ClinVar Miner

Submissions for variant NC_000002.11:g.(?_203384790)_(203421274_?)del

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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 RCV003105665 SCV003792476 pathogenic Primary pulmonary hypertension 2022-07-17 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant disrupts a region of the BMPR2 protein in which other variant(s) (p.Cys420Tyr) have been determined to be pathogenic (PMID: 15146475, 21737554, 21801371, 27453251; Invitae). 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 has not been reported in the literature in individuals affected with BMPR2-related conditions. This variant is a gross deletion of the genomic region encompassing exon(s) 7-12 of the BMPR2 gene. While this deletion is not anticipated to lead to nonsense mediated decay, it is expected to disrupt the C-terminus of the protein.

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