New Step by Step Map For thr777
New Step by Step Map For thr777
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The result of your variant on RNA or protein functionality, depending on experimental proof from submitters.
This value is calculated by NCBI according to knowledge from submitters. Go through our policies for calculating the assessment standing. The quantity of submissions which add to this critique standing is revealed in parentheses.
This day represents the final time this VCV history was up-to-date. The update may be on account of an update to among the list of bundled submitted information (SCVs), or on account of an update that ClinVar produced for the variant like adding HGVS expressions or maybe a rs number.
The global insignificant allele frequency calculated by the a thousand Genomes Task. The minor allele at this area is indicated in parentheses and should be diverse from your allele represented by this VCV file.
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Examine our principles for calculating the thr777 assessment standing. This column also includes a website link for the submitter’s assertion criteria if provided, and the gathering method.
The number of variants in ClinVar that happen to be contained in this gene, by using a backlink to watch the listing of variants.
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The amount of variants in ClinVar for this gene, which includes smaller variants in the gene and larger CNVs that overlap or fully include the gene.
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Stars depict the critique standing, or the level of review supporting the submitted (SCV) report. This worth is calculated by NCBI based upon facts from your submitter.