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NM_002294.3(LAMP2):c.991T>C (p.Cys331Arg) AND Danon disease

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 22, 2023
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:
RCV003508984.2

Allele description [Variation Report for NM_002294.3(LAMP2):c.991T>C (p.Cys331Arg)]

NM_002294.3(LAMP2):c.991T>C (p.Cys331Arg)

Gene:
LAMP2:lysosomal associated membrane protein 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xq24
Genomic location:
Preferred name:
NM_002294.3(LAMP2):c.991T>C (p.Cys331Arg)
HGVS:
  • NC_000023.11:g.120441832A>G
  • NG_007995.1:g.32518T>C
  • NM_001122606.1:c.991T>C
  • NM_002294.3:c.991T>CMANE SELECT
  • NM_013995.2:c.991T>C
  • NP_001116078.1:p.Cys331Arg
  • NP_002285.1:p.Cys331Arg
  • NP_002285.1:p.Cys331Arg
  • NP_054701.1:p.Cys331Arg
  • LRG_749t1:c.991T>C
  • LRG_749t2:c.991T>C
  • LRG_749t3:c.991T>C
  • LRG_749:g.32518T>C
  • LRG_749p1:p.Cys331Arg
  • LRG_749p2:p.Cys331Arg
  • LRG_749p3:p.Cys331Arg
  • NC_000023.10:g.119575687A>G
  • NM_002294.2:c.991T>C
Protein change:
C331R
Molecular consequence:
  • NM_001122606.1:c.991T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002294.3:c.991T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_013995.2:c.991T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Danon disease
Synonyms:
PSEUDOGLYCOGENOSIS II; GSD IIb; LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0010281; MedGen: C0878677; Orphanet: 34587; OMIM: 300257

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004295898Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Nov 22, 2023) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group, Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV004295898.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This sequence change replaces cysteine, which is neutral and slightly polar, with arginine, which is basic and polar, at codon 331 of the LAMP2 protein (p.Cys331Arg). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with LAMP2-related conditions. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt LAMP2 protein function with a positive predictive value of 80%. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024