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

From: CAISMOV24, a new human low-grade serous ovarian carcinoma 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
  1. Chr chromosome, Ref reference nucleic acid, Alt altered nucleic acid, Alt Freq frequency alteration