Total submissions: 2
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Invitae | RCV001859496 | SCV002283014 | likely pathogenic | not provided | 2021-08-05 | criteria provided, single submitter | clinical testing | In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. This variant disrupts the p.Met1778 amino acid residue in ABCA4. Other variant(s) that disrupt this residue have been observed in individuals with ABCA4-related conditions (PMID: 30060493, 32141364; Invitae), which suggests that this may be a clinically significant amino acid residue. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt ABCA4 protein function. ClinVar contains an entry for this variant (Variation ID: 265997). This variant has not been reported in the literature in individuals affected with ABCA4-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces methionine with lysine at codon 1778 of the ABCA4 protein (p.Met1778Lys). The methionine residue is highly conserved and there is a moderate physicochemical difference between methionine and lysine. |
| Bioscientia Institut fuer Medizinische Diagnostik Gmb |
RCV000256375 | SCV000323156 | likely pathogenic | Cone-rod dystrophy 3 | no assertion criteria provided | clinical testing |