rs468879

Variant names:

• chr21-29851746-A-G
• rs468879
• NM_001330994.2:c.118+87637T>C

Variant summary

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

The NM_001330994.2(GRIK1):​c.118+87637T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.348 in 152,080 control chromosomes in the GnomAD database, including 10,617 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 0.35 (10617 hom., cov: 32)
• Consequence: GRIK1 NM_001330994.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0330
• Publications: 1 publications found

Genes affected

GRIK1 (HGNC:4579): (glutamate ionotropic receptor kainate type subunit 1) Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. This gene product belongs to the kainate family of glutamate receptors, which are composed of four subunits and function as ligand-activated ion channels. The subunit encoded by this gene is subject to RNA editing (CAG->CGG; Q->R) within the second transmembrane domain, which is thought to alter the properties of ion flow. Alternative splicing, resulting in transcript variants encoding different isoforms, has been noted for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.543 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001330994.2. 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
	GRIK1	NM_001330994.2	MANE Select	c.118+87637T>C		intron	N/A	NP_001317923.1	E7ENK3
	GRIK1	NM_001330993.2		c.118+87637T>C		intron	N/A	NP_001317922.1	E7EPY9
	GRIK1	NM_001320616.2		c.118+87637T>C		intron	N/A	NP_001307545.1	E9PD61

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GRIK1	ENST00000327783.9	TSL:5 MANE Select	c.118+87637T>C		intron	N/A	ENSP00000327687.4	E7ENK3
	GRIK1	ENST00000399907.6	TSL:1	c.118+87637T>C		intron	N/A	ENSP00000382791.1	P39086-1
	GRIK1	ENST00000389125.7	TSL:1	c.118+87637T>C		intron	N/A	ENSP00000373777.3	P39086-2

Frequencies

GnomAD3 genomes AF: 0.348 AC: 52892 AN: 151962 Hom.: 10587 Cov.: 32

Gnomad AFR AF: 0.549

Gnomad AMI AF: 0.264

Gnomad AMR AF: 0.326

Gnomad ASJ AF: 0.236

Gnomad EAS AF: 0.461

Gnomad SAS AF: 0.398

Gnomad FIN AF: 0.179

Gnomad MID AF: 0.285

Gnomad NFE AF: 0.253

Gnomad OTH AF: 0.312

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

GnomAD4 genome AF: 0.348 AC: 52977 AN: 152080 Hom.: 10617 Cov.: 32 AF XY: 0.347 AC XY: 25778 AN XY: 74348

African (AFR) AF: 0.549 AC: 22771 AN: 41464

American (AMR) AF: 0.326 AC: 4985 AN: 15274

Ashkenazi Jewish (ASJ) AF: 0.236 AC: 819 AN: 3472

East Asian (EAS) AF: 0.461 AC: 2378 AN: 5154

South Asian (SAS) AF: 0.397 AC: 1915 AN: 4818

European-Finnish (FIN) AF: 0.179 AC: 1898 AN: 10600

Middle Eastern (MID) AF: 0.289 AC: 85 AN: 294

European-Non Finnish (NFE) AF: 0.253 AC: 17224 AN: 67984

Other (OTH) AF: 0.314 AC: 663 AN: 2114

Alfa AF: 0.316 Hom.: 1463

Bravo AF: 0.370

Asia WGS AF: 0.449 AC: 1562 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	2.8
DANN	Benign	0.59
PhyloP100		-0.033
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: rs468879; hg19: chr21-31224063;