R46W (p.Arg46Trp) variant of MCM3 (P25205)
R46W (p.Arg46Trp) in MCM3 (P25205) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.74 / 1. The record also includes population frequency data.
R46W (p.Arg46Trp) variant details
- p.Arg46Trp
- TOPMed rs1242946313
- gnomAD rs1242946313
- Missense
- Variant Prioritization Score for Impact Estimate 0.738
- CADD 33.00
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)