M41V (p.Met41Val) variant of CYP11B1 (P15538)
M41V (p.Met41Val) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
M41V (p.Met41Val) variant details
- p.Met41Val
- rs61752794
- gnomAD 8-142875332-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.0817
- CADD 0.14
- Most common in the HGDP:SAN population (allele frequency 0.083)
- Structural context available
- Literature evidence available