P77T (p.Pro77Thr) variant of CYP11B1 (P15538)
P77T (p.Pro77Thr) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data and structural context.
P77T (p.Pro77Thr) variant details
- p.Pro77Thr
- ExAC rs750931191
- TOPMed rs750931191
- gnomAD rs750931191
- Missense
- Variant Prioritization Score for Impact Estimate 0.614
- REVEL 0.59
- CADD 23.70
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available