rs72655373

chr1-247456136-G-A

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001004492.2(OR2B11):c.-3082-1072C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.093 in 152,172 control chromosomes in the GnomAD database, including 789 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 0.093 (789 hom., cov: 32)
• Consequence: OR2B11 NM_001004492.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.09

Genes affected

OR2B11 (HGNC:31249): (olfactory receptor family 2 subfamily B member 11) 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]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.117 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
OR2B11	NM_001004492.2	c.-3082-1072C>T		intron_variant		ENST00000641149.2
OR2B11	NR_169840.1	n.371-1072C>T		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
OR2B11	ENST00000641149.2	c.-3082-1072C>T		intron_variant			NM_001004492.2	P1
OR2B11	ENST00000641527.1	c.-1213-1072C>T		intron_variant				P1
OR2B11	ENST00000641613.1	n.371-1072C>T		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.0931 AC: 14151 AN: 152054 Hom.: 791 Cov.: 32

Gnomad AFR AF: 0.0311

Gnomad AMI AF: 0.172

Gnomad AMR AF: 0.0894

Gnomad ASJ AF: 0.156

Gnomad EAS AF: 0.0649

Gnomad SAS AF: 0.0601

Gnomad FIN AF: 0.172

Gnomad MID AF: 0.0886

Gnomad NFE AF: 0.120

Gnomad OTH AF: 0.0953

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

GnomAD4 genome AF: 0.0930 AC: 14151 AN: 152172 Hom.: 789 Cov.: 32 AF XY: 0.0952 AC XY: 7076 AN XY: 74362

Gnomad4 AFR AF: 0.0312

Gnomad4 AMR AF: 0.0892

Gnomad4 ASJ AF: 0.156

Gnomad4 EAS AF: 0.0650

Gnomad4 SAS AF: 0.0604

Gnomad4 FIN AF: 0.172

Gnomad4 NFE AF: 0.120

Gnomad4 OTH AF: 0.0948

Alfa AF: 0.0581 Hom.: 57

Bravo AF: 0.0853

Asia WGS AF: 0.0630 AC: 219 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
Cadd	Benign	0.48
Dann	Benign	0.57

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs72655373; hg19: chr1-247619438;