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 | 14 | 75130426 | 75130426 | + | Silent | SNP | G | G | C | TCGA-FD-A43X-01A-11D-A23U-08 | TCGA-FD-A43X-10A-01D-A23U-08 | g.chr14:75130426G>C | c.2469C>G | c.(2467-2469)ctC>ctG | p.L823L |
BLCA | 14 | 75130444 | 75130444 | + | Silent | SNP | G | G | A | TCGA-ZF-AA4W-01A-12D-A38G-08 | TCGA-ZF-AA4W-10A-01D-A38J-08 | g.chr14:75130444G>A | c.2451C>T | c.(2449-2451)tgC>tgT | p.C817C |
BLCA | 14 | 75130680 | 75130680 | + | Missense_Mutation | SNP | C | C | G | TCGA-KQ-A41O-01A-12D-A34U-08 | TCGA-KQ-A41O-10D-01D-A34X-08 | g.chr14:75130680C>G | c.2291G>C | c.(2290-2292)gGa>gCa | p.G764A |
BLCA | 14 | 75130693 | 75130693 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-G2-A3VY-01A-11D-A22Z-08 | TCGA-G2-A3VY-10A-01D-A22Z-08 | g.chr14:75130693G>A | c.2278C>T | c.(2278-2280)Cag>Tag | p.Q760* |
BLCA | 14 | 75131623 | 75131623 | + | Silent | SNP | C | C | G | TCGA-KQ-A41O-01A-12D-A34U-08 | TCGA-KQ-A41O-10D-01D-A34X-08 | g.chr14:75131623C>G | c.2109G>C | c.(2107-2109)ctG>ctC | p.L703L |
BLCA | 14 | 75134072 | 75134072 | + | Missense_Mutation | SNP | C | C | T | TCGA-E7-A7XN-01A-11D-A34U-08 | TCGA-E7-A7XN-10A-01D-A34X-08 | g.chr14:75134072C>T | c.2053G>A | c.(2053-2055)Gaa>Aaa | p.E685K |
BLCA | 14 | 75138126 | 75138126 | + | Missense_Mutation | SNP | A | A | C | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr14:75138126A>C | c.1483T>G | c.(1483-1485)Ttc>Gtc | p.F495V |
BLCA | 14 | 75142403 | 75142403 | + | Splice_Site | SNP | T | T | A | TCGA-GV-A3QI-01A-11D-A21Z-08 | TCGA-GV-A3QI-10A-01D-A21Z-08 | g.chr14:75142403T>A | c.1079A>T | c.(1078-1080)aAg>aTg | p.K360M |
BLCA | 14 | 75142407 | 75142407 | + | Missense_Mutation | SNP | G | G | A | TCGA-E7-A97P-01A-11D-A38G-08 | TCGA-E7-A97P-10A-01D-A38J-08 | g.chr14:75142407G>A | c.1075C>T | c.(1075-1077)Cca>Tca | p.P359S |
BLCA | 14 | 75142466 | 75142466 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-A9SP-01A-11D-A391-08 | TCGA-XF-A9SP-10A-01D-A394-08 | g.chr14:75142466G>C | c.1016C>G | c.(1015-1017)tCt>tGt | p.S339C |
BLCA | 14 | 75143291 | 75143291 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A3SO-01A-11D-A22Z-08 | TCGA-FD-A3SO-10A-01D-A22Z-08 | g.chr14:75143291G>A | c.646C>T | c.(646-648)Cat>Tat | p.H216Y |
BRCA | 14 | 75130698 | 75130698 | + | Missense_Mutation | SNP | G | G | A | TCGA-C8-A26Y-01A-11D-A16D-09 | TCGA-C8-A26Y-10A-01D-A16D-09 | g.chr14:75130698G>A | c.2273C>T | c.(2272-2274)tCc>tTc | p.S758F |
BRCA | 14 | 75136706 | 75136706 | + | Missense_Mutation | SNP | C | C | A | TCGA-E2-A1LI-01A-12D-A159-09 | TCGA-E2-A1LI-11A-23D-A17G-09 | g.chr14:75136706C>A | c.1732G>T | c.(1732-1734)Gct>Tct | p.A578S |
BRCA | 14 | 75137503 | 75137503 | + | Missense_Mutation | SNP | G | G | C | TCGA-AC-A5XS-01A-11D-A29N-09 | TCGA-AC-A5XS-11A-13D-A29N-09 | g.chr14:75137503G>C | c.1570C>G | c.(1570-1572)Cag>Gag | p.Q524E |
BRCA | 14 | 75142432 | 75142432 | + | Silent | SNP | C | C | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr14:75142432C>T | c.1050G>A | c.(1048-1050)ccG>ccA | p.P350P |
BRCA | 14 | 75142442 | 75142442 | + | Missense_Mutation | SNP | A | A | C | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr14:75142442A>C | c.1040T>G | c.(1039-1041)gTg>gGg | p.V347G |
BRCA | 14 | 75142455 | 75142455 | + | Missense_Mutation | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr14:75142455T>G | c.1027A>C | c.(1027-1029)Acc>Ccc | p.T343P |
CESC | 14 | 75134036 | 75134036 | + | Missense_Mutation | SNP | C | C | T | TCGA-EA-A78R-01A-11D-A32I-09 | TCGA-EA-A78R-10A-01D-A32I-09 | g.chr14:75134036C>T | c.2089G>A | c.(2089-2091)Gag>Aag | p.E697K |
CESC | 14 | 75150065 | 75150065 | + | Missense_Mutation | SNP | C | C | T | TCGA-LP-A4AV-01A-11D-A243-09 | TCGA-LP-A4AV-10A-01D-A243-09 | g.chr14:75150065C>T | c.415G>A | c.(415-417)Gaa>Aaa | p.E139K |
CESC | 14 | 75151318 | 75151318 | + | Missense_Mutation | SNP | G | G | T | TCGA-C5-A1M6-01A-11D-A13W-08 | TCGA-C5-A1M6-10A-01D-A13W-08 | g.chr14:75151318G>T | c.82C>A | c.(82-84)Cgt>Agt | p.R28S |
CESC | 14 | 75151319 | 75151319 | + | Silent | SNP | T | T | A | TCGA-EX-A69L-01A-11D-A32I-09 | TCGA-EX-A69L-10A-01D-A32I-09 | g.chr14:75151319T>A | c.81A>T | c.(79-81)gcA>gcT | p.A27A |
CHOL | 14 | 75137486 | 75137486 | + | Missense_Mutation | SNP | G | G | T | TCGA-YR-A95A-01A-12D-A417-09 | TCGA-YR-A95A-10A-01D-A41A-09 | g.chr14:75137486G>T | c.1587C>A | c.(1585-1587)ttC>ttA | p.F529L |
COAD | 14 | 75134228 | 75134228 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr14:75134228A>C | c.1984T>G | c.(1984-1986)Ttg>Gtg | p.L662V |
COAD | 14 | 75139800 | 75139800 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr14:75139800C>T | c.1280G>A | c.(1279-1281)cGc>cAc | p.R427H |
COAD | 14 | 75142569 | 75142569 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr14:75142569T>C | c.913A>G | c.(913-915)Acc>Gcc | p.T305A |
COAD | 14 | 75142626 | 75142626 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6931-01A-11D-1924-10 | TCGA-D5-6931-10A-01D-1924-10 | g.chr14:75142626G>A | c.856C>T | c.(856-858)Cgc>Tgc | p.R286C |
COAD | 14 | 75150177 | 75150177 | + | Silent | SNP | G | G | A | TCGA-D5-6535-01A-11D-1719-10 | TCGA-D5-6535-10A-01D-1719-10 | g.chr14:75150177G>A | c.303C>T | c.(301-303)caC>caT | p.H101H |
COAD | 14 | 75150178 | 75150178 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6539-01A-11D-1719-10 | TCGA-D5-6539-10A-01D-1719-10 | g.chr14:75150178T>C | c.302A>G | c.(301-303)cAc>cGc | p.H101R |
COAD | 14 | 75151212 | 75151212 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-5666-01A-01D-1650-10 | TCGA-A6-5666-10A-01D-1650-10 | g.chr14:75151212G>A | c.188C>T | c.(187-189)tCc>tTc | p.S63F |
COAD | 14 | 75151288 | 75151288 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr14:75151288G>A | c.112C>T | c.(112-114)Cgc>Tgc | p.R38C |
COADREAD | 14 | 75134228 | 75134228 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr14:75134228A>C | c.1984T>G | c.(1984-1986)Ttg>Gtg | p.L662V |
COADREAD | 14 | 75139800 | 75139800 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr14:75139800C>T | c.1280G>A | c.(1279-1281)cGc>cAc | p.R427H |
COADREAD | 14 | 75142569 | 75142569 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr14:75142569T>C | c.913A>G | c.(913-915)Acc>Gcc | p.T305A |
COADREAD | 14 | 75142626 | 75142626 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6931-01A-11D-1924-10 | TCGA-D5-6931-10A-01D-1924-10 | g.chr14:75142626G>A | c.856C>T | c.(856-858)Cgc>Tgc | p.R286C |
COADREAD | 14 | 75142629 | 75142629 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr14:75142629C>T | c.853G>A | c.(853-855)Gaa>Aaa | p.E285K |
COADREAD | 14 | 75150177 | 75150177 | + | Silent | SNP | G | G | A | TCGA-D5-6535-01A-11D-1719-10 | TCGA-D5-6535-10A-01D-1719-10 | g.chr14:75150177G>A | c.303C>T | c.(301-303)caC>caT | p.H101H |
COADREAD | 14 | 75150178 | 75150178 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6539-01A-11D-1719-10 | TCGA-D5-6539-10A-01D-1719-10 | g.chr14:75150178T>C | c.302A>G | c.(301-303)cAc>cGc | p.H101R |
COADREAD | 14 | 75150178 | 75150178 | + | Missense_Mutation | SNP | T | T | C | TCGA-DY-A1DC-01A-31D-A152-10 | TCGA-DY-A1DC-10A-01D-A152-10 | g.chr14:75150178T>C | c.302A>G | c.(301-303)cAc>cGc | p.H101R |
COADREAD | 14 | 75151212 | 75151212 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-5666-01A-01D-1650-10 | TCGA-A6-5666-10A-01D-1650-10 | g.chr14:75151212G>A | c.188C>T | c.(187-189)tCc>tTc | p.S63F |
COADREAD | 14 | 75151288 | 75151288 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr14:75151288G>A | c.112C>T | c.(112-114)Cgc>Tgc | p.R38C |
GBM | 14 | 75149998 | 75149998 | + | Splice_Site | SNP | C | C | T | TCGA-19-2625-01A-01D-1495-08 | TCGA-19-2625-10A-01D-1495-08 | g.chr14:75149998C>T | | c.e5+1 | |
GBMLGG | 14 | 75134270 | 75134270 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DH-A7UR-01A-11D-A33T-08 | TCGA-DH-A7UR-10A-01D-A33W-08 | g.chr14:75134270G>A | c.1942C>T | c.(1942-1944)Caa>Taa | p.Q648* |
GBMLGG | 14 | 75139581 | 75139581 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:75139581G>A | c.1375C>T | c.(1375-1377)Cat>Tat | p.H459Y |
GBMLGG | 14 | 75139816 | 75139816 | + | Missense_Mutation | SNP | C | C | G | TCGA-DB-5278-01A-01D-1468-08 | TCGA-DB-5278-10A-01D-1468-08 | g.chr14:75139816C>G | c.1264G>C | c.(1264-1266)Gca>Cca | p.A422P |
GBMLGG | 14 | 75140811 | 75140811 | + | Missense_Mutation | SNP | A | A | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:75140811A>T | c.1084T>A | c.(1084-1086)Ttc>Atc | p.F362I |
GBMLGG | 14 | 75149998 | 75149998 | + | Splice_Site | SNP | C | C | T | TCGA-19-2625-01A-01D-1495-08 | TCGA-19-2625-10A-01D-1495-08 | g.chr14:75149998C>T | | c.e5+1 | |
GBMLGG | 14 | 75151317 | 75151317 | + | Missense_Mutation | SNP | C | C | T | TCGA-VW-A8FI-01A-11D-A36O-08 | TCGA-VW-A8FI-10A-01D-A367-08 | g.chr14:75151317C>T | c.83G>A | c.(82-84)cGt>cAt | p.R28H |
HNSC | 14 | 75136663 | 75136663 | + | Missense_Mutation | SNP | C | C | A | TCGA-CN-A63W-01A-11D-A30E-08 | TCGA-CN-A63W-10A-01D-A30H-08 | g.chr14:75136663C>A | c.1775G>T | c.(1774-1776)cGt>cTt | p.R592L |
HNSC | 14 | 75140809 | 75140809 | + | Missense_Mutation | SNP | G | G | T | TCGA-CV-7101-01A-11D-2012-08 | TCGA-CV-7101-10A-01D-2013-08 | g.chr14:75140809G>T | c.1086C>A | c.(1084-1086)ttC>ttA | p.F362L |
HNSC | 14 | 75142422 | 75142422 | + | Missense_Mutation | SNP | A | A | G | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr14:75142422A>G | c.1060T>C | c.(1060-1062)Tac>Cac | p.Y354H |
HNSC | 14 | 75142547 | 75142547 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-KU-A66S-01A-21D-A30E-08 | TCGA-KU-A66S-10A-01D-A30H-08 | g.chr14:75142547C>T | c.935G>A | c.(934-936)tGg>tAg | p.W312* |
HNSC | 14 | 75150018 | 75150018 | + | Silent | SNP | G | G | A | TCGA-CV-5441-01A-01D-1512-08 | TCGA-CV-5441-11A-01D-1512-08 | g.chr14:75150018G>A | c.462C>T | c.(460-462)taC>taT | p.Y154Y |
HNSC | 14 | 75151182 | 75151182 | + | Missense_Mutation | SNP | C | C | A | TCGA-CV-7414-01A-11D-2078-08 | TCGA-CV-7414-10A-01D-2078-08 | g.chr14:75151182C>A | c.218G>T | c.(217-219)gGc>gTc | p.G73V |
KIPAN | 14 | 75136411 | 75136411 | + | Missense_Mutation | SNP | T | T | G | TCGA-CJ-4905-01A-02D-1429-08 | TCGA-CJ-4905-11A-01D-1429-08 | g.chr14:75136411T>G | c.1855A>C | c.(1855-1857)Agt>Cgt | p.S619R |
KIPAN | 14 | 75136696 | 75136696 | + | Missense_Mutation | SNP | G | G | A | TCGA-CW-5591-01A-01D-1534-10 | TCGA-CW-5591-11A-01D-1535-10 | g.chr14:75136696G>A | c.1742C>T | c.(1741-1743)aCc>aTc | p.T581I |
KIRC | 14 | 75136411 | 75136411 | + | Missense_Mutation | SNP | T | T | G | TCGA-CJ-4905-01A-02D-1429-08 | TCGA-CJ-4905-11A-01D-1429-08 | g.chr14:75136411T>G | c.1855A>C | c.(1855-1857)Agt>Cgt | p.S619R |
KIRC | 14 | 75136696 | 75136696 | + | Missense_Mutation | SNP | G | G | A | TCGA-CW-5591-01A-01D-1534-10 | TCGA-CW-5591-11A-01D-1535-10 | g.chr14:75136696G>A | c.1742C>T | c.(1741-1743)aCc>aTc | p.T581I |
LGG | 14 | 75134270 | 75134270 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DH-A7UR-01A-11D-A33T-08 | TCGA-DH-A7UR-10A-01D-A33W-08 | g.chr14:75134270G>A | c.1942C>T | c.(1942-1944)Caa>Taa | p.Q648* |
LGG | 14 | 75139581 | 75139581 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:75139581G>A | c.1375C>T | c.(1375-1377)Cat>Tat | p.H459Y |
LGG | 14 | 75139816 | 75139816 | + | Missense_Mutation | SNP | C | C | G | TCGA-DB-5278-01A-01D-1468-08 | TCGA-DB-5278-10A-01D-1468-08 | g.chr14:75139816C>G | c.1264G>C | c.(1264-1266)Gca>Cca | p.A422P |
LGG | 14 | 75140811 | 75140811 | + | Missense_Mutation | SNP | A | A | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr14:75140811A>T | c.1084T>A | c.(1084-1086)Ttc>Atc | p.F362I |
LGG | 14 | 75151317 | 75151317 | + | Missense_Mutation | SNP | C | C | T | TCGA-VW-A8FI-01A-11D-A36O-08 | TCGA-VW-A8FI-10A-01D-A367-08 | g.chr14:75151317C>T | c.83G>A | c.(82-84)cGt>cAt | p.R28H |
LIHC | 14 | 75130431 | 75130431 | + | Missense_Mutation | SNP | T | T | C | TCGA-ES-A2HS-01A-11D-A183-10 | TCGA-ES-A2HS-11A-11D-A183-10 | g.chr14:75130431T>C | c.2464A>G | c.(2464-2466)Atg>Gtg | p.M822V |
LIHC | 14 | 75130470 | 75130470 | + | Silent | SNP | G | G | A | TCGA-4R-AA8I-01A-11D-A382-10 | TCGA-4R-AA8I-10B-01D-A385-10 | g.chr14:75130470G>A | c.2425C>T | c.(2425-2427)Ctg>Ttg | p.L809L |
LIHC | 14 | 75130767 | 75130767 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-GJ-A9DB-01A-11D-A36X-10 | TCGA-GJ-A9DB-10A-01D-A370-10 | g.chr14:75130767C>T | c.2204G>A | c.(2203-2205)tGg>tAg | p.W735* |
LIHC | 14 | 75139861 | 75139861 | + | Missense_Mutation | SNP | T | T | A | TCGA-DD-AACK-01A-11D-A40R-10 | TCGA-DD-AACK-10A-01D-A40U-10 | g.chr14:75139861T>A | c.1219A>T | c.(1219-1221)Att>Ttt | p.I407F |
LIHC | 14 | 75140804 | 75140804 | + | Missense_Mutation | SNP | A | A | T | TCGA-DD-A11C-01A-11D-A12Z-10 | TCGA-DD-A11C-11A-11D-A12Z-10 | g.chr14:75140804A>T | c.1091T>A | c.(1090-1092)gTg>gAg | p.V364E |
LUAD | 14 | 75130623 | 75130623 | + | Missense_Mutation | SNP | G | G | A | TCGA-99-8025-01A-11D-2238-08 | TCGA-99-8025-10A-01D-2238-08 | g.chr14:75130623G>A | c.2348C>T | c.(2347-2349)aCg>aTg | p.T783M |
LUAD | 14 | 75130730 | 75130730 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr14:75130730C>A | c.2241G>T | c.(2239-2241)gaG>gaT | p.E747D |
LUAD | 14 | 75131573 | 75131573 | + | Missense_Mutation | SNP | A | A | G | TCGA-95-7947-01A-11D-2184-08 | TCGA-95-7947-10A-01D-2184-08 | g.chr14:75131573A>G | c.2159T>C | c.(2158-2160)gTa>gCa | p.V720A |
LUAD | 14 | 75134250 | 75134250 | + | Silent | SNP | C | C | G | TCGA-55-7910-01A-11D-2167-08 | TCGA-55-7910-11A-01D-2167-08 | g.chr14:75134250C>G | c.1962G>C | c.(1960-1962)gcG>gcC | p.A654A |
LUAD | 14 | 75136414 | 75136414 | + | Missense_Mutation | SNP | T | T | C | TCGA-69-7978-01A-11D-2184-08 | TCGA-69-7978-10A-01D-2184-08 | g.chr14:75136414T>C | c.1852A>G | c.(1852-1854)Atg>Gtg | p.M618V |
LUAD | 14 | 75138120 | 75138120 | + | Missense_Mutation | SNP | C | C | A | TCGA-53-7624-01A-11D-2063-08 | TCGA-53-7624-10A-01D-2063-08 | g.chr14:75138120C>A | c.1489G>T | c.(1489-1491)Gat>Tat | p.D497Y |
LUAD | 14 | 75142464 | 75142464 | + | Missense_Mutation | SNP | C | C | T | TCGA-64-1677-01A-01W-0928-08 | TCGA-64-1677-10A-01W-0928-08 | g.chr14:75142464C>T | c.1018G>A | c.(1018-1020)Gag>Aag | p.E340K |
LUAD | 14 | 75142577 | 75142577 | + | Missense_Mutation | SNP | T | T | C | TCGA-05-4395-01A-01D-1265-08 | TCGA-05-4395-10A-01D-1265-08 | g.chr14:75142577T>C | c.905A>G | c.(904-906)tAt>tGt | p.Y302C |
LUAD | 14 | 75142581 | 75142581 | + | Missense_Mutation | SNP | G | G | C | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr14:75142581G>C | c.901C>G | c.(901-903)Ctt>Gtt | p.L301V |
LUAD | 14 | 75142625 | 75142625 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-55-7994-01A-11D-2184-08 | TCGA-55-7994-10A-01D-2184-08 | g.chr14:75142625delC | c.857delG | c.(856-858)cgcfs | p.R286fs |
LUAD | 14 | 75142850 | 75142850 | + | Silent | SNP | G | G | A | TCGA-NJ-A4YI-01A-11D-A25L-08 | TCGA-NJ-A4YI-10A-01D-A25L-08 | g.chr14:75142850G>A | c.826C>T | c.(826-828)Cta>Tta | p.L276L |
LUAD | 14 | 75150054 | 75150054 | + | Silent | SNP | C | C | T | TCGA-50-6590-01A-12D-1855-08 | TCGA-50-6590-11A-01D-1855-08 | g.chr14:75150054C>T | c.426G>A | c.(424-426)gtG>gtA | p.V142V |
LUSC | 14 | 75134184 | 75134184 | + | Silent | SNP | C | C | A | TCGA-37-5819-01A-01D-1632-08 | TCGA-37-5819-10A-01D-1632-08 | g.chr14:75134184C>A | c.2028G>T | c.(2026-2028)gtG>gtT | p.V676V |
LUSC | 14 | 75143291 | 75143291 | + | Missense_Mutation | SNP | G | G | C | TCGA-21-1070-01A-01D-1521-08 | TCGA-21-1070-11A-01D-1521-08 | g.chr14:75143291G>C | c.646C>G | c.(646-648)Cat>Gat | p.H216D |
LUSC | 14 | 75151330 | 75151330 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2785-01A-01D-1522-08 | TCGA-66-2785-11A-01D-1522-08 | g.chr14:75151330C>G | c.70G>C | c.(70-72)Gag>Cag | p.E24Q |
OV | 14 | 75131548 | 75131548 | + | Missense_Mutation | SNP | G | G | C | TCGA-24-1555-01A-01W-0552-10 | TCGA-24-1555-10A-01W-0552-10 | g.chr14:75131548G>C | c.2184C>G | c.(2182-2184)ttC>ttG | p.F728L |
OV | 14 | 75134212 | 75134212 | + | Missense_Mutation | SNP | C | C | T | TCGA-61-1910-01A-01W-0639-09 | TCGA-61-1910-11A-01W-0640-09 | g.chr14:75134212C>T | c.2000G>A | c.(1999-2001)cGg>cAg | p.R667Q |
OV | 14 | 75150179 | 75150179 | + | Missense_Mutation | SNP | G | G | A | TCGA-13-1499-01A-01W-0549-09 | TCGA-13-1499-10A-01W-0549-09 | g.chr14:75150179G>A | c.301C>T | c.(301-303)Cac>Tac | p.H101Y |
PAAD | 14 | 75130641 | 75130641 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr14:75130641G>A | c.2330C>T | c.(2329-2331)gCc>gTc | p.A777V |
PAAD | 14 | 75139533 | 75139533 | + | Splice_Site | SNP | C | C | T | TCGA-3A-A9IJ-01A-11D-A397-08 | TCGA-3A-A9IJ-10A-01D-A39A-08 | g.chr14:75139533C>T | | c.e11+1 | |
PAAD | 14 | 75140748 | 75140748 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr14:75140748G>T | c.1147C>A | c.(1147-1149)Cca>Aca | p.P383T |
PAAD | 14 | 75142502 | 75142502 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr14:75142502G>T | c.980C>A | c.(979-981)tCc>tAc | p.S327Y |
PAAD | 14 | 75142633 | 75142633 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr14:75142633G>A | c.849C>T | c.(847-849)atC>atT | p.I283I |
PAAD | 14 | 75151269 | 75151269 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr14:75151269C>T | c.131G>A | c.(130-132)cGg>cAg | p.R44Q |
PRAD | 14 | 75140771 | 75140771 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr14:75140771C>T | c.1124G>A | c.(1123-1125)cGc>cAc | p.R375H |
PRAD | 14 | 75143386 | 75143386 | + | Missense_Mutation | SNP | G | G | A | TCGA-KK-A59V-01A-11D-A29Q-08 | TCGA-KK-A59V-11A-11D-A29Q-08 | g.chr14:75143386G>A | c.551C>T | c.(550-552)cCg>cTg | p.P184L |
PRAD | 14 | 75151249 | 75151249 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr14:75151249G>A | c.151C>T | c.(151-153)Cgg>Tgg | p.R51W |
READ | 14 | 75142629 | 75142629 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr14:75142629C>T | c.853G>A | c.(853-855)Gaa>Aaa | p.E285K |
READ | 14 | 75150178 | 75150178 | + | Missense_Mutation | SNP | T | T | C | TCGA-DY-A1DC-01A-31D-A152-10 | TCGA-DY-A1DC-10A-01D-A152-10 | g.chr14:75150178T>C | c.302A>G | c.(301-303)cAc>cGc | p.H101R |
SKCM | 14 | 75130447 | 75130447 | + | Silent | SNP | A | A | G | TCGA-DA-A1HY-06A-11D-A19A-08 | TCGA-DA-A1HY-10A-01D-A19A-08 | g.chr14:75130447A>G | c.2448T>C | c.(2446-2448)ggT>ggC | p.G816G |
SKCM | 14 | 75134175 | 75134175 | + | Silent | SNP | G | G | A | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr14:75134175G>A | c.2037C>T | c.(2035-2037)ttC>ttT | p.F679F |
SKCM | 14 | 75136681 | 75136681 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr14:75136681G>A | c.1757C>T | c.(1756-1758)gCc>gTc | p.A586V |
SKCM | 14 | 75136688 | 75136688 | + | Missense_Mutation | SNP | A | A | T | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr14:75136688A>T | c.1750T>A | c.(1750-1752)Ttc>Atc | p.F584I |
SKCM | 14 | 75136738 | 75136738 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr14:75136738G>A | c.1700C>T | c.(1699-1701)tCt>tTt | p.S567F |
SKCM | 14 | 75139618 | 75139618 | + | Silent | SNP | G | G | A | TCGA-EE-A29S-06A-11D-A197-08 | TCGA-EE-A29S-10A-01D-A199-08 | g.chr14:75139618G>A | c.1338C>T | c.(1336-1338)ttC>ttT | p.F446F |
SKCM | 14 | 75139651 | 75139651 | + | Silent | SNP | G | G | A | TCGA-EE-A2MI-06A-11D-A197-08 | TCGA-EE-A2MI-10A-01D-A199-08 | g.chr14:75139651G>A | c.1305C>T | c.(1303-1305)ggC>ggT | p.G435G |
SKCM | 14 | 75142897 | 75142897 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZE-06A-11D-A197-08 | TCGA-FS-A1ZE-10A-01D-A199-08 | g.chr14:75142897G>A | c.779C>T | c.(778-780)tCa>tTa | p.S260L |
SKCM | 14 | 75143345 | 75143345 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZQ-06A-11D-A197-08 | TCGA-FS-A1ZQ-10A-01D-A199-08 | g.chr14:75143345G>A | c.592C>T | c.(592-594)Ccc>Tcc | p.P198S |
SKCM | 14 | 75150111 | 75150111 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr14:75150111G>A | c.369C>T | c.(367-369)tcC>tcT | p.S123S |
SKCM | 14 | 75150160 | 75150160 | + | Missense_Mutation | SNP | A | A | G | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr14:75150160A>G | c.320T>C | c.(319-321)cTa>cCa | p.L107P |
SKCM | 14 | 75151289 | 75151289 | + | Silent | SNP | G | G | A | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr14:75151289G>A | c.111C>T | c.(109-111)gaC>gaT | p.D37D |