V59M (p.Val59Met) variant of ADH1B (P00325)
V59M (p.Val59Met) in ADH1B (P00325) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.05 / 1. The record also includes population frequency data and structural context.
V59M (p.Val59Met) variant details
- p.Val59Met
- TOPMed rs1733934481
- gnomAD rs1733934481
- Missense
- Variant Prioritization Score for Impact Estimate 0.0465
- REVEL 0.03
- CADD 0.09
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available