ClinVar Miner

Submissions for variant NM_014049.4(ACAD9):c.[1298G>A];[151-2A>G]

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institut IMAGINE, Institut National de la Sante et de la Recherche Medicale RCV000201557 SCV000255970 pathogenic Acyl-CoA dehydrogenase 9 deficiency 2015-08-27 no assertion criteria provided clinical testing predicted to be deleterious using three different prediction softwares, namely SIFT, MutationTaster and Polyphen-2

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