ClinVar Miner

Submissions for variant NM_003060.4(SLC22A5):c.1636C>T (p.Gln546Ter)

dbSNP: rs1752804300
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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 RCV001321014 SCV001511827 uncertain significance Renal carnitine transport defect 2022-06-24 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Gln546*) in the SLC22A5 gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 12 amino acid(s) of the SLC22A5 protein. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with SLC22A5-related conditions. ClinVar contains an entry for this variant (Variation ID: 1021279). 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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