rs795011

Positions:

• chr3-12169546-G-T

Variant summary

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

The NM_133625.6(SYN2):​c.1159-211G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.634 in 151,926 control chromosomes in the GnomAD database, including 33,420 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 0.63 (33420 hom., cov: 31)
• Consequence: SYN2 NM_133625.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.175

Genes affected

SYN2 (HGNC:11495): (synapsin II) This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. This member of the synapsin family encodes a neuron-specific phosphoprotein that selectively binds to small synaptic vesicles in the presynaptic nerve terminal. Polymorphisms in this gene are associated with abnormal presynaptic function and related neuronal disorders, including autism, epilepsy, bipolar disorder and schizophrenia. Alternative splicing of this gene results in multiple transcript variants. The tissue inhibitor of metalloproteinase 4 gene is located within an intron of this gene and is transcribed in the opposite direction. [provided by RefSeq, Feb 2014]

SYN2 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.79).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.767 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SYN2	NM_133625.6	c.1159-211G>T		intron_variant		ENST00000621198.5	NP_598328.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SYN2	ENST00000621198.5	c.1159-211G>T		intron_variant		1	NM_133625.6	ENSP00000480050.1
SYN2	ENST00000620175.4	c.1159-211G>T		intron_variant		1		ENSP00000484916.1
SYN2	ENST00000425297.2	n.385-211G>T		intron_variant		5		ENSP00000480038.1
SYN2	ENST00000439861.5	n.778-211G>T		intron_variant		2

Frequencies

GnomAD3 genomes AF: 0.634 AC: 96306 AN: 151806 Hom.: 33407 Cov.: 31

Gnomad AFR AF: 0.324

Gnomad AMI AF: 0.912

Gnomad AMR AF: 0.755

Gnomad ASJ AF: 0.728

Gnomad EAS AF: 0.678

Gnomad SAS AF: 0.788

Gnomad FIN AF: 0.788

Gnomad MID AF: 0.755

Gnomad NFE AF: 0.747

Gnomad OTH AF: 0.693

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

GnomAD4 genome AF: 0.634 AC: 96334 AN: 151926 Hom.: 33420 Cov.: 31 AF XY: 0.640 AC XY: 47567 AN XY: 74276

Gnomad4 AFR AF: 0.323

Gnomad4 AMR AF: 0.755

Gnomad4 ASJ AF: 0.728

Gnomad4 EAS AF: 0.678

Gnomad4 SAS AF: 0.788

Gnomad4 FIN AF: 0.788

Gnomad4 NFE AF: 0.747

Gnomad4 OTH AF: 0.694

Alfa AF: 0.681 Hom.: 4628

Bravo AF: 0.618

Asia WGS AF: 0.710 AC: 2468 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.79
CADD	Benign	1.2
DANN	Benign	0.62

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: rs795011; hg19: chr3-12211046;