Publication Details

Results for Alvarez-Mora2016:

Title Comprehensive molecular testing in patients with high functioning autism spectrum disorder
AuthorsAlvarez-Mora, M.I., Calvo Escalona, R., Puig Navarro, O., Madrigal, I., Quintela, I., Amigo, J., Martinez-Elurbe, D., Linder-Lucht, M., Aznar Lain, G., Carracedo, A., Mila, M., Rodriguez-Revenga, L.
TechnologyTargeted sequencing
Variant sourceTable 2: Rare SNVs identified with amino acid changes, origin and allele frequencies from control population
Cohortscollection of Spanish ASD cases
Subject count21
The number of subjects for this study could not be determined directly from the variant data; the value given is that reported by the authors in the publication.
Variant event count24
Curation notesView
Breakdown by exonic function
FunctionVariant Count
nonframeshift insertion1
nonsynonymous SNV23

What am I looking at?

Summary: Information from the literature piece (e.g. Author, Publisher, DOI) and the study experimental design (e.g. sample size, source of probands, sequencing technology.) For a full list of sources of variants, be sure to check out the publications page. Documentation and description of our work can be found on the help page.

Breakdown by exonic function: We annotated the variants with an effect prediction using ANNOVAR. The functions are categories of variants, such as frameshift variants (i.e. frameshift_elongation (SO:0001909)), loss/gain of stop codon, SNVs and non-frameshift variants. See the full list of possible annotations for exonic variants in the documentation.