rs17841329

chr16-55669099-G-A

Variant summary

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

The NM_001172501.3(SLC6A2):c.275-466G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0614 in 152,212 control chromosomes in the GnomAD database, including 374 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 0.061 (374 hom., cov: 32)
• Consequence: SLC6A2 NM_001172501.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.918

Genes affected

SLC6A2 (HGNC:11048): (solute carrier family 6 member 2) This gene encodes a member of the sodium:neurotransmitter symporter family. This member is a multi-pass membrane protein, which is responsible for reuptake of norepinephrine into presynaptic nerve terminals and is a regulator of norepinephrine homeostasis. Mutations in this gene cause orthostatic intolerance, a syndrome characterized by lightheadedness, fatigue, altered mentation and syncope. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.103 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
SLC6A2	NM_001172501.3	c.275-466G>A		intron_variant		ENST00000568943.6

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
SLC6A2	ENST00000568943.6	c.275-466G>A		intron_variant		1	NM_001172501.3	P1

Frequencies

GnomAD3 genomes AF: 0.0614 AC: 9344 AN: 152094 Hom.: 374 Cov.: 32

Gnomad AFR AF: 0.106

Gnomad AMI AF: 0.0505

Gnomad AMR AF: 0.0374

Gnomad ASJ AF: 0.0625

Gnomad EAS AF: 0.00231

Gnomad SAS AF: 0.0670

Gnomad FIN AF: 0.0163

Gnomad MID AF: 0.0696

Gnomad NFE AF: 0.0511

Gnomad OTH AF: 0.0550

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

GnomAD4 genome AF: 0.0614 AC: 9345 AN: 152212 Hom.: 374 Cov.: 32 AF XY: 0.0594 AC XY: 4422 AN XY: 74416

Gnomad4 AFR AF: 0.106

Gnomad4 AMR AF: 0.0373

Gnomad4 ASJ AF: 0.0625

Gnomad4 EAS AF: 0.00232

Gnomad4 SAS AF: 0.0671

Gnomad4 FIN AF: 0.0163

Gnomad4 NFE AF: 0.0511

Gnomad4 OTH AF: 0.0540

Alfa AF: 0.0548 Hom.: 279

Bravo AF: 0.0651

Asia WGS AF: 0.0340 AC: 118 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
Cadd	Benign	7.1
Dann	Benign	0.61

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: rs17841329; hg19: chr16-55703011;