Little Known Facts About thr777.
Little Known Facts About thr777.
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The result of the variant on RNA or protein purpose, based on experimental proof from submitters.
This value is calculated by NCBI determined by data from submitters. Browse our rules for calculating the critique status. The number of submissions which lead to this overview position is demonstrated in parentheses.
There is absolutely no useful evidence in ClinVar for this variation. When you have generated useful details for this variation, please think about publishing that info to ClinVar.
The worldwide minor allele frequency calculated from the 1000 Genomes Venture. The small allele at this location is indicated in parentheses and could be diverse with the allele represented by this VCV report.
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The mixture germline classification for this variant, ordinarily for your monogenic or Mendelian condition as inside the ACMG/AMP recommendations, or for response to your drug. This benefit is calculated by NCBI according to details from submitters. Read our guidelines for calculating the combination classification.
There thr777 are no citations for germline classification of the variant in ClinVar. If you recognize of citations for this variation, you should take into consideration submitting that details to ClinVar.
The number of variants in ClinVar which are contained within this gene, which has a backlink to check out the listing of variants.
These citations are recognized by LitVar utilizing the rs range, so they may include citations for more than one variant at this place. Please evaluate the LitVar final results meticulously for the variant of curiosity. Document last updated May well 19, 2024
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Stars signify the combination review status, or the level of evaluation supporting the mixture germline classification for this VCV record.
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Stars signify the assessment status, or the extent of evaluate supporting the submitted (SCV) record. This value is calculated by NCBI based on data within the submitter.