G26A (p.Gly26Ala) variant of ALK (ALK tyrosine kinase receptor)
G26A (p.Gly26Ala) in ALK (ALK tyrosine kinase receptor) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
G26A (p.Gly26Ala) variant details
- p.Gly26Ala
- ExAC rs755942639
- gnomAD rs755942639
- Likely benign
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Likely benign (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available