| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0810 | missense_variant | SCRIB | NM_015356.5:c.1720G>C | C | isolated CHD: ASD |
| S0840 | missense_variant | SCRIB | NM_015356.5:c.1720G>C | C | isolated CHD: ASD |
| S0861 | missense_variant | SCRIB | NM_015356.5:c.1720G>C | C | isolated CHD: ASD |
| S0878 | missense_variant | SCRIB | NM_015356.5:c.1720G>C | C | isolated CHD: ASD |