G39W (p.Gly39Trp) variant of KRT5 (Keratin, type II cytoskeletal 5)
G39W (p.Gly39Trp) in KRT5 (Keratin, type II cytoskeletal 5) 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 rs146136560
- ExAC rs146136560
- TOPMed rs146136560
- gnomAD rs146136560
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available