P37T (p.Pro37Thr) variant of CYP11B1 (P15538)
P37T (p.Pro37Thr) 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.
P37T (p.Pro37Thr) variant details
- p.Pro37Thr
- gnomAD 8-142875356-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0875
- CADD 0.97
- Population evidence available
- Structural context available
- Literature evidence available