Publication Details

Results for Xiong2019:

Title Neurological Diseases With Autism Spectrum Disorder: Role of ASD Risk Genes
AuthorsXiong, J., Chen, S., Pang, N., Deng, X., Yang, L., He, F., Wu, L., Chen, C., Yin, F., Peng, J.
TechnologyWhole exome sequencing, targeted sequencing
Variant sourceTable S1: Clinical features and genetic information of all subjects in the cohort (ASD Group)
CohortsPediatric department of Xiangya Hospital at Central South University (2014-2018)
Subject count47
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 count51
Curation notesView
Breakdown by exonic function
FunctionVariant Count
frameshift deletion8
frameshift insertion4
nonsynonymous SNV27

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.