Primary Site >> Stomach Cancer
Gene >> TIAL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436547 |
| Start | 119582473:119582473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.214A>G |
| AA Mutation | p.Lys72Glu(p.K72E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436547 |
| Start | 119579988:119579988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.394A>G |
| AA Mutation | p.Met132Val(p.M132V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000436547 |
| Start | 119579987:119579987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.395T>C |
| AA Mutation | p.Met132Thr(p.M132T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000436547 |
| Start | 119575719:119575719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1074A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000436547 |
| Start | 119577149:119577149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778602887 |
| CDS Mutation | c.792G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000436547 |
| Start | 119577117:119577117(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.824delG |
| AA Mutation | p.Gly275ValfsTer7(p.G275Vfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000436547 |
| Start | 119578791:119578791(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.491delG |
| AA Mutation | p.Gly164ValfsTer28(p.G164Vfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000436547 |
| Start | 119577682:119577682(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.611delA |
| AA Mutation | p.Asn204IlefsTer13(p.N204Ifs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |