ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.878T>C (p.Leu293Pro)

gnomAD frequency: 0.00003  dbSNP: rs886042302
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000332634 SCV000333247 uncertain significance not provided 2015-08-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001279136 SCV001516861 uncertain significance Glucose-6-phosphate transport defect 2023-11-20 criteria provided, single submitter clinical testing This sequence change replaces leucine, which is neutral and non-polar, with proline, which is neutral and non-polar, at codon 293 of the SLC37A4 protein (p.Leu293Pro). This variant is present in population databases (no rsID available, gnomAD 0.007%). This variant has not been reported in the literature in individuals affected with SLC37A4-related conditions. ClinVar contains an entry for this variant (Variation ID: 282064). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt SLC37A4 protein function with a negative predictive value of 95%. 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.
Natera, Inc. RCV001279136 SCV001466215 uncertain significance Glucose-6-phosphate transport defect 2020-04-16 no assertion criteria provided clinical testing

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