5-161364629-C-T

Variant names:

• chr5-161364629-C-T
• rs7724086
• NM_001371727.1:c.542-27860G>A

Variant summary

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

The NM_001371727.1(GABRB2):​c.542-27860G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.167 in 151,970 control chromosomes in the GnomAD database, including 2,916 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 0.17 (2916 hom., cov: 32)
• Consequence: GABRB2 NM_001371727.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.167
• Publications: 3 publications found

Genes affected

GABRB2 (HGNC:4082): (gamma-aminobutyric acid type A receptor subunit beta2) The gamma-aminobutyric acid (GABA) A receptor is a multisubunit chloride channel that mediates the fastest inhibitory synaptic transmission in the central nervous system. This gene encodes GABA A receptor, beta 2 subunit. It is mapped to chromosome 5q34 in a cluster comprised of genes encoding alpha 1 and gamma 2 subunits of the GABA A receptor. Alternative splicing of this gene generates 2 transcript variants, differing by a 114 bp insertion. [provided by RefSeq, Jul 2008]

GABRB2 Gene-Disease associations (from GenCC):

• developmental and epileptic encephalopathy 92

  Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: Labcorp Genetics (formerly Invitae), Illumina, G2P
• undetermined early-onset epileptic encephalopathy

  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=-0.96).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.311 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
GABRB2	NM_001371727.1	c.542-27860G>A		intron_variant	Intron 5 of 9	ENST00000393959.6	NP_001358656.1
GABRB2	NM_021911.3	c.542-27860G>A		intron_variant	Intron 6 of 10		NP_068711.1
GABRB2	NM_000813.3	c.542-27860G>A		intron_variant	Intron 6 of 9		NP_000804.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
GABRB2	ENST00000393959.6	c.542-27860G>A		intron_variant	Intron 5 of 9	1	NM_001371727.1	ENSP00000377531.1

Frequencies

GnomAD3 genomes AF: 0.167 AC: 25318 AN: 151852 Hom.: 2908 Cov.: 32

Gnomad AFR AF: 0.315

Gnomad AMI AF: 0.173

Gnomad AMR AF: 0.139

Gnomad ASJ AF: 0.102

Gnomad EAS AF: 0.213

Gnomad SAS AF: 0.0641

Gnomad FIN AF: 0.176

Gnomad MID AF: 0.136

Gnomad NFE AF: 0.0881

Gnomad OTH AF: 0.177

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

GnomAD4 genome AF: 0.167 AC: 25346 AN: 151970 Hom.: 2916 Cov.: 32 AF XY: 0.168 AC XY: 12506 AN XY: 74292

African (AFR) AF: 0.315 AC: 13055 AN: 41436

American (AMR) AF: 0.139 AC: 2124 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.102 AC: 352 AN: 3466

East Asian (EAS) AF: 0.212 AC: 1097 AN: 5168

South Asian (SAS) AF: 0.0646 AC: 311 AN: 4814

European-Finnish (FIN) AF: 0.176 AC: 1854 AN: 10556

Middle Eastern (MID) AF: 0.136 AC: 40 AN: 294

European-Non Finnish (NFE) AF: 0.0881 AC: 5985 AN: 67942

Other (OTH) AF: 0.176 AC: 371 AN: 2108

Alfa AF: 0.0431 Hom.: 40

Bravo AF: 0.175

Asia WGS AF: 0.145 AC: 502 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	3.7
DANN	Benign	0.42
PhyloP100		-0.17
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: rs7724086; hg19: chr5-160791636;