Table 1 – Decreased polymorphism at the for locus in
asexual population. Characterisation of for SNPs that differed
in frequency across sexual and asexual populations: transcript column
indicated the isoform cluster containing the variant; the region and
position column indicated if the SNP is located within the coding
sequence (CDS) or outside (UTR) and its position considering the longest
transcript sequence figured into bracket; polymorphism indicated the
different bases identified at the SNP position; sexual and asexual
population columns contained the number of reads corresponding to each
variant in brackets. In the last two columns information related to the
type of mutation (synonymous or non-synonymous, when SNPs occurred
within CDS), and aminoacid change (only for the non-synonymous mutation)
are informed.