Considerations To Know About thr777
Considerations To Know About thr777
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The outcome from the variant on RNA or protein functionality, according to experimental evidence from submitters.
This worth is calculated by NCBI based upon details from submitters. Browse our policies for calculating the evaluation standing. The amount of submissions which contribute to this evaluate position is demonstrated in parentheses.
This date represents the last time this VCV document was current. The update could possibly be as a result of an update to on the list of incorporated submitted information (SCVs), or due to an update that ClinVar designed into the variant such as introducing HGVS expressions or simply a rs variety.
The global small allele frequency calculated because of the a thousand Genomes Task. The minor allele at this site is indicated in parentheses and should be different through the allele represented by this VCV history.
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There are no citations for germline classification of the variant in ClinVar. If you know of citations for this variation, please think about submitting that information to ClinVar.
The submitting Group for this submitted (SCV) document. This column also includes the SCV accession and version selection, the date this SCV first appeared in ClinVar, as well as the date thr777 this SCV was very last current in ClinVar.
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Stars characterize the aggregate assessment status, or the extent of assessment supporting the aggregate germline classification for this VCV report.
The volume of variants in ClinVar for this gene, like smaller variants in the gene and bigger CNVs that overlap or completely comprise the gene.
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Stars signify the assessment position, or the extent of critique supporting the submitted (SCV) history. This benefit is calculated by NCBI dependant on facts from the submitter.