V19G (p.Val19Gly) variant of ALK (ALK tyrosine kinase receptor)
V19G (p.Val19Gly) 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.
V19G (p.Val19Gly) variant details
- p.Val19Gly
- rs2148444032
- ClinGen CA346590774
- ClinVar RCV004516682
- Ensembl rs2148444032
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- MutPred 0.33
- 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)