Individual ID | 26637798.01 |
---|---|
Pubmed ID | 26637798 |
Whose mosaic mutation | Female Patient |
Phenotypic Category | 3 |
Age | 15.0 |
Disease | Autism Spectrum Disorders(view all the variants in this disease) |
OMIM ID | 209850 |
Found 1 variant in this database.
Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
---|---|---|---|---|---|---|---|
639 | 6323 | SCN1A | 2 | 166911148 | 166911148 | Autism Spectrum Disorders | HiSeq 2000 |