Q98H (p.Gln98His) variant of SLC22A2 (O15244)
Q98H (p.Gln98His) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
Q98H (p.Gln98His) variant details
- p.Gln98His
- TOPMed rs1297143561
- gnomAD rs1297143561
- Missense
- Variant Prioritization Score for Impact Estimate 0.291
- REVEL 0.26
- CADD 19.90
- PolyPhen-2 0.81
- SIFT 0.13
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available