R13W (p.Arg13Trp) variant of MCM3 (P25205)
R13W (p.Arg13Trp) in MCM3 (P25205) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.65 / 1. The record also includes population frequency data.
R13W (p.Arg13Trp) variant details
- p.Arg13Trp
- ExAC rs753057016
- TOPMed rs753057016
- gnomAD rs753057016
- Missense
- Variant Prioritization Score for Impact Estimate 0.65
- CADD 31.00
- PolyPhen-2 0.95
- SIFT 0.00
- Most common in the REMAINING population (allele frequency 1.7e-05)