ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.5529del (p.Lys1844fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003837968 SCV004632641 pathogenic Neurofibromatosis, type 1 2022-11-28 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Lys1823Argfs*19) in the NF1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in NF1 are known to be pathogenic (PMID: 10712197, 23913538). This variant is not present in population databases (gnomAD no frequency). This premature translational stop signal has been observed in individual(s) with NF1-related conditions (PMID: 31573083). For these reasons, this variant has been classified as Pathogenic.

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