NM_018667.4:c.-268-7764T>C

Variant names:

• chr16-68394423-A-G
• rs8050499
• NM_018667.4:c.-268-7764T>C

Variant summary

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

The NM_018667.4(SMPD3):​c.-268-7764T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.18 in 152,094 control chromosomes in the GnomAD database, including 2,646 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 0.18 (2646 hom., cov: 33)
• Consequence: SMPD3 NM_018667.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0250
• Publications: 11 publications found

Genes affected

SMPD3 (HGNC:14240): (sphingomyelin phosphodiesterase 3) Predicted to enable phosphatidic acid binding activity; phosphatidylserine binding activity; and sphingomyelin phosphodiesterase activity. Predicted to be involved in positive regulation of exosomal secretion and sphingomyelin metabolic process. Predicted to act upstream of or within several processes, including animal organ development; enzyme linked receptor protein signaling pathway; and sphingolipid metabolic process. Predicted to be located in Golgi apparatus and plasma membrane. Predicted to be active in cytoplasm. Biomarker of pulmonary emphysema. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.205 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_018667.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SMPD3	NM_018667.4	MANE Select	c.-268-7764T>C		intron	N/A	NP_061137.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SMPD3	ENST00000219334.10	TSL:1 MANE Select	c.-268-7764T>C		intron	N/A	ENSP00000219334.5
	SMPD3	ENST00000561749.1	TSL:2	c.-206-22036T>C		intron	N/A	ENSP00000457236.1
	SMPD3	ENST00000566723.1	TSL:4	n.91-7764T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.180 AC: 27378 AN: 151976 Hom.: 2638 Cov.: 33

Gnomad AFR AF: 0.209

Gnomad AMI AF: 0.259

Gnomad AMR AF: 0.138

Gnomad ASJ AF: 0.202

Gnomad EAS AF: 0.0694

Gnomad SAS AF: 0.182

Gnomad FIN AF: 0.249

Gnomad MID AF: 0.180

Gnomad NFE AF: 0.168

Gnomad OTH AF: 0.179

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

GnomAD4 genome AF: 0.180 AC: 27407 AN: 152094 Hom.: 2646 Cov.: 33 AF XY: 0.185 AC XY: 13740 AN XY: 74358

African (AFR) AF: 0.209 AC: 8647 AN: 41468

American (AMR) AF: 0.138 AC: 2109 AN: 15286

Ashkenazi Jewish (ASJ) AF: 0.202 AC: 701 AN: 3468

East Asian (EAS) AF: 0.0692 AC: 359 AN: 5190

South Asian (SAS) AF: 0.182 AC: 880 AN: 4832

European-Finnish (FIN) AF: 0.249 AC: 2626 AN: 10548

Middle Eastern (MID) AF: 0.180 AC: 53 AN: 294

European-Non Finnish (NFE) AF: 0.168 AC: 11406 AN: 67984

Other (OTH) AF: 0.185 AC: 390 AN: 2112

Alfa AF: 0.167 Hom.: 6942

Bravo AF: 0.171

Asia WGS AF: 0.173 AC: 603 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	1.3
DANN	Benign	0.54
PhyloP100		0.025
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: rs8050499; hg19: chr16-68428326;