R69W (p.Arg69Trp) variant of HAVCR2 (Q8TDQ0)
R69W (p.Arg69Trp) in HAVCR2 (Q8TDQ0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
R69W (p.Arg69Trp) variant details
- p.Arg69Trp
- NCI-TCGA Cosmic COSV1003
- cosmic curated COSV10032
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.