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Article

The most commonly reported variant in ASXL1 (c.1934dupG;p.Gly646TrpfsX12) is not a somatic alteration

1 Jul 2010

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 20596031
DOI: 10.1038/leu.2010.144

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Related research

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Click a neighbor to travelStep 1 · 12 closest

The most commonly reported variant in ASXL1 (c.1934dupG;p.Gly646TrpfsX12) is not a somatic alterationPMID 20596031Read ↗

Frequent ASXL1 mutations in children and young adults with chronic myeloid leukemia.Semantic proximity Read ↗

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

ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism.Semantic proximity Read ↗

Highly variable mutational profile of ASXL1 in myelofibrosis.Semantic proximity Read ↗

ASXL1 mutation in clonal hematopoiesisSemantic proximity Read ↗

[Clinical Characteristics and Prognosis of Acute Myeloid Leukemia Patients with ASXL1 Gene Mutation].Semantic proximity Read ↗

ASXL1 mutations are infrequent in young patients with primary acute myeloid leukemia and their detection has a limited role in therapeutic risk stratification.Semantic proximity Read ↗

Clinical molecular testing for ASXL1 c.1934dupG p.Gly646fs mutation in hematologic neoplasms in the NGS eraSemantic proximity Read ↗

ASXL1 mutations are prognostically significant in PMF, but not MF following essential thrombocythemia or polycythemia vera.Semantic proximity Read ↗

WASPbase: a database of WAS- and XLT-causing mutations.Semantic proximity Read ↗

A novel de-novo frameshift mutation of the ASXL1 gene in a classic case of Bohring-Opitz syndrome.Semantic proximity Read ↗

BTKbase: a database of XLA-causing mutations. International Study Group.Semantic proximity Read ↗

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