ClinVar Miner

Submissions for variant NM_002225.5(IVD):c.1071_1072del (p.Ala358fs)

dbSNP: rs1891674455
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001047853 SCV001211835 pathogenic Isovaleryl-CoA dehydrogenase deficiency 2019-12-30 criteria provided, single submitter clinical testing This variant is not present in population databases (ExAC no frequency). For these reasons, this variant has been classified as Pathogenic. This variant disrupts the C-terminus of the IVD protein. Other variant(s) that disrupt this region (p.Leu397Phefs*9) have been determined to be pathogenic (PMID: 10713113, 2063866, Invitae). This suggests that variants that disrupt this region of the protein are likely to be causative of disease. This variant has not been reported in the literature in individuals with IVD-related conditions. This sequence change results in a premature translational stop signal in the IVD gene (p.Ala361Argfs*8). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 66 amino acids of the IVD protein.

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