P67S (p.Pro67Ser) variant of SLC22A2 (O15244)
P67S (p.Pro67Ser) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data and structural context.
P67S (p.Pro67Ser) variant details
- p.Pro67Ser
- ExAC rs767622094
- TOPMed rs767622094
- gnomAD rs767622094
- Missense
- Variant Prioritization Score for Impact Estimate 0.191
- REVEL 0.09
- CADD 17.50
- PolyPhen-2 0.23
- SIFT 0.10
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available