ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.5141del (p.Phe1714fs) (rs1596556375)

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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 RCV001001133 SCV001158275 pathogenic Polycystic kidney disease, adult type 2019-03-08 criteria provided, single submitter clinical testing The PKD1 c.5141delT; p.Phe1714fs variant has been described in at least one individual with autosomal dominant polycystic kidney disease (ADPKD; see link to Mayo ADPKD database). It is absent from general population databases (Exome Variant Server and Genome Aggregation Database), indicating it is not a common polymorphism. This variant causes a frameshift by deleting a single nucleotide, so it is predicted to result in a truncated protein or mRNA subject to nonsense-mediated decay. Additionally, several downstream truncating variant have been described in individuals affected with ADPKD and are considered pathogenic (Audrezet 2012, Rossetti 2007). Based on available information, the p.Phe1714fs variant is considered pathogenic. REFERENCES Link to Mayo ADPKD database: Audrezet M et al. Autosomal dominant polycystic kidney disease: comprehensive mutation analysis of PKD1 and PKD2 in 700 unrelated patients. Hum Mutat. 2012 Aug;33(8):1239-50. Rossetti S et al. Comprehensive molecular diagnostics in autosomal dominant polycystic kidney disease. J Am Soc Nephrol. 2007 Jul;18(7):2143-60.

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