CYP2A13 cytochrome P450 family 2 subfamily A member 13

Information
Symbol
CYP2A13
Type
protein-coding
Description
cytochrome P450 family 2 subfamily A member 13
Entrez Gene ID
1553
Genome
hg19
Position
chr19:41,594,356-41,602,100
Genome
hg38
Position
chr19:41,088,451-41,096,195
MIM
608055 OMIM
HGNC
HGNC:2608 HGNC
Ensembl
ENSG00000197838 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 92
Ranking
ClinVar
0
0
0
100
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 CPAD
SYNONYM CYP2A
SYNONYM CYPIIA13
MIM 608055 OMIM
HGNC HGNC:2608 HGNC
Ensembl ENSG00000197838 Ensembl
AllianceGenome HGNC:2608
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000330436.4 hg38 chr19 41,088,451 41,096,195 7,745
ENST00000330436.4 hg19 chr19 41,594,356 41,602,100 7,745
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