R80G (p.Arg80Gly) variant of MRE11 (P49959)
R80G (p.Arg80Gly) in MRE11 (P49959) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R80G (p.Arg80Gly) variant details
- p.Arg80Gly
- cosmic curated COSV10518
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available