APOBEC3H apolipoprotein B mRNA editing enzyme catalytic subunit 3H
Information
- Symbol
- APOBEC3H
- Type
- protein-coding
- Description
- apolipoprotein B mRNA editing enzyme catalytic subunit 3H
- Entrez Gene ID
- 164668
- Genome
- hg19
- Position
- chr22:39,493,280-39,500,003
- Genome
- hg38
- Position
- chr22:39,097,275-39,103,998
- MIM
- 610976 OMIM
- HGNC
- HGNC:24100 HGNC
- Ensembl
- ENSG00000100298 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 30 |
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 | A3H |
| SYNONYM | ARP-10 |
| SYNONYM | ARP10 |
| MIM | 610976 OMIM |
| HGNC | HGNC:24100 HGNC |
| Ensembl | ENSG00000100298 Ensembl |
| AllianceGenome | HGNC:24100 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000421988.6 | hg38 | chr22 | 39,097,224 | 39,102,558 | 5,335 |
| ENST00000348946.8 | hg38 | chr22 | 39,097,224 | 39,104,067 | 6,844 |
| ENST00000401756.5 | hg38 | chr22 | 39,097,275 | 39,103,998 | 6,724 |
| ENST00000613677.4 | hg38 | chr22 | 39,097,224 | 39,102,571 | 5,348 |
| ENST00000613996.1 | hg38 | chr22 | 39,100,279 | 39,102,558 | 2,280 |
| ENST00000442487.8 | hg38 | chr22 | 39,097,244 | 39,104,067 | 6,824 |
| ENST00000421988.6 | hg19 | chr22 | 39,493,229 | 39,498,563 | 5,335 |
| ENST00000613677.4 | hg19 | chr22 | 39,493,229 | 39,498,576 | 5,348 |
| ENST00000348946.8 | hg19 | chr22 | 39,493,229 | 39,500,072 | 6,844 |
| ENST00000442487.8 | hg19 | chr22 | 39,493,249 | 39,500,072 | 6,824 |
| ENST00000401756.5 | hg19 | chr22 | 39,493,280 | 39,500,003 | 6,724 |
| ENST00000613996.1 | hg19 | chr22 | 39,496,284 | 39,498,563 | 2,280 |
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