NM_024408.4(NOTCH2):c.6893G>A (p.Arg2298Gln) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 13, 2017
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:: RCV000405161.6

Allele description [Variation Report for NM_024408.4(NOTCH2):c.6893G>A (p.Arg2298Gln)]

NM_024408.4(NOTCH2):c.6893G>A (p.Arg2298Gln)

Gene:

NOTCH2:notch receptor 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p12

Genomic location:

Preferred name:

NM_024408.4(NOTCH2):c.6893G>A (p.Arg2298Gln)

HGVS:

NC_000001.11:g.119915829C>T
NG_008163.1:g.158825G>A
NM_024408.3:c.6893G>A
NM_024408.4:c.6893G>AMANE SELECT
NP_077719.2:p.Arg2298Gln
NC_000001.10:g.120458452C>T

Protein change:

R2298Q

Links:

dbSNP: rs140832430

NCBI 1000 Genomes Browser:

rs140832430

Molecular consequence:

NM_024408.4:c.6893G>A - missense variant - [Sequence Ontology: SO:0001583]

Observations:

Condition(s)

Synonyms:: none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000345909	Eurofins Ntd Llc (ga)	criteria provided, single submitter (EGL Classification Definitions 2015)	Uncertain significance (Dec 13, 2017)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000345909

Eurofins Ntd Llc (ga)

criteria provided, single submitter

(EGL Classification Definitions 2015)

Uncertain significance
(Dec 13, 2017)

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	3	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Eurofins Ntd Llc (ga), SCV000345909.5

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	3	not provided	not provided	clinical testing	not provided

#	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		3	not provided	not provided	not provided

Last Updated: May 16, 2025

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