CYP2B6 cytochrome P450 family 2 subfamily B member 6

Information
Symbol
CYP2B6
Type
protein-coding
Description
cytochrome P450 family 2 subfamily B member 6
Entrez Gene ID
1555
Genome
hg19
Position
chr19:41,497,187-41,524,303
Genome
hg38
Position
chr19:40,991,282-41,018,398
MIM
123930 OMIM
HGNC
HGNC:2615 HGNC
Ensembl
ENSG00000197408 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 34
drug response 0 18
Uncertain significance 0 64
Ranking
ClinVar
0
4
2
100
14
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 CPB6
SYNONYM CYP2B
SYNONYM CYP2B7
SYNONYM CYP2B7P
SYNONYM CYPIIB6
SYNONYM EFVM
SYNONYM IIB1
SYNONYM P450
MIM 123930 OMIM
HGNC HGNC:2615 HGNC
Ensembl ENSG00000197408 Ensembl
AllianceGenome HGNC:2615
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000593831.1 hg38 chr19 41,003,946 41,017,373 13,428
ENST00000324071.10 hg38 chr19 40,991,282 41,018,398 27,117
ENST00000324071.10 hg19 chr19 41,497,187 41,524,303 27,117
ENST00000593831.1 hg19 chr19 41,509,851 41,523,278 13,428
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