S86R (p.Ser86Arg) variant of KRT3 (Keratin, type II cytoskeletal 3)
S86R (p.Ser86Arg) in KRT3 (Keratin, type II cytoskeletal 3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
S86R (p.Ser86Arg) variant details
- p.Ser86Arg
- TOPMed rs1243912523
- gnomAD rs1243912523
- Missense
- Variant Prioritization Score for Impact Estimate 0.165
- REVEL 0.17
- CADD 0.94
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available