D91G (p.Asp91Gly) variant of ABCG2 (Q9UNQ0)
D91G (p.Asp91Gly) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.73 / 1. The record also includes population frequency data and structural context.
D91G (p.Asp91Gly) variant details
- p.Asp91Gly
- cosmic curated COSV52946
- TOPMed rs755380197
- gnomAD rs755380197
- Missense
- Variant Prioritization Score for Impact Estimate 0.73
- REVEL 0.79
- CADD 28.00
- PolyPhen-2 0.65
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 7.2e-06)
- Structural context available