ClinVar Miner

Submissions for variant NM_001243133.2(NLRP3):c.2902A>G (p.Ser968Gly)

gnomAD frequency: 0.00001  dbSNP: rs1408232607
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001046560 SCV001210465 uncertain significance Cryopyrin associated periodic syndrome 2019-11-21 criteria provided, single submitter clinical testing Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. 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. This variant has not been reported in the literature in individuals with NLRP3-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces serine with glycine at codon 970 of the NLRP3 protein (p.Ser970Gly). The serine residue is moderately conserved and there is a small physicochemical difference between serine and glycine.
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002264156 SCV002542627 uncertain significance Autoinflammatory syndrome 2018-05-01 criteria provided, single submitter clinical testing

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