V7A (p.Val7Ala) variant of ADH1B (P00325)
V7A (p.Val7Ala) in ADH1B (P00325) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
V7A (p.Val7Ala) variant details
- p.Val7Ala
- TOPMed rs1160577696
- gnomAD rs1160577696
- Missense
- Variant Prioritization Score for Impact Estimate 0.292
- REVEL 0.19
- CADD 21.80
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available