chr3-190562376-T-G

Variant names:

• chr3-190562376-T-G
• rs3773981
• NM_002182.4:c.-1-1913T>G

Variant summary

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

The NM_002182.4(IL1RAP):​c.-1-1913T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.228 in 151,876 control chromosomes in the GnomAD database, including 4,909 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 0.23 (4909 hom., cov: 31)
• Consequence: IL1RAP NM_002182.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.304
• Publications: 5 publications found

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

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.403 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_002182.4. 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
	IL1RAP	NM_002182.4	MANE Select	c.-1-1913T>G		intron	N/A	NP_002173.1
	IL1RAP	NM_001167931.2		c.-1-1913T>G		intron	N/A	NP_001161403.1
	IL1RAP	NM_001364879.1		c.-1-1913T>G		intron	N/A	NP_001351808.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	IL1RAP	ENST00000447382.6	TSL:1 MANE Select	c.-1-1913T>G		intron	N/A	ENSP00000390541.1
	IL1RAP	ENST00000317757.8	TSL:1	c.-1-1913T>G		intron	N/A	ENSP00000314807.3
	IL1RAP	ENST00000072516.7	TSL:1	c.-1-1913T>G		intron	N/A	ENSP00000072516.3

Frequencies

GnomAD3 genomes AF: 0.228 AC: 34643 AN: 151760 Hom.: 4897 Cov.: 31

Gnomad AFR AF: 0.408

Gnomad AMI AF: 0.128

Gnomad AMR AF: 0.175

Gnomad ASJ AF: 0.153

Gnomad EAS AF: 0.195

Gnomad SAS AF: 0.0976

Gnomad FIN AF: 0.160

Gnomad MID AF: 0.139

Gnomad NFE AF: 0.160

Gnomad OTH AF: 0.193

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

GnomAD4 genome AF: 0.228 AC: 34690 AN: 151876 Hom.: 4909 Cov.: 31 AF XY: 0.226 AC XY: 16772 AN XY: 74262

African (AFR) AF: 0.408 AC: 16873 AN: 41376

American (AMR) AF: 0.175 AC: 2667 AN: 15260

Ashkenazi Jewish (ASJ) AF: 0.153 AC: 531 AN: 3470

East Asian (EAS) AF: 0.195 AC: 1007 AN: 5164

South Asian (SAS) AF: 0.0975 AC: 469 AN: 4810

European-Finnish (FIN) AF: 0.160 AC: 1680 AN: 10518

Middle Eastern (MID) AF: 0.143 AC: 42 AN: 294

European-Non Finnish (NFE) AF: 0.160 AC: 10899 AN: 67962

Other (OTH) AF: 0.192 AC: 405 AN: 2110

Alfa AF: 0.228 Hom.: 1239

Bravo AF: 0.238

Asia WGS AF: 0.160 AC: 559 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
CADD	Benign	1.8
DANN	Benign	0.78
PhyloP100		-0.30
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: rs3773981; hg19: chr3-190280165;