Primary Site >> Stomach Cancer
Gene >> UQCRFS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304863 |
| Start | 29207561:29207561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.812T>C |
| AA Mutation | p.Val271Ala(p.V271A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304863 |
| Start | 29208095:29208095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148167893 |
| CDS Mutation | c.278G>A |
| AA Mutation | p.Arg93His(p.R93H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304863 |
| Start | 29208055:29208055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.318C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304863 |
| Start | 29208010:29208010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.363T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304863 |
| Start | 29207569:29207569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.804C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304863 |
| Start | 29207650:29207650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746611014 |
| CDS Mutation | c.723A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |