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46;XX;t(7;14)(p15;q24)dn AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 20, 2016
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:
RCV000258620.2

Allele description [Variation Report for 46;XX;t(7;14)(p15;q24)dn]

46;XX;t(7;14)(p15;q24)dn

Variant type:
Translocation
Cytogenetic location:
14q24
Preferred name:
46;XX;t(7;14)(p15;q24)dn

Condition(s)

Name:
Hypertelorism
Identifiers:
MedGen: C0020534; OMIM: 145400; Human Phenotype Ontology: HP:0000316
Name:
Triphalangeal thumb (TPT)
Identifiers:
MedGen: C0241397; Human Phenotype Ontology: HP:0001199
Name:
Global developmental delay (DD)
Identifiers:
MedGen: C0557874; Human Phenotype Ontology: HP:0001263
Name:
Motor delay
Synonyms:
Motor retardation; motor developmental delay
Identifiers:
MedGen: C1854301; Human Phenotype Ontology: HP:0001270
Name:
Low-set ears
Identifiers:
MedGen: C0239234; Human Phenotype Ontology: HP:0000369
Name:
Anteriorly placed anus
Identifiers:
MedGen: C1838705; Human Phenotype Ontology: HP:0001545
Name:
Broad forehead
Identifiers:
MedGen: C1849089; Human Phenotype Ontology: HP:0000337
Name:
Broad hallux
Identifiers:
MedGen: C1867131; Human Phenotype Ontology: HP:0010055
Name:
Delayed speech and language development
Identifiers:
MedGen: C0454644; Human Phenotype Ontology: HP:0000750
Name:
Frontal bossing
Identifiers:
MedGen: C0221354; Human Phenotype Ontology: HP:0002007
Name:
High forehead
Identifiers:
MedGen: C0239676; Human Phenotype Ontology: HP:0000348
Name:
Joint hypermobility
Identifiers:
MedGen: C1844820; Human Phenotype Ontology: HP:0001382
Name:
Bilateral triphalangeal thumbs
Identifiers:
MedGen: C4021627; Human Phenotype Ontology: HP:0005707
Name:
Finger syndactyly
Identifiers:
MedGen: C0221352; Human Phenotype Ontology: HP:0006101

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000320974Talkowski Laboratory, Center for Human Genetic Research, Massachusetts General Hospital
criteria provided, single submitter

(Talkowski Lab Assertion Criteria for BCA 2016)
Uncertain significance
(Aug 20, 2016)
de novoresearch

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

Talkowski_Lab_Assertion_Criteria_for_BCA_2016.pdf

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedde novoyesnot providednot providednot providednot providednot providedresearch

Citations

PubMed

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.

Redin C, Brand H, Collins RL, Kammin T, Mitchell E, Hodge JC, Hanscom C, Pillalamarri V, Seabra CM, Abbott MA, Abdul-Rahman OA, Aberg E, Adley R, Alcaraz-Estrada SL, Alkuraya FS, An Y, Anderson MA, Antolik C, Anyane-Yeboa K, Atkin JF, Bartell T, Bernstein JA, et al.

Nat Genet. 2017 Jan;49(1):36-45. doi: 10.1038/ng.3720. Epub 2016 Nov 14.

PubMed [citation]
PMID:
27841880
PMCID:
PMC5307971

Details of each submission

From Talkowski Laboratory, Center for Human Genetic Research, Massachusetts General Hospital, SCV000320974.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedresearch PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1de novoyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 30, 2023