NM_000769.4:c.1292-17A>G

Variant names:

• chr10-94852716-A-G
• rs4451645
• NM_000769.4:c.1292-17A>G

Variant summary

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

The NM_000769.4(CYP2C19):​c.1292-17A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00486 in 1,612,882 control chromosomes in the GnomAD database, including 280 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 0.025 (162 hom., cov: 32)
  • Exomes 𝑓: 0.0028 (118 hom.)
• Consequence: CYP2C19 NM_000769.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.13

Genes affected

CYP2C19 (HGNC:2621): (cytochrome P450 family 2 subfamily C member 19) 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 known to metabolize many xenobiotics, including the anticonvulsive drug mephenytoin, omeprazole, diazepam and some barbiturates. Polymorphism within this gene is associated with variable ability to metabolize mephenytoin, known as the poor metabolizer and extensive metabolizer phenotypes. The gene is located within a cluster of cytochrome P450 genes on chromosome 10q24. [provided by RefSeq, Jul 2008]

ENSG00000276490 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.0825 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CYP2C19	NM_000769.4	c.1292-17A>G		intron_variant	Intron 8 of 8	ENST00000371321.9	NP_000760.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CYP2C19	ENST00000371321.9	c.1292-17A>G		intron_variant	Intron 8 of 8	1	NM_000769.4	ENSP00000360372.3
ENSG00000276490	ENST00000464755.1	n.*1050-17A>G		intron_variant	Intron 13 of 13	2		ENSP00000483243.1
CYP2C19	ENST00000645461.1	n.2203-17A>G		intron_variant	Intron 6 of 6

Frequencies

GnomAD3 genomes AF: 0.0248 AC: 3777 AN: 152002 Hom.: 162 Cov.: 32

Gnomad AFR AF: 0.0851

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.0108

Gnomad ASJ AF: 0.000865

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.000415

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.0253

Gnomad NFE AF: 0.000559

Gnomad OTH AF: 0.0187

GnomAD2 exomes AF: 0.00675 AC: 1696 AN: 251102 AF XY: 0.00508

Gnomad AFR exome AF: 0.0866

Gnomad AMR exome AF: 0.00479

Gnomad ASJ exome AF: 0.00109

Gnomad EAS exome AF: 0.00

Gnomad FIN exome AF: 0.00

Gnomad NFE exome AF: 0.000687

Gnomad OTH exome AF: 0.00491

GnomAD4 exome AF: 0.00278 AC: 4060 AN: 1460762 Hom.: 118 Cov.: 31 AF XY: 0.00240 AC XY: 1745 AN XY: 726726

Gnomad4 AFR exome AF: 0.0817 AC: 2730 AN: 33418

Gnomad4 AMR exome AF: 0.00584 AC: 261 AN: 44654

Gnomad4 ASJ exome AF: 0.00123 AC: 32 AN: 26122

Gnomad4 EAS exome AF: 0.00 AC: 0 AN: 39688

Gnomad4 SAS exome AF: 0.000139 AC: 12 AN: 86226

Gnomad4 FIN exome AF: 0.00 AC: 0 AN: 53394

Gnomad4 NFE exome AF: 0.000506 AC: 562 AN: 1111528

Gnomad4 Remaining exome AF: 0.00663 AC: 400 AN: 60328

GnomAD4 genome AF: 0.0248 AC: 3772 AN: 152120 Hom.: 162 Cov.: 32 AF XY: 0.0240 AC XY: 1785 AN XY: 74362

Gnomad4 AFR AF: 0.0848 AC: 0.0848197 AN: 0.0848197

Gnomad4 AMR AF: 0.0108 AC: 0.010797 AN: 0.010797

Gnomad4 ASJ AF: 0.000865 AC: 0.000864553 AN: 0.000864553

Gnomad4 EAS AF: 0.00 AC: 0 AN: 0

Gnomad4 SAS AF: 0.000415 AC: 0.000415282 AN: 0.000415282

Gnomad4 FIN AF: 0.00 AC: 0 AN: 0

Gnomad4 NFE AF: 0.000559 AC: 0.000558922 AN: 0.000558922

Gnomad4 OTH AF: 0.0185 AC: 0.0185361 AN: 0.0185361

Alfa AF: 0.0144 Hom.: 13

Bravo AF: 0.0284

Asia WGS AF: 0.00433 AC: 15 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.48
DANN	Benign	0.26
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

Publications

LitVar

Other links and lift over

dbSNP: rs4451645; hg19: chr10-96612473;