Y39H (p.Tyr39His) variant of VKORC1 (Q9BQB6)
Y39H (p.Tyr39His) in VKORC1 (Q9BQB6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.79 / 1. The record also includes population frequency data and structural context.
Y39H (p.Tyr39His) variant details
- p.Tyr39His
- gnomAD rs2057315224
- Missense
- Variant Prioritization Score for Impact Estimate 0.795
- REVEL 0.88
- CADD 32.00
- Most common in the Non-Finnish European population (allele frequency 1.6e-05)
- Structural context available