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. 2019 May 17;105(2):358–365. doi: 10.3324/haematol.2019.219386

Figure 1.

Figure 1.

Somatic mutations identified in coding exons of five patients in the proximally exposed group. Each numerical number on the bar charts represents the number of variants of each mutation type identified using whole exome sequencing. No splice site variants were identified among these five patients. U-WES: unbiased-whole exome sequencing.