A57G (p.Ala57Gly) variant of SLC22A2 (O15244)
A57G (p.Ala57Gly) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
A57G (p.Ala57Gly) variant details
- p.Ala57Gly
- gnomAD rs1431278103
- Missense
- Variant Prioritization Score for Impact Estimate 0.329
- REVEL 0.23
- CADD 21.90
- PolyPhen-2 0.27
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)
- Structural context available