D109V (p.Asp109Val) variant of MCM6 (Q14566)
D109V (p.Asp109Val) in MCM6 (Q14566) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
D109V (p.Asp109Val) variant details
- p.Asp109Val
- gnomAD rs1680176201
- Missense
- Variant Prioritization Score for Impact Estimate 0.416
- REVEL 0.27
- CADD 24.00
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available