| 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 (#0020113) |
| Phenotype |
myopathy, nemaline, type 6 (NEM-6) |
| Phenotype additional |
EM rods and cores, slow progression (diabling>50y), muscle weakness neck/proximal, no cardiac abnormalities |
| Reference |
United States:Bethesda |
| Remarks |
5-generation family, 15 affecteds |
| Geographic origin |
Australia |
| Ethnic origin |
Dutch |
| Gender |
- |
| Inheritance |
familial, autosomal dominant |
| Consanguinity |
- |
| Fam_Pat |
- |
| # reported |
15 |
| CK level |
- |
| Protein data |
- |
| Submitter |
Nyamkhishig Sambuughin |
| Variant data |
| Allele |
Unknown |
| Reported pathogenicity |
No known pathogenicity |
| Concluded pathogenicity |
No known pathogenicity |
| Exon |
1_10 |
| DNA change |
c.= |
| Var_pub_as |
- |
| RNA change |
r.= |
| Protein change |
p.= |
| DB-ID |
TPM1_00000 |
| Variant remarks |
no variants 2nd chromosome |
| Genet_ori |
germline (inherited) |
| Reference |
- |
| Template |
DNA |
| Technique |
SEQ |
| Frequency |
- |
| RE-site |
- |
|
