MIR4307HG MIR4307 host gene
Information
- Symbol
- MIR4307HG
- Type
- ncRNA
- Description
- MIR4307 host gene
- Entrez Gene ID
- 101927081
- Genome
- hg19
- Position
- chr14:27,342,346-27,350,683
- Genome
- hg38
- Position
- chr14:26,873,140-26,881,477
- HGNC
- HGNC:52004 HGNC
- Ensembl
- ENSG00000257612 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
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0 |
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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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| 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 | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000656692.1 | hg38 | chr14 | 26,873,144 | 26,914,741 | 41,598 |
| ENST00000655440.1 | hg38 | chr14 | 26,873,137 | 26,914,739 | 41,603 |
| ENST00000657558.1 | hg38 | chr14 | 26,873,130 | 26,914,736 | 41,607 |
| ENST00000657233.1 | hg38 | chr14 | 26,873,092 | 26,918,594 | 45,503 |
| ENST00000667739.1 | hg38 | chr14 | 26,873,133 | 26,914,747 | 41,615 |
| ENST00000670889.1 | hg38 | chr14 | 26,873,140 | 26,881,477 | 8,338 |
| ENST00000666377.1 | hg38 | chr14 | 26,873,137 | 26,914,740 | 41,604 |
| ENST00000667699.1 | hg38 | chr14 | 26,873,143 | 26,914,633 | 41,491 |
| ENST00000655440.1 | hg19 | chr14 | 27,342,343 | 27,383,945 | 41,603 |
| ENST00000667739.1 | hg19 | chr14 | 27,342,339 | 27,383,953 | 41,615 |
| ENST00000657558.1 | hg19 | chr14 | 27,342,336 | 27,383,942 | 41,607 |
| ENST00000666377.1 | hg19 | chr14 | 27,342,343 | 27,383,946 | 41,604 |
| ENST00000670889.1 | hg19 | chr14 | 27,342,346 | 27,350,683 | 8,338 |
| ENST00000667699.1 | hg19 | chr14 | 27,342,349 | 27,383,839 | 41,491 |
| ENST00000656692.1 | hg19 | chr14 | 27,342,350 | 27,383,947 | 41,598 |
| ENST00000657233.1 | hg19 | chr14 | 27,342,298 | 27,387,800 | 45,503 |
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