NM_001365276.2(TNXB):c.11531-25T>C AND Ehlers-Danlos syndrome due to tenascin-X deficiency

Germline classification:: Benign (1 submission)
Last evaluated:: Sep 10, 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:: RCV001838590.3

Allele description [Variation Report for NM_001365276.2(TNXB):c.11531-25T>C]

NM_001365276.2(TNXB):c.11531-25T>C

Genes:

LOC106780803:tenascin XB recombination region [Gene]
TNXB:tenascin XB [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p21.33

Genomic location:

Preferred name:

NM_001365276.2(TNXB):c.11531-25T>C

HGVS:

NC_000006.12:g.32043581A>G
NG_007941.3:g.10277A>G
NG_008337.2:g.70794T>C
NG_045227.1:g.2074A>G
NM_001365276.2:c.11531-25T>CMANE SELECT
NM_019105.8:c.11525-25T>C
NM_032470.4:c.818-25T>C
LRG_829:g.10277A>G
NC_000006.11:g.32011358A>G
NM_019105.6:c.11525-25T>C

Links:

dbSNP: rs2856451

NCBI 1000 Genomes Browser:

rs2856451

Molecular consequence:

NM_001365276.2:c.11531-25T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_019105.8:c.11525-25T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_032470.4:c.818-25T>C - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: Ehlers-Danlos syndrome due to tenascin-X deficiency (EDSCLL1)
Synonyms:: Ehlers-Danlos-like syndrome due to tenascin-X deficiency; EDS due to TNX deficiency; TNX deficiency; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0011670; MedGen: C1848029; Orphanet: 230839; OMIM: 606408

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002098626	Genome-Nilou Lab	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Sep 10, 2021)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002098626

Genome-Nilou Lab

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Sep 10, 2021)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	no	not provided	not provided	not provided	not provided	not provided	clinical 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 Genome-Nilou Lab, SCV002098626.1

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

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	no	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 1, 2024

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