K97N (p.Lys97Asn) variant of ABCG2 (Q9UNQ0)
K97N (p.Lys97Asn) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
K97N (p.Lys97Asn) variant details
- p.Lys97Asn
- TOPMed rs1368759015
- gnomAD rs1368759015
- Missense
- Variant Prioritization Score for Impact Estimate 0.574
- REVEL 0.49
- CADD 23.40
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available