G78A (p.Gly78Ala) variant of KRT17 (Keratin, type I cytoskeletal 17)
G78A (p.Gly78Ala) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The record also includes population frequency data and structural context.
G78A (p.Gly78Ala) variant details
- p.Gly78Ala
- 1000Genomes rs11553454
- ExAC rs11553454
- TOPMed rs11553454
- gnomAD rs11553454
- Missense
- Population evidence available
- Structural context available