A77T (p.Ala77Thr) variant of ABCG2 (Q9UNQ0)
A77T (p.Ala77Thr) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.80 / 1. The record also includes population frequency data and structural context.
A77T (p.Ala77Thr) variant details
- p.Ala77Thr
- ExAC rs747978861
- TOPMed rs747978861
- gnomAD rs747978861
- Missense
- Variant Prioritization Score for Impact Estimate 0.805
- REVEL 0.83
- CADD 25.70
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the East Asian population (allele frequency 0.0001)
- Structural context available