E51D (p.Glu51Asp) variant of CDH2 (Cadherin-2)
E51D (p.Glu51Asp) 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 variant effect predictions and structural context.
E51D (p.Glu51Asp) variant details
- p.Glu51Asp
- NCI-TCGA Cosmic COSV5227
- NCI-TCGA Cosmic COSV9929
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.14
- MetaSVM -1.00
- SIFT 0.16
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available