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NM_000138.5(FBN1):c.8461A>C (p.Lys2821Gln) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Mar 21, 2017
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:
RCV000181634.2

Allele description [Variation Report for NM_000138.5(FBN1):c.8461A>C (p.Lys2821Gln)]

NM_000138.5(FBN1):c.8461A>C (p.Lys2821Gln)

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.8461A>C (p.Lys2821Gln)
Other names:
p.K2821Q:AAG>CAG
HGVS:
  • NC_000015.10:g.48411145T>G
  • NG_008805.2:g.239644A>C
  • NM_000138.5:c.8461A>CMANE SELECT
  • NP_000129.3:p.Lys2821Gln
  • NP_000129.3:p.Lys2821Gln
  • LRG_778t1:c.8461A>C
  • LRG_778:g.239644A>C
  • LRG_778p1:p.Lys2821Gln
  • NC_000015.9:g.48703342T>G
  • NM_000138.4:c.8461A>C
Protein change:
K2821Q
Links:
dbSNP: rs794728286
NCBI 1000 Genomes Browser:
rs794728286
Molecular consequence:
  • NM_000138.5:c.8461A>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000233937GeneDx
criteria provided, single submitter

(GeneDx Variant Classification (06012015))
Uncertain significance
(Mar 21, 2017)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From GeneDx, SCV000233937.11

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

A variant of uncertain significance has been identified in the FBN1 gene. The K2821Q variant has not been published as pathogenic or been reported as benign to our knowledge. This variant is not observed in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). The K2821Q variant is a semi-conservative amino acid substitution, which may impact secondary protein structure as these residues differ in some properties. Additionally, this substitution occurs at a position that is conserved across species. Furthermore, in silico analysis predicts this substitution is likely damaging to the protein structure/function. Nevertheless, the K2821Q variant does not affect a Cysteine residue within a calcium-binding EGF-like domain of the FBN1 gene. Cysteine substitutions in the calcium-binding EGF-like domains represent the majority of pathogenic missense changes associated with Marfan syndrome (Collod-Beroud et al., 2003).

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

Last Updated: Nov 3, 2024