G118W (p.Gly118Trp) variant of VSIR (Q9H7M9)
G118W (p.Gly118Trp) in VSIR (Q9H7M9) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G118W (p.Gly118Trp) variant details
- p.Gly118Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available