Primary Site >> Stomach Cancer
Gene >> EPN3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268933 |
| Start | 50540921:50540921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1108T>G |
| AA Mutation | p.Ser370Ala(p.S370A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268933 |
| Start | 50536629:50536629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753177479 |
| CDS Mutation | c.73C>T |
| AA Mutation | p.Arg25Cys(p.R25C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268933 |
| Start | 50540873:50540873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1060G>A |
| AA Mutation | p.Val354Ile(p.V354I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268933 |
| Start | 50536929:50536929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141972412 |
| CDS Mutation | c.373G>A |
| AA Mutation | p.Glu125Lys(p.E125K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268933 |
| Start | 50541670:50541670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1561A>G |
| AA Mutation | p.Lys521Glu(p.K521E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268933 |
| Start | 50541281:50541281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1302C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268933 |
| Start | 50541305:50541305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372518997 |
| CDS Mutation | c.1326G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |