Q38R (p.Gln38Arg) variant of MCM6 (Q14566)
Q38R (p.Gln38Arg) in MCM6 (Q14566) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
Q38R (p.Gln38Arg) variant details
- p.Gln38Arg
- 1000Genomes rs538983384
- ExAC rs538983384
- gnomAD rs538983384
- Missense
- Variant Prioritization Score for Impact Estimate 0.248
- REVEL 0.07
- CADD 19.90
- Most common in the 1KG:ESN population (allele frequency 0.0049)
- Structural context available