rs4755409

Positions:

• chr11-35415439-A-T

Variant summary

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

The ENST00000278379.9(SLC1A2):​c.17+3511T>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.124 in 152,220 control chromosomes in the GnomAD database, including 1,243 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 0.12 (1243 hom., cov: 33)
• Consequence: SLC1A2 ENST00000278379.9 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.509

Genes affected

SLC1A2 (HGNC:10940): (solute carrier family 1 member 2) This gene encodes a member of a family of solute transporter proteins. The membrane-bound protein is the principal transporter that clears the excitatory neurotransmitter glutamate from the extracellular space at synapses in the central nervous system. Glutamate clearance is necessary for proper synaptic activation and to prevent neuronal damage from excessive activation of glutamate receptors. Improper regulation of this gene is thought to be associated with several neurological disorders. Alternatively spliced transcript variants of this gene have been identified. [provided by RefSeq, Jun 2017]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.8).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.127 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SLC1A2	NM_004171.4	c.17+3511T>A		intron_variant		ENST00000278379.9	NP_004162.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SLC1A2	ENST00000278379.9	c.17+3511T>A		intron_variant		1	NM_004171.4	ENSP00000278379	P4

Frequencies

GnomAD3 genomes AF: 0.124 AC: 18932 AN: 152102 Hom.: 1234 Cov.: 33

Gnomad AFR AF: 0.111

Gnomad AMI AF: 0.0910

Gnomad AMR AF: 0.0921

Gnomad ASJ AF: 0.189

Gnomad EAS AF: 0.0955

Gnomad SAS AF: 0.123

Gnomad FIN AF: 0.193

Gnomad MID AF: 0.152

Gnomad NFE AF: 0.129

Gnomad OTH AF: 0.121

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

GnomAD4 genome AF: 0.124 AC: 18951 AN: 152220 Hom.: 1243 Cov.: 33 AF XY: 0.126 AC XY: 9392 AN XY: 74400

Gnomad4 AFR AF: 0.111

Gnomad4 AMR AF: 0.0920

Gnomad4 ASJ AF: 0.189

Gnomad4 EAS AF: 0.0953

Gnomad4 SAS AF: 0.122

Gnomad4 FIN AF: 0.193

Gnomad4 NFE AF: 0.129

Gnomad4 OTH AF: 0.129

Alfa AF: 0.122 Hom.: 134

Bravo AF: 0.117

Asia WGS AF: 0.123 AC: 426 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.80
CADD	Benign	7.0
DANN	Benign	0.56

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: rs4755409; hg19: chr11-35436986;