ClinVar Miner

Submissions for variant NM_001082486.2(ACD):c.99+3G>A

gnomAD frequency: 0.00001  dbSNP: rs1189416936
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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 RCV001986555 SCV002282014 uncertain significance Dyskeratosis congenita, autosomal dominant 6 2021-04-04 criteria provided, single submitter clinical testing This variant is not present in population databases (ExAC no frequency). This sequence change falls in intron 1 of the ACD gene. It does not directly change the encoded amino acid sequence of the ACD protein. It affects a nucleotide within the consensus splice site of the intron. This variant has not been reported in the literature in individuals with ACD-related conditions. 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. Nucleotide substitutions within the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant is not likely to affect RNA splicing, but this prediction has not been confirmed by published transcriptional studies.

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