P37H (p.Pro37His) variant of CYP11B1 (P15538)
P37H (p.Pro37His) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
P37H (p.Pro37His) variant details
- p.Pro37His
- gnomAD 8-142875355-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0792
- CADD 0.15
- Population evidence available
- Structural context available
- Literature evidence available