ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.3683C>A (p.Ser1228Tyr)

gnomAD frequency: 0.00001  dbSNP: rs755523528
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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 RCV000459491 SCV000547472 uncertain significance Fanconi anemia 2016-11-16 criteria provided, single submitter clinical testing In summary, this variant is a rare missense change that is not predicted to affect protein function. There is no indication that it causes disease, but the available evidence is currently insufficient to prove that conclusively. 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 output the following: (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). The tyrosine amino acid residue is found in multiple mammalian species, suggesting that this missense change does not adversely affect protein function. These predictions have not been confirmed by published functional studies. This variant is present in population databases (rs755523528, ExAC 0.02%) but has not been reported in the literature in individuals with a SLX4-related disease. This sequence change replaces serine with tyrosine at codon 1228 of the SLX4 protein (p.Ser1228Tyr). The serine residue is moderately conserved and there is a large physicochemical difference between serine and tyrosine.

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