P86R (p.Pro86Arg) variant of ADH1B (P00325)
P86R (p.Pro86Arg) in ADH1B (P00325) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
P86R (p.Pro86Arg) variant details
- p.Pro86Arg
- ExAC rs199926877
- TOPMed rs199926877
- gnomAD rs199926877
- Missense
- Variant Prioritization Score for Impact Estimate 0.426
- REVEL 0.20
- CADD 27.20
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Middle Eastern population (allele frequency 0.00017)
- Structural context available