G88D (p.Gly88Asp) variant of KRT9 (Keratin, type I cytoskeletal 9)
G88D (p.Gly88Asp) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
G88D (p.Gly88Asp) variant details
- p.Gly88Asp
- Ensembl rs1452318170
- Missense
- Variant Prioritization Score for Impact Estimate 0.392
- REVEL 0.41
- CADD 17.90
- PolyPhen-2 0.60
- SIFT 0.01
- Most common in the 1KG:MXL population (allele frequency 0.0081)
- Structural context available