A145T (p.Ala145Thr) variant of ABCG2 (Q9UNQ0)
A145T (p.Ala145Thr) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
A145T (p.Ala145Thr) variant details
- p.Ala145Thr
- TOPMed rs947226023
- gnomAD rs947226023
- Missense
- Variant Prioritization Score for Impact Estimate 0.42
- REVEL 0.16
- CADD 25.70
- PolyPhen-2 0.94
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available