S77G (p.Ser77Gly) variant of E2F1 (Transcription factor E2F1)
S77G (p.Ser77Gly) in E2F1 (Transcription factor E2F1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data.
S77G (p.Ser77Gly) variant details
- p.Ser77Gly
- TOPMed rs1429701584
- gnomAD rs1429701584
- Missense
- Variant Prioritization Score for Impact Estimate 0.224
- REVEL 0.08
- CADD 16.60
- PolyPhen-2 0.00
- SIFT 0.40
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.0001)