Primary Site >> Esophagus Cancer
Gene >> CENPH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283006 |
| Start | 69189684:69189684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.50G>C |
| AA Mutation | p.Gly17Ala(p.G17A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |