I78V (p.Ile78Val) variant of ABCG2 (Q9UNQ0)
I78V (p.Ile78Val) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
I78V (p.Ile78Val) variant details
- p.Ile78Val
- TOPMed rs1724971978
- Missense
- Variant Prioritization Score for Impact Estimate 0.456
- REVEL 0.41
- CADD 24.00
- PolyPhen-2 0.89
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available