F57V (p.Phe57Val) variant of KRT10 (Keratin, type I cytoskeletal 10)
F57V (p.Phe57Val) in KRT10 (Keratin, type I cytoskeletal 10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data.
F57V (p.Phe57Val) variant details
- p.Phe57Val
- TOPMed rs1905472558
- gnomAD rs1905472558
- Missense
- Variant Prioritization Score for Impact Estimate 0.317
- REVEL 0.16
- CADD 16.50
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)