M41I (p.Met41Ile) variant of CYP11B1 (P15538)
M41I (p.Met41Ile) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
M41I (p.Met41Ile) variant details
- p.Met41Ile
- gnomAD 8-142875330-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.0911
- CADD 1.47
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available