18-49090685-C-T

Position:

• chr18-49090685-C-T

Variant summary

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

The NM_001353214.3(DYM):​c.2025+6717G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.123 in 151,982 control chromosomes in the GnomAD database, including 1,499 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 0.12 (1499 hom., cov: 31)
• Consequence: DYM NM_001353214.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.122

Genes affected

DYM (HGNC:21317): (dymeclin) This gene encodes a protein which regulates Golgi-associated secretory pathways that are essential to endochondral bone formation during early development. This gene is also believed to play a role in early brain development. This gene is widely expressed in embryos and is particularly abundant in chodrocytes and brain tissues. It encodes a peripheral membrane protein which shuttles between the cytosol and Golgi complex. Mutations in this gene are associated with two types of recessive osteochondrodysplasia: Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia. [provided by RefSeq, Jun 2017]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.265 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
DYM	NM_001353214.3	c.2025+6717G>A		intron_variant		ENST00000675505.1	NP_001340143.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
DYM	ENST00000675505.1	c.2025+6717G>A		intron_variant			NM_001353214.3	ENSP00000501694.1
DYM	ENST00000269445.10	c.1860+6717G>A		intron_variant		1		ENSP00000269445.6
DYM	ENST00000442713.6	c.1290+6717G>A		intron_variant		2		ENSP00000395942.2
DYM	ENST00000577734.1	c.185+2532G>A		intron_variant		3		ENSP00000464163.1

Frequencies

GnomAD3 genomes AF: 0.123 AC: 18719 AN: 151864 Hom.: 1495 Cov.: 31

Gnomad AFR AF: 0.0398

Gnomad AMI AF: 0.269

Gnomad AMR AF: 0.0871

Gnomad ASJ AF: 0.136

Gnomad EAS AF: 0.277

Gnomad SAS AF: 0.238

Gnomad FIN AF: 0.152

Gnomad MID AF: 0.0949

Gnomad NFE AF: 0.156

Gnomad OTH AF: 0.112

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

GnomAD4 genome AF: 0.123 AC: 18725 AN: 151982 Hom.: 1499 Cov.: 31 AF XY: 0.125 AC XY: 9286 AN XY: 74274

Gnomad4 AFR AF: 0.0397

Gnomad4 AMR AF: 0.0870

Gnomad4 ASJ AF: 0.136

Gnomad4 EAS AF: 0.277

Gnomad4 SAS AF: 0.237

Gnomad4 FIN AF: 0.152

Gnomad4 NFE AF: 0.156

Gnomad4 OTH AF: 0.122

Alfa AF: 0.146 Hom.: 348

Bravo AF: 0.112

Asia WGS AF: 0.277 AC: 961 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	3.3
DANN	Benign	0.29

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: rs11873029; hg19: chr18-46617055;