ClinVar Miner

Submissions for variant NM_001164277.2(SLC37A4):c.728G>A (p.Cys243Tyr)

dbSNP: rs1555191076
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000672710 SCV000797844 uncertain significance Glucose-6-phosphate transport defect 2018-02-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000672710 SCV002965226 uncertain significance Glucose-6-phosphate transport defect 2021-07-26 criteria provided, single submitter clinical testing This sequence change replaces cysteine with tyrosine at codon 243 of the SLC37A4 protein (p.Cys243Tyr). The cysteine residue is highly conserved and there is a large physicochemical difference between cysteine and tyrosine. 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. ClinVar contains an entry for this variant (Variation ID: 556676). 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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