N26D (p.Asn26Asp) variant of ABCG2 (Q9UNQ0)
N26D (p.Asn26Asp) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
N26D (p.Asn26Asp) variant details
- p.Asn26Asp
- ExAC rs758463101
- gnomAD rs758463101
- Missense
- Variant Prioritization Score for Impact Estimate 0.168
- REVEL 0.11
- CADD 10.70
- PolyPhen-2 0.01
- SIFT 0.06
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available