G19D (p.Gly19Asp) variant of ABCG2 (Q9UNQ0)
G19D (p.Gly19Asp) in ABCG2 (Q9UNQ0) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G19D (p.Gly19Asp) variant details
- p.Gly19Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available