V41F (p.Val41Phe) variant of SLC22A2 (O15244)
V41F (p.Val41Phe) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data and structural context.
V41F (p.Val41Phe) variant details
- p.Val41Phe
- 1000Genomes rs548362661
- ExAC rs548362661
- TOPMed rs548362661
- gnomAD rs548362661
- Missense
- Variant Prioritization Score for Impact Estimate 0.599
- REVEL 0.56
- CADD 23.50
- PolyPhen-2 0.47
- SIFT 0.06
- Most common in the 1KG:PJL population (allele frequency 0.0052)
- Structural context available