G17S (p.Gly17Ser) variant of KRT9 (Keratin, type I cytoskeletal 9)
G17S (p.Gly17Ser) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
G17S (p.Gly17Ser) variant details
- p.Gly17Ser
- TOPMed rs1907106036
- Missense
- Variant Prioritization Score for Impact Estimate 0.222
- REVEL 0.26
- CADD 14.10
- PolyPhen-2 0.96
- SIFT 0.09
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available