G22D (p.Gly22Asp) variant of ABCG8 (Q9H221)
G22D (p.Gly22Asp) in ABCG8 (Q9H221) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G22D (p.Gly22Asp) variant details
- p.Gly22Asp
- cosmic curated COSV10723
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available