Usage Disclaimer

This resource is not intended to be a comprehensive database of all human splicing mutations and the absence of a variant from the database should not be used to exclude the impact of a variant on splicing. While the variant(s) you have submitted may not be present, there is no substitute for appropriate laboratory testing and/or analyses of splicing mutation with robust bioinformatic methods. We recommend subscribing to MutationForecaster to evaluate the variants present in your genomic sequence for possible splicing effects.

Click here to return to the site homepage.