V37D (p.Val37Asp) variant of ADH1B (P00325)
V37D (p.Val37Asp) in ADH1B (P00325) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data and structural context.
V37D (p.Val37Asp) variant details
- p.Val37Asp
- ExAC rs775558705
- TOPMed rs775558705
- gnomAD rs775558705
- Missense
- Variant Prioritization Score for Impact Estimate 0.562
- REVEL 0.52
- CADD 25.10
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the Latino/Admixed American population (allele frequency 0.0002)
- Structural context available