T71N (p.Thr71Asn) variant of CYP11B1 (P15538)
T71N (p.Thr71Asn) 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 and structural context.
T71N (p.Thr71Asn) variant details
- p.Thr71Asn
- TOPMed rs1425271405
- gnomAD rs1425271405
- Missense
- Variant Prioritization Score for Impact Estimate 0.104
- REVEL 0.07
- CADD 9.27
- PolyPhen-2 0.80
- SIFT 0.71
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available