V68I (p.Val68Ile) variant of CYP11B1 (P15538)
V68I (p.Val68Ile) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
V68I (p.Val68Ile) variant details
- p.Val68Ile
- ExAC rs769810247
- gnomAD rs769810247
- Missense
- Variant Prioritization Score for Impact Estimate 0.121
- REVEL 0.14
- CADD 5.25
- PolyPhen-2 0.01
- SIFT 0.04
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available