ClinVar Miner

Submissions for variant NM_000136.3(FANCC):c.457-10del

dbSNP: rs763416214
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000691188 SCV000818935 uncertain significance Fanconi anemia 2018-04-28 criteria provided, single submitter clinical testing This sequence change falls in intron 5 of the FANCC gene. It does not directly change the encoded amino acid sequence of the FANCC protein. This variant is present in population databases (rs763416214, ExAC 0.002%). This variant has not been reported in the literature in individuals with FANCC-related disease. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site, but this prediction has not been confirmed by published transcriptional studies. 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.

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