D33G (p.Asp33Gly) variant of CDH1 (Cadherin-1)
D33G (p.Asp33Gly) in CDH1 (Cadherin-1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as conflicting interpretations in the context of Hereditary cancer-predisposing syndrome; Hereditary diffuse gastric adenocarcino. The record also includes structural context.
D33G (p.Asp33Gly) variant details
- p.Asp33Gly
- Ensembl rs1597838602
- Conflicting interpretations
- Hereditary cancer-predisposing syndrome; Hereditary diffuse gastric adenocarcino
- Missense
- ClinVar: Conflicting classifications of pathogenicity (Hereditary cancer-predisposing syndrome; Hereditary diffuse gast)
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available