rs2737844

Variant names:

• chr14-64941791-G-A
• rs2737844
• NM_002083.4:c.222+714C>T

Your query was ambiguous. Multiple possible variants found:

• chr14-64941791-G-A
• chr14-64941791-G-C
• chr14-64941791-G-T

Variant summary

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

The NM_002083.4(GPX2):​c.222+714C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.465 in 152,092 control chromosomes in the GnomAD database, including 20,376 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 0.46 (20376 hom., cov: 32)
• Consequence: GPX2 NM_002083.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.258
• Publications: 19 publications found

Genes affected

GPX2 (HGNC:4554): (glutathione peroxidase 2) 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 predominantly expressed in the gastrointestinal tract (also in liver in human), is localized in the cytoplasm, and whose preferred substrate is hydrogen peroxide. Overexpression of this gene is associated with increased differentiation and proliferation in colorectal cancer. 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]

CHURC1-FNTB (HGNC:42960): (CHURC1-FNTB readthrough) This locus represents naturally occurring read-through transcription between the neighboring CHURC1 (churchill domain containing 1) and FNTB (farnesyltransferase, CAAX box, beta) on chromosome 14. The read-through transcript produces a fusion protein that shares sequence identity with each individual gene product. [provided by RefSeq, Feb 2011]

CHURC1 (HGNC:20099): (churchill domain containing 1) Predicted to enable zinc ion binding activity. Predicted to be involved in positive regulation of transcription, DNA-templated. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.797 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_002083.4. 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
	GPX2	NM_002083.4	MANE Select	c.222+714C>T		intron	N/A	NP_002074.2
	CHURC1-FNTB	NM_001202559.1		c.327+15711G>A		intron	N/A	NP_001189488.1	B4DL54
	CHURC1-FNTB	NM_001202558.2		c.6+17665G>A		intron	N/A	NP_001189487.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GPX2	ENST00000389614.6	TSL:1 MANE Select	c.222+714C>T		intron	N/A	ENSP00000374265.5	P18283
	CHURC1-FNTB	ENST00000549987.1	TSL:2	c.246+15711G>A		intron	N/A	ENSP00000447121.2	B4DL54
	GPX2	ENST00000553522.1	TSL:1	n.222+714C>T		intron	N/A	ENSP00000450991.1	G3V323

Frequencies

GnomAD3 genomes AF: 0.464 AC: 70544 AN: 151972 Hom.: 20322 Cov.: 32

Gnomad AFR AF: 0.804

Gnomad AMI AF: 0.421

Gnomad AMR AF: 0.364

Gnomad ASJ AF: 0.384

Gnomad EAS AF: 0.714

Gnomad SAS AF: 0.394

Gnomad FIN AF: 0.355

Gnomad MID AF: 0.377

Gnomad NFE AF: 0.289

Gnomad OTH AF: 0.434

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

GnomAD4 genome AF: 0.465 AC: 70662 AN: 152092 Hom.: 20376 Cov.: 32 AF XY: 0.466 AC XY: 34664 AN XY: 74360

African (AFR) AF: 0.804 AC: 33377 AN: 41488

American (AMR) AF: 0.364 AC: 5571 AN: 15292

Ashkenazi Jewish (ASJ) AF: 0.384 AC: 1333 AN: 3472

East Asian (EAS) AF: 0.713 AC: 3687 AN: 5170

South Asian (SAS) AF: 0.394 AC: 1901 AN: 4826

European-Finnish (FIN) AF: 0.355 AC: 3752 AN: 10572

Middle Eastern (MID) AF: 0.381 AC: 112 AN: 294

European-Non Finnish (NFE) AF: 0.289 AC: 19624 AN: 67962

Other (OTH) AF: 0.438 AC: 924 AN: 2110

Alfa AF: 0.381 Hom.: 2328

Bravo AF: 0.488

Asia WGS AF: 0.560 AC: 1949 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	0.62
DANN	Benign	0.66
PhyloP100		-0.26
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: rs2737844; hg19: chr14-65408509;