Primary Site >> Stomach Cancer
Gene >> COL23A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390654 |
| Start | 178255022:178255022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369107371 |
| CDS Mutation | c.887C>T |
| AA Mutation | p.Ala296Val(p.A296V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390654 |
| Start | 178270344:178270344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.461G>A |
| AA Mutation | p.Gly154Asp(p.G154D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000390654 |
| Start | 178239175:178239175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1586C>T |
| AA Mutation | p.Pro529Leu(p.P529L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000390654 |
| Start | 178560734:178560734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.309A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000390654 |
| Start | 178255015:178255015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.894C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000390654 |
| Start | 178263277:178263277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.570A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000390654 |
| Start | 178560740:178560740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373172383 |
| CDS Mutation | c.303C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |