CYP7A1 cytochrome P450 family 7 subfamily A member 1

Information
Symbol
CYP7A1
Type
protein-coding
Description
cytochrome P450 family 7 subfamily A member 1
Entrez Gene ID
1581
Genome
hg19
Position
chr8:59,402,737-59,412,722
Genome
hg38
Position
chr8:58,490,178-58,500,163
MIM
118455 OMIM
HGNC
HGNC:2651 HGNC
Ensembl
ENSG00000167910 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 36
Likely benign 0 86
Conflicting classifications of pathogenicity 0 16
Uncertain significance 0 212
Ranking
ClinVar
0
0
58
260
2
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 :
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 CP7A
SYNONYM CYP7
SYNONYM CYPVII
MIM 118455 OMIM
HGNC HGNC:2651 HGNC
Ensembl ENSG00000167910 Ensembl
AllianceGenome HGNC:2651
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000301645.4 hg38 chr8 58,490,178 58,500,163 9,986
ENST00000301645.4 hg19 chr8 59,402,737 59,412,722 9,986
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