rs10491141

chr17-46715266-C-G

Variant summary

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

The NM_006178.4(NSF):c.1761+1280C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.15 in 152,156 control chromosomes in the GnomAD database, including 3,401 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 0.15 (3401 hom., cov: 33)
• Consequence: NSF NM_006178.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.362

Genes affected

NSF (HGNC:8016): (N-ethylmaleimide sensitive factor, vesicle fusing ATPase) Enables PDZ domain binding activity and ionotropic glutamate receptor binding activity. Involved in intracellular protein transport; positive regulation of protein catabolic process; and positive regulation of receptor recycling. Located in Golgi apparatus; cytosol; and plasma membrane. Implicated in developmental and epileptic encephalopathy. [provided by Alliance of Genome Resources, Apr 2022]

LRRC37A2 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.75).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.587 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
NSF	NM_006178.4	c.1761+1280C>G		intron_variant		ENST00000398238.8
LRRC37A2	XM_024450773.2	c.4809+164747C>G		intron_variant
NSF	NR_040116.2	n.1828+1280C>G		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
NSF	ENST00000398238.8	c.1761+1280C>G		intron_variant		1	NM_006178.4	P3

Frequencies

GnomAD3 genomes AF: 0.150 AC: 22789 AN: 152038 Hom.: 3375 Cov.: 33

Gnomad AFR AF: 0.290

Gnomad AMI AF: 0.0736

Gnomad AMR AF: 0.236

Gnomad ASJ AF: 0.0683

Gnomad EAS AF: 0.605

Gnomad SAS AF: 0.122

Gnomad FIN AF: 0.0717

Gnomad MID AF: 0.0981

Gnomad NFE AF: 0.0310

Gnomad OTH AF: 0.128

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

GnomAD4 genome AF: 0.150 AC: 22863 AN: 152156 Hom.: 3401 Cov.: 33 AF XY: 0.155 AC XY: 11563 AN XY: 74394

Gnomad4 AFR AF: 0.290

Gnomad4 AMR AF: 0.237

Gnomad4 ASJ AF: 0.0683

Gnomad4 EAS AF: 0.605

Gnomad4 SAS AF: 0.122

Gnomad4 FIN AF: 0.0717

Gnomad4 NFE AF: 0.0311

Gnomad4 OTH AF: 0.129

Alfa AF: 0.0947 Hom.: 207

Bravo AF: 0.177

Asia WGS AF: 0.350 AC: 1215 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.75
Cadd	Benign	11
Dann	Benign	0.76

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: rs10491141; hg19: chr17-44792632;