APOBEC3G apolipoprotein B mRNA editing enzyme catalytic subunit 3G
Information
- Symbol
- APOBEC3G
- Type
- protein-coding
- Description
- apolipoprotein B mRNA editing enzyme catalytic subunit 3G
- Entrez Gene ID
- 60489
- Genome
- hg19
- Position
- chr22:39,473,280-39,483,748
- Genome
- hg38
- Position
- chr22:39,077,275-39,087,743
- MIM
- 607113 OMIM
- HGNC
- HGNC:17357 HGNC
- Ensembl
- ENSG00000239713 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 38 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
38 |
 |
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 | A3G |
| SYNONYM | ARCD |
| SYNONYM | ARP-9 |
| SYNONYM | ARP9 |
| SYNONYM | CEM-15 |
| SYNONYM | CEM15 |
| SYNONYM | MDS019 |
| SYNONYM | bK150C2.7 |
| SYNONYM | dJ494G10.1 |
| MIM | 607113 OMIM |
| HGNC | HGNC:17357 HGNC |
| Ensembl | ENSG00000239713 Ensembl |
| AllianceGenome | HGNC:17357 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000407997.4 | hg38 | chr22 | 39,077,275 | 39,087,743 | 10,469 |
| ENST00000407997.4 | hg19 | chr22 | 39,473,280 | 39,483,748 | 10,469 |
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