APOBEC3D apolipoprotein B mRNA editing enzyme catalytic subunit 3D
Information
- Symbol
- APOBEC3D
- Type
- protein-coding
- Description
- apolipoprotein B mRNA editing enzyme catalytic subunit 3D
- Entrez Gene ID
- 140564
- Genome
- hg19
- Position
- chr22:39,417,132-39,429,282
- Genome
- hg38
- Position
- chr22:39,021,127-39,033,277
- MIM
- 609900 OMIM
- HGNC
- HGNC:17354 HGNC
- Ensembl
- ENSG00000243811 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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62 |
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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 | |||||
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | A3D |
SYNONYM | A3DE |
SYNONYM | APOBEC3DE |
SYNONYM | APOBEC3E |
SYNONYM | ARP6 |
MIM | 609900 OMIM |
HGNC | HGNC:17354 HGNC |
Ensembl | ENSG00000243811 Ensembl |
AllianceGenome | HGNC:17354 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000216099.13 | hg38 | chr22 | 39,021,127 | 39,033,277 | 12,151 |
ENST00000622217.3 | hg38 | chr22 | 39,021,502 | 39,032,316 | 10,815 |
ENST00000427494.6 | hg38 | chr22 | 39,021,113 | 39,033,261 | 12,149 |
ENST00000427494.6 | hg19 | chr22 | 39,417,118 | 39,429,266 | 12,149 |
ENST00000216099.13 | hg19 | chr22 | 39,417,132 | 39,429,282 | 12,151 |
ENST00000622217.3 | hg19 | chr22 | 39,417,507 | 39,428,321 | 10,815 |
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