rs6673002

Variant names:

• chr1-151770799-T-G
• rs6673002
• ENST00000400999.7:c.566-278T>G

Your query was ambiguous. Multiple possible variants found:

• chr1-151770799-T-G
• chr1-151770799-T-C

Variant summary

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

The NM_016178.2(OAZ3):​c.566-278T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.162 in 152,254 control chromosomes in the GnomAD database, including 2,129 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as (no stars).

• Frequency: Genomes: 𝑓 0.16 (2129 hom., cov: 33)
• Consequence: OAZ3 NM_016178.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.382
• Publications: 11 publications found

Genes affected

OAZ3 (HGNC:8097): (ornithine decarboxylase antizyme 3) The protein encoded by this gene belongs to the ornithine decarboxylase antizyme family, which plays a role in cell growth and proliferation by regulating intracellular polyamine levels. Expression of antizymes requires +1 ribosomal frameshifting, which is enhanced by high levels of polyamines. Antizymes in turn bind to and inhibit ornithine decarboxylase (ODC), the key enzyme in polyamine biosynthesis; thus, completing the auto-regulatory circuit. This gene encodes antizyme 3, the third member of the antizyme family. Like antizymes 1 and 2, antizyme 3 inhibits ODC activity and polyamine uptake; however, it does not stimulate ODC degradation. Also, while antizymes 1 and 2 have broad tissue distribution, expression of antizyme 3 is restricted to haploid germ cells in testis, suggesting a distinct role for this antizyme in spermiogenesis. Antizyme 3 gene knockout studies showed that homozygous mutant male mice were infertile, and indicated the likely role of this antizyme in the formation of a rigid connection between the sperm head and tail during spermatogenesis. Alternatively spliced transcript variants encoding different isoforms, including one resulting from the use of non-AUG (CUG) translation initiation codon, have been found for this gene. [provided by RefSeq, Dec 2014]

TDRKH (HGNC:11713): (tudor and KH domain containing) Predicted to enable RNA binding activity. Predicted to be involved in fertilization; gamete generation; and piRNA metabolic process. Predicted to be located in mitochondrion; pi-body; and piP-body. [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=-0.67).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.208 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_016178.2. 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
	OAZ3	NM_016178.2		c.566-278T>G		intron	N/A	NP_057262.2	Q9UMX2-1
	OAZ3	NM_001301371.1		c.470-278T>G		intron	N/A	NP_001288300.1	H0Y7Y4
	OAZ3	NM_001134939.1		c.431-278T>G		intron	N/A	NP_001128411.1	Q9UMX2

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	OAZ3	ENST00000400999.7	TSL:5	c.566-278T>G		intron	N/A	ENSP00000383784.3	Q9UMX2-1
	OAZ3	ENST00000453029.2	TSL:5	c.470-278T>G		intron	N/A	ENSP00000415904.2	H0Y7Y4
	OAZ3	ENST00000321531.10	TSL:5	c.431-278T>G		intron	N/A	ENSP00000313922.5	A0A0G2JH29

Frequencies

GnomAD3 genomes AF: 0.162 AC: 24598 AN: 152136 Hom.: 2122 Cov.: 33

Gnomad AFR AF: 0.211

Gnomad AMI AF: 0.218

Gnomad AMR AF: 0.138

Gnomad ASJ AF: 0.0916

Gnomad EAS AF: 0.115

Gnomad SAS AF: 0.101

Gnomad FIN AF: 0.168

Gnomad MID AF: 0.0728

Gnomad NFE AF: 0.148

Gnomad OTH AF: 0.142

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

GnomAD4 genome AF: 0.162 AC: 24633 AN: 152254 Hom.: 2129 Cov.: 33 AF XY: 0.161 AC XY: 11955 AN XY: 74446

African (AFR) AF: 0.211 AC: 8784 AN: 41544

American (AMR) AF: 0.138 AC: 2104 AN: 15292

Ashkenazi Jewish (ASJ) AF: 0.0916 AC: 318 AN: 3470

East Asian (EAS) AF: 0.115 AC: 598 AN: 5186

South Asian (SAS) AF: 0.101 AC: 486 AN: 4828

European-Finnish (FIN) AF: 0.168 AC: 1778 AN: 10602

Middle Eastern (MID) AF: 0.0748 AC: 22 AN: 294

European-Non Finnish (NFE) AF: 0.148 AC: 10049 AN: 68014

Other (OTH) AF: 0.140 AC: 295 AN: 2112

Alfa AF: 0.153 Hom.: 312

Bravo AF: 0.165

Asia WGS AF: 0.129 AC: 448 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.67
CADD	Benign	9.7
DANN	Benign	0.89
PhyloP100		-0.38
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

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

Other links and lift over

dbSNP: rs6673002;

hg19: chr1-151743275;