The variant table lists short sequence variations like SNPs and indels found within the gene of interest (Figure 14). The table can be filtered by various facets, such as the consequence on the resultant protein, allele frequency or the evidence for the variant, using the filter buttons at the top.
Figure 14. View the variation table for all SNPs, insertions and deletions mapped to this gene.
NotesFor structural variation, such as copy number variation, see the structural variation view.