S76N (p.Ser76Asn) variant of LRP2 (P98164)
S76N (p.Ser76Asn) in LRP2 (P98164) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
S76N (p.Ser76Asn) variant details
- p.Ser76Asn
- Ensembl rs1684836920
- Missense
- Variant Prioritization Score for Impact Estimate 0.0592
- CADD 0.04
- PolyPhen-2 0.01
- SIFT 0.37
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available