CYP1A2 cytochrome P450 family 1 subfamily A member 2
Information
- Symbol
- CYP1A2
- Type
- protein-coding
- Description
- cytochrome P450 family 1 subfamily A member 2
- Entrez Gene ID
- 1544
- Genome
- hg19
- Position
- chr15:75,041,186-75,048,948
- Genome
- hg38
- Position
- chr15:74,748,845-74,756,607
- MIM
- 124060 OMIM
- HGNC
- HGNC:2596 HGNC
- Ensembl
- ENSG00000140505 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 10 | 4 |
| Likely benign | 0 | 10 |
| not provided | 3 | 0 |
| Uncertain significance | 0 | 34 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
48 |
 |
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
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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
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| Category | : |
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| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CP12 |
| SYNONYM | CYPIA2 |
| SYNONYM | P3-450 |
| SYNONYM | P450(PA) |
| MIM | 124060 OMIM |
| HGNC | HGNC:2596 HGNC |
| Ensembl | ENSG00000140505 Ensembl |
| AllianceGenome | HGNC:2596 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000343932.5 | hg38 | chr15 | 74,748,845 | 74,756,607 | 7,763 |
| ENST00000343932.5 | hg19 | chr15 | 75,041,186 | 75,048,948 | 7,763 |
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