rs36021

Positions:

• chr16-55678038-T-A
• chr16-55678038-T-C
• chr16-55678038-T-G

Variant summary

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

The NM_001172501.3(SLC6A2):​c.644+5863T>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.594 in 152,000 control chromosomes in the GnomAD database, including 26,952 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 0.59 (26952 hom., cov: 31)
• Consequence: SLC6A2 NM_001172501.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.44

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=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.65 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
SLC6A2	NM_001172501.3	c.644+5863T>A		intron_variant		ENST00000568943.6

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
SLC6A2	ENST00000568943.6	c.644+5863T>A		intron_variant		1	NM_001172501.3	P1

Frequencies

GnomAD3 genomes AF: 0.594 AC: 90230 AN: 151882 Hom.: 26918 Cov.: 31

Gnomad AFR AF: 0.657

Gnomad AMI AF: 0.695

Gnomad AMR AF: 0.596

Gnomad ASJ AF: 0.607

Gnomad EAS AF: 0.543

Gnomad SAS AF: 0.590

Gnomad FIN AF: 0.552

Gnomad MID AF: 0.602

Gnomad NFE AF: 0.564

Gnomad OTH AF: 0.605

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

GnomAD4 genome AF: 0.594 AC: 90316 AN: 152000 Hom.: 26952 Cov.: 31 AF XY: 0.594 AC XY: 44124 AN XY: 74294

Gnomad4 AFR AF: 0.657

Gnomad4 AMR AF: 0.596

Gnomad4 ASJ AF: 0.607

Gnomad4 EAS AF: 0.542

Gnomad4 SAS AF: 0.589

Gnomad4 FIN AF: 0.552

Gnomad4 NFE AF: 0.564

Gnomad4 OTH AF: 0.605

Alfa AF: 0.571 Hom.: 2935

Bravo AF: 0.600

Asia WGS AF: 0.567 AC: 1970 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.73
DANN	Benign	0.42

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: rs36021; hg19: chr16-55711950;