ClinVar Miner

Submissions for variant NM_000191.3(HMGCL):c.2T>C (p.Met1Thr)

dbSNP: rs2148428492
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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 RCV001954315 SCV002244106 uncertain significance Deficiency of hydroxymethylglutaryl-CoA lyase 2021-08-28 criteria provided, single submitter clinical testing This sequence change affects the initiator methionine of the HMGCL mRNA. The next in-frame methionine is located at codon 4. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with HMGCL-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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