NM_000426.4(LAMA2):c.8982T>C (p.Asp2994=) AND not provided

Clinical significance:Benign (Last evaluated: Mar 29, 2019)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV001682891.1

Allele description [Variation Report for NM_000426.4(LAMA2):c.8982T>C (p.Asp2994=)]

NM_000426.4(LAMA2):c.8982T>C (p.Asp2994=)

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.8982T>C (p.Asp2994=)
HGVS:
  • NC_000006.12:g.129512487T>C
  • NG_008678.1:g.634347T>C
  • NM_000426.3:c.8982T>C
  • NM_000426.4:c.8982T>CMANE SELECT
  • NM_001079823.2:c.8970T>C
  • NP_000417.2:p.Asp2994=
  • NP_000417.3:p.Asp2994=
  • NP_001073291.2:p.Asp2990=
  • LRG_409t1:c.8982T>C
  • LRG_409:g.634347T>C
  • LRG_409p1:p.Asp2994=
  • NC_000006.11:g.129833632T>C
Links:
dbSNP: rs79374915
NCBI 1000 Genomes Browser:
rs79374915
Molecular consequence:
  • NM_000426.3:c.8982T>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_000426.4:c.8982T>C - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001079823.2:c.8970T>C - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001904769GeneDxcriteria provided, single submitter
Benign
(Mar 29, 2019)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From GeneDx, SCV001904769.1

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

Last Updated: Nov 27, 2021

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