G75W (p.Gly75Trp) variant of KRT17 (Keratin, type I cytoskeletal 17)
G75W (p.Gly75Trp) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
G75W (p.Gly75Trp) variant details
- p.Gly75Trp
- gnomAD 17-41620509-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.274
- CADD 5.92
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)
- Structural context available
- Literature evidence available