S97G (p.Ser97Gly) variant of KRT17 (Keratin, type I cytoskeletal 17)
S97G (p.Ser97Gly) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
S97G (p.Ser97Gly) variant details
- p.Ser97Gly
- rs1304366731
- gnomAD 17-41620440-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.0872
- CADD 0.93
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available