R46G (p.Arg46Gly) variant of KRT9 (Keratin, type I cytoskeletal 9)
R46G (p.Arg46Gly) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The record also includes population frequency data and structural context.
R46G (p.Arg46Gly) variant details
- p.Arg46Gly
- 1000Genomes rs546893755
- ExAC rs546893755
- gnomAD rs546893755
- Missense
- Population evidence available
- Structural context available