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Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change.

The column "Note" can have two values: "diff" means that there is a difference between the reference allele variation interval at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence s of this variation in other HGVS names not labeled as "rev".

We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Other supporting variations are listed in the table without ss. The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements. Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Current Build Released April 9, Genomic Placements. Sequence name Change GRCh Help Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele.

Allele: C allele ID: Release Version: Help Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. No publications for rs Help The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements. Genome context:. WordPress Shortcode. Share Email. Top clipped slide. Technology , Business. Download Now Download Download to read offline. Automatisation et gestion de configuration : Les avantages pour la supervision.

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