F18V (p.Phe18Val) variant of SLC22A2 (O15244)
F18V (p.Phe18Val) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data and structural context.
F18V (p.Phe18Val) variant details
- p.Phe18Val
- gnomAD rs1196922904
- Missense
- Variant Prioritization Score for Impact Estimate 0.671
- REVEL 0.70
- CADD 25.50
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available