ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.787_788del (p.Gln263fs)

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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 RCV003637177 SCV004490221 pathogenic Fanconi anemia 2022-12-20 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Gln263Glufs*25) in the FANCG gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in FANCG are known to be pathogenic (PMID: 12552564). For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals affected with FANCG-related conditions. This variant is not present in population databases (gnomAD no frequency).

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