A59S (p.Ala59Ser) variant of UNC13D (Protein unc-13 homolog D)
A59S (p.Ala59Ser) in UNC13D (Protein unc-13 homolog D) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
A59S (p.Ala59Ser) variant details
- p.Ala59Ser
- 1000Genomes rs9904366
- ESP rs9904366
- ExAC rs9904366
- TOPMed rs9904366
- Benign
- Missense
- EBI: Benign (in dbSNP:rs9904366)
- UniProt: Benign (in dbSNP:rs9904366)
- Structural context available