A13G (p.Ala13Gly) variant of MUTYH (Adenine DNA glycosylase)
A13G (p.Ala13Gly) in MUTYH (Adenine DNA glycosylase) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
A13G (p.Ala13Gly) variant details
- p.Ala13Gly
- gnomAD rs587780747
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available