S59S (p.Ser59Ser) variant of HMGCR (P04035)
S59S (p.Ser59Ser) in HMGCR (P04035) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data, published literature, and structural context.
S59S (p.Ser59Ser) variant details
- p.Ser59Ser
- rs1469871771
- gnomAD 5-75343864-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.388
- CADD 14.10
- Most common in the Latino/Admixed American population (allele frequency 2.4e-05)
- Structural context available
- Literature evidence available