ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.3006+4C>G

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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 RCV002904876 SCV003260951 uncertain significance Fanconi anemia 2021-12-21 criteria provided, single submitter clinical testing Variants that disrupt the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. This variant has not been reported in the literature in individuals affected with FANCI-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change falls in intron 27 of the FANCI gene. It does not directly change the encoded amino acid sequence of the FANCI protein. It affects a nucleotide within the consensus splice site.

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