Primary Site >> Esophagus Cancer
Gene >> GP6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000417454 |
| Start | 55014935:55014935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1006G>T |
| AA Mutation | p.Gly336Trp(p.G336W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |