ClinVar Miner

Submissions for variant NM_001182.5(ALDH7A1):c.1267A>G (p.Ile423Val) (rs760266177)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000186743 SCV000240310 uncertain significance not provided 2014-04-02 criteria provided, single submitter clinical testing p.Ile423Val (ATT>GTT): c.1267 A>G in exon 14 of the ALDH7A1 gene (NM_001182.4). The I423V variant has not been published as a mutation, nor has it been reported as a benign polymorphism to our knowledge. It was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. This variant is a conservative amino acid substitution, which is not likely to impact secondary protein structure as these residues share similar properties. It occurs at a position that is conserved across species. In silico analysis is inconsistent in its predictions as to whether or not the variant is damaging to the protein structure/function. Missense mutations in nearby residues (T426P, E427Q/G/D) have been reported in association with pyridoxine-dependent epilepsy, supporting the functional importance of this region of the protein. Therefore, based on the currently available information, it is unclear whether this variant is a pathogenic mutation or a rare benign variant. The variant is found in EPILEPSY panel(s).

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