chr10:96541616:G>A Detail (hg19) (CYP2C19)

Information

Genome

Assembly Position
hg19 chr10:96,541,616-96,541,616
hg38 chr10:94,781,859-94,781,859 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000769.2:c.681G>A NP_000760.1:p.Pro227=
Ensemble ENST00000371321.9:c.681G>A ENST00000371321.9:p.Pro227=
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:0.280
ToMMo:0.299
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:0.310

Prediction

ClinVar

Clinical Significance Likely benign; other
Review star
Show details
Links
Type Database ID Link
Gene MIM 124020 OMIM
HGNC 2621 HGNC
Ensembl ENSG00000165841 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv40259700 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
drug response 2009-06-01 no assertion criteria provided Mephenytoin, poor metabolism of germline Detail
drug response 2009-06-01 no assertion criteria provided Proguanil, poor metabolism of germline Detail
drug response 2018-05-14 no assertion criteria provided germline Detail
other 2018-08-07 criteria provided, single submitter not provided germline Detail
Likely benign 2018-03-09 criteria provided, single submitter not specified germline Detail
drug response practice guideline germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.003 Non-small cell lung carcinoma CYP2C19*2(G681A), CYP2C19*3(G636A), CYP2D6*4(C188T), CYP2D6*2(C2938T, G4268C), C... BeFree 17450472 Detail
<0.001 Non-small cell lung carcinoma CYP2C19*2(G681A), CYP2C19*3(G636A), CYP2D6*4(C188T), CYP2D6*2(C2938T, G4268C), C... BeFree 17450472 Detail
0.002 Non-small cell lung carcinoma CYP2C19*2(G681A), CYP2C19*3(G636A), CYP2D6*4(C188T), CYP2D6*2(C2938T, G4268C), C... BeFree 17450472 Detail
<0.001 Non-small cell lung carcinoma CYP2C19*2(G681A), CYP2C19*3(G636A), CYP2D6*4(C188T), CYP2D6*2(C2938T, G4268C), C... BeFree 17450472 Detail
<0.001 Angina, Unstable This study aimed to evaluate the impact of PON1 Q192R in parallel to that of CYP... BeFree 23993903 Detail
0.020 Malignant neoplasm of breast [Breast cancer treatment outcome with adjuvant tamoxifen relative to patient CYP... GAD 18024866 Detail
0.003 Angina, Unstable This study aimed to evaluate the impact of PON1 Q192R in parallel to that of CYP... BeFree 23993903 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000769.4(CYP2C19):c.681G>A (p.Pro227=) AND Mephenytoin, poor metabolism of ClinVar Detail
NM_000769.4(CYP2C19):c.681G>A (p.Pro227=) AND Proguanil, poor metabolism of ClinVar Detail
NM_000769.4(CYP2C19):c.681G>A (p.Pro227=) AND Clopidogrel response ClinVar Detail
NM_000769.4(CYP2C19):c.681G>A (p.Pro227=) AND not provided ClinVar Detail
NM_000769.4(CYP2C19):c.681G>A (p.Pro227=) AND not specified ClinVar Detail
CYP2C19*2 AND CYP2C19: no function ClinVar Detail
CYP2C19*2(G681A), CYP2C19*3(G636A), CYP2D6*4(C188T), CYP2D6*2(C2938T, G4268C), CYP3AP1*3- G44A and C... DisGeNET Detail
CYP2C19*2(G681A), CYP2C19*3(G636A), CYP2D6*4(C188T), CYP2D6*2(C2938T, G4268C), CYP3AP1*3- G44A and C... DisGeNET Detail
CYP2C19*2(G681A), CYP2C19*3(G636A), CYP2D6*4(C188T), CYP2D6*2(C2938T, G4268C), CYP3AP1*3- G44A and C... DisGeNET Detail
CYP2C19*2(G681A), CYP2C19*3(G636A), CYP2D6*4(C188T), CYP2D6*2(C2938T, G4268C), CYP3AP1*3- G44A and C... DisGeNET Detail
This study aimed to evaluate the impact of PON1 Q192R in parallel to that of CYP2C19*2 (rs4244285) o... DisGeNET Detail
[Breast cancer treatment outcome with adjuvant tamoxifen relative to patient CYP2D6 and CYP2C19 geno... DisGeNET Detail
This study aimed to evaluate the impact of PON1 Q192R in parallel to that of CYP2C19*2 (rs4244285) o... DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs4244285 dbSNP
Genome
hg19
Position
chr10:96,541,616-96,541,616
Variant Type
snv
Reference Allele
G
Alternative Allele
A
Filtering Status (HGVD)
PASS
# of samples (HGVD)
1201
Mean of sample read depth (HGVD)
89.63
Standard deviation of sample read depth (HGVD)
37.63
Number of reference allele (HGVD)
1730
Number of alternative allele (HGVD)
672
Allele Frequency (HGVD)
0.279766860949209
Gene Symbol (HGVD)
CYP2C19
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs4244285
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.2993
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
5017
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
East Asian Chromosome Counts (ExAC)
8624
East Asian Allele Counts (ExAC)
2676
East Asian Heterozygous Counts (ExAC)
1856
East Asian Homozygous Counts (ExAC)
410
East Asian Allele Frequency (ExAC)
0.3102968460111317
Chromosome Counts in All Race (ExAC)
119422
Allele Counts in All Race (ExAC)
22168
Heterozygous Counts in All Race (ExAC)
17260
Homozygous Counts in All Race (ExAC)
2454
Allele Frequency in All Race (ExAC)
0.18562743883036625
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