G89V (p.Gly89Val) variant of KRT9 (Keratin, type I cytoskeletal 9)
G89V (p.Gly89Val) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
G89V (p.Gly89Val) variant details
- p.Gly89Val
- gnomAD rs1172582138
- Missense
- Variant Prioritization Score for Impact Estimate 0.383
- REVEL 0.41
- CADD 15.30
- PolyPhen-2 0.11
- SIFT 0.01
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available