ClinVar Miner

Submissions for variant NM_001199138.2(NLRC4):c.2908T>C (p.Phe970Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV003448830 SCV004176593 uncertain significance Familial cold autoinflammatory syndrome 4 2023-03-01 criteria provided, single submitter clinical testing The missense c.2908T>C (p.Phe970Leu) variant in NLRC4 gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.Phe970Leu variant is novel (not in any individuals) in gnomAD Exomes and 1000 Genomes. This variant has not been reported to the ClinVar database. The amino acid change p.Phe970Leu in NLRC4 is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. The amino acid Phe at position 970 is changed to a Leu changing protein sequence and it might alter its composition and physico-chemical properties. For these reasons, this variant has been classified as Variant of Uncertain Significance (VUS).

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