H9R (p.His9Arg) variant of HMGCR (P04035)
H9R (p.His9Arg) in HMGCR (P04035) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.65 / 1. The record also includes population frequency data and structural context.
H9R (p.His9Arg) variant details
- p.His9Arg
- gnomAD rs1399840363
- Missense
- Variant Prioritization Score for Impact Estimate 0.652
- REVEL 0.67
- CADD 26.20
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available