Variant chr5-132484278-T-C details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_StrongBP6_ModerateBA1

The NM_002198.3(IRF1):c.853+84A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.335 in 1,517,182 control chromosomes in the GnomAD database, including 86,768 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

Frequency

Genomes: 𝑓 0.38 ( 11049 hom., cov: 31)

Exomes 𝑓: 0.33 ( 75719 hom. )

Consequence

IRF1
NM_002198.3 intron

Scores

Clinical Significance

Benign criteria provided, single submitter B:1

Conservation

PhyloP100: -0.0240

Variant links:

Genes affected

IRF1 (HGNC:6116): (interferon regulatory factor 1) The protein encoded by this gene is a transcriptional regulator and tumor suppressor, serving as an activator of genes involved in both innate and acquired immune responses. The encoded protein activates the transcription of genes involved in the body's response to viruses and bacteria, playing a role in cell proliferation, apoptosis, the immune response, and DNA damage response. This protein represses the transcription of several other genes. As a tumor suppressor, it both suppresses tumor cell growth and stimulates an immune response against tumor cells. Defects in this gene have been associated with gastric cancer, myelogenous leukemia, and lung cancer. [provided by RefSeq, Aug 2017]

IRF1 links:

IRF1-AS1 (HGNC:33838): (colitis associated IRF1 antisense regulator of intestinal homeostasis)

IRF1-AS1 links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -14 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.82).

BP6

Variant 5-132484278-T-C is Benign according to our data. Variant chr5-132484278-T-C is described in ClinVar as [Benign]. Clinvar id is 2688398.Status of the report is criteria_provided_single_submitter, 1 stars.

BA1

GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.479 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
IRF1	NM_002198.3 linkuse as main transcript	c.853+84A>G		intron_variant		ENST00000245414.9	NP_002189.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
IRF1	ENST00000245414.9 linkuse as main transcript	c.853+84A>G		intron_variant		1	NM_002198.3	ENSP00000245414	P1
IRF1-AS1	ENST00000612967.2 linkuse as main transcript	n.281-1914T>C		intron_variant, non_coding_transcript_variant		1

Frequencies

GnomAD3 genomes

AF:

0.376

AC:

56928

AN:

151302

Hom.:

11036

Cov.:

show subpopulations

Gnomad AFR

AF:

0.484

Gnomad AMI

AF:

0.228

Gnomad AMR

AF:

0.342

Gnomad ASJ

AF:

0.318

Gnomad EAS

AF:

0.358

Gnomad SAS

AF:

0.408

Gnomad FIN

AF:

0.327

Gnomad MID

AF:

0.481

Gnomad NFE

AF:

0.331

Gnomad OTH

AF:

0.358

GnomAD4 exome

AF:

0.331

AC:

451736

AN:

1365760

Hom.:

75719

Cov.:

AF XY:

0.332

AC XY:

224842

AN XY:

677758

show subpopulations

Gnomad4 AFR exome

AF:

0.481

Gnomad4 AMR exome

AF:

0.320

Gnomad4 ASJ exome

AF:

0.301

Gnomad4 EAS exome

AF:

0.329

Gnomad4 SAS exome

AF:

0.378

Gnomad4 FIN exome

AF:

0.326

Gnomad4 NFE exome

AF:

0.323

Gnomad4 OTH exome

AF:

0.340

GnomAD4 genome

AF:

0.376

AC:

56985

AN:

151422

Hom.:

11049

Cov.:

AF XY:

0.375

AC XY:

27756

AN XY:

73976

show subpopulations

Gnomad4 AFR

AF:

0.484

Gnomad4 AMR

AF:

0.342

Gnomad4 ASJ

AF:

0.318

Gnomad4 EAS

AF:

0.357

Gnomad4 SAS

AF:

0.409

Gnomad4 FIN

AF:

0.327

Gnomad4 NFE

AF:

0.331

Gnomad4 OTH

AF:

0.358

Alfa

AF:

0.157

Hom.:

270

Bravo

AF:

0.381

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

LINK: link

Submissions by phenotype

not specified

Benign:1

Benign, criteria provided, single submitter

clinical testing

Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan

Jan 24, 2024

This variant is classified as Benign based on local population frequency. This variant was detected in 58% of patients studied by a panel of primary immunodeficiencies. Number of patients: 51. Only high quality variants are reported. -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.82

CADD

Benign

4.6

DANN

Benign

0.72

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

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

LitVar

Other links and lift over