| Individual ID | 28714951.100 |
|---|---|
| Pubmed ID | 28714951 |
| Whose mosaic mutation | Patient |
| Phenotypic Category | 3 |
| 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 |
|---|---|---|---|---|---|---|---|
| 29424 | 343069 | HNRNPCL1 | 1 | 12907860 | 12907860 | Autism Spectrum Disorders | MiSeq |