ClinVar Miner

Submissions for variant NM_182760.4(SUMF1):c.726-1G>A

dbSNP: rs1215549413
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001236822 SCV001409560 likely pathogenic Multiple sulfatase deficiency 2022-06-23 criteria provided, single submitter clinical testing This sequence change affects an acceptor splice site in intron 5 of the SUMF1 gene. It is expected to disrupt RNA splicing. Variants that disrupt the donor or acceptor splice site typically lead to a loss of protein function (PMID: 16199547), and loss-of-function variants in SUMF1 are known to be pathogenic (PMID: 12757705, 12757706, 25885655). In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. ClinVar contains an entry for this variant (Variation ID: 962890). This variant has not been reported in the literature in individuals affected with SUMF1-related conditions. This variant is not present in population databases (gnomAD no frequency).

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