rs4844486

Variant names:

• chr1-209671172-A-C
• rs4844486
• ENST00000441672.2:n.284-8111T>G

Your query was ambiguous. Multiple possible variants found:

• chr1-209671172-A-C
• chr1-209671172-A-T

Variant summary

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

The ENST00000441672.2(HSD11B1-AS1):​n.284-8111T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.652 in 152,126 control chromosomes in the GnomAD database, including 33,789 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 0.65 (33789 hom., cov: 33)
• Consequence: HSD11B1-AS1 ENST00000441672.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.240
• Publications: 14 publications found

Genes affected

HSD11B1-AS1 (HGNC:54053): (HSD11B1 antisense RNA 1)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.8).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.734 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000441672.2. 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
	HSD11B1-AS1	NR_134509.1		n.97-8111T>G		intron	N/A
	HSD11B1-AS1	NR_134510.1		n.67-8111T>G		intron	N/A
	HSD11B1-AS1	NR_134511.1		n.28+4050T>G		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	HSD11B1-AS1	ENST00000441672.2	TSL:3	n.284-8111T>G		intron	N/A
	HSD11B1-AS1	ENST00000445272.8	TSL:5	n.124+4050T>G		intron	N/A
	HSD11B1-AS1	ENST00000774900.1		n.122-8111T>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.652 AC: 99137 AN: 152008 Hom.: 33774 Cov.: 33

Gnomad AFR AF: 0.447

Gnomad AMI AF: 0.681

Gnomad AMR AF: 0.707

Gnomad ASJ AF: 0.853

Gnomad EAS AF: 0.559

Gnomad SAS AF: 0.749

Gnomad FIN AF: 0.743

Gnomad MID AF: 0.766

Gnomad NFE AF: 0.739

Gnomad OTH AF: 0.671

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

GnomAD4 genome AF: 0.652 AC: 99189 AN: 152126 Hom.: 33789 Cov.: 33 AF XY: 0.656 AC XY: 48794 AN XY: 74348

African (AFR) AF: 0.447 AC: 18558 AN: 41508

American (AMR) AF: 0.707 AC: 10810 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.853 AC: 2960 AN: 3472

East Asian (EAS) AF: 0.560 AC: 2890 AN: 5164

South Asian (SAS) AF: 0.750 AC: 3617 AN: 4824

European-Finnish (FIN) AF: 0.743 AC: 7857 AN: 10574

Middle Eastern (MID) AF: 0.769 AC: 226 AN: 294

European-Non Finnish (NFE) AF: 0.739 AC: 50232 AN: 67974

Other (OTH) AF: 0.672 AC: 1418 AN: 2110

Alfa AF: 0.713 Hom.: 169345

Bravo AF: 0.640

Asia WGS AF: 0.631 AC: 2192 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.80
CADD	Benign	6.5
DANN	Benign	0.79
PhyloP100		-0.24

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: rs4844486;

hg19: chr1-209844517;