ClinVar Miner

Submissions for variant NM_145725.3(TRAF3):c.297+18_297+19inv

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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 RCV002611841 SCV003508948 uncertain significance Herpes simplex encephalitis, susceptibility to, 3 2022-06-11 criteria provided, single submitter clinical testing Information on the frequency of this variant in the gnomAD database is not available, as this variant may be reported differently in the database. This sequence change falls in intron 3 of the TRAF3 gene. It does not directly change the encoded amino acid sequence of the TRAF3 protein. This variant has not been reported in the literature in individuals affected with TRAF3-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the effect of this variant on mRNA splicing is currently unknown. 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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