R90G (p.Arg90Gly) variant of SLC22A2 (O15244)
R90G (p.Arg90Gly) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
R90G (p.Arg90Gly) variant details
- p.Arg90Gly
- ESP rs148841179
- ExAC rs148841179
- TOPMed rs148841179
- gnomAD rs148841179
- Missense
- Variant Prioritization Score for Impact Estimate 0.176
- REVEL 0.13
- CADD 9.68
- PolyPhen-2 0.01
- SIFT 0.16
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available