Q18R (p.Gln18Arg) variant of SLC22A1 (O15245)
Q18R (p.Gln18Arg) in SLC22A1 (O15245) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data and structural context.
Q18R (p.Gln18Arg) variant details
- p.Gln18Arg
- gnomAD rs1328983401
- Missense
- Variant Prioritization Score for Impact Estimate 0.749
- REVEL 0.94
- CADD 25.70
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 6.3e-06)
- Structural context available