NC_000005.9:g.(?_88625195)_(90796047_?)inv AND Intellectual disability, autosomal dominant 20

Germline classification:: Pathogenic (1 submission)
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:: RCV002286878.1

Allele description [Variation Report for NC_000005.9:g.(?_88625195)_(90796047_?)inv]

NC_000005.9:g.(?_88625195)_(90796047_?)inv

Genes:

MEF2C:myocyte enhancer factor 2C [Gene - OMIM - HGNC]
LYSMD3:LysM domain containing 3 [Gene - HGNC]
POLR3G:RNA polymerase III subunit G [Gene - OMIM - HGNC]
ADGRV1:adhesion G protein-coupled receptor V1 [Gene - OMIM - HGNC]
ARRDC3:arrestin domain containing 3 [Gene - OMIM - HGNC]
CETN3:centrin 3 [Gene - OMIM - HGNC]
LUCAT1:lung cancer associated transcript 1 [Gene - OMIM - HGNC]
MBLAC2:metallo-beta-lactamase domain containing 2 [Gene - HGNC]

Variant type:

Inversion

Cytogenetic location:

5q14.3

Genomic location:

Chr5: 88625195 - 90796047 (on Assembly GRCh37)

Preferred name:

NC_000005.9:g.(?_88625195)_(90796047_?)inv

HGVS:

NC_000005.9:g.(?_88625195)_(90796047_?)inv

Condition(s)

Name:: Intellectual disability, autosomal dominant 20 (NEDHSIL)
Synonyms:: NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE
Identifiers:: MONDO: MONDO:0013266; MedGen: C3150700; Orphanet: 228384; OMIM: 613443

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002576805	Equipe Genetique des Anomalies du Developpement, Université de Bourgogne	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic	de novo	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

SCV002576805

Equipe Genetique des Anomalies du Developpement, Université de Bourgogne

criteria provided, single submitter

(ACMG Guidelines, 2015)

Pathogenic

de novo

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	de novo	yes	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 Equipe Genetique des Anomalies du Developpement, Université de Bourgogne, SCV002576805.1

#	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	de novo	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Feb 4, 2024

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