rs4397202

chr6-168575196-C-T

Variant summary

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

The NM_001166412.2(SMOC2):c.638-23622C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.084 in 152,192 control chromosomes in the GnomAD database, including 832 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 0.084 (832 hom., cov: 33)
• Consequence: SMOC2 NM_001166412.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.12

Genes affected

SMOC2 (HGNC:20323): (SPARC related modular calcium binding 2) This gene encodes a member of the SPARC family (secreted protein acidic and rich in cysteine/osteonectin/BM-40), which are highly expressed during embryogenesis and wound healing. The gene product is a matricellular protein which promotes matrix assembly and can stimulate endothelial cell proliferation and migration, as well as angiogenic activity. Associated with pulmonary function, this secretory gene product contains a Kazal domain, two thymoglobulin type-1 domains, and two EF-hand calcium-binding domains. The encoded protein may serve as a target for controlling angiogenesis in tumor growth and myocardial ischemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

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 (AFR) allele frequency at 95% confidence interval = 0.175 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
SMOC2	NM_001166412.2	c.638-23622C>T		intron_variant		ENST00000356284.7
SMOC2	NM_022138.3	c.671-23622C>T		intron_variant
SMOC2	XM_011536065.2	c.671-23622C>T		intron_variant
SMOC2	XM_011536066.2	c.638-23622C>T		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
SMOC2	ENST00000356284.7	c.638-23622C>T		intron_variant		1	NM_001166412.2	P3
SMOC2	ENST00000354536.9	c.671-23622C>T		intron_variant		1		A1

Frequencies

GnomAD3 genomes AF: 0.0841 AC: 12788 AN: 152074 Hom.: 838 Cov.: 33

Gnomad AFR AF: 0.179

Gnomad AMI AF: 0.0374

Gnomad AMR AF: 0.0348

Gnomad ASJ AF: 0.0343

Gnomad EAS AF: 0.164

Gnomad SAS AF: 0.0682

Gnomad FIN AF: 0.0360

Gnomad MID AF: 0.0570

Gnomad NFE AF: 0.0439

Gnomad OTH AF: 0.0651

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

GnomAD4 genome AF: 0.0840 AC: 12786 AN: 152192 Hom.: 832 Cov.: 33 AF XY: 0.0829 AC XY: 6171 AN XY: 74400

Gnomad4 AFR AF: 0.179

Gnomad4 AMR AF: 0.0348

Gnomad4 ASJ AF: 0.0343

Gnomad4 EAS AF: 0.164

Gnomad4 SAS AF: 0.0676

Gnomad4 FIN AF: 0.0360

Gnomad4 NFE AF: 0.0438

Gnomad4 OTH AF: 0.0644

Alfa AF: 0.0655 Hom.: 72

Bravo AF: 0.0900

Asia WGS AF: 0.105 AC: 364 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	0.55
Dann	Benign	0.57

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: rs4397202; hg19: chr6-168975876;