ClinVar Miner

Submissions for variant NM_022489.4(INF2):c.1336dup (p.Leu446fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000798510 SCV000938129 uncertain significance Focal segmental glomerulosclerosis 5; Charcot-Marie-Tooth disease, dominant intermediate E 2018-10-23 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Leu446Profs*7) in the INF2 gene. It is expected to result in an absent or disrupted protein product. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate insufficient coverage at this position in the ExAC database. This variant has not been reported in the literature in individuals with INF2-related disease. The current clinical and genetic evidence is not sufficient to establish whether loss-of-function variants in INF2 cause disease. 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.

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