NM_001004452.1:c.28T>C

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 2P and 2B. PM2BP4_Moderate

The NM_001004452.1(OR1J4):​c.28T>C​(p.Ser10Pro) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 15/22 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. S10A) has been classified as Uncertain significance.

Frequency

Genomes: not found (cov: 32)

Consequence

OR1J4
NM_001004452.1 missense

Scores

3
15

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: -0.130

Publications

0 publications found
Variant links:
Genes affected
OR1J4 (HGNC:8211): (olfactory receptor family 1 subfamily J member 4) 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]
OR1J2 (HGNC:8209): (olfactory receptor family 1 subfamily J 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]

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

PM2
Very rare variant in population databases, with high coverage;
BP4
Computational evidence support a benign effect (MetaRNN=0.14134619).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001004452.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.
GeneTranscriptTagsHGVScHGVSpEffectExon RankProteinUniProt
OR1J4
NM_001004452.1
MANE Select
c.28T>Cp.Ser10Pro
missense
Exon 1 of 1NP_001004452.1A0A126GW06

Ensembl Transcripts

Sel.
GeneTranscriptTagsHGVScHGVSpEffectExon RankProteinUniProt
OR1J4
ENST00000340750.1
TSL:6 MANE Select
c.28T>Cp.Ser10Pro
missense
Exon 1 of 1ENSP00000343521.1Q8NGS1
ENSG00000234156
ENST00000431442.3
TSL:3
n.1362+16298T>C
intron
N/A
ENSG00000234156
ENST00000723589.1
n.1044+49983T>C
intron
N/A

Frequencies

GnomAD3 genomes
Cov.:
32
GnomAD4 exome
Cov.:
32
GnomAD4 genome
Cov.:
32
Alfa
AF:
0.0000611
Hom.:
0

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name
Calibrated prediction
Score
Prediction
AlphaMissense
Benign
0.11
BayesDel_addAF
Benign
-0.19
T
BayesDel_noAF
Benign
-0.51
CADD
Benign
15
DANN
Benign
0.90
DEOGEN2
Benign
0.18
T
Eigen
Benign
-0.94
Eigen_PC
Benign
-0.94
FATHMM_MKL
Benign
0.034
N
LIST_S2
Benign
0.24
T
M_CAP
Benign
0.0013
T
MetaRNN
Benign
0.14
T
MetaSVM
Benign
-0.95
T
MutationAssessor
Benign
1.3
L
PhyloP100
-0.13
PrimateAI
Benign
0.34
T
PROVEAN
Uncertain
-3.3
D
REVEL
Benign
0.18
Sift
Uncertain
0.024
D
Sift4G
Uncertain
0.022
D
Polyphen
0.083
B
Vest4
0.25
MVP
0.38
MPC
0.038
ClinPred
0.26
T
GERP RS
4.0
PromoterAI
-0.0014
Neutral
Varity_R
0.27
gMVP
0.17
Mutation Taster
=93/7
polymorphism

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

Other links and lift over

dbSNP: rs776519812; hg19: chr9-125281447; API