Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Blueprint Genetics | RCV000208170 | SCV000263757 | uncertain significance | Primary familial hypertrophic cardiomyopathy | 2015-04-07 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000482813 | SCV000574087 | uncertain significance | not provided | 2017-03-16 | criteria provided, single submitter | clinical testing | A variant of uncertain significance has been identified in the ACTC1 gene. The K375R variant has not been published as pathogenic or been reported as benign to our knowledge. This variant is not observed in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). This substitution occurs at a position that is conserved across species and in silico analysis suggests that this variant is probably damaging to the protein structure/function. However, the K375R variant is a conservative amino acid substitution, which is not likely to impact secondary protein structure as these residues share similar properties. |