G96D (p.Gly96Asp) variant of LRP2 (P98164)
G96D (p.Gly96Asp) in LRP2 (P98164) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
G96D (p.Gly96Asp) variant details
- p.Gly96Asp
- cosmic curated COSV10505
- gnomAD rs1203496853
- Missense
- Variant Prioritization Score for Impact Estimate 0.496
- CADD 24.20
- PolyPhen-2 1.00
- SIFT 0.02
- Most common in the African/African-American population (allele frequency 0.00041)
- Structural context available