S28T (p.Ser28Thr) variant of KRT17 (Keratin, type I cytoskeletal 17)
S28T (p.Ser28Thr) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and structural context.
S28T (p.Ser28Thr) variant details
- p.Ser28Thr
- Ensembl rs1908657901
- Missense
- Variant Prioritization Score for Impact Estimate 0.41
- REVEL 0.29
- CADD 21.50
- PolyPhen-2 0.05
- SIFT 0.06
- Most common in the 1KG:MSL population (allele frequency 0.013)
- Structural context available