ClinVar Miner

Submissions for variant NM_020166.5(MCCC1):c.1126del (p.Thr376fs)

dbSNP: rs2530166841
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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 RCV003879924 SCV004684552 pathogenic 3-methylcrotonyl-CoA carboxylase 1 deficiency 2024-01-18 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Thr376Leufs*27) in the MCCC1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in MCCC1 are known to be pathogenic (PMID: 11181649, 15359379, 22642865). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with MCCC1-related conditions. For these reasons, this variant has been classified as Pathogenic.
Fulgent Genetics, Fulgent Genetics RCV003879924 SCV005661958 likely pathogenic 3-methylcrotonyl-CoA carboxylase 1 deficiency 2024-05-25 criteria provided, single submitter clinical testing

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