Primary Site >> Stomach Cancer
Gene >> SNAI3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332281 |
| Start | 88681690:88681690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.101G>A |
| AA Mutation | p.Cys34Tyr(p.C34Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332281 |
| Start | 88681634:88681634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs45506693 |
| CDS Mutation | c.157G>A |
| AA Mutation | p.Gly53Ser(p.G53S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332281 |
| Start | 88678554:88678554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201681397 |
| CDS Mutation | c.773C>T |
| AA Mutation | p.Thr258Met(p.T258M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332281 |
| Start | 88678485:88678485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147688628 |
| CDS Mutation | c.842C>T |
| AA Mutation | p.Ala281Val(p.A281V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000332281 |
| Start | 88681598:88681598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776627093 |
| CDS Mutation | c.193G>A |
| AA Mutation | p.Val65Ile(p.V65I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332281 |
| Start | 88681482:88681482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.309A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332281 |
| Start | 88681530:88681530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.261C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332281 |
| Start | 88681428:88681428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.363C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000332281 |
| Start | 88681674:88681674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762818249 |
| CDS Mutation | c.117G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |