The pathogenic mutations were downloaded from the publicly-available dataset (ClinVar). Then the coding variants are annotated and get the GERP score and related gene name. User then can provide gene name to get the list and type of pathogenic variant on that gene. Firstly ask: "Alexa, ask pathogen mutation", followed by "show me a random mutation" or "tell me a mutation from CTCF" (or another gene name).
“Alexa, ask pathogen mutation to tell me mutations from CTCF”
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