BGI 5053 PDF

Personnel changes at BAM were also a decisive factor in our decision to rethink our UK equity allocation policy to avoid finding ourselves in a position where one manager could tilt the balance either through under or over-performance. SG has been retained in a new structure that divides the UK equity assets among three managers with equal portions, instead of two. George Harvey, head of sales and business development at BAM says it was an asset allocation review by LRT, not underperformance that led to Barings being fired. While the existential threat of climate change has dominated the agenda in recent years, the pandemic has renewed focus on social and governance issues. Site powered by Webvision Cloud. Skip to main content Skip to navigation.

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All alleles are reported in the Forward orientation. HGVS names are in the Aliases tab. Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors. For more information see Help documentation. The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted.

See here for details. The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology.

When no protein placement is available, only the transcript is listed. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible. Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession i. More information is available on the project page including descriptions, data access, and terms of use.

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. Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Current Build Released April 21, 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. Not Reported in ClinVar. 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 Sequence View not displayed for indexing robots.

East Asian. Ashkenazi Jewish. South Asian. Genetic variation in the Estonian population. UK 10K study - Twins. Latin American 1. Latin American 2. Genome of the Netherlands Release 5. Genome of the Netherlands. Northern Sweden. A Vietnamese Genetic Variation Database.

The Danish reference pan genome.

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LRT drops Baring AM from £500m UK equity mandate

All alleles are reported in the Forward orientation. HGVS names are in the Aliases tab. Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors. For more information see Help documentation.

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