ClinVar Miner

Submissions for variant NM_080632.3(UPF3B):c.263+19_263+20delinsAA

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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 RCV003878872 SCV004679208 uncertain significance Syndromic X-linked intellectual disability 14 2023-01-26 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. Experimental studies and prediction algorithms are not available or were not evaluated, and the effect of this variant on mRNA splicing is currently unknown. This variant has not been reported in the literature in individuals affected with UPF3B-related conditions. 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 2 of the UPF3B gene. It does not directly change the encoded amino acid sequence of the UPF3B protein.

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