NM_016083.6:c.1359G>C

Variant names:

• chr6-88143916-C-G
• rs1049353
• NM_016083.6:c.1359G>C
• CNR1 p.Thr453Thr

Variant summary

Our verdict is

Likely benign

-3 Likely Benign

-7

-6

-1

0

+5

+6

+9

+10

BenignB

Likely BenignLB

UncertainVUS

Likely PathogenicLP

PathogenicP

. The variant received -3 ACMG points: 2P and 5B. PM2BP4_StrongBP7

The NM_016083.6(CNR1):​c.1359G>C​(p.Thr453Thr) variant causes a synonymous 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. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 32)
• Consequence: CNR1 NM_016083.6 synonymous
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.884
• Publications: 0 publications found

Genes affected

CNR1 (HGNC:2159): (cannabinoid receptor 1) This gene encodes one of two cannabinoid receptors. The cannabinoids, principally delta-9-tetrahydrocannabinol and synthetic analogs, are psychoactive ingredients of marijuana. The cannabinoid receptors are members of the guanine-nucleotide-binding protein (G-protein) coupled receptor family, which inhibit adenylate cyclase activity in a dose-dependent, stereoselective and pertussis toxin-sensitive manner. The two receptors have been found to be involved in the cannabinoid-induced CNS effects (including alterations in mood and cognition) experienced by users of marijuana. Multiple transcript variants encoding two different protein isoforms have been described for this gene. [provided by RefSeq, May 2009]

ENSG00000298549 (HGNC:):

ACMG classification

Our verdict: Likely_benign. The variant received -3 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.64).
• BP7: Synonymous conserved (PhyloP=-0.884 with no splicing effect.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_016083.6. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CNR1	NM_016083.6	MANE Select	c.1359G>C	p.Thr453Thr	synonymous	Exon 2 of 2	NP_057167.2
	CNR1	NM_001160226.3		c.1359G>C	p.Thr453Thr	synonymous	Exon 3 of 3	NP_001153698.1	P21554-1
	CNR1	NM_001160258.3		c.1359G>C	p.Thr453Thr	synonymous	Exon 4 of 4	NP_001153730.1	P21554-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CNR1	ENST00000369501.3	TSL:1 MANE Select	c.1359G>C	p.Thr453Thr	synonymous	Exon 2 of 2	ENSP00000358513.2	P21554-1
	CNR1	ENST00000428600.3	TSL:1	c.1359G>C	p.Thr453Thr	synonymous	Exon 2 of 2	ENSP00000412192.2	P21554-1
	CNR1	ENST00000468898.2	TSL:1	c.1260G>C	p.Thr420Thr	synonymous	Exon 2 of 2	ENSP00000420188.1	P21554-3

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 37

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.64
CADD	Benign	0.76
DANN	Benign	0.73
PhyloP100		-0.88

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.12		Details are displayed if max score is > 0.2

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs1049353;

hg19: chr6-88853635;

ACMG debug oncogenicity

ACGS debug oncogenicity

ACMG debug germline