ClinVar Miner

Submissions for variant NM_001099403.2(PRDM8):c.1279_1284del (p.Ala427_Ala428del)

dbSNP: rs1738619565
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001209220 SCV001380644 uncertain significance Early-onset Lafora body disease 2019-05-20 criteria provided, single submitter clinical testing This variant, c.1279_1284del, results in the deletion of 2 amino acid(s) of the PRDM8 protein (p.Ala427_Ala428del), but otherwise preserves the integrity of the reading frame. 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 for this variant, and the functional significance of the affected amino acid(s) is currently unknown. This variant has not been reported in the literature in individuals with PRDM8-related conditions. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate insufficient coverage at this position in the ExAC database.

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