NM_022455.5(NSD1):c.3109C>T (p.Gln1037Ter) AND Sotos syndrome

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:: RCV003232372.9

Allele description [Variation Report for NM_022455.5(NSD1):c.3109C>T (p.Gln1037Ter)]

NM_022455.5(NSD1):c.3109C>T (p.Gln1037Ter)

Gene:

NSD1:nuclear receptor binding SET domain protein 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

5q35.3

Genomic location:

Preferred name:

NM_022455.5(NSD1):c.3109C>T (p.Gln1037Ter)

HGVS:

NC_000005.10:g.177211508C>T
NG_009821.1:g.83430C>T
NM_001365684.2:c.2236C>T
NM_001409301.1:c.3109C>T
NM_001409302.1:c.3109C>T
NM_001409303.1:c.3109C>T
NM_001409304.1:c.2689C>T
NM_001409305.1:c.2356C>T
NM_001409306.1:c.2236C>T
NM_001409307.1:c.2236C>T
NM_001409308.1:c.2236C>T
NM_001409309.1:c.2236C>T
NM_022455.5:c.3109C>TMANE SELECT
NM_172349.5:c.2236C>T
NP_001352613.1:p.Gln768Ter
NP_001352613.2:p.Gln746Ter
NP_001396230.1:p.Gln1037Ter
NP_001396231.1:p.Gln1037Ter
NP_001396232.1:p.Gln1037Ter
NP_001396233.1:p.Gln897Ter
NP_001396234.1:p.Gln786Ter
NP_001396235.1:p.Gln746Ter
NP_001396236.1:p.Gln746Ter
NP_001396237.1:p.Gln746Ter
NP_001396238.1:p.Gln746Ter
NP_071900.2:p.Gln1037Ter
NP_071900.2:p.Gln1037Ter
NP_758859.1:p.Gln768Ter
NP_758859.2:p.Gln746Ter
LRG_512t1:c.3109C>T
LRG_512:g.83430C>T
LRG_512p1:p.Gln1037Ter
NC_000005.9:g.176638509C>T
NM_001365684.1:c.2302C>T
NM_022455.4:c.3109C>T
NM_172349.3:c.2302C>T

Protein change:

Q1037*

Links:

dbSNP: rs2149847258

NCBI 1000 Genomes Browser:

rs2149847258

Molecular consequence:

NM_001365684.2:c.2236C>T - nonsense - [Sequence Ontology: SO:0001587]
NM_001409301.1:c.3109C>T - nonsense - [Sequence Ontology: SO:0001587]
NM_001409302.1:c.3109C>T - nonsense - [Sequence Ontology: SO:0001587]
NM_001409303.1:c.3109C>T - nonsense - [Sequence Ontology: SO:0001587]
NM_001409304.1:c.2689C>T - nonsense - [Sequence Ontology: SO:0001587]
NM_001409305.1:c.2356C>T - nonsense - [Sequence Ontology: SO:0001587]
NM_001409306.1:c.2236C>T - nonsense - [Sequence Ontology: SO:0001587]
NM_001409307.1:c.2236C>T - nonsense - [Sequence Ontology: SO:0001587]
NM_001409308.1:c.2236C>T - nonsense - [Sequence Ontology: SO:0001587]
NM_001409309.1:c.2236C>T - nonsense - [Sequence Ontology: SO:0001587]
NM_022455.5:c.3109C>T - nonsense - [Sequence Ontology: SO:0001587]
NM_172349.5:c.2236C>T - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:: Sotos syndrome (SOTOS)
Synonyms:: Sotos' syndrome; Cerebral gigantism; Distinctive facial appearance, overgrowth in childhood, and learning disabilities or delayed development; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0019349; MedGen: C0175695; Orphanet: 821; OMIM: 117550

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001737086	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

SCV001737086

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, SCV001737086.1

#	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: Nov 3, 2024

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