N42T (p.Asn42Thr) variant of TNFRSF9 (Q07011)
N42T (p.Asn42Thr) 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.
N42T (p.Asn42Thr) variant details
- p.Asn42Thr
- NCI-TCGA Cosmic COSV6634
- cosmic curated COSV66348
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available