Primary Site >> Esophagus Cancer
Gene >> HOXA9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343483 |
| Start | 27165157:27165157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.301G>C |
| AA Mutation | p.Ala101Pro(p.A101P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |