| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1928 | missense_variant | EPRS | NM_004446.3:c.924C>A | C/C | non-isolated CHD: ASD, VSD |
| S1929 | missense_variant | EPRS | NM_004446.3:c.924C>A | A/C | non-isolated CHD: ASD, VSD |
| S1930 | missense_variant | EPRS | NM_004446.3:c.924C>A | A/A | non-isolated CHD: ASD, VSD |