P42S (p.Pro42Ser) variant of TNFRSF13B (O14836)
P42S (p.Pro42Ser) in TNFRSF13B (O14836) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
P42S (p.Pro42Ser) variant details
- p.Pro42Ser
- NCI-TCGA Cosmic COSV5542
- cosmic curated COSV55427
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.