Y49H (p.Tyr49His) variant of SLC18A2 (Q05940)
Y49H (p.Tyr49His) in SLC18A2 (Q05940) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
Y49H (p.Tyr49His) variant details
- p.Tyr49His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available