R6C (p.Arg6Cys) variant of CDH1 (Cadherin-1)
R6C (p.Arg6Cys) 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 diffuse gastric adenocarcinoma. The record also includes population frequency data and structural context.
R6C (p.Arg6Cys) variant details
- p.Arg6Cys
- Ensembl rs2152113958
- Uncertain significance
- Hereditary diffuse gastric adenocarcinoma
- Missense
- ClinVar: Uncertain significance (Hereditary diffuse gastric adenocarcinoma)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available