ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.1154A>G (p.His385Arg)

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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 RCV003025227 SCV003345095 uncertain significance Fanconi anemia 2021-09-29 criteria provided, single submitter clinical testing This sequence change replaces histidine with arginine at codon 385 of the FANCA protein (p.His385Arg). The histidine residue is weakly conserved and there is a small physicochemical difference between histidine and arginine. This variant is present in population databases (rs143262599, ExAC 0.05%). This variant has not been reported in the literature in individuals affected with FANCA-related conditions. 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: "Benign"; Align-GVGD: "Class C0"). 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 RCV005019580 SCV005646659 uncertain significance Fanconi anemia complementation group A 2024-05-13 criteria provided, single submitter clinical testing

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