C110F (p.Cys110Phe) variant of HAVCR2 (Q8TDQ0)
C110F (p.Cys110Phe) in HAVCR2 (Q8TDQ0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
C110F (p.Cys110Phe) variant details
- p.Cys110Phe
- NCI-TCGA Cosmic COSV1044
- TOPMed rs1757256363
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.