V199A (p.Val199Ala) variant of E2F1 (Transcription factor E2F1)
V199A (p.Val199Ala) in E2F1 (Transcription factor E2F1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
V199A (p.Val199Ala) variant details
- p.Val199Ala
- NCI-TCGA Cosmic COSV9986
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.