G10D (p.Gly10Asp) variant of HMGCR (P04035)
G10D (p.Gly10Asp) 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.
G10D (p.Gly10Asp) variant details
- p.Gly10Asp
- NCI-TCGA TCGA novel
- Ensembl rs2150352999
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available