ClinVar Miner

Submissions for variant NM_001204.7(BMPR2):c.894G>A (p.Trp298Ter)

dbSNP: rs2106008336
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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 RCV001874756 SCV002144408 pathogenic Primary pulmonary hypertension 2021-03-26 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This nonsense change has been observed in individual(s) with pulmonary arterial hypertension (PMID: 31727138, 27630060). This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Trp298*) in the BMPR2 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in BMPR2 are known to be pathogenic (PMID: 16429395).

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