ClinVar Miner

Submissions for variant NM_004895.4(NLRP3):c.2499-8T>A (rs199858933)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000413925 SCV000491464 uncertain significance not specified 2016-09-15 criteria provided, single submitter clinical testing The c.2499-8T>A variant in the NLRP3 gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. This variant, which occurs at a nucleotide that is not conserved across species, may reduce the quality of the splice acceptor site in intron 5, leading to abnormal gene splicing. However, since the natural splice acceptor site for intron 5 is not well predicted by splicing algorithms, the effect of this substitution is difficult to predict. The c.2499-8T>A variant was not observed in approximately 6500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. We interpret the maternally inherited c.2499-8T>A splicing variant as a variant of uncertain significance.
Invitae RCV000941778 SCV001087676 likely benign not provided 2018-08-01 criteria provided, single submitter clinical testing

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