S86G (p.Ser86Gly) variant of KRT3 (Keratin, type II cytoskeletal 3)
S86G (p.Ser86Gly) in KRT3 (Keratin, type II cytoskeletal 3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
S86G (p.Ser86Gly) variant details
- p.Ser86Gly
- ExAC rs758760315
- gnomAD rs758760315
- Missense
- Variant Prioritization Score for Impact Estimate 0.0879
- REVEL 0.04
- CADD 3.87
- PolyPhen-2 0.00
- SIFT 0.44
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available