S37F (p.Ser37Phe) variant of KRT9 (Keratin, type I cytoskeletal 9)
S37F (p.Ser37Phe) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
S37F (p.Ser37Phe) variant details
- p.Ser37Phe
- ExAC rs779444299
- TOPMed rs779444299
- gnomAD rs779444299
- Missense
- Variant Prioritization Score for Impact Estimate 0.4
- REVEL 0.28
- CADD 16.70
- PolyPhen-2 0.01
- SIFT 0.00
- Most common in the East Asian population (allele frequency 0.00015)
- Structural context available