Discriminating a common somatic ASXL1 mutation (c.1934dup; p.G646Wfs*12) from artifact in myeloid malignancies using NGS

Leukemia. 2018 Aug;32(8):1874-1878. doi: 10.1038/s41375-018-0193-y. Epub 2018 Jun 29.
No abstract available

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Artifacts
  • Biomarkers, Tumor / genetics*
  • Diagnosis, Differential
  • Gene Duplication*
  • Hematologic Neoplasms / diagnosis*
  • Hematologic Neoplasms / genetics
  • High-Throughput Nucleotide Sequencing / methods
  • High-Throughput Nucleotide Sequencing / standards*
  • Humans
  • Molecular Diagnostic Techniques
  • Mutation*
  • Myeloproliferative Disorders / diagnosis*
  • Myeloproliferative Disorders / genetics
  • Prognosis
  • Repressor Proteins / genetics*

Substances

  • ASXL1 protein, human
  • Biomarkers, Tumor
  • Repressor Proteins