C6R (p.Cys6Arg) variant of ABCC2 (Q92887)
C6R (p.Cys6Arg) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data and structural context.
C6R (p.Cys6Arg) variant details
- p.Cys6Arg
- TOPMed rs1208413085
- gnomAD rs1208413085
- Missense
- Variant Prioritization Score for Impact Estimate 0.659
- CADD 29.20
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available