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

Table 4

Extra mutations identified using the SureSeq Solid Tumour panel in FFPE gDNA.

Cell line	Gene	Variant	Variant allele frequency	Read depth
639V	TP53 (NM_000546.5)	c.113C>A	5.10%	294
KU-19-19		c.1129A>C	6.64%	271
LUCC3		c.1129A>C	5.10%	255