Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory for Molecular Medicine, |
RCV000219596 | SCV000272584 | uncertain significance | not specified | 2015-05-18 | criteria provided, single submitter | clinical testing | The p.Pro4212His variant in TTN has not been previously reported in individuals with cardiomyopathy or in large population studies. Computational prediction too ls and conservation analysis suggest that this variant may impact the protein, t hough this information is not predictive enough to determine pathogenicity. In s ummary, the clinical significance of the p.Pro4212His variant is uncertain. |
Revvity Omics, |
RCV003137811 | SCV003824108 | uncertain significance | not provided | 2020-06-23 | criteria provided, single submitter | clinical testing |