X-123437634-T-C

Position:

• chrX-123437634-T-C

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000620443.2(GRIA3):​c.2076+9495T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.208 in 110,585 control chromosomes in the GnomAD database, including 1,703 homozygotes. There are 6,589 hemizygotes in GnomAD. 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 0.21 (1703 hom., 6589 hem., cov: 22)
• Consequence: GRIA3 ENST00000620443.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0200

Genes affected

GRIA3 (HGNC:4573): (glutamate ionotropic receptor AMPA type subunit 3) Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. These receptors are heteromeric protein complexes composed of multiple subunits, arranged to form ligand-gated ion channels. The classification of glutamate receptors is based on their activation by different pharmacologic agonists. The subunit encoded by this gene belongs to a family of AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate)-sensitive glutamate receptors, and is subject to RNA editing (AGA->GGA; R->G). Alternative splicing at this locus results in different isoforms, which may vary in their signal transduction properties. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.277 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
GRIA3	NM_000828.5	c.2076+9495T>C		intron_variant		ENST00000622768.5	NP_000819.4
GRIA3	NM_007325.5	c.2076+9495T>C		intron_variant		ENST00000620443.2	NP_015564.5

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
GRIA3	ENST00000620443.2	c.2076+9495T>C		intron_variant		1	NM_007325.5	ENSP00000478489	P4
GRIA3	ENST00000622768.5	c.2076+9495T>C		intron_variant		5	NM_000828.5	ENSP00000481554	A1
GRIA3	ENST00000620581.4	c.2076+9495T>C		intron_variant, NMD_transcript_variant		1		ENSP00000481875

Frequencies

GnomAD3 genomes AF: 0.208 AC: 23043 AN: 110531 Hom.: 1700 Cov.: 22 AF XY: 0.201 AC XY: 6586 AN XY: 32779

Gnomad AFR AF: 0.219

Gnomad AMI AF: 0.260

Gnomad AMR AF: 0.229

Gnomad ASJ AF: 0.178

Gnomad EAS AF: 0.243

Gnomad SAS AF: 0.299

Gnomad FIN AF: 0.126

Gnomad MID AF: 0.193

Gnomad NFE AF: 0.201

Gnomad OTH AF: 0.212

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

GnomAD4 genome AF: 0.208 AC: 23047 AN: 110585 Hom.: 1703 Cov.: 22 AF XY: 0.201 AC XY: 6589 AN XY: 32843

Gnomad4 AFR AF: 0.219

Gnomad4 AMR AF: 0.230

Gnomad4 ASJ AF: 0.178

Gnomad4 EAS AF: 0.244

Gnomad4 SAS AF: 0.295

Gnomad4 FIN AF: 0.126

Gnomad4 NFE AF: 0.201

Gnomad4 OTH AF: 0.211

Alfa AF: 0.196 Hom.: 1354

Bravo AF: 0.221

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	1.1
DANN	Benign	0.78

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

Publications

LitVar

Other links and lift over

dbSNP: rs551166; hg19: chrX-122571485;