F63L (p.Phe63Leu) variant of KRT17 (Keratin, type I cytoskeletal 17)
F63L (p.Phe63Leu) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
F63L (p.Phe63Leu) variant details
- p.Phe63Leu
- TOPMed rs1421493202
- gnomAD rs1421493202
- Missense
- Variant Prioritization Score for Impact Estimate 0.277
- REVEL 0.41
- CADD 0.76
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available