Primary Site >> Esophagus Cancer
Gene >> IFNG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000229135 |
| Start | 68159583:68159583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.33G>T |
| AA Mutation | p.Gln11His(p.Q11H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |