A136S (p.Ala136Ser) variant of CDH2 (Cadherin-2)
A136S (p.Ala136Ser) 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.
A136S (p.Ala136Ser) variant details
- p.Ala136Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.11
- MetaSVM -1.04
- SIFT 0.54
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available