A genetic resource for genes and mutations related to epilepsy

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SNVs and InDels
Gene region	exonic intronic 5-UTR 3-UTR splicing intergenic upstream downstream
Effect	nonsynonymous        synonymous        frameshift        stoploss        stopgain
Mutation type	SNV        deletion        insertion
Inheritance	de novo        maternal        paternal        familial
Enter your gene symbol list (like this)

• Data content
• Chromosome
• Mutation type
• CNV
• Gender
• Age of onset
• Inheritance

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Last updated: Jul 6, 2014