| ID | Consequence | Gene/Location | Detail | Geno Type | CHD Type |
|---|---|---|---|---|---|
| S4019 | missense_variant | TGFβ1 | NM_000660.7:c.74G>C | G/G | non-isolated CHD: TS, VSD |
| S4020 | missense_variant | TGFβ1 | NM_000660.7:c.74G>C | G/C | non-isolated CHD: TS, VSD |
| S4021 | missense_variant | TGFβ1 | NM_000660.7:c.74G>C | C/C | non-isolated CHD: TS, VSD |
| S4022 | missense_variant | TGFβ1 | NM_000660.7:c.74G>C | G | non-isolated CHD: TS, VSD |
| S4023 | missense_variant | TGFβ1 | NM_000660.7:c.74G>C | C | non-isolated CHD: TS, VSD |