Next-generation sequencing traces human induced pluripotent stem cell lines clonally generated from heterogeneous cancer tissue

Table 6 Chromosome number, genome position, reference vs single-nucleotide variant, novelty vs dbSNP135, gene symbol, and mutation types of single-nucleotide variants

SNV No.	Chromo-some No.	Genome position	Ref.|SNV	Novel/known	Gene symbol	Mutation types
1	chr2	37336419	C|T	Novel	EIF2AK2	Missense
2	chr2	179408086	A|G	Novel	TTN	Missense
3	chr3	41705179	A|C	Novel	ULK4	Missense
4	chr5	112769527	C|T	Novel	TSSK1B	Missense
5	chr5	180048626	C|T	Novel	FLT4	Missense
6	chr6	31947203	T|C	Novel	STK19	Missense
7	chr7	23808650	G|T	Novel	STK31	Missense
8	chr7	98490141	G|C	Novel	TRRAP	Missense
9	chr12	1009680	C|T	Novel	WNK1	Missense
10	chr16	23690401	C|T	Novel	PLK1	Missense
11	chr17	8789811	G|A	Novel	PIK3R5	Nonsense
12	chr17	37881392	A|G	Novel	ERBB2	Missense
13	chr19	2046399	G|A	Novel	MKNK2	Missense

Ref.: The allele of the human reference genome hg19; SNV: Single-nucleotide variant.