ClinVar Miner

Submissions for variant NM_004387.4(NKX2-5):c.377_378del (p.Glu126fs)

dbSNP: rs2113902216
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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 RCV001904166 SCV002124077 pathogenic Atrial septal defect 7 2023-07-13 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with NKX2-5-related conditions. For these reasons, this variant has been classified as Pathogenic. This variant disrupts a region of the NKX2-5 protein in which other variant(s) (p.Ala262Argfs*32) have been determined to be pathogenic (PMID: 22920929). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Glu126Glyfs*26) in the NKX2-5 gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 199 amino acid(s) of the NKX2-5 protein.

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