Indicators on thr777 You Should Know
Indicators on thr777 You Should Know
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The effect of your variant on RNA or protein functionality, based on experimental proof from submitters.
This worth is calculated by NCBI according to data from submitters. Browse our regulations for calculating the critique status. The volume of submissions which lead to this review standing is proven in parentheses.
There is absolutely no useful evidence in ClinVar for this variation. In case you have created practical information for this variation, please think about submitting that data to ClinVar.
The worldwide minimal allele frequency calculated because of the one thousand Genomes Venture. The minor allele at this location is indicated in parentheses and could be diverse through the allele represented by this VCV document.
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There won't be any citations for germline classification of this variant in ClinVar. If you recognize of citations for this variation, please look at submitting that information to ClinVar.
The submitting Business for this submitted (SCV) document. This column also contains the SCV accession and Model quantity, the day this SCV 1st appeared in ClinVar, as well as date this SCV was last up to date in ClinVar.
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Stars depict the aggregate review standing, or the level of evaluate supporting the mixture germline classification for this VCV document.
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