E39D (p.Glu39Asp) variant of CYP11B1 (P15538)
E39D (p.Glu39Asp) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
E39D (p.Glu39Asp) variant details
- p.Glu39Asp
- gnomAD 8-142875369-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.104
- CADD 3.32
- Population evidence available
- Structural context available
- Literature evidence available