L14V (p.Leu14Val) variant of CDH1 (Cadherin-1)
L14V (p.Leu14Val) in CDH1 (Cadherin-1) is a missense change. Clinical records from ClinVar and UniProt describe it as conflicting interpretations in the context of Hereditary diffuse gastric adenocarcinoma; Hereditary cancer-predisposing syndro. The record also includes structural context.
L14V (p.Leu14Val) variant details
- p.Leu14Val
- gnomAD rs1192852993
- Conflicting interpretations
- Hereditary diffuse gastric adenocarcinoma; Hereditary cancer-predisposing syndro
- Missense
- ClinVar: Conflicting classifications of pathogenicity (Hereditary diffuse gastric adenocarcinoma; Hereditary cancer-pre)
- UniProt: Conflicting interpretations
- Structural context available