ClinVar Miner

Submissions for variant NM_004453.4(ETFDH):c.1169del (p.Gly390fs)

dbSNP: rs1774519872
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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 RCV001047294 SCV001211241 pathogenic Multiple acyl-CoA dehydrogenase deficiency 2023-01-14 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Gly390Valfs*3) in the ETFDH gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in ETFDH are known to be pathogenic (PMID: 16510302, 23785301). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with ETFDH-related conditions. ClinVar contains an entry for this variant (Variation ID: 844449). For these reasons, this variant has been classified as Pathogenic.

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