Primary Site >> Stomach Cancer
Gene >> EHF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257831 |
| Start | 34649058:34649058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.383T>C |
| AA Mutation | p.Val128Ala(p.V128A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257831 |
| Start | 34658861:34658861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775169543 |
| CDS Mutation | c.833G>A |
| AA Mutation | p.Arg278His(p.R278H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257831 |
| Start | 34658574:34658574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.649C>T |
| AA Mutation | p.Leu217Phe(p.L217F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257831 |
| Start | 34646581:34646581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.240C>G |
| AA Mutation | p.Ile80Met(p.I80M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257831 |
| Start | 34658882:34658882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.854T>C |
| AA Mutation | p.Val285Ala(p.V285A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257831 |
| Start | 34658630:34658630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747033466 |
| CDS Mutation | c.705C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |