8-15196915-G-A

Position:

• chr8-15196915-G-A

Variant summary

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

The NM_139167.4(SGCZ):​c.39+40670C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.369 in 152,128 control chromosomes in the GnomAD database, including 11,897 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 0.37 (11897 hom., cov: 33)
• Consequence: SGCZ NM_139167.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.877

Genes affected

SGCZ (HGNC:14075): (sarcoglycan zeta) The zeta-sarcoglycan gene measures over 465 kb and localizes to 8p22. This protein is part of the sarcoglycan complex, a group of 6 proteins. The sarcoglycans are all N-glycosylated transmembrane proteins with a short intra-cellular domain, a single transmembrane region and a large extra-cellular domain containing a carboxyl-terminal cluster with several conserved cysteine residues. The sarcoglycan complex is part of the dystrophin-associated glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extra-cellular matrix. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.02).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.454 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
SGCZ	NM_139167.4	c.39+40670C>T		intron_variant		ENST00000382080.6
SGCZ	NM_001322879.2	c.39+40670C>T		intron_variant
SGCZ	NM_001322880.2	c.39+40670C>T		intron_variant
SGCZ	NM_001322881.2	c.-90+40670C>T		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
SGCZ	ENST00000382080.6	c.39+40670C>T		intron_variant		5	NM_139167.4	P1

Frequencies

GnomAD3 genomes AF: 0.369 AC: 56143 AN: 152010 Hom.: 11896 Cov.: 33

Gnomad AFR AF: 0.197

Gnomad AMI AF: 0.352

Gnomad AMR AF: 0.290

Gnomad ASJ AF: 0.472

Gnomad EAS AF: 0.200

Gnomad SAS AF: 0.353

Gnomad FIN AF: 0.649

Gnomad MID AF: 0.328

Gnomad NFE AF: 0.458

Gnomad OTH AF: 0.359

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

GnomAD4 genome AF: 0.369 AC: 56177 AN: 152128 Hom.: 11897 Cov.: 33 AF XY: 0.376 AC XY: 27942 AN XY: 74364

Gnomad4 AFR AF: 0.197

Gnomad4 AMR AF: 0.290

Gnomad4 ASJ AF: 0.472

Gnomad4 EAS AF: 0.200

Gnomad4 SAS AF: 0.352

Gnomad4 FIN AF: 0.649

Gnomad4 NFE AF: 0.458

Gnomad4 OTH AF: 0.365

Alfa AF: 0.408 Hom.: 7244

Bravo AF: 0.332

Asia WGS AF: 0.339 AC: 1181 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.17
DANN	Benign	0.60

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: rs12680924; hg19: chr8-15054424;