U.S. flag

An official website of the United States government

NM_000138.5(FBN1):c.5917+3A>C AND Marfan syndrome

Germline classification:
Uncertain significance (2 submissions)
Last evaluated:
Mar 1, 2021
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV000663832.2

Allele description [Variation Report for NM_000138.5(FBN1):c.5917+3A>C]

NM_000138.5(FBN1):c.5917+3A>C

Gene:
FBN1:fibrillin 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
15q21.1
Genomic location:
Preferred name:
NM_000138.5(FBN1):c.5917+3A>C
HGVS:
  • NC_000015.10:g.48445373T>G
  • NG_008805.2:g.205416A>C
  • NM_000138.5:c.5917+3A>CMANE SELECT
  • LRG_778t1:c.5917+3A>C
  • LRG_778:g.205416A>C
  • NC_000015.9:g.48737570T>G
  • NM_000138.4:c.5917+3A>C
Links:
dbSNP: rs202158568
NCBI 1000 Genomes Browser:
rs202158568
Molecular consequence:
  • NM_000138.5:c.5917+3A>C - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Marfan syndrome (MFS)
Synonyms:
MARFAN SYNDROME, TYPE I; Marfan syndrome type 1; Marfan's syndrome; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0007947; MedGen: C0024796; Orphanet: 284963; Orphanet: 558; OMIM: 154700

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000787189Center for Medical Genetics Ghent, University of Ghent
no assertion criteria provided
Uncertain significance
(Nov 7, 2017) 		germlineclinical testing

SCV002025371Centre of Medical Genetics, University of Antwerp
criteria provided, single submitter

(Submitter's publication)		Uncertain significance
(Mar 1, 2021) 		unknownresearch

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing
not providedunknownyesnot providednot providednot providednot providednot providedresearch

Details of each submission

From Center for Medical Genetics Ghent, University of Ghent, SCV000787189.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

From Centre of Medical Genetics, University of Antwerp, SCV002025371.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedresearchnot provided

Description

PM2, PP6, PP4

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Dec 11, 2022