V5G (p.Val5Gly) variant of SLC22A2 (O15244)
V5G (p.Val5Gly) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data and structural context.
V5G (p.Val5Gly) variant details
- p.Val5Gly
- gnomAD rs1783323890
- Missense
- Variant Prioritization Score for Impact Estimate 0.517
- REVEL 0.55
- CADD 24.10
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available