thr777 Can Be Fun For Anyone
thr777 Can Be Fun For Anyone
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The effect of the variant on RNA or protein functionality, according to experimental proof from submitters.
This price is calculated by NCBI based upon data from submitters. Examine our procedures for calculating the evaluate standing. The quantity of submissions which lead to this evaluate position is demonstrated in parentheses.
There is not any practical proof in ClinVar for this variation. If you have created functional info for this variation, be sure to think about distributing that knowledge to ClinVar.
The worldwide insignificant allele frequency calculated with the 1000 Genomes Venture. The minimal allele at this area is indicated in parentheses and should be various with the allele represented by this VCV report.
The ailment with the classification, furnished by the submitter for this submitted (SCV) history. This column also involves the afflicted standing and allele origin of people noticed with this particular variant.
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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 contemplate submitting that info to ClinVar.
The publishing Firm for this submitted (SCV) document. This column also features the SCV accession and Edition number, the date this SCV first appeared in ClinVar, plus the date that this SCV was past up to date in ClinVar.
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