G190W (p.Gly190Trp) variant of ITPR2 (Q14571)
G190W (p.Gly190Trp) in ITPR2 (Q14571) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G190W (p.Gly190Trp) variant details
- p.Gly190Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available