Why am I directed to curated evidence for a variant different than the one I searched for?

The indexed data in Mastermind is transcript-agnostic, meaning that articles containing cDNA or protein matches are matched to all valid transcripts for maximal sensitivity. Mastermind stores genomic coordinates and transcript information, and these data are used to inform and refine search results. In cases where no curated data is found for a specific search, users may be redirected to curated data for a similar variant on the canonical transcript. This can occur when the searched variant may have alternate nomenclature or is represented differently on another transcript.