Primary Site >> Esophagus Cancer
Gene >> HMGCS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369406 |
| Start | 119755552:119755552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1062A>C |
| AA Mutation | p.Lys354Asn(p.K354N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |