Primary Site >> Stomach Cancer
Gene >> TNKS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310430 |
| Start | 9763189:9763189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150495385 |
| CDS Mutation | c.3317C>T |
| AA Mutation | p.Thr1106Met(p.T1106M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310430 |
| Start | 9764740:9764740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3397A>G |
| AA Mutation | p.Arg1133Gly(p.R1133G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310430 |
| Start | 9556406:9556406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.467C>T |
| AA Mutation | p.Ala156Val(p.A156V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310430 |
| Start | 9761589:9761589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3227G>A |
| AA Mutation | p.Arg1076His(p.R1076H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000310430 |
| Start | 9764718:9764718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3375G>A |
| AA Mutation | p.Met1125Ile(p.M1125I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000310430 |
| Start | 9735082:9735082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2531C>T |
| AA Mutation | p.Ala844Val(p.A844V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310430 |
| Start | 9748176:9748176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2796G>C |
| AA Mutation | p.Lys932Asn(p.K932N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310430 |
| Start | 9706865:9706865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1324G>A |
| AA Mutation | p.Ala442Thr(p.A442T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310430 |
| Start | 9751784:9751784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3008C>T |
| AA Mutation | p.Ala1003Val(p.A1003V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310430 |
| Start | 9751618:9751618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2842A>G |
| AA Mutation | p.Ile948Val(p.I948V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310430 |
| Start | 9751676:9751676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2900C>A |
| AA Mutation | p.Pro967His(p.P967H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310430 |
| Start | 9706926:9706926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs551035523 |
| CDS Mutation | c.1385C>T |
| AA Mutation | p.Thr462Ile(p.T462I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310430 |
| Start | 9709962:9709962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1586C>T |
| AA Mutation | p.Ala529Val(p.A529V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310430 |
| Start | 9733363:9733363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749980147 |
| CDS Mutation | c.2232T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310430 |
| Start | 9751785:9751785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201607807 |
| CDS Mutation | c.3009C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310430 |
| Start | 9556029:9556029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.90A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310430 |
| Start | 9731009:9731009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2121T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310430 |
| Start | 9776718:9776718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370002383 |
| CDS Mutation | c.3966C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310430 |
| Start | 9764724:9764724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3381T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310430 |
| Start | 9580241:9580241(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759481250 |
| CDS Mutation | c.756G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310430 |
| Start | 9751689:9751689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2913A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310430 |
| Start | 9766381:9766381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747152187 |
| CDS Mutation | c.3696A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310430 |
| Start | 9708430:9708430(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1522delA |
| AA Mutation | p.Thr508HisfsTer33(p.T508Hfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310430 |
| Start | 9710034:9710034(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1664delA |
| AA Mutation | p.Asn555IlefsTer5(p.N555Ifs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000310430 |
| Start | 9766332:9766332(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3650delA |
| AA Mutation | p.Asn1217ThrfsTer38(p.N1217Tfs*38) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000310430 |
| Start | 9704702:9704702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747680650 |
| CDS Mutation | c.1147C>T |
| AA Mutation | p.Arg383Ter(p.R383*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |