F37L (p.Phe37Leu) variant of HMGCR (P04035)
F37L (p.Phe37Leu) 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.
F37L (p.Phe37Leu) variant details
- p.Phe37Leu
- NCI-TCGA Cosmic COSV5531
- cosmic curated COSV55317
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available