rs11747112

Variant names:

• chr5-159347601-C-G
• rs11747112
• ENST00000515337.1:n.831C>G

Your query was ambiguous. Multiple possible variants found:

• chr5-159347601-C-G
• chr5-159347601-C-T

Variant summary

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

The ENST00000515337.1(IL12B-AS1):​n.831C>G variant causes a non coding transcript exon change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.112 in 152,112 control chromosomes in the GnomAD database, including 1,114 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 0.11 (1114 hom., cov: 32)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: IL12B-AS1 ENST00000515337.1 non_coding_transcript_exon
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.467
• Publications: 7 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=-0.91).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.141 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000515337.1. 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
	IL12B-AS1	NR_037889.1		n.831C>G		non_coding_transcript_exon	Exon 3 of 5

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	IL12B-AS1	ENST00000515337.1	TSL:2	n.831C>G		non_coding_transcript_exon	Exon 3 of 5
	IL12B-AS1	ENST00000635333.1	TSL:5	n.160C>G		non_coding_transcript_exon	Exon 2 of 8
	IL12B-AS1	ENST00000641150.1		n.410C>G		non_coding_transcript_exon	Exon 3 of 5

Frequencies

GnomAD3 genomes AF: 0.112 AC: 17018 AN: 151994 Hom.: 1117 Cov.: 32

Gnomad AFR AF: 0.0648

Gnomad AMI AF: 0.147

Gnomad AMR AF: 0.105

Gnomad ASJ AF: 0.235

Gnomad EAS AF: 0.0916

Gnomad SAS AF: 0.0602

Gnomad FIN AF: 0.0887

Gnomad MID AF: 0.133

Gnomad NFE AF: 0.144

Gnomad OTH AF: 0.128

GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 2 Hom.: 0 Cov.: 0 AF XY: 0.00 AC XY: 0 AN XY: 2

African (AFR) AC: 0 AN: 0

American (AMR) AC: 0 AN: 0

Ashkenazi Jewish (ASJ) AC: 0 AN: 0

East Asian (EAS) AC: 0 AN: 0

South Asian (SAS) AC: 0 AN: 0

European-Finnish (FIN) AC: 0 AN: 0

Middle Eastern (MID) AC: 0 AN: 0

European-Non Finnish (NFE) AC: 0 AN: 0

Other (OTH) AF: 0.00 AC: 0 AN: 2

GnomAD4 genome AF: 0.112 AC: 17009 AN: 152112 Hom.: 1114 Cov.: 32 AF XY: 0.108 AC XY: 8021 AN XY: 74362

African (AFR) AF: 0.0646 AC: 2682 AN: 41488

American (AMR) AF: 0.105 AC: 1608 AN: 15284

Ashkenazi Jewish (ASJ) AF: 0.235 AC: 814 AN: 3470

East Asian (EAS) AF: 0.0908 AC: 470 AN: 5176

South Asian (SAS) AF: 0.0598 AC: 288 AN: 4814

European-Finnish (FIN) AF: 0.0887 AC: 938 AN: 10578

Middle Eastern (MID) AF: 0.136 AC: 40 AN: 294

European-Non Finnish (NFE) AF: 0.144 AC: 9769 AN: 67988

Other (OTH) AF: 0.126 AC: 266 AN: 2108

Alfa AF: 0.0520 Hom.: 49

Bravo AF: 0.114

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.97
DANN	Benign	0.61
PhyloP100		-0.47

Splicing

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs11747112;

hg19: chr5-158774609;