Primary Site >> Stomach Cancer
Gene >> WARS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355338 |
| Start | 100335009:100335009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773270850 |
| CDS Mutation | c.1282G>A |
| AA Mutation | p.Gly428Ser(p.G428S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355338 |
| Start | 100334900:100334900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1391G>T |
| AA Mutation | p.Arg464Leu(p.R464L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355338 |
| Start | 100369101:100369101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.85G>A |
| AA Mutation | p.Gly29Arg(p.G29R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355338 |
| Start | 100353818:100353818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751522726 |
| CDS Mutation | c.594C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355338 |
| Start | 100342545:100342545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.966C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355338 |
| Start | 100369093:100369093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774738389 |
| CDS Mutation | c.93G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355338 |
| Start | 100354501:100354501(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.488delG |
| AA Mutation | p.Gly163AlafsTer9(p.G163Afs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |