ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.940T>C (p.Ser314Pro)

gnomAD frequency: 0.00001  dbSNP: rs1365079218
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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 RCV001874194 SCV002121260 uncertain significance Glucose-6-phosphate transport defect 2021-08-14 criteria provided, single submitter clinical testing This sequence change replaces serine with proline at codon 314 of the SLC37A4 protein (p.Ser314Pro). The serine residue is highly conserved and there is a moderate physicochemical difference between serine and proline. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with SLC37A4-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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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