ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.929G>A (p.Arg310Gln)

gnomAD frequency: 0.00003  dbSNP: rs759447034
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000702365 SCV000831217 uncertain significance Fanconi anemia 2022-08-22 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. 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: "Tolerated"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). ClinVar contains an entry for this variant (Variation ID: 579152). This missense change has been observed in individual(s) with idiopathic aplastic anemia or breast cancer (PMID: 24763404, 30613976). This variant is present in population databases (rs759447034, gnomAD 0.01%). This sequence change replaces arginine, which is basic and polar, with glutamine, which is neutral and polar, at codon 310 of the SLX4 protein (p.Arg310Gln).
Fulgent Genetics, Fulgent Genetics RCV002499261 SCV002782377 uncertain significance Fanconi anemia complementation group P 2021-07-30 criteria provided, single submitter clinical testing

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