S76G (p.Ser76Gly) variant of LRP2 (P98164)
S76G (p.Ser76Gly) in LRP2 (P98164) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
S76G (p.Ser76Gly) variant details
- p.Ser76Gly
- gnomAD rs1318993740
- Missense
- Variant Prioritization Score for Impact Estimate 0.304
- CADD 7.02
- PolyPhen-2 0.01
- SIFT 0.13
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available