To whom it may concern,

Currently, we perform an exom sequencing on samples from patients and tried to 
identify the mutations that caused a genetic disorder.  I just received the 
exom sequencing data with about 700 candidate variants.  The only information 
of these variants are chromosome and physical location.  I was wondering if 
there were some ways that I could import the list of these variants (chromosome 
and location) into UCSC browser and identified the genes that variants were 
located and pull out the sequences flanking the variants.  Is there any esay 
way to tell if a variant cause synonymous, nonsynonymous, or nonsense 
alterations?

Thanks.

Dongchuan Guo, PhD
Assistant Professor
Department of Internal Medicine
The University of Texas Medical School at Houston
Tel: 713-500-6849

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