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NM_007327.4(GRIN1):c.950C>T (p.Thr317Ile) AND Intellectual disability, autosomal dominant 8

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Sep 27, 2023
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:
RCV004546865.2

Allele description [Variation Report for NM_007327.4(GRIN1):c.950C>T (p.Thr317Ile)]

NM_007327.4(GRIN1):c.950C>T (p.Thr317Ile)

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.950C>T (p.Thr317Ile)
HGVS:
  • NC_000009.12:g.137157019C>T
  • NG_011507.1:g.22863C>T
  • NM_000832.7:c.950C>T
  • NM_001185090.2:c.1013C>T
  • NM_001185091.2:c.1013C>T
  • NM_007327.4:c.950C>TMANE SELECT
  • NM_021569.4:c.950C>T
  • NP_000823.4:p.Thr317Ile
  • NP_001172019.1:p.Thr338Ile
  • NP_001172020.1:p.Thr338Ile
  • NP_015566.1:p.Thr317Ile
  • NP_067544.1:p.Thr317Ile
  • NC_000009.11:g.140051471C>T
Protein change:
T317I
Molecular consequence:
  • NM_000832.7:c.950C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001185090.2:c.1013C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001185091.2:c.1013C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007327.4:c.950C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_021569.4:c.950C>T - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Name:
Intellectual disability, autosomal dominant 8 (NDHMSD)
Synonyms:
Mental retardation, autosomal dominant 8; Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant
Identifiers:
MONDO: MONDO:0013655; MedGen: C3280282; OMIM: 614254

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005040853MVZ Medizinische Genetik Mainz
criteria provided, single submitter

(UK Practice Guidelines For Variant Classification V4 01 2020)		Uncertain significance
(Sep 27, 2023) 		germlineclinical testing

Citation Link

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Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not providednot providednot providednot providedclinical testing

Details of each submission

From MVZ Medizinische Genetik Mainz, SCV005040853.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided

Description

ACMG Criteria: PS4SUP,PM2_SUP,PP2,PP3

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided1not providednot providednot provided

Last Updated: Jun 2, 2024