NM_003580.4:c.1126-15_1126-12dupTTTT

Variant names:

• chr8-58601546-G-GAAAA
• rs33942423
• NM_003580.4:c.1126-15_1126-12dupTTTT

Variant summary

Our verdict is Benign. Variant got -8 ACMG points: 0P and 8B. BA1

The NM_003580.4(NSMAF):​c.1126-15_1126-12dupTTTT variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0835 in 1,399,740 control chromosomes in the GnomAD database, including 280 homozygotes. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.013 (34 hom., cov: 0)
  • Exomes 𝑓: 0.091 (246 hom.)
• Consequence: NSMAF NM_003580.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.861

Genes affected

NSMAF (HGNC:8017): (neutral sphingomyelinase activation associated factor) This gene encodes a WD-repeat protein that binds the cytoplasmic sphingomyelinase activation domain of the 55kD tumor necrosis factor receptor. This protein is required for TNF-mediated activation of neutral sphingomyelinase and may play a role in regulating TNF-induced cellular responses such as inflammation. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2009]

ACMG classification

Verdict is Benign. Variant got -8 ACMG points.

• BA1: GnomAdExome4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.103 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
NSMAF	NM_003580.4	c.1126-15_1126-12dupTTTT		intron_variant	Intron 14 of 30	ENST00000038176.8	NP_003571.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
NSMAF	ENST00000038176.8	c.1126-12_1126-11insTTTT		intron_variant	Intron 14 of 30	1	NM_003580.4	ENSP00000038176.3
NSMAF	ENST00000427130.6	c.1219-12_1219-11insTTTT		intron_variant	Intron 14 of 30	2		ENSP00000411012.2
NSMAF	ENST00000519858.1	n.665-12_665-11insTTTT		intron_variant	Intron 7 of 8	3
NSMAF	ENST00000649465.1	n.*1252-12_*1252-11insTTTT		intron_variant	Intron 16 of 32			ENSP00000498107.1

Frequencies

GnomAD3 genomes AF: 0.0134 AC: 1813 AN: 135432 Hom.: 34 Cov.: 0

Gnomad AFR AF: 0.00432

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00944

Gnomad ASJ AF: 0.0308

Gnomad EAS AF: 0.00333

Gnomad SAS AF: 0.0461

Gnomad FIN AF: 0.00432

Gnomad MID AF: 0.0321

Gnomad NFE AF: 0.0183

Gnomad OTH AF: 0.0118

GnomAD3 exomes AF: 0.0591 AC: 5991 AN: 101380 Hom.: 181 AF XY: 0.0571 AC XY: 3156 AN XY: 55258

Gnomad AFR exome AF: 0.0311

Gnomad AMR exome AF: 0.0956

Gnomad ASJ exome AF: 0.0595

Gnomad EAS exome AF: 0.0717

Gnomad SAS exome AF: 0.0599

Gnomad FIN exome AF: 0.0241

Gnomad NFE exome AF: 0.0600

Gnomad OTH exome AF: 0.0680

GnomAD4 exome AF: 0.0910 AC: 115024 AN: 1264290 Hom.: 246 Cov.: 32 AF XY: 0.0910 AC XY: 56761 AN XY: 623816

Gnomad4 AFR exome AF: 0.0291

Gnomad4 AMR exome AF: 0.107

Gnomad4 ASJ exome AF: 0.108

Gnomad4 EAS exome AF: 0.0713

Gnomad4 SAS exome AF: 0.105

Gnomad4 FIN exome AF: 0.0508

Gnomad4 NFE exome AF: 0.0932

Gnomad4 OTH exome AF: 0.0952

GnomAD4 genome AF: 0.0134 AC: 1810 AN: 135450 Hom.: 34 Cov.: 0 AF XY: 0.0134 AC XY: 871 AN XY: 65172

Gnomad4 AFR AF: 0.00431

Gnomad4 AMR AF: 0.00944

Gnomad4 ASJ AF: 0.0308

Gnomad4 EAS AF: 0.00333

Gnomad4 SAS AF: 0.0459

Gnomad4 FIN AF: 0.00432

Gnomad4 NFE AF: 0.0183

Gnomad4 OTH AF: 0.0117

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs33942423; hg19: chr8-59514105;