G3C (p.Gly3Cys) variant of TNFRSF13B (O14836)
G3C (p.Gly3Cys) in TNFRSF13B (O14836) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
G3C (p.Gly3Cys) variant details
- p.Gly3Cys
- NCI-TCGA Cosmic COSV9989
- cosmic curated COSV99891
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.