| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S0795 | missense_variant | NKX2-5 | NM_004387.4:c.160G>A | A | isolated CHD: TOF |
| S0796 | missense_variant | NKX2-5 | NM_004387.4:c.160G>A | A | isolated CHD: TOF |
| S0797 | missense_variant | NKX2-5 | NM_004387.4:c.160G>A | A | isolated CHD: TOF |