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NM_001105206.3(LAMA4):c.188C>T (p.Ala63Val) AND Primary dilated cardiomyopathy

Germline classification:
Likely benign (1 submission)
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:
RCV001293181.1

Allele description [Variation Report for NM_001105206.3(LAMA4):c.188C>T (p.Ala63Val)]

NM_001105206.3(LAMA4):c.188C>T (p.Ala63Val)

Genes:
LAMA4-AS1:LAMA4 antisense RNA 1 [Gene - HGNC]
LAMA4:laminin subunit alpha 4 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
6q21
Genomic location:
Preferred name:
NM_001105206.3(LAMA4):c.188C>T (p.Ala63Val)
HGVS:
  • NC_000006.12:g.112253963G>A
  • NG_008209.1:g.5664C>T
  • NM_001105206.3:c.188C>TMANE SELECT
  • NM_001105207.3:c.188C>T
  • NM_001105208.3:c.188C>T
  • NM_001105209.3:c.188C>T
  • NM_002290.3:c.188C>T
  • NM_002290.5:c.188C>T
  • NP_001098676.2:p.Ala63Val
  • NP_001098677.2:p.Ala63Val
  • NP_001098678.1:p.Ala63Val
  • NP_001098679.1:p.Ala63Val
  • NP_002281.3:p.Ala63Val
  • LRG_433t2:c.188C>T
  • LRG_433:g.5664C>T
  • NC_000006.11:g.112575165G>A
  • NM_001105209.2:c.188C>T
Protein change:
A63V
Links:
dbSNP: rs370868386
NCBI 1000 Genomes Browser:
rs370868386
Molecular consequence:
  • NM_001105206.3:c.188C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001105207.3:c.188C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001105208.3:c.188C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001105209.3:c.188C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002290.5:c.188C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Primary dilated cardiomyopathy (DCM)
Synonyms:
Dilated Cardiomyopathy
Identifiers:
EFO: EFO_0000407; MONDO: MONDO:0005021; MeSH: D002311; MedGen: C0007193; Human Phenotype Ontology: HP:0001644

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001434179Genetics and Genomics Program, Sidra Medicine
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely benignunknownresearch

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownyes1not providednot providednot providednot providedresearch

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 Genetics and Genomics Program, Sidra Medicine, SCV001434179.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedresearch PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providednot providednot provided1not providednot providednot provided

Last Updated: Sep 29, 2024