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Representative single-nucleotide variations (SNVs) observed in cell lines. (A) PC9; +49C>T (variant allele frequency (VAF]): 8%) and (B) MKN45; +52A>G (VAF: 47%) detected by next-generation sequencing. (C,D) Sanger electropherograms depicting SNVs PC9, +49C>T (C) and MKN45, +52A>G (D).
