rs2885373

Variant names:

• chr3-190628679-T-C
• rs2885373
• NM_002182.4:c.903-671T>C

Variant summary

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

The NM_002182.4(IL1RAP):​c.903-671T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.9 in 152,302 control chromosomes in the GnomAD database, including 61,831 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 0.90 (61831 hom., cov: 33)
• Consequence: IL1RAP NM_002182.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.21
• Publications: 8 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=-0.89).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.976 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.903-671T>C		intron	N/A	NP_002173.1
	IL1RAP	NM_001167931.2		c.903-671T>C		intron	N/A	NP_001161403.1
	IL1RAP	NM_001364879.1		c.903-671T>C		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.903-671T>C		intron	N/A	ENSP00000390541.1
	IL1RAP	ENST00000317757.8	TSL:1	c.903-671T>C		intron	N/A	ENSP00000314807.3
	IL1RAP	ENST00000072516.7	TSL:1	c.903-671T>C		intron	N/A	ENSP00000072516.3

Frequencies

GnomAD3 genomes AF: 0.899 AC: 136875 AN: 152184 Hom.: 61764 Cov.: 33

Gnomad AFR AF: 0.970

Gnomad AMI AF: 0.748

Gnomad AMR AF: 0.907

Gnomad ASJ AF: 0.884

Gnomad EAS AF: 0.999

Gnomad SAS AF: 0.950

Gnomad FIN AF: 0.849

Gnomad MID AF: 0.886

Gnomad NFE AF: 0.855

Gnomad OTH AF: 0.877

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

GnomAD4 genome AF: 0.900 AC: 137001 AN: 152302 Hom.: 61831 Cov.: 33 AF XY: 0.903 AC XY: 67220 AN XY: 74472

African (AFR) AF: 0.971 AC: 40345 AN: 41568

American (AMR) AF: 0.908 AC: 13882 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.884 AC: 3066 AN: 3470

East Asian (EAS) AF: 0.999 AC: 5174 AN: 5178

South Asian (SAS) AF: 0.950 AC: 4592 AN: 4832

European-Finnish (FIN) AF: 0.849 AC: 9009 AN: 10612

Middle Eastern (MID) AF: 0.891 AC: 262 AN: 294

European-Non Finnish (NFE) AF: 0.855 AC: 58133 AN: 68026

Other (OTH) AF: 0.878 AC: 1856 AN: 2114

Alfa AF: 0.871 Hom.: 29208

Bravo AF: 0.905

Asia WGS AF: 0.967 AC: 3365 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	0.52
DANN	Benign	0.65
PhyloP100		-1.2
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: rs2885373; hg19: chr3-190346468;