F101L (p.Phe101Leu) variant of SLC22A2 (O15244)
F101L (p.Phe101Leu) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
F101L (p.Phe101Leu) variant details
- p.Phe101Leu
- TOPMed rs1013323019
- gnomAD rs1013323019
- Missense
- Variant Prioritization Score for Impact Estimate 0.239
- REVEL 0.12
- CADD 12.60
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available