U.S. flag

An official website of the United States government

NM_024529.5(CDC73):c.-4dup AND Hyperparathyroidism 2 with jaw tumors

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 14, 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:
RCV000401688.12

Allele description [Variation Report for NM_024529.5(CDC73):c.-4dup]

NM_024529.5(CDC73):c.-4dup

Gene:
CDC73:cell division cycle 73 [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
1q31.2
Genomic location:
Preferred name:
NM_024529.5(CDC73):c.-4dup
HGVS:
  • NC_000001.11:g.193122197dup
  • NG_012691.1:g.5240dup
  • NM_024529.5:c.-4dupMANE SELECT
  • LRG_507t1:c.-4dup
  • LRG_507:g.5240dup
  • NC_000001.10:g.193091319_193091320insG
  • NC_000001.10:g.193091327dup
  • NM_024529.4:c.-4dup
  • NM_024529.4:c.-4dupG
  • NM_024529.5:c.-4dupGMANE SELECT
Links:
dbSNP: rs545666726
NCBI 1000 Genomes Browser:
rs545666726
Molecular consequence:
  • NM_024529.5:c.-4dup - 5 prime UTR variant - [Sequence Ontology: SO:0001623]

Condition(s)

Name:
Hyperparathyroidism 2 with jaw tumors
Synonyms:
HYPERPARATHYROIDISM, FAMILIAL PRIMARY, WITH MULTIPLE OSSIFYING JAW FIBROMAS; HYPERPARATHYROIDISM-JAW TUMOR SYNDROME, HEREDITARY; Hyperparathyroidism 2
Identifiers:
MONDO: MONDO:0007768; MedGen: C1704981; Orphanet: 99880; OMIM: 145001

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
SCV000352113Illumina Laboratory Services, Illumina
criteria provided, single submitter

(ICSL Variant Classification 20161018)		Uncertain significance
(Jun 14, 2016) 		germlineclinical testing

ICSL_Variant_Classification_20161018.pdf

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Illumina Laboratory Services, Illumina, SCV000352113.2

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

Last Updated: Nov 24, 2024