rs1167768

Variant names:

• chr9-98569110-G-A
• rs1167768
• NM_005458.8:c.459+8825C>T

Your query was ambiguous. Multiple possible variants found:

• chr9-98569110-G-A
• chr9-98569110-G-C
• chr9-98569110-G-T

Variant summary

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

The NM_005458.8(GABBR2):​c.459+8825C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.294 in 151,998 control chromosomes in the GnomAD database, including 7,487 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 0.29 (7487 hom., cov: 32)
• Consequence: GABBR2 NM_005458.8 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0760
• Publications: 7 publications found

Genes affected

GABBR2 (HGNC:4507): (gamma-aminobutyric acid type B receptor subunit 2) The multi-pass membrane protein encoded by this gene belongs to the G-protein coupled receptor 3 family and GABA-B receptor subfamily. The GABA-B receptors inhibit neuronal activity through G protein-coupled second-messenger systems, which regulate the release of neurotransmitters, and the activity of ion channels and adenylyl cyclase. This receptor subunit forms an active heterodimeric complex with GABA-B receptor subunit 1, neither of which is effective on its own. Allelic variants of this gene have been associated with nicotine dependence.[provided by RefSeq, Jan 2010]

GABBR2 Gene-Disease associations (from GenCC):

• developmental and epileptic encephalopathy, 59

  Inheritance: AD Classification: STRONG, MODERATE Submitted by: G2P, Ambry Genetics, Labcorp Genetics (formerly Invitae)
• neurodevelopmental disorder with poor language and loss of hand skills

  Inheritance: AD Classification: STRONG Submitted by: Labcorp Genetics (formerly Invitae)
• complex neurodevelopmental disorder

  Inheritance: AD Classification: MODERATE Submitted by: ClinGen
• atypical Rett syndrome

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.596 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_005458.8. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GABBR2	NM_005458.8	MANE Select	c.459+8825C>T		intron	N/A	NP_005449.5

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GABBR2	ENST00000259455.4	TSL:1 MANE Select	c.459+8825C>T		intron	N/A	ENSP00000259455.2	O75899
	GABBR2	ENST00000931526.1		c.459+8825C>T		intron	N/A	ENSP00000601585.1
	GABBR2	ENST00000947376.1		c.459+8825C>T		intron	N/A	ENSP00000617435.1

Frequencies

GnomAD3 genomes AF: 0.294 AC: 44726 AN: 151880 Hom.: 7486 Cov.: 32

Gnomad AFR AF: 0.173

Gnomad AMI AF: 0.344

Gnomad AMR AF: 0.416

Gnomad ASJ AF: 0.298

Gnomad EAS AF: 0.612

Gnomad SAS AF: 0.284

Gnomad FIN AF: 0.396

Gnomad MID AF: 0.316

Gnomad NFE AF: 0.301

Gnomad OTH AF: 0.307

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

GnomAD4 genome AF: 0.294 AC: 44739 AN: 151998 Hom.: 7487 Cov.: 32 AF XY: 0.304 AC XY: 22555 AN XY: 74254

African (AFR) AF: 0.173 AC: 7155 AN: 41460

American (AMR) AF: 0.416 AC: 6348 AN: 15274

Ashkenazi Jewish (ASJ) AF: 0.298 AC: 1033 AN: 3468

East Asian (EAS) AF: 0.614 AC: 3169 AN: 5164

South Asian (SAS) AF: 0.283 AC: 1361 AN: 4812

European-Finnish (FIN) AF: 0.396 AC: 4177 AN: 10536

Middle Eastern (MID) AF: 0.323 AC: 95 AN: 294

European-Non Finnish (NFE) AF: 0.301 AC: 20442 AN: 67976

Other (OTH) AF: 0.307 AC: 647 AN: 2108

Alfa AF: 0.256 Hom.: 1347

Bravo AF: 0.293

Asia WGS AF: 0.430 AC: 1493 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	0.52
DANN	Benign	0.57
PhyloP100		-0.076
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: rs1167768; hg19: chr9-101331392;