| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S1918 | missense_variant | EPRS | NM_004446.3:c.924C>A | C/C | isolated CHD: VSD |
| S1919 | missense_variant | EPRS | NM_004446.3:c.924C>A | A/C | isolated CHD: VSD |
| S1920 | missense_variant | EPRS | NM_004446.3:c.924C>A | A/A | isolated CHD: VSD |