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. 2020 Jun 12;4:PO.20.00067. doi: 10.1200/PO.20.00067

FIG 2.

FIG 2.

Presence of the heterozygous DPYD p.R235Q (c.704G>A) variant in the patient’s germline genome. (A) Whole-genome sequencing reads identified the heterozygous single-nucleotide variant (C>T on the + DNA strand depicted) in DPYD. Sequencing reads matching the reference sequence are shown in gray. Data were displayed using Integrated Genomics Viewer. (B) Sanger sequencing confirmed the presence of the heterozygous single-nucleotide variant (G>A on the − coding strand) in DPYD as identified by the arrow.