D127G (p.Asp127Gly) variant of TNFRSF9 (Q07011)
D127G (p.Asp127Gly) in TNFRSF9 (Q07011) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D127G (p.Asp127Gly) variant details
- p.Asp127Gly
- NCI-TCGA Cosmic COSV1010
- cosmic curated COSV10109
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available