D71G (p.Asp71Gly) variant of TNFRSF1A (P19438)
D71G (p.Asp71Gly) 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.
D71G (p.Asp71Gly) variant details
- p.Asp71Gly
- NCI-TCGA Cosmic COSV5082
- cosmic curated COSV50828
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available