NM_001204.7(BMPR2):c.2442_2443del (p.His814fs) 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:: RCV000488686.2

Allele description [Variation Report for NM_001204.7(BMPR2):c.2442_2443del (p.His814fs)]

NM_001204.7(BMPR2):c.2442_2443del (p.His814fs)

Gene:

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

Variant type:

Microsatellite

Cytogenetic location:

2q33.2

Genomic location:

Preferred name:

NM_001204.7(BMPR2):c.2442_2443del (p.His814fs)

HGVS:

NC_000002.12:g.202556105CA[1]
NG_009363.1:g.184779CA[1]
NM_001204.7:c.2442_2443delMANE SELECT
NP_001195.2:p.H814Qfs*3
NP_001195.2:p.His814fs
LRG_712t1:c.2442_2443del
LRG_712:g.184779CA[1]
NC_000002.11:g.203420828CA[1]
NM_001204.6:c.2442_2443delCA

Protein change:

H814fs

Links:

dbSNP: rs1085307385

NCBI 1000 Genomes Browser:

rs1085307385

Molecular consequence:

NM_001204.7:c.2442_2443del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:: Pulmonary hypertension, primary, 1
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
SCV000576288	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

SCV000576288

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

Genetics and genomics of pulmonary arterial hypertension.

Machado RD, Eickelberg O, Elliott CG, Geraci MW, Hanaoka M, Loyd JE, Newman JH, Phillips JA 3rd, Soubrier F, Trembath RC, Chung WK.

J Am Coll Cardiol. 2009 Jun 30;54(1 Suppl):S32-S42. doi: 10.1016/j.jacc.2009.04.015. Review.

PubMed [citation]

PMID:: 19555857
PMCID:: PMC3725550

Details of each submission

From Rare Disease Genomics Group, St George's University of London, SCV000576288.1

#	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: Feb 20, 2024

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