| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4122 | missense_variant | HOXB1 | NM_002144.4:c.309A>T | A/A | isolated CHD: DORV |
| S4123 | missense_variant | HOXB1 | NM_002144.4:c.309A>T | A/T | isolated CHD: DORV |
| S4124 | missense_variant | HOXB1 | NM_002144.4:c.309A>T | T/T | isolated CHD: DORV |