T17S (p.Thr17Ser) variant of ABCG2 (Q9UNQ0)
T17S (p.Thr17Ser) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
T17S (p.Thr17Ser) variant details
- p.Thr17Ser
- gnomAD rs1313475538
- Missense
- Variant Prioritization Score for Impact Estimate 0.183
- REVEL 0.13
- CADD 3.43
- PolyPhen-2 0.00
- SIFT 0.40
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available