D148N (p.Asp148Asn) variant of E2F1 (Transcription factor E2F1)
D148N (p.Asp148Asn) in E2F1 (Transcription factor E2F1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
D148N (p.Asp148Asn) variant details
- p.Asp148Asn
- NCI-TCGA Cosmic COSV5853
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.