V17F (p.Val17Phe) variant of LRP2 (P98164)
V17F (p.Val17Phe) in LRP2 (P98164) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
V17F (p.Val17Phe) variant details
- p.Val17Phe
- gnomAD rs1238825402
- Missense
- Variant Prioritization Score for Impact Estimate 0.345
- CADD 15.40
- PolyPhen-2 0.00
- SIFT 0.72
- Most common in the East Asian population (allele frequency 0.00015)
- Structural context available