thr777 Options
thr777 Options
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The influence in the variant on RNA or protein perform, depending on experimental evidence from submitters.
This benefit is calculated by NCBI determined by info from submitters. Study our rules for calculating the evaluate status. The quantity of submissions which contribute to this evaluate position is revealed in parentheses.
This date represents the final time this VCV report was up-to-date. The update could possibly be as a consequence of an update to one of several included submitted data (SCVs), or as a result of an update that ClinVar built for the variant for instance introducing HGVS expressions or a rs quantity.
The global minor allele frequency calculated by the a thousand Genomes Challenge. The minimal allele at this spot is indicated in parentheses and will be diverse from your 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, remember to look at distributing that data to ClinVar.
The quantity of variants in ClinVar which have been contained in this gene, by using a website link to view the listing of variants.
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Aberrant five' splice sites in human disease genes: mutation sample, nucleotide composition and comparison of computational instruments that predict their utilization.
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The quantity of variants in ClinVar for this gene, which includes smaller variants in the gene and larger CNVs that overlap or fully thr777 incorporate the gene.
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The internet site is safe. The https:// makes sure that you're connecting to the Formal Site Which any facts you deliver is encrypted and transmitted securely.