Whole genome sequencing reveals 9 single nucleotide variants (SNVs) that lie outside predicted open reading frames between early clinical isolate A and late clinical isolate G.

All high-confidence SNVs that were found outside of predicted open reading frames between early clinical isolate A and late clinical isolate G are listed. Their genome coordinates, the base pair substitution, the most proximal gene(s), the position of the mutation relative to that gene, as well as the gene homolog in S. cerevisiae are listed.