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.
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