Primary Site >> Stomach Cancer
Gene >> ELAVL3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359227 |
| Start | 11454603:11454603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761571357 |
| CDS Mutation | c.1027G>A |
| AA Mutation | p.Ala343Thr(p.A343T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359227 |
| Start | 11466782:11466782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.55G>A |
| AA Mutation | p.Gly19Ser(p.G19S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359227 |
| Start | 11458554:11458554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370390792 |
| CDS Mutation | c.391G>A |
| AA Mutation | p.Gly131Arg(p.G131R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359227 |
| Start | 11458495:11458495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.450C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359227 |
| Start | 11466732:11466732(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144461011 |
| CDS Mutation | c.105C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359227 |
| Start | 11454817:11454817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546123062 |
| CDS Mutation | c.813G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359227 |
| Start | 11454736:11454736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768770817 |
| CDS Mutation | c.894C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359227 |
| Start | 11466790:11466790(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs751148694 |
| CDS Mutation | c.47delG |
| AA Mutation | p.Gly16AlafsTer35(p.G16Afs*35) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |