G132V (p.Gly132Val) variant of ABCG2 (Q9UNQ0)
G132V (p.Gly132Val) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data and structural context.
G132V (p.Gly132Val) variant details
- p.Gly132Val
- TOPMed rs1026965987
- gnomAD rs1026965987
- Missense
- Variant Prioritization Score for Impact Estimate 0.755
- REVEL 0.88
- CADD 23.10
- PolyPhen-2 0.68
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 4.4e-05)
- Structural context available