rs4921492

Variant names:

• chr5-159405269-C-A
• rs4921492
• ENST00000635333.1:n.328-11255C>A

Your query was ambiguous. Multiple possible variants found:

• chr5-159405269-C-A
• chr5-159405269-C-G

Variant summary

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

The ENST00000641150.1(IL12B-AS1):​n.533-11255C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.333 in 151,922 control chromosomes in the GnomAD database, including 8,382 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 0.33 (8382 hom., cov: 31)
• Consequence: IL12B-AS1 ENST00000641150.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.28
• Publications: 12 publications found

Genes affected

IL12B-AS1 (HGNC:58156):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.362 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000641150.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	IL12B-AS1	ENST00000635333.1	TSL:5	n.328-11255C>A		intron	N/A
	IL12B-AS1	ENST00000641150.1		n.533-11255C>A		intron	N/A
	IL12B-AS1	ENST00000648969.1		n.54-11255C>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.333 AC: 50484 AN: 151802 Hom.: 8365 Cov.: 31

Gnomad AFR AF: 0.316

Gnomad AMI AF: 0.345

Gnomad AMR AF: 0.293

Gnomad ASJ AF: 0.239

Gnomad EAS AF: 0.375

Gnomad SAS AF: 0.362

Gnomad FIN AF: 0.319

Gnomad MID AF: 0.335

Gnomad NFE AF: 0.353

Gnomad OTH AF: 0.345

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

GnomAD4 genome AF: 0.333 AC: 50537 AN: 151922 Hom.: 8382 Cov.: 31 AF XY: 0.330 AC XY: 24513 AN XY: 74224

African (AFR) AF: 0.316 AC: 13091 AN: 41416

American (AMR) AF: 0.293 AC: 4464 AN: 15256

Ashkenazi Jewish (ASJ) AF: 0.239 AC: 827 AN: 3464

East Asian (EAS) AF: 0.376 AC: 1933 AN: 5144

South Asian (SAS) AF: 0.361 AC: 1736 AN: 4804

European-Finnish (FIN) AF: 0.319 AC: 3369 AN: 10570

Middle Eastern (MID) AF: 0.354 AC: 104 AN: 294

European-Non Finnish (NFE) AF: 0.353 AC: 23962 AN: 67956

Other (OTH) AF: 0.349 AC: 736 AN: 2106

Alfa AF: 0.301 Hom.: 2528

Bravo AF: 0.331

Asia WGS AF: 0.395 AC: 1373 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	0.59
DANN	Benign	0.72
PhyloP100		-1.3

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs4921492; hg19: chr5-158832277;