rs2195817

chr15-27016500-A-Gchr15-27016500-A-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_033223.5(GABRG3):c.203-10254A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.558 in 151,912 control chromosomes in the GnomAD database, including 24,130 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.56 (24130 hom., cov: 31)
• Consequence: GABRG3 NM_033223.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.369

Genes affected

GABRG3 (HGNC:4088): (gamma-aminobutyric acid type A receptor subunit gamma3) This gene encodes a gamma-aminobutyric acid (GABA) receptor. GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. GABA-A receptors are pentameric, consisting of proteins from several subunit classes: alpha, beta, gamma, delta and rho. The protein encoded by this gene is a gamma subunit, which contains the benzodiazepine binding site. Two transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Aug 2012]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.0).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.629 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
GABRG3	NM_033223.5	c.203-10254A>G		intron_variant		ENST00000615808.5
GABRG3	NM_001270873.2	c.203-10254A>G		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
GABRG3	ENST00000615808.5	c.203-10254A>G		intron_variant		1	NM_033223.5	P1
GABRG3	ENST00000555083.5	c.203-10254A>G		intron_variant		2
GABRG3	ENST00000553440.1	n.295-10254A>G		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.558 AC: 84661 AN: 151792 Hom.: 24095 Cov.: 31

Gnomad AFR AF: 0.635

Gnomad AMI AF: 0.490

Gnomad AMR AF: 0.473

Gnomad ASJ AF: 0.539

Gnomad EAS AF: 0.283

Gnomad SAS AF: 0.554

Gnomad FIN AF: 0.478

Gnomad MID AF: 0.604

Gnomad NFE AF: 0.564

Gnomad OTH AF: 0.570

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.558 AC: 84749 AN: 151912 Hom.: 24130 Cov.: 31 AF XY: 0.551 AC XY: 40909 AN XY: 74272

Gnomad4 AFR AF: 0.636

Gnomad4 AMR AF: 0.472

Gnomad4 ASJ AF: 0.539

Gnomad4 EAS AF: 0.282

Gnomad4 SAS AF: 0.554

Gnomad4 FIN AF: 0.478

Gnomad4 NFE AF: 0.564

Gnomad4 OTH AF: 0.571

Alfa AF: 0.550 Hom.: 4961

Bravo AF: 0.556

Asia WGS AF: 0.429 AC: 1495 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
Cadd	Benign	6.2
Dann	Benign	0.77

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs2195817; hg19: chr15-27261647;