p.Leu16 Leu17insMet variant of LRP5 (O75197)
p.Leu16 Leu17insMet in LRP5 (O75197) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data, published literature, and structural context.
p.Leu16 Leu17insMet variant details
- rs2098589305
- gnomAD 11-68312760-C-CTG
- Inframe Insertion
- Variant Prioritization Score for Impact Estimate 0.418
- CADD 9.79
- Most common in the Ashkenazi Jewish population (allele frequency 0.00011)
- Structural context available
- Literature evidence available