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 | 17 | 15496728 | 15496728 | + | Silent | SNP | G | G | A | TCGA-XF-A9T0-01A-11D-A391-08 | TCGA-XF-A9T0-10A-01D-A394-08 | g.chr17:15496728G>A | c.1929C>T | c.(1927-1929)ttC>ttT | p.F643F |
BLCA | 17 | 15501958 | 15501975 | + | Splice_Site | DEL | ATCCCAGTATCTGCAGGA | ATCCCAGTATCTGCAGGA | - | TCGA-G2-A3VY-01A-11D-A22Z-08 | TCGA-G2-A3VY-10A-01D-A22Z-08 | g.chr17:15501958_15501975delATCCCAGTATCTGCAGGA | c.1434_1443delTCCTGCAGATACTGGGAT | c.(1432-1443)agtcctgcagat>ag | p.SPAD478del |
BLCA | 17 | 15516018 | 15516018 | + | Silent | SNP | C | C | T | TCGA-FD-A43P-01A-31D-A23U-08 | TCGA-FD-A43P-10A-01D-A23U-08 | g.chr17:15516018C>T | c.1119G>A | c.(1117-1119)acG>acA | p.T373T |
BLCA | 17 | 15516099 | 15516099 | + | Missense_Mutation | SNP | A | A | C | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr17:15516099A>C | c.1038T>G | c.(1036-1038)aaT>aaG | p.N346K |
BLCA | 17 | 15522516 | 15522516 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A6TA-01A-12D-A339-08 | TCGA-FD-A6TA-10A-21D-A339-08 | g.chr17:15522516G>A | c.311C>T | c.(310-312)tCc>tTc | p.S104F |
BLCA | 17 | 15522668 | 15522668 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-A9T8-01A-11D-A391-08 | TCGA-XF-A9T8-10A-01D-A394-08 | g.chr17:15522668C>G | c.159G>C | c.(157-159)caG>caC | p.Q53H |
BLCA | 17 | 15522810 | 15522810 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-DK-A3IN-01A-11D-A20D-08 | TCGA-DK-A3IN-10A-01D-A20D-08 | g.chr17:15522810G>C | c.17C>G | c.(16-18)tCa>tGa | p.S6* |
BRCA | 17 | 15508674 | 15508674 | + | Silent | SNP | T | T | A | TCGA-A8-A06X-01A-21W-A019-09 | TCGA-A8-A06X-10A-01W-A021-09 | g.chr17:15508674T>A | c.1296A>T | c.(1294-1296)cgA>cgT | p.R432R |
BRCA | 17 | 15516055 | 15516055 | + | Missense_Mutation | SNP | C | C | G | TCGA-D8-A27H-01A-11D-A16D-09 | TCGA-D8-A27H-10A-01D-A16D-09 | g.chr17:15516055C>G | c.1082G>C | c.(1081-1083)aGc>aCc | p.S361T |
BRCA | 17 | 15517307 | 15517307 | + | Missense_Mutation | SNP | C | C | T | TCGA-D8-A27V-01A-12D-A17D-09 | TCGA-D8-A27V-10A-01D-A17D-09 | g.chr17:15517307C>T | c.711G>A | c.(709-711)atG>atA | p.M237I |
BRCA | 17 | 15519016 | 15519016 | + | Missense_Mutation | SNP | G | G | A | TCGA-BH-A0HF-01A-11W-A071-09 | TCGA-BH-A0HF-10A-01W-A071-09 | g.chr17:15519016G>A | c.613C>T | c.(613-615)Ctt>Ttt | p.L205F |
BRCA | 17 | 15522583 | 15522583 | + | Missense_Mutation | SNP | C | C | T | TCGA-EW-A1PB-01A-11D-A142-09 | TCGA-EW-A1PB-10A-01D-A142-09 | g.chr17:15522583C>T | c.244G>A | c.(244-246)Gga>Aga | p.G82R |
BRCA | 17 | 15522759 | 15522759 | + | Missense_Mutation | SNP | A | A | T | TCGA-AQ-A0Y5-01A-11D-A14K-09 | TCGA-AQ-A0Y5-10A-01D-A17G-09 | g.chr17:15522759A>T | c.68T>A | c.(67-69)aTc>aAc | p.I23N |
CESC | 17 | 15519028 | 15519028 | + | Missense_Mutation | SNP | G | G | C | TCGA-IR-A3LK-01A-12D-A20U-09 | TCGA-IR-A3LK-10A-01D-A20U-09 | g.chr17:15519028G>C | c.601C>G | c.(601-603)Cag>Gag | p.Q201E |
COAD | 17 | 15492480 | 15492480 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr17:15492480C>T | c.2068G>A | c.(2068-2070)Gaa>Aaa | p.E690K |
COAD | 17 | 15492514 | 15492514 | + | Silent | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:15492514A>G | c.2034T>C | c.(2032-2034)ttT>ttC | p.F678F |
COAD | 17 | 15496685 | 15496685 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr17:15496685C>T | c.1972G>A | c.(1972-1974)Gat>Aat | p.D658N |
COAD | 17 | 15498090 | 15498090 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6676-01A-11D-1835-10 | TCGA-CM-6676-10A-01D-1835-10 | g.chr17:15498090G>A | c.1819C>T | c.(1819-1821)Cgc>Tgc | p.R607C |
COAD | 17 | 15498128 | 15498128 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00O-01A-02W-A00E-09 | TCGA-AA-A00O-10A-01W-A00E-09 | g.chr17:15498128C>T | c.1781G>A | c.(1780-1782)gGc>gAc | p.G594D |
COAD | 17 | 15501877 | 15501877 | + | Silent | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr17:15501877G>A | c.1524C>T | c.(1522-1524)ctC>ctT | p.L508L |
COAD | 17 | 15508543 | 15508543 | + | Missense_Mutation | SNP | C | C | G | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr17:15508543C>G | c.1427G>C | c.(1426-1428)aGt>aCt | p.S476T |
COAD | 17 | 15510989 | 15510989 | + | Silent | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr17:15510989G>A | c.1131C>T | c.(1129-1131)taC>taT | p.Y377Y |
COAD | 17 | 15516054 | 15516054 | + | Silent | SNP | G | G | A | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr17:15516054G>A | c.1083C>T | c.(1081-1083)agC>agT | p.S361S |
COAD | 17 | 15516134 | 15516134 | + | Missense_Mutation | SNP | A | A | G | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr17:15516134A>G | c.1003T>C | c.(1003-1005)Tcc>Ccc | p.S335P |
COAD | 17 | 15519036 | 15519036 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr17:15519036G>A | c.593C>T | c.(592-594)gCc>gTc | p.A198V |
COAD | 17 | 15519055 | 15519055 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr17:15519055A>G | c.574T>C | c.(574-576)Tca>Cca | p.S192P |
COAD | 17 | 15519091 | 15519091 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr17:15519091delA | c.538delT | c.(538-540)tccfs | p.S180fs |
COAD | 17 | 15522438 | 15522441 | + | Frame_Shift_Del | DEL | TGGG | TGGG | - | TCGA-CM-6165-01A-11D-1650-10 | TCGA-CM-6165-10A-01D-1650-10 | g.chr17:15522438_15522441delTGGG | c.386_389delCCCA | c.(385-390)acccagfs | p.TQ129fs |
COAD | 17 | 15522450 | 15522450 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr17:15522450G>A | c.377C>T | c.(376-378)gCg>gTg | p.A126V |
COADREAD | 17 | 15492480 | 15492480 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr17:15492480C>T | c.2068G>A | c.(2068-2070)Gaa>Aaa | p.E690K |
COADREAD | 17 | 15492480 | 15492480 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr17:15492480C>A | c.2068G>T | c.(2068-2070)Gaa>Taa | p.E690* |
COADREAD | 17 | 15492514 | 15492514 | + | Silent | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:15492514A>G | c.2034T>C | c.(2032-2034)ttT>ttC | p.F678F |
COADREAD | 17 | 15496685 | 15496685 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr17:15496685C>T | c.1972G>A | c.(1972-1974)Gat>Aat | p.D658N |
COADREAD | 17 | 15498090 | 15498090 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6676-01A-11D-1835-10 | TCGA-CM-6676-10A-01D-1835-10 | g.chr17:15498090G>A | c.1819C>T | c.(1819-1821)Cgc>Tgc | p.R607C |
COADREAD | 17 | 15498128 | 15498128 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00O-01A-02W-A00E-09 | TCGA-AA-A00O-10A-01W-A00E-09 | g.chr17:15498128C>T | c.1781G>A | c.(1780-1782)gGc>gAc | p.G594D |
COADREAD | 17 | 15501877 | 15501877 | + | Silent | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr17:15501877G>A | c.1524C>T | c.(1522-1524)ctC>ctT | p.L508L |
COADREAD | 17 | 15508543 | 15508543 | + | Missense_Mutation | SNP | C | C | G | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr17:15508543C>G | c.1427G>C | c.(1426-1428)aGt>aCt | p.S476T |
COADREAD | 17 | 15510989 | 15510989 | + | Silent | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr17:15510989G>A | c.1131C>T | c.(1129-1131)taC>taT | p.Y377Y |
COADREAD | 17 | 15516054 | 15516054 | + | Silent | SNP | G | G | A | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr17:15516054G>A | c.1083C>T | c.(1081-1083)agC>agT | p.S361S |
COADREAD | 17 | 15516134 | 15516134 | + | Missense_Mutation | SNP | A | A | G | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr17:15516134A>G | c.1003T>C | c.(1003-1005)Tcc>Ccc | p.S335P |
COADREAD | 17 | 15519036 | 15519036 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr17:15519036G>A | c.593C>T | c.(592-594)gCc>gTc | p.A198V |
COADREAD | 17 | 15519055 | 15519055 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr17:15519055A>G | c.574T>C | c.(574-576)Tca>Cca | p.S192P |
COADREAD | 17 | 15519091 | 15519091 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr17:15519091delA | c.538delT | c.(538-540)tccfs | p.S180fs |
COADREAD | 17 | 15522438 | 15522441 | + | Frame_Shift_Del | DEL | TGGG | TGGG | - | TCGA-CM-6165-01A-11D-1650-10 | TCGA-CM-6165-10A-01D-1650-10 | g.chr17:15522438_15522441delTGGG | c.386_389delCCCA | c.(385-390)acccagfs | p.TQ129fs |
COADREAD | 17 | 15522450 | 15522450 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr17:15522450G>A | c.377C>T | c.(376-378)gCg>gTg | p.A126V |
DLBC | 17 | 15519029 | 15519029 | + | Silent | SNP | A | A | C | TCGA-GR-7353-01A-11D-2210-10 | TCGA-GR-7353-10A-01D-2210-10 | g.chr17:15519029A>C | c.600T>G | c.(598-600)acT>acG | p.T200T |
DLBC | 17 | 15519066 | 15519066 | + | Missense_Mutation | SNP | T | T | G | TCGA-FF-8061-01A-11D-2210-10 | TCGA-FF-8061-10A-01D-2210-10 | g.chr17:15519066T>G | c.563A>C | c.(562-564)aAg>aCg | p.K188T |
ESCA | 17 | 15510949 | 15510949 | + | Missense_Mutation | SNP | C | C | A | TCGA-S8-A6BV-01A-21D-A31U-09 | TCGA-S8-A6BV-10A-01D-A31U-09 | g.chr17:15510949C>A | c.1171G>T | c.(1171-1173)Gtc>Ttc | p.V391F |
ESCA | 17 | 15522728 | 15522728 | + | Silent | SNP | G | G | T | TCGA-V5-A7RC-01B-11D-A403-09 | TCGA-V5-A7RC-10A-01D-A403-09 | g.chr17:15522728G>T | c.99C>A | c.(97-99)gtC>gtA | p.V33V |
GBM | 17 | 15517208 | 15517208 | + | Silent | SNP | C | C | T | TCGA-14-0813-01A-01W-0424-08 | TCGA-14-0813-10A-01W-0424-08 | g.chr17:15517208C>T | c.810G>A | c.(808-810)ggG>ggA | p.G270G |
GBMLGG | 17 | 15496762 | 15496762 | + | Missense_Mutation | SNP | C | C | T | TCGA-CS-4943-01A-01D-1468-08 | TCGA-CS-4943-10A-01D-1468-08 | g.chr17:15496762C>T | c.1895G>A | c.(1894-1896)tGt>tAt | p.C632Y |
GBMLGG | 17 | 15510968 | 15510968 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:15510968C>T | c.1152G>A | c.(1150-1152)caG>caA | p.Q384Q |
GBMLGG | 17 | 15510998 | 15510998 | + | Splice_Site | SNP | C | C | A | TCGA-DU-7298-01A-11D-2024-08 | TCGA-DU-7298-10A-01D-2024-08 | g.chr17:15510998C>A | | c.e6-1 | |
GBMLGG | 17 | 15517208 | 15517208 | + | Silent | SNP | C | C | T | TCGA-14-0813-01A-01W-0424-08 | TCGA-14-0813-10A-01W-0424-08 | g.chr17:15517208C>T | c.810G>A | c.(808-810)ggG>ggA | p.G270G |
GBMLGG | 17 | 15518967 | 15518967 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:15518967G>T | c.662C>A | c.(661-663)tCt>tAt | p.S221Y |
GBMLGG | 17 | 15522425 | 15522425 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:15522425C>T | c.402G>A | c.(400-402)gcG>gcA | p.A134A |
HNSC | 17 | 15492481 | 15492481 | + | Silent | SNP | G | G | T | TCGA-KU-A66S-01A-21D-A30E-08 | TCGA-KU-A66S-10A-01D-A30H-08 | g.chr17:15492481G>T | c.2067C>A | c.(2065-2067)atC>atA | p.I689I |
HNSC | 17 | 15496704 | 15496704 | + | Missense_Mutation | SNP | T | T | C | TCGA-CV-A6JY-01A-11D-A31L-08 | TCGA-CV-A6JY-10A-01D-A31J-08 | g.chr17:15496704T>C | c.1953A>G | c.(1951-1953)atA>atG | p.I651M |
HNSC | 17 | 15498141 | 15498141 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-A45W-01A-11D-A25D-08 | TCGA-CV-A45W-10A-01D-A25E-08 | g.chr17:15498141C>T | c.1768G>A | c.(1768-1770)Gga>Aga | p.G590R |
HNSC | 17 | 15517267 | 15517267 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-7245-01A-11D-2012-08 | TCGA-CV-7245-10A-01D-2013-08 | g.chr17:15517267C>G | c.751G>C | c.(751-753)Ggg>Cgg | p.G251R |
HNSC | 17 | 15522822 | 15522822 | + | Missense_Mutation | SNP | T | T | C | TCGA-CN-5359-01A-01D-1434-08 | TCGA-CN-5359-10A-01D-1434-08 | g.chr17:15522822T>C | c.5A>G | c.(4-6)gAa>gGa | p.E2G |
KIPAN | 17 | 15498178 | 15498178 | + | Silent | SNP | C | C | T | TCGA-CJ-5678-01A-11D-1534-10 | TCGA-CJ-5678-11A-01D-1534-10 | g.chr17:15498178C>T | c.1731G>A | c.(1729-1731)gtG>gtA | p.V577V |
KIPAN | 17 | 15516051 | 15516051 | + | Missense_Mutation | SNP | C | C | T | TCGA-B0-5116-01A-02D-1421-08 | TCGA-B0-5116-11A-01D-1421-08 | g.chr17:15516051C>T | c.1086G>A | c.(1084-1086)atG>atA | p.M362I |
KIRC | 17 | 15498178 | 15498178 | + | Silent | SNP | C | C | T | TCGA-CJ-5678-01A-11D-1534-10 | TCGA-CJ-5678-11A-01D-1534-10 | g.chr17:15498178C>T | c.1731G>A | c.(1729-1731)gtG>gtA | p.V577V |
KIRC | 17 | 15516051 | 15516051 | + | Missense_Mutation | SNP | C | C | T | TCGA-B0-5116-01A-02D-1421-08 | TCGA-B0-5116-11A-01D-1421-08 | g.chr17:15516051C>T | c.1086G>A | c.(1084-1086)atG>atA | p.M362I |
LGG | 17 | 15496762 | 15496762 | + | Missense_Mutation | SNP | C | C | T | TCGA-CS-4943-01A-01D-1468-08 | TCGA-CS-4943-10A-01D-1468-08 | g.chr17:15496762C>T | c.1895G>A | c.(1894-1896)tGt>tAt | p.C632Y |
LGG | 17 | 15510968 | 15510968 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:15510968C>T | c.1152G>A | c.(1150-1152)caG>caA | p.Q384Q |
LGG | 17 | 15510998 | 15510998 | + | Splice_Site | SNP | C | C | A | TCGA-DU-7298-01A-11D-2024-08 | TCGA-DU-7298-10A-01D-2024-08 | g.chr17:15510998C>A | | c.e6-1 | |
LGG | 17 | 15518967 | 15518967 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:15518967G>T | c.662C>A | c.(661-663)tCt>tAt | p.S221Y |
LGG | 17 | 15522425 | 15522425 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:15522425C>T | c.402G>A | c.(400-402)gcG>gcA | p.A134A |
LIHC | 17 | 15492292 | 15492292 | + | Silent | SNP | C | C | T | TCGA-WQ-A9G7-01A-11D-A36X-10 | TCGA-WQ-A9G7-10A-01D-A370-10 | g.chr17:15492292C>T | c.2256G>A | c.(2254-2256)gtG>gtA | p.V752V |
LIHC | 17 | 15508540 | 15508541 | + | Frame_Shift_Del | DEL | AT | AT | - | TCGA-MI-A75H-01A-11D-A32G-10 | TCGA-MI-A75H-10A-01D-A32G-10 | g.chr17:15508540_15508541delAT | c.1429_1430delAT | c.(1429-1431)atcfs | p.I477fs |
LIHC | 17 | 15510886 | 15510886 | + | Splice_Site | SNP | A | A | T | TCGA-FV-A2QQ-01A-11D-A22F-10 | TCGA-FV-A2QQ-10B-01D-A22F-10 | g.chr17:15510886A>T | | c.e6+1 | |
LIHC | 17 | 15516062 | 15516062 | + | Missense_Mutation | SNP | C | C | A | TCGA-DD-AAE3-01A-11D-A40R-10 | TCGA-DD-AAE3-10A-01D-A40U-10 | g.chr17:15516062C>A | c.1075G>T | c.(1075-1077)Ggg>Tgg | p.G359W |
LUAD | 17 | 15496778 | 15496778 | + | Missense_Mutation | SNP | G | G | A | TCGA-75-6203-01A-11D-1753-08 | TCGA-75-6203-10A-01D-1753-08 | g.chr17:15496778G>A | c.1879C>T | c.(1879-1881)Cgg>Tgg | p.R627W |
LUAD | 17 | 15498129 | 15498129 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr17:15498129C>A | c.1780G>T | c.(1780-1782)Ggc>Tgc | p.G594C |
LUAD | 17 | 15499942 | 15499942 | + | Silent | SNP | C | C | T | TCGA-44-2657-01A-01D-1105-08 | TCGA-44-2657-10A-01D-1105-08 | g.chr17:15499942C>T | c.1590G>A | c.(1588-1590)acG>acA | p.T530T |
LUAD | 17 | 15516139 | 15516139 | + | Splice_Site | SNP | T | T | G | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr17:15516139T>G | | c.e5-2 | |
LUAD | 17 | 15522458 | 15522458 | + | Silent | SNP | A | A | G | TCGA-MP-A4TK-01A-11D-A24P-08 | TCGA-MP-A4TK-10A-01D-A24P-08 | g.chr17:15522458A>G | c.369T>C | c.(367-369)taT>taC | p.Y123Y |
LUAD | 17 | 15522550 | 15522550 | + | Missense_Mutation | SNP | C | C | G | TCGA-17-Z055-01A-01W-0747-08 | TCGA-17-Z055-11A-01W-0747-08 | g.chr17:15522550C>G | c.277G>C | c.(277-279)Gac>Cac | p.D93H |
LUSC | 17 | 15516031 | 15516031 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-22-5471-01A-01D-1632-08 | TCGA-22-5471-11A-01D-1632-08 | g.chr17:15516031C>T | c.1106G>A | c.(1105-1107)tGg>tAg | p.W369* |
OV | 17 | 15501919 | 15501919 | + | Missense_Mutation | SNP | G | G | C | TCGA-13-0924-01A-01W-0421-09 | TCGA-13-0924-10A-01W-0421-09 | g.chr17:15501919G>C | c.1482C>G | c.(1480-1482)caC>caG | p.H494Q |
OV | 17 | 15510908 | 15510908 | + | Silent | SNP | A | A | G | TCGA-36-2530-01A-01D-1526-09 | TCGA-36-2530-10A-01D-1526-09 | g.chr17:15510908A>G | c.1212T>C | c.(1210-1212)aaT>aaC | p.N404N |
OV | 17 | 15517314 | 15517314 | + | Missense_Mutation | SNP | G | G | A | TCGA-20-1687-01A-01W-0633-09 | TCGA-20-1687-10A-01W-0633-09 | g.chr17:15517314G>A | c.704C>T | c.(703-705)tCc>tTc | p.S235F |
PAAD | 17 | 15522551 | 15522551 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr17:15522551G>A | c.276C>T | c.(274-276)atC>atT | p.I92I |
PRAD | 17 | 15522583 | 15522583 | + | Missense_Mutation | SNP | C | C | T | TCGA-J9-A8CL-01A-11D-A34U-08 | TCGA-J9-A8CL-10A-01D-A34X-08 | g.chr17:15522583C>T | c.244G>A | c.(244-246)Gga>Aga | p.G82R |
READ | 17 | 15492480 | 15492480 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr17:15492480C>A | c.2068G>T | c.(2068-2070)Gaa>Taa | p.E690* |
SKCM | 17 | 15492462 | 15492462 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr17:15492462G>A | c.2086C>T | c.(2086-2088)Cag>Tag | p.Q696* |
SKCM | 17 | 15510940 | 15510940 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr17:15510940C>T | c.1180G>A | c.(1180-1182)Gag>Aag | p.E394K |
SKCM | 17 | 15516110 | 15516110 | + | Missense_Mutation | SNP | T | T | C | TCGA-FS-A4FC-06A-11D-A24R-08 | TCGA-FS-A4FC-10A-01D-A24R-08 | g.chr17:15516110T>C | c.1027A>G | c.(1027-1029)Aat>Gat | p.N343D |
SKCM | 17 | 15517241 | 15517241 | + | Silent | SNP | A | A | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr17:15517241A>T | c.777T>A | c.(775-777)gtT>gtA | p.V259V |
SKCM | 17 | 15517307 | 15517307 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A5DY-06A-11D-A30X-08 | TCGA-FW-A5DY-11A-12D-A30X-08 | g.chr17:15517307C>T | c.711G>A | c.(709-711)atG>atA | p.M237I |
SKCM | 17 | 15517324 | 15517324 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1I7-06A-22D-A197-08 | TCGA-DA-A1I7-10A-01D-A199-08 | g.chr17:15517324G>A | c.694C>T | c.(694-696)Cgg>Tgg | p.R232W |
SKCM | 17 | 15518999 | 15518999 | + | Silent | SNP | G | G | A | TCGA-D3-A2JP-06A-11D-A19A-08 | TCGA-D3-A2JP-10A-01D-A19A-08 | g.chr17:15518999G>A | c.630C>T | c.(628-630)gcC>gcT | p.A210A |
SKCM | 17 | 15519000 | 15519000 | + | Missense_Mutation | SNP | G | G | T | TCGA-D3-A2JP-06A-11D-A19A-08 | TCGA-D3-A2JP-10A-01D-A19A-08 | g.chr17:15519000G>T | c.629C>A | c.(628-630)gCc>gAc | p.A210D |
SKCM | 17 | 15519013 | 15519013 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3MV-06A-11D-A21A-08 | TCGA-D3-A3MV-10A-01D-A21A-08 | g.chr17:15519013G>A | c.616C>T | c.(616-618)Cct>Tct | p.P206S |
SKCM | 17 | 15519090 | 15519090 | + | Missense_Mutation | SNP | G | G | A | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr17:15519090G>A | c.539C>T | c.(538-540)tCc>tTc | p.S180F |
SKCM | 17 | 15522499 | 15522499 | + | Silent | SNP | A | A | G | TCGA-GN-A265-06A-21D-A197-08 | TCGA-GN-A265-10A-01D-A199-08 | g.chr17:15522499A>G | c.328T>C | c.(328-330)Ttg>Ctg | p.L110L |
SKCM | 17 | 15522746 | 15522746 | + | Silent | SNP | C | C | T | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr17:15522746C>T | c.81G>A | c.(79-81)cgG>cgA | p.R27R |
SKCM | 17 | 15522784 | 15522784 | + | Missense_Mutation | SNP | G | G | A | TCGA-GF-A6C8-06A-12D-A30X-08 | TCGA-GF-A6C8-10A-01D-A30X-08 | g.chr17:15522784G>A | c.43C>T | c.(43-45)Cgt>Tgt | p.R15C |