Primary Site >> Esophagus Cancer
Gene >> NKX2-8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258829 |
| Start | 36581170:36581170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.452C>A |
| AA Mutation | p.Pro151His(p.P151H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |