NM_001172509.2(SATB2):c.1538G>A (p.Ser513Asn) AND Intellectual disability

Germline classification:: Pathogenic (1 submission)
Last evaluated:: Apr 20, 2020
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:: RCV001257666.2

Allele description [Variation Report for NM_001172509.2(SATB2):c.1538G>A (p.Ser513Asn)]

NM_001172509.2(SATB2):c.1538G>A (p.Ser513Asn)

Gene:

SATB2:SATB homeobox 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q33.1

Genomic location:

Preferred name:

NM_001172509.2(SATB2):c.1538G>A (p.Ser513Asn)

HGVS:

NC_000002.12:g.199323807C>T
NG_016976.2:g.152460G>A
NM_001172509.2:c.1538G>AMANE SELECT
NM_001172517.1:c.1538G>A
NM_015265.4:c.1538G>A
NP_001165980.1:p.Ser513Asn
NP_001165988.1:p.Ser513Asn
NP_056080.1:p.Ser513Asn
NC_000002.11:g.200188530C>T
NG_016976.1:g.152460G>A
NM_001172509.1:c.1538G>A

Protein change:

S513N

Links:

dbSNP: rs1687957552

NCBI 1000 Genomes Browser:

rs1687957552

Molecular consequence:

NM_001172509.2:c.1538G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001172517.1:c.1538G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_015265.4:c.1538G>A - missense variant - [Sequence Ontology: SO:0001583]

Observations:

Condition(s)

Name:: Intellectual disability
Synonyms:: Intellectual functioning disability; intellectual disabilities; Intellectual developmental disorder
Identifiers:: MONDO: MONDO:0001071; MeSH: D008607; MedGen: C3714756; Human Phenotype Ontology: HP:0001249

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
SCV001434477	Diagnostic Laboratory, Strasbourg University Hospital	criteria provided, single submitter (ACMG Guidelines, 2015)	Pathogenic (Apr 20, 2020)	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

SCV001434477

Diagnostic Laboratory, Strasbourg University Hospital

criteria provided, single submitter

(ACMG Guidelines, 2015)

Pathogenic
(Apr 20, 2020)

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	1	not provided	not provided	1	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 Diagnostic Laboratory, Strasbourg University Hospital, SCV001434477.1

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

Last Updated: Sep 30, 2023

ClinVar

Relating variation to medicine