ClinVar Miner

Submissions for variant NM_021922.3(FANCE):c.592G>A (p.Gly198Arg)

gnomAD frequency: 0.00003  dbSNP: rs747727711
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000538869 SCV000650820 uncertain significance Fanconi anemia complementation group E 2024-01-24 criteria provided, single submitter clinical testing This sequence change replaces glycine, which is neutral and non-polar, with arginine, which is basic and polar, at codon 198 of the FANCE protein (p.Gly198Arg). This variant is present in population databases (rs747727711, gnomAD 0.07%). This variant has not been reported in the literature in individuals affected with FANCE-related conditions. ClinVar contains an entry for this variant (Variation ID: 471930). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt FANCE protein function with a negative predictive value of 80%. 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.
Fulgent Genetics, Fulgent Genetics RCV000538869 SCV002779246 uncertain significance Fanconi anemia complementation group E 2022-04-01 criteria provided, single submitter clinical testing

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