| 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. |
| Variant data |
| Allele |
Parent #2 |
| Reported pathogenicity |
Pathogenic |
| Concluded pathogenicity |
Probably pathogenic |
| DB-ID |
AKU_00193 |
| Exon |
09i |
| DNA change |
c.650-13T>G |
| RNA change |
r.(?) |
| Protein |
p.(?) |
| Original description |
ivs9-13T>G |
| Links |
- |
| Variant remarks |
aberrant splicing (AS)/exon skipping/cryptic splice site |
| Predicted Mutation Effect** |
- |
| Reference |
Ascher et al. (2019) |
| Mutation HOT-SPOT |
- |
| Allele code |
AKU_TR2_0332b |
| Type |
substitution |
| Re-site |
- |
| Frequency |
- |
| Template |
DNA/RNA |
| Technique |
SEQ |
| Location |
intron |
|
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