G79D (p.Gly79Asp) variant of KRT9 (Keratin, type I cytoskeletal 9)
G79D (p.Gly79Asp) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
G79D (p.Gly79Asp) variant details
- p.Gly79Asp
- Ensembl rs898333521
- Missense
- Variant Prioritization Score for Impact Estimate 0.425
- REVEL 0.47
- CADD 22.30
- PolyPhen-2 0.90
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available