I56M (p.Ile56Met) variant of CLU (Clusterin)
I56M (p.Ile56Met) in CLU (Clusterin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
I56M (p.Ile56Met) variant details
- p.Ile56Met
- TOPMed rs1371918127
- gnomAD rs1371918127
- Missense
- Variant Prioritization Score for Impact Estimate 0.199
- REVEL 0.20
- CADD 9.51
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available