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. 2012 Dec;97(12):1909–1915. doi: 10.3324/haematol.2012.064667

Table 1.

Molecular details of RUNX1 mutations in 94 CN-AML patients. Fifteen CN-AML patients carried RUNX1 mutations. Four out of these 15 patients had several RUNX1 mutations. Sequence variations in the cDNA and protein are indicated with reference to the longest isoform of RUNX1 (NM_001754.4). UPN: Unique Patient Number.

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