V22L (p.Val22Leu) variant of HMGCR (P04035)
V22L (p.Val22Leu) 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.
V22L (p.Val22Leu) variant details
- p.Val22Leu
- NCI-TCGA Cosmic COSV9984
- cosmic curated COSV99843
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available