NM_000152.5(GAA):c.2320G>A (p.Asp774Asn) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 8, 2024
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:: RCV001547359.3

Allele description [Variation Report for NM_000152.5(GAA):c.2320G>A (p.Asp774Asn)]

NM_000152.5(GAA):c.2320G>A (p.Asp774Asn)

Gene:

GAA:alpha glucosidase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17q25.3

Genomic location:

Preferred name:

NM_000152.5(GAA):c.2320G>A (p.Asp774Asn)

HGVS:

NC_000017.11:g.80117098G>A
NG_009822.1:g.20543G>A
NM_000152.5:c.2320G>AMANE SELECT
NM_001079803.3:c.2320G>A
NM_001079804.3:c.2320G>A
NP_000143.2:p.Asp774Asn
NP_001073271.1:p.Asp774Asn
NP_001073272.1:p.Asp774Asn
LRG_673t1:c.2320G>A
LRG_673:g.20543G>A
NC_000017.10:g.78090897G>A
NM_000152.3:c.2320G>A
NM_000152.4:c.2320G>A

Protein change:

D774N

Links:

dbSNP: rs758390382

NCBI 1000 Genomes Browser:

rs758390382

Molecular consequence:

NM_000152.5:c.2320G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001079803.3:c.2320G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001079804.3:c.2320G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001767046	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Jul 8, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001767046

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Jul 8, 2024)

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	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV001767046.2

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

Description

In silico analysis indicates that this missense variant does not alter protein structure/function; Observed with a pathogenic variant in a patient with late-onset glycogen storage disease type II in published literature (PMID: 22958975); This variant is associated with the following publications: (PMID: 19343043, 22253258, 22958975, 33560568)

#	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: Oct 8, 2024

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