H96P (p.His96Pro) variant of TNFRSF13B (O14836)
H96P (p.His96Pro) in TNFRSF13B (O14836) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
H96P (p.His96Pro) variant details
- p.His96Pro
- NCI-TCGA Cosmic COSV5542
- cosmic curated COSV55428
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.