V31A (p.Val31Ala) variant of MRE11 (P49959)
V31A (p.Val31Ala) in MRE11 (P49959) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
V31A (p.Val31Ala) variant details
- p.Val31Ala
- Ensembl rs1061945
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available