CYP3A7-CYP3A51P CYP3A7-CYP3A51P readthrough
Information
- Symbol
- CYP3A7-CYP3A51P
- Type
- protein-coding
- Description
- CYP3A7-CYP3A51P readthrough
- Entrez Gene ID
- 100861540
- Genome
- hg19
- Position
- chr7:99,282,849-99,332,716
- Genome
- hg38
- Position
- chr7:99,685,226-99,735,093
- HGNC
- HGNC:51504 HGNC
- Ensembl
- ENSG00000282301 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 8 |
| Uncertain significance | 0 | 52 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
62 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | CYP3A7 |
| SYNONYM | CYP3A7-3AP1 |
| SYNONYM | CYP3A7-CYP3AP1 |
| SYNONYM | CYP3A7.1L |
| SYNONYM | CYPIIIA7 |
| HGNC | HGNC:51504 HGNC |
| Ensembl | ENSG00000282301 Ensembl |
| AllianceGenome | HGNC:51504 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000620220.6 | hg38 | chr7 | 99,684,957 | 99,735,102 | 50,146 |
| ENST00000611620.4 | hg38 | chr7 | 99,685,226 | 99,735,093 | 49,868 |
| ENST00000620220.6 | hg19 | chr7 | 99,282,580 | 99,332,725 | 50,146 |
| ENST00000611620.4 | hg19 | chr7 | 99,282,849 | 99,332,716 | 49,868 |
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