D33N (p.Asp33Asn) variant of CDH1 (Cadherin-1)
D33N (p.Asp33Asn) in CDH1 (Cadherin-1) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary diffuse gastric adenocarcinoma; Hereditary cancer-predisposing syndro. The record also includes structural context.
D33N (p.Asp33Asn) variant details
- p.Asp33Asn
- Ensembl rs2152114394
- Uncertain significance
- Hereditary diffuse gastric adenocarcinoma; Hereditary cancer-predisposing syndro
- Missense
- ClinVar: Uncertain significance (Hereditary diffuse gastric adenocarcinoma; Hereditary cancer-pre)
- UniProt: Uncertain significance
- Structural context available