Primary Site >> Stomach Cancer
Gene >> OR6C1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379668 |
| Start | 55320808:55320808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.209C>T |
| AA Mutation | p.Ser70Leu(p.S70L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379668 |
| Start | 55320763:55320763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.164C>T |
| AA Mutation | p.Thr55Ile(p.T55I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379668 |
| Start | 55321261:55321261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.662G>A |
| AA Mutation | p.Arg221Lys(p.R221K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379668 |
| Start | 55321280:55321280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.681T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379668 |
| Start | 55320815:55320815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.216A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379668 |
| Start | 55321205:55321205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144216844 |
| CDS Mutation | c.606G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |