Primary Site >> Stomach Cancer
Gene >> TACR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305249 |
| Start | 75120658:75120658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.500A>G |
| AA Mutation | p.Tyr167Cys(p.Y167C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305249 |
| Start | 75049718:75049718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148591370 |
| CDS Mutation | c.938G>A |
| AA Mutation | p.Arg313His(p.R313H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305249 |
| Start | 75198640:75198640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.295T>C |
| AA Mutation | p.Tyr99His(p.Y99H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305249 |
| Start | 75051427:75051427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.756C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305249 |
| Start | 75120677:75120677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.481C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305249 |
| Start | 75120594:75120594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199842504 |
| CDS Mutation | c.564G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |