EIF4B eukaryotic translation initiation factor 4B
Information
- Symbol
- EIF4B
- Type
- protein-coding
- Description
- eukaryotic translation initiation factor 4B
- Entrez Gene ID
- 1975
- Genome
- hg19
- Position
- chr12:53,400,240-53,434,064
- Genome
- hg38
- Position
- chr12:53,006,456-53,040,280
- MIM
- 603928 OMIM
- HGNC
- HGNC:3285 HGNC
- Ensembl
- ENSG00000063046 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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52 |
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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 |
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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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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 |
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SYNONYM | EIF-4B |
SYNONYM | PRO1843 |
MIM | 603928 OMIM |
HGNC | HGNC:3285 HGNC |
Ensembl | ENSG00000063046 Ensembl |
AllianceGenome | HGNC:3285 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000420463.7 | hg38 | chr12 | 53,006,456 | 53,040,280 | 33,825 |
ENST00000262056.14 | hg38 | chr12 | 53,006,456 | 53,042,215 | 35,760 |
ENST00000416762.7 | hg38 | chr12 | 53,006,457 | 53,040,462 | 34,006 |
ENST00000420463.7 | hg19 | chr12 | 53,400,240 | 53,434,064 | 33,825 |
ENST00000262056.14 | hg19 | chr12 | 53,400,240 | 53,435,999 | 35,760 |
ENST00000416762.7 | hg19 | chr12 | 53,400,241 | 53,434,246 | 34,006 |
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