D51H (p.Asp51His) variant of MCM2 (P49736)
D51H (p.Asp51His) 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.
D51H (p.Asp51His) variant details
- p.Asp51His
- NCI-TCGA Cosmic COSV5403
- NCI-TCGA Cosmic COSV9941
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available