C50F (p.Cys50Phe) variant of HMGCR (P04035)
C50F (p.Cys50Phe) in HMGCR (P04035) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
C50F (p.Cys50Phe) variant details
- p.Cys50Phe
- NCI-TCGA Cosmic COSV9984
- cosmic curated COSV99842
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available