A19G (p.Ala19Gly) variant of POLE (Q07864)
A19G (p.Ala19Gly) in POLE (Q07864) 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.
A19G (p.Ala19Gly) variant details
- p.Ala19Gly
- gnomAD rs1395688602
- 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