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| 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 (#0000275) |
| Disease |
- |
| Reference |
- |
| Remarks |
- |
| Variant data |
| Allele |
Unknown |
| Reported pathogenicity |
Probably pathogenic |
| Concluded pathogenicity |
Probably pathogenic |
| Exon |
4 |
| DNA change |
c.2117T>C (View in UCSC Genome Browser) |
| RNA change |
r.(?) |
| Protein |
p.(Phe706Ser) |
| MAPP/PP2 Prior P |
0.815 |
| Prior P |
0.815 |
| IARC Classification |
Class 4: Likely pathogenic |
| InSiGHT Classification |
Class 4: Likely pathogenic |
| Tumour Char LR |
8.660 |
| Segregation LR |
1.930 |
| Odds for causality |
16.713 |
| Posterior P |
0.9866 |
| Reference |
Thompson et al., 2014, InSiGHT |
| Variant remarks |
- |
| Template |
DNA |
| Technique |
SEQ |
| DB-ID |
MSH6_00018 |
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