N69I (p.Asn69Ile) variant of KRT8 (Keratin, type II cytoskeletal 8)
N69I (p.Asn69Ile) in KRT8 (Keratin, type II cytoskeletal 8) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.54 / 1. The record also includes population frequency data.
N69I (p.Asn69Ile) variant details
- p.Asn69Ile
- ExAC rs773747000
- TOPMed rs773747000
- gnomAD rs773747000
- Missense
- Variant Prioritization Score for Impact Estimate 0.543
- CADD 26.60
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)