ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.5029del (p.Val1677fs)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003031469 SCV003318929 pathogenic Neurofibromatosis, type 1 2022-03-02 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals affected with NF1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Val1656Serfs*21) 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).
Baylor Genetics RCV003459704 SCV004199021 likely pathogenic Juvenile myelomonocytic leukemia 2021-08-13 criteria provided, single submitter clinical testing

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