About thr777
About thr777
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The influence on the variant on RNA or protein operate, depending on experimental proof from submitters.
This value is calculated by NCBI dependant on information from submitters. Examine our rules for calculating the evaluate standing. The number of submissions which lead to this evaluation position is proven in parentheses.
There isn't any purposeful evidence in ClinVar for this variation. When you have generated purposeful data for this variation, remember to look at submitting that information to ClinVar.
The global minor allele frequency calculated from the a thousand Genomes Venture. The minimal allele at this site is indicated in parentheses and may be different from the allele represented by this VCV record.
The condition for the classification, supplied by the submitter for this submitted (SCV) file. This column also features the impacted status and allele origin of people noticed using this type of variant.
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Read through our procedures for calculating the overview position. This column also features a connection for the submitter’s assertion criteria if delivered, and the gathering system.
The submitting Business for this submitted (SCV) file. This column also involves the SCV accession and Variation number, the day this SCV initially appeared in ClinVar, along with the day that this SCV was previous up-to-date in ClinVar.
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The volume of variants in ClinVar for this gene, which includes more compact variants throughout the gene and larger CNVs that overlap or completely comprise the gene.
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Stars characterize the assessment status, or the extent of overview supporting the submitted thr777 (SCV) file. This value is calculated by NCBI according to details through the submitter.