chr7-128939148-T-C

Position:

• chr7-128939148-T-C

Variant summary

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

The NM_001098629.3(IRF5):​c.-12+1099T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.407 in 151,590 control chromosomes in the GnomAD database, including 13,114 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 0.41 (13114 hom., cov: 30)
• Consequence: IRF5 NM_001098629.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0770

Genes affected

IRF5 (HGNC:6120): (interferon regulatory factor 5) This gene encodes a member of the interferon regulatory factor (IRF) family, a group of transcription factors with diverse roles, including virus-mediated activation of interferon, and modulation of cell growth, differentiation, apoptosis, and immune system activity. Members of the IRF family are characterized by a conserved N-terminal DNA-binding domain containing tryptophan (W) repeats. Alternative promoter use and alternative splicing result in multiple transcript variants, and a 30-nt indel polymorphism (SNP rs60344245) can result in loss of a 10-aa segment. [provided by RefSeq, Dec 2016]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.455 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
IRF5	NM_001098629.3	c.-12+1099T>C		intron_variant		ENST00000357234.10

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
IRF5	ENST00000357234.10	c.-12+1099T>C		intron_variant		1	NM_001098629.3

Frequencies

GnomAD3 genomes AF: 0.407 AC: 61723 AN: 151472 Hom.: 13113 Cov.: 30

Gnomad AFR AF: 0.327

Gnomad AMI AF: 0.463

Gnomad AMR AF: 0.415

Gnomad ASJ AF: 0.570

Gnomad EAS AF: 0.186

Gnomad SAS AF: 0.432

Gnomad FIN AF: 0.406

Gnomad MID AF: 0.519

Gnomad NFE AF: 0.459

Gnomad OTH AF: 0.455

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

GnomAD4 genome AF: 0.407 AC: 61745 AN: 151590 Hom.: 13114 Cov.: 30 AF XY: 0.402 AC XY: 29766 AN XY: 74062

Gnomad4 AFR AF: 0.327

Gnomad4 AMR AF: 0.414

Gnomad4 ASJ AF: 0.570

Gnomad4 EAS AF: 0.186

Gnomad4 SAS AF: 0.432

Gnomad4 FIN AF: 0.406

Gnomad4 NFE AF: 0.459

Gnomad4 OTH AF: 0.452

Alfa AF: 0.436 Hom.: 2230

Bravo AF: 0.405

Asia WGS AF: 0.292 AC: 1018 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	5.7
DANN	Benign	0.38

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs3807307; hg19: chr7-128579202;