R165W (p.Arg165Trp) variant of E2F1 (Transcription factor E2F1)
R165W (p.Arg165Trp) 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.
R165W (p.Arg165Trp) variant details
- p.Arg165Trp
- NCI-TCGA Cosmic COSV5853
- Ensembl rs2122546139
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available