N66I (p.Asn66Ile) variant of ABCG2 (Q9UNQ0)
N66I (p.Asn66Ile) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
N66I (p.Asn66Ile) variant details
- p.Asn66Ile
- ExAC rs746978396
- gnomAD rs746978396
- Missense
- Variant Prioritization Score for Impact Estimate 0.467
- REVEL 0.43
- CADD 23.50
- PolyPhen-2 0.71
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 7.2e-06)
- Structural context available