chr13:97873688:> Detail (hg19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr13:97,873,688-98,046,374 |
| hg38 | chr13:97,221,434-97,394,120 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
[No Data.]
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| Show details | |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| <0.001 | diabetes mellitus | NA | BeFree | Detail | |
| <0.001 | Meningomyelocele | NA | BeFree | Detail | |
| <0.001 | myopathy | NA | BeFree | Detail | |
| <0.001 | Myotonic dystrophy | NA | BeFree | Detail | |
| <0.001 | tetralogy of Fallot | We used primary cells derived from the RV of infants with TOF to show a direct l... | BeFree | 25916634 | Detail |
| 0.002 | Tobacco use disorder | NA | GAD | Detail | |
| <0.001 | Congenital Myotonic Dystrophy | NA | BeFree | Detail | |
| 0.122 | Alcoholic Intoxication, Chronic | NA | GAD,GWASCAT | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| We used primary cells derived from the RV of infants with TOF to show a direct link between scaRNA l... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- Genome
- hg19
- Position
- chr13:97,873,688-98,046,374
- Variant Type
- snv
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