ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.3985_*2dup (p.Ter1329=)

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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 RCV003062806 SCV003451597 uncertain significance Fanconi anemia 2023-12-11 criteria provided, single submitter clinical testing This variant occurs in a non-coding region of the FANCI gene. It does not change the encoded amino acid sequence of the FANCI protein. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with FANCI-related conditions. ClinVar contains an entry for this variant (Variation ID: 2143809). Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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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