D22G (p.Asp22Gly) variant of ABCC2 (Q92887)
D22G (p.Asp22Gly) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.69 / 1. The record also includes population frequency data and structural context.
D22G (p.Asp22Gly) variant details
- p.Asp22Gly
- ExAC rs769292618
- TOPMed rs769292618
- gnomAD rs769292618
- Missense
- Variant Prioritization Score for Impact Estimate 0.689
- CADD 32.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available