ClinVar Miner

Submissions for variant NM_000191.3(HMGCL):c.610dup (p.Asp204fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Genetics, Suzhou Beikang Medical Laboratory RCV004776494 SCV005387806 likely pathogenic Deficiency of hydroxymethylglutaryl-CoA lyase 2024-10-31 no assertion criteria provided clinical testing This sequence change creates a premature translational stop signal (p.Ile560Hisfs*8) in the HMGCL gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in HMGCL are known to be pathogenic (PMID: 9817922, 17692550, 23465862). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with HMGCL-related conditions.In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. For these reasons, this variant has been classified as Likely Pathogenic.

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