P67L (p.Pro67Leu) variant of SLC22A2 (O15244)
P67L (p.Pro67Leu) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
P67L (p.Pro67Leu) variant details
- p.Pro67Leu
- 1000Genomes rs145369394
- ESP rs145369394
- ExAC rs145369394
- TOPMed rs145369394
- Missense
- Variant Prioritization Score for Impact Estimate 0.0799
- REVEL 0.08
- CADD 0.02
- PolyPhen-2 0.01
- SIFT 1.00
- Most common in the 1KG:ESN population (allele frequency 0.0097)
- Structural context available