Table 2: Additional mutations identified using the SureSeq Solid Tumour panel in fresh gDNA samples.

Cell lineGeneVariantVariant allele frequencyRead depth

97-7TP53 (NM_000546.5)c.853G>A6.22%225
639Vc.1129A>C6.48%355
KU-19-19c.1129A>C7.61%197