I39M (p.Ile39Met) variant of SLCO1B1 (Q9Y6L6)
I39M (p.Ile39Met) in SLCO1B1 (Q9Y6L6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
I39M (p.Ile39Met) variant details
- p.Ile39Met
- gnomAD rs1322023824
- Missense
- Variant Prioritization Score for Impact Estimate 0.121
- REVEL 0.11
- CADD 7.64
- Most common in the Non-Finnish European population (allele frequency 1.6e-05)
- Structural context available