A Simple Key For thr777 Unveiled
A Simple Key For thr777 Unveiled
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The outcome with the variant on RNA or protein operate, based upon experimental evidence from submitters.
This benefit is calculated by NCBI depending on info from submitters. Go through our rules for calculating the critique position. The quantity of submissions which lead to this evaluate status is shown in parentheses.
There isn't any useful evidence in ClinVar for this variation. In case you have produced practical data for this variation, please take into account distributing that knowledge to ClinVar.
The global small allele frequency calculated from the a thousand Genomes Challenge. The minimal allele at this place is indicated in parentheses and will be unique with the allele represented by this VCV history.
The issue with the classification, supplied by the submitter for this submitted (SCV) report. This column also consists of the afflicted position and allele origin of individuals observed with this particular variant.
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There are no citations for germline classification of the variant in ClinVar. If you know of citations for this variation, remember to take into account distributing that data to ClinVar.
The distributing Group for this submitted (SCV) file. This column also contains the SCV accession and Edition amount, the date this SCV first thr777 appeared in ClinVar, and also the day this SCV was final up-to-date in ClinVar.
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Stars signify the combination evaluate standing, or the level of evaluation supporting the combination germline classification for this VCV report.
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