F97L (p.Phe97Leu) variant of KRT3 (Keratin, type II cytoskeletal 3)
F97L (p.Phe97Leu) in KRT3 (Keratin, type II cytoskeletal 3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
F97L (p.Phe97Leu) variant details
- p.Phe97Leu
- ExAC rs751561509
- TOPMed rs751561509
- gnomAD rs751561509
- Missense
- Variant Prioritization Score for Impact Estimate 0.426
- REVEL 0.23
- CADD 15.30
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available