G63D (p.Gly63Asp) variant of KRT13 (Keratin, type I cytoskeletal 13)
G63D (p.Gly63Asp) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
G63D (p.Gly63Asp) variant details
- p.Gly63Asp
- ExAC rs758993002
- TOPMed rs758993002
- gnomAD rs758993002
- Missense
- Variant Prioritization Score for Impact Estimate 0.365
- REVEL 0.33
- CADD 14.60
- PolyPhen-2 0.35
- SIFT 0.05
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available