ClinVar Miner

Submissions for variant NM_001572.5(IRF7):c.183+5_183+6delinsTA

dbSNP: rs1856759233
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001211837 SCV001383397 uncertain significance Immunodeficiency 39 2019-06-07 criteria provided, single submitter clinical testing This sequence change falls in intron 1 of the IRF7 gene. It does not directly change the encoded amino acid sequence of the IRF7 protein, but it affects a nucleotide within the consensus splice site of the intron. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate insufficient coverage at this position in the ExAC database. This variant has not been reported in the literature in individuals with IRF7-related conditions. Nucleotide substitutions within the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site, but this prediction has not been confirmed by published transcriptional studies. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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