ClinVar Miner

Submissions for variant NM_000214.3(JAG1):c.311del (p.Gly104fs)

dbSNP: rs886041782
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000300352 SCV000330537 pathogenic not provided 2017-01-04 criteria provided, single submitter clinical testing The c.311delG pathogenic variant in the JAG1 gene causes a frameshift starting with codon Glycine 104, changes this amino acid to an Alanine residue and creates a premature Stop codon at position 57 of the new reading frame, denoted p.Gly104AlafsX57. This pathogenic variant is predicted to cause loss of normal protein function either through protein truncation or nonsense-mediated mRNA decay. The c.311delG variant was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations.

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