Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000217379 | SCV000272807 | uncertain significance | not specified | 2015-05-16 | criteria provided, single submitter | clinical testing | The p.Leu29407Phe variant in TTN has not been previously reported in individuals with cardiomyopathy, but has been identified in 1/66674 European chromosomes by the Exome Aggregation Consortium (ExAC, http://exac.broadinstitute.org). Comput ational prediction tools and conservation analysis do not provide strong support for or against an impact to the protein. In summary, the clinical significance of the p.Leu29407Phe variant is uncertain. |