G118A (p.Gly118Ala) variant of KRT9 (Keratin, type I cytoskeletal 9)
G118A (p.Gly118Ala) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
G118A (p.Gly118Ala) variant details
- p.Gly118Ala
- TOPMed rs1434499651
- Missense
- Variant Prioritization Score for Impact Estimate 0.336
- REVEL 0.33
- CADD 9.60
- PolyPhen-2 0.02
- SIFT 0.15
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available