NM_144991.3(TSPEAR):c.1754+145_1754+172del AND not provided

Germline classification:: Likely benign (1 submission)
Last evaluated:: Dec 31, 2018
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:: RCV001559591.2

Allele description [Variation Report for NM_144991.3(TSPEAR):c.1754+145_1754+172del]

NM_144991.3(TSPEAR):c.1754+145_1754+172del

Genes:

LOC126653398:CDK7 strongly-dependent group 2 enhancer GRCh37_chr21:45928270-45929469 [Gene]
TSPEAR-AS1:TSPEAR antisense RNA 1 [Gene - HGNC]
TSPEAR:thrombospondin type laminin G domain and EAR repeats [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

21q22.3

Genomic location:

Preferred name:

NM_144991.3(TSPEAR):c.1754+145_1754+172del

HGVS:

NC_000021.9:g.44509039TTCTTTCCACAGGAAGGTCCCCAGGCCA[1]
NG_033806.1:g.207497CTTCCTGTGGAAAGAATGGCCTGGGGAC[1]
NM_001272037.2:c.1550+145_1550+172del
NM_144991.3:c.1754+145_1754+172delMANE SELECT
NC_000021.8:g.45928922TTCTTTCCACAGGAAGGTCCCCAGGCCA[1]

Links:

dbSNP: rs879970586

NCBI 1000 Genomes Browser:

rs879970586

Molecular consequence:

NM_001272037.2:c.1550+145_1550+172del - intron variant - [Sequence Ontology: SO:0001627]
NM_144991.3:c.1754+145_1754+172del - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001781850	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Likely benign (Dec 31, 2018)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001781850

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Likely benign
(Dec 31, 2018)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV001781850.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Dec 24, 2023

ClinVar

Relating variation to medicine