Individual ID | 26395554.01 |
---|---|
Pubmed ID | 26395554 |
Whose mosaic mutation | Father |
Phenotypic Category | 1 |
Disease | Micolissencephaly(view all the variants in this disease) |
OMIM ID | 600112 |
Found 1 variant in this database.
Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
---|---|---|---|---|---|---|---|
34639 | 1778 | DYNC1H1 | 14 | 102452300 | 102452300 | Micolissencephaly | Whole Exome Sequencing Sanger Sequencing |