G55S (p.Gly55Ser) variant of HMGCS2 (P54868)
G55S (p.Gly55Ser) 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.
G55S (p.Gly55Ser) variant details
- p.Gly55Ser
- NCI-TCGA Cosmic COSV1010
- cosmic curated COSV10102
- NCI-TCGA Cosmic COSV6556
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available