IFIT1B interferon induced protein with tetratricopeptide repeats 1B
Information
- Symbol
- IFIT1B
- Type
- protein-coding
- Description
- interferon induced protein with tetratricopeptide repeats 1B
- Entrez Gene ID
- 439996
- Genome
- hg19
- Position
- chr10:91,137,813-91,144,962
- Genome
- hg38
- Position
- chr10:89,378,056-89,385,205
- HGNC
- HGNC:23442 HGNC
- Ensembl
- ENSG00000204010 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 4 |
not provided | 1 | 0 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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58 |
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2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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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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Category | : |
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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 | IFIT1L |
SYNONYM | bA149I23.6 |
HGNC | HGNC:23442 HGNC |
Ensembl | ENSG00000204010 Ensembl |
AllianceGenome | HGNC:23442 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000371809.3 | hg38 | chr10 | 89,378,056 | 89,385,205 | 7,150 |
ENST00000371809.3 | hg19 | chr10 | 91,137,813 | 91,144,962 | 7,150 |
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