The influence of your variant on RNA or protein purpose, based on experimental evidence from submitters.
This benefit is calculated by NCBI dependant on info from submitters. Study our guidelines for calculating the overview standing. The quantity of submissions which add to this critique status is demonstrated in parentheses.
There is absolutely no functional evidence in ClinVar for this variation. If you have produced functional facts for this variation, please take into consideration distributing that data to ClinVar.
The global small allele frequency calculated with the a thousand Genomes Project. The insignificant allele at this spot is indicated in parentheses and may be distinct with the allele represented by this VCV record.
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There won't be any citations for germline classification of the variant in ClinVar. If you already know of citations for this variation, you should look at distributing that facts to ClinVar.
The submitting Firm for this submitted (SCV) history. This column also consists of the SCV accession and thr777 Variation selection, the date this SCV initial appeared in ClinVar, and the date that this SCV was last up to date in ClinVar.
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Stars depict the review standing, or the extent of evaluate supporting the submitted (SCV) document. This benefit is calculated by NCBI based upon info in the submitter.