c.(1762-1764)acG>acA | p.T588T |
COADREAD | 10 | 62634770 | 62634770 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr10:62634770G>A | c.1757C>T | c.(1756-1758)gCc>gTc | p.A586V |
COADREAD | 10 | 62634791 | 62634791 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr10:62634791G>A | c.1736C>T | c.(1735-1737)gCc>gTc | p.A579V |
COADREAD | 10 | 62647977 | 62647977 | + | Silent | SNP | C | C | T | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr10:62647977C>T | c.1449G>A | c.(1447-1449)acG>acA | p.T483T |
COADREAD | 10 | 62648035 | 62648035 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3519-01A-02W-0831-10 | TCGA-AA-3519-10A-01W-0831-10 | g.chr10:62648035G>A | c.1391C>T | c.(1390-1392)aCg>aTg | p.T464M |
COADREAD | 10 | 62648035 | 62648035 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-3602-01A-02W-0833-10 | TCGA-AG-3602-10A-01W-0833-10 | g.chr10:62648035G>A | c.1391C>T | c.(1390-1392)aCg>aTg | p.T464M |
COADREAD | 10 | 62648343 | 62648343 | + | Silent | SNP | G | G | A | TCGA-AA-3660-01A-01D-1719-10 | TCGA-AA-3660-11A-01D-1719-10 | g.chr10:62648343G>A | c.1083C>T | c.(1081-1083)gcC>gcT | p.A361A |
COADREAD | 10 | 62648478 | 62648478 | + | Missense_Mutation | SNP | C | C | G | TCGA-F4-6460-01A-11D-1771-10 | TCGA-F4-6460-10B-01D-1771-10 | g.chr10:62648478C>G | c.948G>C | c.(946-948)caG>caC | p.Q316H |
COADREAD | 10 | 62648827 | 62648828 | + | Frame_Shift_Ins | INS | - | - | AC | TCGA-AH-6644-01A-21D-1826-10 | TCGA-AH-6644-10A-01D-1826-10 | g.chr10:62648827_62648828insAC | c.598_599insGT | c.(598-600)tttfs | p.F200fs |
COADREAD | 10 | 62671217 | 62671217 | + | Silent | SNP | C | C | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr10:62671217C>T | c.84G>A | c.(82-84)acG>acA | p.T28T |
COADREAD | 10 | 62671289 | 62671289 | + | Silent | SNP | G | G | A | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr10:62671289G>A | c.12C>T | c.(10-12)gaC>gaT | p.D4D |
DLBC | 10 | 62631996 | 62631996 | + | Missense_Mutation | SNP | T | T | G | TCGA-FF-A7CR-01A-11D-A382-10 | TCGA-FF-A7CR-10A-01D-A385-10 | g.chr10:62631996T>G | c.1868A>C | c.(1867-1869)aAc>aCc | p.N623T |
ESCA | 10 | 62647970 | 62647970 | + | Splice_Site | SNP | C | C | A | TCGA-L5-A43J-01A-12D-A247-09 | TCGA-L5-A43J-11A-11D-A247-09 | g.chr10:62647970C>A | c.1456G>T | c.(1456-1458)Gac>Tac | p.D486Y |
ESCA | 10 | 62648194 | 62648194 | + | Missense_Mutation | SNP | A | A | G | TCGA-LN-A49O-01A-11D-A247-09 | TCGA-LN-A49O-10A-01D-A247-09 | g.chr10:62648194A>G | c.1232T>C | c.(1231-1233)tTt>tCt | p.F411S |
GBMLGG | 10 | 62648196 | 62648196 | + | Silent | SNP | A | A | G | TCGA-DU-5871-01A-12D-1705-08 | TCGA-DU-5871-10A-01D-1705-08 | g.chr10:62648196A>G | c.1230T>C | c.(1228-1230)ccT>ccC | p.P410P |
HNSC | 10 | 62631312 | 62631312 | + | Missense_Mutation | SNP | T | T | G | TCGA-UP-A6WW-01A-12D-A34J-08 | TCGA-UP-A6WW-10B-01D-A34M-08 | g.chr10:62631312T>G | c.2019A>C | c.(2017-2019)gaA>gaC | p.E673D |
HNSC | 10 | 62631978 | 62631978 | + | Missense_Mutation | SNP | G | G | C | TCGA-CX-7085-01A-21D-2012-08 | TCGA-CX-7085-10A-01D-2013-08 | g.chr10:62631978G>C | c.1886C>G | c.(1885-1887)tCc>tGc | p.S629C |
HNSC | 10 | 62632017 | 62632017 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-5977-01A-11D-1683-08 | TCGA-CV-5977-11A-01D-1683-08 | g.chr10:62632017C>T | c.1847G>A | c.(1846-1848)tGt>tAt | p.C616Y |
HNSC | 10 | 62634740 | 62634740 | + | Missense_Mutation | SNP | T | T | C | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr10:62634740T>C | c.1787A>G | c.(1786-1788)gAa>gGa | p.E596G |
HNSC | 10 | 62647977 | 62647977 | + | Silent | SNP | C | C | T | TCGA-D6-6825-01A-21D-1912-08 | TCGA-D6-6825-10A-01D-1912-08 | g.chr10:62647977C>T | c.1449G>A | c.(1447-1449)acG>acA | p.T483T |
HNSC | 10 | 62647983 | 62647983 | + | Silent | SNP | C | C | T | TCGA-D6-A6EQ-01A-11D-A31L-08 | TCGA-D6-A6EQ-10A-01D-A31J-08 | g.chr10:62647983C>T | c.1443G>A | c.(1441-1443)aaG>aaA | p.K481K |
HNSC | 10 | 62648067 | 62648067 | + | Missense_Mutation | SNP | C | C | A | TCGA-CR-7374-01A-11D-2012-08 | TCGA-CR-7374-10A-01D-2013-08 | g.chr10:62648067C>A | c.1359G>T | c.(1357-1359)atG>atT | p.M453I |
HNSC | 10 | 62648292 | 62648292 | + | Silent | SNP | G | G | A | TCGA-CN-A6V1-01A-12D-A34J-08 | TCGA-CN-A6V1-10B-01D-A34M-08 | g.chr10:62648292G>A | c.1134C>T | c.(1132-1134)ttC>ttT | p.F378F |
HNSC | 10 | 62648571 | 62648571 | + | Silent | SNP | G | G | A | TCGA-CR-7382-01A-11D-2129-08 | TCGA-CR-7382-10A-01D-2129-08 | g.chr10:62648571G>A | c.855C>T | c.(853-855)ctC>ctT | p.L285L |
HNSC | 10 | 62648688 | 62648688 | + | Silent | SNP | T | T | A | TCGA-CV-7242-01A-11D-2012-08 | TCGA-CV-7242-10A-01D-2013-08 | g.chr10:62648688T>A | c.738A>T | c.(736-738)ccA>ccT | p.P246P |
HNSC | 10 | 62648704 | 62648704 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-A6JO-01B-11D-A34J-08 | TCGA-CV-A6JO-10A-01D-A34M-08 | g.chr10:62648704G>A | c.722C>T | c.(721-723)cCg>cTg | p.P241L |
HNSC | 10 | 62648784 | 62648784 | + | Silent | SNP | C | C | T | TCGA-CV-6960-01A-41D-2012-08 | TCGA-CV-6960-10A-01D-2013-08 | g.chr10:62648784C>T | c.642G>A | c.(640-642)ctG>ctA | p.L214L |
HNSC | 10 | 62648790 | 62648790 | + | Silent | SNP | C | C | T | TCGA-DQ-5625-01A-01D-1870-08 | TCGA-DQ-5625-10A-01D-1870-08 | g.chr10:62648790C>T | c.636G>A | c.(634-636)agG>agA | p.R212R |
HNSC | 10 | 62652607 | 62652607 | + | Missense_Mutation | SNP | T | T | C | TCGA-CV-6954-01A-11D-1912-08 | TCGA-CV-6954-10A-01D-1912-08 | g.chr10:62652607T>C | c.443A>G | c.(442-444)gAc>gGc | p.D148G |
HNSC | 10 | 62652608 | 62652608 | + | Missense_Mutation | SNP | C | C | A | TCGA-D6-A4ZB-01A-11D-A25D-08 | TCGA-D6-A4ZB-10A-01D-A25E-08 | g.chr10:62652608C>A | c.442G>T | c.(442-444)Gac>Tac | p.D148Y |
HNSC | 10 | 62670718 | 62670718 | + | Missense_Mutation | SNP | C | C | T | TCGA-BA-5558-01A-01D-1512-08 | TCGA-BA-5558-10A-01D-1512-08 | g.chr10:62670718C>T | c.223G>A | c.(223-225)Gaa>Aaa | p.E75K |
KIPAN | 10 | 62648933 | 62648933 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-B1-5398-01A-02D-1589-08 | TCGA-B1-5398-10A-01D-1589-08 | g.chr10:62648933T>A | c.493A>T | c.(493-495)Aga>Tga | p.R165* |
KIPAN | 10 | 62670721 | 62670721 | + | Missense_Mutation | SNP | C | C | T | TCGA-2Z-A9J5-01A-21D-A382-10 | TCGA-2Z-A9J5-10A-01D-A385-10 | g.chr10:62670721C>T | c.220G>A | c.(220-222)Gat>Aat | p.D74N |
KIRP | 10 | 62648933 | 62648933 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-B1-5398-01A-02D-1589-08 | TCGA-B1-5398-10A-01D-1589-08 | g.chr10:62648933T>A | c.493A>T | c.(493-495)Aga>Tga | p.R165* |
KIRP | 10 | 62670721 | 62670721 | + | Missense_Mutation | SNP | C | C | T | TCGA-2Z-A9J5-01A-21D-A382-10 | TCGA-2Z-A9J5-10A-01D-A385-10 | g.chr10:62670721C>T | c.220G>A | c.(220-222)Gat>Aat | p.D74N |
LGG | 10 | 62648196 | 62648196 | + | Silent | SNP | A | A | G | TCGA-DU-5871-01A-12D-1705-08 | TCGA-DU-5871-10A-01D-1705-08 | g.chr10:62648196A>G | c.1230T>C | c.(1228-1230)ccT>ccC | p.P410P |
LIHC | 10 | 62637748 | 62637748 | + | Missense_Mutation | SNP | C | C | A | TCGA-DD-AADY-01A-11D-A40R-10 | TCGA-DD-AADY-10A-01D-A40U-10 | g.chr10:62637748C>A | c.1644G>T | c.(1642-1644)ttG>ttT | p.L548F |
LIHC | 10 | 62647978 | 62647978 | + | Missense_Mutation | SNP | G | G | A | TCGA-G3-A7M5-01A-11D-A33Q-10 | TCGA-G3-A7M5-10A-01D-A33Q-10 | g.chr10:62647978G>A | c.1448C>T | c.(1447-1449)aCg>aTg | p.T483M |
LIHC | 10 | 62648855 | 62648855 | + | Missense_Mutation | SNP | A | A | G | TCGA-CC-A8HU-01A-11D-A35Z-10 | TCGA-CC-A8HU-10A-01D-A35Z-10 | g.chr10:62648855A>G | c.571T>C | c.(571-573)Ttt>Ctt | p.F191L |
LIHC | 10 | 62671170 | 62671170 | + | Missense_Mutation | SNP | T | T | C | TCGA-BC-A3KG-01A-11D-A20W-10 | TCGA-BC-A3KG-10A-01D-A20W-10 | g.chr10:62671170T>C | c.131A>G | c.(130-132)cAg>cGg | p.Q44R |
LUAD | 10 | 62631267 | 62631267 | + | Missense_Mutation | SNP | G | G | C | TCGA-50-8459-01A-11D-2323-08 | TCGA-50-8459-10A-01D-2323-08 | g.chr10:62631267G>C | c.2064C>G | c.(2062-2064)ttC>ttG | p.F688L |
LUAD | 10 | 62632019 | 62632019 | + | Missense_Mutation | SNP | C | C | A | TCGA-38-4626-01A-01D-1553-08 | TCGA-38-4626-11A-01D-1553-08 | g.chr10:62632019C>A | c.1845G>T | c.(1843-1845)tgG>tgT | p.W615C |
LUAD | 10 | 62634756 | 62634756 | + | Missense_Mutation | SNP | C | C | A | TCGA-91-6848-01A-11D-1945-08 | TCGA-91-6848-11A-01D-1945-08 | g.chr10:62634756C>A | c.1771G>T | c.(1771-1773)Gtg>Ttg | p.V591L |
LUAD | 10 | 62634766 | 62634766 | + | Silent | SNP | G | G | A | TCGA-05-4432-01A-01D-1265-08 | TCGA-05-4432-10A-01D-1265-08 | g.chr10:62634766G>A | c.1761C>T | c.(1759-1761)gcC>gcT | p.A587A |
LUAD | 10 | 62645903 | 62645903 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z007-01A-01W-0746-08 | TCGA-17-Z007-11A-01W-0746-08 | g.chr10:62645903G>T | c.1542C>A | c.(1540-1542)ttC>ttA | p.F514L |
LUAD | 10 | 62648365 | 62648365 | + | Missense_Mutation | SNP | A | A | T | TCGA-49-6767-01A-11D-1855-08 | TCGA-49-6767-11A-01D-1855-08 | g.chr10:62648365A>T | c.1061T>A | c.(1060-1062)gTg>gAg | p.V354E |
LUAD | 10 | 62648417 | 62648417 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z060-01A-01W-0747-08 | TCGA-17-Z060-11A-01W-0747-08 | g.chr10:62648417G>A | c.1009C>T | c.(1009-1011)Ccg>Tcg | p.P337S |
LUAD | 10 | 62652603 | 62652603 | + | Silent | SNP | C | C | A | TCGA-55-A490-01A-11D-A24D-08 | TCGA-55-A490-10A-01D-A24F-08 | g.chr10:62652603C>A | c.447G>T | c.(445-447)ctG>ctT | p.L149L |
LUSC | 10 | 62648181 | 62648181 | + | Silent | SNP | G | G | C | TCGA-34-5231-01A-21D-1817-08 | TCGA-34-5231-10A-01D-1817-08 | g.chr10:62648181G>C | c.1245C>G | c.(1243-1245)ctC>ctG | p.L415L |
LUSC | 10 | 62648482 | 62648482 | + | Missense_Mutation | SNP | T | T | A | TCGA-66-2756-01A-01D-1522-08 | TCGA-66-2756-11A-01D-1522-08 | g.chr10:62648482T>A | c.944A>T | c.(943-945)aAg>aTg | p.K315M |
LUSC | 10 | 62648494 | 62648494 | + | Missense_Mutation | SNP | C | C | A | TCGA-51-4079-01A-01D-1458-08 | TCGA-51-4079-11A-01D-1458-08 | g.chr10:62648494C>A | c.932G>T | c.(931-933)tGt>tTt | p.C311F |
LUSC | 10 | 62652608 | 62652608 | + | Missense_Mutation | SNP | C | C | A | TCGA-33-4583-01A-01D-1441-08 | TCGA-33-4583-11A-01D-1441-08 | g.chr10:62652608C>A | c.442G>T | c.(442-444)Gac>Tac | p.D148Y |
LUSC | 10 | 62652698 | 62652698 | + | Missense_Mutation | SNP | C | C | A | TCGA-63-6202-01A-11D-1817-08 | TCGA-63-6202-10A-01D-1817-08 | g.chr10:62652698C>A | c.352G>T | c.(352-354)Gtg>Ttg | p.V118L |
OV | 10 | 62634789 | 62634789 | + | Missense_Mutation | SNP | C | C | T | TCGA-29-1695-01A-01W-0633-09 | TCGA-29-1695-10A-01W-0633-09 | g.chr10:62634789C>T | c.1738G>A | c.(1738-1740)Gtt>Att | p.V580I |
PAAD | 10 | 62648459 | 62648459 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr10:62648459G>A | c.967C>T | c.(967-969)Cgg>Tgg | p.R323W |
PAAD | 10 | 62670660 | 62670660 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr10:62670660C>T | c.281G>A | c.(280-282)cGc>cAc | p.R94H |
PCPG | 10 | 62648781 | 62648781 | + | Silent | SNP | T | T | C | TCGA-WB-A81D-01A-11D-A35I-08 | TCGA-WB-A81D-10A-01D-A35G-08 | g.chr10:62648781T>C | c.645A>G | c.(643-645)caA>caG | p.Q215Q |
PRAD | 10 | 62648833 | 62648833 | + | Missense_Mutation | SNP | T | T | C | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr10:62648833T>C | c.593A>G | c.(592-594)gAt>gGt | p.D198G |
READ | 10 | 62634763 | 62634763 | + | Silent | SNP | C | C | T | TCGA-AG-A01W-01A-21W-A096-10 | TCGA-AG-A01W-11A-11W-A096-10 | g.chr10:62634763C>T | c.1764G>A | c.(1762-1764)acG>acA | p.T588T |
READ | 10 | 62648035 | 62648035 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-3602-01A-02W-0833-10 | TCGA-AG-3602-10A-01W-0833-10 | g.chr10:62648035G>A | c.1391C>T | c.(1390-1392)aCg>aTg | p.T464M |
READ | 10 | 62648827 | 62648828 | + | Frame_Shift_Ins | INS | - | - | AC | TCGA-AH-6644-01A-21D-1826-10 | TCGA-AH-6644-10A-01D-1826-10 | g.chr10:62648827_62648828insAC | c.598_599insGT | c.(598-600)tttfs | p.F200fs |
SARC | 10 | 62648024 | 62648024 | + | Missense_Mutation | SNP | G | G | A | TCGA-DX-A8BM-01A-11D-A417-09 | TCGA-DX-A8BM-10B-01D-A41A-09 | g.chr10:62648024G>A | c.1402C>T | c.(1402-1404)Cac>Tac | p.H468Y |
SARC | 10 | 62648444 | 62648444 | + | Missense_Mutation | SNP | C | C | T | TCGA-DX-AB2W-01A-11D-A38Z-09 | TCGA-DX-AB2W-10A-01D-A38Z-09 | g.chr10:62648444C>T | c.982G>A | c.(982-984)Gac>Aac | p.D328N |
SKCM | 10 | 62631393 | 62631393 | + | Silent | SNP | G | G | A | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr10:62631393G>A | c.1938C>T | c.(1936-1938)ttC>ttT | p.F646F |
SKCM | 10 | 62631971 | 62631971 | + | Silent | SNP | G | G | A | TCGA-EE-A29H-06A-12D-A197-08 | TCGA-EE-A29H-10A-01D-A199-08 | g.chr10:62631971G>A | c.1893C>T | c.(1891-1893)ttC>ttT | p.F631F |
SKCM | 10 | 62637807 | 62637807 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AF-06A-11D-A196-08 | TCGA-EE-A3AF-10A-01D-A198-08 | g.chr10:62637807G>A | c.1585C>T | c.(1585-1587)Ccg>Tcg | p.P529S |
SKCM | 10 | 62645910 | 62645910 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29W-06A-11D-A196-08 | TCGA-EE-A29W-10A-01D-A198-08 | g.chr10:62645910G>A | c.1535C>T | c.(1534-1536)gCc>gTc | p.A512V |
SKCM | 10 | 62645964 | 62645964 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A3OT-06A-23D-A23B-08 | TCGA-GF-A3OT-10A-01D-A23B-08 | g.chr10:62645964C>T | c.1481G>A | c.(1480-1482)gGa>gAa | p.G494E |
SKCM | 10 | 62647983 | 62647983 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:62647983C>T | c.1443G>A | c.(1441-1443)aaG>aaA | p.K481K |
SKCM | 10 | 62648351 | 62648351 | + | Silent | SNP | G | G | A | TCGA-DA-A1IC-06A-11D-A197-08 | TCGA-DA-A1IC-10A-01D-A199-08 | g.chr10:62648351G>A | c.1075C>T | c.(1075-1077)Ctg>Ttg | p.L359L |
SKCM | 10 | 62648405 | 62648405 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3C8-06A-12D-A19A-08 | TCGA-D3-A3C8-10A-01D-A19A-08 | g.chr10:62648405G>A | c.1021C>T | c.(1021-1023)Cct>Tct | p.P341S |
SKCM | 10 | 62648613 | 62648613 | + | Silent | SNP | G | G | A | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr10:62648613G>A | c.813C>T | c.(811-813)atC>atT | p.I271I |
SKCM | 10 | 62648700 | 62648700 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:62648700G>A | c.726C>T | c.(724-726)gtC>gtT | p.V242V |
SKCM | 10 | 62652648 | 62652648 | + | Silent | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr10:62652648G>A | c.402C>T | c.(400-402)ccC>ccT | p.P134P |
SKCM | 10 | 62652649 | 62652649 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr10:62652649G>A | c.401C>T | c.(400-402)cCc>cTc | p.P134L |
SKCM | 10 | 62652709 | 62652709 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:62652709G>A | c.341C>T | c.(340-342)tCc>tTc | p.S114F |
SKCM | 10 | 62671279 | 62671279 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29R-06A-11D-A197-08 | TCGA-EE-A29R-10A-01D-A199-08 | g.chr10:62671279C>T | c.22G>A | c.(22-24)Gaa>Aaa | p.E8K |