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 | 5 | 107216802 | 107216802 | + | Missense_Mutation | SNP | C | C | T | TCGA-G2-A2EJ-01A-11D-A17V-08 | TCGA-G2-A2EJ-10A-01D-A17V-08 | g.chr5:107216802C>T | c.1901G>A | c.(1900-1902)gGa>gAa | p.G634E |
BLCA | 5 | 107521822 | 107521822 | + | Missense_Mutation | SNP | C | C | G | TCGA-4Z-AA89-01A-11D-A391-08 | TCGA-4Z-AA89-10A-01D-A394-08 | g.chr5:107521822C>G | c.1741G>C | c.(1741-1743)Gac>Cac | p.D581H |
BLCA | 5 | 107521822 | 107521822 | + | Missense_Mutation | SNP | C | C | T | TCGA-G2-A2EO-01A-11D-A17V-08 | TCGA-G2-A2EO-11A-21D-A17V-08 | g.chr5:107521822C>T | c.1741G>A | c.(1741-1743)Gac>Aac | p.D581N |
BLCA | 5 | 107559915 | 107559915 | + | Silent | SNP | T | T | C | TCGA-FD-A3SR-01A-11D-A22Z-08 | TCGA-FD-A3SR-10A-01D-A22Z-08 | g.chr5:107559915T>C | c.1521A>G | c.(1519-1521)tcA>tcG | p.S507S |
BRCA | 5 | 107216824 | 107216824 | + | Missense_Mutation | SNP | A | A | G | TCGA-E9-A1R2-01A-11D-A14G-09 | TCGA-E9-A1R2-10A-01D-A14G-09 | g.chr5:107216824A>G | c.1879T>C | c.(1879-1881)Tgt>Cgt | p.C627R |
BRCA | 5 | 107216863 | 107216863 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-E2-A15A-01A-11D-A12B-09 | TCGA-E2-A15A-10A-01D-A12B-09 | g.chr5:107216863G>A | c.1840C>T | c.(1840-1842)Cga>Tga | p.R614* |
BRCA | 5 | 107559823 | 107559823 | + | Splice_Site | SNP | T | T | A | TCGA-C8-A12L-01A-11D-A10Y-09 | TCGA-C8-A12L-10A-01D-A110-09 | g.chr5:107559823T>A | c.1613A>T | c.(1612-1614)aAg>aTg | p.K538M |
COAD | 5 | 107197434 | 107197434 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr5:107197434G>A | c.2093C>T | c.(2092-2094)gCc>gTc | p.A698V |
COAD | 5 | 107197437 | 107197437 | + | Missense_Mutation | SNP | G | G | C | TCGA-AA-A01Q-01A-01W-A005-10 | TCGA-AA-A01Q-10A-01W-A005-10 | g.chr5:107197437G>C | c.2090C>G | c.(2089-2091)tCt>tGt | p.S697C |
COAD | 5 | 107197555 | 107197555 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr5:107197555C>T | c.1972G>A | c.(1972-1974)Gaa>Aaa | p.E658K |
COAD | 5 | 107521847 | 107521847 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr5:107521847A>C | c.1716T>G | c.(1714-1716)aaT>aaG | p.N572K |
COADREAD | 5 | 107197434 | 107197434 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr5:107197434G>A | c.2093C>T | c.(2092-2094)gCc>gTc | p.A698V |
COADREAD | 5 | 107197437 | 107197437 | + | Missense_Mutation | SNP | G | G | C | TCGA-AA-A01Q-01A-01W-A005-10 | TCGA-AA-A01Q-10A-01W-A005-10 | g.chr5:107197437G>C | c.2090C>G | c.(2089-2091)tCt>tGt | p.S697C |
COADREAD | 5 | 107197555 | 107197555 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr5:107197555C>T | c.1972G>A | c.(1972-1974)Gaa>Aaa | p.E658K |
COADREAD | 5 | 107521847 | 107521847 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr5:107521847A>C | c.1716T>G | c.(1714-1716)aaT>aaG | p.N572K |
COADREAD | 5 | 107521861 | 107521861 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr5:107521861G>T | c.1702C>A | c.(1702-1704)Ctt>Att | p.L568I |
ESCA | 5 | 107521860 | 107521860 | + | Missense_Mutation | SNP | A | A | C | TCGA-L5-A8NL-01A-12D-A37C-09 | TCGA-L5-A8NL-11A-12D-A37F-09 | g.chr5:107521860A>C | c.1703T>G | c.(1702-1704)cTt>cGt | p.L568R |
ESCA | 5 | 107703648 | 107703648 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-IC-A6RE-01A-11D-A33E-09 | TCGA-IC-A6RE-10A-01D-A33H-09 | g.chr5:107703648delA | c.1000delT | c.(1000-1002)tccfs | p.S334fs |
GBM | 5 | 107684192 | 107684192 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-5858-01A-01D-1696-08 | TCGA-06-5858-10A-01D-1696-08 | g.chr5:107684192C>T | c.1414G>A | c.(1414-1416)Ggc>Agc | p.G472S |
GBMLGG | 5 | 107197443 | 107197443 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-8167-01A-11D-2253-08 | TCGA-DU-8167-10A-01D-2253-08 | g.chr5:107197443T>C | c.2084A>G | c.(2083-2085)aAc>aGc | p.N695S |
GBMLGG | 5 | 107684192 | 107684192 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-5858-01A-01D-1696-08 | TCGA-06-5858-10A-01D-1696-08 | g.chr5:107684192C>T | c.1414G>A | c.(1414-1416)Ggc>Agc | p.G472S |
HNSC | 5 | 107216852 | 107216852 | + | Missense_Mutation | SNP | C | C | A | TCGA-BA-A4II-01A-11D-A25Y-08 | TCGA-BA-A4II-10A-01D-A25Y-08 | g.chr5:107216852C>A | c.1851G>T | c.(1849-1851)atG>atT | p.M617I |
HNSC | 5 | 107700445 | 107700445 | + | Silent | SNP | G | G | C | TCGA-CV-7427-01A-11D-2078-08 | TCGA-CV-7427-10A-01D-2078-08 | g.chr5:107700445G>C | c.1368C>G | c.(1366-1368)ctC>ctG | p.L456L |
KICH | 5 | 107700539 | 107700539 | + | Missense_Mutation | SNP | A | A | G | TCGA-KL-8324-01A-11D-2310-10 | TCGA-KL-8324-11A-01D-2310-10 | g.chr5:107700539A>G | c.1274T>C | c.(1273-1275)cTt>cCt | p.L425P |
KIPAN | 5 | 107700539 | 107700539 | + | Missense_Mutation | SNP | A | A | G | TCGA-KL-8324-01A-11D-2310-10 | TCGA-KL-8324-11A-01D-2310-10 | g.chr5:107700539A>G | c.1274T>C | c.(1273-1275)cTt>cCt | p.L425P |
KIPAN | 5 | 107700635 | 107700635 | + | Missense_Mutation | SNP | A | A | T | TCGA-O9-A75Z-01A-11D-A33Q-10 | TCGA-O9-A75Z-10A-01D-A33Q-10 | g.chr5:107700635A>T | c.1178T>A | c.(1177-1179)aTt>aAt | p.I393N |
KIPAN | 5 | 107703606 | 107703606 | + | Missense_Mutation | SNP | C | C | G | TCGA-B0-5693-01A-11D-1534-10 | TCGA-B0-5693-11A-01D-1534-10 | g.chr5:107703606C>G | c.1042G>C | c.(1042-1044)Gtt>Ctt | p.V348L |
KIRC | 5 | 107703606 | 107703606 | + | Missense_Mutation | SNP | C | C | G | TCGA-B0-5693-01A-11D-1534-10 | TCGA-B0-5693-11A-01D-1534-10 | g.chr5:107703606C>G | c.1042G>C | c.(1042-1044)Gtt>Ctt | p.V348L |
KIRP | 5 | 107700635 | 107700635 | + | Missense_Mutation | SNP | A | A | T | TCGA-O9-A75Z-01A-11D-A33Q-10 | TCGA-O9-A75Z-10A-01D-A33Q-10 | g.chr5:107700635A>T | c.1178T>A | c.(1177-1179)aTt>aAt | p.I393N |
LGG | 5 | 107197443 | 107197443 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-8167-01A-11D-2253-08 | TCGA-DU-8167-10A-01D-2253-08 | g.chr5:107197443T>C | c.2084A>G | c.(2083-2085)aAc>aGc | p.N695S |
LIHC | 5 | 107356642 | 107356642 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-DD-AADF-01A-11D-A40R-10 | TCGA-DD-AADF-10A-01D-A40U-10 | g.chr5:107356642A>T | c.1806T>A | c.(1804-1806)tgT>tgA | p.C602* |
LUAD | 5 | 107197455 | 107197455 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr5:107197455C>A | c.2072G>T | c.(2071-2073)gGc>gTc | p.G691V |
LUAD | 5 | 107216863 | 107216863 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-17-Z057-01A-01W-0747-08 | TCGA-17-Z057-11A-01W-0747-08 | g.chr5:107216863G>A | c.1840C>T | c.(1840-1842)Cga>Tga | p.R614* |
LUAD | 5 | 107559923 | 107559923 | + | Missense_Mutation | SNP | C | C | A | TCGA-53-7626-01A-12D-2063-08 | TCGA-53-7626-10A-01D-2063-08 | g.chr5:107559923C>A | c.1513G>T | c.(1513-1515)Gat>Tat | p.D505Y |
LUAD | 5 | 107684233 | 107684233 | + | Splice_Site | SNP | T | T | C | TCGA-MP-A4SV-01A-11D-A24P-08 | TCGA-MP-A4SV-10A-01D-A24P-08 | g.chr5:107684233T>C | | c.e4-2 | |
LUAD | 5 | 107700563 | 107700563 | + | Missense_Mutation | SNP | T | T | C | TCGA-95-7562-01A-11D-2238-08 | TCGA-95-7562-10B-01D-2238-08 | g.chr5:107700563T>C | c.1250A>G | c.(1249-1251)tAt>tGt | p.Y417C |
LUAD | 5 | 107700656 | 107700656 | + | Missense_Mutation | SNP | T | T | C | TCGA-73-4676-01A-01D-1753-08 | TCGA-73-4676-11A-01D-1753-08 | g.chr5:107700656T>C | c.1157A>G | c.(1156-1158)cAg>cGg | p.Q386R |
LUAD | 5 | 107700679 | 107700679 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-7995-01A-11D-2184-08 | TCGA-55-7995-10A-01D-2184-08 | g.chr5:107700679C>A | c.1134G>T | c.(1132-1134)ttG>ttT | p.L378F |
LUSC | 5 | 107521909 | 107521909 | + | Missense_Mutation | SNP | C | C | T | TCGA-18-4086-01A-01D-1352-08 | TCGA-18-4086-11A-01D-1352-08 | g.chr5:107521909C>T | c.1654G>A | c.(1654-1656)Gaa>Aaa | p.E552K |
PAAD | 5 | 107216798 | 107216798 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr5:107216798G>A | c.1905C>T | c.(1903-1905)gcC>gcT | p.A635A |
PAAD | 5 | 107559841 | 107559841 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr5:107559841C>T | c.1595G>A | c.(1594-1596)gGa>gAa | p.G532E |
PRAD | 5 | 107216868 | 107216868 | + | Missense_Mutation | SNP | A | A | G | TCGA-G9-6351-01A-21D-1961-08 | TCGA-G9-6351-10A-01D-1961-08 | g.chr5:107216868A>G | c.1835T>C | c.(1834-1836)aTt>aCt | p.I612T |
PRAD | 5 | 107356650 | 107356650 | + | Missense_Mutation | SNP | C | C | T | TCGA-KK-A7AQ-01A-11D-A33T-08 | TCGA-KK-A7AQ-11A-11D-A33W-08 | g.chr5:107356650C>T | c.1798G>A | c.(1798-1800)Gtg>Atg | p.V600M |
PRAD | 5 | 107700657 | 107700657 | + | Missense_Mutation | SNP | G | G | T | TCGA-ZG-A9L2-01A-31D-A41K-08 | TCGA-ZG-A9L2-10A-01D-A41N-08 | g.chr5:107700657G>T | c.1156C>A | c.(1156-1158)Cag>Aag | p.Q386K |
READ | 5 | 107521861 | 107521861 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr5:107521861G>T | c.1702C>A | c.(1702-1704)Ctt>Att | p.L568I |
SKCM | 5 | 107197446 | 107197446 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A199-06A-11D-A197-08 | TCGA-ER-A199-10A-01D-A199-08 | g.chr5:107197446G>A | c.2081C>T | c.(2080-2082)cCc>cTc | p.P694L |
SKCM | 5 | 107216802 | 107216802 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A51T-06A-11D-A25O-08 | TCGA-D3-A51T-10A-01D-A25O-08 | g.chr5:107216802C>T | c.1901G>A | c.(1900-1902)gGa>gAa | p.G634E |
SKCM | 5 | 107216803 | 107216803 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A51T-06A-11D-A25O-08 | TCGA-D3-A51T-10A-01D-A25O-08 | g.chr5:107216803C>T | c.1900G>A | c.(1900-1902)Gga>Aga | p.G634R |