ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2573G>C (p.Ser858Thr)

gnomAD frequency: 0.00001  dbSNP: rs1291169859
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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 RCV001988454 SCV002273587 uncertain significance Fanconi anemia 2021-04-16 criteria provided, single submitter clinical testing 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. 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 FANCA protein function. This variant has not been reported in the literature in individuals with FANCA-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces serine with threonine at codon 858 of the FANCA protein (p.Ser858Thr). The serine residue is weakly conserved and there is a small physicochemical difference between serine and threonine.

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