E111Q (p.Glu111Gln) variant of TNFRSF9 (Q07011)
E111Q (p.Glu111Gln) 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.
E111Q (p.Glu111Gln) variant details
- p.Glu111Gln
- NCI-TCGA Cosmic COSV6634
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available