R111G (p.Arg111Gly) variant of TERF2 (Q15554)
R111G (p.Arg111Gly) 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.
R111G (p.Arg111Gly) variant details
- p.Arg111Gly
- NCI-TCGA Cosmic COSV5474
- cosmic curated COSV54748
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available