Y89* (p.Tyr89Ter) variant of MCM6 (Q14566)
Y89* (p.Tyr89Ter) in MCM6 (Q14566) is a protein-truncating 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.
Y89* (p.Tyr89Ter) variant details
- p.Tyr89Ter
- gnomAD rs1462836086
- Stop Gained
- Variant Prioritization Score for Impact Estimate 0.416
- CADD 33.00
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available