A91T (p.Ala91Thr) variant of KRT5 (Keratin, type II cytoskeletal 5)
A91T (p.Ala91Thr) in KRT5 (Keratin, type II cytoskeletal 5) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
A91T (p.Ala91Thr) variant details
- p.Ala91Thr
- ESP rs142778320
- ExAC rs142778320
- TOPMed rs142778320
- gnomAD rs142778320
- Missense
- Variant Prioritization Score for Impact Estimate 0.194
- REVEL 0.08
- CADD 15.90
- PolyPhen-2 0.03
- SIFT 0.10
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available