DETAILED NOTES ON THR777

Detailed Notes on thr777

Detailed Notes on thr777

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The result on the variant on RNA or protein functionality, depending on experimental evidence from submitters.

This benefit is calculated by NCBI based upon knowledge from submitters. Go through our principles for calculating the evaluation position. The amount of submissions which add to this critique status is revealed in parentheses.

This day signifies the final time this VCV history was updated. The update could possibly be because of an update to among the list of included submitted records (SCVs), or as a result of an update that ClinVar designed on the variant for instance including HGVS expressions or maybe a rs selection.

The worldwide slight allele frequency calculated with the 1000 Genomes Venture. The minor allele at this area is indicated in parentheses and may be different within the allele represented by this VCV document.

The problem with the classification, furnished by the submitter for this submitted (SCV) report. This column also incorporates the impacted position and allele origin of individuals noticed with this variant.

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There are no citations for germline classification of the variant in ClinVar. If you realize of citations for this variation, make sure you look at publishing that information to ClinVar.

The volume of variants in ClinVar which have been contained in this gene, which has a url to check out the list of variants.

These citations are determined by LitVar utilizing the rs amount, so They could consist of citations for more than one variant at this location. Remember to critique the LitVar final results diligently to your variant of interest. File final up-to-date May 19, 2024 

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Stars depict the mixture overview status, or the extent of overview supporting the aggregate germline classification for this VCV history.

The volume of variants in ClinVar for this gene, which include smaller sized variants throughout the gene and larger CNVs that overlap or thoroughly have the gene.

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