Figure 5.

'Gene details' table in EVA. For a given gene (here NOTCH1) it is possible: (top) to get information about its chromosomic laction, links to useful public databases (Entrez, Pubmed, CCDS, OMIM), areas not captured during the pre sequencing protocol and links to interpretation tools (SNPper, Polyphen 2, Mutation Taster); (bottom): the categorized variations located in that gene for all the individuals of a project.

Coutant et al. BMC Bioinformatics 2012 13(Suppl 14):S9   doi:10.1186/1471-2105-13-S14-S9