F47S (p.Phe47Ser) variant of KRT10 (Keratin, type I cytoskeletal 10)
F47S (p.Phe47Ser) in KRT10 (Keratin, type I cytoskeletal 10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data.
F47S (p.Phe47Ser) variant details
- p.Phe47Ser
- gnomAD rs1231099404
- Missense
- Variant Prioritization Score for Impact Estimate 0.145
- REVEL 0.17
- CADD 3.72
- PolyPhen-2 0.01
- SIFT 0.89
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)