G33K (p.Gly33Lys) variant of MRE11 (P49959)
G33K (p.Gly33Lys) in MRE11 (P49959) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
G33K (p.Gly33Lys) variant details
- p.Gly33Lys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available