ClinVar Miner

Submissions for variant NM_022725.4(FANCF):c.583C>T (p.Arg195Cys)

dbSNP: rs1231820160
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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 RCV001960492 SCV002221525 uncertain significance Fanconi anemia 2021-07-28 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. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C15"). This variant has not been reported in the literature in individuals affected with FANCF-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces arginine with cysteine at codon 195 of the FANCF protein (p.Arg195Cys). The arginine residue is moderately conserved and there is a large physicochemical difference between arginine and cysteine.

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