Individual ID | 25878179.01 |
---|---|
Pubmed ID | 25878179 |
Whose mosaic mutation | Male Patient |
Origin of mosaic mutation in patients | de novo |
Phenotypic Category | 3 |
Disease | Focal Cortical Dysplasias(view all the variants in this disease) |
OMIM ID | 607341 |
Found 1 variant in this database.
Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
---|---|---|---|---|---|---|---|
608 | 2475 | MTOR | 1 | 11210266 | 11210266 | Focal Cortical Dysplasias | Sanger |