Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001055749 | SCV001220154 | likely pathogenic | Autosomal recessive polycystic kidney disease | 2023-05-08 | 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. 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 PKHD1 protein function. ClinVar contains an entry for this variant (Variation ID: 851366). This missense change has been observed in individuals with clinical features of polycystic kidney disease (PMID: 19914852, 27752906; Invitae). This variant is present in population databases (rs776845008, gnomAD 0.002%). This sequence change replaces glycine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 470 of the PKHD1 protein (p.Gly470Val). |
Natera, |
RCV001055749 | SCV002081081 | uncertain significance | Autosomal recessive polycystic kidney disease | 2021-06-29 | no assertion criteria provided | clinical testing |