ClinVar Miner

Submissions for variant NM_000018.4(ACADVL):c.428G>C (p.Gly143Ala)

dbSNP: rs1458941582
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine RCV001200814 SCV001365014 uncertain significance Very long chain acyl-CoA dehydrogenase deficiency 2019-11-01 criteria provided, single submitter clinical testing The NM_000018.3:c.428G>C (NP_000009.1:p.Gly143Ala) [GRCH38: NC_000017.11:g.7221009G>C] variant in ACADVL gene is interpretated to be Uncertain Significance based on ACMG guidelines (PMID: 25741868). This variant has been reported. This variant meets the following evidence codes reported in the ACMG guidelines: PP3
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV001200814 SCV005441939 likely pathogenic Very long chain acyl-CoA dehydrogenase deficiency 2024-12-19 criteria provided, single submitter clinical testing

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