The Fact About thr777 That No One Is Suggesting
The Fact About thr777 That No One Is Suggesting
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The influence on the variant on RNA or protein function, dependant on experimental evidence from submitters.
This worth is calculated by NCBI determined by data from submitters. Browse our procedures for calculating the critique standing. The amount of submissions which add to this overview position is shown in parentheses.
There isn't a practical proof in ClinVar for this variation. In case you have generated useful information for this variation, be sure to take into account publishing that facts to ClinVar.
The global slight allele frequency calculated by the one thousand Genomes Challenge. The small allele at this locale is indicated in parentheses and may be diverse from the allele represented by this VCV file.
The condition for your classification, provided by the submitter for this submitted (SCV) document. This column also involves the impacted status and allele origin of people noticed using this variant.
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There isn't any citations for germline classification of the variant in ClinVar. If you are aware of of citations for this variation, be sure to consider publishing that facts to ClinVar.
The publishing Business for this submitted (SCV) record. This column also includes the SCV accession and Edition number, the date this SCV to start with appeared in ClinVar, along with the day that this SCV was very last updated in ClinVar.
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Stars represent the combination assessment status, or the extent of assessment supporting the combination germline classification for this VCV file.
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Stars depict thr777 the critique standing, or the level of review supporting the submitted (SCV) file. This price is calculated by NCBI dependant on details within the submitter.