G10V (p.Gly10Val) variant of ABCG8 (Q9H221)
G10V (p.Gly10Val) in ABCG8 (Q9H221) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
G10V (p.Gly10Val) variant details
- p.Gly10Val
- gnomAD rs1157337875
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available