EIF3F eukaryotic translation initiation factor 3 subunit F
Information
- Symbol
- EIF3F
- Type
- protein-coding
- Description
- eukaryotic translation initiation factor 3 subunit F
- Entrez Gene ID
- 8665
- Genome
- hg19
- Position
- chr11:7,991,798-8,023,409
- Genome
- hg38
- Position
- chr11:7,970,251-8,001,862
- MIM
- 603914 OMIM
- HGNC
- HGNC:3275 HGNC
- Ensembl
- ENSG00000175390 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Likely pathogenic | 0 | 4 |
Benign | 0 | 18 |
Likely benign | 0 | 28 |
Conflicting classifications of pathogenicity | 0 | 8 |
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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10 |
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82 |
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4 |
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 | EIF3S5 |
SYNONYM | MRT67 |
SYNONYM | eIF3-p47 |
MIM | 603914 OMIM |
HGNC | HGNC:3275 HGNC |
Ensembl | ENSG00000175390 Ensembl |
AllianceGenome | HGNC:3275 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000533626.5 | hg38 | chr11 | 7,970,251 | 8,001,862 | 31,612 |
ENST00000651655.1 | hg38 | chr11 | 7,987,337 | 8,001,852 | 14,516 |
ENST00000531572.2 | hg38 | chr11 | 7,987,337 | 7,996,139 | 8,803 |
ENST00000533626.5 | hg19 | chr11 | 7,991,798 | 8,023,409 | 31,612 |
ENST00000531572.2 | hg19 | chr11 | 8,008,884 | 8,017,686 | 8,803 |
ENST00000651655.1 | hg19 | chr11 | 8,008,884 | 8,023,399 | 14,516 |
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