APOBEC3A apolipoprotein B mRNA editing enzyme catalytic subunit 3A
Information
- Symbol
- APOBEC3A
- Type
- protein-coding
- Description
- apolipoprotein B mRNA editing enzyme catalytic subunit 3A
- Entrez Gene ID
- 200315
- Genome
- hg19
- Position
- chr22:39,348,756-39,359,188
- Genome
- hg38
- Position
- chr22:38,952,751-38,963,183
- MIM
- 607109 OMIM
- HGNC
- HGNC:17343 HGNC
- Ensembl
- ENSG00000128383 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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14 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | A3A |
SYNONYM | ARP3 |
SYNONYM | PHRBN |
SYNONYM | bK150C2.1 |
MIM | 607109 OMIM |
HGNC | HGNC:17343 HGNC |
Ensembl | ENSG00000128383 Ensembl |
AllianceGenome | HGNC:17343 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000249116.7 | hg38 | chr22 | 38,957,609 | 38,963,184 | 5,576 |
ENST00000402255.5 | hg38 | chr22 | 38,952,751 | 38,963,183 | 10,433 |
ENST00000402255.5 | hg19 | chr22 | 39,348,756 | 39,359,188 | 10,433 |
ENST00000249116.7 | hg19 | chr22 | 39,353,614 | 39,359,189 | 5,576 |
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