rs3792797

Variant names:

• chr5-151022330-A-C
• rs3792797
• NM_002084.5:c.87+1589A>C

Your query was ambiguous. Multiple possible variants found:

• chr5-151022330-A-C
• chr5-151022330-A-G
• chr5-151022330-A-T

Variant summary

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

The NM_002084.5(GPX3):​c.87+1589A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.72 in 152,088 control chromosomes in the GnomAD database, including 41,661 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 0.72 (41661 hom., cov: 32)
• Consequence: GPX3 NM_002084.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.389
• Publications: 20 publications found

Genes affected

GPX3 (HGNC:4555): (glutathione peroxidase 3) The protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of organic hydroperoxides and hydrogen peroxide (H2O2) by glutathione, and thereby protect cells against oxidative damage. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. This isozyme is secreted, and is abundantly found in plasma. Downregulation of expression of this gene by promoter hypermethylation has been observed in a wide spectrum of human malignancies, including thyroid cancer, hepatocellular carcinoma and chronic myeloid leukemia. This isozyme is also a selenoprotein, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2016]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.909 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_002084.5. 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
	GPX3	NM_002084.5	MANE Select	c.87+1589A>C		intron	N/A	NP_002075.2
	GPX3	NM_001329790.2		c.114+1476A>C		intron	N/A	NP_001316719.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GPX3	ENST00000388825.9	TSL:1 MANE Select	c.87+1589A>C		intron	N/A	ENSP00000373477.4	P22352
	GPX3	ENST00000521650.5	TSL:2	c.114+1476A>C		intron	N/A	ENSP00000427873.1	E5RG32
	GPX3	ENST00000517973.1	TSL:3	c.87+1589A>C		intron	N/A	ENSP00000429709.1	A0A182DWH9

Frequencies

GnomAD3 genomes AF: 0.721 AC: 109507 AN: 151970 Hom.: 41642 Cov.: 32

Gnomad AFR AF: 0.450

Gnomad AMI AF: 0.944

Gnomad AMR AF: 0.806

Gnomad ASJ AF: 0.780

Gnomad EAS AF: 0.931

Gnomad SAS AF: 0.735

Gnomad FIN AF: 0.810

Gnomad MID AF: 0.772

Gnomad NFE AF: 0.828

Gnomad OTH AF: 0.739

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

GnomAD4 genome AF: 0.720 AC: 109563 AN: 152088 Hom.: 41661 Cov.: 32 AF XY: 0.720 AC XY: 53552 AN XY: 74336

African (AFR) AF: 0.450 AC: 18661 AN: 41446

American (AMR) AF: 0.806 AC: 12328 AN: 15286

Ashkenazi Jewish (ASJ) AF: 0.780 AC: 2707 AN: 3470

East Asian (EAS) AF: 0.931 AC: 4815 AN: 5172

South Asian (SAS) AF: 0.736 AC: 3550 AN: 4826

European-Finnish (FIN) AF: 0.810 AC: 8574 AN: 10580

Middle Eastern (MID) AF: 0.755 AC: 222 AN: 294

European-Non Finnish (NFE) AF: 0.828 AC: 56291 AN: 67994

Other (OTH) AF: 0.737 AC: 1554 AN: 2108

Alfa AF: 0.784 Hom.: 109630

Bravo AF: 0.711

Asia WGS AF: 0.777 AC: 2700 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	7.4
DANN	Benign	0.81
PhyloP100		0.39
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: rs3792797; hg19: chr5-150401891;