Primary Site >> Esophagus Cancer
Gene >> EEF2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3984218:3984218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.136A>G |
| AA Mutation | p.Ile46Val(p.I46V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3980010:3980010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1403A>G |
| AA Mutation | p.Asn468Ser(p.N468S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3982337:3982337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.700G>T |
| AA Mutation | p.Ala234Ser(p.A234S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3980635:3980635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1225C>T |
| AA Mutation | p.Arg409Trp(p.R409W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309311 |
| Start | 3982017:3982017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.827C>T |
| AA Mutation | p.Ser276Leu(p.S276L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309311 |
| Start | 3982034:3982034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201754413 |
| CDS Mutation | c.810C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |