Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001066608 | SCV001231623 | pathogenic | Alagille syndrome due to a JAG1 point mutation | 2019-11-28 | criteria provided, single submitter | clinical testing | This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Cys897Trpfs*55) in the JAG1 gene. It is expected to result in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with JAG1-related conditions. For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in JAG1 are known to be pathogenic (PMID: 11180599). |