G38S (p.Gly38Ser) variant of KRT17 (Keratin, type I cytoskeletal 17)
G38S (p.Gly38Ser) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
G38S (p.Gly38Ser) variant details
- p.Gly38Ser
- ExAC rs757015302
- TOPMed rs757015302
- gnomAD rs757015302
- Missense
- Variant Prioritization Score for Impact Estimate 0.421
- REVEL 0.23
- CADD 17.00
- PolyPhen-2 0.01
- SIFT 0.39
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available