V151D (p.Val151Asp) variant of E2F1 (Transcription factor E2F1)
V151D (p.Val151Asp) in E2F1 (Transcription factor E2F1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
V151D (p.Val151Asp) variant details
- p.Val151Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.