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NM_001134407.3(GRIN2A):c.934T>C (p.Tyr312His) AND Landau-Kleffner syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 20, 2021
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:
RCV001919354.4

Allele description [Variation Report for NM_001134407.3(GRIN2A):c.934T>C (p.Tyr312His)]

NM_001134407.3(GRIN2A):c.934T>C (p.Tyr312His)

Gene:
GRIN2A:glutamate ionotropic receptor NMDA type subunit 2A [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16p13.2
Genomic location:
Preferred name:
NM_001134407.3(GRIN2A):c.934T>C (p.Tyr312His)
HGVS:
  • NC_000016.10:g.9938032A>G
  • NG_011812.2:g.249723T>C
  • NM_000833.5:c.934T>C
  • NM_001134407.3:c.934T>CMANE SELECT
  • NM_001134408.2:c.934T>C
  • NP_000824.1:p.Tyr312His
  • NP_001127879.1:p.Tyr312His
  • NP_001127880.1:p.Tyr312His
  • NC_000016.9:g.10031889A>G
Protein change:
Y312H
Links:
dbSNP: rs2044756352
NCBI 1000 Genomes Browser:
rs2044756352
Molecular consequence:
  • NM_000833.5:c.934T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001134407.3:c.934T>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001134408.2:c.934T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Landau-Kleffner syndrome (FESD)
Synonyms:
Acquired aphasia with convulsive disorder; Acquired epileptiform aphasia; APHASIA, ACQUIRED, WITH EPILEPSY; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0009509; MedGen: C0282512; Orphanet: 1945; Orphanet: 725; Orphanet: 98818; OMIM: 245570

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002192810Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Oct 20, 2021) 		germlineclinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV002192810.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt GRIN2A protein function. This variant has not been reported in the literature in individuals affected with GRIN2A-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces tyrosine with histidine at codon 312 of the GRIN2A protein (p.Tyr312His). The tyrosine residue is weakly conserved and there is a moderate physicochemical difference between tyrosine and histidine.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024