ClinVar Miner

Submissions for variant NM_173660.5(DOK7):c.1387G>T (p.Glu463Ter)

dbSNP: rs745941308
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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 RCV001381053 SCV001579305 pathogenic Fetal akinesia deformation sequence 1; Congenital myasthenic syndrome 10 2020-02-17 criteria provided, single submitter clinical testing This sequence change results in a premature translational stop signal in the DOK7 gene (p.Glu463*). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 42 amino acids of the DOK7 protein. 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 DOK7 protein. Other variant(s) that disrupt this region (p.Pro486Argfs*15) have been determined to be pathogenic (PMID: 29118959). 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 DOK7-related conditions.

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