G87R (p.Gly87Arg) variant of KRT13 (Keratin, type I cytoskeletal 13)
G87R (p.Gly87Arg) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
G87R (p.Gly87Arg) variant details
- p.Gly87Arg
- ExAC rs746998705
- TOPMed rs746998705
- gnomAD rs746998705
- Missense
- Variant Prioritization Score for Impact Estimate 0.47
- REVEL 0.45
- CADD 21.70
- PolyPhen-2 0.55
- SIFT 0.02
- Most common in the African/African-American population (allele frequency 0.00041)
- Structural context available