ClinVar Miner

Submissions for variant NM_138694.4(PKHD1):c.7765_7766delinsT (p.Thr2589fs)

dbSNP: rs1773247172
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001239664 SCV001412553 pathogenic Autosomal recessive polycystic kidney disease 2019-07-26 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in PKHD1 are known to be pathogenic (PMID: 19940839). This variant has not been reported in the literature in individuals with PKHD1-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Thr2589Serfs*2) in the PKHD1 gene. It is expected to result in an absent or disrupted protein product.

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