A89D (p.Ala89Asp) variant of SLC2A2 (P11168)
A89D (p.Ala89Asp) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
A89D (p.Ala89Asp) variant details
- p.Ala89Asp
- Ensembl rs2108256517
- Missense
- Variant Prioritization Score for Impact Estimate 0.333
- REVEL 0.27
- CADD 11.80
- PolyPhen-2 0.00
- SIFT 0.27
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available