ClinVar Miner

Submissions for variant NM_030930.4(UNC93B1):c.1090-5C>A

dbSNP: rs755512821
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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 RCV001209750 SCV001381200 uncertain significance Herpes simplex encephalitis, susceptibility to, 1 2022-01-17 criteria provided, single submitter clinical testing This sequence change falls in intron 8 of the UNC93B1 gene. It does not directly change the encoded amino acid sequence of the UNC93B1 protein. This variant is present in population databases (rs755512821, gnomAD 0.1%). This variant has not been reported in the literature in individuals affected with UNC93B1-related conditions. ClinVar contains an entry for this variant (Variation ID: 940213). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus 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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