Total submissions: 3
| Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
|---|---|---|---|---|---|---|---|---|
| Invitae | RCV000227798 | SCV000283430 | uncertain significance | Beckwith-Wiedemann syndrome | 2023-11-15 | criteria provided, single submitter | clinical testing | This sequence change replaces alanine, which is neutral and non-polar, with glycine, which is neutral and non-polar, at codon 257 of the CDKN1C protein (p.Ala257Gly). The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This variant has not been reported in the literature in individuals affected with CDKN1C-related conditions. ClinVar contains an entry for this variant (Variation ID: 236975). 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 not expected to disrupt CDKN1C protein function with a negative predictive value of 80%. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. |
| Fulgent Genetics, |
RCV002494616 | SCV002784190 | uncertain significance | Beckwith-Wiedemann syndrome; IMAGe syndrome | 2022-05-03 | criteria provided, single submitter | clinical testing | |
| Baylor Genetics | RCV000227798 | SCV004212455 | uncertain significance | Beckwith-Wiedemann syndrome | 2023-06-05 | criteria provided, single submitter | clinical testing |