IFITM1 interferon induced transmembrane protein 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 5 | 0 |
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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6 |
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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
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 |
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SYNONYM | 9-27 |
SYNONYM | CD225 |
SYNONYM | DSPA2a |
SYNONYM | IFI17 |
SYNONYM | LEU13 |
MIM | 604456 OMIM |
HGNC | HGNC:5412 HGNC |
Ensembl | ENSG00000185885 Ensembl |
AllianceGenome | HGNC:5412 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000328221.5 | hg38 | chr11 | 313,527 | 315,240 | 1,714 |
ENST00000679380.1 | hg38 | chr11 | 314,040 | 315,271 | 1,232 |
ENST00000680699.1 | hg38 | chr11 | 314,040 | 314,962 | 923 |
ENST00000680696.1 | hg38 | chr11 | 314,040 | 315,272 | 1,233 |
ENST00000680938.1 | hg38 | chr11 | 314,040 | 315,271 | 1,232 |
ENST00000408968.4 | hg38 | chr11 | 314,040 | 315,272 | 1,233 |
ENST00000681938.1 | hg38 | chr11 | 314,040 | 315,271 | 1,232 |
ENST00000681180.1 | hg38 | chr11 | 314,040 | 315,272 | 1,233 |
ENST00000681426.1 | hg38 | chr11 | 314,040 | 315,272 | 1,233 |
ENST00000680588.1 | hg38 | chr11 | 310,041 | 315,271 | 5,231 |
ENST00000528780.5 | hg38 | chr11 | 313,506 | 315,272 | 1,767 |
ENST00000328221.5 | hg19 | chr11 | 313,527 | 315,240 | 1,714 |
ENST00000679380.1 | hg19 | chr11 | 314,040 | 315,271 | 1,232 |
ENST00000680938.1 | hg19 | chr11 | 314,040 | 315,271 | 1,232 |
ENST00000408968.4 | hg19 | chr11 | 314,040 | 315,272 | 1,233 |
ENST00000528780.5 | hg19 | chr11 | 313,506 | 315,272 | 1,767 |
ENST00000680696.1 | hg19 | chr11 | 314,040 | 315,272 | 1,233 |
ENST00000681426.1 | hg19 | chr11 | 314,040 | 315,272 | 1,233 |
ENST00000681180.1 | hg19 | chr11 | 314,040 | 315,272 | 1,233 |
ENST00000680588.1 | hg19 | chr11 | 310,041 | 315,271 | 5,231 |
ENST00000680699.1 | hg19 | chr11 | 314,040 | 314,962 | 923 |
ENST00000681938.1 | hg19 | chr11 | 314,040 | 315,271 | 1,232 |
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