ClinVar Miner

Submissions for variant NM_001204.7(BMPR2):c.1525G>T (p.Glu509Ter)

dbSNP: rs1085307363
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002528227 SCV003525187 pathogenic Primary pulmonary hypertension 2021-12-17 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Glu509*) 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). For these reasons, this variant has been classified as Pathogenic. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site. ClinVar contains an entry for this variant (Variation ID: 425957). This premature translational stop signal has been observed in individual(s) with pulmonary arterial hypertension (PMID: 25429696). This variant is not present in population databases (gnomAD no frequency).
Rare Disease Genomics Group, St George's University of London RCV000488517 SCV000576258 pathogenic Pulmonary hypertension, primary, 1 no assertion criteria provided literature only

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