CAISMOV24, a new human low-grade serous ovarian carcinoma cell line

BMC Cancer

Table 4 Gene mutations without SNP location record and with high alteration frequencies in CAISMOV24 cell line

Gene	Chr	Position	Depth	Ref	Alt	Alt Freq	Variant Type
AKAP9	chr7	91,652,181	18	C	CAAC	0.39	inframe insertion
HIST1H1D, HIST1H2APS3	chr6	26,235,122	186	G	A	0.39	missense variant, downstream gene variant
AKAP12	chr6	151,674,121	585	A	AGGA	0.41	inframe insertion
SPEN	chr1	16,202,753	20	G	A	0.45	missense variant
NCOR2	chr12	124,812,039	117	G	T	0.47	missense variant
EP400	chr12	132,554,157	32	G	A	0.59	missense variant
ZNF687	chr1	151,259,035	5	G	C	0.60	missense variant, upstream gene variant
NOTCH1	chr9	139,393,579	38	C	T	0.63	missense variant
HMGA1, C6orf1	chr6	34,211,292	59	A	AA	0.78	frameshift variant, feature elongation, downstream gene variant
WHSC1L1	chr8	38,148,080	20	C	T	0.85	missense variant
KIF5B	chr10	32,311,775	7	C	G	1.00	splice donor variant
PPP2R1B	chr11	111,631,542	2	C	T	1.00	splice donor variant
RELN	chr7	103,230,181	2	T	C	1.00	missense variant
AKAP9	chr7	91,652,181	18	C	CAAC	0.39	inframe insertion
HIST1H1D, HIST1H2APS3	chr6	26,235,122	186	G	A	0.39	missense variant, downstream gene variant

Chr chromosome, Ref reference nucleic acid, Alt altered nucleic acid, Alt Freq frequency alteration

ISSN: 1471-2407