N68Y (p.Asn68Tyr) variant of ABCG2 (Q9UNQ0)
N68Y (p.Asn68Tyr) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.59 / 1. The record also includes population frequency data and structural context.
N68Y (p.Asn68Tyr) variant details
- p.Asn68Tyr
- TOPMed rs1294004492
- Missense
- Variant Prioritization Score for Impact Estimate 0.595
- REVEL 0.57
- CADD 26.30
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available