Towards a Next-Generation Sequencing Diagnostic Service for Tumour Genotyping: A Comparison of Panels and Platforms

Table 2

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

Cell line	Gene	Variant	Variant allele frequency	Read depth
97-7	TP53 (NM_000546.5)	c.853G>A	6.22%	225
639V		c.1129A>C	6.48%	355
KU-19-19		c.1129A>C	7.61%	197