NM_022455.5(NSD1):c.3242G>C (p.Gly1081Ala) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 15, 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:: RCV002324804.2

Allele description [Variation Report for NM_022455.5(NSD1):c.3242G>C (p.Gly1081Ala)]

NM_022455.5(NSD1):c.3242G>C (p.Gly1081Ala)

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.3242G>C (p.Gly1081Ala)

HGVS:

NC_000005.10:g.177211641G>C
NG_009821.1:g.83563G>C
NM_001365684.2:c.2369G>C
NM_001409301.1:c.3242G>C
NM_001409302.1:c.3242G>C
NM_001409303.1:c.3242G>C
NM_001409304.1:c.2822G>C
NM_001409305.1:c.2489G>C
NM_001409306.1:c.2369G>C
NM_001409307.1:c.2369G>C
NM_001409308.1:c.2369G>C
NM_001409309.1:c.2369G>C
NM_022455.5:c.3242G>CMANE SELECT
NM_172349.5:c.2369G>C
NP_001352613.1:p.Gly812Ala
NP_001352613.2:p.Gly790Ala
NP_001396230.1:p.Gly1081Ala
NP_001396231.1:p.Gly1081Ala
NP_001396232.1:p.Gly1081Ala
NP_001396233.1:p.Gly941Ala
NP_001396234.1:p.Gly830Ala
NP_001396235.1:p.Gly790Ala
NP_001396236.1:p.Gly790Ala
NP_001396237.1:p.Gly790Ala
NP_001396238.1:p.Gly790Ala
NP_071900.2:p.Gly1081Ala
NP_071900.2:p.Gly1081Ala
NP_758859.1:p.Gly812Ala
NP_758859.2:p.Gly790Ala
LRG_512t1:c.3242G>C
LRG_512:g.83563G>C
LRG_512p1:p.Gly1081Ala
NC_000005.9:g.176638642G>C
NM_001365684.1:c.2435G>C
NM_022455.4:c.3242G>C
NM_172349.3:c.2435G>C

Protein change:

G1081A

Molecular consequence:

NM_001365684.2:c.2369G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001409301.1:c.3242G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001409302.1:c.3242G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001409303.1:c.3242G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001409304.1:c.2822G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001409305.1:c.2489G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001409306.1:c.2369G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001409307.1:c.2369G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001409308.1:c.2369G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001409309.1:c.2369G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_022455.5:c.3242G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_172349.5:c.2369G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002609791	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jul 15, 2020)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002609791

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jul 15, 2020)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV002609791.2

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

Description

The p.G1081A variant (also known as c.3242G>C), located in coding exon 4 of the NSD1 gene, results from a G to C substitution at nucleotide position 3242. The glycine at codon 1081 is replaced by alanine, an amino acid with similar properties. This amino acid position is not well conserved in available vertebrate species, and alanine is the reference amino acid in other vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: May 19, 2024

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