G26D (p.Gly26Asp) variant of KRT13 (Keratin, type I cytoskeletal 13)
G26D (p.Gly26Asp) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data and structural context.
G26D (p.Gly26Asp) variant details
- p.Gly26Asp
- ExAC rs779187731
- TOPMed rs779187731
- gnomAD rs779187731
- Missense
- Variant Prioritization Score for Impact Estimate 0.556
- REVEL 0.41
- CADD 23.10
- PolyPhen-2 0.96
- SIFT 0.07
- Most common in the Middle Eastern population (allele frequency 0.0007)
- Structural context available