rs3773953

Positions:

• chr3-190596931-C-A
• chr3-190596931-C-T

Variant summary

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

The NM_002182.4(IL1RAP):​c.65-7197C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0931 in 152,038 control chromosomes in the GnomAD database, including 720 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 0.093 (720 hom., cov: 32)
• Consequence: IL1RAP NM_002182.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.191

Genes affected

IL1RAP (HGNC:5995): (interleukin 1 receptor accessory protein) This gene encodes a component of the interleukin 1 receptor complex, which initiates signalling events that result in the activation of interleukin 1-responsive genes. Alternative splicing of this gene results in membrane-bound and soluble isoforms differing in their C-terminus. The ratio of soluble to membrane-bound forms increases during acute-phase induction or stress. [provided by RefSeq, Jul 2018]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.115 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
IL1RAP	NM_002182.4	c.65-7197C>A		intron_variant		ENST00000447382.6

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
IL1RAP	ENST00000447382.6	c.65-7197C>A		intron_variant		1	NM_002182.4	P1

Frequencies

GnomAD3 genomes AF: 0.0931 AC: 14145 AN: 151920 Hom.: 719 Cov.: 32

Gnomad AFR AF: 0.118

Gnomad AMI AF: 0.0800

Gnomad AMR AF: 0.0571

Gnomad ASJ AF: 0.0841

Gnomad EAS AF: 0.0214

Gnomad SAS AF: 0.107

Gnomad FIN AF: 0.0641

Gnomad MID AF: 0.0981

Gnomad NFE AF: 0.0957

Gnomad OTH AF: 0.0859

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

GnomAD4 genome AF: 0.0931 AC: 14154 AN: 152038 Hom.: 720 Cov.: 32 AF XY: 0.0910 AC XY: 6767 AN XY: 74326

Gnomad4 AFR AF: 0.118

Gnomad4 AMR AF: 0.0571

Gnomad4 ASJ AF: 0.0841

Gnomad4 EAS AF: 0.0214

Gnomad4 SAS AF: 0.108

Gnomad4 FIN AF: 0.0641

Gnomad4 NFE AF: 0.0957

Gnomad4 OTH AF: 0.0859

Alfa AF: 0.0881 Hom.: 875

Bravo AF: 0.0932

Asia WGS AF: 0.0630 AC: 219 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	1.1
DANN	Benign	0.54

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: rs3773953; hg19: chr3-190314720;