Primary Site >> Stomach Cancer
Gene >> SYT13
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000020926 |
| Start | 45244057:45244057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1276C>A |
| AA Mutation | p.Leu426Met(p.L426M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000020926 |
| Start | 45244287:45244287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1046A>C |
| AA Mutation | p.Lys349Thr(p.K349T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000020926 |
| Start | 45252424:45252424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.843G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000020926 |
| Start | 45252427:45252427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.840A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000020926 |
| Start | 45286118:45286118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.90T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000020926 |
| Start | 45255871:45255871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776357791 |
| CDS Mutation | c.204G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |