1-41912558-T-C

Variant names:

• chr1-41912558-T-C
• rs7554964
• NM_024503.5:c.-801+5855A>G

Variant summary

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

The NM_024503.5(HIVEP3):​c.-801+5855A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.564 in 152,052 control chromosomes in the GnomAD database, including 24,433 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 0.56 (24433 hom., cov: 32)
• Consequence: HIVEP3 NM_024503.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.633
• Publications: 2 publications found

Genes affected

HIVEP3 (HGNC:13561): (HIVEP zinc finger 3) This gene encodes a member of the human immunodeficiency virus type 1 enhancer-binding protein family. Members of this protein family contain multiple zinc finger and acid-rich (ZAS) domains and serine-threonine rich regions. This protein acts as a transcription factor and is able to regulate nuclear factor kappaB-mediated transcription by binding the kappaB motif in target genes. This protein also binds the recombination signal sequence that flanks the V, D, and J regions of immunoglobulin and T-cell receptors. Alternate splicing results in both coding and non-coding transcript variants. [provided by RefSeq, Sep 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.694 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_024503.5. 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
	HIVEP3	NM_024503.5	MANE Select	c.-801+5855A>G		intron	N/A	NP_078779.2
	HIVEP3	NM_001127714.3		c.-721+5855A>G		intron	N/A	NP_001121186.1
	HIVEP3	NR_038260.2		n.510+5855A>G		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	HIVEP3	ENST00000372583.6	TSL:1 MANE Select	c.-801+5855A>G		intron	N/A	ENSP00000361664.1
	HIVEP3	ENST00000372584.5	TSL:1	c.-721+5855A>G		intron	N/A	ENSP00000361665.1
	HIVEP3	ENST00000489103.5	TSL:1	n.231+5855A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.564 AC: 85690 AN: 151934 Hom.: 24402 Cov.: 32

Gnomad AFR AF: 0.619

Gnomad AMI AF: 0.466

Gnomad AMR AF: 0.427

Gnomad ASJ AF: 0.632

Gnomad EAS AF: 0.714

Gnomad SAS AF: 0.530

Gnomad FIN AF: 0.521

Gnomad MID AF: 0.557

Gnomad NFE AF: 0.557

Gnomad OTH AF: 0.538

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

GnomAD4 genome AF: 0.564 AC: 85768 AN: 152052 Hom.: 24433 Cov.: 32 AF XY: 0.560 AC XY: 41630 AN XY: 74308

African (AFR) AF: 0.620 AC: 25696 AN: 41472

American (AMR) AF: 0.426 AC: 6521 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.632 AC: 2193 AN: 3468

East Asian (EAS) AF: 0.714 AC: 3692 AN: 5174

South Asian (SAS) AF: 0.529 AC: 2550 AN: 4820

European-Finnish (FIN) AF: 0.521 AC: 5501 AN: 10554

Middle Eastern (MID) AF: 0.572 AC: 167 AN: 292

European-Non Finnish (NFE) AF: 0.557 AC: 37879 AN: 67964

Other (OTH) AF: 0.543 AC: 1146 AN: 2110

Alfa AF: 0.564 Hom.: 3034

Bravo AF: 0.560

Asia WGS AF: 0.606 AC: 2107 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	0.58
DANN	Benign	0.42
PhyloP100		-0.63
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: rs7554964; hg19: chr1-42378229;