| 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 (#0012426) |
| Phenotype |
myopathy, nemaline, type 1 (NEM-1) |
| Phenotype additional |
muscle hypotonia (1m), facial weakness, lack head control,lax distal joints, scoliosis (1y), delayed motor milestones |
| Reference |
JdD |
| Remarks |
sister of 18382475.F2b ; 2nd cousin parents |
| Geographic origin |
Turkey |
| Ethnic origin |
- |
| Gender |
F |
| Inheritance |
isolated (sporadic) |
| Consanguinity |
- |
| Fam_Pat |
- |
| # reported |
1 |
| CK level |
- |
| Protein data |
- |
| Submitter |
Johan den Dunnen |
| Variant data |
| Allele |
Maternal (confirmed) |
| Reported pathogenicity |
Pathogenic |
| Concluded pathogenicity |
Unknown |
| Exon |
10 |
| DNA change |
c.855delA (View in UCSC Genome Browser, Ensembl) |
| Var_pub_as |
913delA |
| RNA change |
r.(?) |
| Protein change |
p.(*286Asnext*74) |
| Variant remarks |
- |
| Genet_ori |
germline (inherited) |
| DB-ID |
TPM3_00012 |
| Reference |
Lehtokari 2008, (OMIM 0006) |
| Template |
DNA |
| Technique |
SEQ |
| Frequency |
- |
| RE-site |
- |
|
