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.