P37P (p.Pro37Pro) variant of CYP11B1 (P15538)
P37P (p.Pro37Pro) in CYP11B1 (P15538) is a synonymous 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.
P37P (p.Pro37Pro) variant details
- p.Pro37Pro
- gnomAD 8-142875354-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0816
- CADD 0.13
- Most common in the Non-Finnish European population (allele frequency 9.2e-07)
- Structural context available
- Literature evidence available