V36G (p.Val36Gly) variant of MCM3 (P25205)
V36G (p.Val36Gly) in MCM3 (P25205) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.69 / 1. The record also includes population frequency data.
V36G (p.Val36Gly) variant details
- p.Val36Gly
- TOPMed rs1313677046
- Missense
- Variant Prioritization Score for Impact Estimate 0.688
- CADD 32.00
- PolyPhen-2 0.87
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 6e-05)