Y39H (p.Tyr39His) variant of ABCC2 (Q92887)
Y39H (p.Tyr39His) in ABCC2 (Q92887) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data, published literature, and structural context.
Y39H (p.Tyr39His) variant details
- p.Tyr39His
- gnomAD 10-99784689-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.604
- CADD 24.50
- PolyPhen-2 0.17
- SIFT 0.00
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available