NM_000767.5:c.1295-1024A>G

Variant names:

• chr19-41015622-A-G
• rs4802104
• NM_000767.5:c.1295-1024A>G

Variant summary

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

The NM_000767.5(CYP2B6):​c.1295-1024A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.266 in 152,064 control chromosomes in the GnomAD database, including 6,214 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 0.27 (6214 hom., cov: 31)
• Consequence: CYP2B6 NM_000767.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0190
• Publications: 3 publications found

Genes affected

CYP2B6 (HGNC:2615): (cytochrome P450 family 2 subfamily B member 6) This gene, CYP2B6, 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 its expression is induced by phenobarbital. The enzyme is known to metabolize some xenobiotics, such as the anti-cancer drugs cyclophosphamide and ifosphamide. Transcript variants for this gene have been described; however, it has not been resolved whether these transcripts are in fact produced by this gene or by a closely related pseudogene, CYP2B7. Both the gene and the pseudogene are located in the middle of a CYP2A pseudogene found in a large cluster of cytochrome P450 genes from the CYP2A, CYP2B and CYP2F subfamilies on chromosome 19q. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.76).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.418 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_000767.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CYP2B6	NM_000767.5	MANE Select	c.1295-1024A>G		intron	N/A	NP_000758.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CYP2B6	ENST00000324071.10	TSL:1 MANE Select	c.1295-1024A>G		intron	N/A	ENSP00000324648.2
	CYP2B6	ENST00000597612.1	TSL:1	n.648-1024A>G		intron	N/A
	CYP2B6	ENST00000593831.1	TSL:2	c.587-1024A>G		intron	N/A	ENSP00000470582.1

Frequencies

GnomAD3 genomes AF: 0.266 AC: 40379 AN: 151946 Hom.: 6213 Cov.: 31

Gnomad AFR AF: 0.111

Gnomad AMI AF: 0.284

Gnomad AMR AF: 0.354

Gnomad ASJ AF: 0.309

Gnomad EAS AF: 0.433

Gnomad SAS AF: 0.346

Gnomad FIN AF: 0.355

Gnomad MID AF: 0.376

Gnomad NFE AF: 0.305

Gnomad OTH AF: 0.282

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

GnomAD4 genome AF: 0.266 AC: 40390 AN: 152064 Hom.: 6214 Cov.: 31 AF XY: 0.272 AC XY: 20225 AN XY: 74334

African (AFR) AF: 0.111 AC: 4595 AN: 41484

American (AMR) AF: 0.354 AC: 5411 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.309 AC: 1072 AN: 3470

East Asian (EAS) AF: 0.433 AC: 2232 AN: 5156

South Asian (SAS) AF: 0.346 AC: 1666 AN: 4814

European-Finnish (FIN) AF: 0.355 AC: 3756 AN: 10572

Middle Eastern (MID) AF: 0.377 AC: 110 AN: 292

European-Non Finnish (NFE) AF: 0.304 AC: 20697 AN: 67976

Other (OTH) AF: 0.281 AC: 593 AN: 2110

Alfa AF: 0.287 Hom.: 1135

Bravo AF: 0.261

Asia WGS AF: 0.343 AC: 1194 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.76
CADD	Benign	4.5
DANN	Benign	0.88
PhyloP100		0.019
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: rs4802104; hg19: chr19-41521527;