P27A (p.Pro27Ala) variant of CDH1 (Cadherin-1)
P27A (p.Pro27Ala) in CDH1 (Cadherin-1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of Hereditary cancer-predisposing syndrome. The record also includes population frequency data and structural context.
P27A (p.Pro27Ala) variant details
- p.Pro27Ala
- Ensembl rs878854696
- Likely benign
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Likely benign (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available