ClinVar Miner

Submissions for variant NM_000267.3:c.1491_4110+4407del

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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 RCV001048021 SCV001212010 pathogenic Neurofibromatosis, type 1 2019-12-26 criteria provided, single submitter clinical testing This variant results in the deletion of part of exon 13 and exon(s) 14-30 of the NF1 gene. It is expected to disrupt RNA splicing and likely results in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with NF1-related conditions. This variant disrupts the p.Leu695 amino acid residue in NF1. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 10712197, 23404336, 26331193, 23758643). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. Loss-of-function variants in NF1 are known to be pathogenic (PMID: 10712197, 23913538). For these reasons, this variant has been classified as Pathogenic.

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