ClinVar Miner

Submissions for variant NM_138694.4(PKHD1):c.9448T>C (p.Phe3150Leu)

dbSNP: rs2150983802
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001924111 SCV002199439 uncertain significance Autosomal recessive polycystic kidney disease 2021-09-21 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. 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 not expected to disrupt PKHD1 protein function. This variant has not been reported in the literature in individuals affected with PKHD1-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces phenylalanine with leucine at codon 3150 of the PKHD1 protein (p.Phe3150Leu). The phenylalanine residue is weakly conserved and there is a small physicochemical difference between phenylalanine and leucine.

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