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. 2022 Sep 9;17(9):e0274335. doi: 10.1371/journal.pone.0274335

Fig 2. Chromatograms of novel duplications and an insertion detected in PCG patients.

Fig 2

A) A homozygous variant c.629dup detected in PCG050 leading to p.Gly211Argfs*13. B) Chromatogram of homozygous variant c.287dup detected in PCG053 that resulted in protein change i.e., p.Leu97Alafs*127. C) Sequence chromatogram of homozygous variant c.662dup leading to protein change p.Arg222Profs*2 in PCG054. D) Chromatogram showing c.789dup homozygous variant in PCG063 leading to a p.Leu264Alafs*63. E) Homozygous insertion c.758_759insA detected in PCG059 resulting in p.Val254Glyfs*73. All the chromatograms on left side indicate normal sequence while right side of figure shows mutated chromatograms.