The outcome on the variant on RNA or protein function, dependant on experimental proof from submitters.

This worth is calculated by NCBI according to data from submitters. Examine our policies for calculating the assessment position. The volume of submissions which contribute to this evaluate status is demonstrated in parentheses.

There is absolutely no useful evidence in ClinVar for this variation. In case you have produced useful info for this variation, please contemplate submitting that data to ClinVar.

This column includes additional information supporting the classification, like citations, the touch upon classification, and thorough evidence furnished as observations in the variant from the submitter.

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There are no citations for germline classification of the variant in ClinVar. If you are aware of of citations for this variation, be sure thr777 to consider publishing that information and facts to ClinVar.

The quantity of variants in ClinVar which might be contained inside of this gene, with a backlink to check out the listing of variants.

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