S17R (p.Ser17Arg) variant of CYP11B1 (P15538)
S17R (p.Ser17Arg) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
S17R (p.Ser17Arg) variant details
- p.Ser17Arg
- rs1816903838
- gnomAD 8-142875357-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0988
- CADD 2.56
- Population evidence available
- Structural context available
- Literature evidence available