| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0814 | missense_variant | SEMA4G | NM_001203244.1:c.1529G>A | A | isolated CHD: ASD |
| S0844 | missense_variant | SEMA4G | NM_001203244.1:c.1529G>A | A | isolated CHD: ASD |
| S0865 | missense_variant | SEMA4G | NM_001203244.1:c.1529G>A | A | isolated CHD: ASD |