N119T (p.Asn119Thr) variant of HAVCR2 (Q8TDQ0)
N119T (p.Asn119Thr) in HAVCR2 (Q8TDQ0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
N119T (p.Asn119Thr) variant details
- p.Asn119Thr
- NCI-TCGA Cosmic COSV1003
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.