R96G (p.Arg96Gly) variant of ABCG2 (Q9UNQ0)
R96G (p.Arg96Gly) in ABCG2 (Q9UNQ0) 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.
R96G (p.Arg96Gly) variant details
- p.Arg96Gly
- ESP rs149339865
- ExAC rs149339865
- gnomAD rs149339865
- Missense
- Variant Prioritization Score for Impact Estimate 0.661
- REVEL 0.82
- CADD 26.10
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available