H39Y (p.His39Tyr) variant of LRP2 (P98164)
H39Y (p.His39Tyr) in LRP2 (P98164) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
H39Y (p.His39Tyr) variant details
- p.His39Tyr
- gnomAD rs1684891259
- Missense
- Variant Prioritization Score for Impact Estimate 0.0789
- CADD 0.07
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available