NM_001127644.2(GABRA1):c.1069G>A (p.Val357Ile) AND multiple conditions

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 23, 2022
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:: RCV002305090.5

Allele description [Variation Report for NM_001127644.2(GABRA1):c.1069G>A (p.Val357Ile)]

NM_001127644.2(GABRA1):c.1069G>A (p.Val357Ile)

Gene:

GABRA1:gamma-aminobutyric acid type A receptor subunit alpha1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

5q34

Genomic location:

Preferred name:

NM_001127644.2(GABRA1):c.1069G>A (p.Val357Ile)

HGVS:

NC_000005.10:g.161897120G>A
NG_011548.1:g.54930G>A
NM_000806.5:c.1069G>A
NM_001127643.2:c.1069G>A
NM_001127644.2:c.1069G>AMANE SELECT
NM_001127645.2:c.1069G>A
NM_001127648.2:c.1069G>A
NP_000797.2:p.Val357Ile
NP_001121115.1:p.Val357Ile
NP_001121116.1:p.Val357Ile
NP_001121117.1:p.Val357Ile
NP_001121120.1:p.Val357Ile
NC_000005.9:g.161324126G>A

Protein change:

V357I

Links:

dbSNP: rs2532295515

NCBI 1000 Genomes Browser:

rs2532295515

Molecular consequence:

NM_000806.5:c.1069G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001127643.2:c.1069G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001127644.2:c.1069G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001127645.2:c.1069G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001127648.2:c.1069G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Idiopathic generalized epilepsy
Synonyms:: EIG; Generalised epilepsy
Identifiers:: MONDO: MONDO:0005579; MedGen: C0270850; OMIM: 600669; OMIM: PS600669

Name:: Epilepsy, idiopathic generalized, susceptibility to, 13
Synonyms:: EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 5
Identifiers:: MONDO: MONDO:0012627; MedGen: C4013473; Orphanet: 307; Orphanet: 64280; OMIM: 611136

Name:: Epilepsy, childhood absence 4 (ECA4)
Synonyms:: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 4
Identifiers:: MedGen: C1970160; Orphanet: 307

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002591965	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Sep 23, 2022)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002591965

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Sep 23, 2022)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical 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, SCV002591965.4

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical 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 GABRA1 protein function. This variant has not been reported in the literature in individuals affected with GABRA1-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 isoleucine, which is neutral and non-polar, at codon 357 of the GABRA1 protein (p.Val357Ile).

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: May 16, 2025

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