NM_007327.4(GRIN1):c.780C>T (p.Arg260=) AND not provided

Clinical significance:Uncertain significance (Last evaluated: Aug 1, 2016)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000416174.5

Allele description [Variation Report for NM_007327.4(GRIN1):c.780C>T (p.Arg260=)]

NM_007327.4(GRIN1):c.780C>T (p.Arg260=)

Gene:
GRIN1:glutamate ionotropic receptor NMDA type subunit 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q34.3
Genomic location:
Preferred name:
NM_007327.4(GRIN1):c.780C>T (p.Arg260=)
HGVS:
  • NC_000009.12:g.137156777C>T
  • NG_011507.1:g.22621C>T
  • NM_000832.7:c.780C>T
  • NM_001185090.2:c.843C>T
  • NM_001185091.2:c.843C>T
  • NM_007327.4:c.780C>TMANE SELECT
  • NM_021569.4:c.780C>T
  • NP_000823.4:p.Arg260=
  • NP_001172019.1:p.Arg281=
  • NP_001172020.1:p.Arg281=
  • NP_015566.1:p.Arg260=
  • NP_067544.1:p.Arg260=
  • NC_000009.11:g.140051229C>T
  • NM_007327.3:c.780C>T
Links:
dbSNP: rs3181450
NCBI 1000 Genomes Browser:
rs3181450
Molecular consequence:
  • NM_000832.7:c.780C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001185090.2:c.843C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001185091.2:c.843C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_007327.4:c.780C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_021569.4:c.780C>T - synonymous variant - [Sequence Ontology: SO:0001819]
Observations:
1

Condition(s)

Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000493360CeGaT Praxis fuer Humangenetik Tuebingencriteria provided, single submitter
Uncertain significance
(Aug 1, 2016)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not providednot providednot providednot providedclinical testing

Details of each submission

From CeGaT Praxis fuer Humangenetik Tuebingen, SCV000493360.13

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided1not providednot providednot provided

Last Updated: Oct 6, 2021

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