A37V (p.Ala37Val) variant of KRT17 (Keratin, type I cytoskeletal 17)
A37V (p.Ala37Val) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
A37V (p.Ala37Val) variant details
- p.Ala37Val
- gnomAD rs1311792391
- Missense
- Variant Prioritization Score for Impact Estimate 0.269
- REVEL 0.22
- CADD 5.68
- PolyPhen-2 0.01
- SIFT 0.35
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available