Primary Site >> Stomach Cancer
Gene >> EEF2K
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263026 |
| Start | 22280325:22280325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs531682732 |
| CDS Mutation | c.2017G>A |
| AA Mutation | p.Glu673Lys(p.E673K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263026 |
| Start | 22257278:22257278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143471765 |
| CDS Mutation | c.794G>A |
| AA Mutation | p.Arg265His(p.R265H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263026 |
| Start | 22260467:22260467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1237C>T |
| AA Mutation | p.Pro413Ser(p.P413S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263026 |
| Start | 22266848:22266848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1736A>T |
| AA Mutation | p.His579Leu(p.H579L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263026 |
| Start | 22248765:22248765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760638533 |
| CDS Mutation | c.358G>A |
| AA Mutation | p.Val120Ile(p.V120I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263026 |
| Start | 22225822:22225822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148266060 |
| CDS Mutation | c.93C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |