NM_001204.7(BMPR2):c.802dup (p.Thr268fs) AND Pulmonary hypertension, primary, 1

Germline classification:: Pathogenic (1 submission)
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV000488507.2

Allele description [Variation Report for NM_001204.7(BMPR2):c.802dup (p.Thr268fs)]

NM_001204.7(BMPR2):c.802dup (p.Thr268fs)

Gene:

BMPR2:bone morphogenetic protein receptor type 2 [Gene - OMIM - HGNC]

Variant type:

Duplication

Cytogenetic location:

2q33.2

Genomic location:

Preferred name:

NM_001204.7(BMPR2):c.802dup (p.Thr268fs)

HGVS:

NC_000002.12:g.202519002dup
NG_009363.1:g.147676dup
NM_001204.7:c.802dupMANE SELECT
NP_001195.2:p.Thr268fs
LRG_712t1:c.802dup
LRG_712:g.147676dup
LRG_712p1:p.T268Nfs*30
NC_000002.11:g.203383725dup
NM_001204.6:c.802dupA
NP_001195.2:p.T268Nfs*30

Protein change:

T268fs

Links:

dbSNP: rs1085307262

NCBI 1000 Genomes Browser:

rs1085307262

Molecular consequence:

NM_001204.7:c.802dup - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:: Pulmonary hypertension, primary, 1 (PPH1)
Identifiers:: MONDO: MONDO:0024533; MedGen: C4552070; Orphanet: 422; OMIM: 178600

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000576112	Rare Disease Genomics Group, St George's University of London	no assertion criteria provided	Pathogenic	germline	literature only	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000576112

Rare Disease Genomics Group, St George's University of London

no assertion criteria provided

Pathogenic

germline

literature only

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	literature only

Citations

PubMed

Identities and frequencies of BMPR2 mutations in Chinese patients with idiopathic pulmonary arterial hypertension.

Wang H, Cui QQ, Sun K, Song L, Zou YB, Wang XJ, Jia L, Liu X, Gao S, Zhang CN, Hui RT.

Clin Genet. 2010 Feb;77(2):189-92. doi: 10.1111/j.1399-0004.2009.01335.x. Epub 2009 Dec 10. No abstract available.

PubMed [citation]

PMID:: 20002458

Details of each submission

From Rare Disease Genomics Group, St George's University of London, SCV000576112.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	literature only	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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