N26S (p.Asn26Ser) variant of ABCG2 (Q9UNQ0)
N26S (p.Asn26Ser) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
N26S (p.Asn26Ser) variant details
- p.Asn26Ser
- cosmic curated COSV52945
- 1000Genomes rs373683219
- ESP rs373683219
- ExAC rs373683219
- Missense
- Variant Prioritization Score for Impact Estimate 0.0945
- REVEL 0.10
- CADD 0.46
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the 1KG:KHV population (allele frequency 0.005)
- Structural context available