G87C (p.Gly87Cys) variant of HMGCS2 (P54868)
G87C (p.Gly87Cys) in HMGCS2 (P54868) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G87C (p.Gly87Cys) variant details
- p.Gly87Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available