V162A (p.Val162Ala) variant of E2F1 (Transcription factor E2F1)
V162A (p.Val162Ala) in E2F1 (Transcription factor E2F1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V162A (p.Val162Ala) variant details
- p.Val162Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available