Not known Facts About thr777
Not known Facts About thr777
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The outcome of your variant on RNA or protein purpose, based upon experimental evidence from submitters.
This value is calculated by NCBI based on details from submitters. Examine our policies for calculating the critique status. The volume of submissions which lead to this review standing is shown in parentheses.
This day signifies the final time this VCV history was updated. The update could possibly be due to an update to one of several bundled submitted documents (SCVs), or because of an update that ClinVar manufactured to your variant which include incorporating HGVS expressions or possibly a rs range.
The global small allele frequency calculated from the a thousand Genomes Job. The minimal allele at this area is indicated in parentheses and may be different within the allele represented by this VCV report.
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The aggregate germline classification for this variant, commonly for just a monogenic or Mendelian condition as while in the ACMG/AMP guidelines, or for response to some drug. This worth is calculated by NCBI depending on information from submitters. Go through our rules for calculating the aggregate classification.
There aren't any citations for germline classification of this variant in ClinVar. If you are aware of of citations for this variation, please take into account distributing that data to ClinVar.
The distributing organization for this submitted (SCV) document. This column also consists of the SCV accession and Variation amount, the day this SCV 1st appeared in ClinVar, and also the day this SCV was final current in ClinVar.
These citations are determined by LitVar utilizing the rs quantity, so They might consist of citations for multiple variant at this locale. Remember to overview the LitVar success thoroughly for the variant of curiosity. History final up-to-date May 19, 2024
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The internet site is protected. The https:// assures that you're connecting into the official website and that any information you present is encrypted and transmitted securely.
The amount of variants in ClinVar for this gene, including more compact variants inside the gene and bigger CNVs that overlap or completely comprise the gene.
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Stars signify the evaluation status, or the extent of overview supporting the submitted (SCV) file. This worth is calculated by NCBI depending on info in the submitter.