The best Side of thr777
The best Side of thr777
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The problem for the classification, provided by the submitter for this submitted (SCV) file. This column also contains the affected standing and allele origin of individuals observed with this particular variant.
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The amount of variants thr777 in ClinVar for this gene, including lesser variants in the gene and bigger CNVs that overlap or absolutely consist of the gene.
The impact in the variant on RNA or protein functionality, determined by experimental proof from submitters.
The number of variants in ClinVar which might be contained in just this gene, with a website link to watch the listing of variants.
The global insignificant allele frequency calculated with the a thousand Genomes Job. The small allele at this area is indicated in parentheses and may be diverse within the allele represented by this VCV record.
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