Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
ARUP Laboratories, |
RCV000757654 | SCV000885955 | pathogenic | not provided | 2018-03-07 | criteria provided, single submitter | clinical testing | The PKD1 c.8590G>T; p.Glu2864Ter variant has been reported in at least 2 individuals affected with autosomal dominant polycystic kidney disease (Liu 2015). It is absent from general population databases (1000 Genomes Project, Exome Variant Server, and Genome Aggregation Database), indicating it is not a common polymorphism. This variant induces an early termination codon and is predicted to result in a truncated protein or mRNA subject to nonsense-mediated decay. Based on the above information, this variant is considered pathogenic. References: Liu Y et al. Targeted Next-Generation Sequencing for Clinical Diagnosis of 561 Mendelian Diseases. PLoS One. 2015; 10(8): e0133636. |