F32L (p.Phe32Leu) variant of CDH1 (Cadherin-1)
F32L (p.Phe32Leu) in CDH1 (Cadherin-1) 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 population frequency data and structural context.
F32L (p.Phe32Leu) variant details
- p.Phe32Leu
- TOPMed rs1382043754
- gnomAD rs1382043754
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available