ClinVar Miner

Submissions for variant NM_001572.5(IRF7):c.767-8G>A

gnomAD frequency: 0.00001  dbSNP: rs200149783
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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 RCV001065889 SCV001230877 uncertain significance Immunodeficiency 39 2019-04-13 criteria provided, single submitter clinical testing 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. 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. This variant has not been reported in the literature in individuals with IRF7-related conditions. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the ExAC database. This sequence change falls in intron 5 of the IRF7 gene. It does not directly change the encoded amino acid sequence of the IRF7 protein.

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