R13C (p.Arg13Cys) variant of KRT9 (Keratin, type I cytoskeletal 9)
R13C (p.Arg13Cys) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
R13C (p.Arg13Cys) variant details
- p.Arg13Cys
- ExAC rs773447868
- TOPMed rs773447868
- gnomAD rs773447868
- Missense
- Variant Prioritization Score for Impact Estimate 0.263
- REVEL 0.36
- CADD 10.30
- PolyPhen-2 0.01
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available