A86P (p.Ala86Pro) variant of KRT13 (Keratin, type I cytoskeletal 13)
A86P (p.Ala86Pro) in KRT13 (Keratin, type I cytoskeletal 13) 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.
A86P (p.Ala86Pro) variant details
- p.Ala86Pro
- gnomAD rs1181490462
- Missense
- Variant Prioritization Score for Impact Estimate 0.222
- REVEL 0.11
- CADD 15.70
- PolyPhen-2 0.26
- SIFT 0.13
- Most common in the 1KG:MSL population (allele frequency 0.013)
- Structural context available