N29S (p.Asn29Ser) variant of CLU (Clusterin)
N29S (p.Asn29Ser) in CLU (Clusterin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
N29S (p.Asn29Ser) variant details
- p.Asn29Ser
- TOPMed rs775044236
- gnomAD rs775044236
- Missense
- Variant Prioritization Score for Impact Estimate 0.227
- REVEL 0.01
- CADD 5.56
- PolyPhen-2 0.01
- SIFT 0.47
- Most common in the Finnish in Finland (FIN) population (allele frequency 3.7e-05)
- Structural context available