thr777 No Further a Mystery

thr777 No Further a Mystery

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The effect of your variant on RNA or protein operate, based on experimental evidence from submitters.

This benefit is calculated by NCBI based upon details from submitters. Read through our guidelines for calculating the evaluate status. The quantity of submissions which add to this review status is proven in parentheses.

There is not any practical evidence in ClinVar for this variation. When you have generated useful knowledge for this variation, remember to think about publishing that facts to ClinVar.

This column consists of additional information supporting the classification, including citations, the comment on classification, and specific evidence provided as observations in the variant through the submitter.

The issue for that classification, furnished by the submitter for this submitted (SCV) history. This column also consists of the affected status and allele origin of individuals observed with this variant.

The combination germline classification for this variant, typically for your monogenic or Mendelian disorder as inside the ACMG/AMP tips, or for response to a drug. This benefit is calculated by NCBI according to knowledge from submitters. Study our regulations for calculating the mixture classification.

There aren't any citations for germline classification of the variant in ClinVar. If you already know of citations for this thr777 variation, you should contemplate publishing that information and facts to ClinVar.

The number of variants in ClinVar that are contained in just this gene, which has a website link to check out the listing of variants.

These citations are discovered by LitVar using the rs number, so they may include things like citations for more than one variant at this location. You should critique the LitVar outcomes carefully for your personal variant of curiosity. File very last current Might 19, 2024 

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The amount of variants in ClinVar for this gene, which includes smaller variants in the gene and larger CNVs that overlap or entirely contain the gene.

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