S17G (p.Ser17Gly) variant of CYP11B1 (P15538)
S17G (p.Ser17Gly) in CYP11B1 (P15538) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data, published literature, and structural context.
S17G (p.Ser17Gly) variant details
- p.Ser17Gly
- gnomAD 8-142875368-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.297
- CADD 4.51
- Most common in the Non-Finnish European population (allele frequency 9.4e-07)
- Structural context available
- Literature evidence available