| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1907 | missense_variant | EPRS | NM_004446.3:c.924C>A | C/C | isolated CHD: ASD |
| S1908 | missense_variant | EPRS | NM_004446.3:c.924C>A | A/C | isolated CHD: ASD |
| S1909 | missense_variant | EPRS | NM_004446.3:c.924C>A | A/A | isolated CHD: ASD |