V26I (p.Val26Ile) variant of CLU (Clusterin)
V26I (p.Val26Ile) in CLU (Clusterin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.04 / 1. The record also includes population frequency data and structural context.
V26I (p.Val26Ile) variant details
- p.Val26Ile
- rs1170008221
- NCI-TCGA Cosmic COSV5706
- cosmic curated COSV57067
- gnomAD rs1170008221
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.0433
- REVEL 0.03
- CADD 0.19
- PolyPhen-2 0.01
- SIFT 0.53
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Latino/Admixed American population (allele frequency 0.00026)
- Structural context available