A86V (p.Ala86Val) variant of KRT17 (Keratin, type I cytoskeletal 17)
A86V (p.Ala86Val) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
A86V (p.Ala86Val) variant details
- p.Ala86Val
- rs1333332337
- gnomAD 17-41620475-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.314
- CADD 7.38
- Most common in the 1KG:MSL population (allele frequency 0.013)
- Structural context available
- Literature evidence available