A111T (p.Ala111Thr) variant of ABCG2 (Q9UNQ0)
A111T (p.Ala111Thr) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
A111T (p.Ala111Thr) variant details
- p.Ala111Thr
- ExAC rs757687597
- TOPMed rs757687597
- gnomAD rs757687597
- Missense
- Variant Prioritization Score for Impact Estimate 0.353
- REVEL 0.34
- CADD 21.50
- PolyPhen-2 0.83
- SIFT 0.12
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available