G41D (p.Gly41Asp) variant of KRT5 (Keratin, type II cytoskeletal 5)
G41D (p.Gly41Asp) in KRT5 (Keratin, type II cytoskeletal 5) 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.
G41D (p.Gly41Asp) variant details
- p.Gly41Asp
- gnomAD rs1170652770
- Missense
- Variant Prioritization Score for Impact Estimate 0.42
- REVEL 0.44
- CADD 22.10
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available