G26D (p.Gly26Asp) variant of KRT9 (Keratin, type I cytoskeletal 9)
G26D (p.Gly26Asp) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
G26D (p.Gly26Asp) variant details
- p.Gly26Asp
- ExAC rs775365716
- gnomAD rs775365716
- Missense
- Variant Prioritization Score for Impact Estimate 0.298
- REVEL 0.26
- CADD 5.56
- PolyPhen-2 0.03
- SIFT 0.06
- Most common in the African/African-American population (allele frequency 0.00012)
- Structural context available