G39R (p.Gly39Arg) variant of KRT9 (Keratin, type I cytoskeletal 9)
G39R (p.Gly39Arg) in KRT9 (Keratin, type I cytoskeletal 9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
G39R (p.Gly39Arg) variant details
- p.Gly39Arg
- 1000Genomes rs556615807
- ExAC rs556615807
- gnomAD rs556615807
- Missense
- Variant Prioritization Score for Impact Estimate 0.282
- REVEL 0.32
- CADD 7.95
- PolyPhen-2 0.01
- SIFT 0.28
- Most common in the HGDP:YAKUT population (allele frequency 0.04)
- Structural context available