U.S. flag

An official website of the United States government

NM_001457.4(FLNB):c.3350A>G (p.His1117Arg) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 8, 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:
RCV002491435.1

Allele description [Variation Report for NM_001457.4(FLNB):c.3350A>G (p.His1117Arg)]

NM_001457.4(FLNB):c.3350A>G (p.His1117Arg)

Gene:
FLNB:filamin B [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
3p14.3
Genomic location:
Preferred name:
NM_001457.4(FLNB):c.3350A>G (p.His1117Arg)
HGVS:
  • NC_000003.12:g.58123316A>G
  • NG_012801.1:g.119917A>G
  • NM_001164317.2:c.3350A>G
  • NM_001164318.2:c.3350A>G
  • NM_001164319.2:c.3350A>G
  • NM_001457.4:c.3350A>GMANE SELECT
  • NP_001157789.1:p.His1117Arg
  • NP_001157790.1:p.His1117Arg
  • NP_001157791.1:p.His1117Arg
  • NP_001448.2:p.His1117Arg
  • NC_000003.11:g.58109043A>G
  • NC_000003.11:g.58109043A>G
  • NM_001457.3:c.3350A>G
Protein change:
H1117R
Links:
dbSNP: rs779765790
NCBI 1000 Genomes Browser:
rs779765790
Molecular consequence:
  • NM_001164317.2:c.3350A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001164318.2:c.3350A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001164319.2:c.3350A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001457.4:c.3350A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Atelosteogenesis type III
Synonyms:
Atelosteogenesis type 3
Identifiers:
MONDO: MONDO:0007168; MedGen: C3668942; Orphanet: 56305; OMIM: 108721
Name:
Atelosteogenesis type I
Synonyms:
Atelosteogenesis type 1; Giant cell chondrodysplasia; Spondylohumerofemoral hypoplasia
Identifiers:
MONDO: MONDO:0007167; MedGen: C0265283; Orphanet: 1190; OMIM: 108720
Name:
Boomerang dysplasia
Synonyms:
Dwarfism with short, bowed, rigid limbs and characteristic facies; Boomerang-like skeletal dysplasia
Identifiers:
MONDO: MONDO:0007208; MedGen: C0432201; Orphanet: 1263; OMIM: 112310
Name:
Spondylocarpotarsal synostosis syndrome (SCT)
Synonyms:
Spondylocarpotarsal syndrome; Synspondylism congenital; Vertebral fusion with carpal coalition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0010094; MedGen: C1848934; Orphanet: 3275; OMIM: 272460
Name:
Larsen syndrome (LRS)
Synonyms:
Larsen syndrome, dominant type; Bilateral dislocation of the knees, pes cavus, cylindrically shaped fingers and characteristic facies
Identifiers:
MONDO: MONDO:0007875; MedGen: C0175778; Orphanet: 503; OMIM: 150250

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
SCV002775755Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Oct 8, 2021) 		unknownclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot 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 Fulgent Genetics, Fulgent Genetics, SCV002775755.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024