D78Y (p.Asp78Tyr) variant of CDH2 (Cadherin-2)
D78Y (p.Asp78Tyr) in CDH2 (Cadherin-2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D78Y (p.Asp78Tyr) variant details
- p.Asp78Tyr
- NCI-TCGA Cosmic COSV9929
- cosmic curated COSV99296
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available