Primary Site >> Esophagus Cancer
Gene >> CHN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409900 |
| Start | 174877977:174877977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.412A>T |
| AA Mutation | p.Thr138Ser(p.T138S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |