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NM_000426.4(LAMA2):c.3532G>A (p.Ala1178Thr) AND Intellectual disability

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jan 1, 2019
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
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:
RCV001252051.4

Allele description [Variation Report for NM_000426.4(LAMA2):c.3532G>A (p.Ala1178Thr)]

NM_000426.4(LAMA2):c.3532G>A (p.Ala1178Thr)

Gene:
LAMA2:laminin subunit alpha 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
6q22.33
Genomic location:
Preferred name:
NM_000426.4(LAMA2):c.3532G>A (p.Ala1178Thr)
HGVS:
  • NC_000006.12:g.129314775G>A
  • NG_008678.1:g.436635G>A
  • NM_000426.4:c.3532G>AMANE SELECT
  • NM_001079823.2:c.3532G>A
  • NP_000417.2:p.Ala1178Thr
  • NP_000417.3:p.Ala1178Thr
  • NP_001073291.2:p.Ala1178Thr
  • LRG_409t1:c.3532G>A
  • LRG_409:g.436635G>A
  • LRG_409p1:p.Ala1178Thr
  • NC_000006.11:g.129635920G>A
  • NM_000426.3:c.3532G>A
  • p.A1178T
  • p.Ala1178Thr
Protein change:
A1178T
Links:
dbSNP: rs34505698
NCBI 1000 Genomes Browser:
rs34505698
Molecular consequence:
  • NM_000426.4:c.3532G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001079823.2:c.3532G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Intellectual disability
Synonyms:
Intellectual functioning disability; intellectual disabilities; Intellectual developmental disorder
Identifiers:
MONDO: MONDO:0001071; MeSH: D008607; MedGen: C3714756; Human Phenotype Ontology: HP:0001249

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001427799Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille
no assertion criteria provided
Uncertain significance
(Jan 1, 2019) 		unknownclinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee.

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille, SCV001427799.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 24, 2024