I108T (p.Ile108Thr) variant of ABCG2 (Q9UNQ0)
I108T (p.Ile108Thr) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.79 / 1. The record also includes population frequency data and structural context.
I108T (p.Ile108Thr) variant details
- p.Ile108Thr
- TOPMed rs1361699841
- gnomAD rs1361699841
- Missense
- Variant Prioritization Score for Impact Estimate 0.79
- REVEL 0.91
- CADD 25.00
- PolyPhen-2 0.94
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 0.00018)
- Structural context available