ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.1851_1859dup (p.Asp617_Asn619dup)

dbSNP: rs1554843116
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000470276 SCV000552986 uncertain significance Brugada syndrome 4 2016-07-31 criteria provided, single submitter clinical testing In summary, this is a novel sequence change with uncertain impact on protein function. It has been classified as a Variant of Uncertain Significance. Experimental studies investigating the functional effect of this duplication have not been published in the literature. This variant is not present in population databases (ExAC no frequency) and has not been reported in the literature in individuals with a CACNB2-related disease. This sequence change inserts 9 nucleotides in exon 13 of the CACNB2 mRNA (c.1689_1697dupCCACAACGA). This leads to the insertion of 3 amino acid residue(s) in the CACNB2 protein (p.Asp563_Asn565dup) but otherwise preserves the integrity of the reading frame.

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