Documentation

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Publication Details

Results for Valentino2021:

Summary

Title	Exome Sequencing in 200 Intellectual Disability/Autistic Patients: New Candidates and Atypical Presentations
Authors	Valentino, F., Bruno, L.P., Doddato, G., Giliberti, A., Tita, R., Resciniti, S., Fallerini, C., Bruttini, M., Lo Rizzo, C., Mencarelli, M.A., Mari, F., Pinto, A.M., Fava, F., Baldassarri, M., Fabbiani, A., Lamacchia, V., Benetti, E., Zguro, K., Furini, S., Renieri, A., Ariani, F.
Technology	Whole Exome Sequencing
Variant source	Supp Table 2, Table 1, Table 2
Cohorts	200 enrolled families with at least one proband, totaling 574 individuals
Design	Simplex, Multiplex
URL	https://dx.doi.org/10.3390/brainsci11070936
Pubmed	34356170
Subject count	11 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 count	11
Curation notes	View

Breakdown by exonic function

Function	Variant Count
frameshift deletion	1
frameshift insertion	1
nonsynonymous SNV	4
splicing	2
stopgain	3

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.