F18I (p.Phe18Ile) variant of SLC22A2 (O15244)
F18I (p.Phe18Ile) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data and structural context.
F18I (p.Phe18Ile) variant details
- p.Phe18Ile
- gnomAD rs1196922904
- Missense
- Variant Prioritization Score for Impact Estimate 0.657
- REVEL 0.68
- CADD 25.70
- PolyPhen-2 0.82
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available