A118S (p.Ala118Ser) variant of CDH2 (Cadherin-2)
A118S (p.Ala118Ser) in CDH2 (Cadherin-2) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes variant effect predictions and structural context.
A118S (p.Ala118Ser) variant details
- p.Ala118Ser
- 1000Genomes rs17445840
- ESP rs17445840
- ExAC rs17445840
- TOPMed rs17445840
- Benign
- Missense
- MetaLR 0.08
- MetaSVM -1.03
- SIFT 0.37
- EBI: Benign (in dbSNP:rs17445840)
- UniProt: Benign (in dbSNP:rs17445840)
- Structural context available