Primary Site >> Esophagus Cancer
Gene >> CITED2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367651 |
| Start | 139373748:139373748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.197C>A |
| AA Mutation | p.Thr66Lys(p.T66K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |