CYP4F12 cytochrome P450 family 4 subfamily F member 12

Information
Symbol
CYP4F12
Type
protein-coding
Description
cytochrome P450 family 4 subfamily F member 12
Entrez Gene ID
66002
Genome
hg19
Position
chr19:15,783,897-15,807,984
Genome
hg38
Position
chr19:15,673,087-15,697,174
MIM
611485 OMIM
HGNC
HGNC:18857 HGNC
Ensembl
ENSG00000186204 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 10
Uncertain significance 0 64
Ranking
ClinVar
0
0
0
74
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 :
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 CYPIVF12
SYNONYM F22329_1
MIM 611485 OMIM
HGNC HGNC:18857 HGNC
Ensembl ENSG00000186204 Ensembl
AllianceGenome HGNC:18857
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000324632.10 hg38 chr19 15,673,478 15,697,145 23,668
ENST00000550308.6 hg38 chr19 15,673,087 15,697,174 24,088
ENST00000324632.10 hg19 chr19 15,784,288 15,807,955 23,668
ENST00000550308.6 hg19 chr19 15,783,897 15,807,984 24,088
Genome browser