F97Y (p.Phe97Tyr) variant of MCM6 (Q14566)
F97Y (p.Phe97Tyr) in MCM6 (Q14566) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
F97Y (p.Phe97Tyr) variant details
- p.Phe97Tyr
- rs376597944
- ClinGen CA1889317
- ClinVar RCV004419251
- ESP rs376597944
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.349
- REVEL 0.17
- CADD 22.70
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available