Q88H (p.Gln88His) variant of SLC22A2 (O15244)
Q88H (p.Gln88His) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
Q88H (p.Gln88His) variant details
- p.Gln88His
- 1000Genomes rs200904655
- ExAC rs200904655
- TOPMed rs200904655
- gnomAD rs200904655
- Missense
- Variant Prioritization Score for Impact Estimate 0.44
- REVEL 0.34
- CADD 21.90
- PolyPhen-2 0.96
- SIFT 0.14
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available