G82D (p.Gly82Asp) variant of KRT17 (Keratin, type I cytoskeletal 17)
G82D (p.Gly82Asp) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data, published literature, and structural context.
G82D (p.Gly82Asp) variant details
- p.Gly82Asp
- rs1378330109
- gnomAD 17-41620487-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.139
- CADD 8.30
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available
- Literature evidence available