G26R (p.Gly26Arg) variant of ALK (ALK tyrosine kinase receptor)
G26R (p.Gly26Arg) 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 variant effect predictions, published literature, and structural context.
G26R (p.Gly26Arg) variant details
- p.Gly26Arg
- rs1060500214
- ClinGen CA346590737
- ClinVar RCV003358400
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- MutPred 0.15
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)