ClinVar Miner

Submissions for variant NC_000017.10:g.(?_29575992)_(29587543_?)del

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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 RCV001379206 SCV001576958 likely pathogenic Neurofibromatosis, type 1 2020-08-24 criteria provided, single submitter clinical testing This variant is an in-frame deletion of the genomic region encompassing exon(s) 30-33 of the NF1 gene. It preserves the integrity of the reading frame. This variant has not been reported in the literature in individuals with NF1-related conditions. This variant disrupts the p.Arg1391 amino acid residue in NF1. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 27322474, 24789688, Invitae). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic.

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