E39G (p.Glu39Gly) variant of CYP11B1 (P15538)
E39G (p.Glu39Gly) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
E39G (p.Glu39Gly) variant details
- p.Glu39Gly
- gnomAD 8-142875370-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.107
- CADD 3.71
- Most common in the Non-Finnish European population (allele frequency 9.5e-07)
- Structural context available
- Literature evidence available