NM_003490.4:c.1230+128G>C

Variant names:

• chr22-32528746-C-G
• rs135123
• NM_003490.4:c.1230+128G>C

Variant summary

Our verdict is Benign. The variant received -8 ACMG points: 0P and 8B. BA1

The NM_003490.4(SYN3):​c.1230+128G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.179 in 1,346,874 control chromosomes in the GnomAD database, including 22,482 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 0.17 (2236 hom., cov: 33)
  • Exomes 𝑓: 0.18 (20246 hom.)
• Consequence: SYN3 NM_003490.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.32
• Publications: 1 publications found

Genes affected

SYN3 (HGNC:11496): (synapsin III) 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. The protein encoded by this gene shares the synapsin family domain model, with domains A, C, and E exhibiting the highest degree of conservation. The protein contains a unique domain J, located between domains C and E. Based on this gene's localization to 22q12.3, a possible schizophrenia susceptibility locus, and the established neurobiological roles of the synapsins, this family member may represent a candidate gene for schizophrenia. The TIMP3 gene is located within an intron of this gene and is transcribed in the opposite direction. Alternative splicing of this gene results in multiple splice variants that encode different isoforms. [provided by RefSeq, Oct 2008]

ACMG classification

Our verdict: Benign. The variant received -8 ACMG points.

• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.196 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_003490.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SYN3	NM_003490.4	MANE Select	c.1230+128G>C		intron	N/A	NP_003481.3
	SYN3	NM_001369907.1		c.1230+128G>C		intron	N/A	NP_001356836.1
	SYN3	NM_001369908.1		c.1230+128G>C		intron	N/A	NP_001356837.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SYN3	ENST00000358763.7	TSL:5 MANE Select	c.1230+128G>C		intron	N/A	ENSP00000351614.2
	SYN3	ENST00000459990.5	TSL:4	n.291+128G>C		intron	N/A
	SYN3	ENST00000461446.1	TSL:2	n.209+128G>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.167 AC: 25376 AN: 152132 Hom.: 2240 Cov.: 33

Gnomad AFR AF: 0.132

Gnomad AMI AF: 0.253

Gnomad AMR AF: 0.203

Gnomad ASJ AF: 0.182

Gnomad EAS AF: 0.0809

Gnomad SAS AF: 0.142

Gnomad FIN AF: 0.144

Gnomad MID AF: 0.196

Gnomad NFE AF: 0.189

Gnomad OTH AF: 0.178

GnomAD4 exome AF: 0.181 AC: 215822 AN: 1194624 Hom.: 20246 AF XY: 0.180 AC XY: 106266 AN XY: 589740

African (AFR) AF: 0.124 AC: 3355 AN: 26980

American (AMR) AF: 0.213 AC: 6056 AN: 28374

Ashkenazi Jewish (ASJ) AF: 0.190 AC: 3791 AN: 19986

East Asian (EAS) AF: 0.0814 AC: 2850 AN: 35026

South Asian (SAS) AF: 0.148 AC: 9772 AN: 65892

European-Finnish (FIN) AF: 0.144 AC: 5533 AN: 38362

Middle Eastern (MID) AF: 0.175 AC: 846 AN: 4834

European-Non Finnish (NFE) AF: 0.189 AC: 174712 AN: 924456

Other (OTH) AF: 0.176 AC: 8907 AN: 50714

GnomAD4 genome AF: 0.167 AC: 25372 AN: 152250 Hom.: 2236 Cov.: 33 AF XY: 0.165 AC XY: 12278 AN XY: 74436

African (AFR) AF: 0.132 AC: 5486 AN: 41552

American (AMR) AF: 0.202 AC: 3096 AN: 15304

Ashkenazi Jewish (ASJ) AF: 0.182 AC: 631 AN: 3470

East Asian (EAS) AF: 0.0811 AC: 420 AN: 5178

South Asian (SAS) AF: 0.142 AC: 687 AN: 4822

European-Finnish (FIN) AF: 0.144 AC: 1523 AN: 10606

Middle Eastern (MID) AF: 0.194 AC: 57 AN: 294

European-Non Finnish (NFE) AF: 0.189 AC: 12866 AN: 67998

Other (OTH) AF: 0.177 AC: 375 AN: 2114

Alfa AF: 0.0824 Hom.: 116

Bravo AF: 0.172

Asia WGS AF: 0.0940 AC: 327 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
CADD	Benign	0.92
DANN	Benign	0.54
PhyloP100		-1.3
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.21		Details are displayed if max score is > 0.2
DS_DG_spliceai		0.21		Position offset: -47

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs135123; hg19: chr22-32924733;