P67T (p.Pro67Thr) variant of SLC22A2 (O15244)
P67T (p.Pro67Thr) 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.
P67T (p.Pro67Thr) variant details
- p.Pro67Thr
- ExAC rs767622094
- TOPMed rs767622094
- gnomAD rs767622094
- Missense
- Variant Prioritization Score for Impact Estimate 0.194
- REVEL 0.10
- CADD 17.00
- PolyPhen-2 0.23
- SIFT 0.10
- Most common in the Middle Eastern population (allele frequency 0.00035)
- Structural context available