10-94820445-C-G

Variant names:

• chr10-94820445-C-G
• rs4417205
• NM_000769.4:c.820-51C>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.820-51C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.165 in 1,600,518 control chromosomes in the GnomAD database, including 24,130 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 (2516 hom., cov: 31)
  • Exomes 𝑓: 0.16 (21614 hom.)
• Consequence: CYP2C19 NM_000769.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.629
• Publications: 19 publications found

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=-0.91).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.317 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CYP2C19	NM_000769.4	c.820-51C>G		intron_variant	Intron 5 of 8	ENST00000371321.9	NP_000760.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CYP2C19	ENST00000371321.9	c.820-51C>G		intron_variant	Intron 5 of 8	1	NM_000769.4	ENSP00000360372.3
ENSG00000276490	ENST00000464755.1	n.*578-51C>G		intron_variant	Intron 10 of 13	2		ENSP00000483243.1
CYP2C19	ENST00000645461.1	n.1873-22392C>G		intron_variant	Intron 4 of 6

Frequencies

GnomAD3 genomes AF: 0.173 AC: 26308 AN: 152034 Hom.: 2511 Cov.: 31

Gnomad AFR AF: 0.196

Gnomad AMI AF: 0.182

Gnomad AMR AF: 0.133

Gnomad ASJ AF: 0.132

Gnomad EAS AF: 0.311

Gnomad SAS AF: 0.330

Gnomad FIN AF: 0.183

Gnomad MID AF: 0.0918

Gnomad NFE AF: 0.148

Gnomad OTH AF: 0.153

GnomAD2 exomes AF: 0.180 AC: 45111 AN: 250118 AF XY: 0.187

Gnomad AFR exome AF: 0.200

Gnomad AMR exome AF: 0.105

Gnomad ASJ exome AF: 0.133

Gnomad EAS exome AF: 0.310

Gnomad FIN exome AF: 0.171

Gnomad NFE exome AF: 0.147

Gnomad OTH exome AF: 0.157

GnomAD4 exome AF: 0.164 AC: 237559 AN: 1448366 Hom.: 21614 Cov.: 28 AF XY: 0.169 AC XY: 121698 AN XY: 721370

African (AFR) AF: 0.204 AC: 6768 AN: 33232

American (AMR) AF: 0.108 AC: 4805 AN: 44586

Ashkenazi Jewish (ASJ) AF: 0.134 AC: 3494 AN: 25998

East Asian (EAS) AF: 0.303 AC: 11997 AN: 39562

South Asian (SAS) AF: 0.324 AC: 27814 AN: 85880

European-Finnish (FIN) AF: 0.171 AC: 9104 AN: 53288

Middle Eastern (MID) AF: 0.115 AC: 663 AN: 5744

European-Non Finnish (NFE) AF: 0.148 AC: 162839 AN: 1100180

Other (OTH) AF: 0.168 AC: 10075 AN: 59896

GnomAD4 genome AF: 0.173 AC: 26328 AN: 152152 Hom.: 2516 Cov.: 31 AF XY: 0.177 AC XY: 13172 AN XY: 74392

African (AFR) AF: 0.196 AC: 8129 AN: 41486

American (AMR) AF: 0.133 AC: 2036 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.132 AC: 459 AN: 3470

East Asian (EAS) AF: 0.311 AC: 1608 AN: 5170

South Asian (SAS) AF: 0.331 AC: 1594 AN: 4818

European-Finnish (FIN) AF: 0.183 AC: 1941 AN: 10594

Middle Eastern (MID) AF: 0.0918 AC: 27 AN: 294

European-Non Finnish (NFE) AF: 0.148 AC: 10036 AN: 68000

Other (OTH) AF: 0.157 AC: 332 AN: 2112

Alfa AF: 0.146 Hom.: 359

Bravo AF: 0.167

Asia WGS AF: 0.305 AC: 1058 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.68
DANN	Benign	0.66
PhyloP100		-0.63
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.040		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: rs4417205; hg19: chr10-96580202; COSMIC: COSV64907197;