V9M (p.Val9Met) variant of CYP11B1 (P15538)
V9M (p.Val9Met) 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.
V9M (p.Val9Met) variant details
- p.Val9Met
- ESP rs150163594
- TOPMed rs150163594
- gnomAD rs150163594
- Missense
- Variant Prioritization Score for Impact Estimate 0.0996
- REVEL 0.09
- CADD 7.39
- PolyPhen-2 0.10
- SIFT 0.12
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available