L13F (p.Leu13Phe) variant of LRP2 (P98164)
L13F (p.Leu13Phe) in LRP2 (P98164) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
L13F (p.Leu13Phe) variant details
- p.Leu13Phe
- TOPMed rs1255290148
- gnomAD rs1255290148
- Missense
- Variant Prioritization Score for Impact Estimate 0.389
- CADD 20.60
- PolyPhen-2 0.03
- SIFT 0.09
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)
- Structural context available