Primary Site >> Stomach Cancer
Gene >> HRH1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397056 |
| Start | 11259732:11259732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.695C>A |
| AA Mutation | p.Pro232His(p.P232H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397056 |
| Start | 11259673:11259673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.636G>T |
| AA Mutation | p.Lys212Asn(p.K212N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397056 |
| Start | 11260254:11260254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1217A>T |
| AA Mutation | p.His406Leu(p.H406L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397056 |
| Start | 11259714:11259714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.677T>G |
| AA Mutation | p.Leu226Arg(p.L226R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397056 |
| Start | 11260263:11260263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779665353 |
| CDS Mutation | c.1226G>A |
| AA Mutation | p.Arg409His(p.R409H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397056 |
| Start | 11259262:11259262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377397952 |
| CDS Mutation | c.225C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |