ENST00000613780.4 MIAT
Information
- Transcript ID
- ENST00000613780.4
- Genome
- hg38
- Position
- chr22:26,657,520-26,676,475
- Strand
- +
- CDS length
- 0
- Amino acid length
- 0
- Gene symbol
- MIAT
- Gene type
- ncRNA
- Gene description
- myocardial infarction associated transcript
- Gene Entrez Gene ID
- 440823
Variants
Display target variant
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
|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
Exon
| Exon number | Start | Stop |
|---|---|---|
| 1 | 26,657,520 | 26,657,654 |
| 2 | 26,663,316 | 26,663,398 |
| 3 | 26,665,457 | 26,666,937 |
| 4 | 26,667,185 | 26,667,310 |
| 5 | 26,668,158 | 26,676,475 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr22 | 27,053,484 | 27,072,438 | Link |
CDS sequence
Amino sequence