F59C (p.Phe59Cys) variant of SLCO1B1 (Q9Y6L6)
F59C (p.Phe59Cys) in SLCO1B1 (Q9Y6L6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.72 / 1. The record also includes population frequency data and structural context.
F59C (p.Phe59Cys) variant details
- p.Phe59Cys
- TOPMed rs1940771354
- gnomAD rs1940771354
- Missense
- Variant Prioritization Score for Impact Estimate 0.723
- REVEL 0.77
- CADD 29.20
- Most common in the South Asian population (allele frequency 0.00044)
- Structural context available