ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.3835A>G (p.Arg1279Gly)

gnomAD frequency: 0.00001  dbSNP: rs1252550783
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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 RCV001904670 SCV002124772 uncertain significance Fanconi anemia 2022-08-19 criteria provided, single submitter clinical testing This sequence change replaces arginine, which is basic and polar, with glycine, which is neutral and non-polar, at codon 1279 of the SLX4 protein (p.Arg1279Gly). This variant is present in population databases (no rsID available, gnomAD 0.0009%). This variant has not been reported in the literature in individuals affected with SLX4-related conditions. ClinVar contains an entry for this variant (Variation ID: 1360024). Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The glycine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. 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 RCV002489993 SCV002776273 uncertain significance Fanconi anemia complementation group P 2022-03-24 criteria provided, single submitter clinical testing

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