L66V (p.Leu66Val) variant of ABCC2 (Q92887)
L66V (p.Leu66Val) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
L66V (p.Leu66Val) variant details
- p.Leu66Val
- TOPMed rs2037677277
- gnomAD rs2037677277
- Missense
- Variant Prioritization Score for Impact Estimate 0.274
- CADD 12.70
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available