G112C (p.Gly112Cys) variant of TERF2 (Q15554)
G112C (p.Gly112Cys) 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.
G112C (p.Gly112Cys) variant details
- p.Gly112Cys
- NCI-TCGA Cosmic COSV9965
- cosmic curated COSV99651
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available