Q59H (p.Gln59His) variant of CYP11B1 (P15538)
Q59H (p.Gln59His) in CYP11B1 (P15538) 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.
Q59H (p.Gln59His) variant details
- p.Gln59His
- ExAC rs756448189
- gnomAD rs756448189
- Missense
- Variant Prioritization Score for Impact Estimate 0.321
- REVEL 0.33
- CADD 17.10
- PolyPhen-2 0.96
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available