T17A (p.Thr17Ala) variant of ABCG2 (Q9UNQ0)
T17A (p.Thr17Ala) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
T17A (p.Thr17Ala) variant details
- p.Thr17Ala
- gnomAD rs1313475538
- Missense
- Variant Prioritization Score for Impact Estimate 0.23
- REVEL 0.20
- CADD 5.28
- PolyPhen-2 0.06
- SIFT 0.43
- Most common in the Non-Finnish European population (allele frequency 8.1e-06)
- Structural context available