Q29R (p.Gln29Arg) variant of ABCC2 (Q92887)
Q29R (p.Gln29Arg) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.59 / 1. The record also includes population frequency data and structural context.
Q29R (p.Gln29Arg) variant details
- p.Gln29Arg
- ExAC rs761583735
- gnomAD rs761583735
- Missense
- Variant Prioritization Score for Impact Estimate 0.594
- CADD 22.80
- PolyPhen-2 0.22
- SIFT 0.12
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available