rs244960

Positions:

• chr5-155924251-T-A
• chr5-155924251-T-C
• chr5-155924251-T-G

Variant summary

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

The ENST00000517913.5(SGCD):​c.-282+53827T>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.431 in 152,036 control chromosomes in the GnomAD database, including 15,620 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 0.43 (15620 hom., cov: 32)
• Consequence: SGCD ENST00000517913.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.529

Genes affected

SGCD (HGNC:10807): (sarcoglycan delta) The protein encoded by this gene is one of the four known components of the sarcoglycan complex, which is a subcomplex of the dystrophin-glycoprotein complex (DGC). DGC forms a link between the F-actin cytoskeleton and the extracellular matrix. This protein is expressed most abundantly in skeletal and cardiac muscle. Mutations in this gene have been associated with autosomal recessive limb-girdle muscular dystrophy and dilated cardiomyopathy. Alternatively spliced transcript variants encoding distinct isoforms have been observed for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.543 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SGCD	XM_017009724.2	c.-208+195261T>A		intron_variant			XP_016865213.1
SGCD	XM_047417518.1	c.-264+53827T>A		intron_variant			XP_047273474.1
SGCD	XM_047417519.1	c.-208+53827T>A		intron_variant			XP_047273475.1
SGCD	XM_047417520.1	c.-165+195261T>A		intron_variant			XP_047273476.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SGCD	ENST00000517913.5	c.-282+53827T>A		intron_variant		5		ENSP00000429378.1

Frequencies

GnomAD3 genomes AF: 0.432 AC: 65559 AN: 151918 Hom.: 15618 Cov.: 32

Gnomad AFR AF: 0.235

Gnomad AMI AF: 0.748

Gnomad AMR AF: 0.357

Gnomad ASJ AF: 0.475

Gnomad EAS AF: 0.546

Gnomad SAS AF: 0.422

Gnomad FIN AF: 0.467

Gnomad MID AF: 0.380

Gnomad NFE AF: 0.548

Gnomad OTH AF: 0.428

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

GnomAD4 genome AF: 0.431 AC: 65566 AN: 152036 Hom.: 15620 Cov.: 32 AF XY: 0.428 AC XY: 31799 AN XY: 74330

Gnomad4 AFR AF: 0.235

Gnomad4 AMR AF: 0.357

Gnomad4 ASJ AF: 0.475

Gnomad4 EAS AF: 0.546

Gnomad4 SAS AF: 0.423

Gnomad4 FIN AF: 0.467

Gnomad4 NFE AF: 0.548

Gnomad4 OTH AF: 0.433

Alfa AF: 0.472 Hom.: 2211

Bravo AF: 0.414

Asia WGS AF: 0.481 AC: 1675 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	3.9
DANN	Benign	0.73

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs244960; hg19: chr5-155351261;