Q89R (p.Gln89Arg) variant of LRP2 (P98164)
Q89R (p.Gln89Arg) in LRP2 (P98164) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes structural context.
Q89R (p.Gln89Arg) variant details
- p.Gln89Arg
- rs2105513194
- ClinGen CA349173650
- ClinVar RCV001973241
- Ensembl rs2105513194
- Uncertain significance
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.494
- AlphaMissense 0.07
- MetaLR 0.67
- MetaSVM -0.20
- PolyPhen-2 0.00
- SIFT 0.63
- MutPred 0.53
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available