CYP2A7 cytochrome P450 family 2 subfamily A member 7

Information
Symbol
CYP2A7
Type
protein-coding
Description
cytochrome P450 family 2 subfamily A member 7
Entrez Gene ID
1549
Genome
hg19
Position
chr19:41,381,344-41,388,136
Genome
hg38
Position
chr19:40,875,439-40,882,231
MIM
608054 OMIM
HGNC
HGNC:2611 HGNC
Ensembl
ENSG00000198077 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 8
Uncertain significance 0 82
Ranking
ClinVar
0
0
0
106
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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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 CPA7
SYNONYM CPAD
SYNONYM CYP2A
SYNONYM CYPIIA7
SYNONYM P450-IIA4
MIM 608054 OMIM
HGNC HGNC:2611 HGNC
Ensembl ENSG00000198077 Ensembl
AllianceGenome HGNC:2611
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000291764.3 hg38 chr19 40,875,439 40,882,752 7,314
ENST00000301146.9 hg38 chr19 40,875,439 40,882,231 6,793
ENST00000291764.3 hg19 chr19 41,381,344 41,388,657 7,314
ENST00000301146.9 hg19 chr19 41,381,344 41,388,136 6,793
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