ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.410C>G (p.Ser137Cys)

dbSNP: rs1203036492
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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 RCV001945799 SCV002205152 uncertain significance Fanconi anemia 2022-09-22 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 FANCG protein function. ClinVar contains an entry for this variant (Variation ID: 1427018). This variant has not been reported in the literature in individuals affected with FANCG-related conditions. This variant is present in population databases (no rsID available, gnomAD 0.003%). This sequence change replaces serine, which is neutral and polar, with cysteine, which is neutral and slightly polar, at codon 137 of the FANCG protein (p.Ser137Cys).

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