ClinVar Miner

Submissions for variant NM_001572.5(IRF7):c.1128G>A (p.Val376=)

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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 RCV002730477 SCV003010509 uncertain significance Immunodeficiency 39 2023-07-17 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with IRF7-related conditions. This sequence change affects codon 389 of the IRF7 mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the IRF7 protein. This variant is present in population databases (rs771649294, gnomAD 0.006%). ClinVar contains an entry for this variant (Variation ID: 1970312). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site. 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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