![]() ![]() Workflow Using the New Variation Viewer to Explore Human Genetic Variation. Each segment was then evaluated for the following criteria: save. Presented August 13, 2014.NCBI Webinars YouTube playlist. Variation viewer shows where variations occur at the chromosome and gene level, followed by a table of each individual variation: Click on the View below to open up a live version: Protein change: P167L Links: dbSNP: rs886051020 NCBI 1000 Genomes Browser: rs886051020 Molecular consequence: NM_005678.5:c.*712C>T - 3 prime UTR variant - NM_001349454.2:c.524C>T - missense variant - The Single Nucleotide Polymorphism Database (dbSNP) is a free public archive for genetic variation within and across different species developed and hosted by the National Center for Biotechnology Information (NCBI) in collaboration with the National Human Genome Research Institute (NHGRI). Explore genetic variations and their clinical significance.
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