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NM_000152.5(GAA):c.2740dup (p.Gln914fs) AND Glycogen storage disease, type II

Germline classification:
Pathogenic (1 submission)
Last evaluated:
May 4, 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:
RCV002250001.1

Allele description [Variation Report for NM_000152.5(GAA):c.2740dup (p.Gln914fs)]

NM_000152.5(GAA):c.2740dup (p.Gln914fs)

Gene:
GAA:alpha glucosidase [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
17q25.3
Genomic location:
Preferred name:
NM_000152.5(GAA):c.2740dup (p.Gln914fs)
HGVS:
  • NC_000017.11:g.80118746dup
  • NG_009822.1:g.22191dup
  • NM_000152.5:c.2740dupMANE SELECT
  • NM_001079803.3:c.2740dup
  • NM_001079804.3:c.2740dup
  • NP_000143.2:p.Gln914fs
  • NP_001073271.1:p.Gln914fs
  • NP_001073272.1:p.Gln914fs
  • LRG_673:g.22191dup
  • NC_000017.10:g.78092545dup
  • NC_000017.11:g.80118742_80118743insC
Protein change:
Q914fs
Links:
dbSNP: rs745427943
NCBI 1000 Genomes Browser:
rs745427943
Molecular consequence:
  • NM_000152.5:c.2740dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001079803.3:c.2740dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001079804.3:c.2740dup - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:
Glycogen storage disease, type II (GSD2)
Synonyms:
ACID ALPHA-GLUCOSIDASE DEFICIENCY; GLYCOGENOSIS, GENERALIZED, CARDIAC FORM; GSD II; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0009290; MedGen: C0017921; Orphanet: 365; OMIM: 232300

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002516425Mendelics
criteria provided, single submitter

(Mendelics Assertion Criteria 2019)		Pathogenic
(May 4, 2022) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Mendelics, SCV002516425.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Dec 24, 2023