G39W (p.Gly39Trp) variant of PDE6B (P35913)
G39W (p.Gly39Trp) in PDE6B (P35913) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
G39W (p.Gly39Trp) variant details
- p.Gly39Trp
- ESP rs151334566
- ExAC rs151334566
- TOPMed rs151334566
- gnomAD rs151334566
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available