IFITM2 interferon induced transmembrane protein 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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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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 | 1-8D |
SYNONYM | DSPA2c |
MIM | 605578 OMIM |
HGNC | HGNC:5413 HGNC |
Ensembl | ENSG00000185201 Ensembl |
AllianceGenome | HGNC:5413 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000399817.9 | hg38 | chr11 | 308,106 | 309,397 | 1,292 |
ENST00000681833.1 | hg38 | chr11 | 308,193 | 309,395 | 1,203 |
ENST00000680261.1 | hg38 | chr11 | 308,193 | 309,395 | 1,203 |
ENST00000680344.1 | hg38 | chr11 | 308,136 | 309,395 | 1,260 |
ENST00000616316.3 | hg38 | chr11 | 307,816 | 309,395 | 1,580 |
ENST00000602569.2 | hg38 | chr11 | 308,253 | 309,393 | 1,141 |
ENST00000680619.1 | hg38 | chr11 | 308,193 | 309,165 | 973 |
ENST00000533141.1 | hg38 | chr11 | 307,631 | 309,230 | 1,600 |
ENST00000399817.9 | hg19 | chr11 | 308,106 | 309,397 | 1,292 |
ENST00000533141.1 | hg19 | chr11 | 307,631 | 309,230 | 1,600 |
ENST00000602569.2 | hg19 | chr11 | 308,253 | 309,393 | 1,141 |
ENST00000616316.3 | hg19 | chr11 | 307,816 | 309,395 | 1,580 |
ENST00000680261.1 | hg19 | chr11 | 308,193 | 309,395 | 1,203 |
ENST00000680344.1 | hg19 | chr11 | 308,136 | 309,395 | 1,260 |
ENST00000680619.1 | hg19 | chr11 | 308,193 | 309,165 | 973 |
ENST00000681833.1 | hg19 | chr11 | 308,193 | 309,395 | 1,203 |
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