ClinVar Miner

Submissions for variant NM_018062.4(FANCL):c.40dup (p.Leu14fs)

dbSNP: rs761039364
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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 RCV000697873 SCV000826506 pathogenic Fanconi anemia 2023-10-09 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Leu14Profs*13) in the FANCL gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in FANCL are known to be pathogenic (PMID: 19405097, 23613520). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with FANCL-related conditions. ClinVar contains an entry for this variant (Variation ID: 575609). For these reasons, this variant has been classified as Pathogenic.

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