Q59R (p.Gln59Arg) variant of CALCB (P10092)
Q59R (p.Gln59Arg) in CALCB (P10092) 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.
Q59R (p.Gln59Arg) variant details
- p.Gln59Arg
- ExAC rs776636220
- gnomAD rs776636220
- Missense
- Variant Prioritization Score for Impact Estimate 0.444
- REVEL 0.44
- CADD 26.80
- PolyPhen-2 1.00
- SIFT 0.05
- Most common in the Middle Eastern population (allele frequency 0.00017)
- Structural context available