NM_007327.4(GRIN1):c.1776C>T (p.Asn592=) AND not provided

Clinical significance:Likely benign (Last evaluated: Sep 11, 2020)

Review status:2 stars out of maximum of 4 stars

criteria provided, multiple submitters, no conflicts

Based on:
2 submissions [Details]
Record status:
current
Accession:
RCV000866346.6

Allele description [Variation Report for NM_007327.4(GRIN1):c.1776C>T (p.Asn592=)]

NM_007327.4(GRIN1):c.1776C>T (p.Asn592=)

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.1776C>T (p.Asn592=)
HGVS:
  • NC_000009.12:g.137162428C>T
  • NG_011507.1:g.28272C>T
  • NM_000832.7:c.1776C>T
  • NM_001185090.2:c.1839C>T
  • NM_001185091.2:c.1839C>T
  • NM_007327.4:c.1776C>TMANE SELECT
  • NM_021569.4:c.1776C>T
  • NP_000823.4:p.Asn592=
  • NP_001172019.1:p.Asn613=
  • NP_001172020.1:p.Asn613=
  • NP_015566.1:p.Asn592=
  • NP_067544.1:p.Asn592=
  • NC_000009.11:g.140056880C>T
  • NM_007327.3:c.1776C>T
Links:
dbSNP: rs369596145
NCBI 1000 Genomes Browser:
rs369596145
Molecular consequence:
  • NM_000832.7:c.1776C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001185090.2:c.1839C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001185091.2:c.1839C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_007327.4:c.1776C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_021569.4:c.1776C>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
SCV001155861CeGaT Praxis fuer Humangenetik Tuebingencriteria provided, single submitter
Likely benign
(Mar 1, 2019)
germlineclinical testing

Citation Link,

SCV001795674GeneDxcriteria provided, single submitter
Likely benign
(Sep 11, 2020)
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, SCV001155861.7

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

From GeneDx, SCV001795674.1

#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: Oct 6, 2021

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