CYP2A6 cytochrome P450 family 2 subfamily A member 6
Information
- Symbol
- CYP2A6
- Type
- protein-coding
- Description
- cytochrome P450 family 2 subfamily A member 6
- Entrez Gene ID
- 1548
- Genome
- hg19
- Position
- chr19:41,349,446-41,356,352
- Genome
- hg38
- Position
- chr19:40,843,541-40,850,447
- MIM
- 122720 OMIM
- HGNC
- HGNC:2610 HGNC
- Ensembl
- ENSG00000255974 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 8 |
| Likely benign | 0 | 14 |
| drug response | 0 | 4 |
| Uncertain significance | 0 | 38 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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60 |
![]() |
4 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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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| 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 | CPA6 |
| SYNONYM | CYP2A |
| SYNONYM | CYP2A3 |
| SYNONYM | CYPIIA6 |
| SYNONYM | P450C2A |
| SYNONYM | P450PB |
| MIM | 122720 OMIM |
| HGNC | HGNC:2610 HGNC |
| Ensembl | ENSG00000255974 Ensembl |
| AllianceGenome | HGNC:2610 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000301141.10 | hg38 | chr19 | 40,843,541 | 40,850,447 | 6,907 |
| ENST00000301141.10 | hg19 | chr19 | 41,349,446 | 41,356,352 | 6,907 |
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