Genetic Variant OR2G2:p.Leu167Pro (chr1-247588859-T-C) – ACMG Classification: Benign (-12 pts)

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_StrongBA1

The NM_001001915.1(OR2G2):c.500T>C(p.Leu167Pro) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.386 in 1,613,912 control chromosomes in the GnomAD database, including 125,326 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 0.31 ( 8947 hom., cov: 33)

Exomes 𝑓: 0.39 ( 116379 hom. )

Consequence

OR2G2
NM_001001915.1 missense

Scores

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: -0.859

Publications

28 publications found

Variant links:

Genes affected

OR2G2 (HGNC:15007): (olfactory receptor family 2 subfamily G member 2) Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]

OR2G2 links:

ENSG00000236817 (HGNC:):

ENSG00000236817 links:

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ACMG classification

Classification was made for transcript

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

BP4

Computational evidence support a benign effect (MetaRNN=1.9362569E-4).

BA1

GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.5 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001001915.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
OR2G2	NM_001001915.1	MANE Select	c.500T>C	p.Leu167Pro	missense	Exon 1 of 1	NP_001001915.1	Q8NGZ5
LOC102724446	NR_188589.1		n.226-22908A>G		intron	N/A
LOC102724446	NR_188590.1		n.438-22908A>G		intron	N/A

Ensembl Transcripts

Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
OR2G2	ENST00000320065.1	TSL:6 MANE Select	c.500T>C	p.Leu167Pro	missense	Exon 1 of 1	ENSP00000326349.1	Q8NGZ5
ENSG00000236817	ENST00000435333.6	TSL:3	n.295-22908A>G		intron	N/A
ENSG00000236817	ENST00000446347.1	TSL:2	n.438-22908A>G		intron	N/A

Frequencies

GnomAD3 genomes

AF:

0.315

AC:

47849

AN:

152024

Hom.:

8950

Cov.:

show subpopulations

Gnomad AFR

AF:

0.102

Gnomad AMI

AF:

0.410

Gnomad AMR

AF:

0.369

Gnomad ASJ

AF:

0.444

Gnomad EAS

AF:

0.516

Gnomad SAS

AF:

0.294

Gnomad FIN

AF:

0.373

Gnomad MID

AF:

0.386

Gnomad NFE

AF:

0.400

Gnomad OTH

AF:

0.357

GnomAD2 exomes

AF:

0.370

AC:

92829

AN:

250958

AF XY:

0.371

show subpopulations

Gnomad AFR exome

AF:

0.0935

Gnomad AMR exome

AF:

0.374

Gnomad ASJ exome

AF:

0.442

Gnomad EAS exome

AF:

0.527

Gnomad FIN exome

AF:

0.372

Gnomad NFE exome

AF:

0.399

Gnomad OTH exome

AF:

0.393

GnomAD4 exome

AF:

0.394

AC:

575352

AN:

1461770

Hom.:

116379

Cov.:

AF XY:

0.390

AC XY:

283850

AN XY:

727196

show subpopulations

African (AFR)

AF:

0.0941

AC:

3149

AN:

33478

American (AMR)

AF:

0.374

AC:

16728

AN:

44722

Ashkenazi Jewish (ASJ)

AF:

0.440

AC:

11491

AN:

26134

East Asian (EAS)

AF:

0.549

AC:

21791

AN:

39700

South Asian (SAS)

AF:

0.279

AC:

24072

AN:

86256

European-Finnish (FIN)

AF:

0.376

AC:

20100

AN:

53410

Middle Eastern (MID)

AF:

0.365

AC:

2106

AN:

5766

European-Non Finnish (NFE)

AF:

0.407

AC:

452020

AN:

1111912

Other (OTH)

AF:

0.396

AC:

23895

AN:

60392

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.488

Heterozygous variant carriers

21571

43141

64712

86282

107853

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Exome Hom

Variant carriers

13924

27848

41772

55696

69620

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

AF:

0.314

AC:

47847

AN:

152142

Hom.:

8947

Cov.:

AF XY:

0.313

AC XY:

23264

AN XY:

74374

show subpopulations

African (AFR)

AF:

0.102

AC:

4235

AN:

41550

American (AMR)

AF:

0.368

AC:

5628

AN:

15278

Ashkenazi Jewish (ASJ)

AF:

0.444

AC:

1543

AN:

3472

East Asian (EAS)

AF:

0.516

AC:

2667

AN:

5166

South Asian (SAS)

AF:

0.293

AC:

1416

AN:

4828

European-Finnish (FIN)

AF:

0.373

AC:

3943

AN:

10568

Middle Eastern (MID)

AF:

0.374

AC:

110

AN:

294

European-Non Finnish (NFE)

AF:

0.400

AC:

27168

AN:

67962

Other (OTH)

AF:

0.361

AC:

763

AN:

2112

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.501

Heterozygous variant carriers

1582

3164

4747

6329

7911

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome Het

Genome Hom

Variant carriers

476

952

1428

1904

2380

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

Alfa

AF:

0.368

Hom.:

25349

Bravo

AF:

0.311

TwinsUK

AF:

0.416

AC:

1542

ALSPAC

AF:

0.409

AC:

1576

ESP6500AA

AF:

0.106

AC:

465

ESP6500EA

AF:

0.403

AC:

3464

ExAC

AF:

0.362

AC:

43966

Asia WGS

AF:

0.404

AC:

1403

AN:

3478

EpiCase

AF:

0.413

EpiControl

AF:

0.414

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.16

BayesDel_addAF

Benign

-0.60

BayesDel_noAF

Benign

-0.50

CADD

Benign

(source)

DANN

Uncertain

1.0

DEOGEN2

Benign

0.0080

Eigen

Uncertain

0.32

Eigen_PC

Benign

0.16

FATHMM_MKL

Benign

0.063

LIST_S2

Benign

0.33

MetaRNN

Benign

0.00019

MetaSVM

Benign

-1.1

MutationAssessor

Uncertain

2.7

PhyloP100

-0.86

PrimateAI

Benign

0.24

PROVEAN

Pathogenic

-5.8

REVEL

Benign

0.057

Sift

Pathogenic

0.0

Sift4G

Pathogenic

0.0010

Polyphen

1.0

Vest4

0.17

MPC

0.43

ClinPred

0.049

GERP RS

4.3

PromoterAI

-0.0022

Neutral

(source)

Varity_R

0.76

gMVP

0.39

Mutation Taster

=99/1

polymorphism (auto)

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.010

Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Variant Effect in Transcripts

RefSeq Transcripts

Ensembl Transcripts

Frequencies

Age Distribution

Age Distribution

ClinVar

Computational scores

Splicing

Publications

Other links and lift over