V199I (p.Val199Ile) variant of E2F1 (Transcription factor E2F1)
V199I (p.Val199Ile) in E2F1 (Transcription factor E2F1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data.
V199I (p.Val199Ile) variant details
- p.Val199Ile
- ExAC rs771638059
- TOPMed rs771638059
- gnomAD rs771638059
- Missense
- Variant Prioritization Score for Impact Estimate 0.122
- REVEL 0.02
- CADD 0.43
- PolyPhen-2 0.00
- SIFT 0.64
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)