rs7824175

chr8-53231614-C-Gchr8-53231614-C-T

Variant summary

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

The NM_000912.5(OPRK1):c.611-1785G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.166 in 152,112 control chromosomes in the GnomAD database, including 2,948 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 0.17 (2948 hom., cov: 32)
• Consequence: OPRK1 NM_000912.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.862

Genes affected

OPRK1 (HGNC:8154): (opioid receptor kappa 1) This gene encodes an opioid receptor, which is a member of the 7 transmembrane-spanning G protein-coupled receptor family. It functions as a receptor for endogenous ligands, as well as a receptor for various synthetic opioids. Ligand binding results in inhibition of adenylate cyclase activity and neurotransmitter release. This opioid receptor plays a role in the perception of pain and mediating the hypolocomotor, analgesic and aversive actions of synthetic opioids. Variations in this gene have also been associated with alcohol dependence and opiate addiction. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A recent study provided evidence for translational readthrough in this gene, and expression of an additional C-terminally extended isoform via the use of an alternative in-frame translation termination codon. [provided by RefSeq, Dec 2017]

LOC105375836 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.8).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.32 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
OPRK1	NM_000912.5	c.611-1785G>C		intron_variant		ENST00000265572.8
LOC105375836	XR_928877.2	n.4326C>G		non_coding_transcript_exon_variant	3/3
OPRK1	NM_001282904.2	c.344-1785G>C		intron_variant
OPRK1	NM_001318497.2	c.611-1785G>C		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
OPRK1	ENST00000265572.8	c.611-1785G>C		intron_variant		1	NM_000912.5	P1
	ENST00000524425.1	n.671-10914C>G		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.166 AC: 25209 AN: 151994 Hom.: 2937 Cov.: 32

Gnomad AFR AF: 0.324

Gnomad AMI AF: 0.0407

Gnomad AMR AF: 0.224

Gnomad ASJ AF: 0.172

Gnomad EAS AF: 0.0717

Gnomad SAS AF: 0.0883

Gnomad FIN AF: 0.0872

Gnomad MID AF: 0.156

Gnomad NFE AF: 0.0828

Gnomad OTH AF: 0.168

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

GnomAD4 genome AF: 0.166 AC: 25257 AN: 152112 Hom.: 2948 Cov.: 32 AF XY: 0.166 AC XY: 12332 AN XY: 74368

Gnomad4 AFR AF: 0.324

Gnomad4 AMR AF: 0.224

Gnomad4 ASJ AF: 0.172

Gnomad4 EAS AF: 0.0717

Gnomad4 SAS AF: 0.0886

Gnomad4 FIN AF: 0.0872

Gnomad4 NFE AF: 0.0828

Gnomad4 OTH AF: 0.168

Alfa AF: 0.0356 Hom.: 27

Bravo AF: 0.184

Asia WGS AF: 0.100 AC: 347 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.80
Cadd	Benign	6.3
Dann	Benign	0.68

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

Other links and lift over

dbSNP: rs7824175; hg19: chr8-54144174;