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NM_000138.5(FBN1):c.1900T>C (p.Ser634Pro) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 13, 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:
RCV001800851.1

Allele description [Variation Report for NM_000138.5(FBN1):c.1900T>C (p.Ser634Pro)]

NM_000138.5(FBN1):c.1900T>C (p.Ser634Pro)

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.1900T>C (p.Ser634Pro)
HGVS:
  • NC_000015.10:g.48505085A>G
  • NG_008805.2:g.145704T>C
  • NM_000138.5:c.1900T>CMANE SELECT
  • NP_000129.3:p.Ser634Pro
  • NP_000129.3:p.Ser634Pro
  • LRG_778t1:c.1900T>C
  • LRG_778:g.145704T>C
  • LRG_778p1:p.Ser634Pro
  • NC_000015.9:g.48797282A>G
  • NM_000138.4:c.1900T>C
Protein change:
S634P
Links:
dbSNP: rs1566914005
NCBI 1000 Genomes Browser:
rs1566914005
Molecular consequence:
  • NM_000138.5:c.1900T>C - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Name:
Pes planus
Synonyms:
flatfoot
Identifiers:
MONDO: MONDO:0005293; MedGen: C0016202; Human Phenotype Ontology: HP:0001763
Name:
Arachnodactyly
Identifiers:
MedGen: C0003706; Human Phenotype Ontology: HP:0001166
Name:
Mitral valve prolapse
Identifiers:
MONDO: MONDO:0004910; MedGen: C0026267; Human Phenotype Ontology: HP:0001634
Name:
Lens luxation
Identifiers:
MedGen: C0023309; Human Phenotype Ontology: HP:0012019
Name:
Aortic aneurysm
Synonyms:
Aortic aneurysm (disease)
Identifiers:
MONDO: MONDO:0005160; MedGen: C0003486; Human Phenotype Ontology: HP:0004942

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002047384Institute of Human Genetics, University Hospital Muenster
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Dec 13, 2021) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not providednot providednot providednot providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Institute of Human Genetics, University Hospital Muenster, SCV002047384.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)

Description

ACMG categories: PM2,PP3,BP1

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providedbloodnot provided1not providednot providednot provided

Last Updated: Sep 29, 2024