G38G (p.Gly38Gly) variant of KRT18 (Keratin, type I cytoskeletal 18)
G38G (p.Gly38Gly) in KRT18 (Keratin, type I cytoskeletal 18) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, published literature, and structural context.
G38G (p.Gly38Gly) variant details
- p.Gly38Gly
- rs75380684
- gnomAD 12-52949287-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.196
- CADD 16.50
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available
- Literature evidence available