S39N (p.Ser39Asn) variant of KRT10 (Keratin, type I cytoskeletal 10)
S39N (p.Ser39Asn) in KRT10 (Keratin, type I cytoskeletal 10) 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.
S39N (p.Ser39Asn) variant details
- p.Ser39Asn
- ExAC rs770303156
- gnomAD rs770303156
- Missense
- Variant Prioritization Score for Impact Estimate 0.261
- REVEL 0.21
- CADD 19.90
- PolyPhen-2 0.16
- SIFT 0.03
- Most common in the African/African-American population (allele frequency 4.8e-05)