I39N (p.Ile39Asn) variant of SLCO1B1 (Q9Y6L6)
I39N (p.Ile39Asn) in SLCO1B1 (Q9Y6L6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data and structural context.
I39N (p.Ile39Asn) variant details
- p.Ile39Asn
- ESP rs370556411
- ExAC rs370556411
- TOPMed rs370556411
- gnomAD rs370556411
- Missense
- Variant Prioritization Score for Impact Estimate 0.33
- REVEL 0.33
- CADD 23.00
- PolyPhen-2 0.93
- SIFT 0.00
- Most common in the 1KG:IBS population (allele frequency 0.017)
- Structural context available