A108V (p.Ala108Val) variant of E2F1 (Transcription factor E2F1)
A108V (p.Ala108Val) in E2F1 (Transcription factor E2F1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data.
A108V (p.Ala108Val) variant details
- p.Ala108Val
- TOPMed rs1159129500
- gnomAD rs1159129500
- Missense
- Variant Prioritization Score for Impact Estimate 0.14
- REVEL 0.07
- CADD 13.30
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)