ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.6592del (p.Ala2198fs)

dbSNP: rs2151556490
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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 RCV001387634 SCV001588306 pathogenic Neurofibromatosis, type 1 2022-01-21 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 1074365). 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.Ala2177Leufs*2) 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).

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