E93D (p.Glu93Asp) variant of SLC22A2 (O15244)
E93D (p.Glu93Asp) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
E93D (p.Glu93Asp) variant details
- p.Glu93Asp
- TOPMed rs1014024980
- gnomAD rs1014024980
- Missense
- Variant Prioritization Score for Impact Estimate 0.139
- REVEL 0.06
- CADD 11.40
- PolyPhen-2 0.02
- SIFT 0.76
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available