thr777 - An Overview
thr777 - An Overview
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The impact from the variant on RNA or protein perform, determined by experimental proof from submitters.
This price is calculated by NCBI based upon information from submitters. Go through our policies for calculating the critique status. The volume of submissions which lead to this overview status is proven in parentheses.
This day signifies the final time this VCV record was up to date. The update may very well be on account of an update to on the list of integrated submitted records (SCVs), or because of an update that ClinVar built for the variant like incorporating HGVS expressions or possibly a rs range.
The worldwide minimal allele frequency calculated because of the one thousand Genomes Undertaking. The small allele at this location is indicated in parentheses and could be unique from the allele represented by this VCV record.
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The combination germline classification for this variant, typically for any monogenic or Mendelian dysfunction as during the ACMG/AMP guidelines, or for response to a drug. This value is calculated by NCBI depending on knowledge from submitters. Examine our procedures for calculating the combination classification.
There isn't any citations for germline classification of the variant in ClinVar. If you recognize of citations for this variation, you should look at distributing that facts to ClinVar.
The quantity of variants in ClinVar which can be contained inside this gene, that has a website link to see the list of variants.
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The quantity of variants in ClinVar for this gene, such as lesser variants inside the gene and bigger CNVs that overlap or fully incorporate the gene.
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Stars signify the evaluation position, or the extent of overview supporting the submitted (SCV) file. This worth is calculated by NCBI according to information from the submitter.