G98V (p.Gly98Val) variant of KRT9 (Keratin, type I cytoskeletal 9)
G98V (p.Gly98Val) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
G98V (p.Gly98Val) variant details
- p.Gly98Val
- TOPMed rs914181565
- gnomAD rs914181565
- Missense
- Variant Prioritization Score for Impact Estimate 0.421
- REVEL 0.49
- CADD 20.50
- PolyPhen-2 0.97
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available