ClinVar Miner

Submissions for variant NM_005591.4(MRE11):c.544+4A>T

dbSNP: rs2135084555
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002239146 SCV002509518 uncertain significance Ataxia-telangiectasia-like disorder 2023-07-17 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with MRE11-related conditions. This sequence change falls in intron 6 of the MRE11 gene. It does not directly change the encoded amino acid sequence of the MRE11 protein. It affects a nucleotide within the consensus splice site. This variant is not present in population databases (gnomAD no frequency). ClinVar contains an entry for this variant (Variation ID: 1681621). Variants that disrupt 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. 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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