Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV002330175 | SCV002629599 | uncertain significance | Cardiovascular phenotype | 2021-10-04 | criteria provided, single submitter | clinical testing | The c.4289-5C>T intronic variant results from a C to T substitution 5 nucleotides upstream from coding exon 25 in the FLNC gene. This nucleotide position is poorly conserved in available vertebrate species. In silico splice site analysis predicts that this alteration will not have any significant effect on splicing. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear. |
Invitae | RCV003102557 | SCV003473405 | likely benign | Myofibrillar myopathy 5; Distal myopathy with posterior leg and anterior hand involvement; Hypertrophic cardiomyopathy 26; Dilated Cardiomyopathy, Dominant | 2022-09-07 | criteria provided, single submitter | clinical testing |