CYP4A22 cytochrome P450 family 4 subfamily A member 22

Information
Symbol
CYP4A22
Type
protein-coding
Description
cytochrome P450 family 4 subfamily A member 22
Entrez Gene ID
284541
Genome
hg19
Position
chr1:47,603,113-47,615,399
Genome
hg38
Position
chr1:47,137,441-47,149,727
MIM
615341 OMIM
HGNC
HGNC:20575 HGNC
Ensembl
ENSG00000162365 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
association 0 2
Uncertain significance 0 68
Ranking
ClinVar
0
0
0
70
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
MIM 615341 OMIM
HGNC HGNC:20575 HGNC
Ensembl ENSG00000162365 Ensembl
AllianceGenome HGNC:20575
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000294337.7 hg38 chr1 47,137,455 47,146,483 9,029
ENST00000371890.7 hg38 chr1 47,137,450 47,149,275 11,826
ENST00000371891.8 hg38 chr1 47,137,441 47,149,727 12,287
ENST00000619754.4 hg38 chr1 47,137,454 47,147,402 9,949
ENST00000371891.8 hg19 chr1 47,603,113 47,615,399 12,287
ENST00000371890.7 hg19 chr1 47,603,122 47,614,947 11,826
ENST00000619754.4 hg19 chr1 47,603,126 47,613,074 9,949
ENST00000294337.7 hg19 chr1 47,603,127 47,612,155 9,029
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