C122G (p.Cys122Gly) variant of SLC22A2 (O15244)
C122G (p.Cys122Gly) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.80 / 1. The record also includes population frequency data and structural context.
C122G (p.Cys122Gly) variant details
- p.Cys122Gly
- ExAC rs767010128
- TOPMed rs767010128
- gnomAD rs767010128
- Missense
- Variant Prioritization Score for Impact Estimate 0.796
- REVEL 0.92
- CADD 25.20
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available