rs3106652

Variant names:

• chr2-154721910-A-G
• rs3106652
• NM_002239.4:c.919+12091A>G

Variant summary

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

The NM_002239.4(KCNJ3):​c.919+12091A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.253 in 152,050 control chromosomes in the GnomAD database, including 5,058 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 0.25 (5058 hom., cov: 32)
• Consequence: KCNJ3 NM_002239.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.286
• Publications: 5 publications found

Genes affected

KCNJ3 (HGNC:6264): (potassium inwardly rectifying channel subfamily J member 3) Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and plays an important role in regulating heartbeat. It associates with three other G-protein-activated potassium channels to form a heteromultimeric pore-forming complex that also couples to neurotransmitter receptors in the brain and whereby channel activation can inhibit action potential firing by hyperpolarizing the plasma membrane. These multimeric G-protein-gated inwardly-rectifying potassium (GIRK) channels may play a role in the pathophysiology of epilepsy, addiction, Down's syndrome, ataxia, and Parkinson's disease. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, May 2012]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.57).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.287 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
KCNJ3	NM_002239.4	c.919+12091A>G		intron_variant	Intron 2 of 2	ENST00000295101.3	NP_002230.1
KCNJ3	NM_001260508.2	c.702+22433A>G		intron_variant	Intron 1 of 1		NP_001247437.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
KCNJ3	ENST00000295101.3	c.919+12091A>G		intron_variant	Intron 2 of 2	1	NM_002239.4	ENSP00000295101.2
KCNJ3	ENST00000544049.2	c.702+22433A>G		intron_variant	Intron 1 of 1	1		ENSP00000438410.1
KCNJ3	ENST00000651198.1	c.382+12091A>G		intron_variant	Intron 3 of 3			ENSP00000498639.1
KCNJ3	ENST00000493505.1	n.262+12091A>G		intron_variant	Intron 2 of 2	2

Frequencies

GnomAD3 genomes AF: 0.253 AC: 38511 AN: 151932 Hom.: 5051 Cov.: 32

Gnomad AFR AF: 0.199

Gnomad AMI AF: 0.410

Gnomad AMR AF: 0.253

Gnomad ASJ AF: 0.307

Gnomad EAS AF: 0.127

Gnomad SAS AF: 0.227

Gnomad FIN AF: 0.274

Gnomad MID AF: 0.234

Gnomad NFE AF: 0.290

Gnomad OTH AF: 0.257

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

GnomAD4 genome AF: 0.253 AC: 38537 AN: 152050 Hom.: 5058 Cov.: 32 AF XY: 0.252 AC XY: 18725 AN XY: 74350

African (AFR) AF: 0.199 AC: 8236 AN: 41484

American (AMR) AF: 0.253 AC: 3864 AN: 15274

Ashkenazi Jewish (ASJ) AF: 0.307 AC: 1063 AN: 3464

East Asian (EAS) AF: 0.127 AC: 657 AN: 5166

South Asian (SAS) AF: 0.228 AC: 1099 AN: 4824

European-Finnish (FIN) AF: 0.274 AC: 2893 AN: 10568

Middle Eastern (MID) AF: 0.235 AC: 69 AN: 294

European-Non Finnish (NFE) AF: 0.290 AC: 19734 AN: 67954

Other (OTH) AF: 0.260 AC: 548 AN: 2110

Alfa AF: 0.272 Hom.: 4117

Bravo AF: 0.250

Asia WGS AF: 0.204 AC: 707 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.57
CADD	Benign	1.8
DANN	Benign	0.90
PhyloP100		-0.29
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs3106652; hg19: chr2-155578422;