CYP2A7 cytochrome P450 family 2 subfamily A member 7
Information
- Symbol
- CYP2A7
- Type
- protein-coding
- Description
- cytochrome P450 family 2 subfamily A member 7
- Entrez Gene ID
- 1549
- Genome
- hg19
- Position
- chr19:41,381,344-41,388,136
- Genome
- hg38
- Position
- chr19:40,875,439-40,882,231
- MIM
- 608054 OMIM
- HGNC
- HGNC:2611 HGNC
- Ensembl
- ENSG00000198077 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 16 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 82 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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106 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | CPA7 |
SYNONYM | CPAD |
SYNONYM | CYP2A |
SYNONYM | CYPIIA7 |
SYNONYM | P450-IIA4 |
MIM | 608054 OMIM |
HGNC | HGNC:2611 HGNC |
Ensembl | ENSG00000198077 Ensembl |
AllianceGenome | HGNC:2611 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000291764.3 | hg38 | chr19 | 40,875,439 | 40,882,752 | 7,314 |
ENST00000301146.9 | hg38 | chr19 | 40,875,439 | 40,882,231 | 6,793 |
ENST00000291764.3 | hg19 | chr19 | 41,381,344 | 41,388,657 | 7,314 |
ENST00000301146.9 | hg19 | chr19 | 41,381,344 | 41,388,136 | 6,793 |
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