R87G (p.Arg87Gly) variant of SLC22A2 (O15244)
R87G (p.Arg87Gly) in SLC22A2 (O15244) 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.
R87G (p.Arg87Gly) variant details
- p.Arg87Gly
- ExAC rs781590898
- TOPMed rs781590898
- gnomAD rs781590898
- Missense
- Variant Prioritization Score for Impact Estimate 0.0914
- REVEL 0.09
- CADD 3.88
- PolyPhen-2 0.00
- SIFT 0.44
- Most common in the Non-Finnish European population (allele frequency 4.4e-05)
- Structural context available