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NM_198904.4(GABRG2):c.935T>A (p.Val312Asp) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 25, 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:
RCV003801309.2

Allele description [Variation Report for NM_198904.4(GABRG2):c.935T>A (p.Val312Asp)]

NM_198904.4(GABRG2):c.935T>A (p.Val312Asp)

Gene:
GABRG2:gamma-aminobutyric acid type A receptor subunit gamma2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
5q34
Genomic location:
Preferred name:
NM_198904.4(GABRG2):c.935T>A (p.Val312Asp)
HGVS:
  • NC_000005.10:g.162149120T>A
  • NG_009290.1:g.86479T>A
  • NM_000816.3:c.935T>A
  • NM_001375339.1:c.926T>A
  • NM_001375340.1:c.923-2610T>A
  • NM_001375341.1:c.932T>A
  • NM_001375342.1:c.932T>A
  • NM_001375343.1:c.1055T>A
  • NM_001375344.1:c.974T>A
  • NM_001375345.1:c.869T>A
  • NM_001375346.1:c.869T>A
  • NM_001375347.1:c.848T>A
  • NM_001375348.1:c.515T>A
  • NM_001375349.1:c.650T>A
  • NM_001375350.1:c.515T>A
  • NM_198903.2:c.1055T>A
  • NM_198904.4:c.935T>AMANE SELECT
  • NP_000807.2:p.Val312Asp
  • NP_001362268.1:p.Val309Asp
  • NP_001362270.1:p.Val311Asp
  • NP_001362271.1:p.Val311Asp
  • NP_001362272.1:p.Val352Asp
  • NP_001362273.1:p.Val325Asp
  • NP_001362274.1:p.Val290Asp
  • NP_001362275.1:p.Val290Asp
  • NP_001362276.1:p.Val283Asp
  • NP_001362277.1:p.Val172Asp
  • NP_001362278.1:p.Val217Asp
  • NP_001362279.1:p.Val172Asp
  • NP_944493.2:p.Val352Asp
  • NP_944494.1:p.Val312Asp
  • NC_000005.9:g.161576126T>A
Protein change:
V172D
Molecular consequence:
  • NM_001375340.1:c.923-2610T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_000816.3:c.935T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001375339.1:c.926T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001375341.1:c.932T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001375342.1:c.932T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001375343.1:c.1055T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001375344.1:c.974T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001375345.1:c.869T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001375346.1:c.869T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001375347.1:c.848T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001375348.1:c.515T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001375349.1:c.650T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001375350.1:c.515T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198903.2:c.1055T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_198904.4:c.935T>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Epilepsy, childhood absence 2 (ECA2)
Identifiers:
MedGen: C1843244; Orphanet: 64280
Name:
Febrile seizures, familial, 8 (FEB8)
Synonyms:
CONVULSIONS, FAMILIAL FEBRILE, 8
Identifiers:
MONDO: MONDO:0011891; MedGen: C1969810; Orphanet: 36387; OMIM: 607681

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004594246Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Apr 25, 2023) 		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, SCV004594246.1

#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 expected to disrupt GABRG2 protein function. This variant has not been reported in the literature in individuals affected with GABRG2-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces valine, which is neutral and non-polar, with aspartic acid, which is acidic and polar, at codon 312 of the GABRG2 protein (p.Val312Asp).

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

Last Updated: Oct 26, 2024