Primary Site >> Stomach Cancer
Gene >> SSTR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357585 |
| Start | 73170317:73170317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.998G>A |
| AA Mutation | p.Ser333Asn(p.S333N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357585 |
| Start | 73170082:73170082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.763A>G |
| AA Mutation | p.Thr255Ala(p.T255A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357585 |
| Start | 73170347:73170347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752083493 |
| CDS Mutation | c.1028G>A |
| AA Mutation | p.Ser343Asn(p.S343N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357585 |
| Start | 73170157:73170157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779626588 |
| CDS Mutation | c.838G>A |
| AA Mutation | p.Val280Ile(p.V280I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357585 |
| Start | 73169868:73169868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.549C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357585 |
| Start | 73170051:73170051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779529162 |
| CDS Mutation | c.732C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |