NM_000775.4:c.1331-2620A>G

Variant names:

• chr1-59896449-T-C
• rs10889160
• NM_000775.4:c.1331-2620A>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_000775.4(CYP2J2):​c.1331-2620A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.223 in 151,950 control chromosomes in the GnomAD database, including 4,744 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 0.22 (4744 hom., cov: 32)
• Consequence: CYP2J2 NM_000775.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.686
• Publications: 11 publications found

Genes affected

CYP2J2 (HGNC:2634): (cytochrome P450 family 2 subfamily J member 2) This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the endoplasmic reticulum and is thought to be the predominant enzyme responsible for epoxidation of endogenous arachidonic acid in cardiac tissue. Multiple transcript variants have been found for this gene. [provided by RefSeq, Jan 2016]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.02).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.399 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_000775.4. 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
	CYP2J2	NM_000775.4	MANE Select	c.1331-2620A>G		intron	N/A	NP_000766.2
	CYP2J2	NR_134981.2		n.1170-2620A>G		intron	N/A
	CYP2J2	NR_134982.2		n.1509-2620A>G		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CYP2J2	ENST00000371204.4	TSL:1 MANE Select	c.1331-2620A>G		intron	N/A	ENSP00000360247.3	P51589
	CYP2J2	ENST00000905907.1		c.1322-2620A>G		intron	N/A	ENSP00000575966.1
	CYP2J2	ENST00000905910.1		c.1244-2620A>G		intron	N/A	ENSP00000575969.1

Frequencies

GnomAD3 genomes AF: 0.223 AC: 33818 AN: 151834 Hom.: 4729 Cov.: 32

Gnomad AFR AF: 0.404

Gnomad AMI AF: 0.0648

Gnomad AMR AF: 0.184

Gnomad ASJ AF: 0.0868

Gnomad EAS AF: 0.153

Gnomad SAS AF: 0.0981

Gnomad FIN AF: 0.181

Gnomad MID AF: 0.165

Gnomad NFE AF: 0.153

Gnomad OTH AF: 0.181

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

GnomAD4 genome AF: 0.223 AC: 33871 AN: 151950 Hom.: 4744 Cov.: 32 AF XY: 0.220 AC XY: 16367 AN XY: 74280

African (AFR) AF: 0.404 AC: 16720 AN: 41374

American (AMR) AF: 0.184 AC: 2805 AN: 15262

Ashkenazi Jewish (ASJ) AF: 0.0868 AC: 301 AN: 3466

East Asian (EAS) AF: 0.152 AC: 784 AN: 5174

South Asian (SAS) AF: 0.0976 AC: 470 AN: 4816

European-Finnish (FIN) AF: 0.181 AC: 1915 AN: 10572

Middle Eastern (MID) AF: 0.163 AC: 48 AN: 294

European-Non Finnish (NFE) AF: 0.153 AC: 10389 AN: 67972

Other (OTH) AF: 0.180 AC: 380 AN: 2110

Alfa AF: 0.223 Hom.: 705

Bravo AF: 0.230

Asia WGS AF: 0.153 AC: 533 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.54
DANN	Benign	0.45
PhyloP100		-0.69
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs10889160; hg19: chr1-60362121;