G98D (p.Gly98Asp) variant of KRT9 (Keratin, type I cytoskeletal 9)
G98D (p.Gly98Asp) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and structural context.
G98D (p.Gly98Asp) variant details
- p.Gly98Asp
- TOPMed rs914181565
- gnomAD rs914181565
- Missense
- Variant Prioritization Score for Impact Estimate 0.414
- REVEL 0.47
- CADD 20.80
- PolyPhen-2 0.96
- SIFT 0.00
- Most common in the East Asian population (allele frequency 0.00015)
- Structural context available