CYP2F1 cytochrome P450 family 2 subfamily F member 1

Information
Symbol
CYP2F1
Type
protein-coding
Description
cytochrome P450 family 2 subfamily F member 1
Entrez Gene ID
1572
Genome
hg19
Position
chr19:41,620,337-41,634,286
Genome
hg38
Position
chr19:41,114,432-41,128,381
MIM
124070 OMIM
HGNC
HGNC:2632 HGNC
Ensembl
ENSG00000197446 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 2
Uncertain significance 0 72
Ranking
ClinVar
0
0
0
90
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 :
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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 C2F1
SYNONYM CYP2F
SYNONYM CYPIIF1
MIM 124070 OMIM
HGNC HGNC:2632 HGNC
Ensembl ENSG00000197446 Ensembl
AllianceGenome HGNC:2632
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000331105.7 hg38 chr19 41,114,432 41,128,381 13,950
ENST00000331105.7 hg19 chr19 41,620,337 41,634,286 13,950
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