W96R (p.Trp96Arg) variant of SLC22A2 (O15244)
W96R (p.Trp96Arg) 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.
W96R (p.Trp96Arg) variant details
- p.Trp96Arg
- ESP rs368040619
- ExAC rs368040619
- TOPMed rs368040619
- gnomAD rs368040619
- Missense
- Variant Prioritization Score for Impact Estimate 0.656
- REVEL 0.65
- CADD 28.60
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 2.1e-05)
- Structural context available