A86S (p.Ala86Ser) variant of KRT17 (Keratin, type I cytoskeletal 17)
A86S (p.Ala86Ser) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data, published literature, and structural context.
A86S (p.Ala86Ser) variant details
- p.Ala86Ser
- gnomAD 17-41620476-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.227
- CADD 6.49
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available