R55G (p.Arg55Gly) variant of ABCC2 (Q92887)
R55G (p.Arg55Gly) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
R55G (p.Arg55Gly) variant details
- p.Arg55Gly
- ExAC rs768214282
- gnomAD rs768214282
- Missense
- Variant Prioritization Score for Impact Estimate 0.389
- CADD 16.40
- PolyPhen-2 0.00
- SIFT 0.21
- Most common in the East Asian population (allele frequency 5e-05)
- Structural context available