AREL1
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA147513042675130426+SilentSNPGGCTCGA-FD-A43X-01A-11D-A23U-08TCGA-FD-A43X-10A-01D-A23U-08g.chr14:75130426G>Cc.2469C>Gc.(2467-2469)ctC>ctGp.L823L
BLCA147513044475130444+SilentSNPGGATCGA-ZF-AA4W-01A-12D-A38G-08TCGA-ZF-AA4W-10A-01D-A38J-08g.chr14:75130444G>Ac.2451C>Tc.(2449-2451)tgC>tgTp.C817C
BLCA147513068075130680+Missense_MutationSNPCCGTCGA-KQ-A41O-01A-12D-A34U-08TCGA-KQ-A41O-10D-01D-A34X-08g.chr14:75130680C>Gc.2291G>Cc.(2290-2292)gGa>gCap.G764A
BLCA147513069375130693+Nonsense_MutationSNPGGATCGA-G2-A3VY-01A-11D-A22Z-08TCGA-G2-A3VY-10A-01D-A22Z-08g.chr14:75130693G>Ac.2278C>Tc.(2278-2280)Cag>Tagp.Q760*
BLCA147513162375131623+SilentSNPCCGTCGA-KQ-A41O-01A-12D-A34U-08TCGA-KQ-A41O-10D-01D-A34X-08g.chr14:75131623C>Gc.2109G>Cc.(2107-2109)ctG>ctCp.L703L
BLCA147513407275134072+Missense_MutationSNPCCTTCGA-E7-A7XN-01A-11D-A34U-08TCGA-E7-A7XN-10A-01D-A34X-08g.chr14:75134072C>Tc.2053G>Ac.(2053-2055)Gaa>Aaap.E685K
BLCA147513812675138126+Missense_MutationSNPAACTCGA-DK-A6AW-01A-11D-A30E-08TCGA-DK-A6AW-10A-01D-A30H-08g.chr14:75138126A>Cc.1483T>Gc.(1483-1485)Ttc>Gtcp.F495V
BLCA147514240375142403+Splice_SiteSNPTTATCGA-GV-A3QI-01A-11D-A21Z-08TCGA-GV-A3QI-10A-01D-A21Z-08g.chr14:75142403T>Ac.1079A>Tc.(1078-1080)aAg>aTgp.K360M
BLCA147514240775142407+Missense_MutationSNPGGATCGA-E7-A97P-01A-11D-A38G-08TCGA-E7-A97P-10A-01D-A38J-08g.chr14:75142407G>Ac.1075C>Tc.(1075-1077)Cca>Tcap.P359S
BLCA147514246675142466+Missense_MutationSNPGGCTCGA-XF-A9SP-01A-11D-A391-08TCGA-XF-A9SP-10A-01D-A394-08g.chr14:75142466G>Cc.1016C>Gc.(1015-1017)tCt>tGtp.S339C
BLCA147514329175143291+Missense_MutationSNPGGATCGA-FD-A3SO-01A-11D-A22Z-08TCGA-FD-A3SO-10A-01D-A22Z-08g.chr14:75143291G>Ac.646C>Tc.(646-648)Cat>Tatp.H216Y
BRCA147513069875130698+Missense_MutationSNPGGATCGA-C8-A26Y-01A-11D-A16D-09TCGA-C8-A26Y-10A-01D-A16D-09g.chr14:75130698G>Ac.2273C>Tc.(2272-2274)tCc>tTcp.S758F
BRCA147513670675136706+Missense_MutationSNPCCATCGA-E2-A1LI-01A-12D-A159-09TCGA-E2-A1LI-11A-23D-A17G-09g.chr14:75136706C>Ac.1732G>Tc.(1732-1734)Gct>Tctp.A578S
BRCA147513750375137503+Missense_MutationSNPGGCTCGA-AC-A5XS-01A-11D-A29N-09TCGA-AC-A5XS-11A-13D-A29N-09g.chr14:75137503G>Cc.1570C>Gc.(1570-1572)Cag>Gagp.Q524E
BRCA147514243275142432+SilentSNPCCTTCGA-AN-A046-01A-21W-A050-09TCGA-AN-A046-10A-01W-A055-09g.chr14:75142432C>Tc.1050G>Ac.(1048-1050)ccG>ccAp.P350P
BRCA147514244275142442+Missense_MutationSNPAACTCGA-A8-A0A6-01A-12W-A071-09TCGA-A8-A0A6-10A-01W-A071-09g.chr14:75142442A>Cc.1040T>Gc.(1039-1041)gTg>gGgp.V347G
BRCA147514245575142455+Missense_MutationSNPTTGTCGA-A8-A0A6-01A-12W-A071-09TCGA-A8-A0A6-10A-01W-A071-09g.chr14:75142455T>Gc.1027A>Cc.(1027-1029)Acc>Cccp.T343P
CESC147513403675134036+Missense_MutationSNPCCTTCGA-EA-A78R-01A-11D-A32I-09TCGA-EA-A78R-10A-01D-A32I-09g.chr14:75134036C>Tc.2089G>Ac.(2089-2091)Gag>Aagp.E697K
CESC147515006575150065+Missense_MutationSNPCCTTCGA-LP-A4AV-01A-11D-A243-09TCGA-LP-A4AV-10A-01D-A243-09g.chr14:75150065C>Tc.415G>Ac.(415-417)Gaa>Aaap.E139K
CESC147515131875151318+Missense_MutationSNPGGTTCGA-C5-A1M6-01A-11D-A13W-08TCGA-C5-A1M6-10A-01D-A13W-08g.chr14:75151318G>Tc.82C>Ac.(82-84)Cgt>Agtp.R28S
CESC147515131975151319+SilentSNPTTATCGA-EX-A69L-01A-11D-A32I-09TCGA-EX-A69L-10A-01D-A32I-09g.chr14:75151319T>Ac.81A>Tc.(79-81)gcA>gcTp.A27A
CHOL147513748675137486+Missense_MutationSNPGGTTCGA-YR-A95A-01A-12D-A417-09TCGA-YR-A95A-10A-01D-A41A-09g.chr14:75137486G>Tc.1587C>Ac.(1585-1587)ttC>ttAp.F529L
COAD147513422875134228+Missense_MutationSNPAACTCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr14:75134228A>Cc.1984T>Gc.(1984-1986)Ttg>Gtgp.L662V
COAD147513980075139800+Missense_MutationSNPCCTTCGA-CA-6717-01A-11D-1835-10TCGA-CA-6717-10A-01D-1835-10g.chr14:75139800C>Tc.1280G>Ac.(1279-1281)cGc>cAcp.R427H
COAD147514256975142569+Missense_MutationSNPTTCTCGA-AD-6889-01A-11D-1924-10TCGA-AD-6889-10A-01D-1924-10g.chr14:75142569T>Cc.913A>Gc.(913-915)Acc>Gccp.T305A
COAD147514262675142626+Missense_MutationSNPGGATCGA-D5-6931-01A-11D-1924-10TCGA-D5-6931-10A-01D-1924-10g.chr14:75142626G>Ac.856C>Tc.(856-858)Cgc>Tgcp.R286C
COAD147515017775150177+SilentSNPGGATCGA-D5-6535-01A-11D-1719-10TCGA-D5-6535-10A-01D-1719-10g.chr14:75150177G>Ac.303C>Tc.(301-303)caC>caTp.H101H
COAD147515017875150178+Missense_MutationSNPTTCTCGA-D5-6539-01A-11D-1719-10TCGA-D5-6539-10A-01D-1719-10g.chr14:75150178T>Cc.302A>Gc.(301-303)cAc>cGcp.H101R
COAD147515121275151212+Missense_MutationSNPGGATCGA-A6-5666-01A-01D-1650-10TCGA-A6-5666-10A-01D-1650-10g.chr14:75151212G>Ac.188C>Tc.(187-189)tCc>tTcp.S63F
COAD147515128875151288+Missense_MutationSNPGGATCGA-AA-3815-01A-01W-0995-10TCGA-AA-3815-10A-01W-0995-10g.chr14:75151288G>Ac.112C>Tc.(112-114)Cgc>Tgcp.R38C
COADREAD147513422875134228+Missense_MutationSNPAACTCGA-AZ-4315-01A-01D-1408-10TCGA-AZ-4315-10A-01D-1408-10g.chr14:75134228A>Cc.1984T>Gc.(1984-1986)Ttg>Gtgp.L662V
COADREAD147513980075139800+Missense_MutationSNPCCTTCGA-CA-6717-01A-11D-1835-10TCGA-CA-6717-10A-01D-1835-10g.chr14:75139800C>Tc.1280G>Ac.(1279-1281)cGc>cAcp.R427H
COADREAD147514256975142569+Missense_MutationSNPTTCTCGA-AD-6889-01A-11D-1924-10TCGA-AD-6889-10A-01D-1924-10g.chr14:75142569T>Cc.913A>Gc.(913-915)Acc>Gccp.T305A
COADREAD147514262675142626+Missense_MutationSNPGGATCGA-D5-6931-01A-11D-1924-10TCGA-D5-6931-10A-01D-1924-10g.chr14:75142626G>Ac.856C>Tc.(856-858)Cgc>Tgcp.R286C
COADREAD147514262975142629+Missense_MutationSNPCCTTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr14:75142629C>Tc.853G>Ac.(853-855)Gaa>Aaap.E285K
COADREAD147515017775150177+SilentSNPGGATCGA-D5-6535-01A-11D-1719-10TCGA-D5-6535-10A-01D-1719-10g.chr14:75150177G>Ac.303C>Tc.(301-303)caC>caTp.H101H
COADREAD147515017875150178+Missense_MutationSNPTTCTCGA-D5-6539-01A-11D-1719-10TCGA-D5-6539-10A-01D-1719-10g.chr14:75150178T>Cc.302A>Gc.(301-303)cAc>cGcp.H101R
COADREAD147515017875150178+Missense_MutationSNPTTCTCGA-DY-A1DC-01A-31D-A152-10TCGA-DY-A1DC-10A-01D-A152-10g.chr14:75150178T>Cc.302A>Gc.(301-303)cAc>cGcp.H101R
COADREAD147515121275151212+Missense_MutationSNPGGATCGA-A6-5666-01A-01D-1650-10TCGA-A6-5666-10A-01D-1650-10g.chr14:75151212G>Ac.188C>Tc.(187-189)tCc>tTcp.S63F
COADREAD147515128875151288+Missense_MutationSNPGGATCGA-AA-3815-01A-01W-0995-10TCGA-AA-3815-10A-01W-0995-10g.chr14:75151288G>Ac.112C>Tc.(112-114)Cgc>Tgcp.R38C
GBM147514999875149998+Splice_SiteSNPCCTTCGA-19-2625-01A-01D-1495-08TCGA-19-2625-10A-01D-1495-08g.chr14:75149998C>Tc.e5+1
GBMLGG147513427075134270+Nonsense_MutationSNPGGATCGA-DH-A7UR-01A-11D-A33T-08TCGA-DH-A7UR-10A-01D-A33W-08g.chr14:75134270G>Ac.1942C>Tc.(1942-1944)Caa>Taap.Q648*
GBMLGG147513958175139581+Missense_MutationSNPGGATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr14:75139581G>Ac.1375C>Tc.(1375-1377)Cat>Tatp.H459Y
GBMLGG147513981675139816+Missense_MutationSNPCCGTCGA-DB-5278-01A-01D-1468-08TCGA-DB-5278-10A-01D-1468-08g.chr14:75139816C>Gc.1264G>Cc.(1264-1266)Gca>Ccap.A422P
GBMLGG147514081175140811+Missense_MutationSNPAATTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr14:75140811A>Tc.1084T>Ac.(1084-1086)Ttc>Atcp.F362I
GBMLGG147514999875149998+Splice_SiteSNPCCTTCGA-19-2625-01A-01D-1495-08TCGA-19-2625-10A-01D-1495-08g.chr14:75149998C>Tc.e5+1
GBMLGG147515131775151317+Missense_MutationSNPCCTTCGA-VW-A8FI-01A-11D-A36O-08TCGA-VW-A8FI-10A-01D-A367-08g.chr14:75151317C>Tc.83G>Ac.(82-84)cGt>cAtp.R28H
HNSC147513666375136663+Missense_MutationSNPCCATCGA-CN-A63W-01A-11D-A30E-08TCGA-CN-A63W-10A-01D-A30H-08g.chr14:75136663C>Ac.1775G>Tc.(1774-1776)cGt>cTtp.R592L
HNSC147514080975140809+Missense_MutationSNPGGTTCGA-CV-7101-01A-11D-2012-08TCGA-CV-7101-10A-01D-2013-08g.chr14:75140809G>Tc.1086C>Ac.(1084-1086)ttC>ttAp.F362L
HNSC147514242275142422+Missense_MutationSNPAAGTCGA-F7-A624-01A-22D-A30E-08TCGA-F7-A624-10A-01D-A30H-08g.chr14:75142422A>Gc.1060T>Cc.(1060-1062)Tac>Cacp.Y354H
HNSC147514254775142547+Nonsense_MutationSNPCCTTCGA-KU-A66S-01A-21D-A30E-08TCGA-KU-A66S-10A-01D-A30H-08g.chr14:75142547C>Tc.935G>Ac.(934-936)tGg>tAgp.W312*
HNSC147515001875150018+SilentSNPGGATCGA-CV-5441-01A-01D-1512-08TCGA-CV-5441-11A-01D-1512-08g.chr14:75150018G>Ac.462C>Tc.(460-462)taC>taTp.Y154Y
HNSC147515118275151182+Missense_MutationSNPCCATCGA-CV-7414-01A-11D-2078-08TCGA-CV-7414-10A-01D-2078-08g.chr14:75151182C>Ac.218G>Tc.(217-219)gGc>gTcp.G73V
KIPAN147513641175136411+Missense_MutationSNPTTGTCGA-CJ-4905-01A-02D-1429-08TCGA-CJ-4905-11A-01D-1429-08g.chr14:75136411T>Gc.1855A>Cc.(1855-1857)Agt>Cgtp.S619R
KIPAN147513669675136696+Missense_MutationSNPGGATCGA-CW-5591-01A-01D-1534-10TCGA-CW-5591-11A-01D-1535-10g.chr14:75136696G>Ac.1742C>Tc.(1741-1743)aCc>aTcp.T581I
KIRC147513641175136411+Missense_MutationSNPTTGTCGA-CJ-4905-01A-02D-1429-08TCGA-CJ-4905-11A-01D-1429-08g.chr14:75136411T>Gc.1855A>Cc.(1855-1857)Agt>Cgtp.S619R
KIRC147513669675136696+Missense_MutationSNPGGATCGA-CW-5591-01A-01D-1534-10TCGA-CW-5591-11A-01D-1535-10g.chr14:75136696G>Ac.1742C>Tc.(1741-1743)aCc>aTcp.T581I
LGG147513427075134270+Nonsense_MutationSNPGGATCGA-DH-A7UR-01A-11D-A33T-08TCGA-DH-A7UR-10A-01D-A33W-08g.chr14:75134270G>Ac.1942C>Tc.(1942-1944)Caa>Taap.Q648*
LGG147513958175139581+Missense_MutationSNPGGATCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr14:75139581G>Ac.1375C>Tc.(1375-1377)Cat>Tatp.H459Y
LGG147513981675139816+Missense_MutationSNPCCGTCGA-DB-5278-01A-01D-1468-08TCGA-DB-5278-10A-01D-1468-08g.chr14:75139816C>Gc.1264G>Cc.(1264-1266)Gca>Ccap.A422P
LGG147514081175140811+Missense_MutationSNPAATTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr14:75140811A>Tc.1084T>Ac.(1084-1086)Ttc>Atcp.F362I
LGG147515131775151317+Missense_MutationSNPCCTTCGA-VW-A8FI-01A-11D-A36O-08TCGA-VW-A8FI-10A-01D-A367-08g.chr14:75151317C>Tc.83G>Ac.(82-84)cGt>cAtp.R28H
LIHC147513043175130431+Missense_MutationSNPTTCTCGA-ES-A2HS-01A-11D-A183-10TCGA-ES-A2HS-11A-11D-A183-10g.chr14:75130431T>Cc.2464A>Gc.(2464-2466)Atg>Gtgp.M822V
LIHC147513047075130470+SilentSNPGGATCGA-4R-AA8I-01A-11D-A382-10TCGA-4R-AA8I-10B-01D-A385-10g.chr14:75130470G>Ac.2425C>Tc.(2425-2427)Ctg>Ttgp.L809L
LIHC147513076775130767+Nonsense_MutationSNPCCTTCGA-GJ-A9DB-01A-11D-A36X-10TCGA-GJ-A9DB-10A-01D-A370-10g.chr14:75130767C>Tc.2204G>Ac.(2203-2205)tGg>tAgp.W735*
LIHC147513986175139861+Missense_MutationSNPTTATCGA-DD-AACK-01A-11D-A40R-10TCGA-DD-AACK-10A-01D-A40U-10g.chr14:75139861T>Ac.1219A>Tc.(1219-1221)Att>Tttp.I407F
LIHC147514080475140804+Missense_MutationSNPAATTCGA-DD-A11C-01A-11D-A12Z-10TCGA-DD-A11C-11A-11D-A12Z-10g.chr14:75140804A>Tc.1091T>Ac.(1090-1092)gTg>gAgp.V364E
LUAD147513062375130623+Missense_MutationSNPGGATCGA-99-8025-01A-11D-2238-08TCGA-99-8025-10A-01D-2238-08g.chr14:75130623G>Ac.2348C>Tc.(2347-2349)aCg>aTgp.T783M
LUAD147513073075130730+Missense_MutationSNPCCATCGA-17-Z031-01A-01W-0746-08TCGA-17-Z031-11A-01W-0746-08g.chr14:75130730C>Ac.2241G>Tc.(2239-2241)gaG>gaTp.E747D
LUAD147513157375131573+Missense_MutationSNPAAGTCGA-95-7947-01A-11D-2184-08TCGA-95-7947-10A-01D-2184-08g.chr14:75131573A>Gc.2159T>Cc.(2158-2160)gTa>gCap.V720A
LUAD147513425075134250+SilentSNPCCGTCGA-55-7910-01A-11D-2167-08TCGA-55-7910-11A-01D-2167-08g.chr14:75134250C>Gc.1962G>Cc.(1960-1962)gcG>gcCp.A654A
LUAD147513641475136414+Missense_MutationSNPTTCTCGA-69-7978-01A-11D-2184-08TCGA-69-7978-10A-01D-2184-08g.chr14:75136414T>Cc.1852A>Gc.(1852-1854)Atg>Gtgp.M618V
LUAD147513812075138120+Missense_MutationSNPCCATCGA-53-7624-01A-11D-2063-08TCGA-53-7624-10A-01D-2063-08g.chr14:75138120C>Ac.1489G>Tc.(1489-1491)Gat>Tatp.D497Y
LUAD147514246475142464+Missense_MutationSNPCCTTCGA-64-1677-01A-01W-0928-08TCGA-64-1677-10A-01W-0928-08g.chr14:75142464C>Tc.1018G>Ac.(1018-1020)Gag>Aagp.E340K
LUAD147514257775142577+Missense_MutationSNPTTCTCGA-05-4395-01A-01D-1265-08TCGA-05-4395-10A-01D-1265-08g.chr14:75142577T>Cc.905A>Gc.(904-906)tAt>tGtp.Y302C
LUAD147514258175142581+Missense_MutationSNPGGCTCGA-75-5126-01A-01D-1753-08TCGA-75-5126-10A-01D-1753-08g.chr14:75142581G>Cc.901C>Gc.(901-903)Ctt>Gttp.L301V
LUAD147514262575142625+Frame_Shift_DelDELCC-TCGA-55-7994-01A-11D-2184-08TCGA-55-7994-10A-01D-2184-08g.chr14:75142625delCc.857delGc.(856-858)cgcfsp.R286fs
LUAD147514285075142850+SilentSNPGGATCGA-NJ-A4YI-01A-11D-A25L-08TCGA-NJ-A4YI-10A-01D-A25L-08g.chr14:75142850G>Ac.826C>Tc.(826-828)Cta>Ttap.L276L
LUAD147515005475150054+SilentSNPCCTTCGA-50-6590-01A-12D-1855-08TCGA-50-6590-11A-01D-1855-08g.chr14:75150054C>Tc.426G>Ac.(424-426)gtG>gtAp.V142V
LUSC147513418475134184+SilentSNPCCATCGA-37-5819-01A-01D-1632-08TCGA-37-5819-10A-01D-1632-08g.chr14:75134184C>Ac.2028G>Tc.(2026-2028)gtG>gtTp.V676V
LUSC147514329175143291+Missense_MutationSNPGGCTCGA-21-1070-01A-01D-1521-08TCGA-21-1070-11A-01D-1521-08g.chr14:75143291G>Cc.646C>Gc.(646-648)Cat>Gatp.H216D
LUSC147515133075151330+Missense_MutationSNPCCGTCGA-66-2785-01A-01D-1522-08TCGA-66-2785-11A-01D-1522-08g.chr14:75151330C>Gc.70G>Cc.(70-72)Gag>Cagp.E24Q
OV147513154875131548+Missense_MutationSNPGGCTCGA-24-1555-01A-01W-0552-10TCGA-24-1555-10A-01W-0552-10g.chr14:75131548G>Cc.2184C>Gc.(2182-2184)ttC>ttGp.F728L
OV147513421275134212+Missense_MutationSNPCCTTCGA-61-1910-01A-01W-0639-09TCGA-61-1910-11A-01W-0640-09g.chr14:75134212C>Tc.2000G>Ac.(1999-2001)cGg>cAgp.R667Q
OV147515017975150179+Missense_MutationSNPGGATCGA-13-1499-01A-01W-0549-09TCGA-13-1499-10A-01W-0549-09g.chr14:75150179G>Ac.301C>Tc.(301-303)Cac>Tacp.H101Y
PAAD147513064175130641+Missense_MutationSNPGGATCGA-IB-7651-01A-11D-2154-08TCGA-IB-7651-10A-01D-2154-08g.chr14:75130641G>Ac.2330C>Tc.(2329-2331)gCc>gTcp.A777V
PAAD147513953375139533+Splice_SiteSNPCCTTCGA-3A-A9IJ-01A-11D-A397-08TCGA-3A-A9IJ-10A-01D-A39A-08g.chr14:75139533C>Tc.e11+1
PAAD147514074875140748+Missense_MutationSNPGGTTCGA-IB-7651-01A-11D-2154-08TCGA-IB-7651-10A-01D-2154-08g.chr14:75140748G>Tc.1147C>Ac.(1147-1149)Cca>Acap.P383T
PAAD147514250275142502+Missense_MutationSNPGGTTCGA-IB-7651-01A-11D-2154-08TCGA-IB-7651-10A-01D-2154-08g.chr14:75142502G>Tc.980C>Ac.(979-981)tCc>tAcp.S327Y
PAAD147514263375142633+SilentSNPGGATCGA-IB-7651-01A-11D-2154-08TCGA-IB-7651-10A-01D-2154-08g.chr14:75142633G>Ac.849C>Tc.(847-849)atC>atTp.I283I
PAAD147515126975151269+Missense_MutationSNPCCTTCGA-IB-7651-01A-11D-2154-08TCGA-IB-7651-10A-01D-2154-08g.chr14:75151269C>Tc.131G>Ac.(130-132)cGg>cAgp.R44Q
PRAD147514077175140771+Missense_MutationSNPCCTTCGA-XK-AAIW-01A-11D-A41K-08TCGA-XK-AAIW-10A-01D-A41N-08g.chr14:75140771C>Tc.1124G>Ac.(1123-1125)cGc>cAcp.R375H
PRAD147514338675143386+Missense_MutationSNPGGATCGA-KK-A59V-01A-11D-A29Q-08TCGA-KK-A59V-11A-11D-A29Q-08g.chr14:75143386G>Ac.551C>Tc.(550-552)cCg>cTgp.P184L
PRAD147515124975151249+Missense_MutationSNPGGATCGA-XK-AAIW-01A-11D-A41K-08TCGA-XK-AAIW-10A-01D-A41N-08g.chr14:75151249G>Ac.151C>Tc.(151-153)Cgg>Tggp.R51W
READ147514262975142629+Missense_MutationSNPCCTTCGA-AG-A002-01A-01W-A00K-09TCGA-AG-A002-10A-01W-A00K-09g.chr14:75142629C>Tc.853G>Ac.(853-855)Gaa>Aaap.E285K
READ147515017875150178+Missense_MutationSNPTTCTCGA-DY-A1DC-01A-31D-A152-10TCGA-DY-A1DC-10A-01D-A152-10g.chr14:75150178T>Cc.302A>Gc.(301-303)cAc>cGcp.H101R
SKCM147513044775130447+SilentSNPAAGTCGA-DA-A1HY-06A-11D-A19A-08TCGA-DA-A1HY-10A-01D-A19A-08g.chr14:75130447A>Gc.2448T>Cc.(2446-2448)ggT>ggCp.G816G
SKCM147513417575134175+SilentSNPGGATCGA-EE-A2GC-06A-11D-A197-08TCGA-EE-A2GC-10A-01D-A199-08g.chr14:75134175G>Ac.2037C>Tc.(2035-2037)ttC>ttTp.F679F
SKCM147513668175136681+Missense_MutationSNPGGATCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr14:75136681G>Ac.1757C>Tc.(1756-1758)gCc>gTcp.A586V
SKCM147513668875136688+Missense_MutationSNPAATTCGA-FS-A1ZK-06A-11D-A197-08TCGA-FS-A1ZK-10A-01D-A199-08g.chr14:75136688A>Tc.1750T>Ac.(1750-1752)Ttc>Atcp.F584I
SKCM147513673875136738+Missense_MutationSNPGGATCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr14:75136738G>Ac.1700C>Tc.(1699-1701)tCt>tTtp.S567F
SKCM147513961875139618+SilentSNPGGATCGA-EE-A29S-06A-11D-A197-08TCGA-EE-A29S-10A-01D-A199-08g.chr14:75139618G>Ac.1338C>Tc.(1336-1338)ttC>ttTp.F446F
SKCM147513965175139651+SilentSNPGGATCGA-EE-A2MI-06A-11D-A197-08TCGA-EE-A2MI-10A-01D-A199-08g.chr14:75139651G>Ac.1305C>Tc.(1303-1305)ggC>ggTp.G435G
SKCM147514289775142897+Missense_MutationSNPGGATCGA-FS-A1ZE-06A-11D-A197-08TCGA-FS-A1ZE-10A-01D-A199-08g.chr14:75142897G>Ac.779C>Tc.(778-780)tCa>tTap.S260L
SKCM147514334575143345+Missense_MutationSNPGGATCGA-FS-A1ZQ-06A-11D-A197-08TCGA-FS-A1ZQ-10A-01D-A199-08g.chr14:75143345G>Ac.592C>Tc.(592-594)Ccc>Tccp.P198S
SKCM147515011175150111+SilentSNPGGATCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr14:75150111G>Ac.369C>Tc.(367-369)tcC>tcTp.S123S
SKCM147515016075150160+Missense_MutationSNPAAGTCGA-D9-A6EC-06A-11D-A30X-08TCGA-D9-A6EC-10A-01D-A30X-08g.chr14:75150160A>Gc.320T>Cc.(319-321)cTa>cCap.L107P
SKCM147515128975151289+SilentSNPGGATCGA-EE-A2A2-06A-11D-A196-08TCGA-EE-A2A2-10A-01D-A198-08g.chr14:75151289G>Ac.111C>Tc.(109-111)gaC>gaTp.D37D
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-CN147513069575130695single base substitutionGC3_prime_UTR_variant
BLCA-CN147513069575130695single base substitutionGCexon_variant
BLCA-CN147513069575130695single base substitutionGCmissense_variantS598C1793C>G
BLCA-CN147513069575130695single base substitutionGCmissense_variantS759C2276C>G
BLCA-CN147515134975151349single base substitutionGAexon_variant
BLCA-CN147515134975151349single base substitutionGAintron_variant
BLCA-CN147515134975151349single base substitutionGAsynonymous_variantF17F51C>T
BLCA-CN147515134975151349single base substitutionGAupstream_gene_variant
BLCA-US147513069375130693single base substitutionGA3_prime_UTR_variant
BLCA-US147513069375130693single base substitutionGAexon_variant
BLCA-US147513069375130693single base substitutionGAstop_gainedQ599*1795C>T
BLCA-US147513069375130693single base substitutionGAstop_gainedQ760*2278C>T
BLCA-US147514240375142403single base substitutionTAdownstream_gene_variant
BLCA-US147514240375142403single base substitutionTAintron_variant
BLCA-US147514240375142403single base substitutionTAmissense_variantK199M596A>T
BLCA-US147514240375142403single base substitutionTAmissense_variantK360M1079A>T
BLCA-US147514240375142403single base substitutionTAsplice_region_variant
BLCA-US147514329175143291single base substitutionGA3_prime_UTR_variant
BLCA-US147514329175143291single base substitutionGAexon_variant
BLCA-US147514329175143291single base substitutionGAmissense_variantH216Y646C>T
BLCA-US147514329175143291single base substitutionGAmissense_variantH55Y163C>T
BLCA-US147514329175143291single base substitutionGAupstream_gene_variant
BRCA-EU147511649675116496single base substitutionGCdownstream_gene_variant
BRCA-EU147511649875116498single base substitutionCAdownstream_gene_variant
BRCA-EU147511701275117012single base substitutionATdownstream_gene_variant
BRCA-EU147511822075118220single base substitutionCGdownstream_gene_variant
BRCA-EU147512232475122324deletion of <=200bpA-downstream_gene_variant
BRCA-EU147512232475122324deletion of <=200bpA-intron_variant
BRCA-EU147512564375125643single base substitutionTCdownstream_gene_variant
BRCA-EU147512564375125643single base substitutionTCintron_variant
BRCA-EU147512832975128329single base substitutionTC3_prime_UTR_variant
BRCA-EU147512832975128329single base substitutionTCdownstream_gene_variant
BRCA-EU147512832975128329single base substitutionTCintron_variant
BRCA-EU147512914175129141single base substitutionGC3_prime_UTR_variant
BRCA-EU147512914175129141single base substitutionGCdownstream_gene_variant
BRCA-EU147512914175129141single base substitutionGCintron_variant
BRCA-EU147512916575129165single base substitutionTA3_prime_UTR_variant
BRCA-EU147512916575129165single base substitutionTAdownstream_gene_variant
BRCA-EU147512916575129165single base substitutionTAintron_variant
BRCA-EU147512982675129826deletion of <=200bpA-3_prime_UTR_variant
BRCA-EU147512982675129826deletion of <=200bpA-downstream_gene_variant
BRCA-EU147512982675129826deletion of <=200bpA-intron_variant
BRCA-EU147513027975130279single base substitutionGC3_prime_UTR_variant
BRCA-EU147513027975130279single base substitutionGCdownstream_gene_variant
BRCA-EU147513027975130279single base substitutionGCintron_variant
BRCA-EU147513033575130335single base substitutionGA3_prime_UTR_variant
BRCA-EU147513033575130335single base substitutionGAdownstream_gene_variant
BRCA-EU147513033575130335single base substitutionGAintron_variant
BRCA-EU147513057875130578single base substitutionTCexon_variant
BRCA-EU147513057875130578single base substitutionTCintron_variant
BRCA-EU147513128775131287single base substitutionCGintron_variant
BRCA-EU147513128775131287single base substitutionCGupstream_gene_variant
BRCA-EU147513331575133315single base substitutionCGdownstream_gene_variant
BRCA-EU147513331575133315single base substitutionCGintron_variant
BRCA-EU147513331575133315single base substitutionCGupstream_gene_variant
BRCA-EU147513387875133878single base substitutionGAdownstream_gene_variant
BRCA-EU147513387875133878single base substitutionGAintron_variant
BRCA-EU147513387875133878single base substitutionGAupstream_gene_variant
BRCA-EU147513471475134714single base substitutionGTdownstream_gene_variant
BRCA-EU147513471475134714single base substitutionGTintron_variant
BRCA-EU147513471475134714single base substitutionGTupstream_gene_variant
BRCA-EU147513532875135328single base substitutionCGdownstream_gene_variant
BRCA-EU147513532875135328single base substitutionCGintron_variant
BRCA-EU147513532875135328single base substitutionCGupstream_gene_variant
BRCA-EU147513582775135827single base substitutionGCdownstream_gene_variant
BRCA-EU147513582775135827single base substitutionGCintron_variant
BRCA-EU147513582775135827single base substitutionGCupstream_gene_variant
BRCA-EU147513606675136066single base substitutionGAdownstream_gene_variant
BRCA-EU147513606675136066single base substitutionGAintron_variant
BRCA-EU147513606675136066single base substitutionGAupstream_gene_variant
BRCA-EU147513710375137103single base substitutionCTdownstream_gene_variant
BRCA-EU147513710375137103single base substitutionCTintron_variant
BRCA-EU147513728875137288single base substitutionTAdownstream_gene_variant
BRCA-EU147513728875137288single base substitutionTAintron_variant
BRCA-EU147513790675137906single base substitutionCGdownstream_gene_variant
BRCA-EU147513790675137906single base substitutionCGintron_variant
BRCA-EU147513797275137972deletion of <=200bpA-downstream_gene_variant
BRCA-EU147513797275137972deletion of <=200bpA-intron_variant
BRCA-EU147513810775138107single base substitutionTCdownstream_gene_variant
BRCA-EU147513810775138107single base substitutionTCsplice_region_variant
BRCA-EU147514028075140280single base substitutionCTdownstream_gene_variant
BRCA-EU147514028075140280single base substitutionCTintron_variant
BRCA-EU147514066475140664single base substitutionGCdownstream_gene_variant
BRCA-EU147514066475140664single base substitutionGCintron_variant
BRCA-EU147514122075141220single base substitutionGAdownstream_gene_variant
BRCA-EU147514122075141220single base substitutionGAintron_variant
BRCA-EU147514246675142466single base substitutionGAdownstream_gene_variant
BRCA-EU147514246675142466single base substitutionGAexon_variant
BRCA-EU147514246675142466single base substitutionGAmissense_variantS178F533C>T
BRCA-EU147514246675142466single base substitutionGAmissense_variantS339F1016C>T
BRCA-EU147514246675142466single base substitutionGAmissense_variantS86F257C>T
BRCA-EU147514246675142466single base substitutionGAupstream_gene_variant
BRCA-EU147514475475144754single base substitutionCAintron_variant
BRCA-EU147514475475144754single base substitutionCAupstream_gene_variant
BRCA-EU147514489175144891single base substitutionGAexon_variant
BRCA-EU147514489175144891single base substitutionGAintron_variant
BRCA-EU147514489175144891single base substitutionGAupstream_gene_variant
BRCA-EU147514504275145042single base substitutionAGdownstream_gene_variant
BRCA-EU147514504275145042single base substitutionAGintron_variant
BRCA-EU147514504275145042single base substitutionAGupstream_gene_variant
BRCA-EU147514531775145317single base substitutionGAdownstream_gene_variant
BRCA-EU147514531775145317single base substitutionGAintron_variant
BRCA-EU147514531775145317single base substitutionGAupstream_gene_variant
BRCA-EU147514577775145777single base substitutionATdownstream_gene_variant
BRCA-EU147514577775145777single base substitutionATintron_variant
BRCA-EU147514577775145777single base substitutionATupstream_gene_variant
BRCA-EU147514948775149488deletion of <=200bpCT-downstream_gene_variant
BRCA-EU147514948775149488deletion of <=200bpCT-intron_variant
BRCA-EU147515333375153333single base substitutionCGdownstream_gene_variant
BRCA-EU147515333375153333single base substitutionCGintron_variant
BRCA-EU147515333375153333single base substitutionCGupstream_gene_variant
BRCA-EU147515511575155115single base substitutionGCdownstream_gene_variant
BRCA-EU147515511575155115single base substitutionGCintron_variant
BRCA-EU147515511575155115single base substitutionGCupstream_gene_variant
BRCA-EU147515527775155277single base substitutionCTdownstream_gene_variant
BRCA-EU147515527775155277single base substitutionCTintron_variant
BRCA-EU147515527775155277single base substitutionCTupstream_gene_variant
BRCA-EU147515529675155296single base substitutionCGdownstream_gene_variant
BRCA-EU147515529675155296single base substitutionCGintron_variant
BRCA-EU147515529675155296single base substitutionCGupstream_gene_variant
BRCA-EU147515718675157186single base substitutionAGdownstream_gene_variant
BRCA-EU147515718675157186single base substitutionAGintron_variant
BRCA-EU147515718675157186single base substitutionAGupstream_gene_variant
BRCA-EU147515855675158556single base substitutionATdownstream_gene_variant
BRCA-EU147515855675158556single base substitutionATintron_variant
BRCA-EU147516038075160380single base substitutionACintron_variant
BRCA-EU147516215275162152single base substitutionAGintron_variant
BRCA-EU147516575975165759single base substitutionGAintron_variant
BRCA-EU147516626975166269single base substitutionCGintron_variant
BRCA-EU147516727475167274single base substitutionGAintron_variant
BRCA-EU147516796375167963insertion of <=200bp-Aintron_variant
BRCA-EU147516838175168381single base substitutionCTexon_variant
BRCA-EU147516838175168381single base substitutionCTintron_variant
BRCA-EU147516945475169454single base substitutionTCintron_variant
BRCA-EU147517078975170789single base substitutionGCintron_variant
BRCA-EU147518158475181584single base substitutionGTupstream_gene_variant
BRCA-EU147518236975182369single base substitutionGAupstream_gene_variant
BRCA-EU147518464175184641single base substitutionGAupstream_gene_variant
BRCA-FR147511822075118220single base substitutionCGdownstream_gene_variant
BRCA-FR147513600175136001single base substitutionTAdownstream_gene_variant
BRCA-FR147513600175136001single base substitutionTAintron_variant
BRCA-FR147513600175136001single base substitutionTAupstream_gene_variant
BRCA-FR147513757775137577single base substitutionGAdownstream_gene_variant
BRCA-FR147513757775137577single base substitutionGAintron_variant
BRCA-FR147513757775137577single base substitutionGAsplice_region_variant
BRCA-FR147514122075141220single base substitutionGAdownstream_gene_variant
BRCA-FR147514122075141220single base substitutionGAintron_variant
BRCA-FR147514531775145317single base substitutionGAdownstream_gene_variant
BRCA-FR147514531775145317single base substitutionGAintron_variant
BRCA-FR147514531775145317single base substitutionGAupstream_gene_variant
BRCA-FR147515051175150511single base substitutionTCintron_variant
BRCA-FR147515051175150511single base substitutionTCupstream_gene_variant
BRCA-FR147515333375153333single base substitutionCGdownstream_gene_variant
BRCA-FR147515333375153333single base substitutionCGintron_variant
BRCA-FR147515333375153333single base substitutionCGupstream_gene_variant
BRCA-FR147515511575155115single base substitutionGCdownstream_gene_variant
BRCA-FR147515511575155115single base substitutionGCintron_variant
BRCA-FR147515511575155115single base substitutionGCupstream_gene_variant
BRCA-FR147515529675155296single base substitutionCGdownstream_gene_variant
BRCA-FR147515529675155296single base substitutionCGintron_variant
BRCA-FR147515529675155296single base substitutionCGupstream_gene_variant
BRCA-FR147515855675158556single base substitutionATdownstream_gene_variant
BRCA-FR147515855675158556single base substitutionATintron_variant
BRCA-FR147516945475169454single base substitutionTCintron_variant
BRCA-FR147517078975170789single base substitutionGCintron_variant
BRCA-UK147511854675118546single base substitutionGAdownstream_gene_variant
BRCA-UK147513532875135328single base substitutionCGdownstream_gene_variant
BRCA-UK147513532875135328single base substitutionCGintron_variant
BRCA-UK147513532875135328single base substitutionCGupstream_gene_variant
BRCA-UK147516695375166953single base substitutionGCintron_variant
BRCA-UK147518043775180437single base substitutionGAupstream_gene_variant
BRCA-US147513069875130698single base substitutionGA3_prime_UTR_variant
BRCA-US147513069875130698single base substitutionGAexon_variant
BRCA-US147513069875130698single base substitutionGAmissense_variantS597F1790C>T
BRCA-US147513069875130698single base substitutionGAmissense_variantS758F2273C>T
BRCA-US147513670675136706single base substitutionCA3_prime_UTR_variant
BRCA-US147513670675136706single base substitutionCAdownstream_gene_variant
BRCA-US147513670675136706single base substitutionCAexon_variant
BRCA-US147513670675136706single base substitutionCAmissense_variantA417S1249G>T
BRCA-US147513670675136706single base substitutionCAmissense_variantA578S1732G>T
BRCA-US147513750375137503single base substitutionGC3_prime_UTR_variant
BRCA-US147513750375137503single base substitutionGCdownstream_gene_variant
BRCA-US147513750375137503single base substitutionGCexon_variant
BRCA-US147513750375137503single base substitutionGCintron_variant
BRCA-US147513750375137503single base substitutionGCmissense_variantQ363E1087C>G
BRCA-US147513750375137503single base substitutionGCmissense_variantQ524E1570C>G
BRCA-US147514243275142432single base substitutionCTdownstream_gene_variant
BRCA-US147514243275142432single base substitutionCTexon_variant
BRCA-US147514243275142432single base substitutionCTintron_variant
BRCA-US147514243275142432single base substitutionCTsynonymous_variantP189P567G>A
BRCA-US147514243275142432single base substitutionCTsynonymous_variantP350P1050G>A
BRCA-US147514243275142432single base substitutionCTupstream_gene_variant
BRCA-US147514244275142442single base substitutionACdownstream_gene_variant
BRCA-US147514244275142442single base substitutionACexon_variant
BRCA-US147514244275142442single base substitutionACmissense_variantV186G557T>G
BRCA-US147514244275142442single base substitutionACmissense_variantV347G1040T>G
BRCA-US147514244275142442single base substitutionACsplice_donor_variant
BRCA-US147514244275142442single base substitutionACupstream_gene_variant
BRCA-US147514245575142455single base substitutionTGdownstream_gene_variant
BRCA-US147514245575142455single base substitutionTGexon_variant
BRCA-US147514245575142455single base substitutionTGmissense_variantT182P544A>C
BRCA-US147514245575142455single base substitutionTGmissense_variantT343P1027A>C
BRCA-US147514245575142455single base substitutionTGmissense_variantT90P268A>C
BRCA-US147514245575142455single base substitutionTGupstream_gene_variant
BTCA-JP147513642675136426single base substitutionGC3_prime_UTR_variant
BTCA-JP147513642675136426single base substitutionGCdownstream_gene_variant
BTCA-JP147513642675136426single base substitutionGCexon_variant
BTCA-JP147513642675136426single base substitutionGCmissense_variantL453V1357C>G
BTCA-JP147513642675136426single base substitutionGCmissense_variantL614V1840C>G
BTCA-JP147513642675136426single base substitutionGCupstream_gene_variant
BTCA-JP147513669375136693single base substitutionCT3_prime_UTR_variant
BTCA-JP147513669375136693single base substitutionCTdownstream_gene_variant
BTCA-JP147513669375136693single base substitutionCTexon_variant
BTCA-JP147513669375136693single base substitutionCTmissense_variantR421H1262G>A
BTCA-JP147513669375136693single base substitutionCTmissense_variantR582H1745G>A
BTCA-JP147514237675142376single base substitutionTCdownstream_gene_variant
BTCA-JP147514237675142376single base substitutionTCintron_variant
CESC-US147513403675134036single base substitutionCT3_prime_UTR_variant
CESC-US147513403675134036single base substitutionCTdownstream_gene_variant
CESC-US147513403675134036single base substitutionCTexon_variant
CESC-US147513403675134036single base substitutionCTmissense_variantE536K1606G>A
CESC-US147513403675134036single base substitutionCTmissense_variantE697K2089G>A
CESC-US147513403675134036single base substitutionCTupstream_gene_variant
CESC-US147515006575150065single base substitutionCT5_prime_UTR_variant
CESC-US147515006575150065single base substitutionCTdownstream_gene_variant
CESC-US147515006575150065single base substitutionCTexon_variant
CESC-US147515006575150065single base substitutionCTintron_variant
CESC-US147515006575150065single base substitutionCTmissense_variantE139K415G>A
CESC-US147515131875151318single base substitutionGTexon_variant
CESC-US147515131875151318single base substitutionGTintron_variant
CESC-US147515131875151318single base substitutionGTmissense_variantR28S82C>A
CESC-US147515131875151318single base substitutionGTupstream_gene_variant
CESC-US147515131975151319single base substitutionTAexon_variant
CESC-US147515131975151319single base substitutionTAintron_variant
CESC-US147515131975151319single base substitutionTAsynonymous_variantA27A81A>T
CESC-US147515131975151319single base substitutionTAupstream_gene_variant
CESC-US147518271475182714single base substitutionCTupstream_gene_variant
CLLE-ES147514111775141117single base substitutionACdownstream_gene_variant
CLLE-ES147514111775141117single base substitutionACintron_variant
CLLE-ES147514977475149774single base substitutionTCdownstream_gene_variant
CLLE-ES147514977475149774single base substitutionTCintron_variant
CLLE-ES147516404875164048single base substitutionACintron_variant
CLLE-ES147516731975167319single base substitutionAGintron_variant
COAD-US147513422875134228single base substitutionAC3_prime_UTR_variant
COAD-US147513422875134228single base substitutionACdownstream_gene_variant
COAD-US147513422875134228single base substitutionACexon_variant
COAD-US147513422875134228single base substitutionACmissense_variantL501V1501T>G
COAD-US147513422875134228single base substitutionACmissense_variantL662V1984T>G
COAD-US147513422875134228single base substitutionACupstream_gene_variant
COAD-US147514256975142569single base substitutionTC3_prime_UTR_variant
COAD-US147514256975142569single base substitutionTCexon_variant
COAD-US147514256975142569single base substitutionTCmissense_variantT144A430A>G
COAD-US147514256975142569single base substitutionTCmissense_variantT305A913A>G
COAD-US147514256975142569single base substitutionTCmissense_variantT52A154A>G
COAD-US147514256975142569single base substitutionTCupstream_gene_variant
COAD-US147514262675142626single base substitutionGA3_prime_UTR_variant
COAD-US147514262675142626single base substitutionGAexon_variant
COAD-US147514262675142626single base substitutionGAmissense_variantR125C373C>T
COAD-US147514262675142626single base substitutionGAmissense_variantR286C856C>T
COAD-US147514262675142626single base substitutionGAmissense_variantR33C97C>T
COAD-US147514262675142626single base substitutionGAupstream_gene_variant
COAD-US147515121275151212single base substitutionGAexon_variant
COAD-US147515121275151212single base substitutionGAintron_variant
COAD-US147515121275151212single base substitutionGAmissense_variantS63F188C>T
COAD-US147515121275151212single base substitutionGAupstream_gene_variant
COCA-CN147513745275137452single base substitutionGAdownstream_gene_variant
COCA-CN147513745275137452single base substitutionGAexon_variant
COCA-CN147513745275137452single base substitutionGAintron_variant
COCA-CN147513809175138091single base substitutionTAdownstream_gene_variant
COCA-CN147513809175138091single base substitutionTAintron_variant
COCA-CN147514307075143070single base substitutionAGintron_variant
COCA-CN147514307075143070single base substitutionAGupstream_gene_variant
COCA-CN147514480975144809single base substitutionTGintron_variant
COCA-CN147514480975144809single base substitutionTGupstream_gene_variant
COCA-CN147515892275158922single base substitutionGT5_prime_UTR_variant
COCA-CN147515892275158922single base substitutionGTexon_variant
COCA-CN147515892275158922single base substitutionGTintron_variant
COCA-CN147517449275174492single base substitutionTCintron_variant
COCA-CN147517990275179902single base substitutionTCupstream_gene_variant
COCA-CN147518153875181538single base substitutionCTupstream_gene_variant
COCA-CN147518255275182552single base substitutionGTupstream_gene_variant
ESAD-UK147511597375115973single base substitutionGAdownstream_gene_variant
ESAD-UK147511673675116736single base substitutionCAdownstream_gene_variant
ESAD-UK147511797975117979insertion of <=200bp-Tdownstream_gene_variant
ESAD-UK147511829875118298single base substitutionCGdownstream_gene_variant
ESAD-UK147511845475118454insertion of <=200bp-Adownstream_gene_variant
ESAD-UK147512129275121292single base substitutionTGintron_variant
ESAD-UK147512705775127057single base substitutionGAdownstream_gene_variant
ESAD-UK147512705775127057single base substitutionGAexon_variant
ESAD-UK147512705775127057single base substitutionGAintron_variant
ESAD-UK147512733575127335single base substitutionCAdownstream_gene_variant
ESAD-UK147512733575127335single base substitutionCAexon_variant
ESAD-UK147512733575127335single base substitutionCAintron_variant
ESAD-UK147512742775127427single base substitutionGAdownstream_gene_variant
ESAD-UK147512742775127427single base substitutionGAexon_variant
ESAD-UK147512742775127427single base substitutionGAintron_variant
ESAD-UK147512888975128889single base substitutionGA3_prime_UTR_variant
ESAD-UK147512888975128889single base substitutionGAdownstream_gene_variant
ESAD-UK147512888975128889single base substitutionGAintron_variant
ESAD-UK147513288675132886single base substitutionCTdownstream_gene_variant
ESAD-UK147513288675132886single base substitutionCTintron_variant
ESAD-UK147513288675132886single base substitutionCTupstream_gene_variant
ESAD-UK147513421375134213single base substitutionGA3_prime_UTR_variant
ESAD-UK147513421375134213single base substitutionGAdownstream_gene_variant
ESAD-UK147513421375134213single base substitutionGAexon_variant
ESAD-UK147513421375134213single base substitutionGAmissense_variantR506W1516C>T
ESAD-UK147513421375134213single base substitutionGAmissense_variantR667W1999C>T
ESAD-UK147513421375134213single base substitutionGAupstream_gene_variant
ESAD-UK147513617975136179single base substitutionACdownstream_gene_variant
ESAD-UK147513617975136179single base substitutionACintron_variant
ESAD-UK147513617975136179single base substitutionACupstream_gene_variant
ESAD-UK147513770175137701single base substitutionGAdownstream_gene_variant
ESAD-UK147513770175137701single base substitutionGAintron_variant
ESAD-UK147513807075138070single base substitutionATdownstream_gene_variant
ESAD-UK147513807075138070single base substitutionATintron_variant
ESAD-UK147513997875139978single base substitutionCGdownstream_gene_variant
ESAD-UK147513997875139978single base substitutionCGintron_variant
ESAD-UK147514124075141240single base substitutionGAdownstream_gene_variant
ESAD-UK147514124075141240single base substitutionGAintron_variant
ESAD-UK147514280175142801single base substitutionCTintron_variant
ESAD-UK147514280175142801single base substitutionCTupstream_gene_variant
ESAD-UK147514287775142877single base substitutionTC3_prime_UTR_variant
ESAD-UK147514287775142877single base substitutionTCexon_variant
ESAD-UK147514287775142877single base substitutionTCmissense_variantN106D316A>G
ESAD-UK147514287775142877single base substitutionTCmissense_variantN14D40A>G
ESAD-UK147514287775142877single base substitutionTCmissense_variantN267D799A>G
ESAD-UK147514287775142877single base substitutionTCupstream_gene_variant
ESAD-UK147514656775146567insertion of <=200bp-Adownstream_gene_variant
ESAD-UK147514656775146567insertion of <=200bp-Aintron_variant
ESAD-UK147514656775146567insertion of <=200bp-Aupstream_gene_variant
ESAD-UK147515042475150424single base substitutionACintron_variant
ESAD-UK147515042475150424single base substitutionACupstream_gene_variant
ESAD-UK147515128775151287single base substitutionCTexon_variant
ESAD-UK147515128775151287single base substitutionCTintron_variant
ESAD-UK147515128775151287single base substitutionCTmissense_variantR38H113G>A
ESAD-UK147515128775151287single base substitutionCTupstream_gene_variant
ESAD-UK147515181575151815single base substitutionTAintron_variant
ESAD-UK147515181575151815single base substitutionTAupstream_gene_variant
ESAD-UK147515717075157170single base substitutionAGdownstream_gene_variant
ESAD-UK147515717075157170single base substitutionAGintron_variant
ESAD-UK147515717075157170single base substitutionAGupstream_gene_variant
ESAD-UK147516069375160693single base substitutionGAintron_variant
ESAD-UK147516743275167432single base substitutionGAintron_variant
ESAD-UK147516777575167775single base substitutionTCintron_variant
ESAD-UK147517199675171996single base substitutionCTintron_variant
ESAD-UK147517800975178009single base substitutionGAintron_variant
ESAD-UK147518198675181986single base substitutionGAupstream_gene_variant
ESCA-CN147515900775159007single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
ESCA-CN147515900775159007single base substitutionGAexon_variant
ESCA-CN147515900775159007single base substitutionGAintron_variant
GBM-US147514999875149998single base substitutionCTdownstream_gene_variant
GBM-US147514999875149998single base substitutionCTintron_variant
GBM-US147514999875149998single base substitutionCTsplice_donor_variant
KIRC-US147513641175136411single base substitutionTG3_prime_UTR_variant
KIRC-US147513641175136411single base substitutionTGdownstream_gene_variant
KIRC-US147513641175136411single base substitutionTGexon_variant
KIRC-US147513641175136411single base substitutionTGmissense_variantS458R1372A>C
KIRC-US147513641175136411single base substitutionTGmissense_variantS619R1855A>C
KIRC-US147513641175136411single base substitutionTGupstream_gene_variant
KIRC-US147513669675136696single base substitutionGA3_prime_UTR_variant
KIRC-US147513669675136696single base substitutionGAdownstream_gene_variant
KIRC-US147513669675136696single base substitutionGAexon_variant
KIRC-US147513669675136696single base substitutionGAmissense_variantT420I1259C>T
KIRC-US147513669675136696single base substitutionGAmissense_variantT581I1742C>T
LAML-KR147513680575136805single base substitutionCT3_prime_UTR_variant
LAML-KR147513680575136805single base substitutionCTdownstream_gene_variant
LAML-KR147513680575136805single base substitutionCTexon_variant
LAML-KR147513680575136805single base substitutionCTmissense_variantA384T1150G>A
LAML-KR147513680575136805single base substitutionCTmissense_variantA545T1633G>A
LAML-KR147513766475137664single base substitutionTCdownstream_gene_variant
LAML-KR147513766475137664single base substitutionTCintron_variant
LAML-KR147514349575143495single base substitutionATintron_variant
LAML-KR147514349575143495single base substitutionATupstream_gene_variant
LAML-KR147517798275177982single base substitutionTCintron_variant
LAML-KR147518153875181538single base substitutionCTupstream_gene_variant
LAML-KR147518293775182937single base substitutionGAupstream_gene_variant
LGG-US147513981675139816single base substitutionCGdownstream_gene_variant
LGG-US147513981675139816single base substitutionCGexon_variant
LGG-US147513981675139816single base substitutionCGmissense_variantA261P781G>C
LGG-US147513981675139816single base substitutionCGmissense_variantA422P1264G>C
LICA-CN147513059975130599single base substitutionTCexon_variant
LICA-CN147513059975130599single base substitutionTCintron_variant
LICA-CN147513059975130599single base substitutionTCsplice_region_variant
LICA-CN147515005275150052single base substitutionTA5_prime_UTR_premature_start_codon_gain_variant
LICA-CN147515005275150052single base substitutionTAdownstream_gene_variant
LICA-CN147515005275150052single base substitutionTAexon_variant
LICA-CN147515005275150052single base substitutionTAintron_variant
LICA-CN147515005275150052single base substitutionTAmissense_variantK143M428A>T
LICA-CN147515016375150163single base substitutionTC5_prime_UTR_variant
LICA-CN147515016375150163single base substitutionTCexon_variant
LICA-CN147515016375150163single base substitutionTCintron_variant
LICA-CN147515016375150163single base substitutionTCmissense_variantE106G317A>G
LICA-CN147515016375150163single base substitutionTCupstream_gene_variant
LICA-FR147514914975149149single base substitutionTCdownstream_gene_variant
LICA-FR147514914975149149single base substitutionTCintron_variant
LICA-FR147515775975157759single base substitutionTCdownstream_gene_variant
LICA-FR147515775975157759single base substitutionTCintron_variant
LIHC-US147513043175130431single base substitutionTC3_prime_UTR_variant
LIHC-US147513043175130431single base substitutionTCdownstream_gene_variant
LIHC-US147513043175130431single base substitutionTCexon_variant
LIHC-US147513043175130431single base substitutionTCintron_variant
LIHC-US147513043175130431single base substitutionTCmissense_variantM822V2464A>G
LIHC-US147513154075131540single base substitutionTCdownstream_gene_variant
LIHC-US147513154075131540single base substitutionTCmissense_variantK570R1709A>G
LIHC-US147513154075131540single base substitutionTCmissense_variantK731R2192A>G
LIHC-US147513154075131540single base substitutionTCsplice_region_variant
LIHC-US147513154075131540single base substitutionTCupstream_gene_variant
LIHC-US147513670475136704single base substitutionAG3_prime_UTR_variant
LIHC-US147513670475136704single base substitutionAGdownstream_gene_variant
LIHC-US147513670475136704single base substitutionAGexon_variant
LIHC-US147513670475136704single base substitutionAGsynonymous_variantA417A1251T>C
LIHC-US147513670475136704single base substitutionAGsynonymous_variantA578A1734T>C
LIHC-US147513964475139644single base substitutionTCdownstream_gene_variant
LIHC-US147513964475139644single base substitutionTCexon_variant
LIHC-US147513964475139644single base substitutionTCmissense_variantT277A829A>G
LIHC-US147513964475139644single base substitutionTCmissense_variantT438A1312A>G
LIHC-US147514080475140804single base substitutionATdownstream_gene_variant
LIHC-US147514080475140804single base substitutionATexon_variant
LIHC-US147514080475140804single base substitutionATmissense_variantV203E608T>A
LIHC-US147514080475140804single base substitutionATmissense_variantV364E1091T>A
LIHC-US147514080475140804single base substitutionATmissense_variantV97E290T>A
LINC-JP147512634675126346single base substitutionGAdownstream_gene_variant
LINC-JP147512634675126346single base substitutionGAintron_variant
LINC-JP147513054775130547single base substitutionGAexon_variant
LINC-JP147513054775130547single base substitutionGAintron_variant
LINC-JP147513108875131088deletion of <=200bpT-intron_variant
LINC-JP147513108875131088deletion of <=200bpT-upstream_gene_variant
LINC-JP147513254675132546single base substitutionAGdownstream_gene_variant
LINC-JP147513254675132546single base substitutionAGintron_variant
LINC-JP147513254675132546single base substitutionAGupstream_gene_variant
LINC-JP147513756375137563single base substitutionCT3_prime_UTR_variant
LINC-JP147513756375137563single base substitutionCTdownstream_gene_variant
LINC-JP147513756375137563single base substitutionCTexon_variant
LINC-JP147513756375137563single base substitutionCTintron_variant
LINC-JP147513756375137563single base substitutionCTmissense_variantG343R1027G>A
LINC-JP147513756375137563single base substitutionCTmissense_variantG504R1510G>A
LINC-JP147514223575142235single base substitutionTCdownstream_gene_variant
LINC-JP147514223575142235single base substitutionTCintron_variant
LINC-JP147514316775143167single base substitutionTCintron_variant
LINC-JP147514316775143167single base substitutionTCupstream_gene_variant
LINC-JP147514441375144413single base substitutionCGintron_variant
LINC-JP147514441375144413single base substitutionCGupstream_gene_variant
LINC-JP147515003375150033single base substitutionCA5_prime_UTR_premature_start_codon_gain_variant
LINC-JP147515003375150033single base substitutionCAdownstream_gene_variant
LINC-JP147515003375150033single base substitutionCAexon_variant
LINC-JP147515003375150033single base substitutionCAintron_variant
LINC-JP147515003375150033single base substitutionCAsynonymous_variantV149V447G>T
LINC-JP147515008975150089single base substitutionTC5_prime_UTR_variant
LINC-JP147515008975150089single base substitutionTCdownstream_gene_variant
LINC-JP147515008975150089single base substitutionTCexon_variant
LINC-JP147515008975150089single base substitutionTCintron_variant
LINC-JP147515008975150089single base substitutionTCmissense_variantT131A391A>G
LINC-JP147515333675153336single base substitutionGAdownstream_gene_variant
LINC-JP147515333675153336single base substitutionGAintron_variant
LINC-JP147515333675153336single base substitutionGAupstream_gene_variant
LINC-JP147516375075163750single base substitutionACintron_variant
LIRI-JP147511673575116735single base substitutionTCdownstream_gene_variant
LIRI-JP147511710875117108single base substitutionTGdownstream_gene_variant
LIRI-JP147511758875117588single base substitutionTCdownstream_gene_variant
LIRI-JP147511779275117792single base substitutionGCdownstream_gene_variant
LIRI-JP147511873775118737single base substitutionAGdownstream_gene_variant
LIRI-JP147512398475123984single base substitutionCTdownstream_gene_variant
LIRI-JP147512398475123984single base substitutionCTintron_variant
LIRI-JP147512470675124706single base substitutionCTdownstream_gene_variant
LIRI-JP147512470675124706single base substitutionCTintron_variant
LIRI-JP147513137075131370single base substitutionCAintron_variant
LIRI-JP147513137075131370single base substitutionCAupstream_gene_variant
LIRI-JP147513421275134212single base substitutionCA3_prime_UTR_variant
LIRI-JP147513421275134212single base substitutionCAdownstream_gene_variant
LIRI-JP147513421275134212single base substitutionCAexon_variant
LIRI-JP147513421275134212single base substitutionCAmissense_variantR506L1517G>T
LIRI-JP147513421275134212single base substitutionCAmissense_variantR667L2000G>T
LIRI-JP147513421275134212single base substitutionCAupstream_gene_variant
LIRI-JP147513882275138822single base substitutionTAdownstream_gene_variant
LIRI-JP147513882275138822single base substitutionTAintron_variant
LIRI-JP147514296175142972deletion of <=200bpGCCTGTTGGATG-3_prime_UTR_variant
LIRI-JP147514296175142972deletion of <=200bpGCCTGTTGGATG-disruptive_inframe_deletionTSNRQ235K
LIRI-JP147514296175142972deletion of <=200bpGCCTGTTGGATG-disruptive_inframe_deletionTSNRQ74K
LIRI-JP147514296175142972deletion of <=200bpGCCTGTTGGATG-exon_variant
LIRI-JP147514296175142972deletion of <=200bpGCCTGTTGGATG-upstream_gene_variant
LIRI-JP147514489775144897single base substitutionTCexon_variant
LIRI-JP147514489775144897single base substitutionTCintron_variant
LIRI-JP147514489775144897single base substitutionTCupstream_gene_variant
LIRI-JP147514548875145488single base substitutionCAdownstream_gene_variant
LIRI-JP147514548875145488single base substitutionCAintron_variant
LIRI-JP147514548875145488single base substitutionCAupstream_gene_variant
LIRI-JP147514603675146036single base substitutionAGdownstream_gene_variant
LIRI-JP147514603675146036single base substitutionAGintron_variant
LIRI-JP147514603675146036single base substitutionAGupstream_gene_variant
LIRI-JP147514697775146977single base substitutionTCdownstream_gene_variant
LIRI-JP147514697775146977single base substitutionTCintron_variant
LIRI-JP147514697775146977single base substitutionTCupstream_gene_variant
LIRI-JP147514734275147342single base substitutionCTdownstream_gene_variant
LIRI-JP147514734275147342single base substitutionCTintron_variant
LIRI-JP147514734275147342single base substitutionCTupstream_gene_variant
LIRI-JP147515008975150089single base substitutionTA5_prime_UTR_variant
LIRI-JP147515008975150089single base substitutionTAdownstream_gene_variant
LIRI-JP147515008975150089single base substitutionTAexon_variant
LIRI-JP147515008975150089single base substitutionTAintron_variant
LIRI-JP147515008975150089single base substitutionTAmissense_variantT131S391A>T
LIRI-JP147515236475152364single base substitutionCTsplice_acceptor_variant
LIRI-JP147515236475152364single base substitutionCTupstream_gene_variant
LIRI-JP147515501475155014single base substitutionCAdownstream_gene_variant
LIRI-JP147515501475155014single base substitutionCAintron_variant
LIRI-JP147515501475155014single base substitutionCAupstream_gene_variant
LIRI-JP147516427075164270single base substitutionGTintron_variant
LIRI-JP147516612775166127single base substitutionCTintron_variant
LIRI-JP147516804875168048single base substitutionTCintron_variant
LIRI-JP147517111575171115single base substitutionCAintron_variant
LIRI-JP147517163475171634single base substitutionTAintron_variant
LIRI-JP147517534675175346single base substitutionTCintron_variant
LIRI-JP147517789575177895single base substitutionTCintron_variant
LIRI-JP147517810275178102single base substitutionTCintron_variant
LIRI-JP147517841575178415single base substitutionTCintron_variant
LIRI-JP147517915075179150single base substitutionTGintron_variant
LIRI-JP147517953375179533single base substitutionAGintron_variant
LIRI-JP147518074775180747single base substitutionTCupstream_gene_variant
LIRI-JP147518167875181678single base substitutionAGupstream_gene_variant
LIRI-JP147518316575183165single base substitutionTCupstream_gene_variant
LUSC-KR147512651375126513single base substitutionCTdownstream_gene_variant
LUSC-KR147512651375126513single base substitutionCTintron_variant
LUSC-KR147512831675128316single base substitutionAC3_prime_UTR_variant
LUSC-KR147512831675128316single base substitutionACdownstream_gene_variant
LUSC-KR147512831675128316single base substitutionACintron_variant
LUSC-KR147512842575128425single base substitutionGA3_prime_UTR_variant
LUSC-KR147512842575128425single base substitutionGAdownstream_gene_variant
LUSC-KR147512842575128425single base substitutionGAintron_variant
LUSC-KR147513023575130235single base substitutionTG3_prime_UTR_variant
LUSC-KR147513023575130235single base substitutionTGdownstream_gene_variant
LUSC-KR147513023575130235single base substitutionTGintron_variant
LUSC-KR147513766475137664single base substitutionTCdownstream_gene_variant
LUSC-KR147513766475137664single base substitutionTCintron_variant
LUSC-KR147513885075138850single base substitutionCTdownstream_gene_variant
LUSC-KR147513885075138850single base substitutionCTintron_variant
LUSC-KR147513907375139073single base substitutionCGdownstream_gene_variant
LUSC-KR147513907375139073single base substitutionCGintron_variant
LUSC-KR147515457175154571single base substitutionTAdownstream_gene_variant
LUSC-KR147515457175154571single base substitutionTAintron_variant
LUSC-KR147515457175154571single base substitutionTAupstream_gene_variant
LUSC-KR147515508575155085single base substitutionCAdownstream_gene_variant
LUSC-KR147515508575155085single base substitutionCAintron_variant
LUSC-KR147515508575155085single base substitutionCAupstream_gene_variant
LUSC-KR147515582475155824single base substitutionTGdownstream_gene_variant
LUSC-KR147515582475155824single base substitutionTGintron_variant
LUSC-KR147515582475155824single base substitutionTGupstream_gene_variant
LUSC-KR147516038975160389single base substitutionTAintron_variant
LUSC-KR147516071275160712single base substitutionTCintron_variant
LUSC-KR147517074675170746single base substitutionCTintron_variant
LUSC-US147513418475134184single base substitutionCA3_prime_UTR_variant
LUSC-US147513418475134184single base substitutionCAdownstream_gene_variant
LUSC-US147513418475134184single base substitutionCAexon_variant
LUSC-US147513418475134184single base substitutionCAsynonymous_variantV515V1545G>T
LUSC-US147513418475134184single base substitutionCAsynonymous_variantV676V2028G>T
LUSC-US147513418475134184single base substitutionCAupstream_gene_variant
LUSC-US147514329175143291single base substitutionGC3_prime_UTR_variant
LUSC-US147514329175143291single base substitutionGCexon_variant
LUSC-US147514329175143291single base substitutionGCmissense_variantH216D646C>G
LUSC-US147514329175143291single base substitutionGCmissense_variantH55D163C>G
LUSC-US147514329175143291single base substitutionGCupstream_gene_variant
LUSC-US147515133075151330single base substitutionCGexon_variant
LUSC-US147515133075151330single base substitutionCGintron_variant
LUSC-US147515133075151330single base substitutionCGmissense_variantE24Q70G>C
LUSC-US147515133075151330single base substitutionCGupstream_gene_variant
LUSC-US147518161575181615single base substitutionAGupstream_gene_variant
MALY-DE147511882175118821insertion of <=200bp-Tdownstream_gene_variant
MALY-DE147512232475122324insertion of <=200bp-Adownstream_gene_variant
MALY-DE147512232475122324insertion of <=200bp-Aintron_variant
MALY-DE147512768475127684single base substitutionACdownstream_gene_variant
MALY-DE147512768475127684single base substitutionACintron_variant
MALY-DE147512810475128104single base substitutionTC3_prime_UTR_variant
MALY-DE147512810475128104single base substitutionTCdownstream_gene_variant
MALY-DE147512810475128104single base substitutionTCintron_variant
MALY-DE147512925775129257single base substitutionGA3_prime_UTR_variant
MALY-DE147512925775129257single base substitutionGAdownstream_gene_variant
MALY-DE147512925775129257single base substitutionGAintron_variant
MALY-DE147515009175150091single base substitutionAG5_prime_UTR_variant
MALY-DE147515009175150091single base substitutionAGdownstream_gene_variant
MALY-DE147515009175150091single base substitutionAGexon_variant
MALY-DE147515009175150091single base substitutionAGintron_variant
MALY-DE147515009175150091single base substitutionAGmissense_variantF130S389T>C
MALY-DE147515584375155843single base substitutionGAdownstream_gene_variant
MALY-DE147515584375155843single base substitutionGAintron_variant
MALY-DE147515584375155843single base substitutionGAupstream_gene_variant
MALY-DE147517549075175490single base substitutionGAintron_variant
MALY-DE147517879975178799single base substitutionATintron_variant
MELA-AU147511543575115435single base substitutionATdownstream_gene_variant
MELA-AU147511548075115481multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU147511617175116171single base substitutionCTdownstream_gene_variant
MELA-AU147511762475117624single base substitutionGAdownstream_gene_variant
MELA-AU147511797775117978multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU147511843675118436single base substitutionATdownstream_gene_variant
MELA-AU147511848375118483single base substitutionGAdownstream_gene_variant
MELA-AU147511937975119379single base substitutionCTdownstream_gene_variant
MELA-AU147511957775119577single base substitutionGCdownstream_gene_variant
MELA-AU147511957875119579multiple base substitution (>=2bp and <=200bp)GGAAdownstream_gene_variant
MELA-AU147511969575119695single base substitutionCTdownstream_gene_variant
MELA-AU147512060075120600single base substitutionGAintron_variant
MELA-AU147512089675120896single base substitutionGAintron_variant
MELA-AU147512108475121084single base substitutionGAintron_variant
MELA-AU147512151775121517single base substitutionGAintron_variant
MELA-AU147512235675122356single base substitutionGAdownstream_gene_variant
MELA-AU147512235675122356single base substitutionGAintron_variant
MELA-AU147512287775122877single base substitutionCTdownstream_gene_variant
MELA-AU147512287775122877single base substitutionCTintron_variant
MELA-AU147512309775123097single base substitutionCGdownstream_gene_variant
MELA-AU147512309775123097single base substitutionCGintron_variant
MELA-AU147512318875123188single base substitutionGAdownstream_gene_variant
MELA-AU147512318875123188single base substitutionGAintron_variant
MELA-AU147512402175124022multiple base substitution (>=2bp and <=200bp)ACTTdownstream_gene_variant
MELA-AU147512402175124022multiple base substitution (>=2bp and <=200bp)ACTTintron_variant
MELA-AU147512406875124068single base substitutionCTdownstream_gene_variant
MELA-AU147512406875124068single base substitutionCTintron_variant
MELA-AU147512427975124279single base substitutionAGdownstream_gene_variant
MELA-AU147512427975124279single base substitutionAGintron_variant
MELA-AU147512520375125203single base substitutionGAdownstream_gene_variant
MELA-AU147512520375125203single base substitutionGAintron_variant
MELA-AU147512535275125352single base substitutionGAdownstream_gene_variant
MELA-AU147512535275125352single base substitutionGAintron_variant
MELA-AU147512539075125390single base substitutionGAdownstream_gene_variant
MELA-AU147512539075125390single base substitutionGAintron_variant
MELA-AU147512634475126344single base substitutionGAdownstream_gene_variant
MELA-AU147512634475126344single base substitutionGAintron_variant
MELA-AU147512639875126398single base substitutionAGdownstream_gene_variant
MELA-AU147512639875126398single base substitutionAGintron_variant
MELA-AU147512726675127266single base substitutionGAdownstream_gene_variant
MELA-AU147512726675127266single base substitutionGAexon_variant
MELA-AU147512726675127266single base substitutionGAintron_variant
MELA-AU147512753575127535single base substitutionGAdownstream_gene_variant
MELA-AU147512753575127535single base substitutionGAexon_variant
MELA-AU147512753575127535single base substitutionGAintron_variant
MELA-AU147512761575127615single base substitutionCT3_prime_UTR_variant
MELA-AU147512761575127615single base substitutionCTdownstream_gene_variant
MELA-AU147512761575127615single base substitutionCTexon_variant
MELA-AU147512804175128041single base substitutionGA3_prime_UTR_variant
MELA-AU147512804175128041single base substitutionGAdownstream_gene_variant
MELA-AU147512804175128041single base substitutionGAintron_variant
MELA-AU147512858975128589single base substitutionGA3_prime_UTR_variant
MELA-AU147512858975128589single base substitutionGAdownstream_gene_variant
MELA-AU147512858975128589single base substitutionGAintron_variant
MELA-AU147512887375128873single base substitutionGA3_prime_UTR_variant
MELA-AU147512887375128873single base substitutionGAdownstream_gene_variant
MELA-AU147512887375128873single base substitutionGAintron_variant
MELA-AU147512920075129200single base substitutionCT3_prime_UTR_variant
MELA-AU147512920075129200single base substitutionCTdownstream_gene_variant
MELA-AU147512920075129200single base substitutionCTintron_variant
MELA-AU147512987775129877single base substitutionAT3_prime_UTR_variant
MELA-AU147512987775129877single base substitutionATdownstream_gene_variant
MELA-AU147512987775129877single base substitutionATintron_variant
MELA-AU147513001175130011single base substitutionAG3_prime_UTR_variant
MELA-AU147513001175130011single base substitutionAGdownstream_gene_variant
MELA-AU147513001175130011single base substitutionAGintron_variant
MELA-AU147513024875130248single base substitutionGA3_prime_UTR_variant
MELA-AU147513024875130248single base substitutionGAdownstream_gene_variant
MELA-AU147513024875130248single base substitutionGAintron_variant
MELA-AU147513044375130443single base substitutionCT3_prime_UTR_variant
MELA-AU147513044375130443single base substitutionCTdownstream_gene_variant
MELA-AU147513044375130443single base substitutionCTexon_variant
MELA-AU147513044375130443single base substitutionCTintron_variant
MELA-AU147513044375130443single base substitutionCTmissense_variantE818K2452G>A
MELA-AU147513056675130566single base substitutionATexon_variant
MELA-AU147513056675130566single base substitutionATintron_variant
MELA-AU147513063775130637single base substitutionAT3_prime_UTR_variant
MELA-AU147513063775130637single base substitutionATexon_variant
MELA-AU147513063775130637single base substitutionATsynonymous_variantA617A1851T>A
MELA-AU147513063775130637single base substitutionATsynonymous_variantA778A2334T>A
MELA-AU147513082575130825single base substitutionGAintron_variant
MELA-AU147513082575130825single base substitutionGAupstream_gene_variant
MELA-AU147513215775132157single base substitutionGAdownstream_gene_variant
MELA-AU147513215775132157single base substitutionGAintron_variant
MELA-AU147513215775132157single base substitutionGAupstream_gene_variant
MELA-AU147513281575132815single base substitutionGAdownstream_gene_variant
MELA-AU147513281575132815single base substitutionGAintron_variant
MELA-AU147513281575132815single base substitutionGAupstream_gene_variant
MELA-AU147513308275133082single base substitutionGAdownstream_gene_variant
MELA-AU147513308275133082single base substitutionGAintron_variant
MELA-AU147513308275133082single base substitutionGAupstream_gene_variant
MELA-AU147513369275133692single base substitutionGAdownstream_gene_variant
MELA-AU147513369275133692single base substitutionGAintron_variant
MELA-AU147513369275133692single base substitutionGAupstream_gene_variant
MELA-AU147513412175134121single base substitutionGAdownstream_gene_variant
MELA-AU147513412175134121single base substitutionGAintron_variant
MELA-AU147513412175134121single base substitutionGAupstream_gene_variant
MELA-AU147513423875134238single base substitutionGA3_prime_UTR_variant
MELA-AU147513423875134238single base substitutionGAdownstream_gene_variant
MELA-AU147513423875134238single base substitutionGAexon_variant
MELA-AU147513423875134238single base substitutionGAsynonymous_variantF497F1491C>T
MELA-AU147513423875134238single base substitutionGAsynonymous_variantF658F1974C>T
MELA-AU147513423875134238single base substitutionGAupstream_gene_variant
MELA-AU147513436775134367single base substitutionGAdownstream_gene_variant
MELA-AU147513436775134367single base substitutionGAintron_variant
MELA-AU147513436775134367single base substitutionGAupstream_gene_variant
MELA-AU147513517075135170single base substitutionGAdownstream_gene_variant
MELA-AU147513517075135170single base substitutionGAintron_variant
MELA-AU147513517075135170single base substitutionGAupstream_gene_variant
MELA-AU147513630775136307single base substitutionGAdownstream_gene_variant
MELA-AU147513630775136307single base substitutionGAintron_variant
MELA-AU147513630775136307single base substitutionGAupstream_gene_variant
MELA-AU147513681775136817single base substitutionGA3_prime_UTR_variant
MELA-AU147513681775136817single base substitutionGAdownstream_gene_variant
MELA-AU147513681775136817single base substitutionGAexon_variant
MELA-AU147513681775136817single base substitutionGAmissense_variantP380S1138C>T
MELA-AU147513681775136817single base substitutionGAmissense_variantP541S1621C>T
MELA-AU147513688975136889single base substitutionGAdownstream_gene_variant
MELA-AU147513688975136889single base substitutionGAintron_variant
MELA-AU147513693975136939single base substitutionGAdownstream_gene_variant
MELA-AU147513693975136939single base substitutionGAintron_variant
MELA-AU147513704475137044single base substitutionTCdownstream_gene_variant
MELA-AU147513704475137044single base substitutionTCintron_variant
MELA-AU147513707375137073single base substitutionGTdownstream_gene_variant
MELA-AU147513707375137073single base substitutionGTintron_variant
MELA-AU147513913675139136single base substitutionAGdownstream_gene_variant
MELA-AU147513913675139136single base substitutionAGintron_variant
MELA-AU147513951575139515single base substitutionGAdownstream_gene_variant
MELA-AU147513951575139515single base substitutionGAintron_variant
MELA-AU147514083475140834single base substitutionGAdownstream_gene_variant
MELA-AU147514083475140834single base substitutionGAintron_variant
MELA-AU147514152275141522single base substitutionAGdownstream_gene_variant
MELA-AU147514152275141522single base substitutionAGintron_variant
MELA-AU147514245275142452single base substitutionGAdownstream_gene_variant
MELA-AU147514245275142452single base substitutionGAexon_variant
MELA-AU147514245275142452single base substitutionGAmissense_variantP183S547C>T
MELA-AU147514245275142452single base substitutionGAmissense_variantP344S1030C>T
MELA-AU147514245275142452single base substitutionGAmissense_variantP91S271C>T
MELA-AU147514245275142452single base substitutionGAupstream_gene_variant
MELA-AU147514273675142736single base substitutionCGintron_variant
MELA-AU147514273675142736single base substitutionCGupstream_gene_variant
MELA-AU147514323875143238single base substitutionATintron_variant
MELA-AU147514323875143238single base substitutionATupstream_gene_variant
MELA-AU147514371575143715single base substitutionGAintron_variant
MELA-AU147514371575143715single base substitutionGAupstream_gene_variant
MELA-AU147514434075144340single base substitutionGAintron_variant
MELA-AU147514434075144340single base substitutionGAupstream_gene_variant
MELA-AU147514453875144538single base substitutionGAintron_variant
MELA-AU147514453875144538single base substitutionGAupstream_gene_variant
MELA-AU147514457575144575single base substitutionGAintron_variant
MELA-AU147514457575144575single base substitutionGAupstream_gene_variant
MELA-AU147514468075144680single base substitutionGAintron_variant
MELA-AU147514468075144680single base substitutionGAupstream_gene_variant
MELA-AU147514495875144958single base substitutionGAexon_variant
MELA-AU147514495875144958single base substitutionGAintron_variant
MELA-AU147514495875144958single base substitutionGAupstream_gene_variant
MELA-AU147514497375144973single base substitutionGAexon_variant
MELA-AU147514497375144973single base substitutionGAintron_variant
MELA-AU147514497375144973single base substitutionGAupstream_gene_variant
MELA-AU147514499175144991single base substitutionGTexon_variant
MELA-AU147514499175144991single base substitutionGTintron_variant
MELA-AU147514499175144991single base substitutionGTupstream_gene_variant
MELA-AU147514526275145262single base substitutionGAdownstream_gene_variant
MELA-AU147514526275145262single base substitutionGAintron_variant
MELA-AU147514526275145262single base substitutionGAupstream_gene_variant
MELA-AU147514581875145818single base substitutionGAdownstream_gene_variant
MELA-AU147514581875145818single base substitutionGAintron_variant
MELA-AU147514581875145818single base substitutionGAupstream_gene_variant
MELA-AU147514635475146354single base substitutionACdownstream_gene_variant
MELA-AU147514635475146354single base substitutionACintron_variant
MELA-AU147514635475146354single base substitutionACupstream_gene_variant
MELA-AU147514643975146439single base substitutionGAdownstream_gene_variant
MELA-AU147514643975146439single base substitutionGAintron_variant
MELA-AU147514643975146439single base substitutionGAupstream_gene_variant
MELA-AU147514666575146665single base substitutionGAdownstream_gene_variant
MELA-AU147514666575146665single base substitutionGAintron_variant
MELA-AU147514666575146665single base substitutionGAupstream_gene_variant
MELA-AU147514829075148290single base substitutionAGdownstream_gene_variant
MELA-AU147514829075148290single base substitutionAGintron_variant
MELA-AU147514974675149747multiple base substitution (>=2bp and <=200bp)GGATdownstream_gene_variant
MELA-AU147514974675149747multiple base substitution (>=2bp and <=200bp)GGATintron_variant
MELA-AU147514996575149965single base substitutionGAdownstream_gene_variant
MELA-AU147514996575149965single base substitutionGAintron_variant
MELA-AU147515015575150155single base substitutionCT5_prime_UTR_premature_start_codon_gain_variant
MELA-AU147515015575150155single base substitutionCTexon_variant
MELA-AU147515015575150155single base substitutionCTintron_variant
MELA-AU147515015575150155single base substitutionCTmissense_variantV109M325G>A
MELA-AU147515015575150155single base substitutionCTupstream_gene_variant
MELA-AU147515052275150522single base substitutionGAintron_variant
MELA-AU147515052275150522single base substitutionGAupstream_gene_variant
MELA-AU147515068775150687single base substitutionGAintron_variant
MELA-AU147515068775150687single base substitutionGAupstream_gene_variant
MELA-AU147515162975151629single base substitutionGAintron_variant
MELA-AU147515162975151629single base substitutionGAupstream_gene_variant
MELA-AU147515170275151702single base substitutionGAintron_variant
MELA-AU147515170275151702single base substitutionGAupstream_gene_variant
MELA-AU147515215075152150single base substitutionGAintron_variant
MELA-AU147515215075152150single base substitutionGAupstream_gene_variant
MELA-AU147515218875152188single base substitutionCTintron_variant
MELA-AU147515218875152188single base substitutionCTupstream_gene_variant
MELA-AU147515222075152220single base substitutionGAintron_variant
MELA-AU147515222075152220single base substitutionGAupstream_gene_variant
MELA-AU147515280375152803single base substitutionGAdownstream_gene_variant
MELA-AU147515280375152803single base substitutionGAintron_variant
MELA-AU147515280375152803single base substitutionGAupstream_gene_variant
MELA-AU147515483875154838single base substitutionCTdownstream_gene_variant
MELA-AU147515483875154838single base substitutionCTintron_variant
MELA-AU147515483875154838single base substitutionCTupstream_gene_variant
MELA-AU147515620375156203single base substitutionCTdownstream_gene_variant
MELA-AU147515620375156203single base substitutionCTintron_variant
MELA-AU147515620375156203single base substitutionCTupstream_gene_variant
MELA-AU147515708175157081single base substitutionGAdownstream_gene_variant
MELA-AU147515708175157081single base substitutionGAintron_variant
MELA-AU147515708175157081single base substitutionGAupstream_gene_variant
MELA-AU147515708275157082single base substitutionGAdownstream_gene_variant
MELA-AU147515708275157082single base substitutionGAintron_variant
MELA-AU147515708275157082single base substitutionGAupstream_gene_variant
MELA-AU147515715275157152single base substitutionACdownstream_gene_variant
MELA-AU147515715275157152single base substitutionACintron_variant
MELA-AU147515715275157152single base substitutionACupstream_gene_variant
MELA-AU147515789075157890single base substitutionGAdownstream_gene_variant
MELA-AU147515789075157890single base substitutionGAintron_variant
MELA-AU147515834975158349single base substitutionGAdownstream_gene_variant
MELA-AU147515834975158349single base substitutionGAintron_variant
MELA-AU147515867775158677single base substitutionGAdownstream_gene_variant
MELA-AU147515867775158677single base substitutionGAintron_variant
MELA-AU147515900675159006single base substitutionCT5_prime_UTR_variant
MELA-AU147515900675159006single base substitutionCTexon_variant
MELA-AU147515900675159006single base substitutionCTintron_variant
MELA-AU147515911275159112single base substitutionGAintron_variant
MELA-AU147515959175159591single base substitutionTAintron_variant
MELA-AU147515962075159620single base substitutionCTintron_variant
MELA-AU147516004675160046single base substitutionGAintron_variant
MELA-AU147516075075160750single base substitutionGAintron_variant
MELA-AU147516086775160867single base substitutionGAintron_variant
MELA-AU147516090775160907single base substitutionAGintron_variant
MELA-AU147516111775161117single base substitutionGAintron_variant
MELA-AU147516118475161184single base substitutionGAintron_variant
MELA-AU147516130475161304single base substitutionAGintron_variant
MELA-AU147516161175161611single base substitutionGAintron_variant
MELA-AU147516206075162060single base substitutionGAintron_variant
MELA-AU147516243675162436single base substitutionGAintron_variant
MELA-AU147516285775162857single base substitutionGAintron_variant
MELA-AU147516289475162894single base substitutionCTintron_variant
MELA-AU147516308175163081single base substitutionGAintron_variant
MELA-AU147516348775163487single base substitutionGAintron_variant
MELA-AU147516503875165039multiple base substitution (>=2bp and <=200bp)GGACintron_variant
MELA-AU147516654575166545single base substitutionGAintron_variant
MELA-AU147516700375167003single base substitutionGAintron_variant
MELA-AU147516713475167134single base substitutionGAintron_variant
MELA-AU147516724275167242single base substitutionGAintron_variant
MELA-AU147516756575167565single base substitutionGAintron_variant
MELA-AU147516764575167645single base substitutionGAintron_variant
MELA-AU147516769375167693single base substitutionGAintron_variant
MELA-AU147516776475167764single base substitutionGAintron_variant
MELA-AU147516777275167772single base substitutionGAintron_variant
MELA-AU147516807475168074single base substitutionGAintron_variant
MELA-AU147516855775168558multiple base substitution (>=2bp and <=200bp)GGAAintron_variant
MELA-AU147516864375168643single base substitutionGAintron_variant
MELA-AU147516887175168871single base substitutionCTintron_variant
MELA-AU147516902575169025single base substitutionGAintron_variant
MELA-AU147516951375169513single base substitutionGAintron_variant
MELA-AU147516984775169847single base substitutionCTintron_variant
MELA-AU147517056475170564single base substitutionGAintron_variant
MELA-AU147517090375170903single base substitutionGAintron_variant
MELA-AU147517094475170944single base substitutionGAintron_variant
MELA-AU147517223075172230single base substitutionGAintron_variant
MELA-AU147517260475172604single base substitutionGAintron_variant
MELA-AU147517304775173047single base substitutionAGintron_variant
MELA-AU147517315375173153single base substitutionGAintron_variant
MELA-AU147517370075173700single base substitutionCTintron_variant
MELA-AU147517402975174029single base substitutionCTintron_variant
MELA-AU147517474175174741single base substitutionGAintron_variant
MELA-AU147517516175175161single base substitutionACintron_variant
MELA-AU147517573975175739single base substitutionGAintron_variant
MELA-AU147517591975175919single base substitutionGAintron_variant
MELA-AU147517641975176419single base substitutionGAintron_variant
MELA-AU147517660575176605single base substitutionGAintron_variant
MELA-AU147517764175177641single base substitutionATintron_variant
MELA-AU147517785575177855single base substitutionAGintron_variant
MELA-AU147517810575178105single base substitutionGAintron_variant
MELA-AU147517876575178765single base substitutionAGintron_variant
MELA-AU147517977675179776single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
MELA-AU147517977675179776single base substitutionGAexon_variant
MELA-AU147517977675179776single base substitutionGAupstream_gene_variant
MELA-AU147517979875179798single base substitutionGA5_prime_UTR_variant
MELA-AU147517979875179798single base substitutionGAexon_variant
MELA-AU147517979875179798single base substitutionGAupstream_gene_variant
MELA-AU147517981075179810single base substitutionCT5_prime_UTR_variant
MELA-AU147517981075179810single base substitutionCTexon_variant
MELA-AU147517981075179810single base substitutionCTupstream_gene_variant
MELA-AU147517982875179828single base substitutionGAupstream_gene_variant
MELA-AU147518017875180178single base substitutionCTupstream_gene_variant
MELA-AU147518068875180688single base substitutionGAupstream_gene_variant
MELA-AU147518070875180708single base substitutionCTupstream_gene_variant
MELA-AU147518146175181461single base substitutionGAupstream_gene_variant
MELA-AU147518156175181561single base substitutionCAupstream_gene_variant
MELA-AU147518190475181904single base substitutionGAupstream_gene_variant
MELA-AU147518199375181993single base substitutionGAupstream_gene_variant
MELA-AU147518229575182295single base substitutionCTupstream_gene_variant
MELA-AU147518264775182647single base substitutionCTupstream_gene_variant
MELA-AU147518265575182655single base substitutionCTupstream_gene_variant
MELA-AU147518302175183021single base substitutionCTupstream_gene_variant
MELA-AU147518357175183571single base substitutionCTupstream_gene_variant
MELA-AU147518357775183577single base substitutionTAupstream_gene_variant
MELA-AU147518389575183895single base substitutionCTupstream_gene_variant
MELA-AU147518404775184047single base substitutionCTupstream_gene_variant
MELA-AU147518415075184150single base substitutionATupstream_gene_variant
MELA-AU147518430575184305single base substitutionCTupstream_gene_variant
MELA-AU147518437975184379single base substitutionCTupstream_gene_variant
MELA-AU147518446475184464single base substitutionCTupstream_gene_variant
MELA-AU147518454275184542single base substitutionGAupstream_gene_variant
MELA-AU147518462775184627single base substitutionGAupstream_gene_variant
MELA-AU147518466975184669single base substitutionCTupstream_gene_variant
ORCA-IN147517743875177438single base substitutionAGintron_variant
OV-AU147512712775127127single base substitutionTAdownstream_gene_variant
OV-AU147512712775127127single base substitutionTAexon_variant
OV-AU147512712775127127single base substitutionTAintron_variant
OV-AU147512816275128162single base substitutionCG3_prime_UTR_variant
OV-AU147512816275128162single base substitutionCGdownstream_gene_variant
OV-AU147512816275128162single base substitutionCGintron_variant
OV-AU147513501275135012single base substitutionTCdownstream_gene_variant
OV-AU147513501275135012single base substitutionTCintron_variant
OV-AU147513501275135012single base substitutionTCupstream_gene_variant
OV-AU147513751575137515single base substitutionCG3_prime_UTR_variant
OV-AU147513751575137515single base substitutionCGdownstream_gene_variant
OV-AU147513751575137515single base substitutionCGexon_variant
OV-AU147513751575137515single base substitutionCGintron_variant
OV-AU147513751575137515single base substitutionCGmissense_variantD359H1075G>C
OV-AU147513751575137515single base substitutionCGmissense_variantD520H1558G>C
OV-AU147514087275140872single base substitutionGTdownstream_gene_variant
OV-AU147514087275140872single base substitutionGTintron_variant
OV-AU147514443175144431single base substitutionCAintron_variant
OV-AU147514443175144431single base substitutionCAupstream_gene_variant
OV-AU147514470475144704single base substitutionTCintron_variant
OV-AU147514470475144704single base substitutionTCupstream_gene_variant
OV-AU147514503775145037insertion of <=200bp-Adownstream_gene_variant
OV-AU147514503775145037insertion of <=200bp-Aintron_variant
OV-AU147514503775145037insertion of <=200bp-Asplice_region_variant
OV-AU147514503775145037insertion of <=200bp-Aupstream_gene_variant
OV-US147515017975150179single base substitutionGA5_prime_UTR_variant
OV-US147515017975150179single base substitutionGAexon_variant
OV-US147515017975150179single base substitutionGAintron_variant
OV-US147515017975150179single base substitutionGAmissense_variantH101Y301C>T
OV-US147515017975150179single base substitutionGAupstream_gene_variant
PACA-AU147511718275117182single base substitutionGAdownstream_gene_variant
PACA-AU147511883875118838single base substitutionATdownstream_gene_variant
PACA-AU147512092275120922single base substitutionGAintron_variant
PACA-AU147512618575126185single base substitutionCTdownstream_gene_variant
PACA-AU147512618575126185single base substitutionCTintron_variant
PACA-AU147512669775126697single base substitutionATdownstream_gene_variant
PACA-AU147512669775126697single base substitutionATintron_variant
PACA-AU147513687275136872single base substitutionCGdownstream_gene_variant
PACA-AU147513687275136872single base substitutionCGintron_variant
PACA-AU147514164575141645insertion of <=200bp-Cdownstream_gene_variant
PACA-AU147514164575141645insertion of <=200bp-Cintron_variant
PACA-AU147514850975148509deletion of <=200bpG-downstream_gene_variant
PACA-AU147514850975148509deletion of <=200bpG-intron_variant
PACA-AU147515027875150278deletion of <=200bpA-intron_variant
PACA-AU147515027875150278deletion of <=200bpA-upstream_gene_variant
PACA-AU147515225675152256single base substitutionGAintron_variant
PACA-AU147515225675152256single base substitutionGAupstream_gene_variant
PACA-AU147515361275153612deletion of <=200bpT-downstream_gene_variant
PACA-AU147515361275153612deletion of <=200bpT-intron_variant
PACA-AU147515361275153612deletion of <=200bpT-upstream_gene_variant
PACA-AU147517552575175525single base substitutionCAintron_variant
PACA-CA147511979075119790single base substitutionTAdownstream_gene_variant
PACA-CA147513062275130622single base substitutionCT3_prime_UTR_variant
PACA-CA147513062275130622single base substitutionCTexon_variant
PACA-CA147513062275130622single base substitutionCTsynonymous_variantT622T1866G>A
PACA-CA147513062275130622single base substitutionCTsynonymous_variantT783T2349G>A
PACA-CA147513452475134524single base substitutionGAdownstream_gene_variant
PACA-CA147513452475134524single base substitutionGAintron_variant
PACA-CA147513452475134524single base substitutionGAupstream_gene_variant
PACA-CA147514018275140182single base substitutionGAdownstream_gene_variant
PACA-CA147514018275140182single base substitutionGAintron_variant
PACA-CA147514483175144831single base substitutionTGintron_variant
PACA-CA147514483175144831single base substitutionTGupstream_gene_variant
PACA-CA147514874375148743single base substitutionATdownstream_gene_variant
PACA-CA147514874375148743single base substitutionATintron_variant
PACA-CA147515251675152516single base substitutionGAintron_variant
PACA-CA147515251675152516single base substitutionGAupstream_gene_variant
PACA-CA147515403975154039single base substitutionGTdownstream_gene_variant
PACA-CA147515403975154039single base substitutionGTintron_variant
PACA-CA147515403975154039single base substitutionGTupstream_gene_variant
PACA-CA147515664175156641single base substitutionGAdownstream_gene_variant
PACA-CA147515664175156641single base substitutionGAintron_variant
PACA-CA147515664175156641single base substitutionGAupstream_gene_variant
PACA-CA147515885075158850single base substitutionAC5_prime_UTR_premature_start_codon_gain_variant
PACA-CA147515885075158850single base substitutionACexon_variant
PACA-CA147515885075158850single base substitutionACintron_variant
PACA-CA147516577975165779single base substitutionAGintron_variant
PACA-CA147516904275169042single base substitutionCAintron_variant
PACA-CA147517039975170399single base substitutionCTintron_variant
PACA-CA147517888775178887single base substitutionAGintron_variant
PACA-CA147518118475181184single base substitutionAGupstream_gene_variant
PAEN-AU147514836075148360single base substitutionCTdownstream_gene_variant
PAEN-AU147514836075148360single base substitutionCTintron_variant
PAEN-AU147515505775155057single base substitutionGAdownstream_gene_variant
PAEN-AU147515505775155057single base substitutionGAintron_variant
PAEN-AU147515505775155057single base substitutionGAupstream_gene_variant
PAEN-AU147515926475159268deletion of <=200bpACTAT-intron_variant
PAEN-AU147517378675173786single base substitutionTCintron_variant
PAEN-IT147511957575119575single base substitutionCTdownstream_gene_variant
PAEN-IT147517776875177768single base substitutionCAintron_variant
PBCA-DE147512920075129200single base substitutionCT3_prime_UTR_variant
PBCA-DE147512920075129200single base substitutionCTdownstream_gene_variant
PBCA-DE147512920075129200single base substitutionCTintron_variant
PBCA-DE147513295075132950single base substitutionGTdownstream_gene_variant
PBCA-DE147513295075132950single base substitutionGTintron_variant
PBCA-DE147513295075132950single base substitutionGTupstream_gene_variant
PBCA-DE147516385975163860deletion of <=200bpAC-intron_variant
PBCA-DE147517733875177338single base substitutionTAintron_variant
PBCA-DE147518182875181828single base substitutionCTupstream_gene_variant
PBCA-DE147518372675183726single base substitutionCTupstream_gene_variant
PBCA-DE147518388775183887single base substitutionCTupstream_gene_variant
PRAD-CA147513575575135755single base substitutionTCdownstream_gene_variant
PRAD-CA147513575575135755single base substitutionTCintron_variant
PRAD-CA147513575575135755single base substitutionTCupstream_gene_variant
PRAD-CA147514848175148481single base substitutionGAdownstream_gene_variant
PRAD-CA147514848175148481single base substitutionGAintron_variant
PRAD-CA147517272175172721single base substitutionAGintron_variant
PRAD-UK147513453675134536single base substitutionTAdownstream_gene_variant
PRAD-UK147513453675134536single base substitutionTAintron_variant
PRAD-UK147513453675134536single base substitutionTAupstream_gene_variant
PRAD-UK147514090175140901single base substitutionTCdownstream_gene_variant
PRAD-UK147514090175140901single base substitutionTCintron_variant
PRAD-UK147514416775144167single base substitutionCGintron_variant
PRAD-UK147514416775144167single base substitutionCGupstream_gene_variant
PRAD-UK147516488375164883single base substitutionTCintron_variant
PRAD-UK147516547375165473single base substitutionTCexon_variant
PRAD-UK147516547375165473single base substitutionTCintron_variant
PRAD-US147514338675143386single base substitutionGA3_prime_UTR_variant
PRAD-US147514338675143386single base substitutionGAexon_variant
PRAD-US147514338675143386single base substitutionGAmissense_variantP184L551C>T
PRAD-US147514338675143386single base substitutionGAmissense_variantP23L68C>T
PRAD-US147514338675143386single base substitutionGAupstream_gene_variant
RECA-EU147512030075120300single base substitutionTGintron_variant
RECA-EU147512651775126517single base substitutionATdownstream_gene_variant
RECA-EU147512651775126517single base substitutionATintron_variant
RECA-EU147512839175128391single base substitutionAT3_prime_UTR_variant
RECA-EU147512839175128391single base substitutionATdownstream_gene_variant
RECA-EU147512839175128391single base substitutionATintron_variant
RECA-EU147512957475129574single base substitutionGC3_prime_UTR_variant
RECA-EU147512957475129574single base substitutionGCdownstream_gene_variant
RECA-EU147512957475129574single base substitutionGCintron_variant
RECA-EU147514214175142141single base substitutionTAdownstream_gene_variant
RECA-EU147514214175142141single base substitutionTAintron_variant
RECA-EU147518280875182808single base substitutionTCupstream_gene_variant
SKCA-BR147511560175115601single base substitutionGAdownstream_gene_variant
SKCA-BR147511742075117420single base substitutionTCdownstream_gene_variant
SKCA-BR147511744975117449single base substitutionCTdownstream_gene_variant
SKCA-BR147511750075117500single base substitutionACdownstream_gene_variant
SKCA-BR147512239275122392single base substitutionGAdownstream_gene_variant
SKCA-BR147512239275122392single base substitutionGAintron_variant
SKCA-BR147512594075125940insertion of <=200bp-CTdownstream_gene_variant
SKCA-BR147512594075125940insertion of <=200bp-CTintron_variant
SKCA-BR147512594075125941deletion of <=200bpCT-downstream_gene_variant
SKCA-BR147512594075125941deletion of <=200bpCT-intron_variant
SKCA-BR147512726575127265single base substitutionGAdownstream_gene_variant
SKCA-BR147512726575127265single base substitutionGAexon_variant
SKCA-BR147512726575127265single base substitutionGAintron_variant
SKCA-BR147513281575132815single base substitutionGAdownstream_gene_variant
SKCA-BR147513281575132815single base substitutionGAintron_variant
SKCA-BR147513281575132815single base substitutionGAupstream_gene_variant
SKCA-BR147513356875133568single base substitutionGAdownstream_gene_variant
SKCA-BR147513356875133568single base substitutionGAintron_variant
SKCA-BR147513356875133568single base substitutionGAupstream_gene_variant
SKCA-BR147513682375136823single base substitutionGA3_prime_UTR_variant
SKCA-BR147513682375136823single base substitutionGAdownstream_gene_variant
SKCA-BR147513682375136823single base substitutionGAexon_variant
SKCA-BR147513682375136823single base substitutionGAmissense_variantP378S1132C>T
SKCA-BR147513682375136823single base substitutionGAmissense_variantP539S1615C>T
SKCA-BR147513692075136920single base substitutionGAdownstream_gene_variant
SKCA-BR147513692075136920single base substitutionGAintron_variant
SKCA-BR147513756475137564single base substitutionCT3_prime_UTR_variant
SKCA-BR147513756475137564single base substitutionCTdownstream_gene_variant
SKCA-BR147513756475137564single base substitutionCTexon_variant
SKCA-BR147513756475137564single base substitutionCTintron_variant
SKCA-BR147513756475137564single base substitutionCTstop_gainedW342*1026G>A
SKCA-BR147513756475137564single base substitutionCTstop_gainedW503*1509G>A
SKCA-BR147513793975137939single base substitutionTCdownstream_gene_variant
SKCA-BR147513793975137939single base substitutionTCintron_variant
SKCA-BR147513978475139784single base substitutionGAdownstream_gene_variant
SKCA-BR147513978475139784single base substitutionGAexon_variant
SKCA-BR147513978475139784single base substitutionGAsynonymous_variantN271N813C>T
SKCA-BR147513978475139784single base substitutionGAsynonymous_variantN432N1296C>T
SKCA-BR147514347775143477single base substitutionCGintron_variant
SKCA-BR147514347775143477single base substitutionCGupstream_gene_variant
SKCA-BR147514539875145399deletion of <=200bpCA-downstream_gene_variant
SKCA-BR147514539875145399deletion of <=200bpCA-intron_variant
SKCA-BR147514539875145399deletion of <=200bpCA-upstream_gene_variant
SKCA-BR147514816975148169single base substitutionAGdownstream_gene_variant
SKCA-BR147514816975148169single base substitutionAGintron_variant
SKCA-BR147515313875153138single base substitutionAGdownstream_gene_variant
SKCA-BR147515313875153138single base substitutionAGintron_variant
SKCA-BR147515313875153138single base substitutionAGupstream_gene_variant
SKCA-BR147516567175165671single base substitutionGAintron_variant
SKCA-BR147517304675173046single base substitutionAGintron_variant
SKCA-BR147517810575178105single base substitutionGAintron_variant
SKCA-BR147517877775178789deletion of <=200bpAAAAGAAAGAAAG-intron_variant
SKCA-BR147517982875179828single base substitutionGAupstream_gene_variant
SKCA-BR147517987975179879single base substitutionGAupstream_gene_variant
SKCA-BR147518047775180477single base substitutionCTupstream_gene_variant
SKCA-BR147518073175180731single base substitutionTAupstream_gene_variant
SKCA-BR147518372375183724deletion of <=200bpGC-upstream_gene_variant
SKCA-BR147518372675183727deletion of <=200bpCA-upstream_gene_variant
SKCA-BR147518372775183727single base substitutionATupstream_gene_variant
SKCM-US147513044775130447single base substitutionAG3_prime_UTR_variant
SKCM-US147513044775130447single base substitutionAGdownstream_gene_variant
SKCM-US147513044775130447single base substitutionAGexon_variant
SKCM-US147513044775130447single base substitutionAGintron_variant
SKCM-US147513044775130447single base substitutionAGsynonymous_variantG816G2448T>C
SKCM-US147513417575134175single base substitutionGA3_prime_UTR_variant
SKCM-US147513417575134175single base substitutionGAdownstream_gene_variant
SKCM-US147513417575134175single base substitutionGAexon_variant
SKCM-US147513417575134175single base substitutionGAsynonymous_variantF518F1554C>T
SKCM-US147513417575134175single base substitutionGAsynonymous_variantF679F2037C>T
SKCM-US147513417575134175single base substitutionGAupstream_gene_variant
SKCM-US147513668175136681single base substitutionGA3_prime_UTR_variant
SKCM-US147513668175136681single base substitutionGAdownstream_gene_variant
SKCM-US147513668175136681single base substitutionGAexon_variant
SKCM-US147513668175136681single base substitutionGAmissense_variantA425V1274C>T
SKCM-US147513668175136681single base substitutionGAmissense_variantA586V1757C>T
SKCM-US147513668875136688single base substitutionAT3_prime_UTR_variant
SKCM-US147513668875136688single base substitutionATdownstream_gene_variant
SKCM-US147513668875136688single base substitutionATexon_variant
SKCM-US147513668875136688single base substitutionATmissense_variantF423I1267T>A
SKCM-US147513668875136688single base substitutionATmissense_variantF584I1750T>A
SKCM-US147513673875136738single base substitutionGA3_prime_UTR_variant
SKCM-US147513673875136738single base substitutionGAdownstream_gene_variant
SKCM-US147513673875136738single base substitutionGAexon_variant
SKCM-US147513673875136738single base substitutionGAmissense_variantS406F1217C>T
SKCM-US147513673875136738single base substitutionGAmissense_variantS567F1700C>T
SKCM-US147513961875139618single base substitutionGAdownstream_gene_variant
SKCM-US147513961875139618single base substitutionGAexon_variant
SKCM-US147513961875139618single base substitutionGAsynonymous_variantF285F855C>T
SKCM-US147513961875139618single base substitutionGAsynonymous_variantF446F1338C>T
SKCM-US147513965175139651single base substitutionGAdownstream_gene_variant
SKCM-US147513965175139651single base substitutionGAexon_variant
SKCM-US147513965175139651single base substitutionGAsynonymous_variantG274G822C>T
SKCM-US147513965175139651single base substitutionGAsynonymous_variantG435G1305C>T
SKCM-US147514289775142897single base substitutionGA3_prime_UTR_variant
SKCM-US147514289775142897single base substitutionGAexon_variant
SKCM-US147514289775142897single base substitutionGAmissense_variantS260L779C>T
SKCM-US147514289775142897single base substitutionGAmissense_variantS7L20C>T
SKCM-US147514289775142897single base substitutionGAmissense_variantS99L296C>T
SKCM-US147514289775142897single base substitutionGAupstream_gene_variant
SKCM-US147514334575143345single base substitutionGA3_prime_UTR_variant
SKCM-US147514334575143345single base substitutionGAexon_variant
SKCM-US147514334575143345single base substitutionGAmissense_variantP198S592C>T
SKCM-US147514334575143345single base substitutionGAmissense_variantP37S109C>T
SKCM-US147514334575143345single base substitutionGAupstream_gene_variant
SKCM-US147515011175150111single base substitutionGA5_prime_UTR_variant
SKCM-US147515011175150111single base substitutionGAexon_variant
SKCM-US147515011175150111single base substitutionGAintron_variant
SKCM-US147515011175150111single base substitutionGAsynonymous_variantS123S369C>T
SKCM-US147515011175150111single base substitutionGAupstream_gene_variant
SKCM-US147515016075150160single base substitutionAG5_prime_UTR_variant
SKCM-US147515016075150160single base substitutionAGexon_variant
SKCM-US147515016075150160single base substitutionAGintron_variant
SKCM-US147515016075150160single base substitutionAGmissense_variantL107P320T>C
SKCM-US147515016075150160single base substitutionAGupstream_gene_variant
SKCM-US147515122975151229single base substitutionGAexon_variant
SKCM-US147515122975151229single base substitutionGAintron_variant
SKCM-US147515122975151229single base substitutionGAsynonymous_variantP57P171C>T
SKCM-US147515122975151229single base substitutionGAupstream_gene_variant
SKCM-US147515128975151289single base substitutionGAexon_variant
SKCM-US147515128975151289single base substitutionGAintron_variant
SKCM-US147515128975151289single base substitutionGAsynonymous_variantD37D111C>T
SKCM-US147515128975151289single base substitutionGAupstream_gene_variant
SKCM-US147518266875182668single base substitutionCTupstream_gene_variant
STAD-US147513050375130503single base substitutionTC3_prime_UTR_variant
STAD-US147513050375130503single base substitutionTCdownstream_gene_variant
STAD-US147513050375130503single base substitutionTCexon_variant
STAD-US147513050375130503single base substitutionTCintron_variant
STAD-US147513050375130503single base substitutionTCmissense_variantT798A2392A>G
STAD-US147513050575130505single base substitutionGT3_prime_UTR_variant
STAD-US147513050575130505single base substitutionGTdownstream_gene_variant
STAD-US147513050575130505single base substitutionGTexon_variant
STAD-US147513050575130505single base substitutionGTintron_variant
STAD-US147513050575130505single base substitutionGTmissense_variantP797H2390C>A
STAD-US147513423775134239deletion of <=200bpAGA-3_prime_UTR_variant
STAD-US147513423775134239deletion of <=200bpAGA-disruptive_inframe_deletionFY497Y
STAD-US147513423775134239deletion of <=200bpAGA-disruptive_inframe_deletionFY658Y
STAD-US147513423775134239deletion of <=200bpAGA-downstream_gene_variant
STAD-US147513423775134239deletion of <=200bpAGA-exon_variant
STAD-US147513423775134239deletion of <=200bpAGA-upstream_gene_variant
STAD-US147513956575139565single base substitutionAGdownstream_gene_variant
STAD-US147513956575139565single base substitutionAGexon_variant
STAD-US147513956575139565single base substitutionAGmissense_variantL303P908T>C
STAD-US147513956575139565single base substitutionAGmissense_variantL464P1391T>C
STAD-US147513956875139568single base substitutionGCdownstream_gene_variant
STAD-US147513956875139568single base substitutionGCexon_variant
STAD-US147513956875139568single base substitutionGCmissense_variantT302S905C>G
STAD-US147513956875139568single base substitutionGCmissense_variantT463S1388C>G
STAD-US147514079575140795single base substitutionACdownstream_gene_variant
STAD-US147514079575140795single base substitutionACexon_variant
STAD-US147514079575140795single base substitutionACmissense_variantF100C299T>G
STAD-US147514079575140795single base substitutionACmissense_variantF206C617T>G
STAD-US147514079575140795single base substitutionACmissense_variantF367C1100T>G
STAD-US147514250175142501single base substitutionGT3_prime_UTR_variant
STAD-US147514250175142501single base substitutionGTdownstream_gene_variant
STAD-US147514250175142501single base substitutionGTexon_variant
STAD-US147514250175142501single base substitutionGTsynonymous_variantS166S498C>A
STAD-US147514250175142501single base substitutionGTsynonymous_variantS327S981C>A
STAD-US147514250175142501single base substitutionGTsynonymous_variantS74S222C>A
STAD-US147514250175142501single base substitutionGTupstream_gene_variant
STAD-US147514343475143434single base substitutionGA3_prime_UTR_variant
STAD-US147514343475143434single base substitutionGAexon_variant
STAD-US147514343475143434single base substitutionGAmissense_variantT168I503C>T
STAD-US147514343475143434single base substitutionGAmissense_variantT7I20C>T
STAD-US147514343475143434single base substitutionGAupstream_gene_variant
STAD-US147515132375151323single base substitutionGAexon_variant
STAD-US147515132375151323single base substitutionGAintron_variant
STAD-US147515132375151323single base substitutionGAmissense_variantA26V77C>T
STAD-US147515132375151323single base substitutionGAupstream_gene_variant
THCA-SA147513677375136773single base substitutionCT3_prime_UTR_variant
THCA-SA147513677375136773single base substitutionCTdownstream_gene_variant
THCA-SA147513677375136773single base substitutionCTexon_variant
THCA-SA147513677375136773single base substitutionCTsynonymous_variantA394A1182G>A
THCA-SA147513677375136773single base substitutionCTsynonymous_variantA555A1665G>A
THCA-SA147513958675139586single base substitutionCGdownstream_gene_variant
THCA-SA147513958675139586single base substitutionCGexon_variant
THCA-SA147513958675139586single base substitutionCGmissense_variantR296T887G>C
THCA-SA147513958675139586single base substitutionCGmissense_variantR457T1370G>C
THCA-SA147515125275151252single base substitutionCTexon_variant
THCA-SA147515125275151252single base substitutionCTintron_variant
THCA-SA147515125275151252single base substitutionCTmissense_variantV50M148G>A
THCA-SA147515125275151252single base substitutionCTupstream_gene_variant
THCA-SA147515900775159007single base substitutionGA5_prime_UTR_premature_start_codon_gain_variant
THCA-SA147515900775159007single base substitutionGAexon_variant
THCA-SA147515900775159007single base substitutionGAintron_variant
THCA-SA147517973475179734single base substitutionCG5_prime_UTR_variant
THCA-SA147517973475179734single base substitutionCGexon_variant
THCA-SA147517973475179734single base substitutionCGupstream_gene_variant
UCEC-US147513072175130721single base substitutionCT3_prime_UTR_variant
UCEC-US147513072175130721single base substitutionCTexon_variant
UCEC-US147513072175130721single base substitutionCTsynonymous_variantR589R1767G>A
UCEC-US147513072175130721single base substitutionCTsynonymous_variantR750R2250G>A
UCEC-US147513425075134250single base substitutionCT3_prime_UTR_variant
UCEC-US147513425075134250single base substitutionCTdownstream_gene_variant
UCEC-US147513425075134250single base substitutionCTexon_variant
UCEC-US147513425075134250single base substitutionCTsynonymous_variantA493A1479G>A
UCEC-US147513425075134250single base substitutionCTsynonymous_variantA654A1962G>A
UCEC-US147513425075134250single base substitutionCTupstream_gene_variant
UCEC-US147513638775136387single base substitutionCA3_prime_UTR_variant
UCEC-US147513638775136387single base substitutionCAdownstream_gene_variant
UCEC-US147513638775136387single base substitutionCAexon_variant
UCEC-US147513638775136387single base substitutionCAstop_gainedE466*1396G>T
UCEC-US147513638775136387single base substitutionCAstop_gainedE627*1879G>T
UCEC-US147513638775136387single base substitutionCAupstream_gene_variant
UCEC-US147513754475137544single base substitutionCA3_prime_UTR_variant
UCEC-US147513754475137544single base substitutionCAdownstream_gene_variant
UCEC-US147513754475137544single base substitutionCAexon_variant
UCEC-US147513754475137544single base substitutionCAintron_variant
UCEC-US147513754475137544single base substitutionCAmissense_variantW349L1046G>T
UCEC-US147513754475137544single base substitutionCAmissense_variantW510L1529G>T
UCEC-US147513755075137550single base substitutionCT3_prime_UTR_variant
UCEC-US147513755075137550single base substitutionCTdownstream_gene_variant
UCEC-US147513755075137550single base substitutionCTexon_variant
UCEC-US147513755075137550single base substitutionCTintron_variant
UCEC-US147513755075137550single base substitutionCTmissense_variantR347Q1040G>A
UCEC-US147513755075137550single base substitutionCTmissense_variantR508Q1523G>A
UCEC-US147513818775138187single base substitutionCTdownstream_gene_variant
UCEC-US147513818775138187single base substitutionCTsplice_acceptor_variant
UCEC-US147513960575139605single base substitutionGAdownstream_gene_variant
UCEC-US147513960575139605single base substitutionGAexon_variant
UCEC-US147513960575139605single base substitutionGAmissense_variantR290W868C>T
UCEC-US147513960575139605single base substitutionGAmissense_variantR451W1351C>T
UCEC-US147513961475139614single base substitutionGAdownstream_gene_variant
UCEC-US147513961475139614single base substitutionGAexon_variant
UCEC-US147513961475139614single base substitutionGAstop_gainedR287*859C>T
UCEC-US147513961475139614single base substitutionGAstop_gainedR448*1342C>T
UCEC-US147513962375139623single base substitutionAGdownstream_gene_variant
UCEC-US147513962375139623single base substitutionAGexon_variant
UCEC-US147513962375139623single base substitutionAGmissense_variantF284L850T>C
UCEC-US147513962375139623single base substitutionAGmissense_variantF445L1333T>C
UCEC-US147514243275142432single base substitutionCTdownstream_gene_variant
UCEC-US147514243275142432single base substitutionCTexon_variant
UCEC-US147514243275142432single base substitutionCTintron_variant
UCEC-US147514243275142432single base substitutionCTsynonymous_variantP189P567G>A
UCEC-US147514243275142432single base substitutionCTsynonymous_variantP350P1050G>A
UCEC-US147514243275142432single base substitutionCTupstream_gene_variant
UCEC-US147514262575142625single base substitutionCT3_prime_UTR_variant
UCEC-US147514262575142625single base substitutionCTexon_variant
UCEC-US147514262575142625single base substitutionCTmissense_variantR125H374G>A
UCEC-US147514262575142625single base substitutionCTmissense_variantR286H857G>A
UCEC-US147514262575142625single base substitutionCTmissense_variantR33H98G>A
UCEC-US147514262575142625single base substitutionCTupstream_gene_variant
UCEC-US147514337375143373single base substitutionTC3_prime_UTR_variant
UCEC-US147514337375143373single base substitutionTCexon_variant
UCEC-US147514337375143373single base substitutionTCsynonymous_variantQ188Q564A>G
UCEC-US147514337375143373single base substitutionTCsynonymous_variantQ27Q81A>G
UCEC-US147514337375143373single base substitutionTCupstream_gene_variant
UCEC-US147515014775150147single base substitutionAC5_prime_UTR_premature_start_codon_gain_variant
UCEC-US147515014775150147single base substitutionACexon_variant
UCEC-US147515014775150147single base substitutionACintron_variant
UCEC-US147515014775150147single base substitutionACmissense_variantI111M333T>G
UCEC-US147515014775150147single base substitutionACupstream_gene_variant
UCEC-US147515124975151249single base substitutionGAexon_variant
UCEC-US147515124975151249single base substitutionGAintron_variant
UCEC-US147515124975151249single base substitutionGAmissense_variantR51W151C>T
UCEC-US147515124975151249single base substitutionGAupstream_gene_variant
UCEC-US147515125275151252single base substitutionCTexon_variant
UCEC-US147515125275151252single base substitutionCTintron_variant
UCEC-US147515125275151252single base substitutionCTmissense_variantV50M148G>A
UCEC-US147515125275151252single base substitutionCTupstream_gene_variant
UCEC-US147515131775151317single base substitutionCTexon_variant
UCEC-US147515131775151317single base substitutionCTintron_variant
UCEC-US147515131775151317single base substitutionCTmissense_variantR28H83G>A
UCEC-US147515131775151317single base substitutionCTupstream_gene_variant
UCEC-US147515135575151355single base substitutionGTexon_variant
UCEC-US147515135575151355single base substitutionGTintron_variant
UCEC-US147515135575151355single base substitutionGTmissense_variantF15L45C>A
UCEC-US147515135575151355single base substitutionGTupstream_gene_variant
UCEC-US147518019975180199single base substitutionGTupstream_gene_variant
UCEC-US147518164275181642single base substitutionGAupstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
TCGA-D1-A16X-01COSM957795c.564A>Gp.Q188QSubstitution - coding silent14:74676670-74676670-
TCGA-D1-A15X-01COSM957782c.2250G>Ap.R750RSubstitution - coding silent14:74664018-74664018-
SH-0622COSM5018383c.1410delCp.L471fs*6Deletion - Frameshift14:74672843-74672843-
RK109_C01COSM1629401c.2000G>Tp.R667LSubstitution - Missense14:74667509-74667509-
KM12COSM2137893c.1712C>Tp.A571VSubstitution - Missense14:74670023-74670023-
TCGA-AZ-4315-01COSM1371073c.1984T>Gp.L662VSubstitution - Missense14:74667525-74667525-
HCC174COSM3706385c.1510G>Ap.G504RSubstitution - Missense14:74670860-74670860-
LUAD-RT-S01777COSM381937c.2086G>Ap.D696NSubstitution - Missense14:74667336-74667336-
B77COSM1748985c.51C>Tp.F17FSubstitution - coding silent14:74684646-74684646-
TCGA-ES-A2HS-01COSM4910462c.2464A>Gp.M822VSubstitution - Missense14:74663728-74663728-
I2L-P8-Tumor-BiopsyCOSM5362723c.1314C>Gp.T438TSubstitution - coding silent14:74672939-74672939-
I2L-P8-Tumor-OrganoidCOSM5362723c.1314C>Gp.T438TSubstitution - coding silent14:74672939-74672939-
TCGA-D7-6528-01COSM4052403c.1388C>Gp.T463SSubstitution - Missense14:74672865-74672865-
LUAD-NYU284COSM372766c.1309G>Ap.E437KSubstitution - Missense14:74672944-74672944-
TCGA-CW-5591-01COSM470237c.1742C>Tp.T581ISubstitution - Missense14:74669993-74669993-
JVM-2COSM1740067c.1787A>Cp.K596TSubstitution - Missense14:74669948-74669948-
CSCC-31-TCOSM4489726c.351C>Tp.V117VSubstitution - coding silent14:74683426-74683426-
61COSM5740175c.896C>Ap.A299DSubstitution - Missense14:74675883-74675883-
XHDG32COSM4695212c.1664C>Tp.A555VSubstitution - Missense14:74670071-74670071-
SNU-175COSM2137885c.2302G>Ap.A768TSubstitution - Missense14:74663966-74663966-
CSCC-44-TCOSM4534584c.2101G>Ap.E701KSubstitution - Missense14:74667321-74667321-
YUQUESTCOSM5382647c.1999C>Tp.R667WSubstitution - Missense14:74667510-74667510-
YURISACOSM5382649c.1134C>Ap.T378TSubstitution - coding silent14:74674058-74674058-
TCGA-D9-A6EC-06COSM4401381c.320T>Cp.L107PSubstitution - Missense14:74683457-74683457-
PDA_092COSM5003108c.1031C>Tp.P344LSubstitution - Missense14:74675748-74675748-
TCGA-B5-A0JY-01COSM957783c.1962G>Ap.A654ASubstitution - coding silent14:74667547-74667547-
TCGA-BR-4362-01COSM4052401c.2390C>Ap.P797HSubstitution - Missense14:74663802-74663802-
587222COSM261541c.853G>Ap.E285KSubstitution - Missense14:74675926-74675926-
TCGA-BS-A0UF-01COSM957784c.1879G>Tp.E627*Substitution - Nonsense14:74669684-74669684-
TCGA-BR-4257-01COSM4052402c.1391T>Cp.L464PSubstitution - Missense14:74672862-74672862-
TCGA-EE-A2GC-06COSM3886363c.2037C>Tp.F679FSubstitution - coding silent14:74667472-74667472-
TCGA-E2-A1LI-01COSM1477763c.1732G>Tp.A578SSubstitution - Missense14:74670003-74670003-
T2940COSM957797c.151C>Tp.R51WSubstitution - Missense14:74684546-74684546-
CSCC-38-TCOSM4520373c.1056G>Ap.K352KSubstitution - coding silent14:74675723-74675723-
TCGA-BS-A0UF-01COSM957800c.45C>Ap.F15LSubstitution - Missense14:74684652-74684652-
TCGA-D1-A17Q-01COSM957799c.83G>Ap.R28HSubstitution - Missense14:74684614-74684614-
DN14066COSM5962909c.1499-3C>Tp.?Unknown14:74670874-74670874-
TCGA-A6-5666-01COSM1371079c.188C>Tp.S63FSubstitution - Missense14:74684509-74684509-
CN-AML-NR-13-DxCOSM5424827c.1633G>Ap.A545TSubstitution - Missense14:74670102-74670102-
TCGA-A8-A0A6-01COSM3815300c.1040T>Gp.V347GSubstitution - Missense14:74675739-74675739-
BD124TCOSM5493202c.1745G>Ap.R582HSubstitution - Missense14:74669990-74669990-
TCGA-G3-A25U-01COSM4911069c.1312A>Gp.T438ASubstitution - Missense14:74672941-74672941-
SW48COSM2137895c.1579delAp.T527fs*10Deletion - Frameshift14:74670791-74670791-
HCC058TCOSM5804388c.428A>Tp.K143MSubstitution - Missense14:74683349-74683349-
TCGA-AC-A5XS-01COSM4391189c.1570C>Gp.Q524ESubstitution - Missense14:74670800-74670800-
KM12COSM1678131c.1700C>Ap.S567YSubstitution - Missense14:74670035-74670035-
Pa09CCOSM87434c.?p.?Unknown14:74692222-74692222-
CG4COSM5422835c.1453T>Gp.S485ASubstitution - Missense14:74671453-74671453-
B80-13-TumorCOSM1748984c.2276C>Gp.S759CSubstitution - Missense14:74663992-74663992-
CSCC-27-TCOSM4446306c.1423-3C>Tp.?Unknown14:74671486-74671486-
CSCC-16-TCOSM4529619c.1628G>Ap.R543HSubstitution - Missense14:74670107-74670107-
KM12COSM1678131c.1700C>Ap.S567YSubstitution - Missense14:74670035-74670035-
2497780COSM5750931c.2305C>Ap.L769ISubstitution - Missense14:74663963-74663963-
BD228TCOSM5508751c.1840C>Gp.L614VSubstitution - Missense14:74669723-74669723-
QC2-42-T2COSM5656248c.549G>Tp.Q183HSubstitution - Missense14:74676685-74676685-
TCGA-37-5819-01COSM699417c.2028G>Tp.V676VSubstitution - coding silent14:74667481-74667481-
TCGA-BS-A0UF-01COSM957790c.1351C>Tp.R451WSubstitution - Missense14:74672902-74672902-
HCC174TCOSM3706385c.1510G>Ap.G504RSubstitution - Missense14:74670860-74670860-
9087_TCOSM5039099c.501G>Tp.K167NSubstitution - Missense14:74676733-74676733-
CSCC-31-TCOSM4521350c.1107G>Cp.L369LSubstitution - coding silent14:74674085-74674085-
CSCC-27-TCOSM3497971c.779C>Tp.S260LSubstitution - Missense14:74676194-74676194-
TCGA-G2-A3VY-01COSM3793857c.2278C>Tp.Q760*Substitution - Nonsense14:74663990-74663990-
TCGA-GN-A26C-01COSM3497973c.171C>Tp.P57PSubstitution - coding silent14:74684526-74684526-
TCGA-LP-A4AV-01COSM4825513c.415G>Ap.E139KSubstitution - Missense14:74683362-74683362-
1604875COSM141440c.1583G>Ap.R528QSubstitution - Missense14:74670787-74670787-
S00472COSM312259c.2337G>Tp.P779PSubstitution - coding silent14:74663931-74663931-
TCGA-EE-A2MI-06COSM3497970c.1305C>Tp.G435GSubstitution - coding silent14:74672948-74672948-
TCGA-CC-5261-01COSM4933491c.2192A>Gp.K731RSubstitution - Missense14:74664837-74664837-
TCGA-C5-A1M6-01COSM4826586c.82C>Ap.R28SSubstitution - Missense14:74684615-74684615-
TCGA-D1-A17Q-01COSM957788c.1423-1G>Ap.?Unknown14:74671484-74671484-
TCGA-B5-A0K6-01COSM957787c.1522C>Tp.R508WSubstitution - Missense14:74670848-74670848-
TCGA-HU-A4H3-01COSM4052405c.981C>Ap.S327SSubstitution - coding silent14:74675798-74675798-
TCGA-KK-A59V-01COSM4878265c.551C>Tp.P184LSubstitution - Missense14:74676683-74676683-
587222COSM1211884c.1139G>Ap.R380QSubstitution - Missense14:74674053-74674053-
TCGA-D1-A163-01COSM957797c.151C>Tp.R51WSubstitution - Missense14:74684546-74684546-
PT33COSM5909376c.272C>Tp.P91LSubstitution - Missense14:74683505-74683505-
TCGA-FS-A1ZE-06COSM3497971c.779C>Tp.S260LSubstitution - Missense14:74676194-74676194-
B80-13COSM1748984c.2276C>Gp.S759CSubstitution - Missense14:74663992-74663992-
pfg068TCOSM4757617c.124G>Ap.G42RSubstitution - Missense14:74684573-74684573-
PCSI_0083_Pa_PCOSM3377461c.2349G>Ap.T783TSubstitution - coding silent14:74663919-74663919-
53MCOSM5594755c.411T>Cp.R137RSubstitution - coding silent14:74683366-74683366-
TCGA-BR-8081-01COSM4052400c.2392A>Gp.T798ASubstitution - Missense14:74663800-74663800-
HRA19COSM4637718c.1926C>Ap.L642LSubstitution - coding silent14:74667583-74667583-
TCGA-AX-A0J0-01COSM957796c.333T>Gp.I111MSubstitution - Missense14:74683444-74683444-
N744TCOSM236464c.462C>Ap.Y154*Substitution - Nonsense14:74683315-74683315-
YUNEKICOSM5382650c.493C>Tp.P165SSubstitution - Missense14:74676741-74676741-
LUAD-B00915COSM391071c.1207delGp.V403fs*19Deletion - Frameshift14:74673170-74673170-
S00472COSM312259c.2337G>Tp.P779PSubstitution - coding silent14:74663931-74663931-
H322TCOSM1194912c.647A>Cp.H216PSubstitution - Missense14:74676587-74676587-
HCC13TCOSM1607945c.391A>Gp.T131ASubstitution - Missense14:74683386-74683386-
TCGA-FW-A3R5-06COSM3886366c.369C>Tp.S123SSubstitution - coding silent14:74683408-74683408-
PD2127aCOSM51884c.1041G>Ap.V347VSubstitution - coding silent14:74675738-74675738-
TCGA-EX-A69L-01COSM4854746c.81A>Tp.A27ASubstitution - coding silent14:74684616-74684616-
585272COSM321166c.1542C>Gp.I514MSubstitution - Missense14:74670828-74670828-
TCGA-24-1555-01COSM77947c.2184C>Gp.F728LSubstitution - Missense14:74664845-74664845-
PCSI_0083_Pa_XCOSM3377461c.2349G>Ap.T783TSubstitution - coding silent14:74663919-74663919-
TCGA-DA-A1HY-06COSM3497967c.2448T>Cp.G816GSubstitution - coding silent14:74663744-74663744-
TCGA-FS-A1ZQ-06COSM3497972c.592C>Tp.P198SSubstitution - Missense14:74676642-74676642-
TCGA-EA-A78R-01COSM4851993c.2089G>Ap.E697KSubstitution - Missense14:74667333-74667333-
Br27PCOSM40223c.1667G>Ap.G556ESubstitution - Missense14:74670068-74670068-
YUJUBECOSM5382648c.1764C>Tp.I588ISubstitution - coding silent14:74669971-74669971-
TCGA-EE-A29S-06COSM3497969c.1338C>Tp.F446FSubstitution - coding silent14:74672915-74672915-
TCGA-66-2785-01COSM699415c.70G>Cp.E24QSubstitution - Missense14:74684627-74684627-
TCGA-AX-A0J0-01COSM957793c.1050G>Ap.P350PSubstitution - coding silent14:74675729-74675729-
T595COSM4695214c.1008C>Tp.D336DSubstitution - coding silent14:74675771-74675771-
TCGA-C8-A26Y-01COSM3815299c.2273C>Tp.S758FSubstitution - Missense14:74663995-74663995-
PT13COSM5896228c.1000G>Ap.D334NSubstitution - Missense14:74675779-74675779-
ESCC_165COSM5648470c.2200A>Tp.R734WSubstitution - Missense14:74664068-74664068-
TCGA-A5-A0VP-01COSM957785c.1529G>Tp.W510LSubstitution - Missense14:74670841-74670841-
HCC111COSM1607944c.447G>Tp.V149VSubstitution - coding silent14:74683330-74683330-
TCGA-GV-A3QI-01COSM1300825c.1079A>Tp.K360MSubstitution - Missense14:74675700-74675700-
TCGA-AP-A059-01COSM957791c.1342C>Tp.R448*Substitution - Nonsense14:74672911-74672911-
CN-AML-32-TCOSM5424827c.1633G>Ap.A545TSubstitution - Missense14:74670102-74670102-
PT23_1COSM1371079c.188C>Tp.S63FSubstitution - Missense14:74684509-74684509-
LIM1899COSM4639982c.80C>Tp.A27VSubstitution - Missense14:74684617-74684617-
TCGA-13-1499-01COSM75117c.301C>Tp.H101YSubstitution - Missense14:74683476-74683476-
419COSM4431912c.2016G>Cp.V672VSubstitution - coding silent14:74667493-74667493-
RW2982COSM4649531c.680G>Tp.G227VSubstitution - Missense14:74676293-74676293-
CN-AML-NR-32-DxCOSM5424827c.1633G>Ap.A545TSubstitution - Missense14:74670102-74670102-
T3094COSM4695212c.1664C>Tp.A555VSubstitution - Missense14:74670071-74670071-
TCGA-DD-A11C-01COSM4925704c.1091T>Ap.V364ESubstitution - Missense14:74674101-74674101-
TCGA-FD-A3SO-01COSM3793858c.646C>Tp.H216YSubstitution - Missense14:74676588-74676588-
Pat_59_BCOSM5848525c.209delAp.Y70fs*29Deletion - Frameshift14:74684488-74684488-
TCGA-BS-A0UJ-01COSM957792c.1333T>Cp.F445LSubstitution - Missense14:74672920-74672920-
TCGA-21-1070-01COSM699416c.646C>Gp.H216DSubstitution - Missense14:74676588-74676588-
pfg120TCOSM4757614c.1010C>Tp.S337LSubstitution - Missense14:74675769-74675769-
RK101_C01COSM3700901c.391A>Tp.T131SSubstitution - Missense14:74683386-74683386-
TCGA-AP-A0LM-01COSM957794c.857G>Ap.R286HSubstitution - Missense14:74675922-74675922-
PCSI_0083_Pa_P_526COSM3377461c.2349G>Ap.T783TSubstitution - coding silent14:74663919-74663919-
TCGA-AG-A002-01COSM261541c.853G>Ap.E285KSubstitution - Missense14:74675926-74675926-
HCC019TCOSM5820301c.317A>Gp.E106GSubstitution - Missense14:74683460-74683460-
TCGA-19-2625-01COSM3401469c.481+1G>Ap.?Unknown14:74683295-74683295-
LIM1899COSM136977c.1627C>Tp.R543CSubstitution - Missense14:74670108-74670108-
pfg008TCOSM1640154c.1081-2A>Cp.?Unknown14:74674113-74674113-
CSCC-44-TCOSM4523717c.122G>Ap.R41QSubstitution - Missense14:74684575-74684575-
CSCC-29-TCOSM4461977c.1228C>Tp.P410SSubstitution - Missense14:74673149-74673149-
TCGA-FW-A3R5-06COSM3886364c.1757C>Tp.A586VSubstitution - Missense14:74669978-74669978-
T3502COSM4695215c.184G>Cp.V62LSubstitution - Missense14:74684513-74684513-
ATL079COSM5705763c.1373C>Ap.P458QSubstitution - Missense14:74672880-74672880-
HCC063TCOSM5812480c.2369+3A>Gp.?Unknown14:74663896-74663896-
TCGA-F1-6177-01COSM4052407c.77C>Tp.A26VSubstitution - Missense14:74684620-74684620-
Pat_59_BCOSM5848524c.1436C>Tp.T479ISubstitution - Missense14:74671470-74671470-
CSCC-56-TCOSM4514202c.966C>Tp.S322SSubstitution - coding silent14:74675813-74675813-
I2L-P7-Tumor-OrganoidCOSM5362370c.1159-10delTp.?Unknown14:74673228-74673228-
TCGA-FW-A3R5-06COSM3886365c.1700C>Tp.S567FSubstitution - Missense14:74670035-74670035-
TCGA-B5-A11F-01COSM957798c.148G>Ap.V50MSubstitution - Missense14:74684549-74684549-
49MCOSM5591499c.1029C>Tp.T343TSubstitution - coding silent14:74675750-74675750-
TCGA-EE-A2A2-06COSM3497974c.111C>Tp.D37DSubstitution - coding silent14:74684586-74684586-
TCGA-D1-A17Q-01COSM957786c.1523G>Ap.R508QSubstitution - Missense14:74670847-74670847-
HCC111TCOSM1607944c.447G>Tp.V149VSubstitution - coding silent14:74683330-74683330-
3101B7_032_TCOSM1516128c.1489G>Tp.D497YSubstitution - Missense14:74671417-74671417-
SW48COSM4615934c.1054_1056delAAGp.K352delKDeletion - In frame14:74675723-74675725-
CN-AML-CR-18-DxCOSM5424827c.1633G>Ap.A545TSubstitution - Missense14:74670102-74670102-
WSU-HN30COSM4391189c.1570C>Gp.Q524ESubstitution - Missense14:74670800-74670800-
TCGA-DD-A118-01COSM4937876c.1734T>Cp.A578ASubstitution - coding silent14:74670001-74670001-
B77-TumorCOSM1748985c.51C>Tp.F17FSubstitution - coding silent14:74684646-74684646-
AOCS-094-6-XCOSM3983697c.1558G>Cp.D520HSubstitution - Missense14:74670812-74670812-
cSCCP5COSM138053c.2236G>Ap.E746KSubstitution - Missense14:74664032-74664032-
T3094COSM4695213c.1207G>Ap.V403MSubstitution - Missense14:74673170-74673170-
TCGA-AD-6889-01COSM1371075c.913A>Gp.T305ASubstitution - Missense14:74675866-74675866-
TCGA-AN-A046-01COSM957793c.1050G>Ap.P350PSubstitution - coding silent14:74675729-74675729-
TCGA-61-1910-01COSM1323392c.2000G>Ap.R667QSubstitution - Missense14:74667509-74667509-
TCGA-D5-6931-01COSM1371076c.856C>Tp.R286CSubstitution - Missense14:74675923-74675923-
TCGA-DB-5278-01COSM3968915c.1264G>Cp.A422PSubstitution - Missense14:74673113-74673113-
SNU-C4COSM4652542c.2467C>Tp.L823FSubstitution - Missense14:74663725-74663725-
TCGA-FS-A1ZK-06COSM3497968c.1750T>Ap.F584ISubstitution - Missense14:74669985-74669985-
HCC13COSM1607945c.391A>Gp.T131ASubstitution - Missense14:74683386-74683386-
cSCCP6COSM136977c.1627C>Tp.R543CSubstitution - Missense14:74670108-74670108-
UM-SCC-2COSM4599252c.767A>Gp.H256RSubstitution - Missense14:74676206-74676206-
CN-AML-13-TCOSM5424827c.1633G>Ap.A545TSubstitution - Missense14:74670102-74670102-
pfg008TCOSM1640154c.1081-2A>Cp.?Unknown14:74674113-74674113-
1N25-VS-1T25COSM4973355c.235C>Tp.R79*Substitution - Nonsense14:74684462-74684462-
TCGA-HU-A4H0-01COSM4052404c.1100T>Gp.F367CSubstitution - Missense14:74674092-74674092-
CSCC-16-TCOSM4546950c.410G>Ap.R137HSubstitution - Missense14:74683367-74683367-
CSCC-60-TCOSM4459138c.1113C>Tp.I371ISubstitution - coding silent14:74674079-74674079-
TCGA-A5-A0GQ-01COSM957789c.1405C>Ap.H469NSubstitution - Missense14:74672848-74672848-
TCGA-A8-A0A6-01COSM3815301c.1027A>Cp.T343PSubstitution - Missense14:74675752-74675752-
ESCC_54COSM5649732c.2027T>Gp.V676GSubstitution - Missense14:74667482-74667482-
TCGA-D7-6525-01COSM4052406c.503C>Tp.T168ISubstitution - Missense14:74676731-74676731-
TCGA-CJ-4905-01COSM470236c.1855A>Cp.S619RSubstitution - Missense14:74669708-74669708-
SNU-C4COSM4652543c.337G>Ap.V113MSubstitution - Missense14:74683440-74683440-
S01864COSM5671631c.2024A>Gp.E675GSubstitution - Missense14:74667485-74667485-
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.49741714q24.3
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
AG3-UTRSNV.c.2469+142T>C1475130284CM
AGMissensep.L464Pc.1391T>C1475139565STAD
AGSynonymousp.G816Gc.2448T>C1475130447CM
ATMissensep.F584Ic.1750T>A1475136688CM
CAMissensep.A578Sc.1732G>T1475136706BRCA
CAMissensep.R192Lc.575G>T1475143362LUAD
CAMissensep.R667Lc.2000G>T1475134212HC
CAMissensep.W510Lc.1529G>T1475137544UCEC
CASynonymousp.P779Pc.2337G>T1475130634SCLC
CASynonymousp.V676Vc.2028G>T1475134184LUSC
CGATMissensep.P350Hc.1049_1050delinsAT1475142432CM
CGMissensep.A422Pc.1264G>C1475139816LGG
CT3-UTRSNV.c.2469+1226G>A1475129200MB
CTMissensep.E340Kc.1018G>A1475142464LUAD
CTSpliceDonorSNV.c.481+1G>A1475149998GBM
CTSynonymousp.K360Kc.1080G>A1475142402CM
CTSynonymousp.V142Vc.426G>A1475150054LUAD
GA5-UTRSNV.c.1-27495C>T1475179813CM
GAMissensep.A26Vc.77C>T1475151323STAD
GAMissensep.G556Ec.1667G>A1475136771GBM
GAMissensep.H101Yc.301C>T1475150179OV
GAMissensep.L614Fc.1840C>T1475136426BRCA
GAMissensep.P198Sc.592C>T1475143345CM
GAMissensep.R51Wc.151C>T1475151249UCEC
GAMissensep.R557Wc.1669C>T1475136769STAD
GAMissensep.S260Lc.779C>T1475142897CM
GAMissensep.T168Ic.503C>T1475143434STAD
GAMissensep.T581Ic.1742C>T1475136696RCCC
GANonsensep.R577*c.1729C>T1475136709STAD
GASynonymousp.D37Dc.111C>T1475151289CM
GASynonymousp.F446Fc.1338C>T1475139618CM
GASynonymousp.F679Fc.2037C>T1475134175CM
GASynonymousp.G435Gc.1305C>T1475139651CM
GASynonymousp.P57Pc.171C>T1475151229CM
GASynonymousp.Y154Yc.462C>T1475150018HNSC
GCMissensep.F728Lc.2184C>G1475131548OV
GCMissensep.H216Dc.646C>G1475143291LUSC
GCMissensep.I514Mc.1542C>G1475137531SCLC
GCMissensep.L301Vc.901C>G1475142581LUAD
GCMissensep.R246Gc.736C>G1475142940CM
GCMissensep.T463Sc.1388C>G1475139568STAD
GTMissensep.F362Lc.1086C>A1475140809HNSC
GTMissensep.P344Tc.1030C>A1475142452CM
TAMissensep.K360Mc.1079A>T1475142403BLCA
TCMissensep.Y302Cc.905A>G1475142577LUAD
TCMissensep.Y84Cc.251A>G1475150229CM
TGMissensep.S619Rc.1855A>C1475136411RCCC
TGSpliceAcceptorSNV.c.1081-2A>C1475140816STAD