S88W (p.Ser88Trp) variant of ABCG2 (Q9UNQ0)
S88W (p.Ser88Trp) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.71 / 1. The record also includes population frequency data and structural context.
S88W (p.Ser88Trp) variant details
- p.Ser88Trp
- ESP rs200415908
- ExAC rs200415908
- TOPMed rs200415908
- gnomAD rs200415908
- Missense
- Variant Prioritization Score for Impact Estimate 0.713
- REVEL 0.75
- CADD 25.00
- PolyPhen-2 0.99
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available