P32H (p.Pro32His) variant of TNFRSF1A (P19438)
P32H (p.Pro32His) 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.
P32H (p.Pro32His) variant details
- p.Pro32His
- NCI-TCGA Cosmic COSV5082
- cosmic curated COSV50828
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available