T34A (p.Thr34Ala) variant of CYP11B1 (P15538)
T34A (p.Thr34Ala) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
T34A (p.Thr34Ala) variant details
- p.Thr34Ala
- rs780289850
- gnomAD 8-142875341-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.101
- CADD 2.81
- Most common in the South Asian population (allele frequency 3.5e-05)
- Structural context available
- Literature evidence available