ClinVar Miner

Submissions for variant NM_003060.4(SLC22A5):c.1492C>A (p.Leu498Met)

dbSNP: rs183379391
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001912901 SCV002172902 uncertain significance Renal carnitine transport defect 2021-10-14 criteria provided, single submitter clinical testing This sequence change replaces leucine with methionine at codon 498 of the SLC22A5 protein (p.Leu498Met). The leucine residue is highly conserved and there is a small physicochemical difference between leucine and methionine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with SLC22A5-related conditions. 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: "Benign"; 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.
Fulgent Genetics, Fulgent Genetics RCV001912901 SCV002797110 uncertain significance Renal carnitine transport defect 2021-07-06 criteria provided, single submitter clinical testing

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