L50P (p.Leu50Pro) variant of CYP11B1 (P15538)
L50P (p.Leu50Pro) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
L50P (p.Leu50Pro) variant details
- p.Leu50Pro
- rs1816902981
- gnomAD 8-142875337-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.152
- CADD 10.10
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available
- Literature evidence available