G89D (p.Gly89Asp) variant of KRT9 (Keratin, type I cytoskeletal 9)
G89D (p.Gly89Asp) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
G89D (p.Gly89Asp) variant details
- p.Gly89Asp
- gnomAD rs1172582138
- Missense
- Variant Prioritization Score for Impact Estimate 0.397
- REVEL 0.43
- CADD 15.80
- PolyPhen-2 0.22
- SIFT 0.00
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)
- Structural context available