ClinVar Miner

Submissions for variant NM_017849.4(TMEM127):c.370A>T (p.Lys124Ter)

dbSNP: rs1684169953
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001035532 SCV001198861 pathogenic Hereditary pheochromocytoma-paraganglioma 2019-02-08 criteria provided, single submitter clinical testing This sequence change results in a premature translational stop signal in the TMEM127 gene (p.Lys124*). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 115 amino acids of the TMEM127 protein. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with TMEM127-related conditions. This variant disrupts the C-terminus of the TMEM127 protein. Other variant(s) that disrupt this region (p.Gln157*, p.Gln159*) have been determined to be pathogenic (PMID: 22419703, 20154675, Invitae). This suggests that variants that disrupt this region of the protein are likely to be causative of disease. For these reasons, this variant has been classified as Pathogenic.

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