rs7169868

chr15-101842890-T-C

Variant summary

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

The NR_046417.1(OR4F13P):n.31-32T>C variant causes a intron, non coding transcript change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.469 in 151,874 control chromosomes in the GnomAD database, including 17,266 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 0.47 (17266 hom., cov: 31)
  • Failed GnomAD Quality Control
• Consequence: OR4F13P NR_046417.1 intron, non_coding_transcript
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0150

Genes affected

OR4F13P (HGNC:15076): (olfactory receptor family 4 subfamily F member 13 pseudogene) 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=-0.69).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.513 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
OR4F13P	NR_046417.1	n.31-32T>C		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
OR4F13P	ENST00000560066.1	n.31-32T>C		intron_variant, non_coding_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.469 AC: 71158 AN: 151756 Hom.: 17257 Cov.: 31

Gnomad AFR AF: 0.519

Gnomad AMI AF: 0.523

Gnomad AMR AF: 0.433

Gnomad ASJ AF: 0.453

Gnomad EAS AF: 0.0576

Gnomad SAS AF: 0.423

Gnomad FIN AF: 0.359

Gnomad MID AF: 0.459

Gnomad NFE AF: 0.499

Gnomad OTH AF: 0.465

GnomAD4 exome Data not reliable, filtered out with message: AC0 AC: 0 AN: 0 Hom.: 0 Cov.: 0 AC XY: 0 AN XY: 0

GnomAD4 genome AF: 0.469 AC: 71199 AN: 151874 Hom.: 17266 Cov.: 31 AF XY: 0.459 AC XY: 34070 AN XY: 74220

Gnomad4 AFR AF: 0.518

Gnomad4 AMR AF: 0.432

Gnomad4 ASJ AF: 0.453

Gnomad4 EAS AF: 0.0575

Gnomad4 SAS AF: 0.424

Gnomad4 FIN AF: 0.359

Gnomad4 NFE AF: 0.498

Gnomad4 OTH AF: 0.464

Alfa AF: 0.492 Hom.: 9467

Bravo AF: 0.468

Asia WGS AF: 0.324 AC: 1127 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.69
Cadd	Benign	5.7
Dann	Benign	0.87

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs7169868; hg19: chr15-102383093;