D33Y (p.Asp33Tyr) variant of CDH1 (Cadherin-1)
D33Y (p.Asp33Tyr) in CDH1 (Cadherin-1) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes variant effect predictions and structural context.
D33Y (p.Asp33Tyr) variant details
- p.Asp33Tyr
- Ensembl rs2152114394
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- MetaLR 0.03
- MetaSVM -1.06
- SIFT 0.14
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available