H40Y (p.His40Tyr) variant of ABCG2 (Q9UNQ0)
H40Y (p.His40Tyr) in ABCG2 (Q9UNQ0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
H40Y (p.His40Tyr) variant details
- p.His40Tyr
- Ensembl rs561122328
- Missense
- Variant Prioritization Score for Impact Estimate 0.502
- REVEL 0.41
- CADD 22.40
- PolyPhen-2 0.17
- SIFT 0.05
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available