V49G (p.Val49Gly) variant of HAVCR2 (Q8TDQ0)
V49G (p.Val49Gly) in HAVCR2 (Q8TDQ0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
V49G (p.Val49Gly) variant details
- p.Val49Gly
- NCI-TCGA Cosmic COSV5715
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.