A69G (p.Ala69Gly) variant of MCM3 (P25205)
A69G (p.Ala69Gly) 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 and structural context.
A69G (p.Ala69Gly) variant details
- p.Ala69Gly
- TOPMed rs1477822068
- gnomAD rs1477822068
- Missense
- Variant Prioritization Score for Impact Estimate 0.737
- CADD 24.70
- PolyPhen-2 0.03
- SIFT 0.07
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available