D22G (p.Asp22Gly) variant of MCM2 (P49736)
D22G (p.Asp22Gly) in MCM2 (P49736) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D22G (p.Asp22Gly) variant details
- p.Asp22Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available