rs7932905

Variant names:

• chr11-43706027-G-A
• rs7932905
• NM_016142.3:c.160+25040G>A

Your query was ambiguous. Multiple possible variants found:

• chr11-43706027-G-A
• chr11-43706027-G-C

Variant summary

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

The NM_016142.3(HSD17B12):​c.160+25040G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.501 in 151,644 control chromosomes in the GnomAD database, including 19,472 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 0.50 (19472 hom., cov: 29)
• Consequence: HSD17B12 NM_016142.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0540
• Publications: 9 publications found

Genes affected

HSD17B12 (HGNC:18646): (hydroxysteroid 17-beta dehydrogenase 12) This gene encodes a very important 17beta-hydroxysteroid dehydrogenase (17beta-HSD) that converts estrone into estradiol in ovarian tissue. This enzyme is also involved in fatty acid elongation. [provided by RefSeq, Oct 2011]

ENSG00000283341 (HGNC:):

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 (NFE) allele frequency at 95% confidence interval = 0.522 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_016142.3. 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
	HSD17B12	NM_016142.3	MANE Select	c.160+25040G>A		intron	N/A	NP_057226.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	HSD17B12	ENST00000278353.10	TSL:1 MANE Select	c.160+25040G>A		intron	N/A	ENSP00000278353.4
	HSD17B12	ENST00000395700.4	TSL:1	c.160+25040G>A		intron	N/A	ENSP00000379052.4
	HSD17B12	ENST00000637401.1	TSL:4	c.160+25040G>A		intron	N/A	ENSP00000490421.1

Frequencies

GnomAD3 genomes AF: 0.501 AC: 75901 AN: 151526 Hom.: 19444 Cov.: 29

Gnomad AFR AF: 0.520

Gnomad AMI AF: 0.588

Gnomad AMR AF: 0.398

Gnomad ASJ AF: 0.618

Gnomad EAS AF: 0.224

Gnomad SAS AF: 0.451

Gnomad FIN AF: 0.521

Gnomad MID AF: 0.494

Gnomad NFE AF: 0.527

Gnomad OTH AF: 0.498

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

GnomAD4 genome AF: 0.501 AC: 75974 AN: 151644 Hom.: 19472 Cov.: 29 AF XY: 0.495 AC XY: 36655 AN XY: 74116

African (AFR) AF: 0.520 AC: 21488 AN: 41294

American (AMR) AF: 0.397 AC: 6043 AN: 15226

Ashkenazi Jewish (ASJ) AF: 0.618 AC: 2146 AN: 3472

East Asian (EAS) AF: 0.224 AC: 1156 AN: 5150

South Asian (SAS) AF: 0.451 AC: 2166 AN: 4798

European-Finnish (FIN) AF: 0.521 AC: 5475 AN: 10500

Middle Eastern (MID) AF: 0.493 AC: 144 AN: 292

European-Non Finnish (NFE) AF: 0.527 AC: 35777 AN: 67902

Other (OTH) AF: 0.497 AC: 1044 AN: 2100

Alfa AF: 0.517 Hom.: 65845

Bravo AF: 0.493

Asia WGS AF: 0.376 AC: 1314 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	3.4
DANN	Benign	0.81
PhyloP100		-0.054
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: rs7932905; hg19: chr11-43727577;