G96V (p.Gly96Val) variant of KRT9 (Keratin, type I cytoskeletal 9)
G96V (p.Gly96Val) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
G96V (p.Gly96Val) variant details
- p.Gly96Val
- gnomAD rs945694059
- Missense
- Variant Prioritization Score for Impact Estimate 0.442
- REVEL 0.33
- CADD 15.60
- PolyPhen-2 0.03
- SIFT 0.05
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available