NM_133445.3:c.1305-5535A>G

Variant names:

• chr9-101676642-T-C
• rs1323426
• NM_133445.3:c.1305-5535A>G

Variant summary

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

The NM_133445.3(GRIN3A):​c.1305-5535A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.234 in 151,782 control chromosomes in the GnomAD database, including 4,466 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 0.23 (4466 hom., cov: 32)
• Consequence: GRIN3A NM_133445.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.47
• Publications: 0 publications found

Genes affected

GRIN3A (HGNC:16767): (glutamate ionotropic receptor NMDA type subunit 3A) This gene encodes a subunit of the N-methyl-D-aspartate (NMDA) receptors, which belong to the superfamily of glutamate-regulated ion channels, and function in physiological and pathological processes in the central nervous system. This subunit shows greater than 90% identity to the corresponding subunit in rat. Studies in the knockout mouse deficient in this subunit suggest that this gene may be involved in the development of synaptic elements by modulating NMDA receptor activity. [provided by RefSeq, Jul 2008]

ENSG00000299588 (HGNC:):

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 (EAS) allele frequency at 95% confidence interval = 0.546 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_133445.3. 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
	GRIN3A	NM_133445.3	MANE Select	c.1305-5535A>G		intron	N/A	NP_597702.2	Q8TCU5

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GRIN3A	ENST00000361820.6	TSL:1 MANE Select	c.1305-5535A>G		intron	N/A	ENSP00000355155.3	Q8TCU5
	ENSG00000299588	ENST00000764873.1		n.224-48106T>C		intron	N/A
	ENSG00000299588	ENST00000764874.1		n.57+26089T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.234 AC: 35436 AN: 151664 Hom.: 4463 Cov.: 32

Gnomad AFR AF: 0.216

Gnomad AMI AF: 0.324

Gnomad AMR AF: 0.265

Gnomad ASJ AF: 0.212

Gnomad EAS AF: 0.564

Gnomad SAS AF: 0.249

Gnomad FIN AF: 0.192

Gnomad MID AF: 0.152

Gnomad NFE AF: 0.218

Gnomad OTH AF: 0.240

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

GnomAD4 genome AF: 0.234 AC: 35455 AN: 151782 Hom.: 4466 Cov.: 32 AF XY: 0.234 AC XY: 17368 AN XY: 74200

African (AFR) AF: 0.216 AC: 8962 AN: 41458

American (AMR) AF: 0.266 AC: 4052 AN: 15246

Ashkenazi Jewish (ASJ) AF: 0.212 AC: 734 AN: 3466

East Asian (EAS) AF: 0.563 AC: 2895 AN: 5138

South Asian (SAS) AF: 0.248 AC: 1194 AN: 4810

European-Finnish (FIN) AF: 0.192 AC: 2031 AN: 10566

Middle Eastern (MID) AF: 0.163 AC: 48 AN: 294

European-Non Finnish (NFE) AF: 0.218 AC: 14745 AN: 67782

Other (OTH) AF: 0.236 AC: 499 AN: 2112

Alfa AF: 0.213 Hom.: 501

Bravo AF: 0.246

Asia WGS AF: 0.393 AC: 1359 AN: 3468

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	5.5
DANN	Benign	0.49
PhyloP100		1.5
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: rs1323426; hg19: chr9-104438924;