A89G (p.Ala89Gly) variant of LAMP2 (P13473)
A89G (p.Ala89Gly) in LAMP2 (P13473) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
A89G (p.Ala89Gly) variant details
- p.Ala89Gly
- gnomAD rs1321639564
- Missense
- Variant Prioritization Score for Impact Estimate 0.0947
- REVEL 0.05
- CADD 12.60
- PolyPhen-2 0.20
- SIFT 0.04
- Most common in the East Asian population (allele frequency 3.3e-05)
- Structural context available