ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.3224C>T (p.Ser1075Phe)

dbSNP: rs147558074
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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 RCV002037053 SCV002318309 uncertain significance Fanconi anemia 2021-05-04 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals with SLX4-related conditions. This variant is present in population databases (rs147558074, ExAC 0.01%). This sequence change replaces serine with phenylalanine at codon 1075 of the SLX4 protein (p.Ser1075Phe). The serine residue is moderately conserved and there is a large physicochemical difference between serine and phenylalanine. 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 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.

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