Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV001188730 | SCV001355864 | uncertain significance | Cardiomyopathy | 2018-12-11 | criteria provided, single submitter | clinical testing | Variant of Uncertain Significance due to insufficient evidence: This variant causes a deletion of one amino acid from the cytoplasmic domain of the TMEM43 protein. Computational splicing tools suggest that this variant may not impact RNA splicing. To our knowledge, functional assays have not been performed for this variant nor has this variant been reported in individuals affected with cardiovascular disorders in the literature. This variant is rare in the general population and has been identified in 0/277264 chromosomes by the Genome Aggregation Database (gnomAD). Available evidence is insufficient to determine the pathogenicity of this variant conclusively. |