S39T (p.Ser39Thr) variant of KRT2 (P35908)
S39T (p.Ser39Thr) in KRT2 (P35908) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
S39T (p.Ser39Thr) variant details
- p.Ser39Thr
- ESP rs376095204
- TOPMed rs376095204
- gnomAD rs376095204
- Missense
- Variant Prioritization Score for Impact Estimate 0.376
- REVEL 0.34
- CADD 19.20
- PolyPhen-2 0.06
- SIFT 0.07
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available