T37A (p.Thr37Ala) variant of KRT2 (P35908)
T37A (p.Thr37Ala) in KRT2 (P35908) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
T37A (p.Thr37Ala) variant details
- p.Thr37Ala
- ExAC rs749830972
- TOPMed rs749830972
- gnomAD rs749830972
- Missense
- Variant Prioritization Score for Impact Estimate 0.298
- REVEL 0.14
- CADD 7.71
- PolyPhen-2 0.00
- SIFT 0.56
- Most common in the Middle Eastern population (allele frequency 0.0007)
- Structural context available