S32T (p.Ser32Thr) variant of KRT17 (Keratin, type I cytoskeletal 17)
S32T (p.Ser32Thr) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
S32T (p.Ser32Thr) variant details
- p.Ser32Thr
- TOPMed rs1295462977
- gnomAD rs1295462977
- Missense
- Variant Prioritization Score for Impact Estimate 0.177
- REVEL 0.11
- CADD 15.30
- PolyPhen-2 0.01
- SIFT 0.17
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available