ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.8590G>T (p.Glu2864Ter)

dbSNP: rs374629549
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, 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.

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