ClinVar Miner

Submissions for variant NM_012452.3(TNFRSF13B):c.753del (p.Asp252fs)

dbSNP: rs755752100
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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 RCV001345156 SCV001539258 uncertain significance Immunodeficiency, common variable, 2 2024-02-17 criteria provided, single submitter clinical testing This sequence change results in a frameshift in the TNFRSF13B gene (p.Asp252Thrfs*72). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 42 amino acid(s) of the TNFRSF13B protein and extend the protein by 29 additional amino acid residues. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This variant has not been reported in the literature in individuals affected with TNFRSF13B-related conditions. ClinVar contains an entry for this variant (Variation ID: 1041356). Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant 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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