Table 3.
Examples of mutation frequencies in (pediatric) tumors
Malignancy | Mutations (range) | Reference |
---|---|---|
AMLa | 0.37 per Mb (0.01–10) of coding sequence | Lawrence et al., Nature 2013 |
Ependymoma, intracranialb | 12.8 ± 10.6 mutations (range 5 to 34) per tumor | Bettegowda et al., Oncotarget 2013 |
Ependymoma, spinal cordb | 12.9 ± 6.4 mutations (range 2 to 23) per tumor | Bettegowda et al., Oncotarget 2013 |
Ewinga | 0.15 per Mb of coding sequence | Brohl et al., PLoS Genet 2014 |
Glioblastoma multiformeb | 1.4 per Mb | Cancer Genome Atlas Research Network, Nature 2008 |
Glioblastoma, non-brainstem pediatric | 23.5 ± 11.2 mutations (range 4–46) per tumor | Bettegowda et al., Oncotarget 2013 |
MDSb | 3 (0–12) mutations per sample in 104 cancer genes | Haferlach et al., Leukemia 2014 |
Medulloblastoma | 8.3 non-synonymous SNVs per sample 0.35 non-silent mutations per megabase |
Parsons et al., Science 2011 Pugh et al., Nature 2012 |
Neuroblastoma | 0.60 per Mb of coding regions | Pugh et al., Nature Genet 2013 |
Rhabdoid cancers | 0.19 per Mb (0–0.45) of coding regions | Lee et al., J Clin Invest 2012 |
Xanthoastrocytoma, pleomorphicb | 9.5 ± 8.5 mutations (range 1 to 28) per tumor | Bettegowda et al., Oncotarget 2013 |
aTumor samples not specified
bDescribed in adult tumor samples