IFFO1 intermediate filament family orphan 1
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 78 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
80 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | HOM-TES-103 |
| SYNONYM | IFFO |
| MIM | 610495 OMIM |
| HGNC | HGNC:24970 HGNC |
| Ensembl | ENSG00000010295 Ensembl |
| AllianceGenome | HGNC:24970 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000336604.8 | hg38 | chr12 | 6,539,528 | 6,556,071 | 16,544 |
| ENST00000356896.8 | hg38 | chr12 | 6,539,539 | 6,556,073 | 16,535 |
| ENST00000619571.5 | hg38 | chr12 | 6,539,539 | 6,556,042 | 16,504 |
| ENST00000396840.6 | hg38 | chr12 | 6,539,528 | 6,556,071 | 16,544 |
| ENST00000465801.5 | hg38 | chr12 | 6,538,961 | 6,551,900 | 12,940 |
| ENST00000465801.5 | hg19 | chr12 | 6,648,127 | 6,661,066 | 12,940 |
| ENST00000336604.8 | hg19 | chr12 | 6,648,694 | 6,665,237 | 16,544 |
| ENST00000396840.6 | hg19 | chr12 | 6,648,694 | 6,665,237 | 16,544 |
| ENST00000619571.5 | hg19 | chr12 | 6,648,705 | 6,665,208 | 16,504 |
| ENST00000356896.8 | hg19 | chr12 | 6,648,705 | 6,665,239 | 16,535 |
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