P37L (p.Pro37Leu) variant of CYP11B1 (P15538)
P37L (p.Pro37Leu) 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.
P37L (p.Pro37Leu) variant details
- p.Pro37Leu
- rs1369120151
- gnomAD 8-142875355-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0819
- CADD 0.18
- Most common in the Middle Eastern population (allele frequency 0.00023)
- Structural context available
- Literature evidence available