ClinVar Miner

Submissions for variant NM_000214.3(JAG1):c.387+1G>C

dbSNP: rs2514537639
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Department, Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology RCV003986036 SCV004801874 likely pathogenic Alagille syndrome due to a JAG1 point mutation criteria provided, single submitter clinical testing A previously undescribed nucleotide variant creates an alteration of the canonical splice site c.387+1G>C in the JAG1 gene. The variant was observed in heterozygous state in an individual affected with cholestatic liver disease. Loss-of-function variants are reported in patients with Alagille syndrome 1, 118450. The variant is not present in population database (gnomAD no frequency). 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.

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