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The amount of variants in ClinVar which have been contained inside of this gene, which has a url to view the list of variants.
The distributing Group for this submitted (SCV) report. This column also incorporates the SCV accession and Variation number, the day this SCV 1st appeared in ClinVar, plus the day that this SCV was last updated in ClinVar.
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There is absolutely no functional evidence in ClinVar for this variation. In case you have produced practical info for this variation, make sure you take into account distributing that facts to ClinVar.
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So this date may very well be diverse in the day on the “most recent submission” described at the top of this webpage. Assistance Stick to NCBI
The impact with the variant on RNA or protein function, based upon experimental proof from submitters.
The amount of variants in ClinVar that happen to be contained within this gene, using a backlink to perspective the listing of variants.
The worldwide insignificant allele frequency calculated by the 1000 Genomes Task. The minimal allele at this spot is indicated in parentheses and should be unique within the allele represented by this VCV report.
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The worldwide minimal allele frequency calculated via login thr777 the a thousand Genomes Project. The minor allele at this place is indicated in parentheses and will be distinct through the allele represented by this VCV file.
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