C148W (p.Cys148Trp) variant of TERF2 (Q15554)
C148W (p.Cys148Trp) in TERF2 (Q15554) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
C148W (p.Cys148Trp) variant details
- p.Cys148Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available