D148V (p.Asp148Val) variant of E2F1 (Transcription factor E2F1)
D148V (p.Asp148Val) in E2F1 (Transcription factor E2F1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
D148V (p.Asp148Val) variant details
- p.Asp148Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.