15-27178416-G-A

Variant names:

• chr15-27178416-G-A
• rs1378101
• NM_033223.5:c.271-148393G>A

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_033223.5(GABRG3):​c.271-148393G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0707 in 152,174 control chromosomes in the GnomAD database, including 774 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 0.071 (774 hom., cov: 32)
• Consequence: GABRG3 NM_033223.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0110
• Publications: 4 publications found

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

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.169 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_033223.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GABRG3	NM_033223.5	MANE Select	c.271-148393G>A		intron	N/A	NP_150092.2
	GABRG3	NM_001270873.2		c.271-148393G>A		intron	N/A	NP_001257802.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GABRG3	ENST00000615808.5	TSL:1 MANE Select	c.271-148393G>A		intron	N/A	ENSP00000479113.1
	GABRG3	ENST00000555083.5	TSL:2	c.271-148393G>A		intron	N/A	ENSP00000452244.1

Frequencies

GnomAD3 genomes AF: 0.0707 AC: 10754 AN: 152056 Hom.: 773 Cov.: 32

Gnomad AFR AF: 0.172

Gnomad AMI AF: 0.0341

Gnomad AMR AF: 0.0442

Gnomad ASJ AF: 0.0265

Gnomad EAS AF: 0.149

Gnomad SAS AF: 0.0589

Gnomad FIN AF: 0.0145

Gnomad MID AF: 0.0478

Gnomad NFE AF: 0.0219

Gnomad OTH AF: 0.0530

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

GnomAD4 genome AF: 0.0707 AC: 10760 AN: 152174 Hom.: 774 Cov.: 32 AF XY: 0.0697 AC XY: 5184 AN XY: 74404

African (AFR) AF: 0.172 AC: 7144 AN: 41474

American (AMR) AF: 0.0442 AC: 676 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.0265 AC: 92 AN: 3466

East Asian (EAS) AF: 0.148 AC: 763 AN: 5166

South Asian (SAS) AF: 0.0581 AC: 280 AN: 4820

European-Finnish (FIN) AF: 0.0145 AC: 154 AN: 10616

Middle Eastern (MID) AF: 0.0445 AC: 13 AN: 292

European-Non Finnish (NFE) AF: 0.0219 AC: 1491 AN: 68018

Other (OTH) AF: 0.0548 AC: 116 AN: 2116

Alfa AF: 0.0340 Hom.: 479

Bravo AF: 0.0785

Asia WGS AF: 0.123 AC: 426 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	2.2
DANN	Benign	0.58
PhyloP100		-0.011
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs1378101; hg19: chr15-27423563;