NM_001543.5(NDST1):c.1831G>A (p.Gly611Ser) AND Global developmental delay

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Feb 16, 2022
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:: RCV002463649.1

Allele description [Variation Report for NM_001543.5(NDST1):c.1831G>A (p.Gly611Ser)]

NM_001543.5(NDST1):c.1831G>A (p.Gly611Ser)

Gene:

NDST1:N-deacetylase and N-sulfotransferase 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

5q33.1

Genomic location:

Preferred name:

NM_001543.5(NDST1):c.1831G>A (p.Gly611Ser)

HGVS:

NC_000005.10:g.150541651G>A
NG_041806.1:g.48874G>A
NM_001301063.2:c.1831G>A
NM_001543.5:c.1831G>AMANE SELECT
NP_001287992.1:p.Gly611Ser
NP_001534.1:p.Gly611Ser
NC_000005.9:g.149921213G>A
NM_001543.4:c.1831G>A
P52848:p.Gly611Ser

Protein change:

G611S; GLY611SER

Links:

UniProtKB: P52848#VAR_072646; OMIM: 600853.0004; dbSNP: rs606231459

NCBI 1000 Genomes Browser:

rs606231459

Molecular consequence:

NM_001301063.2:c.1831G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001543.5:c.1831G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Global developmental delay (DD)
Synonyms:: Cognitive delay
Identifiers:: MedGen: C0557874; Human Phenotype Ontology: HP:0001263

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002758631	Human Genetics Bochum, Ruhr University Bochum	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic (Feb 16, 2022)	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

SCV002758631

Human Genetics Bochum, Ruhr University Bochum

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic
(Feb 16, 2022)

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	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 Human Genetics Bochum, Ruhr University Bochum, SCV002758631.1

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

Description

ACMG criteria used to clasify this variant: PS4, PM1, PM2_SUP, PP3

#	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: Apr 20, 2025

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