rs6553573

Variant names:

• chr4-167148636-G-A
• rs6553573
• NM_001040159.2:c.189+85349C>T

Your query was ambiguous. Multiple possible variants found:

• chr4-167148636-G-A
• chr4-167148636-G-C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001040159.2(SPOCK3):​c.189+85349C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.794 in 152,004 control chromosomes in the GnomAD database, including 48,021 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 0.79 (48021 hom., cov: 32)
• Consequence: SPOCK3 NM_001040159.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.94
• Publications: 1 publications found

Genes affected

SPOCK3 (HGNC:13565): (SPARC (osteonectin), cwcv and kazal like domains proteoglycan 3) This gene encodes a member of a novel family of calcium-binding proteoglycan proteins that contain thyroglobulin type-1 and Kazal-like domains. The encoded protein and may play a role in adult T-cell leukemia by inhibiting the activity of membrane-type matrix metalloproteinases. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.815 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SPOCK3	NM_001040159.2	c.189+85349C>T		intron_variant	Intron 2 of 10	ENST00000357545.9	NP_001035249.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SPOCK3	ENST00000357545.9	c.189+85349C>T		intron_variant	Intron 2 of 10	1	NM_001040159.2	ENSP00000350153.4

Frequencies

GnomAD3 genomes AF: 0.794 AC: 120630 AN: 151884 Hom.: 47981 Cov.: 32

Gnomad AFR AF: 0.822

Gnomad AMI AF: 0.752

Gnomad AMR AF: 0.752

Gnomad ASJ AF: 0.793

Gnomad EAS AF: 0.774

Gnomad SAS AF: 0.786

Gnomad FIN AF: 0.748

Gnomad MID AF: 0.773

Gnomad NFE AF: 0.797

Gnomad OTH AF: 0.802

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

GnomAD4 genome AF: 0.794 AC: 120724 AN: 152004 Hom.: 48021 Cov.: 32 AF XY: 0.793 AC XY: 58944 AN XY: 74298

African (AFR) AF: 0.822 AC: 34088 AN: 41472

American (AMR) AF: 0.752 AC: 11468 AN: 15260

Ashkenazi Jewish (ASJ) AF: 0.793 AC: 2752 AN: 3470

East Asian (EAS) AF: 0.774 AC: 3988 AN: 5150

South Asian (SAS) AF: 0.785 AC: 3783 AN: 4818

European-Finnish (FIN) AF: 0.748 AC: 7897 AN: 10560

Middle Eastern (MID) AF: 0.764 AC: 220 AN: 288

European-Non Finnish (NFE) AF: 0.797 AC: 54148 AN: 67966

Other (OTH) AF: 0.804 AC: 1696 AN: 2110

Alfa AF: 0.803 Hom.: 10515

Bravo AF: 0.795

Asia WGS AF: 0.784 AC: 2716 AN: 3466

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.11
DANN	Benign	0.60
PhyloP100		-1.9
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs6553573; hg19: chr4-168069787;