G46R (p.Gly46Arg) variant of CYP11B1 (P15538)
G46R (p.Gly46Arg) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
G46R (p.Gly46Arg) variant details
- p.Gly46Arg
- gnomAD 8-142875362-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.085
- CADD 0.62
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available
- Literature evidence available