S46N (p.Ser46Asn) variant of TNFRSF9 (Q07011)
S46N (p.Ser46Asn) in TNFRSF9 (Q07011) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S46N (p.Ser46Asn) variant details
- p.Ser46Asn
- NCI-TCGA Cosmic COSV6634
- cosmic curated COSV66349
- TOPMed rs1639859146
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available