P99L (p.Pro99Leu) variant of CLU (Clusterin)
P99L (p.Pro99Leu) in CLU (Clusterin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
P99L (p.Pro99Leu) variant details
- p.Pro99Leu
- TOPMed rs1388938418
- gnomAD rs1388938418
- Missense
- Variant Prioritization Score for Impact Estimate 0.294
- REVEL 0.08
- CADD 21.70
- PolyPhen-2 0.42
- SIFT 0.14
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available