rs693534

chr12-117346913-G-A

Variant summary

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

The NM_000620.5(NOS1):c.-421+14599C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.365 in 152,026 control chromosomes in the GnomAD database, including 10,353 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 0.36 (10353 hom., cov: 33)
• Consequence: NOS1 NM_000620.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.491

Genes affected

NOS1 (HGNC:7872): (nitric oxide synthase 1) The protein encoded by this gene belongs to the family of nitric oxide synthases, which synthesize nitric oxide from L-arginine. Nitric oxide is a reactive free radical, which acts as a biologic mediator in several processes, including neurotransmission, and antimicrobial and antitumoral activities. In the brain and peripheral nervous system, nitric oxide displays many properties of a neurotransmitter, and has been implicated in neurotoxicity associated with stroke and neurodegenerative diseases, neural regulation of smooth muscle, including peristalsis, and penile erection. This protein is ubiquitously expressed, with high level of expression in skeletal muscle. Multiple transcript variants that differ in the 5' UTR have been described for this gene but the full-length nature of these transcripts is not known. Additionally, alternatively spliced transcript variants encoding different isoforms (some testis-specific) have been found for this gene.[provided by RefSeq, Feb 2011]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.397 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
NOS1	NM_000620.5	c.-421+14599C>T		intron_variant		ENST00000317775.11
NOS1	NM_001204218.2	c.-421+14599C>T		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
NOS1	ENST00000317775.11	c.-421+14599C>T		intron_variant		1	NM_000620.5	P1
NOS1	ENST00000618760.4	c.-421+14599C>T		intron_variant		5
NOS1	ENST00000549189.1	n.471-15424C>T		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.365 AC: 55429 AN: 151910 Hom.: 10337 Cov.: 33

Gnomad AFR AF: 0.327

Gnomad AMI AF: 0.597

Gnomad AMR AF: 0.400

Gnomad ASJ AF: 0.420

Gnomad EAS AF: 0.286

Gnomad SAS AF: 0.412

Gnomad FIN AF: 0.352

Gnomad MID AF: 0.443

Gnomad NFE AF: 0.377

Gnomad OTH AF: 0.391

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

GnomAD4 genome AF: 0.365 AC: 55489 AN: 152026 Hom.: 10353 Cov.: 33 AF XY: 0.365 AC XY: 27089 AN XY: 74302

Gnomad4 AFR AF: 0.327

Gnomad4 AMR AF: 0.401

Gnomad4 ASJ AF: 0.420

Gnomad4 EAS AF: 0.285

Gnomad4 SAS AF: 0.413

Gnomad4 FIN AF: 0.352

Gnomad4 NFE AF: 0.377

Gnomad4 OTH AF: 0.392

Alfa AF: 0.379 Hom.: 5484

Bravo AF: 0.365

Asia WGS AF: 0.348 AC: 1211 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
Cadd	Benign	4.4
Dann	Benign	0.66

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: rs693534; hg19: chr12-117784718;