Y168C (p.Tyr168Cys) variant of E2F1 (Transcription factor E2F1)
Y168C (p.Tyr168Cys) 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.
Y168C (p.Tyr168Cys) variant details
- p.Tyr168Cys
- NCI-TCGA Cosmic COSV5853
- Ensembl rs1762881056
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available