Examine This Report on thr777
Examine This Report on thr777
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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 dependant on knowledge from submitters. Read through our principles for calculating the review position. The quantity of submissions which contribute to this critique status is revealed in parentheses.
There is no practical proof in ClinVar for this variation. In case you have created practical knowledge for this variation, make sure you think about publishing that facts to ClinVar.
The worldwide minor allele frequency calculated because of the 1000 Genomes Undertaking. The small allele at this place is indicated in parentheses and could be unique in the allele represented by this VCV document.
The issue for the classification, furnished by the submitter for this submitted (SCV) document. This column also includes the impacted position and allele origin of individuals observed using this type of variant.
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Browse our procedures for calculating the critique standing. This column also includes thr777 a link to your submitter’s assertion criteria if presented, and the collection method.
The volume of variants in ClinVar that happen to be contained in just this gene, having a url to check out the list of variants.
These citations are determined by LitVar utilizing the rs variety, so They could include things like citations for more than one variant at this spot. Please assessment the LitVar outcomes carefully on your variant of desire. Document previous up-to-date Could 19, 2024
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Stars depict the aggregate review position, or the level of review supporting the combination germline classification for this VCV document.
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Stars stand for the evaluate standing, or the level of evaluation supporting the submitted (SCV) document. This value is calculated by NCBI based on data within the submitter.