ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.5721del (p.Phe1907fs)

dbSNP: rs2151544716
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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 RCV001906208 SCV002170318 pathogenic Neurofibromatosis, type 1 2024-09-19 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Phe1886Leufs*18) 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 neurofibromatosis (PMID: 15146469). This variant is also known as c.5656delT. ClinVar contains an entry for this variant (Variation ID: 1397603). For these reasons, this variant has been classified as Pathogenic.

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