G112R (p.Gly112Arg) variant of KRT9 (Keratin, type I cytoskeletal 9)
G112R (p.Gly112Arg) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
G112R (p.Gly112Arg) variant details
- p.Gly112Arg
- gnomAD rs1907087934
- Missense
- Variant Prioritization Score for Impact Estimate 0.32
- REVEL 0.39
- CADD 13.20
- Most common in the HGDP:FRENCH population (allele frequency 0.019)
- Structural context available