ClinVar Miner

Submissions for variant NM_006892.4(DNMT3B):c.1275CAA[2] (p.Asn427del)

dbSNP: rs752142241
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001959888 SCV002208297 uncertain significance Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency 2021-09-24 criteria provided, single submitter clinical testing This variant, c.1281_1283del, results in the deletion of 1 amino acid(s) of the DNMT3B protein (p.Asn427del), but otherwise preserves the integrity of the reading frame. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the ExAC database. This variant has not been reported in the literature in individuals with DNMT3B-related conditions. 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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