Primary Site >> Stomach Cancer
Gene >> TNK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333602 |
| Start | 195868467:195868467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367962373 |
| CDS Mutation | c.1786G>A |
| AA Mutation | p.Ala596Thr(p.A596T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333602 |
| Start | 195867243:195867243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2908G>A |
| AA Mutation | p.Val970Met(p.V970M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333602 |
| Start | 195867551:195867551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781238826 |
| CDS Mutation | c.2702C>T |
| AA Mutation | p.Ala901Val(p.A901V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333602 |
| Start | 195886992:195886992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.219G>T |
| AA Mutation | p.Lys73Asn(p.K73N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333602 |
| Start | 195883173:195883173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762213900 |
| CDS Mutation | c.593C>T |
| AA Mutation | p.Thr198Met(p.T198M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333602 |
| Start | 195867413:195867413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2840G>A |
| AA Mutation | p.Gly947Asp(p.G947D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333602 |
| Start | 195868358:195868358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757105764 |
| CDS Mutation | c.1895C>T |
| AA Mutation | p.Pro632Leu(p.P632L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333602 |
| Start | 195868269:195868269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371737738 |
| CDS Mutation | c.1984G>A |
| AA Mutation | p.Gly662Arg(p.G662R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333602 |
| Start | 195868001:195868001(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200430444 |
| CDS Mutation | c.2252G>A |
| AA Mutation | p.Arg751His(p.R751H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333602 |
| Start | 195867772:195867772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752101541 |
| CDS Mutation | c.2481C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000333602 |
| Start | 195879111:195879111(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.952delG |
| AA Mutation | p.Val318Ter(p.V318*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000333602 |
| Start | 195867762:195867762(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2491delC |
| AA Mutation | p.Gln831ArgfsTer2(p.Q831Rfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000333602 |
| Start | 195868358:195868358(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs757698430 |
| CDS Mutation | c.1895delC |
| AA Mutation | p.Pro632ArgfsTer84(p.P632Rfs*84) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |