V8I (p.Val8Ile) variant of ABCG2 (Q9UNQ0)
V8I (p.Val8Ile) in ABCG2 (Q9UNQ0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data and structural context.
V8I (p.Val8Ile) variant details
- p.Val8Ile
- rs774014561
- ExAC rs774014561
- TOPMed rs774014561
- gnomAD rs774014561
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.31
- REVEL 0.12
- CADD 12.10
- PolyPhen-2 0.00
- SIFT 0.53
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available