A29G (p.Ala29Gly) variant of ALK (ALK tyrosine kinase receptor)
A29G (p.Ala29Gly) in ALK (ALK tyrosine kinase receptor) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
A29G (p.Ala29Gly) variant details
- p.Ala29Gly
- Ensembl rs1667969126
- NCI-TCGA TCGA novel
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available