CYP2C9 cytochrome P450 family 2 subfamily C member 9

Information
Symbol
CYP2C9
Type
protein-coding
Description
cytochrome P450 family 2 subfamily C member 9
Entrez Gene ID
1559
Genome
hg19
Position
chr10:96,698,415-96,749,848
Genome
hg38
Position
chr10:94,938,658-94,990,091
MIM
601130 OMIM
HGNC
HGNC:2623 HGNC
Ensembl
ENSG00000138109 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 24 14
Likely benign 0 4
association 0 4
drug response; other 0 2
Likely benign; drug response 0 4
Likely benign; drug response; other 0 6
not provided 2 0
Uncertain significance 0 30
Ranking
ClinVar
0
0
14
36
8
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CPC9
SYNONYM CYP2C
SYNONYM CYP2C10
SYNONYM CYPIIC9
SYNONYM P450-2C9
SYNONYM P450IIC9
MIM 601130 OMIM
HGNC HGNC:2623 HGNC
Ensembl ENSG00000138109 Ensembl
AllianceGenome HGNC:2623
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000260682.8 hg38 chr10 94,938,658 94,990,091 51,434
ENST00000461906.1 hg38 chr10 94,938,658 94,943,266 4,609
ENST00000461906.1 hg19 chr10 96,698,415 96,703,023 4,609
ENST00000260682.8 hg19 chr10 96,698,415 96,749,848 51,434
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