rs10248903

chr7-50393986-G-Achr7-50393986-G-C

Variant summary

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

The NM_006060.6(IKZF1):c.850+2123G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.699 in 232,046 control chromosomes in the GnomAD database, including 58,652 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 0.71 (38602 hom., cov: 32)
  • Exomes 𝑓: 0.68 (20050 hom.)
• Consequence: IKZF1 NM_006060.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.97

Genes affected

IKZF1 (HGNC:13176): (IKAROS family zinc finger 1) This gene encodes a transcription factor that belongs to the family of zinc-finger DNA-binding proteins associated with chromatin remodeling. The expression of this protein is restricted to the fetal and adult hemo-lymphopoietic system, and it functions as a regulator of lymphocyte differentiation. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. Most isoforms share a common C-terminal domain, which contains two zinc finger motifs that are required for hetero- or homo-dimerization, and for interactions with other proteins. The isoforms, however, differ in the number of N-terminal zinc finger motifs that bind DNA and in nuclear localization signal presence, resulting in members with and without DNA-binding properties. Only a few isoforms contain the requisite three or more N-terminal zinc motifs that confer high affinity binding to a specific core DNA sequence element in the promoters of target genes. The non-DNA-binding isoforms are largely found in the cytoplasm, and are thought to function as dominant-negative factors. Overexpression of some dominant-negative isoforms have been associated with B-cell malignancies, such as acute lymphoblastic leukemia (ALL). [provided by RefSeq, May 2014]

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.767 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
IKZF1	NM_006060.6	c.850+2123G>A		intron_variant		ENST00000331340.8
LOC124901631	XR_007060322.1			upstream_gene_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
IKZF1	ENST00000331340.8	c.850+2123G>A		intron_variant		1	NM_006060.6	A1
	ENST00000644669.1	n.197-18C>T		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.706 AC: 107255 AN: 151904 Hom.: 38567 Cov.: 32

Gnomad AFR AF: 0.663

Gnomad AMI AF: 0.770

Gnomad AMR AF: 0.638

Gnomad ASJ AF: 0.757

Gnomad EAS AF: 0.277

Gnomad SAS AF: 0.658

Gnomad FIN AF: 0.748

Gnomad MID AF: 0.725

Gnomad NFE AF: 0.773

Gnomad OTH AF: 0.725

GnomAD4 exome AF: 0.684 AC: 54770 AN: 80022 Hom.: 20050 Cov.: 0 AF XY: 0.687 AC XY: 25277 AN XY: 36792

Gnomad4 AFR exome AF: 0.683

Gnomad4 AMR exome AF: 0.623

Gnomad4 ASJ exome AF: 0.764

Gnomad4 EAS exome AF: 0.255

Gnomad4 SAS exome AF: 0.639

Gnomad4 FIN exome AF: 0.641

Gnomad4 NFE exome AF: 0.773

Gnomad4 OTH exome AF: 0.720

GnomAD4 genome AF: 0.706 AC: 107335 AN: 152024 Hom.: 38602 Cov.: 32 AF XY: 0.701 AC XY: 52069 AN XY: 74298

Gnomad4 AFR AF: 0.664

Gnomad4 AMR AF: 0.637

Gnomad4 ASJ AF: 0.757

Gnomad4 EAS AF: 0.278

Gnomad4 SAS AF: 0.658

Gnomad4 FIN AF: 0.748

Gnomad4 NFE AF: 0.773

Gnomad4 OTH AF: 0.719

Alfa AF: 0.748 Hom.: 20130

Bravo AF: 0.696

Asia WGS AF: 0.514 AC: 1790 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
Cadd	Benign	0.55
Dann	Benign	0.37

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: rs10248903; hg19: chr7-50461684;