Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Gene |
RCV000434404 | SCV000535580 | uncertain significance | not provided | 2017-01-04 | criteria provided, single submitter | clinical testing | A variant of uncertain significance has been identified in the COL5A2 gene. The P1380S variant has not been published as a pathogenic variant, nor has it been reported as a benign variant to our knowledge. This variant was not observed with any significant frequency in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project. The P1380S variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. However, this substitution occurs at a position that is only conserved in most mammals and where Serine is the wild type in the guinea pig. Finally, in silico analysis is inconsistent in its predictions as to whether or not the variant is damaging to the protein structure/function. Therefore, based on the currently available information, it is unclear whether this variant is pathogenic or rare benign. This result cannot be interpreted for diagnosis or used for family member screening at this time. |
| Invitae | RCV002230295 | SCV001402027 | likely benign | Ehlers-Danlos syndrome, classic type, 1 | 2023-05-22 | criteria provided, single submitter | clinical testing |