E93G (p.Glu93Gly) variant of SLC22A2 (O15244)
E93G (p.Glu93Gly) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
E93G (p.Glu93Gly) variant details
- p.Glu93Gly
- ExAC rs760196452
- TOPMed rs760196452
- gnomAD rs760196452
- Missense
- Variant Prioritization Score for Impact Estimate 0.294
- REVEL 0.23
- CADD 22.70
- PolyPhen-2 0.67
- SIFT 0.02
- Most common in the Latino/Admixed American population (allele frequency 4.5e-05)
- Structural context available