| About this overview [Show] |
| This detailed view shows all details of the selected patient, including all variants reported in this patient. At the bottom of the page, all variants reported in this patient are listed, with the one you are looking at in bold. The link to the UCSC Genome Browser will show the browser zoomed in to the location of the selected variant. |
| Patient data (#0000721) |
| Patient ID |
AKU_DB_421 |
| Disease |
AKU |
| Reference |
Lee et al. (2022), Taiwan:Taipei |
| Remarks |
Compound heterozygous |
| # Reported |
1 |
| Geographic origin |
Taiwan |
| Patient/Affected_per_Family |
1 |
| Families Patients |
1 |
| Submitter |
Ni-Chung Lee |
| Variant data |
| Allele |
Parent #2 |
| Reported pathogenicity |
Pathogenic |
| Concluded pathogenicity |
Probably pathogenic |
| DB-ID |
AKU_00248 |
| Exon |
01i |
| DNA change |
c.16-2063A>C |
| RNA change |
r.(?) |
| Protein |
p.(Tyr5_Ile6insVal*17) |
| Original description |
in1 pseudoexon |
| Links |
- |
| Variant remarks |
aberrant splicing (AS), pseudogene inclusion |
| Predicted Mutation Effect** |
- |
| Reference |
Lee et al. (2022) |
| Mutation HOT-SPOT |
- |
| Allele code |
AKU_DB_421b |
| Type |
substitution |
| Re-site |
- |
| Frequency |
- |
| Template |
DNA |
| Technique |
SEQ |
| Location |
intron |
|
|
