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 | 4 | 141789490 | 141789490 | + | Silent | SNP | C | C | T | TCGA-ZF-AA4V-01A-11D-A38G-08 | TCGA-ZF-AA4V-10A-01D-A38J-08 | g.chr4:141789490C>T | c.1242G>A | c.(1240-1242)ttG>ttA | p.L414L |
BLCA | 4 | 141832307 | 141832307 | + | Missense_Mutation | SNP | T | T | G | TCGA-G2-A3VY-01A-11D-A22Z-08 | TCGA-G2-A3VY-10A-01D-A22Z-08 | g.chr4:141832307T>G | c.1189A>C | c.(1189-1191)Act>Cct | p.T397P |
BLCA | 4 | 141832393 | 141832393 | + | Missense_Mutation | SNP | G | G | A | TCGA-5N-A9KI-01A-31D-A42E-08 | TCGA-5N-A9KI-10A-01D-A42H-08 | g.chr4:141832393G>A | c.1103C>T | c.(1102-1104)aCt>aTt | p.T368I |
BLCA | 4 | 141870482 | 141870482 | + | Missense_Mutation | SNP | C | C | G | TCGA-ZF-A9RL-01A-11D-A38G-08 | TCGA-ZF-A9RL-10A-01D-A38J-08 | g.chr4:141870482C>G | c.780G>C | c.(778-780)caG>caC | p.Q260H |
BLCA | 4 | 141888843 | 141888843 | + | Silent | SNP | G | G | T | TCGA-DK-A3IK-01A-32D-A21A-08 | TCGA-DK-A3IK-10A-01D-A21A-08 | g.chr4:141888843G>T | c.669C>A | c.(667-669)tcC>tcA | p.S223S |
BLCA | 4 | 141888925 | 141888925 | + | Missense_Mutation | SNP | C | C | T | TCGA-LT-A5Z6-01A-11D-A289-08 | TCGA-LT-A5Z6-10A-01D-A289-08 | g.chr4:141888925C>T | c.587G>A | c.(586-588)gGa>gAa | p.G196E |
BLCA | 4 | 141888947 | 141888947 | + | Missense_Mutation | SNP | C | C | T | TCGA-UY-A9PB-01A-11D-A38G-08 | TCGA-UY-A9PB-10A-01D-A38J-08 | g.chr4:141888947C>T | c.565G>A | c.(565-567)Gtg>Atg | p.V189M |
BLCA | 4 | 142053860 | 142053860 | + | Missense_Mutation | SNP | C | C | T | TCGA-SY-A9G5-01A-11D-A38G-08 | TCGA-SY-A9G5-10A-01D-A38J-08 | g.chr4:142053860C>T | c.103G>A | c.(103-105)Gag>Aag | p.E35K |
BRCA | 4 | 142053860 | 142053860 | + | Missense_Mutation | SNP | C | C | T | TCGA-C8-A3M7-01A-12D-A21Q-09 | TCGA-C8-A3M7-10A-01D-A21Q-09 | g.chr4:142053860C>T | c.103G>A | c.(103-105)Gag>Aag | p.E35K |
CESC | 4 | 142053952 | 142053952 | + | Missense_Mutation | SNP | G | G | A | TCGA-FU-A23K-01A-11D-A16O-08 | TCGA-FU-A23K-10A-01D-A16O-08 | g.chr4:142053952G>A | c.11C>T | c.(10-12)tCt>tTt | p.S4F |
COAD | 4 | 141789415 | 141789415 | + | Nonstop_Mutation | SNP | T | T | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr4:141789415T>G | c.1317A>C | c.(1315-1317)tgA>tgC | p.*439C |
COAD | 4 | 141832470 | 141832470 | + | Silent | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr4:141832470G>A | c.1026C>T | c.(1024-1026)ttC>ttT | p.F342F |
COAD | 4 | 141832470 | 141832470 | + | Silent | SNP | G | G | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr4:141832470G>A | c.1026C>T | c.(1024-1026)ttC>ttT | p.F342F |
COAD | 4 | 141870498 | 141870498 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr4:141870498G>A | c.764C>T | c.(763-765)gCc>gTc | p.A255V |
COAD | 4 | 141888828 | 141888828 | + | Silent | SNP | G | G | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr4:141888828G>T | c.684C>A | c.(682-684)gtC>gtA | p.V228V |
COAD | 4 | 141888889 | 141888889 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr4:141888889G>A | c.623C>T | c.(622-624)tCg>tTg | p.S208L |
COAD | 4 | 141888889 | 141888889 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr4:141888889G>A | c.623C>T | c.(622-624)tCg>tTg | p.S208L |
COAD | 4 | 141888889 | 141888889 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr4:141888889G>A | c.623C>T | c.(622-624)tCg>tTg | p.S208L |
COAD | 4 | 141888889 | 141888889 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr4:141888889G>A | c.623C>T | c.(622-624)tCg>tTg | p.S208L |
COAD | 4 | 141889000 | 141889000 | + | Missense_Mutation | SNP | A | A | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr4:141889000A>T | c.512T>A | c.(511-513)aTt>aAt | p.I171N |
COAD | 4 | 141889014 | 141889014 | + | Silent | SNP | G | G | A | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr4:141889014G>A | c.498C>T | c.(496-498)atC>atT | p.I166I |
COAD | 4 | 142053482 | 142053482 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr4:142053482C>T | c.481G>A | c.(481-483)Gcg>Acg | p.A161T |
COAD | 4 | 142053545 | 142053545 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr4:142053545C>T | c.418G>A | c.(418-420)Gcc>Acc | p.A140T |
COAD | 4 | 142053582 | 142053582 | + | Silent | SNP | C | C | T | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr4:142053582C>T | c.381G>A | c.(379-381)acG>acA | p.T127T |
COAD | 4 | 142053667 | 142053667 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr4:142053667C>T | c.296G>A | c.(295-297)cGc>cAc | p.R99H |
COAD | 4 | 142053774 | 142053774 | + | Silent | SNP | G | G | A | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr4:142053774G>A | c.189C>T | c.(187-189)ggC>ggT | p.G63G |
COADREAD | 4 | 141789415 | 141789415 | + | Nonstop_Mutation | SNP | T | T | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr4:141789415T>G | c.1317A>C | c.(1315-1317)tgA>tgC | p.*439C |
COADREAD | 4 | 141832470 | 141832470 | + | Silent | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr4:141832470G>A | c.1026C>T | c.(1024-1026)ttC>ttT | p.F342F |
COADREAD | 4 | 141832470 | 141832470 | + | Silent | SNP | G | G | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr4:141832470G>A | c.1026C>T | c.(1024-1026)ttC>ttT | p.F342F |
COADREAD | 4 | 141870498 | 141870498 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr4:141870498G>A | c.764C>T | c.(763-765)gCc>gTc | p.A255V |
COADREAD | 4 | 141888805 | 141888805 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:141888805C>T | c.707G>A | c.(706-708)cGa>cAa | p.R236Q |
COADREAD | 4 | 141888828 | 141888828 | + | Silent | SNP | G | G | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr4:141888828G>T | c.684C>A | c.(682-684)gtC>gtA | p.V228V |
COADREAD | 4 | 141888889 | 141888889 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr4:141888889G>A | c.623C>T | c.(622-624)tCg>tTg | p.S208L |
COADREAD | 4 | 141888889 | 141888889 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr4:141888889G>A | c.623C>T | c.(622-624)tCg>tTg | p.S208L |
COADREAD | 4 | 141888889 | 141888889 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr4:141888889G>A | c.623C>T | c.(622-624)tCg>tTg | p.S208L |
COADREAD | 4 | 141888889 | 141888889 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr4:141888889G>A | c.623C>T | c.(622-624)tCg>tTg | p.S208L |
COADREAD | 4 | 141889000 | 141889000 | + | Missense_Mutation | SNP | A | A | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr4:141889000A>T | c.512T>A | c.(511-513)aTt>aAt | p.I171N |
COADREAD | 4 | 141889014 | 141889014 | + | Silent | SNP | G | G | A | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr4:141889014G>A | c.498C>T | c.(496-498)atC>atT | p.I166I |
COADREAD | 4 | 142053482 | 142053482 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr4:142053482C>T | c.481G>A | c.(481-483)Gcg>Acg | p.A161T |
COADREAD | 4 | 142053545 | 142053545 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr4:142053545C>T | c.418G>A | c.(418-420)Gcc>Acc | p.A140T |
COADREAD | 4 | 142053582 | 142053582 | + | Silent | SNP | C | C | T | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr4:142053582C>T | c.381G>A | c.(379-381)acG>acA | p.T127T |
COADREAD | 4 | 142053630 | 142053630 | + | Silent | SNP | C | C | T | TCGA-AH-6544-01A-11D-1826-10 | TCGA-AH-6544-10A-01D-1826-10 | g.chr4:142053630C>T | c.333G>A | c.(331-333)ccG>ccA | p.P111P |
COADREAD | 4 | 142053667 | 142053667 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr4:142053667C>T | c.296G>A | c.(295-297)cGc>cAc | p.R99H |
COADREAD | 4 | 142053774 | 142053774 | + | Silent | SNP | G | G | A | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr4:142053774G>A | c.189C>T | c.(187-189)ggC>ggT | p.G63G |
ESCA | 4 | 141888806 | 141888806 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-2H-A9GI-01A-11D-A37C-09 | TCGA-2H-A9GI-11A-11D-A37F-09 | g.chr4:141888806G>A | c.706C>T | c.(706-708)Cga>Tga | p.R236* |
ESCA | 4 | 142053712 | 142053712 | + | Missense_Mutation | SNP | T | T | C | TCGA-V5-AASW-01A-11D-A403-09 | TCGA-V5-AASW-10A-01D-A403-09 | g.chr4:142053712T>C | c.251A>G | c.(250-252)cAg>cGg | p.Q84R |
ESCA | 4 | 142053867 | 142053867 | + | Silent | SNP | G | G | A | TCGA-L5-A4ON-01A-11D-A27G-09 | TCGA-L5-A4ON-11A-21D-A27G-09 | g.chr4:142053867G>A | c.96C>T | c.(94-96)acC>acT | p.T32T |
GBMLGG | 4 | 141832381 | 141832381 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:141832381G>T | c.1115C>A | c.(1114-1116)gCt>gAt | p.A372D |
GBMLGG | 4 | 141832500 | 141832500 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:141832500G>A | c.996C>T | c.(994-996)gcC>gcT | p.A332A |
GBMLGG | 4 | 141888953 | 141888953 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6405-01A-11D-1705-08 | TCGA-DU-6405-10A-01D-1705-08 | g.chr4:141888953T>C | c.559A>G | c.(559-561)Atc>Gtc | p.I187V |
HNSC | 4 | 141832311 | 141832311 | + | Missense_Mutation | SNP | G | G | C | TCGA-CN-A63U-01A-11D-A30E-08 | TCGA-CN-A63U-10A-01D-A30H-08 | g.chr4:141832311G>C | c.1185C>G | c.(1183-1185)atC>atG | p.I395M |
HNSC | 4 | 141847144 | 141847144 | + | Missense_Mutation | SNP | G | G | T | TCGA-CV-7245-01A-11D-2012-08 | TCGA-CV-7245-10A-01D-2013-08 | g.chr4:141847144G>T | c.974C>A | c.(973-975)gCc>gAc | p.A325D |
HNSC | 4 | 141868813 | 141868813 | + | Silent | SNP | G | G | T | TCGA-CR-7364-01A-11D-2012-08 | TCGA-CR-7364-10A-01D-2013-08 | g.chr4:141868813G>T | c.885C>A | c.(883-885)ccC>ccA | p.P295P |
HNSC | 4 | 141888838 | 141888838 | + | Missense_Mutation | SNP | G | G | T | TCGA-CN-A49A-01A-11D-A24D-08 | TCGA-CN-A49A-10A-01D-A24F-08 | g.chr4:141888838G>T | c.674C>A | c.(673-675)gCa>gAa | p.A225E |
HNSC | 4 | 142053645 | 142053645 | + | Silent | SNP | G | G | T | TCGA-BA-6869-01A-11D-1870-08 | TCGA-BA-6869-10A-01D-1870-08 | g.chr4:142053645G>T | c.318C>A | c.(316-318)acC>acA | p.T106T |
HNSC | 4 | 142053860 | 142053860 | + | Missense_Mutation | SNP | C | C | G | TCGA-CR-6481-01A-11D-1870-08 | TCGA-CR-6481-10A-01D-1870-08 | g.chr4:142053860C>G | c.103G>C | c.(103-105)Gag>Cag | p.E35Q |
KIPAN | 4 | 141832440 | 141832440 | + | Missense_Mutation | SNP | G | G | C | TCGA-G7-6796-01A-11D-1961-08 | TCGA-G7-6796-10A-01D-1962-08 | g.chr4:141832440G>C | c.1056C>G | c.(1054-1056)aaC>aaG | p.N352K |
KIPAN | 4 | 141868823 | 141868823 | + | Missense_Mutation | SNP | C | C | T | TCGA-WN-AB4C-01A-11D-A42J-10 | TCGA-WN-AB4C-10A-01D-A42M-10 | g.chr4:141868823C>T | c.875G>A | c.(874-876)cGg>cAg | p.R292Q |
KIRP | 4 | 141832440 | 141832440 | + | Missense_Mutation | SNP | G | G | C | TCGA-G7-6796-01A-11D-1961-08 | TCGA-G7-6796-10A-01D-1962-08 | g.chr4:141832440G>C | c.1056C>G | c.(1054-1056)aaC>aaG | p.N352K |
KIRP | 4 | 141868823 | 141868823 | + | Missense_Mutation | SNP | C | C | T | TCGA-WN-AB4C-01A-11D-A42J-10 | TCGA-WN-AB4C-10A-01D-A42M-10 | g.chr4:141868823C>T | c.875G>A | c.(874-876)cGg>cAg | p.R292Q |
LGG | 4 | 141832381 | 141832381 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:141832381G>T | c.1115C>A | c.(1114-1116)gCt>gAt | p.A372D |
LGG | 4 | 141832500 | 141832500 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:141832500G>A | c.996C>T | c.(994-996)gcC>gcT | p.A332A |
LGG | 4 | 141888953 | 141888953 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6405-01A-11D-1705-08 | TCGA-DU-6405-10A-01D-1705-08 | g.chr4:141888953T>C | c.559A>G | c.(559-561)Atc>Gtc | p.I187V |
LIHC | 4 | 141868832 | 141868832 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-A39Y-01A-11D-A20W-10 | TCGA-DD-A39Y-11A-11D-A20W-10 | g.chr4:141868832T>C | c.866A>G | c.(865-867)gAc>gGc | p.D289G |
LIHC | 4 | 141888829 | 141888829 | + | Missense_Mutation | SNP | A | A | G | TCGA-CC-A3MB-01A-11D-A20W-10 | TCGA-CC-A3MB-10A-01D-A20W-10 | g.chr4:141888829A>G | c.683T>C | c.(682-684)gTc>gCc | p.V228A |
LIHC | 4 | 141888999 | 141888999 | + | Silent | SNP | A | A | G | TCGA-CC-A7IJ-01A-11D-A33Q-10 | TCGA-CC-A7IJ-10A-01D-A33Q-10 | g.chr4:141888999A>G | c.513T>C | c.(511-513)atT>atC | p.I171I |
LUAD | 4 | 141789440 | 141789440 | + | Missense_Mutation | SNP | T | T | G | TCGA-17-Z014-01A-01W-0746-08 | TCGA-17-Z014-11A-01W-0746-08 | g.chr4:141789440T>G | c.1292A>C | c.(1291-1293)cAg>cCg | p.Q431P |
LUAD | 4 | 141789444 | 141789444 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-6590-01A-12D-1855-08 | TCGA-50-6590-11A-01D-1855-08 | g.chr4:141789444C>A | c.1288G>T | c.(1288-1290)Gac>Tac | p.D430Y |
LUAD | 4 | 141789475 | 141789475 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-8120-01A-11D-2238-08 | TCGA-44-8120-10A-01D-2238-08 | g.chr4:141789475C>A | c.1257G>T | c.(1255-1257)gaG>gaT | p.E419D |
LUAD | 4 | 141832458 | 141832458 | + | Silent | SNP | C | C | A | TCGA-97-7546-01A-11D-2036-08 | TCGA-97-7546-10A-01D-2036-08 | g.chr4:141832458C>A | c.1038G>T | c.(1036-1038)ctG>ctT | p.L346L |
LUAD | 4 | 141847164 | 141847164 | + | Silent | SNP | G | G | A | TCGA-86-7711-01A-11D-2063-08 | TCGA-86-7711-10A-01D-2063-08 | g.chr4:141847164G>A | c.954C>T | c.(952-954)tgC>tgT | p.C318C |
LUAD | 4 | 141847205 | 141847205 | + | Missense_Mutation | SNP | C | C | G | TCGA-99-8028-01A-11D-2238-08 | TCGA-99-8028-10A-01D-2238-08 | g.chr4:141847205C>G | c.913G>C | c.(913-915)Gtt>Ctt | p.V305L |
LUAD | 4 | 141847210 | 141847210 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-7907-01A-11D-2167-08 | TCGA-55-7907-10A-01D-2167-08 | g.chr4:141847210G>T | c.908C>A | c.(907-909)tCc>tAc | p.S303Y |
LUAD | 4 | 141888788 | 141888788 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-7670-01A-11D-2063-08 | TCGA-44-7670-10A-01D-2063-08 | g.chr4:141888788C>A | c.724G>T | c.(724-726)Gat>Tat | p.D242Y |
LUAD | 4 | 141888915 | 141888915 | + | Missense_Mutation | SNP | G | G | T | TCGA-75-5122-01A-01D-1753-08 | TCGA-75-5122-10A-01D-1753-08 | g.chr4:141888915G>T | c.597C>A | c.(595-597)aaC>aaA | p.N199K |
LUAD | 4 | 141888968 | 141888968 | + | Missense_Mutation | SNP | G | G | T | TCGA-91-A4BC-01A-11D-A24D-08 | TCGA-91-A4BC-10A-01D-A24F-08 | g.chr4:141888968G>T | c.544C>A | c.(544-546)Ctg>Atg | p.L182M |
LUAD | 4 | 141889013 | 141889013 | + | Missense_Mutation | SNP | C | C | T | TCGA-73-4670-01A-01D-1265-08 | TCGA-73-4670-11A-01D-1265-08 | g.chr4:141889013C>T | c.499G>A | c.(499-501)Gtg>Atg | p.V167M |
LUSC | 4 | 141888789 | 141888789 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2727-01A-01D-0983-08 | TCGA-66-2727-11A-01D-0983-08 | g.chr4:141888789C>G | c.723G>C | c.(721-723)agG>agC | p.R241S |
OV | 4 | 141889014 | 141889014 | + | Silent | SNP | G | G | A | TCGA-20-0991-01A-03D-0428-08 | TCGA-20-0991-10A-01D-0428-08 | g.chr4:141889014G>A | c.498C>T | c.(496-498)atC>atT | p.I166I |
READ | 4 | 141888805 | 141888805 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:141888805C>T | c.707G>A | c.(706-708)cGa>cAa | p.R236Q |
READ | 4 | 142053630 | 142053630 | + | Silent | SNP | C | C | T | TCGA-AH-6544-01A-11D-1826-10 | TCGA-AH-6544-10A-01D-1826-10 | g.chr4:142053630C>T | c.333G>A | c.(331-333)ccG>ccA | p.P111P |
SARC | 4 | 141847187 | 141847187 | + | Missense_Mutation | SNP | C | C | A | TCGA-QQ-A8VG-01A-11D-A37C-09 | TCGA-QQ-A8VG-10A-01D-A37F-09 | g.chr4:141847187C>A | c.931G>T | c.(931-933)Gac>Tac | p.D311Y |
SARC | 4 | 141888986 | 141888986 | + | Missense_Mutation | SNP | C | C | T | TCGA-QC-A6FX-01A-11D-A32I-09 | TCGA-QC-A6FX-10B-01D-A32I-09 | g.chr4:141888986C>T | c.526G>A | c.(526-528)Ggg>Agg | p.G176R |
SKCM | 4 | 141789438 | 141789438 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A17X-06A-11D-A197-08 | TCGA-EE-A17X-10A-01D-A199-08 | g.chr4:141789438C>T | c.1294G>A | c.(1294-1296)Gac>Aac | p.D432N |
SKCM | 4 | 141789475 | 141789475 | + | Silent | SNP | C | C | T | TCGA-EB-A5SG-06A-11D-A30X-08 | TCGA-EB-A5SG-10A-01D-A30X-08 | g.chr4:141789475C>T | c.1257G>A | c.(1255-1257)gaG>gaA | p.E419E |
SKCM | 4 | 141847198 | 141847198 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr4:141847198G>A | c.920C>T | c.(919-921)cCc>cTc | p.P307L |
SKCM | 4 | 141888811 | 141888811 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr4:141888811C>T | c.701G>A | c.(700-702)aGg>aAg | p.R234K |
SKCM | 4 | 141888920 | 141888920 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr4:141888920G>A | c.592C>T | c.(592-594)Cgg>Tgg | p.R198W |
SKCM | 4 | 141888927 | 141888927 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr4:141888927G>A | c.585C>T | c.(583-585)atC>atT | p.I195I |
SKCM | 4 | 141889002 | 141889002 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr4:141889002C>T | c.510G>A | c.(508-510)atG>atA | p.M170I |
SKCM | 4 | 141889002 | 141889002 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr4:141889002C>T | c.510G>A | c.(508-510)atG>atA | p.M170I |
SKCM | 4 | 141889014 | 141889014 | + | Silent | SNP | G | G | A | TCGA-QB-A6FS-06A-11D-A30X-08 | TCGA-QB-A6FS-10A-01D-A30X-08 | g.chr4:141889014G>A | c.498C>T | c.(496-498)atC>atT | p.I166I |
SKCM | 4 | 142053480 | 142053480 | + | Splice_Site | SNP | C | C | T | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr4:142053480C>T | c.483G>A | c.(481-483)gcG>gcA | p.A161A |
SKCM | 4 | 142053555 | 142053555 | + | Silent | SNP | G | G | A | TCGA-EE-A3JI-06A-11D-A21A-08 | TCGA-EE-A3JI-10A-01D-A21A-08 | g.chr4:142053555G>A | c.408C>T | c.(406-408)ttC>ttT | p.F136F |
SKCM | 4 | 142053624 | 142053624 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZT-06A-11D-A197-08 | TCGA-FS-A1ZT-10A-01D-A199-08 | g.chr4:142053624G>A | c.339C>T | c.(337-339)cgC>cgT | p.R113R |
SKCM | 4 | 142053641 | 142053641 | + | Missense_Mutation | SNP | A | A | G | TCGA-FS-A4FD-06A-11D-A25O-08 | TCGA-FS-A4FD-10B-01D-A25O-08 | g.chr4:142053641A>G | c.322T>C | c.(322-324)Ttc>Ctc | p.F108L |