rs416586

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_StrongBA1

The NM_001005567.3(OR51B5):​c.-360+33242T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.292 in 152,072 control chromosomes in the GnomAD database, including 7,013 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 0.29 ( 7013 hom., cov: 32)

Consequence

OR51B5
NM_001005567.3 intron

Scores

2

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: -0.402
Variant links:
Genes affected
HBE1 (HGNC:4830): (hemoglobin subunit epsilon 1) The epsilon globin gene (HBE) is normally expressed in the embryonic yolk sac: two epsilon chains together with two zeta chains (an alpha-like globin) constitute the embryonic hemoglobin Hb Gower I; two epsilon chains together with two alpha chains form the embryonic Hb Gower II. Both of these embryonic hemoglobins are normally supplanted by fetal, and later, adult hemoglobin. The five beta-like globin genes are found within a 45 kb cluster on chromosome 11 in the following order: 5'-epsilon - G-gamma - A-gamma - delta - beta-3' [provided by RefSeq, Jul 2008]
OR51B5 (HGNC:19599): (olfactory receptor family 51 subfamily B member 5) 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]
HBG2 (HGNC:4832): (hemoglobin subunit gamma 2) The gamma globin genes (HBG1 and HBG2) are normally expressed in the fetal liver, spleen and bone marrow. Two gamma chains together with two alpha chains constitute fetal hemoglobin (HbF) which is normally replaced by adult hemoglobin (HbA) at birth. In some beta-thalassemias and related conditions, gamma chain production continues into adulthood. The two types of gamma chains differ at residue 136 where glycine is found in the G-gamma product (HBG2) and alanine is found in the A-gamma product (HBG1). The former is predominant at birth. The order of the genes in the beta-globin cluster is: 5'- epsilon -- gamma-G -- gamma-A -- delta -- beta--3'. [provided by RefSeq, Jul 2008]

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -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 = 0.398 is higher than 0.05.

Transcripts

RefSeq

Gene Transcript HGVSc HGVSp Effect #exon/exons MANE Protein UniProt
OR51B5NM_001005567.3 linkuse as main transcriptc.-360+33242T>C intron_variant NP_001005567.2 Q9H339Q05CQ2
OR51B5NR_038321.2 linkuse as main transcriptn.84+33242T>C intron_variant

Ensembl

Gene Transcript HGVSc HGVSp Effect #exon/exons TSL MANE Protein Appris UniProt
ENSG00000239920ENST00000380259.7 linkuse as main transcriptn.*739+118498T>C intron_variant 5 ENSP00000369609.3 A0A2U3TZJ3

Frequencies

GnomAD3 genomes
AF:
0.292
AC:
44361
AN:
151954
Hom.:
7001
Cov.:
32
show subpopulations
Gnomad AFR
AF:
0.403
Gnomad AMI
AF:
0.215
Gnomad AMR
AF:
0.290
Gnomad ASJ
AF:
0.209
Gnomad EAS
AF:
0.0634
Gnomad SAS
AF:
0.202
Gnomad FIN
AF:
0.268
Gnomad MID
AF:
0.339
Gnomad NFE
AF:
0.258
Gnomad OTH
AF:
0.276
We have no GnomAD4 exomes data on this position. Probably position not covered by the project.
GnomAD4 genome
AF:
0.292
AC:
44405
AN:
152072
Hom.:
7013
Cov.:
32
AF XY:
0.290
AC XY:
21584
AN XY:
74320
show subpopulations
Gnomad4 AFR
AF:
0.403
Gnomad4 AMR
AF:
0.290
Gnomad4 ASJ
AF:
0.209
Gnomad4 EAS
AF:
0.0628
Gnomad4 SAS
AF:
0.201
Gnomad4 FIN
AF:
0.268
Gnomad4 NFE
AF:
0.258
Gnomad4 OTH
AF:
0.279
Alfa
AF:
0.259
Hom.:
6858
Bravo
AF:
0.293
Asia WGS
AF:
0.159
AC:
553
AN:
3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name
Calibrated prediction
Score
Prediction
BayesDel_noAF
Benign
-0.89
CADD
Benign
0.20
DANN
Benign
0.50

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

Publications

LitVar

Below is the list of publications found by LitVar. It may be empty.

Other links and lift over

dbSNP: rs416586; hg19: chr11-5493557; API