Primary Site >> Stomach Cancer
Gene >> E2F2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361729 |
| Start | 23519033:23519033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.835G>A |
| AA Mutation | p.Val279Met(p.V279M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361729 |
| Start | 23519060:23519060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.808A>G |
| AA Mutation | p.Lys270Glu(p.K270E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361729 |
| Start | 23516428:23516428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201302633 |
| CDS Mutation | c.952C>T |
| AA Mutation | p.Leu318Phe(p.L318F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361729 |
| Start | 23519053:23519053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.815C>A |
| AA Mutation | p.Pro272His(p.P272H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361729 |
| Start | 23516437:23516437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.943G>A |
| AA Mutation | p.Glu315Lys(p.E315K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361729 |
| Start | 23509907:23509907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146034018 |
| CDS Mutation | c.1287C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361729 |
| Start | 23509979:23509979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754726067 |
| CDS Mutation | c.1215A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |