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 |
ACC | 19 | 16859997 | 16859997 | + | Missense_Mutation | SNP | G | G | A | TCGA-OR-A5L9-01A-11D-A29I-10 | TCGA-OR-A5L9-10B-01D-A29L-10 | g.chr19:16859997G>A | c.544G>A | c.(544-546)Gaa>Aaa | p.E182K |
ACC | 19 | 16861150 | 16861150 | + | Missense_Mutation | SNP | T | T | A | TCGA-OR-A5L1-01A-11D-A30A-10 | TCGA-OR-A5L1-10A-01D-A30A-10 | g.chr19:16861150T>A | c.1697T>A | c.(1696-1698)cTc>cAc | p.L566H |
BLCA | 19 | 16860125 | 16860125 | + | Silent | SNP | C | C | G | TCGA-DK-A3IT-01A-31D-A20D-08 | TCGA-DK-A3IT-10A-01D-A20D-08 | g.chr19:16860125C>G | c.672C>G | c.(670-672)ctC>ctG | p.L224L |
BLCA | 19 | 16860125 | 16860125 | + | Silent | SNP | C | C | T | TCGA-BT-A20J-01A-11D-A14W-08 | TCGA-BT-A20J-11A-11D-A14W-08 | g.chr19:16860125C>T | c.672C>T | c.(670-672)ctC>ctT | p.L224L |
BLCA | 19 | 16860181 | 16860181 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-A9RE-01A-11D-A38G-08 | TCGA-ZF-A9RE-10A-01D-A38J-08 | g.chr19:16860181G>A | c.728G>A | c.(727-729)cGc>cAc | p.R243H |
BLCA | 19 | 16860863 | 16860863 | + | Silent | SNP | G | G | A | TCGA-BT-A42B-01A-32D-A23M-08 | TCGA-BT-A42B-10A-01D-A23K-08 | g.chr19:16860863G>A | c.1410G>A | c.(1408-1410)tcG>tcA | p.S470S |
BLCA | 19 | 16870082 | 16870082 | + | Missense_Mutation | SNP | G | G | T | TCGA-G2-AA3B-01A-11D-A391-08 | TCGA-G2-AA3B-10A-01D-A394-08 | g.chr19:16870082G>T | c.1816G>T | c.(1816-1818)Gac>Tac | p.D606Y |
BLCA | 19 | 16872917 | 16872917 | + | Missense_Mutation | SNP | C | C | G | TCGA-ZF-AA4N-01A-11D-A38G-08 | TCGA-ZF-AA4N-10A-01D-A38J-08 | g.chr19:16872917C>G | c.2101C>G | c.(2101-2103)Ctt>Gtt | p.L701V |
BLCA | 19 | 16899841 | 16899841 | + | Missense_Mutation | SNP | C | C | G | TCGA-4Z-AA7W-01A-11D-A391-08 | TCGA-4Z-AA7W-10A-01D-A394-08 | g.chr19:16899841C>G | c.2780C>G | c.(2779-2781)tCt>tGt | p.S927C |
BLCA | 19 | 16902160 | 16902160 | + | Splice_Site | SNP | G | G | C | TCGA-CU-A3YL-01A-11D-A22Z-08 | TCGA-CU-A3YL-10A-01D-A22Z-08 | g.chr19:16902160G>C | | c.e12-1 | |
BLCA | 19 | 16902336 | 16902336 | + | Missense_Mutation | SNP | A | A | G | TCGA-BT-A42E-01A-11D-A23U-08 | TCGA-BT-A42E-10A-01D-A23U-08 | g.chr19:16902336A>G | c.3116A>G | c.(3115-3117)cAt>cGt | p.H1039R |
BLCA | 19 | 16908608 | 16908608 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A3IU-01A-11D-A20D-08 | TCGA-DK-A3IU-10A-01D-A20D-08 | g.chr19:16908608G>A | c.3370G>A | c.(3370-3372)Gat>Aat | p.D1124N |
BLCA | 19 | 16910728 | 16910728 | + | Missense_Mutation | SNP | T | T | C | TCGA-UY-A78K-01A-11D-A339-08 | TCGA-UY-A78K-10A-01D-A339-08 | g.chr19:16910728T>C | c.3491T>C | c.(3490-3492)cTg>cCg | p.L1164P |
BLCA | 19 | 16910736 | 16910736 | + | Silent | SNP | C | C | T | TCGA-4Z-AA7M-01A-11D-A391-08 | TCGA-4Z-AA7M-10A-01D-A394-08 | g.chr19:16910736C>T | c.3499C>T | c.(3499-3501)Ctg>Ttg | p.L1167L |
BLCA | 19 | 16918475 | 16918475 | + | Missense_Mutation | SNP | C | C | T | TCGA-UY-A9PD-01A-11D-A38G-08 | TCGA-UY-A9PD-10A-01D-A38J-08 | g.chr19:16918475C>T | c.3815C>T | c.(3814-3816)aCg>aTg | p.T1272M |
BLCA | 19 | 16918490 | 16918490 | + | Missense_Mutation | SNP | G | G | A | TCGA-G2-A2EL-01A-12D-A18F-08 | TCGA-G2-A2EL-10A-01D-A18F-08 | g.chr19:16918490G>A | c.3830G>A | c.(3829-3831)gGg>gAg | p.G1277E |
BLCA | 19 | 16918496 | 16918496 | + | Missense_Mutation | SNP | T | T | C | TCGA-K4-A6FZ-01A-11D-A31L-08 | TCGA-K4-A6FZ-10A-01D-A31J-08 | g.chr19:16918496T>C | c.3836T>C | c.(3835-3837)gTc>gCc | p.V1279A |
BLCA | 19 | 16918561 | 16918561 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr19:16918561G>A | c.3901G>A | c.(3901-3903)Gca>Aca | p.A1301T |
BLCA | 19 | 16918749 | 16918749 | + | Silent | SNP | C | C | G | TCGA-2F-A9KW-01A-11D-A38G-08 | TCGA-2F-A9KW-10A-01D-A38J-08 | g.chr19:16918749C>G | c.4089C>G | c.(4087-4089)gtC>gtG | p.V1363V |
BLCA | 19 | 16925938 | 16925938 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-AAN0-01A-11D-A42E-08 | TCGA-XF-AAN0-10A-01D-A42H-08 | g.chr19:16925938G>A | c.4493G>A | c.(4492-4494)cGa>cAa | p.R1498Q |
BRCA | 19 | 16860188 | 16860188 | + | Silent | SNP | G | G | A | TCGA-AN-A0XR-01A-11D-A10G-09 | TCGA-AN-A0XR-10A-01D-A117-09 | g.chr19:16860188G>A | c.735G>A | c.(733-735)ccG>ccA | p.P245P |
BRCA | 19 | 16860225 | 16860225 | + | Missense_Mutation | SNP | C | C | G | TCGA-D8-A1J9-01A-11D-A13L-09 | TCGA-D8-A1J9-10A-01D-A13O-09 | g.chr19:16860225C>G | c.772C>G | c.(772-774)Cac>Gac | p.H258D |
BRCA | 19 | 16860392 | 16860392 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-LL-A5YP-01A-21D-A28B-09 | TCGA-LL-A5YP-10A-01D-A28E-09 | g.chr19:16860392C>A | c.939C>A | c.(937-939)tgC>tgA | p.C313* |
BRCA | 19 | 16860608 | 16860608 | + | Silent | SNP | G | G | T | TCGA-AN-A0FW-01A-11W-A050-09 | TCGA-AN-A0FW-10A-01W-A055-09 | g.chr19:16860608G>T | c.1155G>T | c.(1153-1155)ctG>ctT | p.L385L |
BRCA | 19 | 16861091 | 16861091 | + | Missense_Mutation | SNP | G | G | T | TCGA-LL-A5YP-01A-21D-A28B-09 | TCGA-LL-A5YP-10A-01D-A28E-09 | g.chr19:16861091G>T | c.1638G>T | c.(1636-1638)tgG>tgT | p.W546C |
BRCA | 19 | 16870120 | 16870120 | + | Silent | SNP | G | G | A | TCGA-AO-A0J2-01A-11W-A050-09 | TCGA-AO-A0J2-10A-01W-A055-09 | g.chr19:16870120G>A | c.1854G>A | c.(1852-1854)ccG>ccA | p.P618P |
BRCA | 19 | 16870217 | 16870217 | + | Missense_Mutation | SNP | A | A | C | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr19:16870217A>C | c.1951A>C | c.(1951-1953)Acc>Ccc | p.T651P |
BRCA | 19 | 16872911 | 16872911 | + | Silent | SNP | C | C | T | TCGA-D8-A27V-01A-12D-A17D-09 | TCGA-D8-A27V-10A-01D-A17D-09 | g.chr19:16872911C>T | c.2095C>T | c.(2095-2097)Ctg>Ttg | p.L699L |
BRCA | 19 | 16874756 | 16874756 | + | Splice_Site | SNP | G | G | C | TCGA-BH-A0BZ-01A-31D-A12Q-09 | TCGA-BH-A0BZ-11A-61D-A12Q-09 | g.chr19:16874756G>C | c.2251G>C | c.(2251-2253)Ggc>Cgc | p.G751R |
BRCA | 19 | 16902312 | 16902312 | + | Missense_Mutation | SNP | C | C | T | TCGA-A8-A06O-01A-11W-A019-09 | TCGA-A8-A06O-10A-01W-A021-09 | g.chr19:16902312C>T | c.3092C>T | c.(3091-3093)aCg>aTg | p.T1031M |
BRCA | 19 | 16902356 | 16902356 | + | Missense_Mutation | SNP | G | G | C | TCGA-PE-A5DE-01A-11D-A27P-09 | TCGA-PE-A5DE-10A-01D-A27P-09 | g.chr19:16902356G>C | c.3136G>C | c.(3136-3138)Gaa>Caa | p.E1046Q |
BRCA | 19 | 16908579 | 16908579 | + | Missense_Mutation | SNP | C | C | T | TCGA-E9-A54X-01A-11D-A25Q-09 | TCGA-E9-A54X-10A-01D-A25Q-09 | g.chr19:16908579C>T | c.3341C>T | c.(3340-3342)tCg>tTg | p.S1114L |
BRCA | 19 | 16918863 | 16918863 | + | Missense_Mutation | SNP | G | G | C | TCGA-HN-A2NL-01A-11D-A18P-09 | TCGA-HN-A2NL-10A-01D-A18P-09 | g.chr19:16918863G>C | c.4203G>C | c.(4201-4203)caG>caC | p.Q1401H |
BRCA | 19 | 16918910 | 16918910 | + | Missense_Mutation | SNP | T | T | C | TCGA-AR-A1AQ-01A-11D-A12Q-09 | TCGA-AR-A1AQ-10A-01D-A12Q-09 | g.chr19:16918910T>C | c.4250T>C | c.(4249-4251)cTg>cCg | p.L1417P |
BRCA | 19 | 16923622 | 16923622 | + | Missense_Mutation | SNP | T | T | A | TCGA-B6-A400-01A-11D-A23C-09 | TCGA-B6-A400-10A-01D-A23C-09 | g.chr19:16923622T>A | c.4354T>A | c.(4354-4356)Tta>Ata | p.L1452I |
BRCA | 19 | 16926010 | 16926010 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-A7-A26F-01A-21D-A167-09 | TCGA-A7-A26F-10A-01D-A167-09 | g.chr19:16926010G>A | c.4565G>A | c.(4564-4566)tGg>tAg | p.W1522* |
CESC | 19 | 16860666 | 16860666 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-IR-A3LH-01A-21D-A20U-09 | TCGA-IR-A3LH-10A-01D-A20U-09 | g.chr19:16860666C>T | c.1213C>T | c.(1213-1215)Cag>Tag | p.Q405* |
CESC | 19 | 16861134 | 16861134 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr19:16861134G>T | c.1681G>T | c.(1681-1683)Gaa>Taa | p.E561* |
CESC | 19 | 16870140 | 16870140 | + | Missense_Mutation | SNP | G | G | A | TCGA-Q1-A73R-01A-11D-A33O-09 | TCGA-Q1-A73R-10B-01D-A33O-09 | g.chr19:16870140G>A | c.1874G>A | c.(1873-1875)cGc>cAc | p.R625H |
CESC | 19 | 16872844 | 16872844 | + | Missense_Mutation | SNP | G | G | C | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr19:16872844G>C | c.2028G>C | c.(2026-2028)aaG>aaC | p.K676N |
CESC | 19 | 16890254 | 16890254 | + | Silent | SNP | C | C | T | TCGA-IR-A3LA-01A-11D-A22X-09 | TCGA-IR-A3LA-10A-01D-A22X-09 | g.chr19:16890254C>T | c.2709C>T | c.(2707-2709)atC>atT | p.I903I |
CESC | 19 | 16918399 | 16918399 | + | Missense_Mutation | SNP | G | G | A | TCGA-EK-A2GZ-01A-11D-A17W-09 | TCGA-EK-A2GZ-10A-01D-A17W-09 | g.chr19:16918399G>A | c.3739G>A | c.(3739-3741)Gag>Aag | p.E1247K |
CESC | 19 | 16926106 | 16926106 | + | Nonsense_Mutation | SNP | C | C | G | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr19:16926106C>G | c.4661C>G | c.(4660-4662)tCa>tGa | p.S1554* |
COAD | 19 | 16860011 | 16860011 | + | Silent | SNP | C | C | T | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chr19:16860011C>T | c.558C>T | c.(556-558)acC>acT | p.T186T |
COAD | 19 | 16860310 | 16860310 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3831-01A-01W-0900-09 | TCGA-AA-3831-10A-01W-0900-09 | g.chr19:16860310C>T | c.857C>T | c.(856-858)aCg>aTg | p.T286M |
COAD | 19 | 16860311 | 16860311 | + | Silent | SNP | G | G | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr19:16860311G>A | c.858G>A | c.(856-858)acG>acA | p.T286T |
COAD | 19 | 16860328 | 16860328 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr19:16860328C>T | c.875C>T | c.(874-876)gCg>gTg | p.A292V |
COAD | 19 | 16860349 | 16860349 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr19:16860349G>A | c.896G>A | c.(895-897)cGc>cAc | p.R299H |
COAD | 19 | 16860402 | 16860402 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr19:16860402G>A | c.949G>A | c.(949-951)Gaa>Aaa | p.E317K |
COAD | 19 | 16860457 | 16860457 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr19:16860457delC | c.1004delC | c.(1003-1005)accfs | p.T335fs |
COAD | 19 | 16860457 | 16860457 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr19:16860457delC | c.1004delC | c.(1003-1005)accfs | p.T335fs |
COAD | 19 | 16860978 | 16860978 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-2676-01A-01W-0833-10 | TCGA-A6-2676-10A-01W-0833-10 | g.chr19:16860978G>A | c.1525G>A | c.(1525-1527)Gca>Aca | p.A509T |
COAD | 19 | 16861115 | 16861115 | + | Silent | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr19:16861115G>A | c.1662G>A | c.(1660-1662)ccG>ccA | p.P554P |
COAD | 19 | 16861197 | 16861197 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3852-01A-01W-0900-09 | TCGA-AA-3852-10A-01W-0900-09 | g.chr19:16861197G>A | c.1744G>A | c.(1744-1746)Gtg>Atg | p.V582M |
COAD | 19 | 16872816 | 16872816 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr19:16872816G>A | c.2000G>A | c.(1999-2001)cGc>cAc | p.R667H |
COAD | 19 | 16872934 | 16872934 | + | Silent | SNP | G | G | T | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr19:16872934G>T | c.2118G>T | c.(2116-2118)ctG>ctT | p.L706L |
COAD | 19 | 16874747 | 16874747 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-3712-01A-21D-1719-10 | TCGA-AA-3712-11A-01D-1719-10 | g.chr19:16874747G>T | c.2242G>T | c.(2242-2244)Gag>Tag | p.E748* |
COAD | 19 | 16883957 | 16883957 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr19:16883957G>T | c.2431G>T | c.(2431-2433)Gaa>Taa | p.E811* |
COAD | 19 | 16884019 | 16884019 | + | Silent | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr19:16884019C>T | c.2493C>T | c.(2491-2493)tgC>tgT | p.C831C |
COAD | 19 | 16890161 | 16890161 | + | Silent | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr19:16890161C>T | c.2616C>T | c.(2614-2616)acC>acT | p.T872T |
COAD | 19 | 16890222 | 16890222 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr19:16890222G>A | c.2677G>A | c.(2677-2679)Gct>Act | p.A893T |
COAD | 19 | 16899834 | 16899834 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr19:16899834G>A | c.2773G>A | c.(2773-2775)Gcc>Acc | p.A925T |
COAD | 19 | 16899865 | 16899865 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3660-01A-01D-1719-10 | TCGA-AA-3660-11A-01D-1719-10 | g.chr19:16899865A>G | c.2804A>G | c.(2803-2805)cAc>cGc | p.H935R |
COAD | 19 | 16899893 | 16899893 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr19:16899893G>T | c.2832G>T | c.(2830-2832)gaG>gaT | p.E944D |
COAD | 19 | 16902373 | 16902373 | + | Silent | SNP | C | C | T | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr19:16902373C>T | c.3153C>T | c.(3151-3153)gcC>gcT | p.A1051A |
COAD | 19 | 16908586 | 16908586 | + | Silent | SNP | C | C | G | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr19:16908586C>G | c.3348C>G | c.(3346-3348)ggC>ggG | p.G1116G |
COAD | 19 | 16908590 | 16908590 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr19:16908590C>T | c.3352C>T | c.(3352-3354)Cgc>Tgc | p.R1118C |
COAD | 19 | 16910772 | 16910772 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6304-01A-11D-1924-10 | TCGA-G4-6304-10A-01D-1924-10 | g.chr19:16910772C>A | c.3535C>A | c.(3535-3537)Cgc>Agc | p.R1179S |
COAD | 19 | 16910774 | 16910774 | + | Silent | SNP | C | C | T | TCGA-AA-3693-01A-01W-0900-09 | TCGA-AA-3693-10A-01W-0900-09 | g.chr19:16910774C>T | c.3537C>T | c.(3535-3537)cgC>cgT | p.R1179R |
COAD | 19 | 16910774 | 16910774 | + | Silent | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr19:16910774C>T | c.3537C>T | c.(3535-3537)cgC>cgT | p.R1179R |
COAD | 19 | 16910915 | 16910915 | + | Silent | SNP | C | C | T | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr19:16910915C>T | c.3678C>T | c.(3676-3678)taC>taT | p.Y1226Y |
COAD | 19 | 16918475 | 16918475 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr19:16918475C>T | c.3815C>T | c.(3814-3816)aCg>aTg | p.T1272M |
COAD | 19 | 16918475 | 16918475 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6315-01A-11D-1719-10 | TCGA-G4-6315-10A-01D-1720-10 | g.chr19:16918475C>T | c.3815C>T | c.(3814-3816)aCg>aTg | p.T1272M |
COAD | 19 | 16918828 | 16918828 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-A6-2683-01A-01W-0831-10 | TCGA-A6-2683-10A-01W-0831-10 | g.chr19:16918828C>T | c.4168C>T | c.(4168-4170)Cga>Tga | p.R1390* |
COAD | 19 | 16918875 | 16918875 | + | Silent | SNP | C | C | T | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr19:16918875C>T | c.4215C>T | c.(4213-4215)agC>agT | p.S1405S |
COAD | 19 | 16918880 | 16918880 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3819-01A-01W-0900-09 | TCGA-AA-3819-10A-01W-0900-09 | g.chr19:16918880C>T | c.4220C>T | c.(4219-4221)tCt>tTt | p.S1407F |
COAD | 19 | 16918932 | 16918932 | + | Silent | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr19:16918932C>T | c.4272C>T | c.(4270-4272)ttC>ttT | p.F1424F |
COADREAD | 19 | 16860011 | 16860011 | + | Silent | SNP | C | C | T | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chr19:16860011C>T | c.558C>T | c.(556-558)acC>acT | p.T186T |
COADREAD | 19 | 16860310 | 16860310 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3831-01A-01W-0900-09 | TCGA-AA-3831-10A-01W-0900-09 | g.chr19:16860310C>T | c.857C>T | c.(856-858)aCg>aTg | p.T286M |
COADREAD | 19 | 16860311 | 16860311 | + | Silent | SNP | G | G | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr19:16860311G>A | c.858G>A | c.(856-858)acG>acA | p.T286T |
COADREAD | 19 | 16860328 | 16860328 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr19:16860328C>T | c.875C>T | c.(874-876)gCg>gTg | p.A292V |
COADREAD | 19 | 16860349 | 16860349 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr19:16860349G>A | c.896G>A | c.(895-897)cGc>cAc | p.R299H |
COADREAD | 19 | 16860402 | 16860402 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr19:16860402G>A | c.949G>A | c.(949-951)Gaa>Aaa | p.E317K |
COADREAD | 19 | 16860457 | 16860457 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr19:16860457delC | c.1004delC | c.(1003-1005)accfs | p.T335fs |
COADREAD | 19 | 16860457 | 16860457 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr19:16860457delC | c.1004delC | c.(1003-1005)accfs | p.T335fs |
COADREAD | 19 | 16860978 | 16860978 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-2676-01A-01W-0833-10 | TCGA-A6-2676-10A-01W-0833-10 | g.chr19:16860978G>A | c.1525G>A | c.(1525-1527)Gca>Aca | p.A509T |
COADREAD | 19 | 16861115 | 16861115 | + | Silent | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr19:16861115G>A | c.1662G>A | c.(1660-1662)ccG>ccA | p.P554P |
COADREAD | 19 | 16861197 | 16861197 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3852-01A-01W-0900-09 | TCGA-AA-3852-10A-01W-0900-09 | g.chr19:16861197G>A | c.1744G>A | c.(1744-1746)Gtg>Atg | p.V582M |
COADREAD | 19 | 16872816 | 16872816 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr19:16872816G>A | c.2000G>A | c.(1999-2001)cGc>cAc | p.R667H |
COADREAD | 19 | 16872934 | 16872934 | + | Silent | SNP | G | G | T | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr19:16872934G>T | c.2118G>T | c.(2116-2118)ctG>ctT | p.L706L |
COADREAD | 19 | 16874747 | 16874747 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-3712-01A-21D-1719-10 | TCGA-AA-3712-11A-01D-1719-10 | g.chr19:16874747G>T | c.2242G>T | c.(2242-2244)Gag>Tag | p.E748* |
COADREAD | 19 | 16883957 | 16883957 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr19:16883957G>T | c.2431G>T | c.(2431-2433)Gaa>Taa | p.E811* |
COADREAD | 19 | 16884019 | 16884019 | + | Silent | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr19:16884019C>T | c.2493C>T | c.(2491-2493)tgC>tgT | p.C831C |
COADREAD | 19 | 16884050 | 16884050 | + | Missense_Mutation | SNP | G | G | A | TCGA-DC-5337-01A-01D-1657-10 | TCGA-DC-5337-10A-01D-1657-10 | g.chr19:16884050G>A | c.2524G>A | c.(2524-2526)Gca>Aca | p.A842T |
COADREAD | 19 | 16890161 | 16890161 | + | Silent | SNP | C | C | T | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr19:16890161C>T | c.2616C>T | c.(2614-2616)acC>acT | p.T872T |
COADREAD | 19 | 16890222 | 16890222 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr19:16890222G>A | c.2677G>A | c.(2677-2679)Gct>Act | p.A893T |
COADREAD | 19 | 16899834 | 16899834 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr19:16899834G>A | c.2773G>A | c.(2773-2775)Gcc>Acc | p.A925T |
COADREAD | 19 | 16899834 | 16899834 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr19:16899834G>A | c.2773G>A | c.(2773-2775)Gcc>Acc | p.A925T |
COADREAD | 19 | 16899843 | 16899843 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-4007-01A-01W-1073-09 | TCGA-AG-4007-10A-01W-1073-09 | g.chr19:16899843G>T | c.2782G>T | c.(2782-2784)Gct>Tct | p.A928S |
COADREAD | 19 | 16899865 | 16899865 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3660-01A-01D-1719-10 | TCGA-AA-3660-11A-01D-1719-10 | g.chr19:16899865A>G | c.2804A>G | c.(2803-2805)cAc>cGc | p.H935R |
COADREAD | 19 | 16899893 | 16899893 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr19:16899893G>T | c.2832G>T | c.(2830-2832)gaG>gaT | p.E944D |
COADREAD | 19 | 16899951 | 16899951 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr19:16899951C>A | c.2890C>A | c.(2890-2892)Ctt>Att | p.L964I |
COADREAD | 19 | 16902373 | 16902373 | + | Silent | SNP | C | C | T | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr19:16902373C>T | c.3153C>T | c.(3151-3153)gcC>gcT | p.A1051A |
COADREAD | 19 | 16908586 | 16908586 | + | Silent | SNP | C | C | G | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr19:16908586C>G | c.3348C>G | c.(3346-3348)ggC>ggG | p.G1116G |
COADREAD | 19 | 16908590 | 16908590 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr19:16908590C>T | c.3352C>T | c.(3352-3354)Cgc>Tgc | p.R1118C |
COADREAD | 19 | 16910772 | 16910772 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6304-01A-11D-1924-10 | TCGA-G4-6304-10A-01D-1924-10 | g.chr19:16910772C>A | c.3535C>A | c.(3535-3537)Cgc>Agc | p.R1179S |
COADREAD | 19 | 16910774 | 16910774 | + | Silent | SNP | C | C | T | TCGA-AA-3693-01A-01W-0900-09 | TCGA-AA-3693-10A-01W-0900-09 | g.chr19:16910774C>T | c.3537C>T | c.(3535-3537)cgC>cgT | p.R1179R |
COADREAD | 19 | 16910774 | 16910774 | + | Silent | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr19:16910774C>T | c.3537C>T | c.(3535-3537)cgC>cgT | p.R1179R |
COADREAD | 19 | 16910915 | 16910915 | + | Silent | SNP | C | C | T | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr19:16910915C>T | c.3678C>T | c.(3676-3678)taC>taT | p.Y1226Y |
COADREAD | 19 | 16918475 | 16918475 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr19:16918475C>T | c.3815C>T | c.(3814-3816)aCg>aTg | p.T1272M |
COADREAD | 19 | 16918475 | 16918475 | + | Missense_Mutation | SNP | C | C | T | TCGA-CL-5917-01A-11D-1657-10 | TCGA-CL-5917-10A-01D-1657-10 | g.chr19:16918475C>T | c.3815C>T | c.(3814-3816)aCg>aTg | p.T1272M |
COADREAD | 19 | 16918475 | 16918475 | + | Missense_Mutation | SNP | C | C | T | TCGA-G4-6315-01A-11D-1719-10 | TCGA-G4-6315-10A-01D-1720-10 | g.chr19:16918475C>T | c.3815C>T | c.(3814-3816)aCg>aTg | p.T1272M |
COADREAD | 19 | 16918828 | 16918828 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-A6-2683-01A-01W-0831-10 | TCGA-A6-2683-10A-01W-0831-10 | g.chr19:16918828C>T | c.4168C>T | c.(4168-4170)Cga>Tga | p.R1390* |
COADREAD | 19 | 16918875 | 16918875 | + | Silent | SNP | C | C | T | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr19:16918875C>T | c.4215C>T | c.(4213-4215)agC>agT | p.S1405S |
COADREAD | 19 | 16918880 | 16918880 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3819-01A-01W-0900-09 | TCGA-AA-3819-10A-01W-0900-09 | g.chr19:16918880C>T | c.4220C>T | c.(4219-4221)tCt>tTt | p.S1407F |
COADREAD | 19 | 16918932 | 16918932 | + | Silent | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr19:16918932C>T | c.4272C>T | c.(4270-4272)ttC>ttT | p.F1424F |
DLBC | 19 | 16860001 | 16860001 | + | Missense_Mutation | SNP | A | A | T | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr19:16860001A>T | c.548A>T | c.(547-549)cAg>cTg | p.Q183L |
DLBC | 19 | 16860087 | 16860087 | + | Missense_Mutation | SNP | G | G | A | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr19:16860087G>A | c.634G>A | c.(634-636)Gcg>Acg | p.A212T |
DLBC | 19 | 16860558 | 16860558 | + | Missense_Mutation | SNP | G | G | A | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr19:16860558G>A | c.1105G>A | c.(1105-1107)Gtc>Atc | p.V369I |
DLBC | 19 | 16860602 | 16860602 | + | Silent | SNP | T | T | C | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr19:16860602T>C | c.1149T>C | c.(1147-1149)cgT>cgC | p.R383R |
DLBC | 19 | 16860685 | 16860685 | + | Missense_Mutation | SNP | C | C | T | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr19:16860685C>T | c.1232C>T | c.(1231-1233)aCc>aTc | p.T411I |
DLBC | 19 | 16860860 | 16860860 | + | Silent | SNP | C | C | T | TCGA-FA-A4XK-01A-11D-A31X-10 | TCGA-FA-A4XK-10A-01D-A31X-10 | g.chr19:16860860C>T | c.1407C>T | c.(1405-1407)tgC>tgT | p.C469C |
DLBC | 19 | 16872794 | 16872794 | + | Silent | SNP | C | C | T | TCGA-G8-6907-01A-11D-2210-10 | TCGA-G8-6907-14A-01D-2210-10 | g.chr19:16872794C>T | c.1978C>T | c.(1978-1980)Ctg>Ttg | p.L660L |
DLBC | 19 | 16899852 | 16899852 | + | Missense_Mutation | SNP | G | G | T | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr19:16899852G>T | c.2791G>T | c.(2791-2793)Gat>Tat | p.D931Y |
DLBC | 19 | 16918459 | 16918459 | + | Missense_Mutation | SNP | C | C | T | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr19:16918459C>T | c.3799C>T | c.(3799-3801)Cgc>Tgc | p.R1267C |
ESCA | 19 | 16860996 | 16860996 | + | Silent | SNP | C | C | T | TCGA-IG-A3YB-01A-11D-A247-09 | TCGA-IG-A3YB-10A-01D-A247-09 | g.chr19:16860996C>T | c.1543C>T | c.(1543-1545)Ctg>Ttg | p.L515L |
ESCA | 19 | 16883997 | 16883997 | + | Missense_Mutation | SNP | C | C | A | TCGA-LN-A9FP-01A-31D-A387-09 | TCGA-LN-A9FP-10A-01D-A38A-09 | g.chr19:16883997C>A | c.2471C>A | c.(2470-2472)cCa>cAa | p.P824Q |
ESCA | 19 | 16884031 | 16884031 | + | Silent | SNP | G | G | A | TCGA-LN-A4MR-01A-11D-A28B-09 | TCGA-LN-A4MR-10A-01D-A28E-09 | g.chr19:16884031G>A | c.2505G>A | c.(2503-2505)caG>caA | p.Q835Q |
ESCA | 19 | 16902312 | 16902312 | + | Missense_Mutation | SNP | C | C | T | TCGA-R6-A8WC-01A-11D-A37C-09 | TCGA-R6-A8WC-10A-01D-A37F-09 | g.chr19:16902312C>T | c.3092C>T | c.(3091-3093)aCg>aTg | p.T1031M |
ESCA | 19 | 16902329 | 16902329 | + | Missense_Mutation | SNP | A | A | G | TCGA-JY-A93E-01A-11D-A37C-09 | TCGA-JY-A93E-10A-01D-A37F-09 | g.chr19:16902329A>G | c.3109A>G | c.(3109-3111)Aag>Gag | p.K1037E |
ESCA | 19 | 16910773 | 16910773 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr19:16910773G>A | c.3536G>A | c.(3535-3537)cGc>cAc | p.R1179H |
ESCA | 19 | 16918782 | 16918782 | + | Silent | SNP | C | C | T | TCGA-L7-A56G-01A-21D-A27G-09 | TCGA-L7-A56G-10A-01D-A27G-09 | g.chr19:16918782C>T | c.4122C>T | c.(4120-4122)taC>taT | p.Y1374Y |
ESCA | 19 | 16923594 | 16923594 | + | Silent | SNP | C | C | G | TCGA-R6-A6L6-01B-11D-A33E-09 | TCGA-R6-A6L6-10A-01D-A33H-09 | g.chr19:16923594C>G | c.4326C>G | c.(4324-4326)tcC>tcG | p.S1442S |
GBM | 19 | 16860196 | 16860196 | + | Missense_Mutation | SNP | G | G | A | TCGA-26-5136-01B-01D-1486-08 | TCGA-26-5136-10A-01D-1486-08 | g.chr19:16860196G>A | c.743G>A | c.(742-744)cGc>cAc | p.R248H |
GBM | 19 | 16874718 | 16874718 | + | Missense_Mutation | SNP | A | A | G | TCGA-27-2526-01A-01D-1494-08 | TCGA-27-2526-10A-01D-1494-08 | g.chr19:16874718A>G | c.2213A>G | c.(2212-2214)cAc>cGc | p.H738R |
GBM | 19 | 16883984 | 16883984 | + | Missense_Mutation | SNP | G | G | A | TCGA-06-5414-01A-01D-1486-08 | TCGA-06-5414-10A-01D-1486-08 | g.chr19:16883984G>A | c.2458G>A | c.(2458-2460)Gcc>Acc | p.A820T |
GBMLGG | 19 | 16860196 | 16860196 | + | Missense_Mutation | SNP | G | G | A | TCGA-26-5136-01B-01D-1486-08 | TCGA-26-5136-10A-01D-1486-08 | g.chr19:16860196G>A | c.743G>A | c.(742-744)cGc>cAc | p.R248H |
GBMLGG | 19 | 16860397 | 16860397 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-A5TR-01A-11D-A289-08 | TCGA-DU-A5TR-10A-01D-A289-08 | g.chr19:16860397G>A | c.944G>A | c.(943-945)cGc>cAc | p.R315H |
GBMLGG | 19 | 16860740 | 16860740 | + | Silent | SNP | C | C | T | TCGA-DU-7019-01A-11D-2024-08 | TCGA-DU-7019-10A-01D-2024-08 | g.chr19:16860740C>T | c.1287C>T | c.(1285-1287)ttC>ttT | p.F429F |
GBMLGG | 19 | 16860910 | 16860910 | + | Missense_Mutation | SNP | C | C | T | TCGA-HT-A5R9-01A-11D-A289-08 | TCGA-HT-A5R9-10A-01D-A289-08 | g.chr19:16860910C>T | c.1457C>T | c.(1456-1458)cCg>cTg | p.P486L |
GBMLGG | 19 | 16874671 | 16874671 | + | Silent | SNP | G | G | A | TCGA-HW-7495-01A-11D-2024-08 | TCGA-HW-7495-10A-01D-2024-08 | g.chr19:16874671G>A | c.2166G>A | c.(2164-2166)acG>acA | p.T722T |
GBMLGG | 19 | 16874718 | 16874718 | + | Missense_Mutation | SNP | A | A | G | TCGA-27-2526-01A-01D-1494-08 | TCGA-27-2526-10A-01D-1494-08 | g.chr19:16874718A>G | c.2213A>G | c.(2212-2214)cAc>cGc | p.H738R |
GBMLGG | 19 | 16883984 | 16883984 | + | Missense_Mutation | SNP | G | G | A | TCGA-06-5414-01A-01D-1486-08 | TCGA-06-5414-10A-01D-1486-08 | g.chr19:16883984G>A | c.2458G>A | c.(2458-2460)Gcc>Acc | p.A820T |
GBMLGG | 19 | 16902242 | 16902242 | + | Missense_Mutation | SNP | G | G | A | TCGA-TQ-A7RR-01A-21D-A34A-08 | TCGA-TQ-A7RR-10A-01D-A34A-08 | g.chr19:16902242G>A | c.3022G>A | c.(3022-3024)Gtg>Atg | p.V1008M |
GBMLGG | 19 | 16902375 | 16902375 | + | Missense_Mutation | SNP | T | T | C | TCGA-TQ-A7RJ-01A-11D-A33T-08 | TCGA-TQ-A7RJ-10A-01D-A33W-08 | g.chr19:16902375T>C | c.3155T>C | c.(3154-3156)gTc>gCc | p.V1052A |
GBMLGG | 19 | 16905360 | 16905360 | + | Silent | SNP | C | C | T | TCGA-VM-A8C8-01A-11D-A36O-08 | TCGA-VM-A8C8-10A-01D-A367-08 | g.chr19:16905360C>T | c.3300C>T | c.(3298-3300)gcC>gcT | p.A1100A |
GBMLGG | 19 | 16908642 | 16908642 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-S9-A6TS-01A-12D-A33T-08 | TCGA-S9-A6TS-10A-01D-A33W-08 | g.chr19:16908642delT | c.3404delT | c.(3403-3405)gttfs | p.V1135fs |
HNSC | 19 | 16860197 | 16860197 | + | Silent | SNP | C | C | T | TCGA-CQ-A4C6-01A-11D-A25D-08 | TCGA-CQ-A4C6-10A-01D-A25E-08 | g.chr19:16860197C>T | c.744C>T | c.(742-744)cgC>cgT | p.R248R |
HNSC | 19 | 16860198 | 16860198 | + | Missense_Mutation | SNP | G | G | A | TCGA-BA-A6D8-01A-31D-A31L-08 | TCGA-BA-A6D8-10A-01D-A31J-08 | g.chr19:16860198G>A | c.745G>A | c.(745-747)Gac>Aac | p.D249N |
HNSC | 19 | 16860285 | 16860285 | + | Missense_Mutation | SNP | C | C | T | TCGA-BA-A6DA-01A-31D-A31L-08 | TCGA-BA-A6DA-10A-01D-A31J-08 | g.chr19:16860285C>T | c.832C>T | c.(832-834)Ctc>Ttc | p.L278F |
HNSC | 19 | 16860942 | 16860942 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-7261-01A-11D-2012-08 | TCGA-CV-7261-10A-01D-2013-08 | g.chr19:16860942G>A | c.1489G>A | c.(1489-1491)Gga>Aga | p.G497R |
HNSC | 19 | 16861004 | 16861004 | + | Silent | SNP | G | G | A | TCGA-CV-5441-01A-01D-1512-08 | TCGA-CV-5441-11A-01D-1512-08 | g.chr19:16861004G>A | c.1551G>A | c.(1549-1551)ccG>ccA | p.P517P |
HNSC | 19 | 16875993 | 16875993 | + | Silent | SNP | C | C | A | TCGA-CR-6481-01A-11D-1870-08 | TCGA-CR-6481-10A-01D-1870-08 | g.chr19:16875993C>A | c.2400C>A | c.(2398-2400)ctC>ctA | p.L800L |
HNSC | 19 | 16890267 | 16890267 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr19:16890267G>A | c.2722G>A | c.(2722-2724)Gga>Aga | p.G908R |
HNSC | 19 | 16902219 | 16902219 | + | Missense_Mutation | SNP | C | C | T | TCGA-D6-A74Q-01A-11D-A34J-08 | TCGA-D6-A74Q-10A-02D-A34M-08 | g.chr19:16902219C>T | c.2999C>T | c.(2998-3000)tCt>tTt | p.S1000F |
HNSC | 19 | 16902349 | 16902349 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-7103-01A-21D-2012-08 | TCGA-CV-7103-10A-01D-2013-08 | g.chr19:16902349C>G | c.3129C>G | c.(3127-3129)atC>atG | p.I1043M |
HNSC | 19 | 16923646 | 16923655 | + | Frame_Shift_Del | DEL | TGGAGTGTGC | TGGAGTGTGC | - | TCGA-CX-A4AQ-01A-11D-A25D-08 | TCGA-CX-A4AQ-10A-01D-A25E-08 | g.chr19:16923646_16923655delTGGAGTGTGC | c.4378_4387delTGGAGTGTGC | c.(4378-4389)tggagtgtgctgfs | p.WSVL1460fs |
KIPAN | 19 | 16875873 | 16875873 | + | Silent | SNP | C | C | T | TCGA-B0-4819-01A-01D-1361-10 | TCGA-B0-4819-11A-01D-1361-10 | g.chr19:16875873C>T | c.2280C>T | c.(2278-2280)ggC>ggT | p.G760G |
KIPAN | 19 | 16910759 | 16910759 | + | Silent | SNP | G | G | A | TCGA-A3-3313-01A-01D-0966-08 | TCGA-A3-3313-11A-01D-0966-08 | g.chr19:16910759G>A | c.3522G>A | c.(3520-3522)gtG>gtA | p.V1174V |
KIPAN | 19 | 16910780 | 16910780 | + | Silent | SNP | G | G | T | TCGA-BP-4351-01A-01D-1366-10 | TCGA-BP-4351-11A-01D-1366-10 | g.chr19:16910780G>T | c.3543G>T | c.(3541-3543)ggG>ggT | p.G1181G |
KIPAN | 19 | 16918705 | 16918705 | + | Missense_Mutation | SNP | G | G | A | TCGA-B9-4113-01A-01D-1252-08 | TCGA-B9-4113-11A-01D-1252-08 | g.chr19:16918705G>A | c.4045G>A | c.(4045-4047)Gag>Aag | p.E1349K |
KIRC | 19 | 16875873 | 16875873 | + | Silent | SNP | C | C | T | TCGA-B0-4819-01A-01D-1361-10 | TCGA-B0-4819-11A-01D-1361-10 | g.chr19:16875873C>T | c.2280C>T | c.(2278-2280)ggC>ggT | p.G760G |
KIRC | 19 | 16910759 | 16910759 | + | Silent | SNP | G | G | A | TCGA-A3-3313-01A-01D-0966-08 | TCGA-A3-3313-11A-01D-0966-08 | g.chr19:16910759G>A | c.3522G>A | c.(3520-3522)gtG>gtA | p.V1174V |
KIRC | 19 | 16910780 | 16910780 | + | Silent | SNP | G | G | T | TCGA-BP-4351-01A-01D-1366-10 | TCGA-BP-4351-11A-01D-1366-10 | g.chr19:16910780G>T | c.3543G>T | c.(3541-3543)ggG>ggT | p.G1181G |
KIRP | 19 | 16918705 | 16918705 | + | Missense_Mutation | SNP | G | G | A | TCGA-B9-4113-01A-01D-1252-08 | TCGA-B9-4113-11A-01D-1252-08 | g.chr19:16918705G>A | c.4045G>A | c.(4045-4047)Gag>Aag | p.E1349K |
LGG | 19 | 16860397 | 16860397 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-A5TR-01A-11D-A289-08 | TCGA-DU-A5TR-10A-01D-A289-08 | g.chr19:16860397G>A | c.944G>A | c.(943-945)cGc>cAc | p.R315H |
LGG | 19 | 16860740 | 16860740 | + | Silent | SNP | C | C | T | TCGA-DU-7019-01A-11D-2024-08 | TCGA-DU-7019-10A-01D-2024-08 | g.chr19:16860740C>T | c.1287C>T | c.(1285-1287)ttC>ttT | p.F429F |
LGG | 19 | 16860910 | 16860910 | + | Missense_Mutation | SNP | C | C | T | TCGA-HT-A5R9-01A-11D-A289-08 | TCGA-HT-A5R9-10A-01D-A289-08 | g.chr19:16860910C>T | c.1457C>T | c.(1456-1458)cCg>cTg | p.P486L |
LGG | 19 | 16874671 | 16874671 | + | Silent | SNP | G | G | A | TCGA-HW-7495-01A-11D-2024-08 | TCGA-HW-7495-10A-01D-2024-08 | g.chr19:16874671G>A | c.2166G>A | c.(2164-2166)acG>acA | p.T722T |
LGG | 19 | 16902242 | 16902242 | + | Missense_Mutation | SNP | G | G | A | TCGA-TQ-A7RR-01A-21D-A34A-08 | TCGA-TQ-A7RR-10A-01D-A34A-08 | g.chr19:16902242G>A | c.3022G>A | c.(3022-3024)Gtg>Atg | p.V1008M |
LGG | 19 | 16902375 | 16902375 | + | Missense_Mutation | SNP | T | T | C | TCGA-TQ-A7RJ-01A-11D-A33T-08 | TCGA-TQ-A7RJ-10A-01D-A33W-08 | g.chr19:16902375T>C | c.3155T>C | c.(3154-3156)gTc>gCc | p.V1052A |
LGG | 19 | 16905360 | 16905360 | + | Silent | SNP | C | C | T | TCGA-VM-A8C8-01A-11D-A36O-08 | TCGA-VM-A8C8-10A-01D-A367-08 | g.chr19:16905360C>T | c.3300C>T | c.(3298-3300)gcC>gcT | p.A1100A |
LGG | 19 | 16908642 | 16908642 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-S9-A6TS-01A-12D-A33T-08 | TCGA-S9-A6TS-10A-01D-A33W-08 | g.chr19:16908642delT | c.3404delT | c.(3403-3405)gttfs | p.V1135fs |
LIHC | 19 | 16860649 | 16860649 | + | Missense_Mutation | SNP | T | T | C | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chr19:16860649T>C | c.1196T>C | c.(1195-1197)cTg>cCg | p.L399P |
LIHC | 19 | 16908642 | 16908642 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-DD-A1EG-01A-11D-A20W-10 | TCGA-DD-A1EG-10A-01D-A20W-10 | g.chr19:16908642delT | c.3404delT | c.(3403-3405)gttfs | p.V1135fs |
LIHC | 19 | 16918475 | 16918475 | + | Missense_Mutation | SNP | C | C | T | TCGA-KR-A7K0-01A-12D-A33Q-10 | TCGA-KR-A7K0-10A-01D-A33Q-10 | g.chr19:16918475C>T | c.3815C>T | c.(3814-3816)aCg>aTg | p.T1272M |
LIHC | 19 | 16918939 | 16918939 | + | Missense_Mutation | SNP | A | A | G | TCGA-HP-A5N0-01A-11D-A28X-10 | TCGA-HP-A5N0-10A-01D-A28X-10 | g.chr19:16918939A>G | c.4279A>G | c.(4279-4281)Agc>Ggc | p.S1427G |
LUAD | 19 | 16860107 | 16860107 | + | Silent | SNP | T | T | G | TCGA-17-Z023-01A-01W-0746-08 | TCGA-17-Z023-11A-01W-0746-08 | g.chr19:16860107T>G | c.654T>G | c.(652-654)gcT>gcG | p.A218A |
LUAD | 19 | 16860134 | 16860134 | + | Silent | SNP | C | C | G | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr19:16860134C>G | c.681C>G | c.(679-681)ctC>ctG | p.L227L |
LUAD | 19 | 16860465 | 16860465 | + | Missense_Mutation | SNP | G | G | T | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr19:16860465G>T | c.1012G>T | c.(1012-1014)Gta>Tta | p.V338L |
LUAD | 19 | 16861059 | 16861059 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-7281-01A-11D-2036-08 | TCGA-55-7281-10A-01D-2036-08 | g.chr19:16861059C>A | c.1606C>A | c.(1606-1608)Ctg>Atg | p.L536M |
LUAD | 19 | 16870093 | 16870093 | + | Silent | SNP | G | G | T | TCGA-17-Z049-01A-01W-0746-08 | TCGA-17-Z049-11A-01W-0747-08 | g.chr19:16870093G>T | c.1827G>T | c.(1825-1827)ctG>ctT | p.L609L |
LUAD | 19 | 16870183 | 16870183 | + | Silent | SNP | A | A | G | TCGA-62-A471-01A-12D-A24D-08 | TCGA-62-A471-10A-01D-A24F-08 | g.chr19:16870183A>G | c.1917A>G | c.(1915-1917)ggA>ggG | p.G639G |
LUAD | 19 | 16874686 | 16874686 | + | Silent | SNP | G | G | T | TCGA-17-Z045-01A-01W-0746-08 | TCGA-17-Z045-11A-01W-0747-08 | g.chr19:16874686G>T | c.2181G>T | c.(2179-2181)cgG>cgT | p.R727R |
LUAD | 19 | 16874726 | 16874726 | + | Missense_Mutation | SNP | C | C | A | TCGA-97-7938-01A-11D-2167-08 | TCGA-97-7938-10A-01D-2167-08 | g.chr19:16874726C>A | c.2221C>A | c.(2221-2223)Cgc>Agc | p.R741S |
LUAD | 19 | 16874727 | 16874727 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-7281-01A-11D-2036-08 | TCGA-55-7281-10A-01D-2036-08 | g.chr19:16874727G>T | c.2222G>T | c.(2221-2223)cGc>cTc | p.R741L |
LUAD | 19 | 16890214 | 16890214 | + | Missense_Mutation | SNP | G | G | A | TCGA-78-7159-01A-11D-2036-08 | TCGA-78-7159-10A-01D-2036-08 | g.chr19:16890214G>A | c.2669G>A | c.(2668-2670)gGc>gAc | p.G890D |
LUAD | 19 | 16899898 | 16899898 | + | Missense_Mutation | SNP | T | T | G | TCGA-64-1681-01A-11D-2063-08 | TCGA-64-1681-10A-01D-2063-08 | g.chr19:16899898T>G | c.2837T>G | c.(2836-2838)tTt>tGt | p.F946C |
LUAD | 19 | 16902312 | 16902312 | + | Missense_Mutation | SNP | C | C | T | TCGA-86-8585-01A-11D-2393-08 | TCGA-86-8585-10A-01D-2393-08 | g.chr19:16902312C>T | c.3092C>T | c.(3091-3093)aCg>aTg | p.T1031M |
LUAD | 19 | 16902383 | 16902383 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z015-01A-01W-0746-08 | TCGA-17-Z015-11A-01W-0746-08 | g.chr19:16902383C>A | c.3163C>A | c.(3163-3165)Cag>Aag | p.Q1055K |
LUAD | 19 | 16910854 | 16910854 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-8119-01A-11D-2238-08 | TCGA-44-8119-10A-01D-2238-08 | g.chr19:16910854G>T | c.3617G>T | c.(3616-3618)cGg>cTg | p.R1206L |
LUAD | 19 | 16910855 | 16910855 | + | Silent | SNP | G | G | A | TCGA-05-4424-01A-22D-1855-08 | TCGA-05-4424-10A-01D-1855-08 | g.chr19:16910855G>A | c.3618G>A | c.(3616-3618)cgG>cgA | p.R1206R |
LUAD | 19 | 16910888 | 16910888 | + | Silent | SNP | C | C | G | TCGA-44-3918-01A-01D-1105-08 | TCGA-44-3918-11A-01D-1105-08 | g.chr19:16910888C>G | c.3651C>G | c.(3649-3651)ctC>ctG | p.L1217L |
LUAD | 19 | 16923619 | 16923619 | + | Missense_Mutation | SNP | G | G | T | TCGA-86-8054-01A-11D-2238-08 | TCGA-86-8054-10A-01D-2238-08 | g.chr19:16923619G>T | c.4351G>T | c.(4351-4353)Ggc>Tgc | p.G1451C |
LUAD | 19 | 16925862 | 16925862 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z045-01A-01W-0746-08 | TCGA-17-Z045-11A-01W-0747-08 | g.chr19:16925862G>T | c.4417G>T | c.(4417-4419)Gtc>Ttc | p.V1473F |
LUAD | 19 | 16925938 | 16925938 | + | Missense_Mutation | SNP | G | G | T | TCGA-95-7043-01A-11D-1945-08 | TCGA-95-7043-10A-01D-1946-08 | g.chr19:16925938G>T | c.4493G>T | c.(4492-4494)cGa>cTa | p.R1498L |
LUSC | 19 | 16860592 | 16860592 | + | Nonsense_Mutation | SNP | C | C | G | TCGA-34-5236-01A-21D-1817-08 | TCGA-34-5236-10A-01D-1817-08 | g.chr19:16860592C>G | c.1139C>G | c.(1138-1140)tCa>tGa | p.S380* |
LUSC | 19 | 16861050 | 16861050 | + | Missense_Mutation | SNP | C | C | A | TCGA-39-5024-01A-21D-1817-08 | TCGA-39-5024-11A-01D-1817-08 | g.chr19:16861050C>A | c.1597C>A | c.(1597-1599)Cca>Aca | p.P533T |
LUSC | 19 | 16884028 | 16884028 | + | Silent | SNP | C | C | A | TCGA-70-6722-01A-11D-1817-08 | TCGA-70-6722-10A-01D-1817-08 | g.chr19:16884028C>A | c.2502C>A | c.(2500-2502)gcC>gcA | p.A834A |
LUSC | 19 | 16908679 | 16908679 | + | Silent | SNP | C | C | T | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr19:16908679C>T | c.3441C>T | c.(3439-3441)tcC>tcT | p.S1147S |
LUSC | 19 | 16910739 | 16910739 | + | Missense_Mutation | SNP | G | G | A | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr19:16910739G>A | c.3502G>A | c.(3502-3504)Gaa>Aaa | p.E1168K |
LUSC | 19 | 16910814 | 16910814 | + | Missense_Mutation | SNP | T | T | G | TCGA-37-4133-01A-01D-1352-08 | TCGA-37-4133-10A-01D-1352-08 | g.chr19:16910814T>G | c.3577T>G | c.(3577-3579)Tct>Gct | p.S1193A |
LUSC | 19 | 16910890 | 16910890 | + | Missense_Mutation | SNP | C | C | G | TCGA-21-1076-01A-02D-1521-08 | TCGA-21-1076-11A-01D-1521-08 | g.chr19:16910890C>G | c.3653C>G | c.(3652-3654)aCc>aGc | p.T1218S |
LUSC | 19 | 16918790 | 16918790 | + | Missense_Mutation | SNP | C | C | A | TCGA-60-2698-01A-01D-1522-08 | TCGA-60-2698-11A-01D-1522-08 | g.chr19:16918790C>A | c.4130C>A | c.(4129-4131)gCa>gAa | p.A1377E |
OV | 19 | 16860175 | 16860175 | + | Missense_Mutation | SNP | C | C | G | TCGA-23-1124-01A-01W-0488-09 | TCGA-23-1124-10A-01W-0488-09 | g.chr19:16860175C>G | c.722C>G | c.(721-723)aCc>aGc | p.T241S |
OV | 19 | 16870240 | 16870240 | + | Splice_Site | SNP | G | G | A | TCGA-25-1628-01A-01W-0615-10 | TCGA-25-1628-10A-01W-0615-10 | g.chr19:16870240G>A | | c.e5+1 | |
OV | 19 | 16918641 | 16918641 | + | Missense_Mutation | SNP | C | C | G | TCGA-13-2066-01A-01D-1526-09 | TCGA-13-2066-10A-01D-1526-09 | g.chr19:16918641C>G | c.3981C>G | c.(3979-3981)atC>atG | p.I1327M |
PAAD | 19 | 16860012 | 16860012 | + | Missense_Mutation | SNP | G | G | A | TCGA-F2-A7TX-01A-33D-A38G-08 | TCGA-F2-A7TX-10B-01D-A38J-08 | g.chr19:16860012G>A | c.559G>A | c.(559-561)Gtc>Atc | p.V187I |
PAAD | 19 | 16884049 | 16884049 | + | Silent | SNP | C | C | T | TCGA-FB-AAQ3-01A-11D-A40W-08 | TCGA-FB-AAQ3-11A-11D-A40W-08 | g.chr19:16884049C>T | c.2523C>T | c.(2521-2523)tgC>tgT | p.C841C |
PAAD | 19 | 16884050 | 16884050 | + | Missense_Mutation | SNP | G | G | A | TCGA-US-A77J-01A-11D-A32N-08 | TCGA-US-A77J-11A-11D-A32N-08 | g.chr19:16884050G>A | c.2524G>A | c.(2524-2526)Gca>Aca | p.A842T |
PAAD | 19 | 16899861 | 16899861 | + | Silent | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr19:16899861C>T | c.2800C>T | c.(2800-2802)Ctg>Ttg | p.L934L |
PAAD | 19 | 16905360 | 16905360 | + | Silent | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr19:16905360C>T | c.3300C>T | c.(3298-3300)gcC>gcT | p.A1100A |
PAAD | 19 | 16908642 | 16908642 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-3E-AAAY-01A-11D-A38G-08 | TCGA-3E-AAAY-10A-01D-A38J-08 | g.chr19:16908642delT | c.3404delT | c.(3403-3405)gttfs | p.V1135fs |
PAAD | 19 | 16908642 | 16908642 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-F2-A8YN-01A-11D-A377-08 | TCGA-F2-A8YN-10A-01D-A37A-08 | g.chr19:16908642delT | c.3404delT | c.(3403-3405)gttfs | p.V1135fs |
PAAD | 19 | 16908642 | 16908642 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-IB-AAUP-01A-11D-A377-08 | TCGA-IB-AAUP-10A-01D-A37A-08 | g.chr19:16908642delT | c.3404delT | c.(3403-3405)gttfs | p.V1135fs |
PAAD | 19 | 16908642 | 16908642 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-YB-A89D-01A-12D-A36O-08 | TCGA-YB-A89D-10A-01D-A367-08 | g.chr19:16908642delT | c.3404delT | c.(3403-3405)gttfs | p.V1135fs |
PAAD | 19 | 16910925 | 16910925 | + | Missense_Mutation | SNP | C | C | T | TCGA-2J-AAB8-01A-12D-A40W-08 | TCGA-2J-AAB8-10A-01D-A40W-08 | g.chr19:16910925C>T | c.3688C>T | c.(3688-3690)Ccc>Tcc | p.P1230S |
PAAD | 19 | 16926085 | 16926085 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr19:16926085C>T | c.4640C>T | c.(4639-4641)gCc>gTc | p.A1547V |
PCPG | 19 | 16902242 | 16902242 | + | Missense_Mutation | SNP | G | G | A | TCGA-SQ-A6I6-01A-11D-A35I-08 | TCGA-SQ-A6I6-10A-01D-A35G-08 | g.chr19:16902242G>A | c.3022G>A | c.(3022-3024)Gtg>Atg | p.V1008M |
PRAD | 19 | 16860227 | 16860227 | + | Silent | SNP | C | C | T | TCGA-KC-A7FD-01A-11D-A33T-08 | TCGA-KC-A7FD-10A-01D-A33W-08 | g.chr19:16860227C>T | c.774C>T | c.(772-774)caC>caT | p.H258H |
PRAD | 19 | 16860790 | 16860790 | + | Missense_Mutation | SNP | G | G | C | TCGA-X4-A8KS-01A-12D-A364-08 | TCGA-X4-A8KS-10A-01D-A362-08 | g.chr19:16860790G>C | c.1337G>C | c.(1336-1338)cGc>cCc | p.R446P |
PRAD | 19 | 16860827 | 16860827 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-J9-A52C-01A-11D-A26M-08 | TCGA-J9-A52C-10A-01D-A26K-08 | g.chr19:16860827delC | c.1374delC | c.(1372-1374)tgcfs | p.C458fs |
PRAD | 19 | 16861005 | 16861005 | + | Missense_Mutation | SNP | G | G | C | TCGA-EJ-7791-01A-11D-2114-08 | TCGA-EJ-7791-10A-01D-2115-08 | g.chr19:16861005G>C | c.1552G>C | c.(1552-1554)Gtg>Ctg | p.V518L |
PRAD | 19 | 16872810 | 16872810 | + | Missense_Mutation | SNP | G | G | A | TCGA-HC-8259-01A-11D-2260-08 | TCGA-HC-8259-10A-01D-2260-08 | g.chr19:16872810G>A | c.1994G>A | c.(1993-1995)cGt>cAt | p.R665H |
PRAD | 19 | 16902377 | 16902377 | + | Missense_Mutation | SNP | T | T | G | TCGA-G9-6499-01A-12D-1961-08 | TCGA-G9-6499-10A-01D-1961-08 | g.chr19:16902377T>G | c.3157T>G | c.(3157-3159)Tca>Gca | p.S1053A |
PRAD | 19 | 16908688 | 16908688 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr19:16908688G>A | c.3450G>A | c.(3448-3450)gcG>gcA | p.A1150A |
PRAD | 19 | 16918719 | 16918719 | + | Silent | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr19:16918719C>T | c.4059C>T | c.(4057-4059)agC>agT | p.S1353S |
PRAD | 19 | 16918888 | 16918888 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr19:16918888G>A | c.4228G>A | c.(4228-4230)Gcc>Acc | p.A1410T |
READ | 19 | 16884050 | 16884050 | + | Missense_Mutation | SNP | G | G | A | TCGA-DC-5337-01A-01D-1657-10 | TCGA-DC-5337-10A-01D-1657-10 | g.chr19:16884050G>A | c.2524G>A | c.(2524-2526)Gca>Aca | p.A842T |
READ | 19 | 16899834 | 16899834 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr19:16899834G>A | c.2773G>A | c.(2773-2775)Gcc>Acc | p.A925T |
READ | 19 | 16899843 | 16899843 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-4007-01A-01W-1073-09 | TCGA-AG-4007-10A-01W-1073-09 | g.chr19:16899843G>T | c.2782G>T | c.(2782-2784)Gct>Tct | p.A928S |
READ | 19 | 16899951 | 16899951 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr19:16899951C>A | c.2890C>A | c.(2890-2892)Ctt>Att | p.L964I |
READ | 19 | 16918475 | 16918475 | + | Missense_Mutation | SNP | C | C | T | TCGA-CL-5917-01A-11D-1657-10 | TCGA-CL-5917-10A-01D-1657-10 | g.chr19:16918475C>T | c.3815C>T | c.(3814-3816)aCg>aTg | p.T1272M |
SARC | 19 | 16860069 | 16860069 | + | Silent | SNP | A | A | C | TCGA-WK-A8XT-01A-11D-A37C-09 | TCGA-WK-A8XT-10A-01D-A37F-09 | g.chr19:16860069A>C | c.616A>C | c.(616-618)Agg>Cgg | p.R206R |
SARC | 19 | 16860451 | 16860451 | + | Missense_Mutation | SNP | A | A | G | TCGA-DX-A23Y-01A-11D-A27P-09 | TCGA-DX-A23Y-10A-01D-A27P-09 | g.chr19:16860451A>G | c.998A>G | c.(997-999)cAg>cGg | p.Q333R |
SARC | 19 | 16860994 | 16860994 | + | Missense_Mutation | SNP | C | C | T | TCGA-3B-A9HT-01A-11D-A38Z-09 | TCGA-3B-A9HT-10A-01D-A38Z-09 | g.chr19:16860994C>T | c.1541C>T | c.(1540-1542)aCg>aTg | p.T514M |
SARC | 19 | 16861027 | 16861027 | + | Missense_Mutation | SNP | C | C | T | TCGA-QC-AA9N-01A-11D-A38Z-09 | TCGA-QC-AA9N-10A-01D-A38Z-09 | g.chr19:16861027C>T | c.1574C>T | c.(1573-1575)gCc>gTc | p.A525V |
SARC | 19 | 16918668 | 16918668 | + | Silent | SNP | C | C | T | TCGA-LI-A9QH-01A-11D-A37C-09 | TCGA-LI-A9QH-10A-01D-A37F-09 | g.chr19:16918668C>T | c.4008C>T | c.(4006-4008)atC>atT | p.I1336I |
SKCM | 19 | 16859961 | 16859961 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1I5-06A-11D-A197-08 | TCGA-DA-A1I5-10A-01D-A199-08 | g.chr19:16859961G>A | c.508G>A | c.(508-510)Gag>Aag | p.E170K |
SKCM | 19 | 16859997 | 16859997 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16859997G>A | c.544G>A | c.(544-546)Gaa>Aaa | p.E182K |
SKCM | 19 | 16860003 | 16860003 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A42L-06A-11D-A24R-08 | TCGA-ER-A42L-10A-01D-A24R-08 | g.chr19:16860003G>A | c.550G>A | c.(550-552)Gga>Aga | p.G184R |
SKCM | 19 | 16860010 | 16860010 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr19:16860010C>T | c.557C>T | c.(556-558)aCc>aTc | p.T186I |
SKCM | 19 | 16860024 | 16860024 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr19:16860024G>A | c.571G>A | c.(571-573)Gag>Aag | p.E191K |
SKCM | 19 | 16860201 | 16860201 | + | Silent | SNP | T | T | C | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16860201T>C | c.748T>C | c.(748-750)Ttg>Ctg | p.L250L |
SKCM | 19 | 16860284 | 16860284 | + | Silent | SNP | C | C | T | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr19:16860284C>T | c.831C>T | c.(829-831)gtC>gtT | p.V277V |
SKCM | 19 | 16860285 | 16860285 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr19:16860285C>T | c.832C>T | c.(832-834)Ctc>Ttc | p.L278F |
SKCM | 19 | 16860305 | 16860305 | + | Silent | SNP | G | G | A | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chr19:16860305G>A | c.852G>A | c.(850-852)ctG>ctA | p.L284L |
SKCM | 19 | 16860357 | 16860357 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MU-06A-21D-A196-08 | TCGA-EE-A2MU-10A-01D-A198-08 | g.chr19:16860357C>T | c.904C>T | c.(904-906)Ctt>Ttt | p.L302F |
SKCM | 19 | 16860407 | 16860407 | + | Silent | SNP | C | C | T | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr19:16860407C>T | c.954C>T | c.(952-954)ctC>ctT | p.L318L |
SKCM | 19 | 16860407 | 16860407 | + | Silent | SNP | C | C | T | TCGA-D3-A5GL-06A-11D-A27K-08 | TCGA-D3-A5GL-10A-01D-A27N-08 | g.chr19:16860407C>T | c.954C>T | c.(952-954)ctC>ctT | p.L318L |
SKCM | 19 | 16860421 | 16860421 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr19:16860421G>A | c.968G>A | c.(967-969)gGg>gAg | p.G323E |
SKCM | 19 | 16860439 | 16860439 | + | Missense_Mutation | SNP | A | A | C | TCGA-D9-A3Z1-06A-11D-A23B-08 | TCGA-D9-A3Z1-10A-01D-A23B-08 | g.chr19:16860439A>C | c.986A>C | c.(985-987)gAt>gCt | p.D329A |
SKCM | 19 | 16860477 | 16860477 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MI-06A-11D-A197-08 | TCGA-EE-A2MI-10A-01D-A199-08 | g.chr19:16860477C>T | c.1024C>T | c.(1024-1026)Ccc>Tcc | p.P342S |
SKCM | 19 | 16860478 | 16860478 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MI-06A-11D-A197-08 | TCGA-EE-A2MI-10A-01D-A199-08 | g.chr19:16860478C>T | c.1025C>T | c.(1024-1026)cCc>cTc | p.P342L |
SKCM | 19 | 16860484 | 16860484 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29N-06A-12D-A197-08 | TCGA-EE-A29N-10A-01D-A199-08 | g.chr19:16860484G>A | c.1031G>A | c.(1030-1032)gGc>gAc | p.G344D |
SKCM | 19 | 16860660 | 16860660 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JF-06A-11D-A196-08 | TCGA-D3-A2JF-10A-01D-A198-08 | g.chr19:16860660C>T | c.1207C>T | c.(1207-1209)Cct>Tct | p.P403S |
SKCM | 19 | 16860664 | 16860664 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr19:16860664C>T | c.1211C>T | c.(1210-1212)gCc>gTc | p.A404V |
SKCM | 19 | 16860679 | 16860679 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZQ-06A-11D-A197-08 | TCGA-FS-A1ZQ-10A-01D-A199-08 | g.chr19:16860679C>T | c.1226C>T | c.(1225-1227)gCc>gTc | p.A409V |
SKCM | 19 | 16860716 | 16860716 | + | Silent | SNP | C | C | T | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr19:16860716C>T | c.1263C>T | c.(1261-1263)ctC>ctT | p.L421L |
SKCM | 19 | 16860798 | 16860798 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MI-06A-11D-A197-08 | TCGA-EE-A2MI-10A-01D-A199-08 | g.chr19:16860798C>T | c.1345C>T | c.(1345-1347)Cgg>Tgg | p.R449W |
SKCM | 19 | 16860799 | 16860799 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A19S-06A-11D-A196-08 | TCGA-ER-A19S-10A-01D-A198-08 | g.chr19:16860799G>A | c.1346G>A | c.(1345-1347)cGg>cAg | p.R449Q |
SKCM | 19 | 16860808 | 16860808 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A51T-06A-11D-A25O-08 | TCGA-D3-A51T-10A-01D-A25O-08 | g.chr19:16860808C>T | c.1355C>T | c.(1354-1356)cCc>cTc | p.P452L |
SKCM | 19 | 16860837 | 16860837 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A1Q7-06A-11D-A19A-08 | TCGA-D3-A1Q7-10A-01D-A19A-08 | g.chr19:16860837G>A | c.1384G>A | c.(1384-1386)Gtg>Atg | p.V462M |
SKCM | 19 | 16860848 | 16860848 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16860848C>T | c.1395C>T | c.(1393-1395)atC>atT | p.I465I |
SKCM | 19 | 16860876 | 16860876 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29R-06A-11D-A197-08 | TCGA-EE-A29R-10A-01D-A199-08 | g.chr19:16860876G>A | c.1423G>A | c.(1423-1425)Gtt>Att | p.V475I |
SKCM | 19 | 16860911 | 16860911 | + | Silent | SNP | G | G | A | TCGA-RP-A693-06A-13D-A30X-08 | TCGA-RP-A693-10A-01D-A30X-08 | g.chr19:16860911G>A | c.1458G>A | c.(1456-1458)ccG>ccA | p.P486P |
SKCM | 19 | 16860935 | 16860935 | + | Silent | SNP | C | C | T | TCGA-D3-A3MR-06A-11D-A21A-08 | TCGA-D3-A3MR-10A-01D-A21A-08 | g.chr19:16860935C>T | c.1482C>T | c.(1480-1482)ccC>ccT | p.P494P |
SKCM | 19 | 16860953 | 16860953 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16860953C>T | c.1500C>T | c.(1498-1500)ggC>ggT | p.G500G |
SKCM | 19 | 16860971 | 16860971 | + | Silent | SNP | C | C | T | TCGA-EE-A17Y-06A-11D-A196-08 | TCGA-EE-A17Y-10B-01D-A198-08 | g.chr19:16860971C>T | c.1518C>T | c.(1516-1518)ctC>ctT | p.L506L |
SKCM | 19 | 16861034 | 16861034 | + | Silent | SNP | C | C | T | TCGA-FS-A1ZE-06A-11D-A197-08 | TCGA-FS-A1ZE-10A-01D-A199-08 | g.chr19:16861034C>T | c.1581C>T | c.(1579-1581)ctC>ctT | p.L527L |
SKCM | 19 | 16861050 | 16861050 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr19:16861050C>T | c.1597C>T | c.(1597-1599)Cca>Tca | p.P533S |
SKCM | 19 | 16861084 | 16861084 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16861084G>A | c.1631G>A | c.(1630-1632)cGg>cAg | p.R544Q |
SKCM | 19 | 16861094 | 16861094 | + | Silent | SNP | C | C | G | TCGA-DA-A1HY-06A-11D-A19A-08 | TCGA-DA-A1HY-10A-01D-A19A-08 | g.chr19:16861094C>G | c.1641C>G | c.(1639-1641)gcC>gcG | p.A547A |
SKCM | 19 | 16861191 | 16861191 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr19:16861191G>A | c.1738G>A | c.(1738-1740)Gcc>Acc | p.A580T |
SKCM | 19 | 16861220 | 16861220 | + | Silent | SNP | C | C | T | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr19:16861220C>T | c.1767C>T | c.(1765-1767)tcC>tcT | p.S589S |
SKCM | 19 | 16870130 | 16870130 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr19:16870130G>A | c.1864G>A | c.(1864-1866)Gag>Aag | p.E622K |
SKCM | 19 | 16870169 | 16870169 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16870169C>T | c.1903C>T | c.(1903-1905)Cgt>Tgt | p.R635C |
SKCM | 19 | 16872877 | 16872877 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZC-06A-11D-A197-08 | TCGA-FS-A1ZC-10A-01D-A199-08 | g.chr19:16872877G>A | c.2061G>A | c.(2059-2061)ggG>ggA | p.G687G |
SKCM | 19 | 16874664 | 16874664 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A4F0-06A-11D-A24R-08 | TCGA-FS-A4F0-10A-01D-A24R-08 | g.chr19:16874664C>T | c.2159C>T | c.(2158-2160)tCa>tTa | p.S720L |
SKCM | 19 | 16875863 | 16875863 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29B-06A-11D-A197-08 | TCGA-EE-A29B-10A-01D-A199-08 | g.chr19:16875863C>T | c.2270C>T | c.(2269-2271)tCc>tTc | p.S757F |
SKCM | 19 | 16875863 | 16875863 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AE-06A-11D-A196-08 | TCGA-EE-A3AE-10A-01D-A198-08 | g.chr19:16875863C>T | c.2270C>T | c.(2269-2271)tCc>tTc | p.S757F |
SKCM | 19 | 16875870 | 16875870 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr19:16875870G>A | c.2277G>A | c.(2275-2277)cgG>cgA | p.R759R |
SKCM | 19 | 16875962 | 16875962 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16875962C>T | c.2369C>T | c.(2368-2370)gCc>gTc | p.A790V |
SKCM | 19 | 16883983 | 16883983 | + | Silent | SNP | C | C | T | TCGA-FS-A4F5-06A-11D-A25O-08 | TCGA-FS-A4F5-10B-01D-A25O-08 | g.chr19:16883983C>T | c.2457C>T | c.(2455-2457)ttC>ttT | p.F819F |
SKCM | 19 | 16884082 | 16884082 | + | Silent | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr19:16884082C>T | c.2556C>T | c.(2554-2556)ttC>ttT | p.F852F |
SKCM | 19 | 16884103 | 16884103 | + | Silent | SNP | C | C | T | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr19:16884103C>T | c.2577C>T | c.(2575-2577)ccC>ccT | p.P859P |
SKCM | 19 | 16899851 | 16899851 | + | Silent | SNP | G | G | A | TCGA-EE-A2GM-06B-11D-A196-08 | TCGA-EE-A2GM-10A-01D-A198-08 | g.chr19:16899851G>A | c.2790G>A | c.(2788-2790)aaG>aaA | p.K930K |
SKCM | 19 | 16899852 | 16899852 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A2NG-06A-11D-A196-08 | TCGA-ER-A2NG-10A-01D-A198-08 | g.chr19:16899852G>A | c.2791G>A | c.(2791-2793)Gat>Aat | p.D931N |
SKCM | 19 | 16899890 | 16899890 | + | Missense_Mutation | SNP | G | G | T | TCGA-EE-A184-06A-11D-A196-08 | TCGA-EE-A184-10B-01D-A198-08 | g.chr19:16899890G>T | c.2829G>T | c.(2827-2829)caG>caT | p.Q943H |
SKCM | 19 | 16899909 | 16899909 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A19D-06A-11D-A197-08 | TCGA-ER-A19D-10A-01D-A199-08 | g.chr19:16899909G>A | c.2848G>A | c.(2848-2850)Gat>Aat | p.D950N |
SKCM | 19 | 16902221 | 16902221 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr19:16902221G>A | c.3001G>A | c.(3001-3003)Gat>Aat | p.D1001N |
SKCM | 19 | 16902222 | 16902222 | + | Missense_Mutation | SNP | A | A | T | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr19:16902222A>T | c.3002A>T | c.(3001-3003)gAt>gTt | p.D1001V |
SKCM | 19 | 16902224 | 16902224 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JO-06A-11D-A196-08 | TCGA-D3-A2JO-10A-01D-A198-08 | g.chr19:16902224C>T | c.3004C>T | c.(3004-3006)Cct>Tct | p.P1002S |
SKCM | 19 | 16902315 | 16902315 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MI-06A-11D-A197-08 | TCGA-EE-A2MI-10A-01D-A199-08 | g.chr19:16902315G>A | c.3095G>A | c.(3094-3096)gGa>gAa | p.G1032E |
SKCM | 19 | 16902353 | 16902353 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MC-06A-12D-A197-08 | TCGA-EE-A2MC-10A-01D-A199-08 | g.chr19:16902353G>A | c.3133G>A | c.(3133-3135)Gaa>Aaa | p.E1045K |
SKCM | 19 | 16902356 | 16902356 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1YY-06A-11D-A197-08 | TCGA-FS-A1YY-10A-01D-A199-08 | g.chr19:16902356G>A | c.3136G>A | c.(3136-3138)Gaa>Aaa | p.E1046K |
SKCM | 19 | 16905281 | 16905281 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr19:16905281C>T | c.3221C>T | c.(3220-3222)tCc>tTc | p.S1074F |
SKCM | 19 | 16908556 | 16908556 | + | Silent | SNP | G | G | A | TCGA-EE-A2ML-06A-11D-A197-08 | TCGA-EE-A2ML-10A-01D-A199-08 | g.chr19:16908556G>A | c.3318G>A | c.(3316-3318)tcG>tcA | p.S1106S |
SKCM | 19 | 16908590 | 16908590 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A17X-06A-11D-A197-08 | TCGA-EE-A17X-10A-01D-A199-08 | g.chr19:16908590C>T | c.3352C>T | c.(3352-3354)Cgc>Tgc | p.R1118C |
SKCM | 19 | 16908608 | 16908608 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1I2-06A-21D-A19A-08 | TCGA-DA-A1I2-10A-01D-A19A-08 | g.chr19:16908608G>A | c.3370G>A | c.(3370-3372)Gat>Aat | p.D1124N |
SKCM | 19 | 16908642 | 16908642 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-EE-A2MF-06A-11D-A21A-08 | TCGA-EE-A2MF-10B-01D-A21A-08 | g.chr19:16908642delT | c.3404delT | c.(3403-3405)gttfs | p.V1135fs |
SKCM | 19 | 16908642 | 16908642 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-ER-A3ES-06A-11D-A20D-08 | TCGA-ER-A3ES-10A-01D-A20D-08 | g.chr19:16908642delT | c.3404delT | c.(3403-3405)gttfs | p.V1135fs |
SKCM | 19 | 16908678 | 16908678 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1HW-06A-11D-A19A-08 | TCGA-DA-A1HW-10A-01D-A19A-08 | g.chr19:16908678C>T | c.3440C>T | c.(3439-3441)tCc>tTc | p.S1147F |
SKCM | 19 | 16908679 | 16908679 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16908679C>T | c.3441C>T | c.(3439-3441)tcC>tcT | p.S1147S |
SKCM | 19 | 16908680 | 16908680 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16908680C>T | c.3442C>T | c.(3442-3444)Ctt>Ttt | p.L1148F |
SKCM | 19 | 16910720 | 16910720 | + | Silent | SNP | G | G | A | TCGA-EE-A2M8-06A-12D-A196-08 | TCGA-EE-A2M8-10A-01D-A198-08 | g.chr19:16910720G>A | c.3483G>A | c.(3481-3483)ggG>ggA | p.G1161G |
SKCM | 19 | 16910720 | 16910720 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16910720G>A | c.3483G>A | c.(3481-3483)ggG>ggA | p.G1161G |
SKCM | 19 | 16910772 | 16910772 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16910772C>T | c.3535C>T | c.(3535-3537)Cgc>Tgc | p.R1179C |
SKCM | 19 | 16910778 | 16910778 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3CB-06A-11D-A196-08 | TCGA-D3-A3CB-10A-01D-A198-08 | g.chr19:16910778G>A | c.3541G>A | c.(3541-3543)Ggg>Agg | p.G1181R |
SKCM | 19 | 16910856 | 16910856 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr19:16910856G>A | c.3619G>A | c.(3619-3621)Gtg>Atg | p.V1207M |
SKCM | 19 | 16910870 | 16910870 | + | Silent | SNP | T | T | C | TCGA-EE-A29N-06A-12D-A197-08 | TCGA-EE-A29N-10A-01D-A199-08 | g.chr19:16910870T>C | c.3633T>C | c.(3631-3633)ttT>ttC | p.F1211F |
SKCM | 19 | 16910916 | 16910916 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A4U9-06A-11D-A32N-08 | TCGA-GN-A4U9-10B-01D-A32N-08 | g.chr19:16910916G>A | c.3679G>A | c.(3679-3681)Gtc>Atc | p.V1227I |
SKCM | 19 | 16918402 | 16918402 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr19:16918402G>A | c.3742G>A | c.(3742-3744)Gaa>Aaa | p.E1248K |
SKCM | 19 | 16918482 | 16918482 | + | Silent | SNP | C | C | T | TCGA-EE-A29V-06A-12D-A197-08 | TCGA-EE-A29V-10A-01D-A199-08 | g.chr19:16918482C>T | c.3822C>T | c.(3820-3822)ctC>ctT | p.L1274L |
SKCM | 19 | 16918508 | 16918508 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A3F8-06A-11D-A20D-08 | TCGA-DA-A3F8-10A-01D-A20D-08 | g.chr19:16918508C>T | c.3848C>T | c.(3847-3849)cCc>cTc | p.P1283L |
SKCM | 19 | 16918517 | 16918517 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2A0-06A-11D-A196-08 | TCGA-EE-A2A0-10A-01D-A198-08 | g.chr19:16918517C>T | c.3857C>T | c.(3856-3858)tCc>tTc | p.S1286F |
SKCM | 19 | 16918540 | 16918540 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr19:16918540C>T | c.3880C>T | c.(3880-3882)Ccc>Tcc | p.P1294S |
SKCM | 19 | 16918626 | 16918626 | + | Silent | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr19:16918626C>T | c.3966C>T | c.(3964-3966)gtC>gtT | p.V1322V |
SKCM | 19 | 16918651 | 16918651 | + | Missense_Mutation | SNP | G | G | T | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr19:16918651G>T | c.3991G>T | c.(3991-3993)Gac>Tac | p.D1331Y |
SKCM | 19 | 16918718 | 16918718 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr19:16918718G>A | c.4058G>A | c.(4057-4059)aGc>aAc | p.S1353N |
SKCM | 19 | 16918807 | 16918807 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3MR-06A-11D-A21A-08 | TCGA-D3-A3MR-10A-01D-A21A-08 | g.chr19:16918807C>T | c.4147C>T | c.(4147-4149)Ccc>Tcc | p.P1383S |
SKCM | 19 | 16918926 | 16918926 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr19:16918926G>A | c.4266G>A | c.(4264-4266)tgG>tgA | p.W1422* |
SKCM | 19 | 16918926 | 16918926 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16918926G>A | c.4266G>A | c.(4264-4266)tgG>tgA | p.W1422* |
SKCM | 19 | 16923627 | 16923627 | + | Silent | SNP | G | G | A | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr19:16923627G>A | c.4359G>A | c.(4357-4359)aaG>aaA | p.K1453K |
SKCM | 19 | 16925901 | 16925901 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16925901G>A | c.4456G>A | c.(4456-4458)Ggc>Agc | p.G1486S |
SKCM | 19 | 16925942 | 16925942 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr19:16925942G>A | c.4497G>A | c.(4495-4497)gaG>gaA | p.E1499E |
SKCM | 19 | 16926096 | 16926096 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JA-06A-11D-A20D-08 | TCGA-EE-A3JA-10A-01D-A20D-08 | g.chr19:16926096G>A | c.4651G>A | c.(4651-4653)Gaa>Aaa | p.E1551K |