Indicators on thr777 You Should Know
Indicators on thr777 You Should Know
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The effect of the variant on RNA or protein functionality, according to experimental proof from submitters.
This benefit is calculated by NCBI based upon knowledge from submitters. Go through our guidelines for calculating the review position. The amount of submissions which add to this overview status is demonstrated in parentheses.
There isn't a useful evidence in ClinVar for this variation. Should you have produced practical info for this variation, remember to take into account distributing that info to ClinVar.
The global insignificant allele frequency calculated via the a thousand Genomes Task. The slight allele at this place is indicated in parentheses and may be distinctive within the allele represented by this VCV report.
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There are no citations for germline classification of the variant in ClinVar. If you know of citations for this variation, please consider publishing that information and facts to ClinVar.
The publishing Firm for this submitted (SCV) record. This column also incorporates the SCV accession and Edition selection, the date this SCV to start with appeared in ClinVar, and the date this SCV was final up-to-date in ClinVar.
These citations are recognized by LitVar utilizing the rs number, so They might involve citations for more than one variant at this place. Remember to assessment the LitVar success very carefully to your variant of curiosity. Document very last current Might 19, 2024
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