The impact on the variant on RNA or protein function, according to experimental evidence from submitters.
This value is calculated by NCBI determined by data from submitters. Study our policies for calculating the critique status. The quantity of submissions which contribute to this critique status is revealed in parentheses.
There is absolutely no functional evidence in ClinVar for this variation. When you've got produced purposeful facts for this variation, be sure to take into consideration publishing that facts to ClinVar.
The worldwide small allele frequency calculated through the 1000 Genomes Challenge. The minimal allele at this site is indicated in parentheses and will be distinctive in the allele represented by this VCV record.
The issue for the classification, provided by the submitter for this submitted (SCV) file. This column also consists of the influenced status and allele origin of individuals noticed with this particular variant.
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There are no citations for germline classification of this variant in ClinVar. If you realize of citations for this variation, make sure you contemplate submitting that information to ClinVar.
The quantity of variants in ClinVar which might be contained inside of this gene, with a connection to watch the listing of variants.
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Stars symbolize the overview position, or the extent of evaluation supporting the submitted (SCV) report. This benefit is calculated by NCBI according to information in the submitter.