DDI2
Mutation - TCGA
TypeChromosomeStart PositionEnd PositionStrandVariant ClassificationVariant TypeReference AlleleTumor_seq Allele 1Tumor_seq Allele 2Tumor Sample BarcodeMatched Norm Sample BarcodeGenome ChangecDNA ChangeCodon ChangeProtein Change
BLCA11595692615956926+Missense_MutationSNPAAGTCGA-XF-A9SJ-01A-11D-A391-08TCGA-XF-A9SJ-10A-01D-A394-08g.chr1:15956926A>Gc.375A>Gc.(373-375)atA>atGp.I125M
BLCA11595693915956939+Nonsense_MutationSNPCCTTCGA-DK-A1AC-01A-11D-A13W-08TCGA-DK-A1AC-10A-01D-A13W-08g.chr1:15956939C>Tc.388C>Tc.(388-390)Cag>Tagp.Q130*
BLCA11595993315959933+Splice_SiteSNPGGCTCGA-FD-A3SN-01A-12D-A22Z-08TCGA-FD-A3SN-10A-01D-A22Z-08g.chr1:15959933G>Cc.e4-1
BLCA11596001715960017+Missense_MutationSNPCCGTCGA-MV-A51V-01A-11D-A26M-08TCGA-MV-A51V-10A-01D-A26K-08g.chr1:15960017C>Gc.589C>Gc.(589-591)Ccc>Gccp.P197A
BLCA11597826415978264+Missense_MutationSNPCCGTCGA-XF-A9SL-01A-11D-A391-08TCGA-XF-A9SL-10A-01D-A394-08g.chr1:15978264C>Gc.1057C>Gc.(1057-1059)Ctt>Gttp.L353V
BLCA11597826715978267+Missense_MutationSNPCCGTCGA-DK-A3IL-01A-11D-A20D-08TCGA-DK-A3IL-10A-01D-A20D-08g.chr1:15978267C>Gc.1060C>Gc.(1060-1062)Cct>Gctp.P354A
BLCA11597836915978369+Missense_MutationSNPCCGTCGA-FD-A3SN-01A-12D-A22Z-08TCGA-FD-A3SN-10A-01D-A22Z-08g.chr1:15978369C>Gc.1162C>Gc.(1162-1164)Caa>Gaap.Q388E
BRCA11595696315956963+Missense_MutationSNPCCGTCGA-C8-A3M8-01A-11D-A20S-09TCGA-C8-A3M8-10A-01D-A20S-09g.chr1:15956963C>Gc.412C>Gc.(412-414)Ctc>Gtcp.L138V
BRCA11597837815978378+Missense_MutationSNPGGTTCGA-AO-A0J3-01A-11W-A050-09TCGA-AO-A0J3-10A-01W-A055-09g.chr1:15978378G>Tc.1171G>Tc.(1171-1173)Gca>Tcap.A391S
CESC11595993315959933+Splice_SiteSNPGGTTCGA-DS-A5RQ-01A-11D-A28B-09TCGA-DS-A5RQ-10A-01D-A28E-09g.chr1:15959933G>Tc.e4-1
CESC11597827015978270+Missense_MutationSNPGGATCGA-UC-A7PF-01A-11D-A351-09TCGA-UC-A7PF-11A-31D-A351-09g.chr1:15978270G>Ac.1063G>Ac.(1063-1065)Gag>Aagp.E355K
CESC11597834715978347+SilentSNPCCTTCGA-DS-A1OA-01A-11D-A16Y-08TCGA-DS-A1OA-10A-01D-A16Y-08g.chr1:15978347C>Tc.1140C>Tc.(1138-1140)gaC>gaTp.D380D
COAD11595685515956855+Missense_MutationSNPCCTTCGA-AA-A022-01A-21W-A096-10TCGA-AA-A022-11A-11W-A096-10g.chr1:15956855C>Tc.304C>Tc.(304-306)Cct>Tctp.P102S
COAD11596483015964830+Missense_MutationSNPAATTCGA-AA-3833-01A-01W-0900-09TCGA-AA-3833-10A-01W-0900-09g.chr1:15964830A>Tc.661A>Tc.(661-663)Ata>Ttap.I221L
COADREAD11595685515956855+Missense_MutationSNPCCTTCGA-AA-A022-01A-21W-A096-10TCGA-AA-A022-11A-11W-A096-10g.chr1:15956855C>Tc.304C>Tc.(304-306)Cct>Tctp.P102S
COADREAD11596483015964830+Missense_MutationSNPAATTCGA-AA-3833-01A-01W-0900-09TCGA-AA-3833-10A-01W-0900-09g.chr1:15964830A>Tc.661A>Tc.(661-663)Ata>Ttap.I221L
GBM11597832715978327+SilentSNPCCATCGA-19-1790-01B-01D-1353-08TCGA-19-1790-10B-01D-1353-08g.chr1:15978327C>Ac.1120C>Ac.(1120-1122)Cgg>Aggp.R374R
GBMLGG11595698915956989+SilentSNPGGATCGA-E1-5322-01A-01D-1468-08TCGA-E1-5322-10A-01D-1468-08g.chr1:15956989G>Ac.438G>Ac.(436-438)ccG>ccAp.P146P
GBMLGG11596486115964861+Missense_MutationSNPGGTTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr1:15964861G>Tc.692G>Tc.(691-693)gGc>gTcp.G231V
GBMLGG11597832715978327+SilentSNPCCATCGA-19-1790-01B-01D-1353-08TCGA-19-1790-10B-01D-1353-08g.chr1:15978327C>Ac.1120C>Ac.(1120-1122)Cgg>Aggp.R374R
HNSC11595683915956839+SilentSNPCCTTCGA-CN-6998-01A-23D-2012-08TCGA-CN-6998-10A-01D-2013-08g.chr1:15956839C>Tc.288C>Tc.(286-288)ttC>ttTp.F96F
HNSC11595691015956910+Missense_MutationSNPCCTTCGA-CV-6935-01A-11D-1912-08TCGA-CV-6935-10A-01D-1912-08g.chr1:15956910C>Tc.359C>Tc.(358-360)tCa>tTap.S120L
HNSC11595996515959965+SilentSNPGGATCGA-CV-6954-01A-11D-1912-08TCGA-CV-6954-10A-01D-1912-08g.chr1:15959965G>Ac.537G>Ac.(535-537)caG>caAp.Q179Q
HNSC11598311915983119+SilentSNPGGATCGA-CV-6961-01A-21D-1912-08TCGA-CV-6961-10A-01D-1912-08g.chr1:15983119G>Ac.1191G>Ac.(1189-1191)caG>caAp.Q397Q
KIPAN11595683915956839+SilentSNPCCTTCGA-IZ-8196-01A-11D-2396-08TCGA-IZ-8196-10A-01D-2396-08g.chr1:15956839C>Tc.288C>Tc.(286-288)ttC>ttTp.F96F
KIPAN11595685015956850+Missense_MutationSNPCCATCGA-HE-7128-01A-11D-1961-08TCGA-HE-7128-10A-01D-1962-08g.chr1:15956850C>Ac.299C>Ac.(298-300)gCt>gAtp.A100D
KIPAN11595702115957021+Missense_MutationSNPCCTTCGA-A4-7288-01A-11D-2136-08TCGA-A4-7288-11A-01D-2136-08g.chr1:15957021C>Tc.470C>Tc.(469-471)cCa>cTap.P157L
KIRP11595683915956839+SilentSNPCCTTCGA-IZ-8196-01A-11D-2396-08TCGA-IZ-8196-10A-01D-2396-08g.chr1:15956839C>Tc.288C>Tc.(286-288)ttC>ttTp.F96F
KIRP11595685015956850+Missense_MutationSNPCCATCGA-HE-7128-01A-11D-1961-08TCGA-HE-7128-10A-01D-1962-08g.chr1:15956850C>Ac.299C>Ac.(298-300)gCt>gAtp.A100D
KIRP11595702115957021+Missense_MutationSNPCCTTCGA-A4-7288-01A-11D-2136-08TCGA-A4-7288-11A-01D-2136-08g.chr1:15957021C>Tc.470C>Tc.(469-471)cCa>cTap.P157L
LGG11595698915956989+SilentSNPGGATCGA-E1-5322-01A-01D-1468-08TCGA-E1-5322-10A-01D-1468-08g.chr1:15956989G>Ac.438G>Ac.(436-438)ccG>ccAp.P146P
LGG11596486115964861+Missense_MutationSNPGGTTCGA-DU-6392-01A-11D-1705-08TCGA-DU-6392-10A-01D-1705-08g.chr1:15964861G>Tc.692G>Tc.(691-693)gGc>gTcp.G231V
LIHC11595996715959967+Missense_MutationSNPAAGTCGA-DD-A39Y-01A-11D-A20W-10TCGA-DD-A39Y-11A-11D-A20W-10g.chr1:15959967A>Gc.539A>Gc.(538-540)cAg>cGgp.Q180R
LUAD11595318715953187+SilentSNPCCTTCGA-91-6831-01A-11D-1855-08TCGA-91-6831-11A-02D-1855-08g.chr1:15953187C>Tc.162C>Tc.(160-162)ctC>ctTp.L54L
LUAD11595696615956966+Nonsense_MutationSNPCCTTCGA-50-5051-01A-21D-1855-08TCGA-50-5051-10A-01D-1855-08g.chr1:15956966C>Tc.415C>Tc.(415-417)Cga>Tgap.R139*
LUAD11595994515959945+Missense_MutationSNPAAGTCGA-05-4427-01A-21D-1855-08TCGA-05-4427-10A-01D-1855-08g.chr1:15959945A>Gc.517A>Gc.(517-519)Aga>Ggap.R173G
LUAD11597013415970134+Missense_MutationSNPGGTTCGA-17-Z031-01A-01W-0746-08TCGA-17-Z031-11A-01W-0746-08g.chr1:15970134G>Tc.878G>Tc.(877-879)aGg>aTgp.R293M
LUSC11595682215956822+Missense_MutationSNPTTGTCGA-22-5482-01A-01D-1632-08TCGA-22-5482-11A-01D-1632-08g.chr1:15956822T>Gc.271T>Gc.(271-273)Tta>Gtap.L91V
LUSC11595692115956921+Missense_MutationSNPGGCTCGA-56-5897-01A-11D-1632-08TCGA-56-5897-10A-01D-1632-08g.chr1:15956921G>Cc.370G>Cc.(370-372)Gaa>Caap.E124Q
OV11595319515953195+Missense_MutationSNPAAGTCGA-30-1856-01A-01W-0639-09TCGA-30-1856-10A-01W-0639-09g.chr1:15953195A>Gc.170A>Gc.(169-171)aAc>aGcp.N57S
OV11595701715957017+Missense_MutationSNPAATTCGA-29-2434-01A-01D-1526-09TCGA-29-2434-10A-01D-1526-09g.chr1:15957017A>Tc.466A>Tc.(466-468)Aat>Tatp.N156Y
OV11596484615964846+Missense_MutationSNPCCGTCGA-30-1718-01A-01W-0633-09TCGA-30-1718-10A-01W-0633-09g.chr1:15964846C>Gc.677C>Gc.(676-678)gCt>gGtp.A226G
PCPG11595691815956918+Missense_MutationSNPGGATCGA-SR-A6MZ-01A-11D-A35I-08TCGA-SR-A6MZ-10A-01D-A35G-08g.chr1:15956918G>Ac.367G>Ac.(367-369)Gga>Agap.G123R
SKCM11595325515953255+Missense_MutationSNPAATTCGA-D3-A3ML-06A-11D-A21A-08TCGA-D3-A3ML-10A-01D-A21A-08g.chr1:15953255A>Tc.230A>Tc.(229-231)aAg>aTgp.K77M
SKCM11596001815960018+Missense_MutationSNPCCTTCGA-EE-A3J7-06A-11D-A20D-08TCGA-EE-A3J7-10A-01D-A20D-08g.chr1:15960018C>Tc.590C>Tc.(589-591)cCc>cTcp.P197L
SKCM11596004715960047+Missense_MutationSNPGGATCGA-ER-A19P-06A-11D-A196-08TCGA-ER-A19P-10A-01D-A198-08g.chr1:15960047G>Ac.619G>Ac.(619-621)Gaa>Aaap.E207K
SKCM11597626315976263+Missense_MutationSNPTTGTCGA-D9-A6EC-06A-11D-A30X-08TCGA-D9-A6EC-10A-01D-A30X-08g.chr1:15976263T>Gc.938T>Gc.(937-939)cTt>cGtp.L313R
SKCM11597820515978205+Missense_MutationSNPCCTTCGA-D3-A5GO-06A-12D-A27K-08TCGA-D3-A5GO-10A-01D-A27N-08g.chr1:15978205C>Tc.998C>Tc.(997-999)tCc>tTcp.S333F
SKCM11597820615978206+SilentSNPCCTTCGA-FW-A3R5-06A-11D-A23B-08TCGA-FW-A3R5-10A-01D-A23B-08g.chr1:15978206C>Tc.999C>Tc.(997-999)tcC>tcTp.S333S
Mutation - ICGC
Project CodeChromosomeChromosome StartChromosome EndMutation TypeMutated from AlleleMutated to AlleleConsequence TypeAA MutationCDS Mutation
BLCA-CN11598774415987744single base substitutionCA3_prime_UTR_variant
BLCA-CN11598774415987744single base substitutionCAdownstream_gene_variant
BLCA-US11595693915956939single base substitutionCTdownstream_gene_variant
BLCA-US11595693915956939single base substitutionCTexon_variant
BLCA-US11595693915956939single base substitutionCTstop_gainedQ130*388C>T
BLCA-US11595993315959933single base substitutionGCsplice_acceptor_variant
BLCA-US11597826715978267single base substitutionCG3_prime_UTR_variant
BLCA-US11597826715978267single base substitutionCGdownstream_gene_variant
BLCA-US11597826715978267single base substitutionCGmissense_variantP354A1060C>G
BLCA-US11597826715978267single base substitutionCGupstream_gene_variant
BLCA-US11597836915978369single base substitutionCG3_prime_UTR_variant
BLCA-US11597836915978369single base substitutionCGdownstream_gene_variant
BLCA-US11597836915978369single base substitutionCGexon_variant
BLCA-US11597836915978369single base substitutionCGmissense_variantQ388E1162C>G
BLCA-US11598646215986462single base substitutionCG3_prime_UTR_variant
BLCA-US11598646215986462single base substitutionCGdownstream_gene_variant
BLCA-US11598651915986519single base substitutionTC3_prime_UTR_variant
BLCA-US11598651915986519single base substitutionTCdownstream_gene_variant
BLCA-US11598658115986581single base substitutionCA3_prime_UTR_variant
BLCA-US11598658115986581single base substitutionCAdownstream_gene_variant
BLCA-US11598725315987253single base substitutionCA3_prime_UTR_variant
BLCA-US11598725315987253single base substitutionCAdownstream_gene_variant
BLCA-US11598744115987441single base substitutionCT3_prime_UTR_variant
BLCA-US11598744115987441single base substitutionCTdownstream_gene_variant
BRCA-EU11593924415939244single base substitutionGAupstream_gene_variant
BRCA-EU11593986715939867single base substitutionTAupstream_gene_variant
BRCA-EU11594011615940116single base substitutionGCupstream_gene_variant
BRCA-EU11594023015940230single base substitutionATupstream_gene_variant
BRCA-EU11594180315941803single base substitutionTAupstream_gene_variant
BRCA-EU11594560615945606insertion of <=200bp-Tintron_variant
BRCA-EU11594591515945915single base substitutionCTintron_variant
BRCA-EU11594685815946858single base substitutionAGintron_variant
BRCA-EU11594849115948491single base substitutionGAintron_variant
BRCA-EU11594869115948691single base substitutionGTintron_variant
BRCA-EU11594889215948892single base substitutionCTintron_variant
BRCA-EU11594935215949352single base substitutionGAintron_variant
BRCA-EU11594936415949364single base substitutionGAintron_variant
BRCA-EU11595129615951296deletion of <=200bpG-intron_variant
BRCA-EU11595292615952926single base substitutionCGintron_variant
BRCA-EU11595292615952926single base substitutionCGupstream_gene_variant
BRCA-EU11595354015953540single base substitutionCGexon_variant
BRCA-EU11595354015953540single base substitutionCGintron_variant
BRCA-EU11595354015953540single base substitutionCGupstream_gene_variant
BRCA-EU11595385215953852single base substitutionGAdownstream_gene_variant
BRCA-EU11595385215953852single base substitutionGAintron_variant
BRCA-EU11595385215953852single base substitutionGAupstream_gene_variant
BRCA-EU11595397815953978single base substitutionGAdownstream_gene_variant
BRCA-EU11595397815953978single base substitutionGAintron_variant
BRCA-EU11595397815953978single base substitutionGAupstream_gene_variant
BRCA-EU11595794415957944single base substitutionCGdownstream_gene_variant
BRCA-EU11595794415957944single base substitutionCGintron_variant
BRCA-EU11595880915958809single base substitutionCTintron_variant
BRCA-EU11595949015959490single base substitutionCTintron_variant
BRCA-EU11595982815959828single base substitutionCAintron_variant
BRCA-EU11596093815960938single base substitutionCTdownstream_gene_variant
BRCA-EU11596093815960938single base substitutionCTintron_variant
BRCA-EU11596180015961800single base substitutionCGdownstream_gene_variant
BRCA-EU11596180015961800single base substitutionCGintron_variant
BRCA-EU11596263215962632insertion of <=200bp-Tdownstream_gene_variant
BRCA-EU11596263215962632insertion of <=200bp-Tintron_variant
BRCA-EU11596311915963119single base substitutionAGdownstream_gene_variant
BRCA-EU11596311915963119single base substitutionAGintron_variant
BRCA-EU11596404915964049single base substitutionGCdownstream_gene_variant
BRCA-EU11596404915964049single base substitutionGCintron_variant
BRCA-EU11596483615964836single base substitutionAGdownstream_gene_variant
BRCA-EU11596483615964836single base substitutionAGintron_variant
BRCA-EU11596483615964836single base substitutionAGmissense_variantM223V667A>G
BRCA-EU11596656615966566deletion of <=200bpA-intron_variant
BRCA-EU11596740615967406single base substitutionAGintron_variant
BRCA-EU11596873315968733single base substitutionAGintron_variant
BRCA-EU11596963915969639single base substitutionGAintron_variant
BRCA-EU11597274515972745single base substitutionGAintron_variant
BRCA-EU11597367315973673single base substitutionCTintron_variant
BRCA-EU11597367315973673single base substitutionCTupstream_gene_variant
BRCA-EU11597422515974225single base substitutionGTintron_variant
BRCA-EU11597422515974225single base substitutionGTupstream_gene_variant
BRCA-EU11597585115975851single base substitutionTCintron_variant
BRCA-EU11597585115975851single base substitutionTCupstream_gene_variant
BRCA-EU11597715115977151single base substitutionGCdownstream_gene_variant
BRCA-EU11597715115977151single base substitutionGCintron_variant
BRCA-EU11597715115977151single base substitutionGCupstream_gene_variant
BRCA-EU11597724815977248single base substitutionATdownstream_gene_variant
BRCA-EU11597724815977248single base substitutionATintron_variant
BRCA-EU11597724815977248single base substitutionATupstream_gene_variant
BRCA-EU11597816915978169single base substitutionCTdownstream_gene_variant
BRCA-EU11597816915978169single base substitutionCTintron_variant
BRCA-EU11597816915978169single base substitutionCTupstream_gene_variant
BRCA-EU11597984815979848single base substitutionGAdownstream_gene_variant
BRCA-EU11597984815979848single base substitutionGAintron_variant
BRCA-EU11598075915980759single base substitutionGAdownstream_gene_variant
BRCA-EU11598075915980759single base substitutionGAintron_variant
BRCA-EU11598194815981948single base substitutionCGintron_variant
BRCA-EU11598207015982070single base substitutionATintron_variant
BRCA-EU11598241915982419deletion of <=200bpA-intron_variant
BRCA-EU11598243015982430deletion of <=200bpA-intron_variant
BRCA-EU11598249515982495single base substitutionATintron_variant
BRCA-EU11598253615982536single base substitutionAGintron_variant
BRCA-EU11598303715983037single base substitutionGAexon_variant
BRCA-EU11598303715983037single base substitutionGAintron_variant
BRCA-EU11598546115985461insertion of <=200bp-Tdownstream_gene_variant
BRCA-EU11598546115985461insertion of <=200bp-Tintron_variant
BRCA-EU11598641315986413single base substitutionCT3_prime_UTR_variant
BRCA-EU11598641315986413single base substitutionCTdownstream_gene_variant
BRCA-EU11598684715986847single base substitutionGA3_prime_UTR_variant
BRCA-EU11598684715986847single base substitutionGAdownstream_gene_variant
BRCA-EU11598777015987770single base substitutionGC3_prime_UTR_variant
BRCA-EU11598777015987770single base substitutionGCdownstream_gene_variant
BRCA-EU11599159315991593single base substitutionCT3_prime_UTR_variant
BRCA-EU11599159315991593single base substitutionCTdownstream_gene_variant
BRCA-EU11599255915992559single base substitutionGA3_prime_UTR_variant
BRCA-EU11599490815994908single base substitutionGT3_prime_UTR_variant
BRCA-EU11599518815995188single base substitutionAC3_prime_UTR_variant
BRCA-EU11599643015996430single base substitutionCTdownstream_gene_variant
BRCA-EU11599672715996727single base substitutionGCdownstream_gene_variant
BRCA-EU11599721015997210deletion of <=200bpA-downstream_gene_variant
BRCA-EU11599785315997853single base substitutionCGdownstream_gene_variant
BRCA-EU11599854915998549single base substitutionGAdownstream_gene_variant
BRCA-EU11599890015998900single base substitutionGAdownstream_gene_variant
BRCA-EU11599891415998914single base substitutionCAdownstream_gene_variant
BRCA-EU11599930715999307single base substitutionGTdownstream_gene_variant
BRCA-EU11599946515999465single base substitutionAGdownstream_gene_variant
BRCA-FR11595292615952926single base substitutionCGintron_variant
BRCA-FR11595292615952926single base substitutionCGupstream_gene_variant
BRCA-FR11595572415955724single base substitutionGCdownstream_gene_variant
BRCA-FR11595572415955724single base substitutionGCintron_variant
BRCA-FR11595572415955724single base substitutionGCupstream_gene_variant
BRCA-FR11596404915964049single base substitutionGCdownstream_gene_variant
BRCA-FR11596404915964049single base substitutionGCintron_variant
BRCA-FR11597816915978169single base substitutionCTdownstream_gene_variant
BRCA-FR11597816915978169single base substitutionCTintron_variant
BRCA-FR11597816915978169single base substitutionCTupstream_gene_variant
BRCA-FR11598303715983037single base substitutionGAexon_variant
BRCA-FR11598303715983037single base substitutionGAintron_variant
BRCA-FR11599082715990827single base substitutionGA3_prime_UTR_variant
BRCA-FR11599082715990827single base substitutionGAdownstream_gene_variant
BRCA-FR11599490815994908single base substitutionGT3_prime_UTR_variant
BRCA-FR11599793915997939single base substitutionGAdownstream_gene_variant
BRCA-FR11599854915998549single base substitutionGAdownstream_gene_variant
BRCA-UK11594023015940230single base substitutionATupstream_gene_variant
BRCA-UK11595385215953852single base substitutionGAdownstream_gene_variant
BRCA-UK11595385215953852single base substitutionGAintron_variant
BRCA-UK11595385215953852single base substitutionGAupstream_gene_variant
BRCA-UK11596978715969787single base substitutionAGintron_variant
BRCA-US11595696315956963single base substitutionCGdownstream_gene_variant
BRCA-US11595696315956963single base substitutionCGexon_variant
BRCA-US11595696315956963single base substitutionCGmissense_variantL138V412C>G
BRCA-US11597837815978378single base substitutionGT3_prime_UTR_variant
BRCA-US11597837815978378single base substitutionGTdownstream_gene_variant
BRCA-US11597837815978378single base substitutionGTexon_variant
BRCA-US11597837815978378single base substitutionGTmissense_variantA391S1171G>T
BRCA-US11598746415987464single base substitutionTC3_prime_UTR_variant
BRCA-US11598746415987464single base substitutionTCdownstream_gene_variant
BRCA-US11598781815987818single base substitutionCT3_prime_UTR_variant
BRCA-US11598781815987818single base substitutionCTdownstream_gene_variant
BRCA-US11598807915988079single base substitutionTC3_prime_UTR_variant
BRCA-US11598807915988079single base substitutionTCdownstream_gene_variant
BTCA-JP11594440115944401deletion of <=200bpG-intron_variant
BTCA-JP11598645615986457deletion of <=200bpCT-3_prime_UTR_variant
BTCA-JP11598645615986457deletion of <=200bpCT-downstream_gene_variant
BTCA-JP11598688515986885single base substitutionAG3_prime_UTR_variant
BTCA-JP11598688515986885single base substitutionAGdownstream_gene_variant
BTCA-JP11598747115987471single base substitutionGA3_prime_UTR_variant
BTCA-JP11598747115987471single base substitutionGAdownstream_gene_variant
BTCA-JP11598815815988158single base substitutionGC3_prime_UTR_variant
BTCA-JP11598815815988158single base substitutionGCdownstream_gene_variant
CESC-US11595993315959933single base substitutionGTsplice_acceptor_variant
CESC-US11597827015978270single base substitutionGA3_prime_UTR_variant
CESC-US11597827015978270single base substitutionGAdownstream_gene_variant
CESC-US11597827015978270single base substitutionGAmissense_variantE355K1063G>A
CESC-US11597827015978270single base substitutionGAupstream_gene_variant
CESC-US11597834715978347single base substitutionCT3_prime_UTR_variant
CESC-US11597834715978347single base substitutionCTdownstream_gene_variant
CESC-US11597834715978347single base substitutionCTexon_variant
CESC-US11597834715978347single base substitutionCTsynonymous_variantD380D1140C>T
CLLE-ES11594393115943931single base substitutionCTupstream_gene_variant
CLLE-ES11594885915948859single base substitutionGAintron_variant
CLLE-ES11595782515957825single base substitutionGAdownstream_gene_variant
CLLE-ES11595782515957825single base substitutionGAintron_variant
CLLE-ES11595934615959346single base substitutionTGintron_variant
CLLE-ES11596452415964524single base substitutionAGdownstream_gene_variant
CLLE-ES11596452415964524single base substitutionAGintron_variant
CLLE-ES11599157515991575single base substitutionGA3_prime_UTR_variant
CLLE-ES11599157515991575single base substitutionGAdownstream_gene_variant
CLLE-ES11599791515997915single base substitutionGAdownstream_gene_variant
COAD-US11595687415956874single base substitutionGAdownstream_gene_variant
COAD-US11595687415956874single base substitutionGAexon_variant
COAD-US11595687415956874single base substitutionGAmissense_variantR108Q323G>A
COAD-US11595687415956874single base substitutionGAupstream_gene_variant
COAD-US11595997715959977single base substitutionCTexon_variant
COAD-US11595997715959977single base substitutionCTsynonymous_variantA183A549C>T
COAD-US11598654715986547single base substitutionTC3_prime_UTR_variant
COAD-US11598654715986547single base substitutionTCdownstream_gene_variant
COAD-US11598686815986868single base substitutionGA3_prime_UTR_variant
COAD-US11598686815986868single base substitutionGAdownstream_gene_variant
COAD-US11598749815987498single base substitutionAT3_prime_UTR_variant
COAD-US11598749815987498single base substitutionATdownstream_gene_variant
COCA-CN11595324915953249single base substitutionGAexon_variant
COCA-CN11595324915953249single base substitutionGAmissense_variantR75Q224G>A
COCA-CN11595324915953249single base substitutionGAupstream_gene_variant
COCA-CN11595997215959972single base substitutionCTexon_variant
COCA-CN11595997215959972single base substitutionCTstop_gainedR182*544C>T
COCA-CN11596049515960495single base substitutionCTexon_variant
COCA-CN11596049515960495single base substitutionCTintron_variant
COCA-CN11596633115966331single base substitutionCTintron_variant
COCA-CN11598645515986455single base substitutionGA3_prime_UTR_variant
COCA-CN11598645515986455single base substitutionGAdownstream_gene_variant
COCA-CN11598726215987262single base substitutionTG3_prime_UTR_variant
COCA-CN11598726215987262single base substitutionTGdownstream_gene_variant
COCA-CN11598726315987263single base substitutionTG3_prime_UTR_variant
COCA-CN11598726315987263single base substitutionTGdownstream_gene_variant
COCA-CN11598819015988190single base substitutionCT3_prime_UTR_variant
COCA-CN11598819015988190single base substitutionCTdownstream_gene_variant
EOPC-DE11596768715967687single base substitutionCTintron_variant
EOPC-DE11597032715970327single base substitutionGAintron_variant
ESAD-UK11594086915940869single base substitutionTAupstream_gene_variant
ESAD-UK11594087015940870single base substitutionGAupstream_gene_variant
ESAD-UK11594511115945111single base substitutionAGintron_variant
ESAD-UK11595005315950053insertion of <=200bp-TTAintron_variant
ESAD-UK11595311215953112single base substitutionGAintron_variant
ESAD-UK11595311215953112single base substitutionGAupstream_gene_variant
ESAD-UK11595402615954026single base substitutionGAdownstream_gene_variant
ESAD-UK11595402615954026single base substitutionGAintron_variant
ESAD-UK11595402615954026single base substitutionGAupstream_gene_variant
ESAD-UK11595651815956518single base substitutionCTdownstream_gene_variant
ESAD-UK11595651815956518single base substitutionCTintron_variant
ESAD-UK11595651815956518single base substitutionCTupstream_gene_variant
ESAD-UK11595660115956601single base substitutionGAdownstream_gene_variant
ESAD-UK11595660115956601single base substitutionGAintron_variant
ESAD-UK11595660115956601single base substitutionGAupstream_gene_variant
ESAD-UK11595762815957628single base substitutionAGdownstream_gene_variant
ESAD-UK11595762815957628single base substitutionAGintron_variant
ESAD-UK11595812015958120single base substitutionTCdownstream_gene_variant
ESAD-UK11595812015958120single base substitutionTCintron_variant
ESAD-UK11596154615961546single base substitutionGAdownstream_gene_variant
ESAD-UK11596154615961546single base substitutionGAintron_variant
ESAD-UK11596363415963634single base substitutionGCdownstream_gene_variant
ESAD-UK11596363415963634single base substitutionGCintron_variant
ESAD-UK11596408315964083single base substitutionGCdownstream_gene_variant
ESAD-UK11596408315964083single base substitutionGCintron_variant
ESAD-UK11596559815965598single base substitutionGAdownstream_gene_variant
ESAD-UK11596559815965598single base substitutionGAintron_variant
ESAD-UK11596572515965725single base substitutionGAdownstream_gene_variant
ESAD-UK11596572515965725single base substitutionGAintron_variant
ESAD-UK11596651615966516single base substitutionAGintron_variant
ESAD-UK11596877015968770single base substitutionCTintron_variant
ESAD-UK11596928015969280single base substitutionGAintron_variant
ESAD-UK11597079715970797single base substitutionAGintron_variant
ESAD-UK11597446715974467single base substitutionATintron_variant
ESAD-UK11597446715974467single base substitutionATupstream_gene_variant
ESAD-UK11597616215976162single base substitutionGAintron_variant
ESAD-UK11597616215976162single base substitutionGAupstream_gene_variant
ESAD-UK11597971615979716single base substitutionTCdownstream_gene_variant
ESAD-UK11597971615979716single base substitutionTCintron_variant
ESAD-UK11598004615980046single base substitutionATdownstream_gene_variant
ESAD-UK11598004615980046single base substitutionATintron_variant
ESAD-UK11598191215981912single base substitutionGCintron_variant
ESAD-UK11598269515982695single base substitutionTAintron_variant
ESAD-UK11599309915993099single base substitutionGA3_prime_UTR_variant
ESAD-UK11599680915996809single base substitutionGCdownstream_gene_variant
ESAD-UK11600010716000107single base substitutionGAdownstream_gene_variant
ESCA-CN11596484215964842single base substitutionGCdownstream_gene_variant
ESCA-CN11596484215964842single base substitutionGCintron_variant
ESCA-CN11596484215964842single base substitutionGCmissense_variantE225Q673G>C
ESCA-CN11598749115987491single base substitutionAT3_prime_UTR_variant
ESCA-CN11598749115987491single base substitutionATdownstream_gene_variant
GACA-CN11595704715957047single base substitutionGAdownstream_gene_variant
GACA-CN11595704715957047single base substitutionGAexon_variant
GACA-CN11595704715957047single base substitutionGAmissense_variantG166R496G>A
GBM-US11597832715978327single base substitutionCA3_prime_UTR_variant
GBM-US11597832715978327single base substitutionCAdownstream_gene_variant
GBM-US11597832715978327single base substitutionCAsynonymous_variantR374R1120C>A
GBM-US11597832715978327single base substitutionCAupstream_gene_variant
KIRC-US11598720615987206deletion of <=200bpT-3_prime_UTR_variant
KIRC-US11598720615987206deletion of <=200bpT-downstream_gene_variant
KIRP-US11595683915956839single base substitutionCTdownstream_gene_variant
KIRP-US11595683915956839single base substitutionCTexon_variant
KIRP-US11595683915956839single base substitutionCTsynonymous_variantF96F288C>T
KIRP-US11595683915956839single base substitutionCTupstream_gene_variant
KIRP-US11595685015956850single base substitutionCAdownstream_gene_variant
KIRP-US11595685015956850single base substitutionCAexon_variant
KIRP-US11595685015956850single base substitutionCAmissense_variantA100D299C>A
KIRP-US11595685015956850single base substitutionCAupstream_gene_variant
KIRP-US11595693315956933single base substitutionTGdownstream_gene_variant
KIRP-US11595693315956933single base substitutionTGexon_variant
KIRP-US11595693315956933single base substitutionTGmissense_variantS128A382T>G
KIRP-US11595702115957021single base substitutionCTdownstream_gene_variant
KIRP-US11595702115957021single base substitutionCTexon_variant
KIRP-US11595702115957021single base substitutionCTmissense_variantP157L470C>T
KIRP-US11598764815987648single base substitutionTC3_prime_UTR_variant
KIRP-US11598764815987648single base substitutionTCdownstream_gene_variant
LAML-KR11594587815945878single base substitutionCTintron_variant
LAML-KR11594605615946056single base substitutionGAintron_variant
LGG-US11595698915956989single base substitutionGAdownstream_gene_variant
LGG-US11595698915956989single base substitutionGAexon_variant
LGG-US11595698915956989single base substitutionGAsynonymous_variantP146P438G>A
LICA-FR11595570715955707single base substitutionCTdownstream_gene_variant
LICA-FR11595570715955707single base substitutionCTintron_variant
LICA-FR11595570715955707single base substitutionCTupstream_gene_variant
LICA-FR11597677015976770single base substitutionAGdownstream_gene_variant
LICA-FR11597677015976770single base substitutionAGintron_variant
LICA-FR11597677015976770single base substitutionAGupstream_gene_variant
LICA-FR11598752515987525single base substitutionGA3_prime_UTR_variant
LICA-FR11598752515987525single base substitutionGAdownstream_gene_variant
LIHC-US11598676415986764single base substitutionCA3_prime_UTR_variant
LIHC-US11598676415986764single base substitutionCAdownstream_gene_variant
LINC-JP11594924915949249single base substitutionGCintron_variant
LINC-JP11595173515951735single base substitutionATintron_variant
LINC-JP11595915815959158single base substitutionGTintron_variant
LINC-JP11596889815968898single base substitutionAGintron_variant
LINC-JP11596932315969323single base substitutionGAintron_variant
LINC-JP11597278815972788single base substitutionAGintron_variant
LINC-JP11597372615973726single base substitutionTGintron_variant
LINC-JP11597372615973726single base substitutionTGupstream_gene_variant
LINC-JP11598701415987014single base substitutionAG3_prime_UTR_variant
LINC-JP11598701415987014single base substitutionAGdownstream_gene_variant
LINC-JP11598756815987568single base substitutionAG3_prime_UTR_variant
LINC-JP11598756815987568single base substitutionAGdownstream_gene_variant
LINC-JP11598774215987742single base substitutionTG3_prime_UTR_variant
LINC-JP11598774215987742single base substitutionTGdownstream_gene_variant
LINC-JP11599215815992158single base substitutionAT3_prime_UTR_variant
LINC-JP11599215815992158single base substitutionATdownstream_gene_variant
LINC-JP11599491915994919single base substitutionAG3_prime_UTR_variant
LIRI-JP11594090315940903single base substitutionGAupstream_gene_variant
LIRI-JP11594096815940968single base substitutionGAupstream_gene_variant
LIRI-JP11594146215941462single base substitutionCGupstream_gene_variant
LIRI-JP11594221715942217single base substitutionCGupstream_gene_variant
LIRI-JP11594284015942840single base substitutionGTupstream_gene_variant
LIRI-JP11594563615945636single base substitutionGAintron_variant
LIRI-JP11594665215946652single base substitutionAGintron_variant
LIRI-JP11594748115947481single base substitutionTCintron_variant
LIRI-JP11595136115951361single base substitutionAGintron_variant
LIRI-JP11595314315953143single base substitutionGAintron_variant
LIRI-JP11595314315953143single base substitutionGAupstream_gene_variant
LIRI-JP11595356215953562single base substitutionAGdownstream_gene_variant
LIRI-JP11595356215953562single base substitutionAGintron_variant
LIRI-JP11595356215953562single base substitutionAGupstream_gene_variant
LIRI-JP11595506215955062single base substitutionTAdownstream_gene_variant
LIRI-JP11595506215955062single base substitutionTAintron_variant
LIRI-JP11595506215955062single base substitutionTAupstream_gene_variant
LIRI-JP11595746515957465single base substitutionACdownstream_gene_variant
LIRI-JP11595746515957465single base substitutionACintron_variant
LIRI-JP11596088915960889single base substitutionAGdownstream_gene_variant
LIRI-JP11596088915960889single base substitutionAGintron_variant
LIRI-JP11596181615961816single base substitutionATdownstream_gene_variant
LIRI-JP11596181615961816single base substitutionATintron_variant
LIRI-JP11596181715961817single base substitutionATdownstream_gene_variant
LIRI-JP11596181715961817single base substitutionATintron_variant
LIRI-JP11596465915964659single base substitutionAGdownstream_gene_variant
LIRI-JP11596465915964659single base substitutionAGintron_variant
LIRI-JP11596509415965094single base substitutionAGdownstream_gene_variant
LIRI-JP11596509415965094single base substitutionAGintron_variant
LIRI-JP11596718515967185single base substitutionTGintron_variant
LIRI-JP11596828815968288single base substitutionAGintron_variant
LIRI-JP11597185015971850single base substitutionGTintron_variant
LIRI-JP11597240215972402single base substitutionTAintron_variant
LIRI-JP11597290115972901single base substitutionGTintron_variant
LIRI-JP11597357915973579single base substitutionAGintron_variant
LIRI-JP11597357915973579single base substitutionAGupstream_gene_variant
LIRI-JP11597403615974036single base substitutionAGintron_variant
LIRI-JP11597403615974036single base substitutionAGupstream_gene_variant
LIRI-JP11597418315974183single base substitutionGAintron_variant
LIRI-JP11597418315974183single base substitutionGAupstream_gene_variant
LIRI-JP11597507515975075single base substitutionACintron_variant
LIRI-JP11597507515975075single base substitutionACupstream_gene_variant
LIRI-JP11597780615977806single base substitutionATdownstream_gene_variant
LIRI-JP11597780615977806single base substitutionATintron_variant
LIRI-JP11597780615977806single base substitutionATupstream_gene_variant
LIRI-JP11597820115978201single base substitutionTAdownstream_gene_variant
LIRI-JP11597820115978201single base substitutionTAmissense_variantC332S994T>A
LIRI-JP11597820115978201single base substitutionTAsplice_region_variant
LIRI-JP11597820115978201single base substitutionTAupstream_gene_variant
LIRI-JP11597944015979440single base substitutionCTdownstream_gene_variant
LIRI-JP11597944015979440single base substitutionCTintron_variant
LIRI-JP11598034715980347single base substitutionTGdownstream_gene_variant
LIRI-JP11598034715980347single base substitutionTGintron_variant
LIRI-JP11598080015980800single base substitutionGTdownstream_gene_variant
LIRI-JP11598080015980800single base substitutionGTintron_variant
LIRI-JP11598110315981103single base substitutionAGdownstream_gene_variant
LIRI-JP11598110315981103single base substitutionAGintron_variant
LIRI-JP11598259815982598single base substitutionAGintron_variant
LIRI-JP11598327515983275single base substitutionAGexon_variant
LIRI-JP11598327515983275single base substitutionAGintron_variant
LIRI-JP11598437515984375single base substitutionTGdownstream_gene_variant
LIRI-JP11598437515984375single base substitutionTGintron_variant
LIRI-JP11598454215984542single base substitutionGCdownstream_gene_variant
LIRI-JP11598454215984542single base substitutionGCintron_variant
LIRI-JP11598588715985887single base substitutionTCdownstream_gene_variant
LIRI-JP11598588715985887single base substitutionTCintron_variant
LIRI-JP11598640215986402single base substitutionCT3_prime_UTR_variant
LIRI-JP11598640215986402single base substitutionCTdownstream_gene_variant
LIRI-JP11598754315987543single base substitutionGT3_prime_UTR_variant
LIRI-JP11598754315987543single base substitutionGTdownstream_gene_variant
LIRI-JP11598770215987702single base substitutionAG3_prime_UTR_variant
LIRI-JP11598770215987702single base substitutionAGdownstream_gene_variant
LIRI-JP11599015915990159single base substitutionAT3_prime_UTR_variant
LIRI-JP11599015915990159single base substitutionATdownstream_gene_variant
LIRI-JP11599703115997031single base substitutionGAdownstream_gene_variant
LIRI-JP11599881015998810single base substitutionCAdownstream_gene_variant
LUSC-KR11594398215943982single base substitutionCGupstream_gene_variant
LUSC-KR11594869015948690single base substitutionCTintron_variant
LUSC-KR11595264615952646single base substitutionAGintron_variant
LUSC-KR11595264615952646single base substitutionAGupstream_gene_variant
LUSC-KR11595994815959948single base substitutionGTexon_variant
LUSC-KR11595994815959948single base substitutionGTmissense_variantV174F520G>T
LUSC-KR11597081315970813single base substitutionCTintron_variant
LUSC-KR11597402515974025single base substitutionGAintron_variant
LUSC-KR11597402515974025single base substitutionGAupstream_gene_variant
LUSC-KR11597429015974290single base substitutionCGintron_variant
LUSC-KR11597429015974290single base substitutionCGupstream_gene_variant
LUSC-KR11597512615975126single base substitutionGTintron_variant
LUSC-KR11597512615975126single base substitutionGTupstream_gene_variant
LUSC-KR11597699915976999single base substitutionGTdownstream_gene_variant
LUSC-KR11597699915976999single base substitutionGTintron_variant
LUSC-KR11597699915976999single base substitutionGTupstream_gene_variant
LUSC-KR11598431315984313single base substitutionCGdownstream_gene_variant
LUSC-KR11598431315984313single base substitutionCGintron_variant
LUSC-KR11598530315985303single base substitutionGCdownstream_gene_variant
LUSC-KR11598530315985303single base substitutionGCintron_variant
LUSC-KR11598717515987175single base substitutionAG3_prime_UTR_variant
LUSC-KR11598717515987175single base substitutionAGdownstream_gene_variant
LUSC-KR11598747315987473single base substitutionTC3_prime_UTR_variant
LUSC-KR11598747315987473single base substitutionTCdownstream_gene_variant
LUSC-KR11598801715988017single base substitutionGA3_prime_UTR_variant
LUSC-KR11598801715988017single base substitutionGAdownstream_gene_variant
LUSC-KR11599371415993714single base substitutionTA3_prime_UTR_variant
LUSC-KR11599484015994840single base substitutionAG3_prime_UTR_variant
LUSC-KR11599869115998691single base substitutionGAdownstream_gene_variant
LUSC-KR11600031316000313single base substitutionCTdownstream_gene_variant
LUSC-US11595682215956822single base substitutionTGdownstream_gene_variant
LUSC-US11595682215956822single base substitutionTGmissense_variantL91V271T>G
LUSC-US11595682215956822single base substitutionTGsplice_region_variant
LUSC-US11595682215956822single base substitutionTGupstream_gene_variant
LUSC-US11595692115956921single base substitutionGCdownstream_gene_variant
LUSC-US11595692115956921single base substitutionGCexon_variant
LUSC-US11595692115956921single base substitutionGCmissense_variantE124Q370G>C
LUSC-US11598658915986589single base substitutionGT3_prime_UTR_variant
LUSC-US11598658915986589single base substitutionGTdownstream_gene_variant
LUSC-US11598728015987280single base substitutionCT3_prime_UTR_variant
LUSC-US11598728015987280single base substitutionCTdownstream_gene_variant
LUSC-US11598790715987907single base substitutionCT3_prime_UTR_variant
LUSC-US11598790715987907single base substitutionCTdownstream_gene_variant
MALY-DE11594014215940142single base substitutionTAupstream_gene_variant
MALY-DE11594116415941164single base substitutionGCupstream_gene_variant
MALY-DE11596564915965649single base substitutionGAdownstream_gene_variant
MALY-DE11596564915965649single base substitutionGAintron_variant
MALY-DE11597811615978116single base substitutionTGdownstream_gene_variant
MALY-DE11597811615978116single base substitutionTGintron_variant
MALY-DE11597811615978116single base substitutionTGupstream_gene_variant
MALY-DE11599365015993650single base substitutionCT3_prime_UTR_variant
MALY-DE11599809615998096single base substitutionAGdownstream_gene_variant
MELA-AU11593919815939198single base substitutionGAupstream_gene_variant
MELA-AU11593994615939946single base substitutionCTupstream_gene_variant
MELA-AU11594014215940142single base substitutionTAupstream_gene_variant
MELA-AU11594016815940168single base substitutionCTupstream_gene_variant
MELA-AU11594028815940288single base substitutionAGupstream_gene_variant
MELA-AU11594038515940385single base substitutionCTupstream_gene_variant
MELA-AU11594044715940447single base substitutionGAupstream_gene_variant
MELA-AU11594058315940583single base substitutionCTupstream_gene_variant
MELA-AU11594078715940787single base substitutionCTupstream_gene_variant
MELA-AU11594095015940950single base substitutionGAupstream_gene_variant
MELA-AU11594105115941051single base substitutionGAupstream_gene_variant
MELA-AU11594166815941668single base substitutionACupstream_gene_variant
MELA-AU11594173515941736multiple base substitution (>=2bp and <=200bp)GGAAupstream_gene_variant
MELA-AU11594238015942380single base substitutionCTupstream_gene_variant
MELA-AU11594370015943700single base substitutionGAupstream_gene_variant
MELA-AU11594370215943702single base substitutionTAupstream_gene_variant
MELA-AU11594378715943787single base substitutionCTupstream_gene_variant
MELA-AU11594627115946271single base substitutionCTintron_variant
MELA-AU11594709315947093single base substitutionCTintron_variant
MELA-AU11594714515947145single base substitutionCGintron_variant
MELA-AU11594795515947955single base substitutionCTintron_variant
MELA-AU11594854715948548multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU11594861315948613single base substitutionGTintron_variant
MELA-AU11595052315950523single base substitutionCTintron_variant
MELA-AU11595115715951157single base substitutionGAintron_variant
MELA-AU11595130715951307single base substitutionAGintron_variant
MELA-AU11595154315951543single base substitutionCTintron_variant
MELA-AU11595171515951715single base substitutionCTintron_variant
MELA-AU11595206715952067single base substitutionCTintron_variant
MELA-AU11595206715952067single base substitutionCTupstream_gene_variant
MELA-AU11595286515952865single base substitutionGAintron_variant
MELA-AU11595286515952865single base substitutionGAupstream_gene_variant
MELA-AU11595287815952878single base substitutionCTintron_variant
MELA-AU11595287815952878single base substitutionCTupstream_gene_variant
MELA-AU11595316615953166single base substitutionCTsplice_region_variant
MELA-AU11595316615953166single base substitutionCTupstream_gene_variant
MELA-AU11595508915955089single base substitutionGAdownstream_gene_variant
MELA-AU11595508915955089single base substitutionGAintron_variant
MELA-AU11595508915955089single base substitutionGAupstream_gene_variant
MELA-AU11595543115955431single base substitutionCTdownstream_gene_variant
MELA-AU11595543115955431single base substitutionCTintron_variant
MELA-AU11595543115955431single base substitutionCTupstream_gene_variant
MELA-AU11595548315955483single base substitutionCTdownstream_gene_variant
MELA-AU11595548315955483single base substitutionCTintron_variant
MELA-AU11595548315955483single base substitutionCTupstream_gene_variant
MELA-AU11595591715955917single base substitutionCTdownstream_gene_variant
MELA-AU11595591715955917single base substitutionCTintron_variant
MELA-AU11595591715955917single base substitutionCTupstream_gene_variant
MELA-AU11595611015956110single base substitutionTGdownstream_gene_variant
MELA-AU11595611015956110single base substitutionTGintron_variant
MELA-AU11595611015956110single base substitutionTGupstream_gene_variant
MELA-AU11595625615956256single base substitutionCTdownstream_gene_variant
MELA-AU11595625615956256single base substitutionCTintron_variant
MELA-AU11595625615956256single base substitutionCTupstream_gene_variant
MELA-AU11595661815956618single base substitutionCTdownstream_gene_variant
MELA-AU11595661815956618single base substitutionCTintron_variant
MELA-AU11595661815956618single base substitutionCTupstream_gene_variant
MELA-AU11595696615956966single base substitutionCTdownstream_gene_variant
MELA-AU11595696615956966single base substitutionCTexon_variant
MELA-AU11595696615956966single base substitutionCTstop_gainedR139*415C>T
MELA-AU11595771215957713multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU11595771215957713multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU11595774815957748single base substitutionTCdownstream_gene_variant
MELA-AU11595774815957748single base substitutionTCintron_variant
MELA-AU11595825815958258single base substitutionCTdownstream_gene_variant
MELA-AU11595825815958258single base substitutionCTintron_variant
MELA-AU11595852315958523single base substitutionAGdownstream_gene_variant
MELA-AU11595852315958523single base substitutionAGintron_variant
MELA-AU11596010815960108single base substitutionCTexon_variant
MELA-AU11596010815960108single base substitutionCTintron_variant
MELA-AU11596114115961141single base substitutionCTdownstream_gene_variant
MELA-AU11596114115961141single base substitutionCTintron_variant
MELA-AU11596190415961904single base substitutionCTdownstream_gene_variant
MELA-AU11596190415961904single base substitutionCTintron_variant
MELA-AU11596193815961938single base substitutionTGdownstream_gene_variant
MELA-AU11596193815961938single base substitutionTGintron_variant
MELA-AU11596211415962114single base substitutionGAdownstream_gene_variant
MELA-AU11596211415962114single base substitutionGAintron_variant
MELA-AU11596214515962145single base substitutionCTdownstream_gene_variant
MELA-AU11596214515962145single base substitutionCTintron_variant
MELA-AU11596215415962154single base substitutionCTdownstream_gene_variant
MELA-AU11596215415962154single base substitutionCTintron_variant
MELA-AU11596248015962480single base substitutionCTdownstream_gene_variant
MELA-AU11596248015962480single base substitutionCTintron_variant
MELA-AU11596281915962819single base substitutionCTdownstream_gene_variant
MELA-AU11596281915962819single base substitutionCTintron_variant
MELA-AU11596353015963530single base substitutionCTdownstream_gene_variant
MELA-AU11596353015963530single base substitutionCTintron_variant
MELA-AU11596353615963536single base substitutionCTdownstream_gene_variant
MELA-AU11596353615963536single base substitutionCTintron_variant
MELA-AU11596365815963659multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU11596365815963659multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU11596371815963718single base substitutionCTdownstream_gene_variant
MELA-AU11596371815963718single base substitutionCTintron_variant
MELA-AU11596487515964875single base substitutionCTdownstream_gene_variant
MELA-AU11596487515964875single base substitutionCTintron_variant
MELA-AU11596487515964875single base substitutionCTmissense_variantL236F706C>T
MELA-AU11596496015964960single base substitutionCTdownstream_gene_variant
MELA-AU11596496015964960single base substitutionCTintron_variant
MELA-AU11596515315965153single base substitutionCTdownstream_gene_variant
MELA-AU11596515315965153single base substitutionCTintron_variant
MELA-AU11596584215965842single base substitutionGAintron_variant
MELA-AU11596615415966154single base substitutionCTintron_variant
MELA-AU11596638615966386single base substitutionCTintron_variant
MELA-AU11596692715966927single base substitutionCTintron_variant
MELA-AU11596706515967065single base substitutionCTintron_variant
MELA-AU11596715315967153single base substitutionTCintron_variant
MELA-AU11596749315967493single base substitutionGAintron_variant
MELA-AU11596825315968253single base substitutionCTintron_variant
MELA-AU11596836215968362single base substitutionAGintron_variant
MELA-AU11596905515969055single base substitutionCTintron_variant
MELA-AU11596934215969342single base substitutionCTintron_variant
MELA-AU11596993015969930single base substitutionCTintron_variant
MELA-AU11597081015970810single base substitutionCTintron_variant
MELA-AU11597103115971031single base substitutionCTintron_variant
MELA-AU11597119115971191single base substitutionCTintron_variant
MELA-AU11597127415971274single base substitutionGAintron_variant
MELA-AU11597150715971507single base substitutionCTintron_variant
MELA-AU11597211115972111single base substitutionCTintron_variant
MELA-AU11597243515972435single base substitutionCTintron_variant
MELA-AU11597251415972515multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU11597272515972725single base substitutionCTintron_variant
MELA-AU11597292915972929single base substitutionCTintron_variant
MELA-AU11597314115973141single base substitutionCTintron_variant
MELA-AU11597354015973540single base substitutionCTintron_variant
MELA-AU11597354015973540single base substitutionCTupstream_gene_variant
MELA-AU11597381815973818deletion of <=200bpT-intron_variant
MELA-AU11597381815973818deletion of <=200bpT-upstream_gene_variant
MELA-AU11597391715973917single base substitutionTGintron_variant
MELA-AU11597391715973917single base substitutionTGupstream_gene_variant
MELA-AU11597470115974701single base substitutionCTintron_variant
MELA-AU11597470115974701single base substitutionCTupstream_gene_variant
MELA-AU11597510615975106single base substitutionCTintron_variant
MELA-AU11597510615975106single base substitutionCTupstream_gene_variant
MELA-AU11597563815975638single base substitutionCTintron_variant
MELA-AU11597563815975638single base substitutionCTupstream_gene_variant
MELA-AU11597582615975826single base substitutionCTintron_variant
MELA-AU11597582615975826single base substitutionCTupstream_gene_variant
MELA-AU11597595415975954single base substitutionCTintron_variant
MELA-AU11597595415975954single base substitutionCTupstream_gene_variant
MELA-AU11597668815976688single base substitutionATdownstream_gene_variant
MELA-AU11597668815976688single base substitutionATintron_variant
MELA-AU11597668815976688single base substitutionATupstream_gene_variant
MELA-AU11597694815976948single base substitutionCTdownstream_gene_variant
MELA-AU11597694815976948single base substitutionCTintron_variant
MELA-AU11597694815976948single base substitutionCTupstream_gene_variant
MELA-AU11597847615978476single base substitutionCTdownstream_gene_variant
MELA-AU11597847615978476single base substitutionCTintron_variant
MELA-AU11597888215978882single base substitutionCTdownstream_gene_variant
MELA-AU11597888215978882single base substitutionCTintron_variant
MELA-AU11597950215979502single base substitutionACdownstream_gene_variant
MELA-AU11597950215979502single base substitutionACintron_variant
MELA-AU11597958415979584single base substitutionGCdownstream_gene_variant
MELA-AU11597958415979584single base substitutionGCintron_variant
MELA-AU11598067215980672single base substitutionCTdownstream_gene_variant
MELA-AU11598067215980672single base substitutionCTintron_variant
MELA-AU11598083915980839single base substitutionTCdownstream_gene_variant
MELA-AU11598083915980839single base substitutionTCintron_variant
MELA-AU11598117115981171single base substitutionAGdownstream_gene_variant
MELA-AU11598117115981171single base substitutionAGintron_variant
MELA-AU11598136215981362single base substitutionGAintron_variant
MELA-AU11598137415981374single base substitutionCTintron_variant
MELA-AU11598175915981759single base substitutionCTintron_variant
MELA-AU11598191215981912single base substitutionGTintron_variant
MELA-AU11598191715981917single base substitutionCTintron_variant
MELA-AU11598249515982495single base substitutionATintron_variant
MELA-AU11598266015982660single base substitutionAGintron_variant
MELA-AU11598270515982705single base substitutionCTintron_variant
MELA-AU11598277515982775single base substitutionCTintron_variant
MELA-AU11598334815983348single base substitutionATexon_variant
MELA-AU11598334815983348single base substitutionATintron_variant
MELA-AU11598448915984489single base substitutionAGdownstream_gene_variant
MELA-AU11598448915984489single base substitutionAGintron_variant
MELA-AU11598504715985047single base substitutionCTdownstream_gene_variant
MELA-AU11598504715985047single base substitutionCTintron_variant
MELA-AU11598537015985370single base substitutionTAdownstream_gene_variant
MELA-AU11598537015985370single base substitutionTAintron_variant
MELA-AU11598545415985455multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU11598545415985455multiple base substitution (>=2bp and <=200bp)CCTTintron_variant
MELA-AU11598590115985901single base substitutionCTdownstream_gene_variant
MELA-AU11598590115985901single base substitutionCTintron_variant
MELA-AU11598630915986309single base substitutionCTdownstream_gene_variant
MELA-AU11598630915986309single base substitutionCTintron_variant
MELA-AU11598704915987049single base substitutionGA3_prime_UTR_variant
MELA-AU11598704915987049single base substitutionGAdownstream_gene_variant
MELA-AU11598799315987993deletion of <=200bpC-3_prime_UTR_variant
MELA-AU11598799315987993deletion of <=200bpC-downstream_gene_variant
MELA-AU11598916015989160single base substitutionCT3_prime_UTR_variant
MELA-AU11598916015989160single base substitutionCTdownstream_gene_variant
MELA-AU11598924015989241multiple base substitution (>=2bp and <=200bp)CCTT3_prime_UTR_variant
MELA-AU11598924015989241multiple base substitution (>=2bp and <=200bp)CCTTdownstream_gene_variant
MELA-AU11599023015990230single base substitutionTC3_prime_UTR_variant
MELA-AU11599023015990230single base substitutionTCdownstream_gene_variant
MELA-AU11599046315990463single base substitutionTC3_prime_UTR_variant
MELA-AU11599046315990463single base substitutionTCdownstream_gene_variant
MELA-AU11599056115990561single base substitutionCT3_prime_UTR_variant
MELA-AU11599056115990561single base substitutionCTdownstream_gene_variant
MELA-AU11599070015990700single base substitutionCT3_prime_UTR_variant
MELA-AU11599070015990700single base substitutionCTdownstream_gene_variant
MELA-AU11599103515991035single base substitutionCT3_prime_UTR_variant
MELA-AU11599103515991035single base substitutionCTdownstream_gene_variant
MELA-AU11599148215991482single base substitutionCT3_prime_UTR_variant
MELA-AU11599148215991482single base substitutionCTdownstream_gene_variant
MELA-AU11599251715992517single base substitutionCT3_prime_UTR_variant
MELA-AU11599251715992517single base substitutionCTdownstream_gene_variant
MELA-AU11599337415993374single base substitutionGA3_prime_UTR_variant
MELA-AU11599341415993414single base substitutionTA3_prime_UTR_variant
MELA-AU11599361615993616single base substitutionCT3_prime_UTR_variant
MELA-AU11599419115994191deletion of <=200bpT-3_prime_UTR_variant
MELA-AU11599449815994498single base substitutionCT3_prime_UTR_variant
MELA-AU11599474615994746single base substitutionGA3_prime_UTR_variant
MELA-AU11599649815996498single base substitutionCTdownstream_gene_variant
MELA-AU11599650815996508single base substitutionCTdownstream_gene_variant
MELA-AU11599714615997146single base substitutionCTdownstream_gene_variant
MELA-AU11599724215997242single base substitutionGAdownstream_gene_variant
MELA-AU11599777015997770single base substitutionCTdownstream_gene_variant
MELA-AU11599856915998569single base substitutionGAdownstream_gene_variant
MELA-AU11599876215998762single base substitutionACdownstream_gene_variant
MELA-AU11599906215999062single base substitutionCTdownstream_gene_variant
MELA-AU11599910515999105single base substitutionGAdownstream_gene_variant
MELA-AU11599940115999401single base substitutionCTdownstream_gene_variant
MELA-AU11599946915999469single base substitutionCTdownstream_gene_variant
MELA-AU11599966915999669single base substitutionTAdownstream_gene_variant
MELA-AU11599977715999777single base substitutionCTdownstream_gene_variant
MELA-AU11600045416000454single base substitutionCTdownstream_gene_variant
MELA-AU11600053616000536single base substitutionCTdownstream_gene_variant
ORCA-IN11593920715939207single base substitutionTCupstream_gene_variant
ORCA-IN11594799615947996single base substitutionCTintron_variant
ORCA-IN11595623915956239deletion of <=200bpC-downstream_gene_variant
ORCA-IN11595623915956239deletion of <=200bpC-intron_variant
ORCA-IN11595623915956239deletion of <=200bpC-upstream_gene_variant
ORCA-IN11595687915956879single base substitutionCAdownstream_gene_variant
ORCA-IN11595687915956879single base substitutionCAexon_variant
ORCA-IN11595687915956879single base substitutionCAmissense_variantR110S328C>A
ORCA-IN11595687915956879single base substitutionCAupstream_gene_variant
ORCA-IN11595999515959995single base substitutionGTexon_variant
ORCA-IN11595999515959995single base substitutionGTmissense_variantR189S567G>T
ORCA-IN11596121815961218single base substitutionGAdownstream_gene_variant
ORCA-IN11596121815961218single base substitutionGAintron_variant
ORCA-IN11599537415995374single base substitutionCG3_prime_UTR_variant
ORCA-IN11599990215999902single base substitutionCTdownstream_gene_variant
OV-AU11593964015939640single base substitutionAGupstream_gene_variant
OV-AU11594091715940917single base substitutionCGupstream_gene_variant
OV-AU11594100515941005single base substitutionCAupstream_gene_variant
OV-AU11594723815947238single base substitutionTGintron_variant
OV-AU11594803315948033single base substitutionCTintron_variant
OV-AU11595107315951073single base substitutionCTintron_variant
OV-AU11595198515951985single base substitutionCTintron_variant
OV-AU11595198515951985single base substitutionCTupstream_gene_variant
OV-AU11595581215955812single base substitutionCTdownstream_gene_variant
OV-AU11595581215955812single base substitutionCTintron_variant
OV-AU11595581215955812single base substitutionCTupstream_gene_variant
OV-AU11596211015962110single base substitutionGCdownstream_gene_variant
OV-AU11596211015962110single base substitutionGCintron_variant
OV-AU11597446815974468single base substitutionTAintron_variant
OV-AU11597446815974468single base substitutionTAupstream_gene_variant
OV-AU11597951815979518single base substitutionCTdownstream_gene_variant
OV-AU11597951815979518single base substitutionCTintron_variant
OV-AU11598235015982350single base substitutionGAintron_variant
OV-AU11598927115989271single base substitutionCT3_prime_UTR_variant
OV-AU11598927115989271single base substitutionCTdownstream_gene_variant
OV-AU11599720715997207single base substitutionACdownstream_gene_variant
OV-AU11599959215999592single base substitutionGTdownstream_gene_variant
OV-US11598657715986577single base substitutionCG3_prime_UTR_variant
OV-US11598657715986577single base substitutionCGdownstream_gene_variant
PACA-AU11593948515939485single base substitutionGAupstream_gene_variant
PACA-AU11594275515942755single base substitutionCTupstream_gene_variant
PACA-AU11594846415948464single base substitutionAGintron_variant
PACA-AU11595357715953577single base substitutionTCdownstream_gene_variant
PACA-AU11595357715953577single base substitutionTCintron_variant
PACA-AU11595357715953577single base substitutionTCupstream_gene_variant
PACA-AU11597012315970123single base substitutionGT3_prime_UTR_variant
PACA-AU11597012315970123single base substitutionGTmissense_variantK289N867G>T
PACA-AU11597433115974331single base substitutionCTintron_variant
PACA-AU11597433115974331single base substitutionCTupstream_gene_variant
PACA-AU11597717315977173single base substitutionAGdownstream_gene_variant
PACA-AU11597717315977173single base substitutionAGintron_variant
PACA-AU11597717315977173single base substitutionAGupstream_gene_variant
PACA-AU11597717415977174single base substitutionGAdownstream_gene_variant
PACA-AU11597717415977174single base substitutionGAintron_variant
PACA-AU11597717415977174single base substitutionGAupstream_gene_variant
PACA-AU11598163315981633single base substitutionGTintron_variant
PACA-AU11598175115981751single base substitutionTCintron_variant
PACA-AU11598641315986413single base substitutionCT3_prime_UTR_variant
PACA-AU11598641315986413single base substitutionCTdownstream_gene_variant
PACA-AU11598863015988630single base substitutionTC3_prime_UTR_variant
PACA-AU11598863015988630single base substitutionTCdownstream_gene_variant
PACA-AU11599371415993714single base substitutionTA3_prime_UTR_variant
PACA-AU11600035916000359single base substitutionGAdownstream_gene_variant
PACA-CA11595513515955135single base substitutionGTdownstream_gene_variant
PACA-CA11595513515955135single base substitutionGTintron_variant
PACA-CA11595513515955135single base substitutionGTupstream_gene_variant
PACA-CA11595742415957424single base substitutionCTdownstream_gene_variant
PACA-CA11595742415957424single base substitutionCTintron_variant
PACA-CA11596471415964714single base substitutionACdownstream_gene_variant
PACA-CA11596471415964714single base substitutionACintron_variant
PACA-CA11597030815970308single base substitutionGCintron_variant
PACA-CA11597056215970562single base substitutionACintron_variant
PACA-CA11597382715973827single base substitutionGCintron_variant
PACA-CA11597382715973827single base substitutionGCupstream_gene_variant
PACA-CA11597445915974459insertion of <=200bp-Aintron_variant
PACA-CA11597445915974459insertion of <=200bp-Aupstream_gene_variant
PACA-CA11597633915976339deletion of <=200bpT-downstream_gene_variant
PACA-CA11597633915976339deletion of <=200bpT-intron_variant
PACA-CA11597633915976339deletion of <=200bpT-upstream_gene_variant
PACA-CA11597787815977878single base substitutionAGdownstream_gene_variant
PACA-CA11597787815977878single base substitutionAGintron_variant
PACA-CA11597787815977878single base substitutionAGupstream_gene_variant
PACA-CA11597941615979416single base substitutionCTdownstream_gene_variant
PACA-CA11597941615979416single base substitutionCTintron_variant
PACA-CA11598243015982430deletion of <=200bpA-intron_variant
PACA-CA11598369515983695single base substitutionCAdownstream_gene_variant
PACA-CA11598369515983695single base substitutionCAintron_variant
PACA-CA11598546215985462single base substitutionTGdownstream_gene_variant
PACA-CA11598546215985462single base substitutionTGintron_variant
PACA-CA11598789615987899deletion of <=200bpTAAG-3_prime_UTR_variant
PACA-CA11598789615987899deletion of <=200bpTAAG-downstream_gene_variant
PACA-CA11599112515991125single base substitutionCT3_prime_UTR_variant
PACA-CA11599112515991125single base substitutionCTdownstream_gene_variant
PACA-CA11599371415993714single base substitutionTA3_prime_UTR_variant
PAEN-IT11594629115946291single base substitutionCGintron_variant
PAEN-IT11595600715956007single base substitutionACdownstream_gene_variant
PAEN-IT11595600715956007single base substitutionACintron_variant
PAEN-IT11595600715956007single base substitutionACupstream_gene_variant
PBCA-DE11594424115944241single base substitutionGCexon_variant
PBCA-DE11594424115944241single base substitutionGCmissense_variantE26Q76G>C
PBCA-DE11595005315950055deletion of <=200bpTTA-intron_variant
PBCA-DE11595289915952899single base substitutionGAintron_variant
PBCA-DE11595289915952899single base substitutionGAupstream_gene_variant
PBCA-DE11595727815957278single base substitutionTGdownstream_gene_variant
PBCA-DE11595727815957278single base substitutionTGintron_variant
PBCA-DE11596592415965924single base substitutionGTintron_variant
PBCA-DE11597006915970069single base substitutionGT3_prime_UTR_variant
PBCA-DE11597006915970069single base substitutionGTmissense_variantM271I813G>T
PBCA-DE11600020516000205insertion of <=200bp-Tdownstream_gene_variant
PRAD-UK11596018015960180single base substitutionAGexon_variant
PRAD-UK11596018015960180single base substitutionAGintron_variant
PRAD-UK11598093815980938single base substitutionGAdownstream_gene_variant
PRAD-UK11598093815980938single base substitutionGAintron_variant
PRAD-UK11598202915982029single base substitutionCTintron_variant
PRAD-UK11598383715983837single base substitutionAGdownstream_gene_variant
PRAD-UK11598383715983837single base substitutionAGintron_variant
PRAD-UK11598827715988277single base substitutionAG3_prime_UTR_variant
PRAD-UK11598827715988277single base substitutionAGdownstream_gene_variant
PRAD-UK11599968115999681deletion of <=200bpT-downstream_gene_variant
PRAD-US11598765715987657single base substitutionAG3_prime_UTR_variant
PRAD-US11598765715987657single base substitutionAGdownstream_gene_variant
READ-US11598728415987284single base substitutionTC3_prime_UTR_variant
READ-US11598728415987284single base substitutionTCdownstream_gene_variant
RECA-EU11594898815948988single base substitutionGCintron_variant
RECA-EU11595203515952035single base substitutionTCintron_variant
RECA-EU11595203515952035single base substitutionTCupstream_gene_variant
RECA-EU11596522215965222single base substitutionGCdownstream_gene_variant
RECA-EU11596522215965222single base substitutionGCintron_variant
RECA-EU11597158415971584single base substitutionCTintron_variant
RECA-EU11598126815981268single base substitutionCAdownstream_gene_variant
RECA-EU11598126815981268single base substitutionCAintron_variant
RECA-EU11598291415982914single base substitutionAGintron_variant
RECA-EU11598291415982914single base substitutionAGsplice_acceptor_variant
RECA-EU11599163715991637single base substitutionAC3_prime_UTR_variant
RECA-EU11599163715991637single base substitutionACdownstream_gene_variant
RECA-EU11599776215997762single base substitutionTCdownstream_gene_variant
SKCA-BR11593919115939191single base substitutionAGupstream_gene_variant
SKCA-BR11594038615940386insertion of <=200bp-CTupstream_gene_variant
SKCA-BR11594068815940700deletion of <=200bpCTTTTTTTTTTTT-upstream_gene_variant
SKCA-BR11594412515944125single base substitutionAG5_prime_UTR_variant
SKCA-BR11594412515944125single base substitutionAGexon_variant
SKCA-BR11594665815946658single base substitutionGTintron_variant
SKCA-BR11594692215946922insertion of <=200bp-TCintron_variant
SKCA-BR11594877815948778single base substitutionCTintron_variant
SKCA-BR11594977215949772single base substitutionCTintron_variant
SKCA-BR11594988215949882single base substitutionCTintron_variant
SKCA-BR11595276415952764single base substitutionATintron_variant
SKCA-BR11595276415952764single base substitutionATupstream_gene_variant
SKCA-BR11595552615955526single base substitutionGAdownstream_gene_variant
SKCA-BR11595552615955526single base substitutionGAintron_variant
SKCA-BR11595552615955526single base substitutionGAupstream_gene_variant
SKCA-BR11595622115956222deletion of <=200bpAT-downstream_gene_variant
SKCA-BR11595622115956222deletion of <=200bpAT-intron_variant
SKCA-BR11595622115956222deletion of <=200bpAT-upstream_gene_variant
SKCA-BR11595758415957584single base substitutionTCdownstream_gene_variant
SKCA-BR11595758415957584single base substitutionTCintron_variant
SKCA-BR11596098015960980single base substitutionAGdownstream_gene_variant
SKCA-BR11596098015960980single base substitutionAGintron_variant
SKCA-BR11596392515963925single base substitutionCTdownstream_gene_variant
SKCA-BR11596392515963925single base substitutionCTintron_variant
SKCA-BR11596845015968453deletion of <=200bpCAAA-intron_variant
SKCA-BR11597096915970969single base substitutionCTintron_variant
SKCA-BR11597108215971082single base substitutionGTintron_variant
SKCA-BR11597147515971475single base substitutionCTintron_variant
SKCA-BR11597229215972292single base substitutionGAintron_variant
SKCA-BR11597236215972362insertion of <=200bp-CAintron_variant
SKCA-BR11597314615973146single base substitutionCTintron_variant
SKCA-BR11597532915975329insertion of <=200bp-CAAintron_variant
SKCA-BR11597532915975329insertion of <=200bp-CAAupstream_gene_variant
SKCA-BR11597563015975630single base substitutionGCintron_variant
SKCA-BR11597563015975630single base substitutionGCupstream_gene_variant
SKCA-BR11597624415976244single base substitutionCT3_prime_UTR_variant
SKCA-BR11597624415976244single base substitutionCTmissense_variantP307S919C>T
SKCA-BR11597624415976244single base substitutionCTupstream_gene_variant
SKCA-BR11597894115978945deletion of <=200bpCGGAG-downstream_gene_variant
SKCA-BR11597894115978945deletion of <=200bpCGGAG-intron_variant
SKCA-BR11597895915978959single base substitutionGAdownstream_gene_variant
SKCA-BR11597895915978959single base substitutionGAintron_variant
SKCA-BR11598115215981153deletion of <=200bpCA-downstream_gene_variant
SKCA-BR11598115215981153deletion of <=200bpCA-intron_variant
SKCA-BR11598144715981447single base substitutionCTintron_variant
SKCA-BR11598581615985816single base substitutionTAdownstream_gene_variant
SKCA-BR11598581615985816single base substitutionTAintron_variant
SKCA-BR11598602015986020single base substitutionTAdownstream_gene_variant
SKCA-BR11598602015986020single base substitutionTAintron_variant
SKCA-BR11598641515986415single base substitutionGA3_prime_UTR_variant
SKCA-BR11598641515986415single base substitutionGAdownstream_gene_variant
SKCA-BR11598641615986416single base substitutionGA3_prime_UTR_variant
SKCA-BR11598641615986416single base substitutionGAdownstream_gene_variant
SKCA-BR11598771915987719single base substitutionCT3_prime_UTR_variant
SKCA-BR11598771915987719single base substitutionCTdownstream_gene_variant
SKCA-BR11599092915990930deletion of <=200bpCA-3_prime_UTR_variant
SKCA-BR11599092915990930deletion of <=200bpCA-downstream_gene_variant
SKCA-BR11599287115992871single base substitutionCT3_prime_UTR_variant
SKCA-BR11599479915994799single base substitutionCT3_prime_UTR_variant
SKCA-BR11599487615994877deletion of <=200bpAT-3_prime_UTR_variant
SKCA-BR11599895715998957single base substitutionGAdownstream_gene_variant
SKCM-US11595325515953255single base substitutionATexon_variant
SKCM-US11595325515953255single base substitutionATmissense_variantK77M230A>T
SKCM-US11595325515953255single base substitutionATupstream_gene_variant
SKCM-US11596001815960018single base substitutionCTexon_variant
SKCM-US11596001815960018single base substitutionCTmissense_variantP197L590C>T
SKCM-US11596004715960047single base substitutionGAexon_variant
SKCM-US11596004715960047single base substitutionGAmissense_variantE207K619G>A
SKCM-US11597626315976263single base substitutionTG3_prime_UTR_variant
SKCM-US11597626315976263single base substitutionTGmissense_variantL313R938T>G
SKCM-US11597626315976263single base substitutionTGupstream_gene_variant
SKCM-US11597820515978205single base substitutionCT3_prime_UTR_variant
SKCM-US11597820515978205single base substitutionCTdownstream_gene_variant
SKCM-US11597820515978205single base substitutionCTmissense_variantS333F998C>T
SKCM-US11597820515978205single base substitutionCTupstream_gene_variant
SKCM-US11597820615978206single base substitutionCT3_prime_UTR_variant
SKCM-US11597820615978206single base substitutionCTdownstream_gene_variant
SKCM-US11597820615978206single base substitutionCTsynonymous_variantS333S999C>T
SKCM-US11597820615978206single base substitutionCTupstream_gene_variant
SKCM-US11597836615978366single base substitutionCT3_prime_UTR_variant
SKCM-US11597836615978366single base substitutionCTdownstream_gene_variant
SKCM-US11597836615978366single base substitutionCTexon_variant
SKCM-US11597836615978366single base substitutionCTmissense_variantL387F1159C>T
SKCM-US11598743115987431single base substitutionGA3_prime_UTR_variant
SKCM-US11598743115987431single base substitutionGAdownstream_gene_variant
SKCM-US11598749215987492single base substitutionGA3_prime_UTR_variant
SKCM-US11598749215987492single base substitutionGAdownstream_gene_variant
SKCM-US11598802415988024single base substitutionAG3_prime_UTR_variant
SKCM-US11598802415988024single base substitutionAGdownstream_gene_variant
STAD-US11596491415964914single base substitutionGAdownstream_gene_variant
STAD-US11596491415964914single base substitutionGAintron_variant
STAD-US11596491415964914single base substitutionGAmissense_variantA249T745G>A
STAD-US11598651815986518single base substitutionCT3_prime_UTR_variant
STAD-US11598651815986518single base substitutionCTdownstream_gene_variant
STAD-US11598690915986909single base substitutionAG3_prime_UTR_variant
STAD-US11598690915986909single base substitutionAGdownstream_gene_variant
STAD-US11598734615987346single base substitutionAG3_prime_UTR_variant
STAD-US11598734615987346single base substitutionAGdownstream_gene_variant
STAD-US11598741315987413single base substitutionGA3_prime_UTR_variant
STAD-US11598741315987413single base substitutionGAdownstream_gene_variant
THCA-SA11595700715957007single base substitutionGAdownstream_gene_variant
THCA-SA11595700715957007single base substitutionGAexon_variant
THCA-SA11595700715957007single base substitutionGAsynonymous_variantL152L456G>A
UCEC-US11595324815953248single base substitutionCTexon_variant
UCEC-US11595324815953248single base substitutionCTstop_gainedR75*223C>T
UCEC-US11595324815953248single base substitutionCTupstream_gene_variant
UCEC-US11595690315956903single base substitutionTGdownstream_gene_variant
UCEC-US11595690315956903single base substitutionTGexon_variant
UCEC-US11595690315956903single base substitutionTGmissense_variantS118A352T>G
UCEC-US11595690315956903single base substitutionTGupstream_gene_variant
UCEC-US11595701415957014single base substitutionCTdownstream_gene_variant
UCEC-US11595701415957014single base substitutionCTexon_variant
UCEC-US11595701415957014single base substitutionCTmissense_variantR155C463C>T
UCEC-US11596487815964878single base substitutionTCdownstream_gene_variant
UCEC-US11596487815964878single base substitutionTCintron_variant
UCEC-US11596487815964878single base substitutionTCmissense_variantY237H709T>C
UCEC-US11597626715976267single base substitutionGC3_prime_UTR_variant
UCEC-US11597626715976267single base substitutionGCmissense_variantE314D942G>C
UCEC-US11597626715976267single base substitutionGCupstream_gene_variant
UCEC-US11598691115986911single base substitutionCT3_prime_UTR_variant
UCEC-US11598691115986911single base substitutionCTdownstream_gene_variant
UCEC-US11598815015988150single base substitutionGA3_prime_UTR_variant
UCEC-US11598815015988150single base substitutionGAdownstream_gene_variant
Mutation - COSMIC
Sample NameMutation IDMutation CDSMutation AAMutation DescriptionMutation Genome PositionMutation Strand
ICGC_0034COSM218341c.867G>Tp.K289NSubstitution - Missense1:15643628-15643628+
GC9_TCOSM146415c.496G>Ap.G166RSubstitution - Missense1:15630552-15630552+
8057513COSM218341c.867G>Tp.K289NSubstitution - Missense1:15643628-15643628+
TCGA-AP-A0LD-01COSM898046c.709T>Cp.Y237HSubstitution - Missense1:15638383-15638383+
H650COSM1194696c.328C>Tp.R110CSubstitution - Missense1:15630384-15630384+
TCGA-A4-7288-01COSM3984375c.470C>Tp.P157LSubstitution - Missense1:15630526-15630526+
RK304_C01COSM4779066c.994T>Ap.C332SSubstitution - Missense1:15651706-15651706+
Sample_1COSM3750496c.549C>Tp.A183ASubstitution - coding silent1:15633482-15633482+
TCGA-AM-5820-01COSM3750496c.549C>Tp.A183ASubstitution - coding silent1:15633482-15633482+
TCGA-DK-A3IL-01COSM1295320c.1060C>Gp.P354ASubstitution - Missense1:15651772-15651772+
TCGA-EE-A3J7-06COSM3863224c.590C>Tp.P197LSubstitution - Missense1:15633523-15633523+
TCGA-A5-A0GW-01COSM898056c.830G>Ap.R277QSubstitution - Missense1:15643591-15643591+
PTC_177COSM5959136c.456G>Ap.L152LSubstitution - coding silent1:15630512-15630512+
TCGA-BR-8680-01COSM4023980c.745G>Ap.A249TSubstitution - Missense1:15638419-15638419+
LPJ041COSM1316009c.815G>Tp.R272ISubstitution - Missense1:15643576-15643576+
TCGA-56-5897-01COSM675951c.370G>Cp.E124QSubstitution - Missense1:15630426-15630426+
OSCC-GB_00940111COSM4891531c.328C>Ap.R110SSubstitution - Missense1:15630384-15630384+
TCGA-FD-A3SN-01COSM3788910c.506-1G>Cp.?Unknown1:15633438-15633438+
TCGA-IZ-8196-01COSM3984373c.288C>Tp.F96FSubstitution - coding silent1:15630344-15630344+
8057501COSM218341c.867G>Tp.K289NSubstitution - Missense1:15643628-15643628+
OSCC-GB_00210111COSM3710361c.567G>Tp.R189SSubstitution - Missense1:15633500-15633500+
ATL059COSM898045c.463C>Tp.R155CSubstitution - Missense1:15630519-15630519+
S00943COSM310502c.493A>Tp.S165CSubstitution - Missense1:15630549-15630549+
H358COSM1194152c.1000A>Tp.I334FSubstitution - Missense1:15651712-15651712+
TCGA-D3-A5GO-06COSM3476596c.998C>Tp.S333FSubstitution - Missense1:15651710-15651710+
PT37COSM5917130c.940G>Ap.E314KSubstitution - Missense1:15649770-15649770+
TCGA-FD-A3SN-01COSM3788911c.1162C>Gp.Q388ESubstitution - Missense1:15651874-15651874+
LUAD-CHTN-Z4716ACOSM361344c.1050C>Tp.T350TSubstitution - coding silent1:15651762-15651762+
CSCC-29-TCOSM4456258c.1002C>Tp.I334ISubstitution - coding silent1:15651714-15651714+
MO_1215COSM5552949c.530A>Gp.E177GSubstitution - Missense1:15633463-15633463+
TCGA-22-5482-01COSM675952c.271T>Gp.L91VSubstitution - Missense1:15630327-15630327+
YURUSCOSM1687040c.1195C>Tp.P399SSubstitution - Missense1:15656628-15656628+
YULADCOSM5378113c.1120C>Tp.R374WSubstitution - Missense1:15651832-15651832+
TCGA-A5-A0GP-01COSM898044c.352T>Gp.S118ASubstitution - Missense1:15630408-15630408+
Pat_59_ACOSM5844134c.211G>Ap.V71ISubstitution - Missense1:15626741-15626741+
TCGA-DK-A1AC-01COSM1295317c.388C>Tp.Q130*Substitution - Nonsense1:15630444-15630444+
TCGA-D1-A17Q-01COSM898058c.942G>Cp.E314DSubstitution - Missense1:15649772-15649772+
21TCOSM3710361c.567G>Tp.R189SSubstitution - Missense1:15633500-15633500+
ICGC_MB126COSM302034c.76G>Cp.E26QSubstitution - Missense1:15617746-15617746+
TCGA-FW-A3R5-06COSM3863232c.999C>Tp.S333SSubstitution - coding silent1:15651711-15651711+
TCGA-D9-A6EC-06COSM4401703c.938T>Gp.L313RSubstitution - Missense1:15649768-15649768+
WA42COSM239535c.934A>Gp.I312VSubstitution - Missense1:15649764-15649764+
C086COSM5529625c.40G>Tp.E14*Substitution - Nonsense1:15617710-15617710+
RMS112_COSM4987630c.1181C>Ap.A394ESubstitution - Missense1:15651893-15651893+
DLD1COSM4622193c.495T>Cp.S165SSubstitution - coding silent1:15630551-15630551+
587342COSM1203200c.800G>Tp.R267MSubstitution - Missense1:15643561-15643561+
TCGA-29-2434-01COSM1319831c.466A>Tp.N156YSubstitution - Missense1:15630522-15630522+
T55COSM4676697c.912delTp.L306fs*31Deletion - Frameshift1:15649742-15649742+
8014753COSM218341c.867G>Tp.K289NSubstitution - Missense1:15643628-15643628+
YUSCACOSM5378110c.932C>Tp.S311FSubstitution - Missense1:15649762-15649762+
TCGA-D3-A3ML-06COSM3476559c.230A>Tp.K77MSubstitution - Missense1:15626760-15626760+
T3225COSM3965938c.438G>Ap.P146PSubstitution - coding silent1:15630494-15630494+
T3080COSM4676696c.826C>Tp.R276CSubstitution - Missense1:15643587-15643587+
TCGA-GN-A26C-01COSM3476598c.1159C>Tp.L387FSubstitution - Missense1:15651871-15651871+
ICGC_MB15COSM215478c.813G>Tp.M271ISubstitution - Missense1:15643574-15643574+
TCGA-AA-3833-01COSM271200c.661A>Tp.I221LSubstitution - Missense1:15638335-15638335+
TCGA-AZ-4615-01COSM2084672c.323G>Ap.R108QSubstitution - Missense1:15630379-15630379+
TCGA-UC-A7PF-01COSM4830402c.1063G>Ap.E355KSubstitution - Missense1:15651775-15651775+
SJHGG010324COSM4970000c.829C>Tp.R277WSubstitution - Missense1:15643590-15643590+
ESO-610COSM1249864c.680C>Tp.P227LSubstitution - Missense1:15638354-15638354+
LUAD-F00365COSM340532c.765C>Gp.A255ASubstitution - coding silent1:15643526-15643526+
TCGA-19-1790-01COSM3399875c.1120C>Ap.R374RSubstitution - coding silent1:15651832-15651832+
CRC-33TCOSM5479500c.224G>Ap.R75QSubstitution - Missense1:15626754-15626754+
TCGA-ER-A19P-06COSM3476569c.619G>Ap.E207KSubstitution - Missense1:15633552-15633552+
TCGA-C8-A3M8-01COSM3802428c.412C>Gp.L138VSubstitution - Missense1:15630468-15630468+
LUAD-CHTN-Z4716ACOSM361343c.827G>Tp.R276LSubstitution - Missense1:15643588-15643588+
ESCC_BICR_033TCOSM5439671c.673G>Cp.E225QSubstitution - Missense1:15638347-15638347+
TCGA-AO-A0J3-01COSM424289c.1171G>Tp.A391SSubstitution - Missense1:15651883-15651883+
8014573COSM218341c.867G>Tp.K289NSubstitution - Missense1:15643628-15643628+
5COSM529835c.415C>Tp.R139*Substitution - Nonsense1:15630471-15630471+
TCGA-30-1856-01COSM1319832c.170A>Gp.N57SSubstitution - Missense1:15626700-15626700+
TCGA-HE-A5NK-01COSM4908459c.382T>Gp.S128ASubstitution - Missense1:15630438-15630438+
8066081COSM218341c.867G>Tp.K289NSubstitution - Missense1:15643628-15643628+
8066067COSM218341c.867G>Tp.K289NSubstitution - Missense1:15643628-15643628+
TCGA-E1-5322-01COSM3965938c.438G>Ap.P146PSubstitution - coding silent1:15630494-15630494+
B52COSM1745161c.627_632+17del23p.?Unknown1:15633560-15633582+
T55COSM898045c.463C>Tp.R155CSubstitution - Missense1:15630519-15630519+
SNUH_G26_S1COSM3677419c.1124C>Tp.P375LSubstitution - Missense1:15651836-15651836+
MD-319COSM302034c.76G>Cp.E26QSubstitution - Missense1:15617746-15617746+
TCGA-HE-7128-01COSM3984374c.299C>Ap.A100DSubstitution - Missense1:15630355-15630355+
TCGA-DS-A1OA-01COSM4843100c.1140C>Tp.D380DSubstitution - coding silent1:15651852-15651852+
TCGA-AP-A056-01COSM898045c.463C>Tp.R155CSubstitution - Missense1:15630519-15630519+
TCGA-A5-A0VP-01COSM898035c.223C>Tp.R75*Substitution - Nonsense1:15626753-15626753+
TCGA-30-1718-01COSM1319829c.677C>Gp.A226GSubstitution - Missense1:15638351-15638351+
T8COSM3750496c.549C>Tp.A183ASubstitution - coding silent1:15633482-15633482+
YUGASPCOSM1685487c.420_421insAp.M141fs*8Insertion - Frameshift1:15630476-15630477+
YUAKERCOSM1687039c.1060C>Tp.P354SSubstitution - Missense1:15651772-15651772+
STC252COSM5052699c.384T>Cp.S128SSubstitution - coding silent1:15630440-15630440+
12MCOSM3476598c.1159C>Tp.L387FSubstitution - Missense1:15651871-15651871+
LUAD-RT-S01813COSM382958c.367G>Tp.G123*Substitution - Nonsense1:15630423-15630423+
Mutation - CGAP
UNIGENECYTOBANDOMIMSNP
Hs.718796;Hs.718814;Hs.718817;Hs.718822;Hs.718824;Hs.718828;Hs.718832;Hs.718835;Hs.718838;Hs.718842;Hs.718847;Hs.718849;Hs.718850;Hs.7188571p36.21
Mutation - IntOGen
Mutated from(ref)Mutated to(alt)Consequence TypeAA MutationCDS MutationChrPosCancer
AGMissensep.R173Gc.517A>G115959945LUAD
AT3-UTRSNV.c.1197+7034A>T115990159HC
ATMissensep.K77Mc.230A>T115953255CM
ATMissensep.S165Cc.493A>T115957044SCLC
CASynonymousp.R374Rc.1120C>A115978327GBM
CGMissensep.P354Ac.1060C>G115978267BLCA
CTMissensep.A368Vc.1103C>T115978310BRCA
CTMissensep.L387Fc.1159C>T115978366CM
CTMissensep.P197Lc.590C>T115960018CM
CTMissensep.P227Lc.680C>T115964849ESCA
CTMissensep.S120Lc.359C>T115956910HNSC
CTNonsensep.R139*c.415C>T115956966LUAD
CTNonsensep.R75*c.223C>T115953248UCEC
CTSynonymousp.F96Fc.288C>T115956839HNSC
CTSynonymousp.L54Lc.162C>T115953187LUAD
CTSynonymousp.S118Sc.354C>T115956905CM
GAMissensep.E207Kc.619G>A115960047CM
GASynonymousp.Q179Qc.537G>A115959965HNSC
GASynonymousp.Q397Qc.1191G>A115983119HNSC
GCMissensep.E124Qc.370G>C115956921LUSC
GCMissensep.E26Qc.76G>C115944241MB
GTMissensep.A391Sc.1171G>T115978378BRCA
GTMissensep.K289Nc.867G>T115970123PAAD
GTMissensep.M271Ic.813G>T115970069MB
GTSpliceDonorSNV.c.1197+50G>T115983175LUAD
TCMissensep.Y237Hc.709T>C115964878UCEC
TGMissensep.L91Vc.271T>G115956822LUSC
TGMissensep.S118Ac.352T>G115956903UCEC