G67S (p.Gly67Ser) variant of KRT9 (Keratin, type I cytoskeletal 9)
G67S (p.Gly67Ser) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
G67S (p.Gly67Ser) variant details
- p.Gly67Ser
- gnomAD rs1465106739
- Missense
- Variant Prioritization Score for Impact Estimate 0.351
- REVEL 0.28
- CADD 0.10
- PolyPhen-2 0.01
- SIFT 0.28
- Most common in the 1KG:MXL population (allele frequency 0.0081)
- Structural context available