R13P (p.Arg13Pro) variant of KRT9 (Keratin, type I cytoskeletal 9)
R13P (p.Arg13Pro) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
R13P (p.Arg13Pro) variant details
- p.Arg13Pro
- ExAC rs749091007
- TOPMed rs749091007
- gnomAD rs749091007
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available