Q141P (p.Gln141Pro) variant of ABCG2 (Q9UNQ0)
Q141P (p.Gln141Pro) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
Q141P (p.Gln141Pro) variant details
- p.Gln141Pro
- ExAC rs769050167
- gnomAD rs769050167
- Missense
- Variant Prioritization Score for Impact Estimate 0.379
- REVEL 0.19
- CADD 25.60
- PolyPhen-2 0.61
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available