Q79R (p.Gln79Arg) variant of LRP2 (P98164)
Q79R (p.Gln79Arg) in LRP2 (P98164) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data and structural context.
Q79R (p.Gln79Arg) variant details
- p.Gln79Arg
- ExAC rs778655445
- TOPMed rs778655445
- gnomAD rs778655445
- Missense
- Variant Prioritization Score for Impact Estimate 0.0682
- CADD 0.02
- PolyPhen-2 0.12
- SIFT 0.62
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available