Primary Site >> Stomach Cancer
Gene >> EIF3F
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309828 |
| Start | 7994990:7994990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.754A>G |
| AA Mutation | p.Ile252Val(p.I252V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309828 |
| Start | 7987464:7987464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.112G>C |
| AA Mutation | p.Val38Leu(p.V38L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309828 |
| Start | 7987688:7987688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.336T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309828 |
| Start | 7987373:7987373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148453570 |
| CDS Mutation | c.21A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309828 |
| Start | 7987469:7987469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767170137 |
| CDS Mutation | c.117C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309828 |
| Start | 7987589:7987589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.237T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |