Y69H (p.Tyr69His) variant of TNFRSF1A (P19438)
Y69H (p.Tyr69His) in TNFRSF1A (P19438) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
Y69H (p.Tyr69His) variant details
- p.Tyr69His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available